Tag | Content |
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EnhancerAtlas ID | HS158-48858 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr6:56239660-56240430 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RORA | MA0071.1 | chr6:56239978-56239988 | ATCAAGGTCA | + | 6.02 | SP2 | MA0516.2 | chr6:56240402-56240419 | CTAAGCCCTGCCCACAC | + | 6.17 |
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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 |
GH06I056374 | chr6 | 56239095 | 56240880 |
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Enhancer Sequence | TTACTCATTT CTGGTCACCT AGAACTTGGT GAGATTCTTT AGACTCTCAT GAACAGATGA 60 TTCTCCAGGT GGAAATTTGC CAGGAAACTT TGCTGAGGGA AATAAACAGT TTCAACCCTC 120 ATCTAGTGTC ACTGTCCCAG AGAACAGGAA TCCCACCACA TGCCTGAGTA GAGCCTTACA 180 TGATGCCAGA ACTCTTGGGA CATATGGACT CAGCCAGAGG CAGAAAGCCA GTTTGAAAGA 240 AAAGTGAGAG AACGCCAGAG CCAAAGGGGA AAAAGAGAAA GAATGTTAGA GACCGAGAAA 300 GGAAAAGTAT GAAATTACAT CAAGGTCAGC AAAACCCTAG TATAAATAGT AACAGCTGTA 360 TGCTGAGTCC CCACAGGAGT CTGTCCTGGA TATTTTCCAC TTGGCCCTCC AGATCCACCC 420 TCCTCACTTC TCCACCCAGC TCTCTAACTG AGGAGGCTGA ACCGTATGGA CTGACTGAAT 480 CAGCTCCTTG TCCACTCGCT TCCAATTGAG TTCAGCCAGT GGTAGGCACC CGTGGAAGAA 540 GGATAGGAGG AAAGTGAGTC TGAGATTATT TTCCCTGCCT CCTTCCTGGC CAGATGACAG 600 CTCTCACCAA GCAGTCTTCT CTGGAAAGGC ACGGCCTCCA GGTTCTAGTC ACCTCCCCTT 660 CTTCTTGCCC TGTCAGGATG AGGGTGGTGG GCACTCTCTG CTGTTCTAGT CCAGTGCATG 720 GTGCCATTAT TTTATGGTTC CCCTAAGCCC TGCCCACACT TTGTAACAAG 770
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