Tag | Content |
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EnhancerAtlas ID | HS047-18019 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:52714750-52715930 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr19:52715341-52715353 | GTTTGTTTGTTT | + | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 52715075 | 52715537 | chr19 | 52715783 | 52715853 |
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| Number: 2 | ID | Chromosome | Start | End |
GH19I052213 | chr19 | 52715281 | 52715430 | GH19I052212 | chr19 | 52715722 | 52719219 |
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Enhancer Sequence | TCTCTGCCTC CTTGGAAGCT CCAAGCTCCC ATCTCAGCTC CAACCTTCTC TAAAGCCTCA 60 GACTCCTTTT GGTCTAGCTG GGGCCCAAAT GCCCCTGAAC TCTCTCCACT CCCACTCCTG 120 CTTACCACCT GATAGGCCAC ATCCTCGAGA GTTGGTCTCT GGACACGGCC ACGTGTCAGT 180 TTACCCACCT CTGCCCCCTT GCTCACTTAG GAATTGAGAT GATGACAGGT CCTCCTTCCC 240 ACTGGTTAAT GTGAGGATTT AAAAGAATTA TCACACATAA AGTGCTTAGA GCAAAATCTG 300 GAACATAAAA ACTTTCAGCA ACTTACATCT GATGGTATCT CCAGCCTGTC CCAGGTCCAG 360 TGCCTTTGGC AGATAAACCA CCTCAGTTTT CAGCCTCCTG CTCGTCTACT TTGCAAACGA 420 TTGACCGTCA AGCCCGGGTT TGAGCCTGAC TCACTCCAGA ACTCTGGTTT ATGGCTGTAC 480 ACTTGCTTAG ATACTTACAC TGGCCCCCAC CGCCTTTGAT CGAAGCAATT GCTGCTGAAA 540 AATAAAGCCT TTCTGTGGCT CTAGACCTGC CTCTTAGTTA AGCAGTTTTT TGTTTGTTTG 600 TTTTTTGAGA TAGGATCTCG CTCTGTCATC CAGGCTGAAG TGCACTGGTG CAGTCATAGC 660 CCACTGCAGC CTCAACCTCC TGGGCTCAAG CATTCCTCCT GCCTTAGCCT CTCAAATAGC 720 TGGGACCACA GGTGTGCAAC ACCACGCTGG GCTCATTTTT TATTTTTGGC AGAGATGGGG 780 TCTCACTATG TTGCTCAGGC TGGTCTTGAA CTCCTGGGCT CAAGCAATCC TCCTGCCTTG 840 GTCTTCCAAA GTGTTCAGAT TACAGGTATG AGCCACTGTG CCTGGCTCGT TGGTTAAGCA 900 ATTTTTATGG GAATGATGTA ATCGTCAGCA CTTAGCATTG ACTAGATTTA TTATGCGCAA 960 TCTGCGAAGT GTCTCACACA CACTATTTTC ATTTAAACCT CATGCGGACC TGTGGGGTAG 1020 GTACTGTTAC TATCAGCTCC GTTTCATAGG GCTGGGAAGA CAGAGAGGGG GTCATCACTT 1080 GCCCAAGGTC ATTCAGCTAA AACCTGGACC CACACAACTG CAGAGTCTGT GCTTGCTCCT 1140 CTCTGCCATA CTGCCTGCTG CCTCAGGATC CCCGTCCCCG 1180
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