Tag | Content |
---|
EnhancerAtlas ID | HS012-13820 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr15:102067630-102069190 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH15I101527 | chr15 | 102067697 | 102069556 |
|
Enhancer Sequence | AGGTGTGAGC CACCATGCCC AGCTAATTTT TGTATTTTTA GTAGAGACAG GGTTTTGCCA 60 TGTTGCCCAG GCTGGCCTTG AACTCCTGAG CACAAGCGAT CCGCCCACCT CAGCCTCACA 120 AAGTGCTGGG ATTACAGGCA TGAGCCACCG TGCCCAGCCA AAGTTGTGGT TTTAAGCAGG 180 ATGTTCCAAA GTCCAGTGGT TATGACCAAA CGCCACACAG AGACAGAAGC CTCCCGCACA 240 GCCCCAACTC CCAGCAGCCA TGGTGTTCCA GGTCCTCCAA AGTCAGCTTC TCCTCCAGGA 300 GGCCACTGAG CTCCCCAGCT GCGGGGCTGA GGCCACACAG CCCTGTGCGG TTCATCTGCC 360 ATCCGGGCCC TTCTTCCTCT TCTGAGCTTC ACAGTTAGCC CAGGGAAGAA AACAGGCGTG 420 TCTTCCACAA ACCCTGAAGG GAATGGGAAG TGCCAACAGT GAGAAGGACT TAGATGTAAA 480 GGATTTACAC ACGGTCACGG CATTTCCACA ACCCTCTGGG CACCTGAGTA CACGTGTGCA 540 GACACACCCC CAGATGGGGG CGAGGGGTGG GGTGCCCCAG CTATTCACAC CTAACCATGA 600 GCGTGTGAGG CAGCAACACT TAAAGGCCAC TTGCTTTCCG CAGCATCTCG ATGGAGCAGG 660 AGCCTGCCTG GGGCATCTCC AGGCAGCTTG GCTGAGCACC CAGGACTGAG TGCAACCCTC 720 AGCGTTTACA TTTTTTAGTA CTATTCACTA AGAGAGAGAG AGACAGAGAG ACAGTGATAG 780 AGACAGGGAA GGACAGAGAC AAAGAGAGCA ATGGGTGAAG AAAGAGCAAG CAAGCAGGGA 840 TGTCGGACAT TTCACACAAC GCAGTCACCA GGGAGGCAAG AACACTTACA GAACAGTTTG 900 AGCCAAAGAG TCACTCAGGG ACAGGAACAG CAATTTCTTA AATATTTAAA GCAGACACCC 960 TGTGAGCGGC TGTGGAGGCG GCTCTTTGTT AATATTTAAC ACGAGCTGGG CAGTTGCCGG 1020 GAAAACAGCT GTTTACAGGA GAGATTAACC AATATTCATC ATTGCTCAAA GCTGTGGGGA 1080 GGCTTCAGGG GACAGGCAGC TGCCGGTATT TCTAGAATAC AGCAGCTCAA GGCCACAGGG 1140 CTGGGGAGGC TCACGGTGTC CCCAGGGTGC ATGAAAACTG TAAACAGGCA GTTCGGGGTC 1200 ACCTACCCTG CTCCAGAATC ACGGTTTGCA GGAAACCCAG CCCTGCAGCT GGGCCTGGGT 1260 GGTGGCTGCT GGCCGGCCAG CCAGCACCTC GCTGGACAGC TGCGTCCCAC AGTCCCAGGC 1320 TGGGCTGTCC TTCAGGCCCA TCCACAGTCC CAGGCAGACT CCTCGTGCAC TCCCTGCATG 1380 AAGTCGGGGG CAGGTGCTCG AAAGTAGAGG GGTTCCCACT GATGGAAAGT GTCACCAGCC 1440 TGCCTGCGAA TCCCCCAGCT CACACTTGGG CTTGCAGGGA CACCAGCCAG GCCGTCTTGC 1500 AGAGAAGACA AGCTGCCTAT TTTCAGGGGC TATGAGTCTT GTTCATGACA GTTTTCTCCT 1560
|