| Tag | Content |
|---|
EnhancerAtlas ID | HS113-12234 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr15:40441830-40443200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr15:40442616-40442627 | AACAGCTGCAG | + | 6.02 | | Tcf12 | MA0521.1 | chr15:40442616-40442627 | AACAGCTGCAG | + | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_37146 | chr15:40441604-40443774 | HSMMtube |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I040149 | chr15 | 40441941 | 40443169 |
|
Enhancer Sequence | CAGTGGCTGC CTTCCTGACA CAGCTTTTGT CAGGCTCTCT CATTGCTGTA GTCTCTCAAT 60
GGGCTCCAGG AGCAAATCTT AACTCTCTTC CCATCAGAAC TAGGGGTAGC AGCTTCCCCT 120
TGTTGCCAGT TTCTAAGTTC TTCACTATCC ATGTTTGTTC CCTTTAATCC CATCCCTTCC 180
ATAGTAAATT TTCCCTTCAT TTATTTATTT CACGGACAGT GAATCATTGG TTTCCTGCTA 240
GGACCCTGAT GATACAGATG GTGTCTCCGT TAGAAATGAA TCTGGCTTCC ATAACAGCGA 300
GCCTTACAAA CAGTGGCTTA AGCAAATAGG TCTTTTTATC CACATTATGA GAAGTCTGGG 360
GGTGGTAGTT CCAGGATGGT GCAAAAGCTC CATGATGCTG TCATAAAGCC AGGCTCTCCC 420
TTTCCACTCT CCTTTCCCTT AACCTGTTGG CTTTTGTCTT TCTGCCTTCA CCTCATGGCC 480
ACAAGATGCT GCCCAGCTCT AGACATTCCA CCTATCTTCA AAGTAGGAAG AAGGGCAAAA 540
GGGCCATGCC AACCATGTCT CTTCTGCCCC AGTCTTCTCC AGACTTCCAT TTGGGTCATA 600
CCTGGATCAC AGGACTACTC CTGGATGCAA GGGAGGCCGA GAAATCGGGG AACACATTTG 660
TCATGACTGA GTTGGGCAAA TCATGACTCA TTGCTCGGGG CACTCCTGGC ACATTGCCAT 720
CCCAACCACT CACTCTGTTA ACAAAGGAGA GCAGGGAGAA TTGGTTTTGG GCAGGCCATG 780
AATACTAACA GCTGCAGTGA AGCTTCCGAA GGCTGGGGAG GCAGCCTGTG TACAATGTGA 840
CAGTGAACAG AAACTGAGAC AAGCTGGTGG AGAGCCGTGT CTGTACCCAG AGATAGGTTT 900
TAGGGATACA CTGTCCCTAA AACTACCTCA TGCCCAGTTC CCCACTTTAG TGAGAATGAT 960
CAAGACCACA AGGTGTAGAG ACAAACCCTA GACACAGTCA GAAGACTCCT CTGGAAATCT 1020
TCCACAGCCA CCTTAGCATT TCTCTCTCCC TCCTCCACGT GCCCCGGCTT CATATGATAC 1080
TCCTGCTAAG TCTCTGACCC CACTGTGTTG CAATTATCTT TCCACACAAG GCTGTCCTCA 1140
CCCACTAGAC CAGGGGCTAC TTGGGGACAG AAATTCTGTC TTGTTTGTAT TTGTGATCCC 1200
TTGCCCAGTT AGTGCCTGAC ATAAAATAAC AATAACAAAT GCTCAATAAG GGCAAGGCGC 1260
GGTGGCTTAT GCCTGTAATC CCAGCACTTT GGGAGGCTGT TGCAGGAGAA TTGCTTGAGG 1320
CCTGGCAGTC AACATCACCC TGTGCAACAT AGCAAGACCC TGTCTCTACA 1370
|
