Tag | Content |
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EnhancerAtlas ID | HS099-00254 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr1:15294720-15296270 |
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) |
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 | ACGCAACCTG GATCCCTCAC ATGCGCAGTT CACAAGAGGG TTCGTGCTCC TATGAGAGTC 60 TAATGCCATC GCTGCTGATC AGACAGGAGG TGGAGCTCCG GCGGTAATGT GAGTGATGGG 120 GAGCAGCTGT AAATACAGAT GAAACTTCGC TCGCTCGCCC CTCACCTCCT GCTGTGCAGC 180 CTGCTTCCTA AGAGGCCAGG GACCAGTACC AGTCCATGGC CTGGGGCTTG GGGACCCCGT 240 GTGAAGCCAC TGCATTGTGT CACTTTGTTA CAACAAGAAT GGGAAACGAA CCAGGCCCTC 300 TCTTTCCCTG GACTTGGCAG CCCTAAACAC TGCCCTCTCT CAGGGCTTAG GACACGTGAG 360 GGTCATCTGT TTCCTTTAGA AACGCCTGCA GGGCACAGCA GCCAGCACGG GGCGGGTGGA 420 GTTAGCTAGC ACTGACTGAG CATGGAGCAG AAGAAAGGAT CCGGAGTTTC CTCTCCTTAC 480 TGGAAGGACT AAGGCCTGTG GGAGCCTTTT CCCTGCCACA GAGTGAGTCA CCTGCCTTAC 540 ACTGAAAGAA ACACAACTTT ATTATTTAAT TTGCTCATTC ACCAAATGTT CCCTGAAAGC 600 TTCCCTACCC CAAAGCTTGT GCCGATGCCT GTGGTTCAGA GCATTCCAGG CCCTGCTCAG 660 AGTCTAGGGA CATGCCTGAA ACCTACGACA CACTCAGTGT ACCTTACTTG AATCCTATTT 720 TTCCAAGTGG CCAACCAGGC CTGTAGATGA GAGTCTATCC CATAGGCATT CCTGCTTCAA 780 GGAGTTCTAG GCTGCAGAGA CTGTCTTAAG TCCAGCGGGG TCGGTGGGGC TGGAAGACTA 840 AAGCTCCCAG CAGGTGCAGC CATGCCCTGG CTGCCTTTGC AGATGTCACC AGGCCTGCAG 900 ACAGTGGGGT AGTAGGTGGC CTGAGAGGCT GTTGAATAGA ACGATGTGTC ATCTGTGCTG 960 GGGCGGCCAT GCCCACTTGC TTTCTTAGAC ACACATCCTT GTCACCACAG CACTGTGTGG 1020 GTTTGAAAAG CTACTTGATG TTTCCTGTGT CCCTTCCCAC ATCCGCACTC CATTCTTAGT 1080 CTCATTCCCT CCATCAAAGA CGTGTTCATC TTCTATGCAG TTCATCACCT GGGGTTGAAT 1140 GTGTATGTTC CTCTTTAGTA AATTCATACG CTTGAAGCTA CTGCTGTTTC TTTAGCCTGG 1200 TGGCTCTCGG GGCTGCTGCA GGGGGCCCAC CCTGAGCCAG CCCCTCGGTC CCACAGCCCT 1260 GACGTAGAAG ACTCTTTGCT GGTAAATCTC GGAACTCACT GGAAGCTTCC ACAAAGTTTA 1320 ACTCTACAGA CAGAATGTCT TCCTTACATA CTACCGGCTG CTTTTAAATA TTGTTAACAG 1380 ATCCCCCTTA AAGGCTTCTT AGACTCCACA TTTTGATCCA GTTGATAATA ATTGATGGTC 1440 AGGTGGAAGA ATTGCCCAGG CTCTGTTGTT GTTCTGTTAT AGTTGCCACT GGACCTGCTT 1500 TCAGCACCCT CACCCTGGCT GCTTCAGAGG GCAGCTGGAT TCCTAAAAAG 1550
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