Tag | Content |
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EnhancerAtlas ID | HS139-10650 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr11:110435590-110437210 |
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) |
Crx | MA0467.1 | chr11:110436984-110436995 | GAGAGGATTAG | + | 6.02 | HEY2 | MA0649.1 | chr11:110436589-110436599 | GACACGTGCC | + | 6.02 | Npas2 | MA0626.1 | chr11:110436589-110436599 | GACACGTGCC | - | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I110564 | chr11 | 110435352 | 110436928 |
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Enhancer Sequence | TCTAAAGTTT TTGATAGGTG GAAAACATCC GCTCCCATGG TACCCAGCTG AGTTTAGGCC 60 TAGAAGTGTT AAGCTGGACC ATACAGGCTG CCCCTCCTCC AGCCAGACAT GGGGGTTCAG 120 CCTGATAGCC CAGGGCTCCT TGTTATTGCC CTACAGAGGA GTGTTCAAAA CATAAAAGTG 180 GTCTGAGAAA GGCAGCAATC TTGTTTTCTC ATGTCTCCTT AGTTTATGGA GAAGCCAAAA 240 AACTCCATAA CAAATATTCA AATCCAGACC CTGTCTCCAC CCTGAGATGG GTCCCCAGAG 300 CCTGAGTGAG ATGCGATATA ATCTGGAGAG GGAGGAGATG AGGGCAGGAT GAAGTGGCGT 360 GGGAGGCGGG GTGGAAAGTG TAAGGTCCTT GCCTGGCTGT GGTATCAGCA GTGAGTCCAG 420 CAAGCAAAGG GTGTTAAGGG AATGAACTTG ATCCTTGAGG CCTCAAAGCA GGAGTGGTCT 480 CTGTTCTCTG TGTATATCTG AGAGAGGAGT TGGGAGGTGA GGAGGCAGCA AAGATAAGAG 540 GCCAGTGGCT GGGTGTCGTA TTACAAAGCT GAGAGGAAGA AGCGAAGAAA CGAAGAGCTC 600 TCTCAAGAAA GATCAGAGAA AGCTGTGATT ATGCAATATG CCCACTGCAG ACAGACAGGC 660 GGCACTGGCC CTTCATCTTT CTTAACCTCA GATTCCGAGA GAGCCTTTGT AGCCTGGTCA 720 GTCACACACA GGCATGGGCT GGGCTGGGCT GGGGTGAACG TCAAAGCCCT GGCAGGTCTC 780 ACTCTGGATA AGAGGGTAAA CCTGGGGAAA ACCGAAGACA TTTCCAGGTT AGGGAACTGA 840 TGCTCAGCCA CAAGCCTGGT TATCAGTTTC CCACATTTAG CCCCCTTCAA GTTGCCCCCA 900 CCCTCCCAAC CAAGTACCCC AGGCCTCTAA AGCTCCAGCA CTGCAGATGG TAGCGTGTGC 960 AGTGCCCCAA CCTGCCACAC ACTTGGCAGG CCCCACCCAG ACACGTGCCA ACTTGAGCTT 1020 GGTAAAGAGT GAAACCGCAA TCCATCCGGC AGTTGTTTTG TCTGCATGAC ACCAAACCAA 1080 CCAGTTATTT ACACTGGTGC CACACGGTAA GGAGAGCTAT TTTGACTCAA ACCAGCTCCT 1140 TGGACATTGT GGAGCCTGCG CTTGGTACCA CATGGAAGGA AGGTAAAGAC GTGTCAGAGA 1200 CTTCCTCAGA TTCAGGCTGA GTCAAACATC ACTGCCCTGA CTGAAACTGG GCACTGTTTT 1260 GGGTTGCCCC AATCTTAAGG CTCAAGCATT TTTGTTCACT GCCACAGCTC TGAGTATATG 1320 TATGGCCTCT GTGGGTGTCC CTGGGTGCCA GGAGTTACAC AGAGCAGAAG GAACACCGCG 1380 CTGTGCTTGC AACTGAGAGG ATTAGAAACC AAAGCAGCAC AGACACAGAT CCTCACCTAA 1440 GACAGCACTT GGCATTGGAG AAGGGTTGCA GGGAAGTGGG TCTCTGGGTC ATAACCTGGA 1500 CGTGGCTTAT CCCCAGGGTG GGTTCTCAGT AAATGTCAAA TCACCAGCTT CTTGCGTGGG 1560 CAAATGCCAG GAATAAATGT GGACCATGGA GAAGGCACGA GAAACATCCT GCCACTTCCT 1620
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