- Basic information
- CohesinDB ID: CDBP00418008
- Locus: chr21-35225613-35229873
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Data sourse: ENCSR000BLD, ENCSR230ZWH, GSE72082, ENCSR000BSB, ENCSR000BLY, GSE105028, GSE131606, GSE108869, GSE25021, ENCSR917QNE, ENCSR000EFJ, GSE165895, GSE93080, GSE67783, ENCSR000BKV, GSE138405, GSE206145-NatGen2015, GSE112028, GSE138105, ENCSR703TNG, GSE116344, ENCSR879KXD, ENCSR000EHW, GSE206145, GSE62063, ENCSR000BMY, ENCSR635OSG, ENCSR000BTQ, ENCSR167MTG, GSE129526, ENCSR000HPG, GSE111913, GSE155324, ENCSR054FKH, ENCSR000EDE, ENCSR153HNT, GSE68388, GSE83726, GSE126990, GSE50893, ENCSR000ECS
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Cell type: RH4, GM10847, GM2610, SLK, GM19240, HSPC, Liver, HuCC-T1, H9-hESC, B-cell, GM2630, RPE, Fibroblast, GM12890, HeLa-S3, GM2255, IMR-90, K-562, GM18486, HFFc6, H1-hESC, SNYDER, GM18505, Lymphoblast, GM12878, GM12891, GM2588, SK-N-SH, GM19239, HeLa-Tet-On, RT-112, Ramos, MCF-7, GM12892, Hela-Kyoto, HCT-116, Hep-G2, GM18951
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 22% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.578
- Subunit: NIPBL,SA1,Rad21,SMC1,SA2,Mau2,SMC3
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CTCF binding site: CTCF
CTCF motif: False
- Genomic location: Intergenic
- 3D genome
- TAD boundary: non-Boundary
- Chromatin hubs: Hub
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Hi-C loops: True
Hi-ChIP loops: False
ChIA-PET loops: True
- Compartment:
84% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): Enhancer
- Super enhancer (SEdb): True
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Chromatin annotation:
"7_Enh": 33%,
"15_Quies": 28%,
Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
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Co-bound Transcriptional factors: FOXO1, CBFA2T2, MEF2B, PGR, HDAC1, NKX2-2, FOXA2, EBF1, ID3, MEIS2, MTA2, FOXA1, FOXF1, ERG3, PBX2, HOXB13, MEF2A, CREBBP, ZNF274, SMARCA4, ARID1B, ZNF184, GRHL3, PROX1, RXRA, GATA3, HMBOX1, TAL1, CBFA2T3, MAFB, NKX3-1, GATA1, PBX3, STAT3, IKZF1, HAND2, NR2F6, CDX2, PDX1, PML, NR2F2, KMT2A, CEBPD, NR2F1, TRIM28, ESR1, PKNOX1, C11orf30, STAT5A, KLF16, PHOX2B, TCF12, MAFK, BCL11A, EP300, BAF155, SP1, AR, DPF2, ZBTB40, GATA2, TRIM24, SOX6, NCOR1, BRD4, PHIP, JUND, FOXP1, TEAD4, MEF2D, ADNP, FOSL2
- Target gene symbol (double-evidenced CRMs): SMIM11A,RUNX1
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000205670,
ENSG00000159216,
- Related loop:
chr21:34350000-34375000~~chr21:35200000-35225000,
chr21:34350000-34375000~~chr21:35225000-35250000,
chr21:34525000-34550000~~chr21:35200000-35225000,
chr21:34725000-34750000~~chr21:35200000-35225000,
chr21:34766515-34767688~~chr21:35234194-35236987,
chr21:34875000-34900000~~chr21:35200000-35225000,
chr21:34875000-34900000~~chr21:35225000-35250000,
chr21:34900000-34925000~~chr21:35200000-35225000,
chr21:35050000-35075000~~chr21:35200000-35225000,
chr21:35050000-35075000~~chr21:35225000-35250000,
chr21:35050055-35052229~~chr21:35226410-35228579,
chr21:35050056-35052270~~chr21:35226396-35228810,
chr21:35050107-35052241~~chr21:35221744-35223755,
chr21:35050233-35052173~~chr21:35222102-35223621,
chr21:35050370-35052249~~chr21:35226507-35228618,
chr21:35188702-35190920~~chr21:35226847-35228785,
chr21:35188826-35191178~~chr21:35226396-35228810,
chr21:35200000-35225000~~chr21:35375000-35400000,
chr21:35200000-35225000~~chr21:35400000-35425000,
chr21:35200000-35225000~~chr21:35825000-35850000,
chr21:35200000-35225000~~chr21:35925000-35950000,
chr21:35200000-35225000~~chr21:36025000-36050000,
chr21:35204264-35206999~~chr21:35221664-35223363,
chr21:35225000-35250000~~chr21:35350000-35375000,
chr21:35226847-35228785~~chr21:35339309-35341219,
chr21:35226847-35228785~~chr21:35399325-35401608,