Tag | Content |
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EnhancerAtlas ID | HS141-06840 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr15:102067370-102069360 |
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 | TCTCACCCAG GAAGGAGGAA TCTAAACAAA CTCAGCTGCC AGTGGCTCCC CCATAGCGAC 60 AGTTTGAGGC CGGATTCACT GAAGTTTTCA CAGATGAGTC TAGGTAAAGT TGTGGGGGTT 120 TTTGCTGTTG TTTTGTTTTG TTTTGTTTCT TTGAGACAGG GTCTCAGTCT GTCGCCCAGG 180 CTGGAGTGCA GTTGAGTGAT CTTGGCTCAC TGCAGACTCC AACTCCTGGA TTCAAGTGAT 240 TCTCCTGCCT CAGCCACCCA AGGTGTGAGC CACCATGCCC AGCTAATTTT TGTATTTTTA 300 GTAGAGACAG GGTTTTGCCA TGTTGCCCAG GCTGGCCTTG AACTCCTGAG CACAAGCGAT 360 CCGCCCACCT CAGCCTCACA AAGTGCTGGG ATTACAGGCA TGAGCCACCG TGCCCAGCCA 420 AAGTTGTGGT TTTAAGCAGG ATGTTCCAAA GTCCAGTGGT TATGACCAAA CGCCACACAG 480 AGACAGAAGC CTCCCGCACA GCCCCAACTC CCAGCAGCCA TGGTGTTCCA GGTCCTCCAA 540 AGTCAGCTTC TCCTCCAGGA GGCCACTGAG CTCCCCAGCT GCGGGGCTGA GGCCACACAG 600 CCCTGTGCGG TTCATCTGCC ATCCGGGCCC TTCTTCCTCT TCTGAGCTTC ACAGTTAGCC 660 CAGGGAAGAA AACAGGCGTG TCTTCCACAA ACCCTGAAGG GAATGGGAAG TGCCAACAGT 720 GAGAAGGACT TAGATGTAAA GGATTTACAC ACGGTCACGG CATTTCCACA ACCCTCTGGG 780 CACCTGAGTA CACGTGTGCA GACACACCCC CAGATGGGGG CGAGGGGTGG GGTGCCCCAG 840 CTATTCACAC CTAACCATGA GCGTGTGAGG CAGCAACACT TAAAGGCCAC TTGCTTTCCG 900 CAGCATCTCG ATGGAGCAGG AGCCTGCCTG GGGCATCTCC AGGCAGCTTG GCTGAGCACC 960 CAGGACTGAG TGCAACCCTC AGCGTTTACA TTTTTTAGTA CTATTCACTA AGAGAGAGAG 1020 AGACAGAGAG ACAGTGATAG AGACAGGGAA GGACAGAGAC AAAGAGAGCA ATGGGTGAAG 1080 AAAGAGCAAG CAAGCAGGGA TGTCGGACAT TTCACACAAC GCAGTCACCA GGGAGGCAAG 1140 AACACTTACA GAACAGTTTG AGCCAAAGAG TCACTCAGGG ACAGGAACAG CAATTTCTTA 1200 AATATTTAAA GCAGACACCC TGTGAGCGGC TGTGGAGGCG GCTCTTTGTT AATATTTAAC 1260 ACGAGCTGGG CAGTTGCCGG GAAAACAGCT GTTTACAGGA GAGATTAACC AATATTCATC 1320 ATTGCTCAAA GCTGTGGGGA GGCTTCAGGG GACAGGCAGC TGCCGGTATT TCTAGAATAC 1380 AGCAGCTCAA GGCCACAGGG CTGGGGAGGC TCACGGTGTC CCCAGGGTGC ATGAAAACTG 1440 TAAACAGGCA GTTCGGGGTC ACCTACCCTG CTCCAGAATC ACGGTTTGCA GGAAACCCAG 1500 CCCTGCAGCT GGGCCTGGGT GGTGGCTGCT GGCCGGCCAG CCAGCACCTC GCTGGACAGC 1560 TGCGTCCCAC AGTCCCAGGC TGGGCTGTCC TTCAGGCCCA TCCACAGTCC CAGGCAGACT 1620 CCTCGTGCAC TCCCTGCATG AAGTCGGGGG CAGGTGCTCG AAAGTAGAGG GGTTCCCACT 1680 GATGGAAAGT GTCACCAGCC TGCCTGCGAA TCCCCCAGCT CACACTTGGG CTTGCAGGGA 1740 CACCAGCCAG GCCGTCTTGC AGAGAAGACA AGCTGCCTAT TTTCAGGGGC TATGAGTCTT 1800 GTTCATGACA GTTTTCTCCT CTATGTGCCA AACATTCAAG AGCCTGGCCA TTTTCACACA 1860 GCCCCATAGC CTGGGTGAAT CAGGCCTCAC TCCCCTGTAC TTCCTTCCAA ACATTCTATC 1920 ACTCCCAACA CCCTCCACCC AGGCCTCATG GAACTACACA CAGATCACGC TTGGGCCCAA 1980 CTGGATGCGG 1990
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