Tag | Content |
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EnhancerAtlas ID | HS129-17330 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr19:868950-870420 |
Target genes | Number: 57 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr19:869558-869569 | TGTGACTCATT | + | 6.62 | MYC | MA0147.3 | chr19:869240-869252 | CGCCACGTGCCC | + | 6.74 | Nr2f6(var.2) | MA0728.1 | chr19:870344-870359 | GAGGTCAGGAGTTCA | + | 6.22 | Nr2f6(var.2) | MA0728.1 | chr19:870077-870092 | TGACCTCTTGCCCCC | - | 6.4 |
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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 |
GH19I000868 | chr19 | 868078 | 874050 |
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Enhancer Sequence | CGGGAGAGGG GAGAACGTGA GGGAGGCCTG GGCACCACGA GGCCAGGTTC CGGCAGGGGC 60 ATCTGTCCAC AGGCGGGGGT GGAGGGAATG GCCGGCCTCA CACCATCTGC CAGGTGGGCC 120 CAGATGTCTG TGAACAGTGA GGTGGGAGGT GCGGGACCAC CTGAGACAGG CCCAGTAAAG 180 GGGGCGGGAC CCCCCACACG GAGGAGGGTT GGTCTCCCAG GTGCCTGGGG AGCTTGAGGC 240 TTAGAGACCC AGTAAAGGGG ACGGGGCCCA CACAGGGACG AGGGTCGGTC CGCCACGTGC 300 CCGGGGAGCC TGAGGTGCAG GGAAGGTGCT TGTGACGCTC CCATTTGAGG CTGGACAGAA 360 GCAGGTACAT GGGGACTTCC ACACCACCTC TGCCCAGACA CCCGGCCTGG AGGTGCCGGG 420 ACCTCTGAAC GACAAGATTC TGGTGGCAAA AGCTGCCCTC GGTGGTGGGT GGGGGACCTG 480 GGTCTGGGTG GGGGTGGGCC GGCTTATTCT GCTCTCATTA AATATCTGAA ATTTTCCCAG 540 TTTACAAGCC TCTGACGTAA CCGTCCTCTC TTTCCATCAA GTCTTTTCCT GAAACCCAAA 600 CCCTCGTGTG TGACTCATTA GGAGGCCCCT CCCACAGTGA GCACGAGGAA GAAAATGCTG 660 GAGGTCCTAG AGCCAAGCCA GGGCGCCTTC CCGGAGGTCC CGGAGCCAAG CCGGGGGTGC 720 CTTCCCTGGA GGTCCTGGAG CCGAGCCGGG GCCTTCCCCG GAGCAGGGCT GCTGGAGGTT 780 CACTTCATTT TCTTCCTTTT GCTCATCTGT GTTTTCTAAA ATTCCAGCCC TGAGCAATCA 840 GTGGCTCAGA GGGTTTGCAT GTGCTCCTTG TCAAACGTGT GTCTGAAACA GGCTGGGGGT 900 CTGACGGGCC TGGGTTCAAA TCCTGACTCG GCCACTTCCT GACCGCGTGA CCCCAGATGA 960 GTGGGGTGAC AAGGTCCCAC CCTTTCCAGG CTGGGTTTCC TCACCGTGAA ATGGGGTGAC 1020 AAGGTCCCAC CTCACAGGGC TGCTGGGCAG CCAGGGTCAG CTCAGCACAC TTGGGTTGCC 1080 CAAACCCCGC ACATTCCAGA GAAAGGCCAG CCCCGGGCCC TGCAAGGTGA CCTCTTGCCC 1140 CCGGGAGATC CTCCTGATGA GGTGTCTGCT CAGCAGGGCC CTGGGCCATA TGCTAAGGCG 1200 TCTCTCTCCA TCCACAGAGG GATCTACGGC GAGGCCTGAC ATCCAGGGGG GCCAGAGACT 1260 AAGGGCAGAG GCTAAGGCAG GGCGCCCTGT ACAGCGAGGC CAACACACAA TCAGGAAACA 1320 CCAAGGCAAG GCCGGGGCGG TGGCTCACAC CTGTAATCCC AGCACTTTGG GAGGGCGAGG 1380 CAGGTGGATC ACCTGAGGTC AGGAGTTCAA GACCAGCCTG GCCAACATTG CAAAACCGCC 1440 TCTATACCAA AAATACAAAA AATACCTAGG 1470
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