Tag | Content |
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EnhancerAtlas ID | HS047-08002 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr12:54580370-54581600 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF3 | MA0522.2 | chr12:54580625-54580635 | AACACCTGCT | + | 6.02 |
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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 |
GH12I054187 | chr12 | 54580941 | 54581090 |
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Enhancer Sequence | GCCTCAGCCT CCCAAAGTGC TGGGATTACA AACGTGAGCT ACCGTGCCCA GCCTGGGAAT 60 CTGTATTTTA AACAAGCTTC CCAGGGTGAT TCTGATGGTT GGTGAAGGCT GAGAACCACT 120 GTGTGTCACC ATGGTTACCG TCGTCTTAAT GAATTCCTTT TGCCTCCCCA GCTAAACTTG 180 GGCAGATCAA GAGCCAGGCC TTGTTCAATC TCCCTCCATA AGCCCAAGGT CCTGGCCCTT 240 ATTAGGTACT CAACAAACAC CTGCTCAGCA ATGTCCATCT TCTTTTTCAC TTTTGTTTAA 300 AACTACCTTC TGTGCTGGGC ACAGTGGCTC ATGCCTGTAA TCCCAGCACT TTGAGAGGCC 360 AAGGCAGAAG AATTGCTTGA GGCCAGGAGT TCAAGACCAG CCTGGCTGAC ATAATGAGAC 420 CCCATCTGTA AATATAAAAA TAAAATAAAC AGCTTTTACC AAGGAGGCAC TCCTGATGGA 480 TCCTTCTCCA CTTCTATATC CTGAGTTCAC TCAAGGCTTA GCTGCCCACT TTGCACTCTG 540 CTTGTTTTCC AGACTCTGGG TCTGTGCCCA TCATATGTGT GCCTCCCATG CGACAAGGAC 600 CATTGTCATT CCTTCCTCTC AACTTTCTGC CTGGGTCAGG AGTGACTTCT CCAAGATAAG 660 AACTCAAGGT TGACACAACA GCTCGATAAA CCTATTTTCT CACCCTAGCC TAGGGGAAGT 720 GGGAGAGAAA AGAAATCAGA GGCCCAACTT AGGAAGTCCT TCCCTGACTG TCTCAGTAGT 780 CTTTAACTGA TCTGTTGTCC AGGTGGCTAC CCAGGACAAA CTGGGCTCAT ACAAAAGCTG 840 AGAAGGGTGC TGTGGAGAAC GCCAGTGTTT CAGGGGACCT TGCTTTGCAT CTCCCCATGC 900 AACACCAACA TTAGCAGATT GGCTGCTCCA GCTCTAGAAT CTCGAGAAGT CTTGAGCCCA 960 CCTTTGACAT TTAGACACCT GTGTTGGAAA CAGCAAGGCT GGGGAAAAGA GTGGCAAGAT 1020 ACTACTTTCA TTGTTCCATA ACTTCAAAGC CTGATCTCAT AGCAAGAGCC ACAGGCTGGA 1080 AGTCAATTGA TTTGAATTCT ACTCCTGTTT CATCTCTAAG AAGGTTCTCT TGAGCAACTC 1140 ATTTAACTCT CTTCTCTATG GAAAATCACA TACTCCATCC AACCTACCAC CTGTTAACTC 1200 ATTTTTTTTT TCAATACTTA TGAGTCTCTT 1230
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