Tag | Content |
---|
EnhancerAtlas ID | HS047-32497 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr8:29230060-29231480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYB | MA0100.3 | chr8:29230356-29230366 | GACAGTTGGT | - | 6.02 | ZNF263 | MA0528.1 | chr8:29230401-29230422 | CGGGGAGGAGGAGAAGGGAAG | + | 6.16 | ZNF263 | MA0528.1 | chr8:29230647-29230668 | CTTCCCTTCTCCTCCTCATCA | - | 6.3 | ZNF263 | MA0528.1 | chr8:29230404-29230425 | GGAGGAGGAGAAGGGAAGGAA | + | 7.55 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr8 | 29230223 | 29230556 | chr8 | 29230447 | 29231437 | chr8 | 29230784 | 29230978 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH08I029372 | chr8 | 29229801 | 29231737 |
|
Enhancer Sequence | TATGACGGGG ACCATGCGAT TGCTCCCAAT TTACAGATGA GGACAGTGAG GAACGCACAG 60 CTTAGGTCAC TCCCTGAGGT TCTCTGGTAG GAGCTTGCAG GTGGTAAGCT CAGGTGGGCT 120 CGCCCCAGAG ACTCTTGAAA CCTCCACAGT GCTCACTGAT GTGCACAGGT GGAAGGGCCG 180 TGGATAGCCC TTCAGAGACG CAGCAAGCCT CTGTGACCGG CCCAGGGGTG AGCAGGAGGT 240 GAGCTCTGAT AGGCTGTTGG GGAGATGGCC TTCACAGGCA GTTCTTTGTA CCCAGAGACA 300 GTTGGTTACC CAGGGGAAAT CCTTCCTGAC CATGGAAATC CCGGGGAGGA GGAGAAGGGA 360 AGGAAGTGGA GAGGCTGCAG GGAGGTGCGG GCCCCCAGCG CCAGGGGTGC AGAGTGGGCA 420 GGCCGGGTGC TAACTGCCCA GGGGTGTGGC AAGCAGGGCC CTTGCTAAGG GTGCTTCCCA 480 GACAGCCGCT GCAGGCTGTG GCCTTGATCA GGGAGAGTGG GAGATGAGTG CCCTTGTAGC 540 CCGTAAGGGG CCGGGGCTCA GCGAATGGAG CTGCTCTCGG CAGGAGGCTT CCCTTCTCCT 600 CCTCATCACA TCCGCTGGAG TGAAAGGAAG AAAAGGATCT CAGGAAGAAG GCCGAGTGGG 660 AGCAGGCCCT GTGCAGCCGC AGGCCCCCCA GTCCCCCTTC TGTCTCTTAC ATAACAGAAG 720 AGACTGCTCT CTCCCGGCTC TCCAGGCGAG GAAGCCGAGT GTGTCTGCTG CGTGTGTGTT 780 TCTGCTGCCA GCCACTGCCC AGAGGGGCCA CCGGGCGCGT CACAGCCTCT TCAGCCTAGT 840 ACTGAGGGCG GAGGAACTCC TGACTCATCC TCAGCCCTGA GTACTGCAGA GCCGCTGGCC 900 AGCTGCCTGC CTGGGTCACA CGGCTGCCTC TGATGGCCGG AACCTAGCAG AAGGGGGGCT 960 TTCGGAGCCC CTTTCCACAG GCAGTCCCGG CCGGTGGGGA AGAGGATCCC ACCGTGGTTT 1020 TGCAAAGAAG ATAACGCCAT GTTATTATGC ATTCATGCTA CAAAGACATA GTGACTCCCA 1080 GAAGGGCTGG GTGCTGCTCT GGGCAGTGGA GCCACAGCAG CGAAAAAAAT GAATGAGAAA 1140 CCCTGCACTT GAGGATCACA TGTTTCTAGT GAATGAATGA GTGATGCTAA CCAGATTCGT 1200 GAAAATTCTA TGCAGCCTGA AGCTGAGGTT GTCCCATGGG GCATCCCCAT CCTGTGCCCT 1260 GCCTCCACTC CAGACCCTGT GCTGCCTGGG CTACCTTATC TTGCCTCCTG GTCCTGGCCA 1320 CCCCTGGAGT CAGTACAAAT TATATGGAAG GCCAAGATTA GATCCAGAGC TGTGGGCCTC 1380 TTCTACCTGC CTGGCTCACA TCACAGCCTC CAAAAGGAAC 1420
|