| Tag | Content |
|---|
EnhancerAtlas ID | HS098-20879 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr15:102067690-102069600 |
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 | TGTTGCCCAG GCTGGCCTTG AACTCCTGAG CACAAGCGAT CCGCCCACCT CAGCCTCACA 60
AAGTGCTGGG ATTACAGGCA TGAGCCACCG TGCCCAGCCA AAGTTGTGGT TTTAAGCAGG 120
ATGTTCCAAA GTCCAGTGGT TATGACCAAA CGCCACACAG AGACAGAAGC CTCCCGCACA 180
GCCCCAACTC CCAGCAGCCA TGGTGTTCCA GGTCCTCCAA AGTCAGCTTC TCCTCCAGGA 240
GGCCACTGAG CTCCCCAGCT GCGGGGCTGA GGCCACACAG CCCTGTGCGG TTCATCTGCC 300
ATCCGGGCCC TTCTTCCTCT TCTGAGCTTC ACAGTTAGCC CAGGGAAGAA AACAGGCGTG 360
TCTTCCACAA ACCCTGAAGG GAATGGGAAG TGCCAACAGT GAGAAGGACT TAGATGTAAA 420
GGATTTACAC ACGGTCACGG CATTTCCACA ACCCTCTGGG CACCTGAGTA CACGTGTGCA 480
GACACACCCC CAGATGGGGG CGAGGGGTGG GGTGCCCCAG CTATTCACAC CTAACCATGA 540
GCGTGTGAGG CAGCAACACT TAAAGGCCAC TTGCTTTCCG CAGCATCTCG ATGGAGCAGG 600
AGCCTGCCTG GGGCATCTCC AGGCAGCTTG GCTGAGCACC CAGGACTGAG TGCAACCCTC 660
AGCGTTTACA TTTTTTAGTA CTATTCACTA AGAGAGAGAG AGACAGAGAG ACAGTGATAG 720
AGACAGGGAA GGACAGAGAC AAAGAGAGCA ATGGGTGAAG AAAGAGCAAG CAAGCAGGGA 780
TGTCGGACAT TTCACACAAC GCAGTCACCA GGGAGGCAAG AACACTTACA GAACAGTTTG 840
AGCCAAAGAG TCACTCAGGG ACAGGAACAG CAATTTCTTA AATATTTAAA GCAGACACCC 900
TGTGAGCGGC TGTGGAGGCG GCTCTTTGTT AATATTTAAC ACGAGCTGGG CAGTTGCCGG 960
GAAAACAGCT GTTTACAGGA GAGATTAACC AATATTCATC ATTGCTCAAA GCTGTGGGGA 1020
GGCTTCAGGG GACAGGCAGC TGCCGGTATT TCTAGAATAC AGCAGCTCAA GGCCACAGGG 1080
CTGGGGAGGC TCACGGTGTC CCCAGGGTGC ATGAAAACTG TAAACAGGCA GTTCGGGGTC 1140
ACCTACCCTG CTCCAGAATC ACGGTTTGCA GGAAACCCAG CCCTGCAGCT GGGCCTGGGT 1200
GGTGGCTGCT GGCCGGCCAG CCAGCACCTC GCTGGACAGC TGCGTCCCAC AGTCCCAGGC 1260
TGGGCTGTCC TTCAGGCCCA TCCACAGTCC CAGGCAGACT CCTCGTGCAC TCCCTGCATG 1320
AAGTCGGGGG CAGGTGCTCG AAAGTAGAGG GGTTCCCACT GATGGAAAGT GTCACCAGCC 1380
TGCCTGCGAA TCCCCCAGCT CACACTTGGG CTTGCAGGGA CACCAGCCAG GCCGTCTTGC 1440
AGAGAAGACA AGCTGCCTAT TTTCAGGGGC TATGAGTCTT GTTCATGACA GTTTTCTCCT 1500
CTATGTGCCA AACATTCAAG AGCCTGGCCA TTTTCACACA GCCCCATAGC CTGGGTGAAT 1560
CAGGCCTCAC TCCCCTGTAC TTCCTTCCAA ACATTCTATC ACTCCCAACA CCCTCCACCC 1620
AGGCCTCATG GAACTACACA CAGATCACGC TTGGGCCCAA CTGGATGCGG AATCCCAGCT 1680
CAGGACCAAG GAATGCTGCT GCTGTCTCCA CAATGCCCTA GACCTGCAAC CCTGGGCGCT 1740
TCCTGGCATA CCACTGCCCA CTCTGCCCAC ACCACAGCTG ACTGACTCCT AATGGCTCTT 1800
CAAACAGTTG TTTGCACACC TGACCATTTA TTATAAAGGA AGAAGCGCCG AACAGCACGT 1860
GCTGCTCTGA GGAATCTGTA CAAGAATTGG GGCTCTGCGT ATTAATCTTT 1910
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