Tag | Content |
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EnhancerAtlas ID | HS158-08759 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr10:120427320-120428990 |
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) |
CTCF | MA0139.1 | chr10:120428248-120428267 | TTCTGCCACCTACTGGCTG | - | 6.83 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 120427655 | 120427929 | chr10 | 120427979 | 120428114 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I118668 | chr10 | 120428407 | 120430021 |
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Enhancer Sequence | GTGTGTGTAT TCAGACATGC AAAGGAAGAC AAAGGTTTTT AAAGGTAAAA TGAGAAGGAT 60 TATATAATTG TTTTGAAATA ATTGTCCTTG GCTACTAAGA TCAATAACAA GGGTGACGCC 120 AGTCCAAGGT TGGACAGGCA GTTGCTAGGC AGATGTCCTT GCAGAAGTAT TTGTTGTGTA 180 AGGTTGTGAT AGCCTTTGTG CAAGGTTGTG GGTTTGCAGG CTTTTGTGAT ACTTTTTGTA 240 TCCAAGGCGT CCAAGTGTGA GAACACTTCC TTCATGAACT TCCCCGGCTC TCTTGTGTTT 300 TCAACACAAG AGATTCCATT TTGATTGACA ACTTTCATAC AATATAGAAA TTAGAACCTG 360 AGACCTAATC TAGCCCACCT GTCCCCACGT GTGGTGGGCC CACCATGCAC AGCCAAGTCA 420 CCTGGAGCAT GAGGCTGAAA TGCAGGTTTC TGGGCCCTGC TCCAGACCTG CAGACTCAGA 480 ATCTCAGGGA GGTAGGGAGG GGTGGGGAGG GTAAAAGCTG CATTACTGAC TAGCTCCCTT 540 AGTGACAGTT CAGCACGCTG ATGTTCAGGG ATGCCCTCTT CTTGCCAAGG AGAAAACAGA 600 AGCGCAGTCT GTTGGCCAAG GGCCCTCAGC CAGGGAACAT CAGGACCTGG GGCACAGCTC 660 TAGGAAACGC TGTTGTTGCT GAGAGTGGGG GCAAGGGGCA CTGGCCAGAC CTGGATTTGT 720 GGGAGGCGGC TGACATGAGG CTCTGGACTT CTGCAGCAAG ACGGACATCA GGGAACCTGG 780 GCTTCCAGCA AGCAGCTCTT TTAGCCAGCA CAGTAGATGC ACTCCAGGTG GTGGGGTCTC 840 AGTCCAGTGG GGTCTTCAGG AGAAAGCAAG GCTCCTAGGC TGGAGTCTAG TTTCAGGTGG 900 GGCTGTGATT GGGGTCTGGC CATCGTGGTT CTGCCACCTA CTGGCTGTGT AACTCCGGGT 960 ACCTCTCTGA GCCTTAACTC CTCGTCTGAA AACAGAATAA TCAGAGTACC TACTTCTTGG 1020 GGTAGCTGTG GGGTGGGGCA TGAGATGGCA CTGGCTGTTC AGTGTTTGCC TCTCAGGTCC 1080 TTCTTGACTC CTTGGGGCTG AATTTATGTT CTCATCACTC CGTTTCTGAG CAGATGAGGA 1140 AGAAGGAGGG TGGAACTCTA GCTCCAACTC TGCTCCCTGA CCTAAGTATC CCAACCCCTC 1200 CCAGGTTGGG GACAGAGCCC TTCCATCACG TAGCTCTCGG TCCCACCGGA CTCTTTGCTT 1260 AGGAAGAGGC TGCCTGCCCC CATCGTGGTT AGGTGCTAAC TCATTCTCTG CTTTATCTAT 1320 CACATCTCTA ACTGCCCATC AGAGCCCATT AGACCAGAAT GAGACTCCCA GGGTGGCCGC 1380 AGAGCAGCAG CATTTCAGCT CATCAGAGGA AGCTGCCAAA TGAGCCAGTC TGAGCAGCAT 1440 TTGGGGGTAG ATGTTCGCTT CCTATTAACA GGCTAAATTG CGGAAGTGGC TCAGAGTTTC 1500 ATTCCCACTG TGCCACTCCC TGGGGTCTGC AGCGTGGCCT GGGAGAAAAA GGCACAGCCT 1560 CGGGGTCAGA CCCGAGTTGG ACCCAGCTCT GTCCCCTGGT ACCTGAGGGA CTCTGGATAA 1620 ATTACTGGAT TTCTCTGAAC TCCACTTATC CCATTTGTAA AACAGGATTA 1670
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