- Basic information
- CohesinDB ID: CDBP00418123
- Locus: chr21-35520216-35522630
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Data sourse: ENCSR000BLD, ENCSR000BKV, GSE86191, GSE25021, ENCSR000BLY, ENCSR879KXD, GSE105028, GSE206145-NatGen2015, ENCSR000ECE, GSE206145, ENCSR153HNT, GSE83726, GSE116344, GSE106870, GSE145327, GSE97394, GSE64758
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Cell type: H1-hESC, Fibroblast, HCT-116, RH4, HEK293T, Hep-G2, HUES64, K-562, SK-N-SH, CVI-hiPSC, H9-hESC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 5% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.878
- Subunit: NIPBL,SA1,Rad21,SA2
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CTCF binding site: CTCF
CTCF motif: True
- Genomic location: Intergenic
- 3D genome
- TAD boundary: Boundary
- Chromatin hubs: Hub
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Hi-C loops: True
Hi-ChIP loops: True
ChIA-PET loops: True
- Compartment:
80% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
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Chromatin annotation:
"15_Quies": 67%,
"7_Enh": 18%,
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: SOX2, NME2, MEIS2, FOXA1, PBX2, CHD7, ZSCAN4, TP63, CDX2, TRIM28, ESR1, OCA2, TP73, CTCF, TCF12, JUN, BAF155, GATA6, ZNF350, TEAD4, PDX1, TFAP2C, NANOG, CHD8, ZSCAN5D, MYCN, POU5F1, CTBP1, ZNF317, DUX4, ZNF134, SP4, ERG, MYC, SMARCA4, RFX1, ARID1B, RAD21, GRHL3, STAT3, XRCC5, IKZF1, RCOR1, NR3C1, CREB1, EZH2, HDAC2, GATA2, RUNX1, CTNNB1, SMC1A, HDAC1, EZH2phosphoT487, ZFX, SMAD3, CBX8, ERG3, ZNF18, ZNF384, NOTCH1, NRF1, ARNT, ATF2, ZNF518A, CBFA2T3, ZNF10, FOS, MED1, MYB, SCRT2, NIPBL, BCL11A, HNF4A, NR4A1, RBM25, ATF7, POU2F3, ASH2L, HNRNPLL, BCOR, FOXP1, CBFA2T2, PPARG, FOXA2, ZNF207, CREM, MEIS1, RBBP5, WT1, HOXB13, KDM1A, YY1, RELA, MCM3, HIF1A, TAL1, MAX, NRIP1, ZNF143, GATA1, GFI1B, TCF7L2, TP53, PKNOX1, AR, ZBTB16, RNF2, BRD4, JUND, MAZ
- Target gene symbol (double-evidenced CRMs): SMIM11A,RUNX1,SETD4,CLIC6
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000205670,
ENSG00000159212,
ENSG00000159216,
ENSG00000185917,
- Related loop:
chr21:34350000-34375000~~chr21:35500000-35525000,
chr21:34350000-34375000~~chr21:35525000-35550000,
chr21:34675000-34700000~~chr21:35500000-35525000,
chr21:34700000-34725000~~chr21:35500000-35525000,
chr21:34725000-34750000~~chr21:35500000-35525000,
chr21:34750000-34775000~~chr21:35500000-35525000,
chr21:34775000-34800000~~chr21:35500000-35525000,
chr21:34850000-34875000~~chr21:35500000-35525000,
chr21:34875000-34900000~~chr21:35500000-35525000,
chr21:35025000-35050000~~chr21:35500000-35525000,
chr21:35050000-35075000~~chr21:35500000-35525000,
chr21:35250000-35275000~~chr21:35500000-35525000,
chr21:35400000-35425000~~chr21:35500000-35525000,
chr21:35400000-35425000~~chr21:35525000-35550000,
chr21:35500000-35525000~~chr21:35775000-35800000,
chr21:35500000-35525000~~chr21:35825000-35850000,
chr21:35500000-35525000~~chr21:35925000-35950000,
chr21:35500000-35525000~~chr21:36025000-36050000,
chr21:35525000-35550000~~chr21:35800000-35825000,
chr21:35525000-35550000~~chr21:35825000-35850000,