Tag | Content |
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EnhancerAtlas ID | HS158-02763 | Organism | Homo sapiens | Tissue/cell | Pancreas | Coordinate | chr1:94444670-94446120 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6 | MA0677.1 | chr1:94445306-94445320 | AAGGTCCAAGGTCA | + | 6.24 |
| | 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 |
GH01I093978 | chr1 | 94443865 | 94446690 |
| Enhancer Sequence | TGAATGAAAG GATGTCTATT CATCAGATTT CCATGGAACC ATGCCATCAG GGAGTATCGT 60 GAAGGCAAGT TGTCCTGGCT CCCCACCTCC GTCCTGGCCC CGCTGCTCTC TGCTTGGCTG 120 TGTATGCACA GCCCTGCGGG TGCCTGCCTC CAGGTGGGAA CCACTCCTGG GCTCTCTGCA 180 TATGGCTTCA GCATTGTTTC AACCCCCTTC TCCATCCTAC CTTGCTGTTA CAGTCCCAAG 240 ATTTGTTTCT CACTAGTGTT TTAGGTCCTG CAACTGCACT GTGTTTTTGA GAAGAGAGTC 300 TGACATGTAT ACGCAGTACA TGCCATTTGG CCTTTGCTTG ATACCTGTCT GCTCCTCTGC 360 TGTTCTTTTT AATTAAAAGG GAGAGAGGTA TGTATGCGGG CTGGAGCAGG ACTGGGGCCG 420 TTAAGACTTG AGCCTGGTCC TGGCTCTGGC ATTCAGTTTC CCTCTGACCT CAGGCAAGTT 480 CCCTAAACCT TGGCTTTTTT ATGGGCTTTA GTGAGTAGCC TGGCTGTTTC TTGGAAAACA 540 TGTTAAATAT GTTGAAAATG CTAAATATTG AAAATACTTT CTCAGCTGCA TCCTTTGGCA 600 AATTCCAGAT TCCTTCCTAT CCGTCTTTGG TTTTGCAAGG TCCAAGGTCA GATATCCTAG 660 TTTCCCTCTG CCTAAGCCTC TTCAGTTAGC TGGCCCAGTT TTCAGGGAAA TAGGAATATG 720 AGGCATAGAC ATTCATTAAT TGTAGCTGTT AAAATTCCCA AGCAAATCCA AGTAGAATGT 780 GGTTATGAAA GCCAAGGCCT GTTGCCAAAG AAAGATGTGT GTGTGTGTGT GTGTGTGTGT 840 GTGCATGTGC ACGTGCATGT GCGTGCATTG TGGGATATGT GCTTGTTATA TAACTTCTGA 900 TCCTTGATCC CTGGATGTTA TCCAGTGAGT AGCTGGTTGG ATTTGGGGCT TAACATGGCT 960 TGGGAGCTGT TTGGAGCCTT GGTGGGAACT AGATGACTCT GTGTTGTCTC AATCCTGCTG 1020 TGTAAATAGT CTCTTTCCCT GATCCATCTG CCACAGCCCA GCTGCTTTTC AGCTCCAGTG 1080 ATCCTGCTTA CTGATTCTCC TAGAGACAGA GATCTGAATG GTTGGTGAGG AGCCCATCCC 1140 AGGCTGGCAG GAAGGATTCT GGGCACTCTG GGGACATCTT TAATGGACTG TACCGTAAGA 1200 TATTTTCAGT GTGGGACTTC CAAGCTTGCT CTGTCAAGGA ACTTTAACAT CCTGTGCAGC 1260 TGCTTGAGTT CTCTGGAGAG AGCTGTCTGT CCCACCTGAG CTGAGTTCCC TTCCCCCTCT 1320 AAACTAAGCT CCTTCCTCCT CTAAACTAAG CTCCTTCCTC AGAGCTGACC CAGGGCCCAC 1380 TGCTGCCGCC AGTGCACAGG GGCCTGCAGG CCTGTTACAG CATTGGCTTA GTCTGGAAGG 1440 TCATATATCT 1450
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