Tag | Content |
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EnhancerAtlas ID | HS095-13997 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr18:55724280-55725300 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GSC | MA0648.1 | chr18:55725025-55725035 | GCTAATCCCC | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAATTACCTT TTTTTCTTAC CTTTTGAGCC AGGGGTAAAG TCAGGCACGG TGACCCTGCA 60 TTCCACACCT TGGATAATCC ATCCACCTTC AGAAATGCCC CTGGCTTCGT GAAATGCACA 120 TGCTCCCTTT CTCCAGGGAG GTGACCCGAA TATGCAGCTA AGTATTGCAA GGATTTCTGG 180 GTAATATTAC ACCTGAAAGG AGGTTTTTTT TTTTTTTAAT TATCTGGTGA TTTATGACTA 240 AATAGGCTAT GTCTCTCAAA ACATTGAACC TGCAATGGGC AAGAAAGAAC AGGATGACTA 300 CAATGAACCT TCTATTTGGA AAAGGGGAAA ATAAGACACT CACAGTGGGG TAGCTGGCTG 360 AACAGGAACA GCTGGGAGCG TTTGCTTTGG TCAGCCGGTC TGGCAGCTTG CCTCTGCTGA 420 AGTCCGTCCA GGGTGAGAAT CTCGCTTGGT CATTGTCCTC TGCAGCTGCA CCTGGATGGG 480 GTAGGCACTG GCAAAGCTCC TTTTCTTGGG TGCTGCTTGG CATTAGTCTG GGGCTTCAGG 540 ATTGGTTGTC TTGGGGTTGA ATAGCCACAG GCTTGTTCCA GCCTTACTGA GAATGTCTTT 600 GGCAAAACTG CTCCCAGGAA AACTCAGGCT CTGAGTTTTG TGTCTAGTCA ATTCCATGGG 660 CTGGTAATGG CAGCCAGTGA TCTCACCTAG ATGAGGTCTG TGGTTCTGGG AATTCCTGGG 720 TCTTAACAGT AAGTCCCACA GCCCTGCTAA TCCCCACCAC ATCTGCCTTG AGGCAATTTT 780 AAAATAGCCT AGAATGAAGA GGCACACAGT TTTGGGTCTA ACAGACAACA GGGGCAGTTT 840 AACCCACTCT GCTTTTGCTC TCTGGTGTAT CAAGAATGAG CAACTTCCCC ACACTGGGAT 900 TGTGGGACTC TGAGTACCCA CTTCCCTTCA CTCAGCCATT CCAATTTCTT AAAGCAATTT 960 TTAAAAAATG GTGGTAAGGC CGGCCGCGGT GGCTCACGCC TGTAATCCCA GCACTTTGGG 1020
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