Tag | Content |
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EnhancerAtlas ID | HS047-15455 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr17:79466510-79467530 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr17:79467322-79467337 | AGGTCAGCCTGTCCT | + | 7.24 | INSM1 | MA0155.1 | chr17:79467114-79467126 | TGCCAGGGGGCA | + | 6.62 | ZIC3 | MA0697.1 | chr17:79466793-79466808 | GAGCAGCAGGGGGCC | - | 6 | ZIC4 | MA0751.1 | chr17:79466793-79466808 | GAGCAGCAGGGGGCC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 79467092 | 79467468 | chr17 | 79466809 | 79466898 | chr17 | 79466947 | 79467007 |
| Enhancer Sequence | GTCCTGCAGC CACGAGGGGA GGGGACGCCA CAAATCCGGG TGCCGACCCG GGCCAGGAGA 60 GTCGGGAAAT GGGCCTTGGC TGGGACCCAG GCCGACTCTG ATCCCGCGGG CCTCGTAGCC 120 CCTCCAGCCC TCGGCCATGC AAAGTGGGGG TCCCACGGGA TGAGCCCCAG TGTGGGAGCC 180 CAGCTCGGAC AGACATCACC CCTCAGTCCC CCGACCCTCC GCCCCAGGAG AGAAGCTGGA 240 CGCTTGCCTG GGCGACCAGG TCCAGGCCAC CCTAGGCAGT GAGGAGCAGC AGGGGGCCAT 300 GGCGAGAGGA CAGGGAGGGC CTCTGTTGGG CCTCGGAGGT GGAGACCCCA CTGCTGAGCC 360 ACAGCTGGGG CATGCATTGG CTTTCTTCTG AGCATCTGTC TGGGGAACCG CCGTGGGAGG 420 AGCAGAGCCC CTCGGGCACT GGTAGGGAAG CCAGGCTGCC AACAGCCCTG CCACCCTGGC 480 TGCAGGTTCT GGAGCCGGGG ACCCTCTAGG CTGAAGTTCT CCAAGTGGGT TGAGCCCAGG 540 TATCCGTTTA TCCTAGGTAG GCCTCCATGC CTGAAGGTCC CGGGCTCCTC TGGACCACCC 600 GTCCTGCCAG GGGGCAGACA GGCCTCCTGT CCCTTCCTGT TCTGTTCTGC TCCCTAAACT 660 CCAAGCTAAG TGTGTCCCTG GGCAGCTGGG TCTTAAGAGC CTGAAAGGCT GCATGGAGTC 720 TGTTTGTTCG TTCAGAGGAA TCTCAGCTAT TTCCTGGGAG GCTCCATCTG AGCCTGGTAG 780 GTCCCGGATG AGGGGTGGGT GGCCCGGTGA GCAGGTCAGC CTGTCCTCAG GGGCTTGCAG 840 CACACCCGCC AGGGTGGCAA TTATCCAAAA TATAGAAAAC AAGTGCCACT GAGGATGTGA 900 AGCAACTGGA ACTCTTGTCC ACTGCCGATG GGAATGCAAG ATGAGGCAGC TGCTGTGGAG 960 AACTGTTGGT TCCTCAGAAA GGTGCACAGA ATGACCCTAT GACCAGCAGT CCACGCCGGC 1020
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