Tag | Content |
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EnhancerAtlas ID | HS158-13429 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr12:66135580-66136580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:66136546-66136564 | GCCTCCTTTCCTCCTTCC | - | 6.31 | RREB1 | MA0073.1 | chr12:66135805-66135825 | CCCGCCAACACCCCCACCCC | + | 6.57 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I065740 | chr12 | 66134138 | 66136996 |
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Enhancer Sequence | CTCGCCGCGC TCTAAAGTTA AGTTGTATCT CCTTCCCGCC GCGAGTCTCC TTCCACAGAC 60 CCGCCGGAGC TGCCGGGACG GGCGCTGCGC GGGACTGGGC GTTAGGTGCT CCCGGCTGGT 120 TCCGGCGAGC AGCCCCCACC CCTCGCCCAC GCTCGGGGTT AGAGACCCCA GCACCCCACG 180 CAGACGGCCC GGGCTTAGAC CTCTCCACGT CGCTGTGGCG CGCGCCCCGC CAACACCCCC 240 ACCCCACGCG CAGCCCGTGT CTTCTTTACC CCCGCGCACT TAACGCAGGG CGCACGCACG 300 CATCCCGGCC CCCTCACACT CACACTGCGT CTTCTGTCAC ACCCCCTGTC GCACACACAC 360 TGTTCTCTGA CTCCCACCAT CTCCTGTCTC ACACCCACTC CAGTTTCGTG TTGAGCGGCC 420 GCCAGTTCTC CCTCGGTCGC GCCGGCGCAC GCTCGTCCCC TTCTGCCCCG GAGCCCGCCC 480 GCGCCGCACG GTGGCCCCTT GCGCTGGCCT GATCGTGGGA ACCAGGCGGG GCCCCAGCGT 540 CCCTGCCCCT GCCCGGTCAT CCATCTCCCT CCCGGTCGGC CAGCCGAGAC TTCAAAGGCG 600 CCTCCTCCGG CCGGGCCTGC CAAACCCCGA CGCAGCCTGG ATGTGGGCCG GGGGCGCTCC 660 CCGGCGGGGG GAGGCCGGGC CAGGGCGCGT CTGGGGCCGG CTCCGTCCTT AGTGCGGCGG 720 CGGCGGACTC CAGAGCTGAC CGCGGGGCCA CCCCCGCCGC GGCCGGGCCA CGCGCGGGCC 780 ACCCGGGAGC TTCTACCAGC CCAGCGAGCA CGCGCCGGCG GGAGGGGGGC CTCATTTTCA 840 TGGCAAGGGA AATCCGGATA AGGATGGACT CCTTTCGGAG GAGAATGGGA ACGCGCTAGT 900 CCTGGTGCCT GACCCTCTCT CCTAAAGAAA ATGAGTCTCC CCTGGAGCTT AAGCCATATT 960 TCCTTCGCCT CCTTTCCTCC TTCCCATTCG GACACCCCTA 1000
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