| Tag | Content |
|---|
EnhancerAtlas ID | HS158-00851 | Organism | Homo sapiens | Tissue/cell | Pancreas | Coordinate | chr1:20692560-20693620 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr1:20692610-20692621 | CCGCAGCTGTC | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH01I020367 | chr1 | 20692601 | 20692750 | | GH01I020366 | chr1 | 20693127 | 20693202 |
| Enhancer Sequence | CGAGCACCCT CCCCAACCCC TGCGCGCGCG CTCCTCCAAA CCCCGCAAAG CCGCAGCTGT 60
CCTTAACCCA CAATCCTGCC AATTAAACCG CTCCCTCCGG CTCTGGCTGC GGCTGCTGAC 120
GTCGGAAGAT CCAGGCGAGG CGAGGCCGCC GCCTACGCGG GTGGGGTTGG GAGAGGCGAC 180
GGCCCCCTCC TCGGGCCCCG CGGCCGTCGG TCAGTCAGCC GGCGGCAACA CGAGCCCGCA 240
CTAGACCCAA GCGCCGCCCG TCGGTCCCCA CTCCCGACGG GCCTCGCATT CCTGGTCCTC 300
CACCTTCTGC CAAGACCCTG CCCACGCTTC CCGCACCAGC CTTAGGTCCC GAGGTCCCCA 360
ACTTTGGCGA AGATCCCGCC TGGGCTCCCC GCATCTTCCC TTGGTCCCAA GGTCCCCAAC 420
TTGTCGCCAA GACCCCGCCT GGGCTCCCAG CACCGCCCCT CGCGCTCGGG GTCTCCCGCC 480
CCACGCCAAG TCAGCAAATG CACCCCAGGT TCTGCCTCTC GCGCTGCCGC TCCGCGACCC 540
CCACTCCGAG TTCCCCGCGT CCCAGCATCC CAAGTGCGCT CCCAGCACCC TCCGCGCCCC 600
GACCGCGCAC GCCCCGCGGA CGCCGCGCCG CGACCCCGCT GGGTCCCCCG CCCTCCCGGC 660
AGCCTCCGCG CGCTCGGTCC TCGGTTTCCC CTCTCCGAGC GTCGCTGGCT CTGTCTCCAC 720
GAAGGCGTCG CAGTGGGAAC CGGGAGGGGG CACATTAAGA GCAATTAGCC TGCGCACACT 780
TGGCAGCGAT ACCTTAATAA ATAATAGTCT GAAAGTCATG TAAATAAATA TTAGAGCGCA 840
TTACGCGGGC AGGAGGCGCG GCACGGGGCC CGCGAGCTGG TGGCGAGACA CCGCCGCCTC 900
TCGGGATTGG CACGTGCAGG CGGGGGCCCG AGATCCCCGC GCCCCGGCGG CCTGCGACCC 960
GCTGCCAGGG GCCGGGCAGG CAGGGGTGGA GGGAGAGGCC CGGGGAAGGA GCCCCAGGGA 1020
GACAGAGAAA GCCACAGAAA GAAATAGGGA GAGGGGAGGG 1060
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