Tag | Content |
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EnhancerAtlas ID | HS093-11025 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr15:102067680-102069100 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr15:102068653-102068663 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr15:102068653-102068663 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr15:102068653-102068663 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr15:102068653-102068663 | AACAGCTGTT | - | 6.02 | Nr5a2 | MA0505.1 | chr15:102067700-102067715 | GCTGGCCTTGAACTC | - | 8.25 |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I101527 | chr15 | 102067697 | 102069556 |
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Enhancer Sequence | GGTTTTGCCA TGTTGCCCAG GCTGGCCTTG AACTCCTGAG CACAAGCGAT CCGCCCACCT 60 CAGCCTCACA AAGTGCTGGG ATTACAGGCA TGAGCCACCG TGCCCAGCCA AAGTTGTGGT 120 TTTAAGCAGG ATGTTCCAAA GTCCAGTGGT TATGACCAAA CGCCACACAG AGACAGAAGC 180 CTCCCGCACA GCCCCAACTC CCAGCAGCCA TGGTGTTCCA GGTCCTCCAA AGTCAGCTTC 240 TCCTCCAGGA GGCCACTGAG CTCCCCAGCT GCGGGGCTGA GGCCACACAG CCCTGTGCGG 300 TTCATCTGCC ATCCGGGCCC TTCTTCCTCT TCTGAGCTTC ACAGTTAGCC CAGGGAAGAA 360 AACAGGCGTG TCTTCCACAA ACCCTGAAGG GAATGGGAAG TGCCAACAGT GAGAAGGACT 420 TAGATGTAAA GGATTTACAC ACGGTCACGG CATTTCCACA ACCCTCTGGG CACCTGAGTA 480 CACGTGTGCA GACACACCCC CAGATGGGGG CGAGGGGTGG GGTGCCCCAG CTATTCACAC 540 CTAACCATGA GCGTGTGAGG CAGCAACACT TAAAGGCCAC TTGCTTTCCG CAGCATCTCG 600 ATGGAGCAGG AGCCTGCCTG GGGCATCTCC AGGCAGCTTG GCTGAGCACC CAGGACTGAG 660 TGCAACCCTC AGCGTTTACA TTTTTTAGTA CTATTCACTA AGAGAGAGAG AGACAGAGAG 720 ACAGTGATAG AGACAGGGAA GGACAGAGAC AAAGAGAGCA ATGGGTGAAG AAAGAGCAAG 780 CAAGCAGGGA TGTCGGACAT TTCACACAAC GCAGTCACCA GGGAGGCAAG AACACTTACA 840 GAACAGTTTG AGCCAAAGAG TCACTCAGGG ACAGGAACAG CAATTTCTTA AATATTTAAA 900 GCAGACACCC TGTGAGCGGC TGTGGAGGCG GCTCTTTGTT AATATTTAAC ACGAGCTGGG 960 CAGTTGCCGG GAAAACAGCT GTTTACAGGA GAGATTAACC AATATTCATC ATTGCTCAAA 1020 GCTGTGGGGA GGCTTCAGGG GACAGGCAGC TGCCGGTATT TCTAGAATAC AGCAGCTCAA 1080 GGCCACAGGG CTGGGGAGGC TCACGGTGTC CCCAGGGTGC ATGAAAACTG TAAACAGGCA 1140 GTTCGGGGTC ACCTACCCTG CTCCAGAATC ACGGTTTGCA GGAAACCCAG CCCTGCAGCT 1200 GGGCCTGGGT GGTGGCTGCT GGCCGGCCAG CCAGCACCTC GCTGGACAGC TGCGTCCCAC 1260 AGTCCCAGGC TGGGCTGTCC TTCAGGCCCA TCCACAGTCC CAGGCAGACT CCTCGTGCAC 1320 TCCCTGCATG AAGTCGGGGG CAGGTGCTCG AAAGTAGAGG GGTTCCCACT GATGGAAAGT 1380 GTCACCAGCC TGCCTGCGAA TCCCCCAGCT CACACTTGGG 1420
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