Tag | Content |
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EnhancerAtlas ID | HS052-18005 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr19:1324300-1326000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NRF1 | MA0506.1 | chr19:1325387-1325398 | GCGCCTGCGCG | + | 6.14 | PLAG1 | MA0163.1 | chr19:1325633-1325647 | GGGGGCCTGGGGGG | + | 6.28 | RFX1 | MA0509.2 | chr19:1325441-1325457 | CGTTGCCAAGACAACG | + | 6.03 | RFX2 | MA0600.2 | chr19:1325441-1325457 | CGTTGCCAAGACAACG | - | 6.16 | RFX2 | MA0600.2 | chr19:1325441-1325457 | CGTTGCCAAGACAACG | + | 6.2 | RFX5 | MA0510.2 | chr19:1325441-1325457 | CGTTGCCAAGACAACG | + | 6.23 | RFX5 | MA0510.2 | chr19:1325441-1325457 | CGTTGCCAAGACAACG | - | 6.23 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I001324 | chr19 | 1324339 | 1325941 |
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Enhancer Sequence | TACCCTCGGG GAGCCTACAG GACGTGAGCT TGAAAGAGCT GGTTATCTCC CCGTCTCTCT 60 GTCTCTCTCT GTCTTGGAAA TGTCTAAGGG GGCAGGCAGG AGGGCTTCCT GGAGGAGGGG 120 TCCTTTGAGC TGAGTTCAGA AGGGCGAGAA GGAGCCAGGT TTCTCATGGA GCAGCCAATG 180 CAAAGGGCTG GGGGCCACCT GGAGCCTGGT GTGTCCTTCG GGCAGCTGGT GTGGCTGGAG 240 CAGGGGATGC CAAGCCTGCT GAGGGCTTCA TGGGCCGCAG GGAGGAGTTT GGTTTTTCTC 300 CTGAGGGCAC TGGGGAGCCA CAGCAGAGTT TAGAGCAGAA GAAGGACACA ATTTGTGCCC 360 TGTGCCCGTG GTGAGCGGCG AGCAGGGAGG GCTGCCTGGA GGCGGGTAAG GACCTCAGAG 420 CGGAATTCTG CCACAGTGAA GCTTTGGAGG AAATCTTTCT TCCTTTTCTC TTCTTTTCCC 480 ATCACGGGTT GAGAAATTGG AGGGAGGGGC ATTGCTGGGG CTTCCTGTGC CCGCGTGTGC 540 GGGGGGTTCT GGGGCCTGCT GCCTGCCTGA GCCAGCCCCT TTTCCCGCCA GAGGCCTCTC 600 GTCAGTCCCC GGGGGGGCCC AGTGGTGACC TTGGGCCTCG GGGAACATCC AGACCTGGGT 660 CAGTGGCCTC GGCAAGTGCC CGGGGGATCC GCCCTCCGGT CCCCGTGCCA GTTTCCACAG 720 CGGGACAGGG GGGTCCCGGG GGCCGGGAGT CCGCAGCCCC GAAGACCTAC GCTGCCGCCA 780 GCCACACCCC TGGGGGTCCG ACCCTCCTGG GTCCCACTTT ACAGATGGAG GAACTGAGGC 840 GGTGACTCTA ATCTTCGCCC GGCCTGAGTC GCGGGGCTGG AACCCGCAGC GTTTGCCGAT 900 TCCCAGGGCC CGAGCGCTCC GGCGAGTGTG TGTGTAACGC CCTCTCCCTG GACGCCTCGA 960 GTTTAGGAAA CGGCGGAGCC GCCCGGATTG AAATTCTCGG CCCGTGCACG CCCGGCGGAG 1020 AAATCCATGA CGCATTGTTT AGACAGACGC CTTTAAACCG CGCCGCGGCG GGGGGCGGCG 1080 GCCGGGGGCG CCTGCGCGGG GAAGGTCACC CTTTTTTTCT GCACAAAGGT CAGCCGTAGA 1140 CCGTTGCCAA GACAACGGCC GGCGTAAAGA TGGAGGCTTA AGGAGAACAG ACAGTTCCCC 1200 TCCCGAAGAT GCCCCGTGCA AAGGGCCCGG CCGTGGGCTT GGGAGGCTCA GGGGGTGTGA 1260 GGAGCTGAGC GCCGGAGCAG AGAGAGCGGA GAGTGGGGCG CTGGGATGGC TCTGGGAGGC 1320 CAGGAAGGAA TGCGGGGGCC TGGGGGGCAG ATCTTGGCTC AGGCCCTGCC AGGCTGTCTT 1380 CAAACCAATG AGCCTCAGGG TTCCTGGCTG TGAAATGGGA ACAACGTCTG CCCTTCAGGG 1440 TAGGCATCTC CAGGCTGGTC TGGTGTGGGA ACCGCTGTGT TAAACATGCA GACTCCAGCC 1500 AGGCGCCGTG GCTCACACCA ACGGGGCACA GTGGCTCACA CCAACAGGGC ACAGTAGCTC 1560 ACACCCGCCG GGCACGGTGG TTCACACCAG CCGGGCACGG TGGCTCACAC CCGCCGGGCA 1620 CAGTGGTTCA CGCCAGCCAG GCACAGTGGC TCAAACCCGC TGGGCACAGT GGCTCACACC 1680 AACGGGGCAC AGTGGCTCAC 1700
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