Tag | Content |
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EnhancerAtlas ID | HS184-08350 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:102285000-102286000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr12:102285870-102285881 | ATATTTACTTA | - | 6.14 | FOXC1 | MA0032.2 | chr12:102285927-102285938 | ATATTTACTTA | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 102285059 | 102285855 | chr12 | 102285250 | 102285626 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I101888 | chr12 | 102282578 | 102287673 |
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Enhancer Sequence | GAATTATGTT TTTTTTAGAT TCTAAGTCCC TATCAATCAT CCAAGCAATT AGTGTATGAG 60 TTTGGAACAA TCTAATAAAT TTCAGGCTGG AGACACACAT GATGTTGCAT TTTGTTAGCA 120 TCTAAGTTCC TCCAATAAAC CATAATTCTA GGCTTTGGAA TATTTAAATC CTGTGTATCC 180 AGTAACTTAA AGAACAAAGT TTGACCAAGC TTCAGAAAGT CTTCTATTAT CCAGCATGTT 240 TTCTTTGTAT CGTTTTCATT CCTTTCAGTA TCAAGTGATT ATTCACTAGC TTAACATCAT 300 AAATTAGTTT GAAGTAGGAT GTTACACAAA CGACTTGGAA TTTTCCACAG TCTGCTTAAC 360 TTGCAGAAAT GTAAATACAG GAAATGTGGA CATAAACGGA TTTCCTAGGC ACAACCTACC 420 CCTAAAATAA CTGTGTATAC ATAACAGCCT CAACAGCTTC TGAACCACAG GCAAATGAAC 480 AATTTGCTGG CCTTGTCCTC TTTACAGTTT CCAGAAAGTG CCTTATTAGC AAGGAGGCAA 540 ATCAGGTGGT GGGTGGAGCT GGGCAGGGCC CACTGCACTG CAGAAACTGT GTGGTGCAGA 600 ATGATGTGGT AGGAGCTGGG TAGAGAGACT ACTGCTGCCA GGCTGGGAAG CAACTGGTTT 660 TGCCTCTCAC TCATTCTCCA GTGTACTGAA TCAGGCACCC AGGCACAGTT AGGCCACCCA 720 AATACTACTA CCTCTGCCCT TGCATGATGG AATCATTTAG CTTGAGCTTA AAAAAAATAA 780 ATAAATAAAA AGAGGTTACC CACAGGGTCT CTTGGTTACC TCTTAGTGTT TACTTATCTG 840 GATTCCAGTA TCACCAGAAT ATGTGACTTA ATATTTACTT ATGTATGCTG TCCAAAAAAG 900 CAAAAAACAA ACCAACAAAA GTAAAAAATA TTTACTTAAT ATATAAAATC AGACGTGGAA 960 AGACATAAGA ACATTTTTCA TTGAGAGGTA AGAGCTATTT 1000
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