Tag | Content |
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EnhancerAtlas ID | HS129-12241 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr14:93192130-93193160 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr14:93192604-93192615 | AAGTAAACAAA | + | 6.62 | ZNF263 | MA0528.1 | chr14:93193051-93193072 | TCCCTCGCTTCCTCCTCCCCA | - | 6.06 | ZNF263 | MA0528.1 | chr14:93193045-93193066 | TCCTTCTCCCTCGCTTCCTCC | - | 6.76 | ZNF263 | MA0528.1 | chr14:93193048-93193069 | TTCTCCCTCGCTTCCTCCTCC | - | 7.65 |
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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 |
GH14I092723 | chr14 | 93189754 | 93193617 |
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Enhancer Sequence | GCTGGTCTCA AACTCCTGAC CTCAGGTGAT CCACCTACCT TGGTCTCCCA AAGTGATGAA 60 ATTACAGGTG TGAGCCACCA CACCTGGCCA CGGATTTTTT TAAATATAAA AGTGATATTG 120 TGCAACAACA TGGATTAATC TCAAAACACC ATAAGTTATG AGCTCATCTG ACCGGGCACA 180 GTGGCTCATA CCTGTAATCC CAGCACTTTG GGAGGCTGAG GCAGGTGGAT CATCAGAGGT 240 CAGGAGATCG AGACCAGTCT GGCTAACATG GTAAAACCCT GTCTCTACTA AAAATACAAA 300 AATTAGCCGG GCGTGGTGGC AGGTGCCTGT AATCCCAGCT ATTCGGGAGG CTGAGACAGG 360 AGAATCGCTT AAACCCAGGA GGCGGAGACT GCAGTGAGCT GAGATCACGC CATTGCACTC 420 CAGGCTGGGC AACAAGATTG AGGCTCTGTC TCAAAAAAAA AAAAAAAATT AAATAAGTAA 480 ACAAATAGCT TGTGAGAAAC AGACTGTGAG TCACCACCAC CTCCTTCCTG CACTCCCTGG 540 CCACTCCCTC TCGCCTCCGT CACTGCAGTC TGCCCAGCCT GTCTTTGGCC CCGCCAGCCT 600 CGATTTTTGC CCCTTGGCCC ACAAAACCTC AAATATCTAC TATCTGGCCC TTTATAGAAA 660 AAAACTCTGC AGGCCCCAGT CTTGAGCCAG ACAGCAATGG TGAGGCTCTG AGTGTGTGGG 720 GGTGGGGAAG GGGCTTGCCA GGAGCACACA GAGTGAGGAG CTCCCTGTTC TTGTCATTGG 780 TGACATGGCG CCTGTCCAAC CCTTTATCTA CTTCTGAGTG GAGAGGTTCT GTCAAAGGGA 840 AAGAAAGGGA GAGTTGCTGA CTGGGCCTTC TCCTCCTAAC ACGCCTCACC ATGCCCTCAC 900 CCTACCTTGC CGGTCTCCTT CTCCCTCGCT TCCTCCTCCC CATCTACCTG GGCCATGCAC 960 TGTCCTTGCA TGCCCTGTGG CCACCTTCCT TTCCACCAGG GCCCTGGCTT TGCTCAGATG 1020 ACCTACCCAG 1030
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