| Tag | Content |
|---|
EnhancerAtlas ID | HS034-10074 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr15:63664210-63665360 |
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 | ACAGCTGGAT GAATGCTCAA AAACTGACTG CAGCACCCAC ACCAAGGACC TGAACGTGCC 60
CACAACCCTT CCTGCCTCCT TCCGGTCATC TTCATCCCCC ACAGGGCACA TATTCTGATA 120
CCTTAGCAGG CTGGAGTTTG TCCTTAGCTC ACATGACAAC CTGACCTGCA GCTGTCCTCA 180
GTTCACAGCA AGTGAAGCTG CCGGGCTCAG CGGGATTGAT GCGGGACTGA TTTCCGGCGG 240
GGAAGGTCCA TGTCACATCA TCCCCAGCCT CTCTCTCATG ATGCCACCTC AGCCATGCTA 300
AGCCCAGCAG CCATTCAGCT GCTGTTTCAG CACCCTAGGA GGGGCTCAAA GAGGTGGCGC 360
TGGCCCCATC TTGGCAGTCA GATGGTCCTC CTCTCTCCAG GGAGGAGCCA TCCATGCAGT 420
CAGCCTGGTG ACTCAGCTAT GAGGATGTAG GGGTAGAACT CCCTTTTTTG TACTTCTAAA 480
AGTCCTACCA TGTGTGCCAG ACAGTGGGAG GCCCCTGGAG AATGACTCAG CAGTGTACGT 540
GCAAAGAAGC TGAGTTCTGC ACATGAGCCA CCATGCCCAG CACGGAGCCT TTGGTTGGAC 600
TTGCCCCATT CAGTGCGGCC CTTATTGCTT GGAAGCCGTT TCCCTCCAGC ACTTATGCTG 660
GGCCCTCTGT CTACCTGTGC AGCCCTGAGC ACAGGTGCCA GCTGCCAGCC AGGACCTAAG 720
GAGGAGCTAG CCAAGACCTC AGGAGGAGTT TGCCTCCTTA GCTGTCTTCC ATCTGTCCTC 780
TCCTGCACGT CCCCTCTGAG GGCTGACTCC ACATCACACA TGCCCATGTC ACTAATAAAA 840
ACCAGACTTG CCTTTGTGCT TACCCCATGC ATGTCCATGC ATCATTAGAC TCTGCCCTCT 900
GCTTCCTCAG CAAAGAGCTG CTCTAATTAT GCAGGGTAGG AGGGACAGAG GGCTGGCCAG 960
AGCTAGTGGT CAGGGAGAAA TGCTTCTGGA CAGGTCAGTG TGGCTGCACT GAGAAGCCCG 1020
CCCTTGGCGA ACACCACGTC ATGATGAAGA GGCAGTTAAG ATTCTCTTCC CAGCCAGTCA 1080
TGGTGGCTCA CACCTGTAAT CCCAACACTT TGAGAGGCCG AGGTGGGCAG AACACTTGAG 1140
ATCAGGAGTT 1150
|
