Tag | Content |
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EnhancerAtlas ID | HS108-08536 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:110435390-110437070 |
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 | CTCCTACCTC TGAGAAACCC GAGCAGTCTG AGACCTTGGA AGGACGGTCC CTGCTCACTG 60 CAGTCCACGT CTTTGAGAAG AGCTACAAGA GGGCAATCTT TTTCTTTTTC CTTGCTTTAA 120 AGTACAGTCC CTCTTAAGAG CAGAGGGGGC AGGCAGGGAG TCTCTTTATG ATGCAGATTG 180 CCGATTTGTG ATGGGAATGA TCTAAAGTTT TTGATAGGTG GAAAACATCC GCTCCCATGG 240 TACCCAGCTG AGTTTAGGCC TAGAAGTGTT AAGCTGGACC ATACAGGCTG CCCCTCCTCC 300 AGCCAGACAT GGGGGTTCAG CCTGATAGCC CAGGGCTCCT TGTTATTGCC CTACAGAGGA 360 GTGTTCAAAA CATAAAAGTG GTCTGAGAAA GGCAGCAATC TTGTTTTCTC ATGTCTCCTT 420 AGTTTATGGA GAAGCCAAAA AACTCCATAA CAAATATTCA AATCCAGACC CTGTCTCCAC 480 CCTGAGATGG GTCCCCAGAG CCTGAGTGAG ATGCGATATA ATCTGGAGAG GGAGGAGATG 540 AGGGCAGGAT GAAGTGGCGT GGGAGGCGGG GTGGAAAGTG TAAGGTCCTT GCCTGGCTGT 600 GGTATCAGCA GTGAGTCCAG CAAGCAAAGG GTGTTAAGGG AATGAACTTG ATCCTTGAGG 660 CCTCAAAGCA GGAGTGGTCT CTGTTCTCTG TGTATATCTG AGAGAGGAGT TGGGAGGTGA 720 GGAGGCAGCA AAGATAAGAG GCCAGTGGCT GGGTGTCGTA TTACAAAGCT GAGAGGAAGA 780 AGCGAAGAAA CGAAGAGCTC TCTCAAGAAA GATCAGAGAA AGCTGTGATT ATGCAATATG 840 CCCACTGCAG ACAGACAGGC GGCACTGGCC CTTCATCTTT CTTAACCTCA GATTCCGAGA 900 GAGCCTTTGT AGCCTGGTCA GTCACACACA GGCATGGGCT GGGCTGGGCT GGGGTGAACG 960 TCAAAGCCCT GGCAGGTCTC ACTCTGGATA AGAGGGTAAA CCTGGGGAAA ACCGAAGACA 1020 TTTCCAGGTT AGGGAACTGA TGCTCAGCCA CAAGCCTGGT TATCAGTTTC CCACATTTAG 1080 CCCCCTTCAA GTTGCCCCCA CCCTCCCAAC CAAGTACCCC AGGCCTCTAA AGCTCCAGCA 1140 CTGCAGATGG TAGCGTGTGC AGTGCCCCAA CCTGCCACAC ACTTGGCAGG CCCCACCCAG 1200 ACACGTGCCA ACTTGAGCTT GGTAAAGAGT GAAACCGCAA TCCATCCGGC AGTTGTTTTG 1260 TCTGCATGAC ACCAAACCAA CCAGTTATTT ACACTGGTGC CACACGGTAA GGAGAGCTAT 1320 TTTGACTCAA ACCAGCTCCT TGGACATTGT GGAGCCTGCG CTTGGTACCA CATGGAAGGA 1380 AGGTAAAGAC GTGTCAGAGA CTTCCTCAGA TTCAGGCTGA GTCAAACATC ACTGCCCTGA 1440 CTGAAACTGG GCACTGTTTT GGGTTGCCCC AATCTTAAGG CTCAAGCATT TTTGTTCACT 1500 GCCACAGCTC TGAGTATATG TATGGCCTCT GTGGGTGTCC CTGGGTGCCA GGAGTTACAC 1560 AGAGCAGAAG GAACACCGCG CTGTGCTTGC AACTGAGAGG ATTAGAAACC AAAGCAGCAC 1620 AGACACAGAT CCTCACCTAA GACAGCACTT GGCATTGGAG AAGGGTTGCA GGGAAGTGGG 1680
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