Tag | Content |
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EnhancerAtlas ID | HS095-25371 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr6:2588930-2590370 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2A | MA0003.3 | chr6:2589712-2589723 | TGCCTGAGGCT | - | 6.32 |
| | 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 |
GH06I002588 | chr6 | 2588901 | 2590336 |
| Enhancer Sequence | TAGGCATTGT CAGAGGGAAG GTCTAGGGCT GAAGGCTGTT GTTCAGATTT TTTTGTCCCA 60 CGGTGTGTTC CCTTGATGTA GTGCTCTCCC CCTTTTCCTG TGGATGTGGC TTCCTGTGAG 120 CTGAACTGCA GTGATTGTTG TCTCTGTTAT GGGTCTAGCC ACCCAGCGAG TCTACCTGGC 180 ACTGGGCTGT TACTGGAGGT TGTCTGCATG GAGTCCTGGA ATGTGAATTA TCTATGGGTC 240 TCTCAGCTGT GGATACCAGC GCCTGTTCTG GTGGAGGTGG CAGAGGGTGC ATTGGACTCT 300 GTAAGGGTCC TTCGGTTTGG TGGTTTAATG CTCTATTTTT GTGCTGGTTG GCCTCTTACC 360 AGGAGGTGAT GCTTTCCAGA AAGCATCAGC TGTAGTAGTG TGGAGAGGGA CCAGTGGTGG 420 GAGGGGCCCT AGAACTCCCA AGATTATATG TCCTTTGTCT TCCCCTACCA GGGTGGATAG 480 GGAAGGACCA TCAGGTGTGG GCGGAGCTAG GCGTGTCTGA GCTCAGCCTC TCCTTGGGCA 540 GGTCTTGCTG CGGCTGCTGT GGTGGGTGAG GGTGAGAGTC CAGGGTCACT GGAGTTGTGT 600 ACCTAGAAGG ATTAAGGCTG CCTCTGTTGA GTCATGCAGG TTGTCAGGGA GGTGGGGGAA 660 AGCTGGCAGT CACAGGTTTC ATCCAGCTCC CACGCAAACC AAAAAGCCAG TCTCACTCCC 720 ACCGTGCTCC CCAACAGCCC TGAGTCTGTT TTTAGGTGGA GGGTGAGACG GGCTTGAAAA 780 CTTGCCTGAG GCTACCTGCC TCCCAGCTGT GAGAGAGAAG GGCTTTCATT TATGCCCCAT 840 CCCCCCACCC CCACTGTGAA GTCTGCATGC CTGATTCGCG CCCTCCCCTG AATTCTGGCC 900 AGGAGGCTTC TTGTTCTCTT CAAATTGTTA CAAAGTTCAG CTAGAGAATT CCTTCTCCTT 960 GTAGAGTGTT ACCCCCTGCC CCTCAGGCCA CCTTCCTGCT GGATCCCTGT GGTGCCAGGC 1020 AGGAATGGGC TGCTAGGGGA CCCAAAGAGC TCCCAGGGCC TTTCTGCTGC TTTCTCTACC 1080 CCTGTGTTTT GCTGGGCTCT CTAACTTGAC TCAGCTCCAG GTAAAGTCAG AAACTTCTCC 1140 CACAAACAGA TCTTCAGCTT CTCCAGTGGG GGAGAGGGGG GAGTGTTTGG AAGAGGGGGG 1200 TTTCCCTTTC CCACTTCTGC AGTTGGGGCA TTCACAGTAT TTGGGGTGTC TCCTGGGTCC 1260 TGCAGGAGGA ATCCACTTCC TTCAGAGGGT CTGTGGATCC TCTTAGTTTT GCTGGTTTGT 1320 TCTTGCAGTG GATCTAAAGC TCAGATTCAC AGTGCGAGAC TCTGCATGCT GCTCTCTCCG 1380 GAGATGCAAT CTAATCCTGC CTCCCGTCCA CCATGATCCC AGGCATTTTT TCATATATTT 1440
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