Tag | Content |
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EnhancerAtlas ID | HS062-16265 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr9:5763870-5765410 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr9:5764716-5764731 | GTTTTAAAAATAGAA | + | 6.49 | MYB | MA0100.3 | chr9:5764482-5764492 | GACAGTTGGT | - | 6.02 |
| | 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 |
GH09I005763 | chr9 | 5763565 | 5765157 |
| Enhancer Sequence | AACAATTCTC TTCTTATAAA GGGGCAAGAA TTAATGAGCT TAAACTTAGA AAAATAGAAA 60 TGTCCTGTTT TGACACCATG ATTGTGTTTA AGGAATTCAT AGTCAAATTT TCTGTTTATA 120 TCTTTAATTT GGAAGAATTC AGACAGATTC CTTTGAATAT CATAAAGTAA CATTGCAGAG 180 ATATTTTTTC CATTGTCCAT AAATAGGCCT AAAACAGATT AATGAGTTCA GAGTAGTGTT 240 TTGAAATTTT AATATATTGA AGAAATTTAA TATGTATATT AGAATACATG TAATAGGAAC 300 ATGGAAGAAA TATTACATAA GATTATTGAA ATATTACATA AGAAACATAG CAAAGAAAGT 360 ATTATTTGAG ATATTAGTGA GTTTGAGCTT CTCACAACAG TAGATTTGTT TCCTTTCAGT 420 GTGGGTTACT GAGGGGACAC TTATTAGAGC ATGGTCATAA CAGAGCACCT TGAGCTAGTC 480 TTCCCCAAAG CAAGCTGAGA AGGCTCAGGC CTGCCACAGC AAAGACCCTC ATAGCACACA 540 GTTTTTCTCA AAATAATGGC TTCTTTGCAA CTCCTGAAAA TTTATTTCAT TAGCTATTTG 600 ACAAAAGGGC TTGACAGTTG GTTATTTGAT AGGCTACACT TAAAGATTCT TTCCAGTTAC 660 TGCAAAGTTG TTTCCATTGA TGTAAGAAGC TAACCATAAA CCTGGTTTCA ATCTCTGCCT 720 GAAGCAGATT TCCTGTCAGC TTCTTTGCTT CATGACAATG AACTGAAACC AGAGGAGACA 780 CTCAAGCAGA GGCCAGGTGG CCTTGAAGTA TGATTCCATG GCTAACCCTA AAGAAAAAGA 840 CATAGGGTTT TAAAAATAGA ATCAAAATAA ATGCAGCTGT TTTTTGGTTC CGGGTCACTC 900 CCTGCAACTT CACTGTATCT CCCTGACAAT GTAATTTTTT TCTGCAACAG AATTCCTAAG 960 TTGCTATGGA TTGGCAGATA ATAATTACAA TTACAGTTGT CTATTAGGCA CCTTTCCATA 1020 AAGACCAAGA TAGGCAGGTT AAATTTGTGA AAGAAAAATG GAGGATTCTG AATGTGCAGC 1080 AGAACTTTAC TACTTGCTAT TGCCCAAAGC AAAGATTCTA GTCACATCCT CAGAAAACTC 1140 TGCAACAGGA GACAGACCTG ACCTATTTTG GAGTCAGGCA AACCTCCCTT TTTTTTCTTC 1200 CTTTTCTGCT GATCTTCAAC AATTTACTTA ACTCAGTTTC CTCACTTGTA AAATACAAAT 1260 GATATGCCTA TCTGCAGAGT CACTGGGAGA AATAAATGAA ATGACTTAAA GTATATGTAT 1320 GCTATCTGGC ATGTAGTAGG AGTTTAATAA ATTATAGTTT ACATACACCA GAAGAGTACT 1380 TGCCTCGCTT TTCCTTGTAT GGTACTTTTT AATCTTATTA TTAAACTAAC CCCTGTGGTG 1440 GTGTGGCTAC ATTCTTTGAG TTTAGAAAAC GAGATAAAGA ATTGCTCATA TCTTCCCAAA 1500 TTGTGTAGTA TAAAAAGAAT GCTGTCCTGG TTGTTTTTTG 1540
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