- Basic information
- CohesinDB ID: CDBP00417363
- Locus: chr21-33532796-33533465
-
Data sourse: GSE206145-NatGen2015, GSE120943, GSE67783, GSE98367
-
Cell type: Monocytes, Fibroblast, HSPC, Macrophage
- 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,SMC1
-
CTCF binding site: non-CTCF
CTCF motif: False
- Genomic location: Intragenic
- 3D genome
- TAD boundary: Boundary
- Chromatin hubs: Hub
-
Hi-C loops: True
Hi-ChIP loops: False
ChIA-PET loops: True
- Compartment:
88% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): False
-
Chromatin annotation:
"4_Tx": 76%,
"5_TxWk": 21%,
Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
-
Co-bound Transcriptional factors: ZNF426, ZNF697, SOX2, MEIS2, XBP1, FOXA1, RBFOX2, SRSF4, PBX2, LEO1, HDGF, ATF3, NFIC, ZFP64, ZNF362, ATF4, GLYR1, ZNF189, HDAC3, CDX2, JMJD1C, TRIM28, ZNF573, SNAI2, NFE2L2, SMAD5, ESR1, OCA2, HNF1B, CTCF, JUN, POU2F1, MNT, GATA6, PAX8, DPF2, IRF4, TRIM24, SOX6, DDX20, U2AF2, TEAD4, ZNF555, ZNF175, GATAD2A, PDX1, EED, POU2F2, CHD8, TOP2A, ZNF317, ZBTB17, DUX4, ZBTB48, ZMYND11, STAT1, ZSCAN5A, SAP130, NBN, ERG, MYC, ONECUT1, SMARCA4, EZH1, ARID1B, ZNF180, GRHL3, NKX2-1, GABPA, APC, XRCC5, NKX3-1, NFE2, DNMT3B, DACH1, NR3C1, CEBPB, KMT2A, EZH2, ZNF652, EBF3, NFE2L1, GABPB1, ELF4, SPI1, IRF1, ZNF182, SMARCA5, HCFC1R1, ATF1, RUNX1, MAFG, SMC1A, CEBPA, AFF4, ZFX, ZNF770, ZNF384, EWSR1, CDK6, GATA4, ZNF184, ARNT, BACH1, ZNF781, ATF2, PRDM9, ZEB2, HMBOX1, ZNF518A, ETV6, SUPT5H, CDK8, ZEB1, PML, CEBPD, SCRT2, C11orf30, STAT5A, ZNF22, RBM22, MAFK, BCL11A, USF1, ARID2, REST, ATF7, HOXA9, FOXP1, SMC3, ZNF34, STAG1, ZNF783, ZNF394, FOXA2, AGO1, MTA3, CBX3, PAF1, E2F8, ZNF600, ZSCAN16, GTF2B, MAFF, WT1, ZBTB33, HOXB13, RELA, NEUROD1, HIF1A, OTX2, TAL1, ZNF143, AGO2, GATA1, CEBPG, ZNF592, NR2F2, ZBTB6, PKNOX1, ZNF334, PHOX2B, PAX3-FOXO1, AR, MYNN, NCOR1, NOTCH3, BRD4, JUND, ILF3, ZBTB26, MAZ, ZSCAN23, ZZZ3, ZNF24, ZNF316
- Target gene symbol (double-evidenced CRMs): AP000311.1,URB1,ITSN1,PAXBP1,IFNGR2,SLC5A3,MRPS6,GART,SYNJ1
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 12
- Number of somatic mutations (non-coding): 3
- Related genes and loops
- Related gene:
ENSG00000142207,
ENSG00000159082,
ENSG00000159086,
ENSG00000159128,
ENSG00000159131,
ENSG00000249209,
ENSG00000205726,
ENSG00000243927,
ENSG00000198743,
- Related loop:
chr21:29025000-29050000~~chr21:33525000-33550000,
chr21:32325000-32350000~~chr21:33525000-33550000,
chr21:32350000-32375000~~chr21:33525000-33550000,
chr21:32725000-32750000~~chr21:33525000-33550000,
chr21:32750000-32775000~~chr21:33525000-33550000,
chr21:33375000-33400000~~chr21:33525000-33550000,
chr21:33525000-33550000~~chr21:33675000-33700000,
chr21:33525000-33550000~~chr21:34050000-34075000,