Tag | Content |
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EnhancerAtlas ID | HS158-09046 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr10:129239390-129240730 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr10:129239931-129239945 | ATTCCCTGGGGACA | + | 6.01 | Gfi1b | MA0483.1 | chr10:129240136-129240147 | GGCTGTGATTT | - | 6.02 | RREB1 | MA0073.1 | chr10:129239956-129239976 | CCCCCCACCACCCCCACTGT | + | 6.58 | RREB1 | MA0073.1 | chr10:129239945-129239965 | ACACCAGCCACCCCCCCACC | + | 6.59 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 129240040 | 129240200 | chr10 | 129240200 | 129240600 |
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| Number: 2 | ID | Chromosome | Start | End |
GH10I127440 | chr10 | 129239181 | 129239973 | GH10I127441 | chr10 | 129240041 | 129240230 |
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Enhancer Sequence | CAGTTGTGCC AAGTGGCAGA ATTGATCACA GCTGACTTGT GTGAAAAGAA GTCCAAGGAC 60 ACAAGCACAC ACGTGACAGG CACAGAGCCA GCACAGTGCA TCTTCTGTCC CTGCCCTTGG 120 TGGCCCAAGC ATCCTTCTAG GGTCCTTGCA AGCAGCAGGG CTAGGGGCAG CCCCACGAGG 180 GCTGCCTCCC CACGGCTGGC CCTAGCACCC TCAGCAAATC CACAGGAACT CACCAAGGTC 240 AGAGCACAGA ACCTTGGCGG TGCTTCTCAG CATCTGGCCC AGTGTCAGCT TGAACCTTCC 300 AGCACCAGGA GGCGGAGAAT CCGAACCTCC CACTGGGGGA CAGGCTTACT ATTCTTGGTC 360 CAGCCCAGCA ACCTGTCTGT CTACGCAGAG GGCACCTCCT CCAGGGGACG GGTGCCGGCA 420 AGGTCTGTGA GGACAGTCAG ACACCTGAAG TTTCCTAGCA GGCGGCTGCG TGCCAGTGAC 480 CAGCCATGCG CAGGAGGGGA GGTGCGGGGG AGGAGGTTCA CAGGAACAGA AGCAGCAACC 540 CATTCCCTGG GGACAACACC AGCCACCCCC CCACCACCCC CACTGTAGTG TCCTCCTTGC 600 CCTTCCCCCC TGCGGGCCTC CCCTGCACCC CAGCTTCTGC AAAGGTTTTC CCTCCTCACC 660 CCTGTGGCTG GGTTCGGTTT CCTACTTGAT TTGCATCATC AACAATTTCC TGACCTTTAG 720 CTGAGCCTCT CCAGCCAGAG CCTCCAGGCT GTGATTTGCA TCTCAGCAGT CCAGCCTCCT 780 CAGCTCTCTG AGTCAGAATG TGCCCTCCCT GGGATGCAGG GAGGCCAGGA GAAGCACCTT 840 AGGAGACCCC AAATCTCTCT TGCCAGCACA TTCACCTTCA GAGAGCCCAG CGCTTCACCC 900 GGCCTTTCCT GACTTCCCAC AGCAGTTTTG CTGCCTGGAA CAAGGCCATT TCTTCAGAGG 960 AGGTGCAGCT CCTGGGCGCT TGGCTCCCCC GACAGCACAG GACAGTTCTG GAAATAGACC 1020 TGTTGGCCTG GCTCTGTCAC TCATTTACCA GAGGGCCTGA ATCTTCCTCC CAAGCCTAGT 1080 TCCCATTTCC TCCTTCCAGC CTCAGTAACC TCCAGACTGG CCCTGGCACA GCTGACTCCT 1140 CCTGGGGCAG ACATTGAAGC CTATGTGCTC TGTTGCTCAC CCAAACCAGC ACAGCGCATC 1200 CACCAGGCCC CCAGACCCAG CCGCAGCCCC AAGCCCAGAG CTGCCCACTC ACCTGCCTGC 1260 CCTTCCTTGG GGGAGAACGT TGACCCCTCC TTTTTGGCTG GGTTAATACG TTTTCTAATT 1320 ACTCCTGCGT CAGAGTATTT 1340
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