| Tag | Content |
|---|
EnhancerAtlas ID | HS158-10931 | Organism | Homo sapiens | Tissue/cell | Pancreas | Coordinate | chr11:70994840-70996500 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT1 | MA0137.3 | chr11:70995965-70995976 | TTTCTAGGAAA | + | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH11I071282 | chr11 | 70993621 | 70996192 |
| Enhancer Sequence | TGGCCAGGCT GGTCTTGAAC TTCTAACCTC AGGTGATCCG CCCACCTTGG CCTCCCAAAG 60
TGCTAGGATT ATAGGCATGA GCCCCCACGC CTGGCCCCTA AGTGATTTTT CTATATCAAA 120
CACCAAGAAG AAACAGGGGC AGCGGAATGG AAGGCTCGGC TGCTTTCGGA CAGGGGAGAG 180
GTCAGCTTCT CAGAGCCTTC TTGACCTTCA GCCTCTGAGG CTCGTATCGG GAGGAGGGGC 240
CCCGCTGACG CTGTTGAGTG CCAGCTGCCT GGGTTCAGAA CAGGCCAGGC TGGTTGGGTT 300
GGTTGTGTGT GGGAGAATCA GGAAGAGGGA GCTTGTTCAT AATCCAGCTC GTTTACCCAA 360
CAAACAATAA AACAGAAGGC AGGATTGTTC GGAGATGCCG GATGGCAGCC ATGAGAAAGA 420
CCCCACTGGT CTGAGAGGTC TGTGCAGGAA TGCACGGAGC CTGGGAAACA CAGAGAGGTA 480
TGGGGCCTGA GGGTGAGGAC GCAGGACAGG TTAGGGACGG GTGGCGCTGG GTGCTGGCTC 540
TGGCAGAGAG CAAGCCAACT GGGGGCATTT CTTTCCAGCC CCGTGGCTGA TGGTCTCGCC 600
GTGCGTGATG GTGAATTTTA TGTGTCGCCT TGATGGGACC TTGGGGGTGC TCAGACATTT 660
GGTCAAGCCT CTGTGTTTGC GAGGATGTTT CTGGATGGGA CTAGCATTCA AATCTGCAGA 720
CCGAGGCAAG CAGAGTGTCC TCCCCGCAGA AGGTGGGCCT CACCTCATCC ATCAGGGGCC 780
TGAATAGAAT AAAAAGTTGA AGAGGAGAGA ATTATTTGCC TCTGCCTGTC TTCAAGGTGG 840
AACCATAGGT CTTCTCCTGC CTTTGGACTT AGACTCAGCA GAAAGAGCAC CTCCCCTGGC 900
CAATGCTTTT GGCAGGATTC CAGAATGTGC ACTCCTGGAG CCCTGGACCA CGGCTGGCTT 960
GGTTCCAGCC CATCTGTGAC CATCTCTCCT AGGATGCTGG GATGTTCTGT GGGGCCAAGC 1020
TAGGGCTACT TGCCTACTTC TGCTGCAAGG GAGGGGTCAG CCCCATGGGA ACCATAAGTG 1080
TGGGGATTGG GGCAGCCTGA TTCTCTAGGA AGAACTGCTG CCCTCTTTCT AGGAAAAAGG 1140
AGAAGGGATT TCAGGCAGCC CAAGCTAACA GAGGCCTGCT GTGCACTTGT GTGTTCTGAG 1200
CACTGGCTAG GAAGTGCAGG GCTTCCAAGA AGACCTAAAA TTCATGAGAA CCAAGACAAG 1260
GCAGTGAAGG TGTGATCCTG ATAAAAGGTG ACCAAGACAA GGCAGTGAAC GTGTCATCCT 1320
GATAAAAGGT GACTGCAGGG GCTGCCCAGG GCAGGGAGGG CTCAGCCTGG AGTGGGTCCA 1380
TCCCGTCCTT GAGTCATTCT GTCCTTCCCC TCATCTGACA GGTGCCTGGC TCTTTGTTCT 1440
TCCTTCATCG TGGGGGACAA GGGTGCAGGG GACGACGTGT TCATTTTCCT CTCCTATGCT 1500
CAGCTCACGG CCCCCGCCCT CCACTCCCCG CCTCACACTG ATCACTTTCC CATTCAGCAG 1560
GTTCGATGCA CGCACAGGAT GCACGCGCCT CCTTGCAGAA CACCGTGTGG GGCTTCCAGT 1620
GAGCGCTTCA TATTGTAAAT GCCACTGTGC CCCGGATCCC 1660
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