Tag | Content |
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EnhancerAtlas ID | HS047-27447 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr5:132124120-132125530 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr5:132124412-132124423 | TTCTTATCTGT | + | 6.14 | Gata1 | MA0035.3 | chr5:132124412-132124423 | TTCTTATCTGT | + | 6.62 | HNF4G | MA0484.1 | chr5:132124605-132124620 | AGAGTTCAGAGTTCA | + | 6.11 | LMX1B | MA0703.2 | chr5:132124644-132124655 | TTAATTAAAAT | - | 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 |
GH05I132788 | chr5 | 132123792 | 132125460 |
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Enhancer Sequence | TTCATGATCT CCAGACAGCT TACCTGACAG GGTACTTGGA AGCTACATTG CATTAAGATA 60 ATTTCCCACA TGACAAAACA ATGATTTGCC TCTAGGGCTG GGCACATTGC TATCTGAAAA 120 AACTGGAGTC TGTTAGAAAA GAAAGAGAAT GGCTGTTGGG TAGGTGCCTG AAGGCACAAG 180 AGTTCACTTA GTCTGGCCTT CTGACTCCAG GTCAGGCAGG CTGAGTTCAT TTTAGATAAA 240 GGAAAGTGTC TGTTTTTCTG GTGAATTATG GATTTGGGGC CTGTAGAATT TGTTCTTATC 300 TGTGAAGTCC CACTTGGAGG GGAGGGGAAG GGCTGGCTCA CTTCTCAGGA TCCTGCTGGC 360 CCAGGTTATG ACTATAGAAG TTCCTCAACA ATTGAACACT GGGGTCATTT ACACAACAAA 420 GATTTACTGA GCGCTTACAG TGTGCCATGG GCATGAAGGT AAAGAAGGCA TGGATGCTGC 480 CTGCCAGAGT TCAGAGTTCA ACAGGCAAGC ACACATAAAA AGTATTAATT AAAATAATAC 540 ACAGACCAAC TTGACCACCC CTTTAAGAAA TCTGCCCTCA GTCAAGCAAA ATATGCTAAG 600 AATAAGATAA AAGGGCAAAA TACCAGCGTT ACAAAGCCCA AATCCTGAGC CACCTGGTAC 660 CAGCAGCCTG CTCCGGTCTC TCACTGCCAA CTTTTACCTA GTTCTTCCTT GTTCTCACCT 720 CACTCACCTT GCCCGCCCAG GGTGACATTC CTTTAGTTTT CTGCTGGCCT CCAGAACCCT 780 GTGTCTTGGC CATCCCCATT GTTCTTGCTC TCCTTGCCTC AGCAATCCTA CTGAAGGCAT 840 ACTGGTGGAC ACCTGATGGC TCAACCTGGC TCTCACCCTC CCAGTGTGTG CTCTGCTAGA 900 GCAAATGCTT CGCCCCCAGC CCAGGCTGTC TTGGTGGGAC CCAGACCATC ACAAATCAGG 960 AAGCACACTG CCCTGGTACC CCCTGCCAGG GATCCAGGGG AGAATGAGAG GAGGGAGATC 1020 GTCCCTGGAG ATGACATTTG GGCTGAGGCT TAAATACTAA TTTGCTCTGG TCAGCAGCAG 1080 TTTCAAACAC AAACGATGAG CCCACCCAAG GCAAAGACAC TCTCCAGGAA TGAAGCCAGG 1140 GCCTTGGGGA GCTACATTAG CTCTTCCAGG CCACCACTGA GAGAATGACA GCAGGTCAAC 1200 TCACATTACA CGAAATCCAT CTGCTTTCTC GGCATGCTCC TGAGCTGCCC AGAGTTTCAT 1260 GAGAAAAAAA AAGTATCACC AGCCCTGGTG CCTGACAGCA CTACATCCTG ATGCTTCCCT 1320 GCTCAGCAGG CCTCCCAGAG CTGCCTGGAA ATCCTGCACT TGTTTCTGGC CACCATCCTG 1380 TCCCTTCTCC ACAGCAGCAG CCCCAAATAT 1410
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