Tag | Content |
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EnhancerAtlas ID | HS095-14204 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr18:77990940-77992620 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr18:77992432-77992447 | AATGCTGAGTCATAG | - | 7.33 | Nfe2l2 | MA0150.2 | chr18:77992434-77992449 | TGCTGAGTCATAGGT | - | 6.36 | RUNX1 | MA0002.2 | chr18:77992219-77992230 | AAACCACAGAA | - | 6.32 | TFAP4 | MA0691.1 | chr18:77991517-77991527 | AACAGCTGAT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CACGCAGGGA CCCCAGCTGC TCATCTCCTG AGGAGTGGAG TGGGGCTTCG TCAACATACC 60 ATTTATTTCA ATTGCATCTC TCTGATGTCT GCTGCTCCTG TCCATGCAGA CACACAGTGT 120 CACCTTCCAG GCAAACTATC CTACCTCTGA CAAAGGAGAA CATTCATGCA AAGTTTTTAA 180 ACAAAACAAA GCCACCTGAG GAGGTACAGG ATTTAACATT CAGCATCAAT CACTCATGTG 240 CCACCGCATA GCCGGTGACT GGAACCGGCG GGTCTCACAC AGGACCCAGG AGGCCTGTCC 300 CCACAGCTGG GCCTGCACTC CCTCTCATCC CTGCACCAGT ACAGGTGCTG ATGGGCCCAA 360 GGTGACTGCA GGCCATGGGG GTCAGTGCCA CTTCCTCTCC CTCATGAAGG ACCACTTTGA 420 AGCCAGAGAA GTTTATTTTG TCCCAAGGAA ACACCCCCTT ATTATTGCAG ACACCAGCAA 480 GGCATGAGGT CAGGACTGTG GGTGGAAAGC CAGTCAGGGA GGCCCCTGAG CCACGGGATA 540 CAGGTGCTAA CATTGCTTTT GTTTCCAAAT CCTCTAGAAC AGCTGATCAC CTAAAAATGA 600 CAGCTGTAAC AGCCCCAAAC TCCTTTCACA GCCTTAACCA GGAACCTCAG GGGCCTCACA 660 CCCGCACCCA GGTCCCCAGA AAGGGGCCTC TTGAGGGCTT ATGCACAGGC GTACTGTCCA 720 TCCTGTCTCA GAAGCAAAGG CAAAAAGAGA GATCTCACAC CTTAGAACTG ACTGATTTAT 780 AACCCAGCTT TTGACAAGCG TACTGATGTG ATAAGACAGA AAATAAATGC ACCCATTCAG 840 CAGGCAGGCT TTTAGGAGGA GCGGAGAGAT TCACACAGTG CTCTGACGGC CCTCGAGACA 900 CAAAGGCTTC ACGAACACCC TCCGAGTGTA GAAGGGATGA GCTGCCAACC AGGCAACCCA 960 GGCACACCTC CCAGGCTGAA GGTGGAGTGG AAGCTCTTGG CCCTGCGGGT GTCCACAGCT 1020 CACCATGAGT GAAGCTGCTG TGAGGTCTTC ATTCCACATG TCAAGTTCAG GCACGTTTTC 1080 CAAGAAAGAT TGTCCAACTT TCATTGTACA CAAAGGGCCC CAGCACAGCG ATGTCCTGGA 1140 CCTCTGGCAC AGTGTCAGGC CTGTTCTCAT CTCAGGTCCC AGCTTCTCCC ACAACATCCA 1200 GCCCACCAGA GGGACCCCAG AGATTGATCA GCTGGTGTGA ACTCAAGGAA AGCCAGGAAA 1260 TGCATAAGAA CAGCCAATCA AACCACAGAA TTCGAAGAAG GGTTGTGAAA GCCCTTCACA 1320 CATCAGCAGT AGGGACCTTA AATTCTGTAA GATAAAGGAT CTTTTCTGAT TTTGATTAAT 1380 CCACAAATAG CTAATAAGTT GTGGTTCAAG GCCTCCAGGA CCTACAACTG CCTCACCCCA 1440 AATCCAGACA GGGGTCACAG TCTCTGTGTA CACCAGAGCC AGGAACAATC CCAATGCTGA 1500 GTCATAGGTA AGATCAATGA CCGAGATCAC CCCCATAGGG CAGACTTGCA TCACTGAAAG 1560 CCAGTATTAG TGGGGCATGG TGGTGTGCAC CTGTAGTCCC AGCTACTCGG GAGGGAGGCT 1620 GAGACAGGAG GATCACTCAA GCCCAGGTGA GTGACTGGTG AGACTCACCA GTCACCAAGT 1680
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