Tag | Content |
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EnhancerAtlas ID | HS154-00262 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr1:15294730-15296290 |
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) |
BCL6B | MA0731.1 | chr1:15296255-15296272 | TGGATTCCTAAAAAGAA | - | 6.19 | RARA(var.2) | MA0730.1 | chr1:15295068-15295085 | AGGACACGTGAGGGTCA | + | 6.03 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26798 | chr1:15294684-15296104 | Esophagus | SE_53292 | chr1:15293321-15296336 | Spleen |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I014967 | chr1 | 15294172 | 15298701 |
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Enhancer Sequence | GATCCCTCAC ATGCGCAGTT CACAAGAGGG TTCGTGCTCC TATGAGAGTC TAATGCCATC 60 GCTGCTGATC AGACAGGAGG TGGAGCTCCG GCGGTAATGT GAGTGATGGG GAGCAGCTGT 120 AAATACAGAT GAAACTTCGC TCGCTCGCCC CTCACCTCCT GCTGTGCAGC CTGCTTCCTA 180 AGAGGCCAGG GACCAGTACC AGTCCATGGC CTGGGGCTTG GGGACCCCGT GTGAAGCCAC 240 TGCATTGTGT CACTTTGTTA CAACAAGAAT GGGAAACGAA CCAGGCCCTC TCTTTCCCTG 300 GACTTGGCAG CCCTAAACAC TGCCCTCTCT CAGGGCTTAG GACACGTGAG GGTCATCTGT 360 TTCCTTTAGA AACGCCTGCA GGGCACAGCA GCCAGCACGG GGCGGGTGGA GTTAGCTAGC 420 ACTGACTGAG CATGGAGCAG AAGAAAGGAT CCGGAGTTTC CTCTCCTTAC TGGAAGGACT 480 AAGGCCTGTG GGAGCCTTTT CCCTGCCACA GAGTGAGTCA CCTGCCTTAC ACTGAAAGAA 540 ACACAACTTT ATTATTTAAT TTGCTCATTC ACCAAATGTT CCCTGAAAGC TTCCCTACCC 600 CAAAGCTTGT GCCGATGCCT GTGGTTCAGA GCATTCCAGG CCCTGCTCAG AGTCTAGGGA 660 CATGCCTGAA ACCTACGACA CACTCAGTGT ACCTTACTTG AATCCTATTT TTCCAAGTGG 720 CCAACCAGGC CTGTAGATGA GAGTCTATCC CATAGGCATT CCTGCTTCAA GGAGTTCTAG 780 GCTGCAGAGA CTGTCTTAAG TCCAGCGGGG TCGGTGGGGC TGGAAGACTA AAGCTCCCAG 840 CAGGTGCAGC CATGCCCTGG CTGCCTTTGC AGATGTCACC AGGCCTGCAG ACAGTGGGGT 900 AGTAGGTGGC CTGAGAGGCT GTTGAATAGA ACGATGTGTC ATCTGTGCTG GGGCGGCCAT 960 GCCCACTTGC TTTCTTAGAC ACACATCCTT GTCACCACAG CACTGTGTGG GTTTGAAAAG 1020 CTACTTGATG TTTCCTGTGT CCCTTCCCAC ATCCGCACTC CATTCTTAGT CTCATTCCCT 1080 CCATCAAAGA CGTGTTCATC TTCTATGCAG TTCATCACCT GGGGTTGAAT GTGTATGTTC 1140 CTCTTTAGTA AATTCATACG CTTGAAGCTA CTGCTGTTTC TTTAGCCTGG TGGCTCTCGG 1200 GGCTGCTGCA GGGGGCCCAC CCTGAGCCAG CCCCTCGGTC CCACAGCCCT GACGTAGAAG 1260 ACTCTTTGCT GGTAAATCTC GGAACTCACT GGAAGCTTCC ACAAAGTTTA ACTCTACAGA 1320 CAGAATGTCT TCCTTACATA CTACCGGCTG CTTTTAAATA TTGTTAACAG ATCCCCCTTA 1380 AAGGCTTCTT AGACTCCACA TTTTGATCCA GTTGATAATA ATTGATGGTC AGGTGGAAGA 1440 ATTGCCCAGG CTCTGTTGTT GTTCTGTTAT AGTTGCCACT GGACCTGCTT TCAGCACCCT 1500 CACCCTGGCT GCTTCAGAGG GCAGCTGGAT TCCTAAAAAG AACCCATGCC CTAATGCACA 1560
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