Tag | Content |
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EnhancerAtlas ID | HS010-02383 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr2:60577950-60579050 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr2:60578811-60578826 | GGCTTCAAGGCCAGC | + | 6.04 | Zfx | MA0146.2 | chr2:60578654-60578668 | CAGGCCCGGGCCCC | - | 6.53 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_10203 | chr2:60575803-60587586 | CD19_Primary | SE_11013 | chr2:60573029-60602381 | CD20 | SE_58937 | chr2:60522660-60600011 | Ly3 | SE_59847 | chr2:60562998-60600524 | Ly4 | SE_60566 | chr2:60563072-60599761 | DHL6 | SE_61071 | chr2:60538412-60598655 | HBL1 | SE_61833 | chr2:60563001-60600536 | Toledo | SE_62777 | chr2:60563017-60600237 | Tonsil |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I060348 | chr2 | 60575658 | 60584772 |
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Enhancer Sequence | TGCTCACCAG CTGCAGTGAA ATTGCTGTGT TGGGAGGGTC CTTCAAAGCT CCTTTATGCC 60 CTACTATGCC TAGCTCAGGG CTAGGCACAT AAAAATGCTT AAATAAGTGC TTCTTGGTTG 120 GCTGCCCTTC CATAACCTTC TCCAGTCCTG CCTGGAGCTG AAAGCACGTG CCCTACTTAC 180 AGCTCCAACG TGTGAGGAGA GGCCCTGCAC TCTCACTTCC TCAGACACAT TTTTAGAGAA 240 TCATCTGAGC CCCGGGGGCA ACGATGCAAG TTTCCATCTG TGGTATGCCA GGCCTCCCAT 300 CACCTCAGCC TTTCAACTTG GTGGGAGAGA AAATATCATG GGCTAGGAAT CAGGAGACTT 360 GGATTTCCTG CAGCTGTGTC CCCAACTTGC TGTGCAACCC TCAACAAGAC ACTCATCCTC 420 TCCAAGCCTC GTTCTTCTCA TCTTTAGAAT GAGGAGATGG CCCAGGTGAT CTTCCAGGGA 480 TCTGCCCACA CCAGCACGGC CCTCAGCCAG TCCCTTCCAG CCTCAGCTGT GCAGACATTG 540 TGTGCTATGG GGATGAGGGC CACTTTGCAC CCAGGAAGGC ACCTGCACTC CCCCTGGACC 600 TGTGCCCATT AGCGTGTTGA TCCCAGCTAA AATGGCACAG CCTTGCCACA GTCACACAAC 660 ATTGCATGAG CATCTTGGGG CAACAATTCT TTCCCCTGGG GCCACAGGCC CGGGCCCCAG 720 AGGCAGCTGC CTGCCCGAAG CAAGACTTAG CCTTTCCTGG TAAGTCAAGA GAAGCCTAAG 780 TGAGGTCTCC TTGATGATCC AGATATGGAT CCCATGACAC CTAAGGACAC ATCTAGGGAG 840 GCTAGACTAC CCACCGATGT AGGCTTCAAG GCCAGCACTG CTCTCACTCA CATCCTTGAA 900 GCAGGTGGCA CCAGAATGGG GAATTGTGTG GTTCCCAAGA GCCTCTGTGG GGGAATTCCT 960 CTCCATTCCT CTCTGCCCGA CTGCCCTCCT CACCTGCTTC CACCTGCTGT TAGAAACAGG 1020 AGAGATGTGA CCTGGAAGGC ACCTCCAAGA CCATCTGGTC CACCCTCTTT GTCTACAGAT 1080 TCAGAAACTG AGTCCAGAGA 1100
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