Tag | Content |
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EnhancerAtlas ID | HS129-16636 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr17:80890610-80892120 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr17:80890794-80890805 | ATATTTACATA | - | 6.62 |
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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 |
GH17I082931 | chr17 | 80889160 | 80891485 |
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Enhancer Sequence | AGTGAGGCTC TGCTTTTCAT GACTTCCTTT CCGATTAAGC CTAAGTAGCT CATGTATTAA 60 AGAAAAAGTC ATCAGACACA GAGATCAGAA TTCCAGGAAA TGATCTTCCA GTGCGTTCTG 120 GGTCAGTTAT GGTGACTGTA AATACCGTCA TCACAGCTGG CCCTCAAAAT AACGCAATAA 180 TAACATATTT ACATAATGAC ATATTATGAC TGTAAGTGCA GTCAGCCCCA TCTGGGGCTG 240 AGGCGGGGGC CCTGCTGTGC ACTCTCCCCC CAGCTATCCC ACCGGGCCAG GGGTGGGCCT 300 CAGGGTTGTG CTGGGAGCCG CAGGGCCTGA AGGGGCCTCG GCTGTACGGG GATGAGACTC 360 GCAGGGGAGA GGGCAGAGGC CGGTGACCTG GCGAGGACTT GCCCAGGAGA TTGGAGCTCC 420 TTGCTTCTGC GCCACGCGGA TGCCCCAGGC TGGTCTCAGC TGGGTTGTTG GCTCTGAGTG 480 GTCATCTCGT TGCTGCCATA TTTTCTTGCT TCATTGAATT TCACCGTGTT GGGCCAGTCT 540 TTTTTTTTTT TTTTTTTTGA GACAGGGTCT AGCTCTGTTT CCCAGGCTGG AGTGCAGTGG 600 CACAATCACA GCTCACTGCA GCCTCTACCT CAGCCTCCCA AGTATCTGGG ACTACAGGCA 660 TGCGCTGTAG TCTAATGTAC GGCTAATGTT TGTATTTTTA GTAGAGACAG GATTTCACTA 720 TGTTTCCCAG GCTGGTCTTG AACTCCTGGC CCCAAGTGCC TGCCTTGGCC TCCTAAAGTG 780 CTAGGATTAC AGGTGTGAGC CACTGCGTCT GGCCTGGATA TATTTGTATC TGGGGCACGT 840 TGGGTCATCC GGAGACAGCG TGGTCTGTTT TTGGGGGCAC TGCTTTTTTT TTGTTTGTTT 900 TGAGATGGAG TCTTGCTCTG TTGCCCAGGG TGTAGTGCAG TGGCTCGATT TCAGCTCACC 960 GCAACCCCGT CCCGGGTTCA AGCAGTTCTC TCGCAGACTT CTGAGTAGCT GAGATTACAG 1020 CTGTGCACCA TCACACCTGG CTGATTGTTT GTATTGTTAG TAGATACAGG GTTTCACCAC 1080 ATTGGTCAGG CTGGTCTCGA ACTCCTGACC TCAAGTGACC TGCCCACCTC GGCCTCCCAA 1140 AGTGCTGGGA TTACAGGCGT GAGCCACTGA GCCTGGCTTG GGCGCTACTC TTAAGCTGTC 1200 AGGTGGACCC AGAGCTGTGC TGGTCTCCAG GGTTTTCTGC CCCTTTAAGG TCTCTGCTCC 1260 CTGGCGCTTC CCTTCCCACC GCTGCTGGGG CAGTGCCGGG GCTTCTGGCC ATCTTTTGGG 1320 TGGTTCGTCC CCAGCCTTGG ACAGCGTCCT CGTACTCAGG TACTGGCTGA CCCAGGCCCA 1380 GGTTAGTCCT CAGCGGCCCC CAGGAAGCCC CCTCTGGTGC TCAGAACCTG AGCGAGCTCT 1440 GCAGACTTGG AATTTCCCGC TTCTCACCAC GGGCTTCCCG CTGGAGTCTG CCACCTGCTG 1500 GACTTGGCTC 1510
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