| Tag | Content |
|---|
EnhancerAtlas ID | HS098-19639 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr15:63664130-63665270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr15:63664375-63664386 | CTGCAGCTGTC | - | 6.62 | | NFE2L1 | MA0089.2 | chr15:63664729-63664744 | GAATGACTCAGCAGT | + | 7.6 | | Nfe2l2 | MA0150.2 | chr15:63664727-63664742 | GAGAATGACTCAGCA | + | 7.52 | | Tcf12 | MA0521.1 | chr15:63664375-63664386 | CTGCAGCTGTC | - | 6.14 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_23470 | chr15:63664748-63665298 | Colon_Crypt_1 | | SE_26934 | chr15:63662910-63667912 | Esophagus | | SE_50638 | chr15:63664022-63665272 | Sigmoid_Colon | | SE_56234 | chr15:63662896-63668892 | u87 | | SE_64951 | chr15:63663016-63666252 | NHEK |
|
| | 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 |
| GH15I063370 | chr15 | 63663161 | 63668065 |
|
Enhancer Sequence | AATCTCCCAG CCAGCTGGAA CTTTGTAACT CTTTTATTGA ATATGAAATA TATACCGAAA 60
AGTGTGTAGA CCATAAGCAA ACAGCTGGAT GAATGCTCAA AAACTGACTG CAGCACCCAC 120
ACCAAGGACC TGAACGTGCC CACAACCCTT CCTGCCTCCT TCCGGTCATC TTCATCCCCC 180
ACAGGGCACA TATTCTGATA CCTTAGCAGG CTGGAGTTTG TCCTTAGCTC ACATGACAAC 240
CTGACCTGCA GCTGTCCTCA GTTCACAGCA AGTGAAGCTG CCGGGCTCAG CGGGATTGAT 300
GCGGGACTGA TTTCCGGCGG GGAAGGTCCA TGTCACATCA TCCCCAGCCT CTCTCTCATG 360
ATGCCACCTC AGCCATGCTA AGCCCAGCAG CCATTCAGCT GCTGTTTCAG CACCCTAGGA 420
GGGGCTCAAA GAGGTGGCGC TGGCCCCATC TTGGCAGTCA GATGGTCCTC CTCTCTCCAG 480
GGAGGAGCCA TCCATGCAGT CAGCCTGGTG ACTCAGCTAT GAGGATGTAG GGGTAGAACT 540
CCCTTTTTTG TACTTCTAAA AGTCCTACCA TGTGTGCCAG ACAGTGGGAG GCCCCTGGAG 600
AATGACTCAG CAGTGTACGT GCAAAGAAGC TGAGTTCTGC ACATGAGCCA CCATGCCCAG 660
CACGGAGCCT TTGGTTGGAC TTGCCCCATT CAGTGCGGCC CTTATTGCTT GGAAGCCGTT 720
TCCCTCCAGC ACTTATGCTG GGCCCTCTGT CTACCTGTGC AGCCCTGAGC ACAGGTGCCA 780
GCTGCCAGCC AGGACCTAAG GAGGAGCTAG CCAAGACCTC AGGAGGAGTT TGCCTCCTTA 840
GCTGTCTTCC ATCTGTCCTC TCCTGCACGT CCCCTCTGAG GGCTGACTCC ACATCACACA 900
TGCCCATGTC ACTAATAAAA ACCAGACTTG CCTTTGTGCT TACCCCATGC ATGTCCATGC 960
ATCATTAGAC TCTGCCCTCT GCTTCCTCAG CAAAGAGCTG CTCTAATTAT GCAGGGTAGG 1020
AGGGACAGAG GGCTGGCCAG AGCTAGTGGT CAGGGAGAAA TGCTTCTGGA CAGGTCAGTG 1080
TGGCTGCACT GAGAAGCCCG CCCTTGGCGA ACACCACGTC ATGATGAAGA GGCAGTTAAG 1140
|
