- Basic information
- CohesinDB ID: CDBP00420888
- Locus: chr21-44062415-44062878
-
Data sourse: GSE206145-NatGen2015, GSE67783, ENCSR153HNT, GSE86191
-
Cell type: K-562, Fibroblast, HCT-116, HSPC
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 1% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.956
- Subunit: SA1,Rad21
-
CTCF binding site: CTCF
CTCF motif: False
- Genomic location: Intragenic
- 3D genome
- TAD boundary: non-Boundary
- Chromatin hubs: Hub
-
Hi-C loops: True
Hi-ChIP loops: True
ChIA-PET loops: True
- Compartment:
62% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
-
Chromatin annotation:
"4_Tx": 64%,
"5_TxWk": 32%,
Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
-
Co-bound Transcriptional factors: FOXO1, NME2, XBP1, FOXA1, LEO1, PBX2, ZFHX2, TFAP4, HDGF, ATF3, HNRNPUL1, ATF4, MECOM, PAX5, MAF, JMJD1C, ELF1, TRIM28, BCLAF1, LMO2, ESR1, OCA2, MLL, CTCF, TCF12, JUN, BAF155, ARID5B, LMO1, TFAP2C, RBPJ, GLIS1, POU2F2, CHD8, MYCN, POU5F1, ZNF263, RUNX1T1, CDK7, ZBTB48, ZSCAN5A, DUX4, ERG2, SP4, ERG, PBX1, ZNF341, MYC, RAD21, FOXP2, GRHL3, GABPA, STAT3, PRDM14, IKZF1, NFE2, DNMT3B, ZNF750, NR3C1, CEBPB, STAT5B, KMT2A, CREB1, EZH2, BMPR1A, SPI1, GATA2, MXD3, FLI1, NCOA2, RUNX1, SMC1A, MAFG, BCL6, CEBPA, ZFX, SMAD3, TET2, ERG3, PRPF4, NOTCH1, RUNX2, ARNT, NRF1, SUPT5H, CHD1, CDK8, TEAD3, TERF1, CEBPD, MYB, ZNF3, C11orf30, EVI1, STAT5A, RBM22, SP1, BCL11A, NR4A1, BCOR, TCF3, STAG1, MLLT1, SKI, TRP47, FOXA2, AGO1, CREM, MEIS1, PAF1, ZNF600, GTF2B, WT1, ESR2, ZBTB33, MEF2C, KDM1A, ZNF19, RELA, NEUROD1, SP140, TCF4, HIF1A, GATA3, TAL1, MAX, NRIP1, ZNF143, AGO2, GATA1, CEBPG, BCL11B, NCOA3, MED, ZNF334, EGR2, TBX21, AR, TAF1, EGR1, HSF1, NCOR1, JUND, BRD4, MAZ, AHR
- Target gene symbol (double-evidenced CRMs): SUMO3,AGPAT3,TRPM2,PKNOX1,RRP1,PFKL,TSPEAR,TRAPPC10,DNMT3L,PTTG1IP,GATD3A,CFAP410,LRRC3,UBE2G2
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 1
- Number of somatic mutations (non-coding): 1
- Related genes and loops
- Related gene:
ENSG00000160199,
ENSG00000160214,
ENSG00000160216,
ENSG00000160218,
ENSG00000160221,
ENSG00000142182,
ENSG00000141959,
ENSG00000160226,
ENSG00000142185,
ENSG00000160233,
ENSG00000175894,
ENSG00000184787,
ENSG00000184900,
ENSG00000183255,
- Related loop:
chr21:43000000-43025000~~chr21:44050000-44075000,
chr21:43175000-43200000~~chr21:44050000-44075000,
chr21:43325000-43350000~~chr21:44050000-44075000,
chr21:43350000-43375000~~chr21:44050000-44075000,
chr21:43800000-43825000~~chr21:44050000-44075000,
chr21:43950000-43975000~~chr21:44050000-44075000,
chr21:44011649-44014659~~chr21:44065052-44066225,
chr21:44050000-44075000~~chr21:44175000-44200000,
chr21:44050000-44075000~~chr21:44250000-44275000,
chr21:44050000-44075000~~chr21:44275000-44300000,
chr21:44050000-44075000~~chr21:44300000-44325000,
chr21:44050000-44075000~~chr21:44425000-44450000,
chr21:44050000-44075000~~chr21:44450000-44475000,
chr21:44050000-44075000~~chr21:44475000-44500000,
chr21:44050000-44075000~~chr21:44800000-44825000,
chr21:44050000-44075000~~chr21:44850000-44875000,
chr21:5125000-5150000~~chr21:44050000-44075000,