Tag | Content |
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EnhancerAtlas ID | HS129-17953 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr19:17401490-17402930 |
Target genes | Number: 27 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr19:17402284-17402296 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr19:17402288-17402300 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr19:17401776-17401788 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr19:17401780-17401792 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr19:17401784-17401796 | AAACAAACAAAC | - | 6.32 | SOX10 | MA0442.2 | chr19:17402253-17402264 | GTCTTTGTTTT | - | 6.14 | Zfx | MA0146.2 | chr19:17401534-17401548 | GAGGCCGAGGCGGG | - | 6.01 |
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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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Enhancer Sequence | TAGGTGAGGT GCGGTGGATC ACGCCTGTAA CCCCAGCACT TTGGGAGGCC GAGGCGGGTG 60 GATCACGAGG TCAGGAGTTC CAAGACCAGT CTGGCCAAGA TGGTGAAACC CCGTCTCTAC 120 TAAAAATACA AAAATTAGCT GGGCGTAGTG GCAGGAGCCT GTAATCCCAG CTACTCCAGT 180 GGCTGAGGCA GGAAAATTTC CTGAACCCGG GGGGCGGAGG TTGCAGTGAG CCGAGATCGT 240 GCCACTGCAC TCCAGCCTGG GCGACAGAGT GAGACTCTGT CTCAAAAAAC AAACAAACAA 300 ACAAACAAAA ACAAAACCAA AACCCAACTA AAAGACAGAT TTGGTGGTTT CAAAAGAAAA 360 GTCTTCTTGA CAAAGGTGGC CCTAAACCAA GCTGAAAGAT ATAACACGGG AATAGTAAAA 420 GGTCCTGACT TGCTGGGTGG GGTTGGATGA GTCGAATTCA ATGAACCAGT GGGTGGCAGG 480 CATTCAACAC ACAGCCTGGA AAACAGTGGG CACTCAATTA TGGCAGCTCT AATTCCATGC 540 AACACCCACT GATCTTCACC TAAACCTCGG TTGGATCTCT TCCGGCCAGG GAAGGGCTCA 600 TCTCGTTTTT TTTTGAGAAG GAGTATCGCC TTGTTGCGCA GGCTGGAGTG CAGTGGTACG 660 ATCTCAGCTG ACCGCAACCT CCACTTCCTG GGTTCAAGCG ATTCTCCTGC CTCAGGCTCC 720 CCGAGTAGCT GGGACCACAG GCGCGTGCCA CCATTCCTGG CTTGTCTTTG TTTTTTGTTG 780 TTGTTGTTGT TGTTGTTTGT TTGTTTGTTT TAGATGGAGT CTCGCTCTGT CACCCAGGCT 840 GGAGTGCAGT GGCACGATCT CGGCTCACTG TAATTTCCGC CTCCCGGGTT CACGCCATTC 900 TTCTGCCACA GCCTCCCGAG TAGCTGGGAC TACAGGCGCC CGCCACCACG CCCAGCTAAT 960 TTTTTGTATT TTTTACTAGA GACGGGGTTT CACTGTGTTA GCCAGGATGG TCTCGATCTC 1020 CTGACCTCGT GATCCCCCCA CCTCTGCCTC CCAAAGTGCT GGGATTACAG GCGTGAACCA 1080 CCGCGCCTGG CCTGTCTGCA TTTTTAAATA GAGACGGGGT TTCACCATTT TGGCCAGGCT 1140 GTTCTCGAAC TCCTGACCTC AGGCGATACT CCTCGGCCTC CCAAAGTGCT GGGATTACAG 1200 GCGTGAGTCA CCACGTCCGG CCGGGGTCAC CTCTTGATAA GTTGCCTCCT GCCCTGGGGG 1260 ATACTGTCCA AGGAGCCTCA GCCTTCTGAG GTACGAGGGG AAATTCAGGA AGCTAACGTG 1320 GACACCAGAC ATTGTCGAAG TCGATCCTGA GCGCGAGGCA CCAGCCTGAG CCCAGTCTGC 1380 AGATGGGAAA ACTGAGGCTC CAGGCGGCGA ACACCCTGCC CTGTGGTCAC CCAGCACAGG 1440
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