| Tag | Content |
|---|
EnhancerAtlas ID | HS176-13963 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr15:63664140-63665520 |
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 | CCAGCTGGAA CTTTGTAACT CTTTTATTGA ATATGAAATA TATACCGAAA AGTGTGTAGA 60
CCATAAGCAA ACAGCTGGAT GAATGCTCAA AAACTGACTG CAGCACCCAC ACCAAGGACC 120
TGAACGTGCC CACAACCCTT CCTGCCTCCT TCCGGTCATC TTCATCCCCC ACAGGGCACA 180
TATTCTGATA CCTTAGCAGG CTGGAGTTTG TCCTTAGCTC ACATGACAAC CTGACCTGCA 240
GCTGTCCTCA GTTCACAGCA AGTGAAGCTG CCGGGCTCAG CGGGATTGAT GCGGGACTGA 300
TTTCCGGCGG GGAAGGTCCA TGTCACATCA TCCCCAGCCT CTCTCTCATG ATGCCACCTC 360
AGCCATGCTA AGCCCAGCAG CCATTCAGCT GCTGTTTCAG CACCCTAGGA GGGGCTCAAA 420
GAGGTGGCGC TGGCCCCATC TTGGCAGTCA GATGGTCCTC CTCTCTCCAG GGAGGAGCCA 480
TCCATGCAGT CAGCCTGGTG ACTCAGCTAT GAGGATGTAG GGGTAGAACT CCCTTTTTTG 540
TACTTCTAAA AGTCCTACCA TGTGTGCCAG ACAGTGGGAG GCCCCTGGAG AATGACTCAG 600
CAGTGTACGT GCAAAGAAGC TGAGTTCTGC ACATGAGCCA CCATGCCCAG CACGGAGCCT 660
TTGGTTGGAC TTGCCCCATT CAGTGCGGCC CTTATTGCTT GGAAGCCGTT TCCCTCCAGC 720
ACTTATGCTG GGCCCTCTGT CTACCTGTGC AGCCCTGAGC ACAGGTGCCA GCTGCCAGCC 780
AGGACCTAAG GAGGAGCTAG CCAAGACCTC AGGAGGAGTT TGCCTCCTTA GCTGTCTTCC 840
ATCTGTCCTC TCCTGCACGT CCCCTCTGAG GGCTGACTCC ACATCACACA TGCCCATGTC 900
ACTAATAAAA ACCAGACTTG CCTTTGTGCT TACCCCATGC ATGTCCATGC ATCATTAGAC 960
TCTGCCCTCT GCTTCCTCAG CAAAGAGCTG CTCTAATTAT GCAGGGTAGG AGGGACAGAG 1020
GGCTGGCCAG AGCTAGTGGT CAGGGAGAAA TGCTTCTGGA CAGGTCAGTG TGGCTGCACT 1080
GAGAAGCCCG CCCTTGGCGA ACACCACGTC ATGATGAAGA GGCAGTTAAG ATTCTCTTCC 1140
CAGCCAGTCA TGGTGGCTCA CACCTGTAAT CCCAACACTT TGAGAGGCCG AGGTGGGCAG 1200
AACACTTGAG ATCAGGAGTT CGAGACCAGC CTGGCCATCA TGGTGAAACC CCATCTCTAA 1260
TAAAAATACA GAAATTAGCC GGGCGTGATG GCACACCCCT GTAATCCCAG CTACTTGGGA 1320
GGCTGAGGCA GGAGAATCCC TTGGACCCAG GAAGCAGAGG TTGCAGTGAG CCAAGATCAC 1380
|
