- Basic information
- CohesinDB ID: CDBP00418747
- Locus: chr21-37145513-37146764
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Data sourse: ENCSR000BLD, ENCSR000BTU, GSE67783, ENCSR000BKV, GSE72082, ENCSR000BSB, GSE129526, ENCSR000BLY, GSE105028, ENCSR000ECE, ENCSR000EHX, ENCSR153HNT, GSE121355, GSE68388, GSE116344, GSE25021, GSE50893
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Cell type: MCF-7, GM2630, H1-hESC, HCT-116, RH4, GM2610, Ishikawa, GM19238, SK-N-SH, K-562, HSPC, HuCC-T1, H9-hESC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 4% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.856
- Subunit: SA1,Rad21,SMC1
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CTCF binding site: CTCF
CTCF motif: False
- Genomic location: Intragenic
- 3D genome
- TAD boundary: Boundary
- Chromatin hubs: non-Hub
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Hi-C loops: False
Hi-ChIP loops: False
ChIA-PET loops: True
- Compartment:
90% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): False
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Chromatin annotation:
"4_Tx": 48%,
"5_TxWk": 32%,
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: PGR, ZSCAN5C, ZNF660, SOX2, MEIS2, XBP1, PATZ1, FOXA1, ZNF101, PBX2, LEO1, ZFHX2, ZNF596, ATF3, NFIC, ZFP64, ZNF362, CHD7, ZBTB44, RUNX3, IKZF3, ZNF189, MZF1, ZNF467, ZNF629, TEAD1, TRIM28, ZNF121, KLF6, KLF10, ESR1, CTCF, TCF12, JUN, EP300, ZNF695, GATA6, DPF2, SOX4, ZNF423, ZNF528, TEAD4, PDX1, RBPJ, EED, GLIS1, NANOG, CHD8, MYCN, POU5F1, ZSCAN21, ZBTB17, ZBTB48, ZSCAN5A, ZNF317, SRF, ERG2, HIC1, HOXC5, ZBTB21, ZNF329, ZNF341, NFKB2, MYC, ETS1, EOMES, TSHZ1, SMARCA4, RAD21, RXRA, NKX2-1, STAT3, NKX3-1, ZNF398, RCOR1, ZNF639, NR2F6, VDR, NR3C1, CEBPB, CREB1, EZH2, KLF8, FEZF1, EBF3, ZHX2, SPI1, HDAC2, SIX2, FLI1, SMARCA5, MRTFB, ZNF554, CEBPA, NKX2-2, HDAC1, ZFX, SMAD3, ZNF770, ERG3, ZNF18, ZNF549, PRDM10, MEF2A, SMARCC1, ZNF35, ZNF384, RUNX2, OSR2, ZNF184, PBX4, DAXX, ARNT, ATF2, ETV6, MAFB, ZNF10, SUPT5H, CDK8, FOS, MED1, ZNF680, SUPT16H, KLF9, SETDB1, RBM22, BCL11A, SP1, PHIP, FOXP1, SMC3, STAG1, ZNF394, CREM, EBF1, PAF1, ZNF600, ZSCAN16, ZNF692, ZNF30, WT1, ZNF574, MEF2C, CDK9, KDM1A, YY1, RELA, NEUROD1, JUNB, ISL1, ZIC2, HIF1A, OTX2, BATF, TAL1, MAX, HAND2, CEBPG, SP7, NR2F2, TP53, PKNOX1, ZSCAN22, NFKB1, EGR2, ELF3, T, ZNF843, AR, ZNF324, ZBTB42, HSF1, NOTCH3, BRD4, JUND, ILF3, MAZ, ZSCAN23, MEF2D, ZNF24
- Target gene symbol (double-evidenced CRMs): TTC3
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 24
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000182670,
- Related loop:
chr21:33500000-33525000~~chr21:37150000-37175000,
chr21:37150000-37175000~~chr21:37250000-37275000,
chr21:37150000-37175000~~chr21:37275000-37300000,
chr21:37150000-37175000~~chr21:37350000-37375000,
chr21:37150000-37175000~~chr21:37375000-37400000,
chr21:37150000-37175000~~chr21:37450000-37475000,
chr21:37150000-37175000~~chr21:37500000-37525000,
chr21:37150000-37175000~~chr21:37575000-37600000,
chr21:37150000-37175000~~chr21:37625000-37650000,
chr21:37150000-37175000~~chr21:37650000-37675000,
chr21:37150000-37175000~~chr21:37900000-37925000,
chr21:37150000-37175000~~chr21:38150000-38175000,
chr21:37150000-37175000~~chr21:38325000-38350000,
chr21:37150000-37175000~~chr21:38350000-38375000,