| Tag | Content |
|---|
EnhancerAtlas ID | HS051-09256 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr15:63664180-63665260 |
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 | TATACCGAAA AGTGTGTAGA CCATAAGCAA ACAGCTGGAT GAATGCTCAA AAACTGACTG 60
CAGCACCCAC ACCAAGGACC TGAACGTGCC CACAACCCTT CCTGCCTCCT TCCGGTCATC 120
TTCATCCCCC ACAGGGCACA TATTCTGATA CCTTAGCAGG CTGGAGTTTG TCCTTAGCTC 180
ACATGACAAC CTGACCTGCA GCTGTCCTCA GTTCACAGCA AGTGAAGCTG CCGGGCTCAG 240
CGGGATTGAT GCGGGACTGA TTTCCGGCGG GGAAGGTCCA TGTCACATCA TCCCCAGCCT 300
CTCTCTCATG ATGCCACCTC AGCCATGCTA AGCCCAGCAG CCATTCAGCT GCTGTTTCAG 360
CACCCTAGGA GGGGCTCAAA GAGGTGGCGC TGGCCCCATC TTGGCAGTCA GATGGTCCTC 420
CTCTCTCCAG GGAGGAGCCA TCCATGCAGT CAGCCTGGTG ACTCAGCTAT GAGGATGTAG 480
GGGTAGAACT CCCTTTTTTG TACTTCTAAA AGTCCTACCA TGTGTGCCAG ACAGTGGGAG 540
GCCCCTGGAG AATGACTCAG CAGTGTACGT GCAAAGAAGC TGAGTTCTGC ACATGAGCCA 600
CCATGCCCAG CACGGAGCCT TTGGTTGGAC TTGCCCCATT CAGTGCGGCC CTTATTGCTT 660
GGAAGCCGTT TCCCTCCAGC ACTTATGCTG GGCCCTCTGT CTACCTGTGC AGCCCTGAGC 720
ACAGGTGCCA GCTGCCAGCC AGGACCTAAG GAGGAGCTAG CCAAGACCTC AGGAGGAGTT 780
TGCCTCCTTA GCTGTCTTCC ATCTGTCCTC TCCTGCACGT CCCCTCTGAG GGCTGACTCC 840
ACATCACACA TGCCCATGTC ACTAATAAAA ACCAGACTTG CCTTTGTGCT TACCCCATGC 900
ATGTCCATGC ATCATTAGAC TCTGCCCTCT GCTTCCTCAG CAAAGAGCTG CTCTAATTAT 960
GCAGGGTAGG AGGGACAGAG GGCTGGCCAG AGCTAGTGGT CAGGGAGAAA TGCTTCTGGA 1020
CAGGTCAGTG TGGCTGCACT GAGAAGCCCG CCCTTGGCGA ACACCACGTC ATGATGAAGA 1080
|
