Tag | Content |
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EnhancerAtlas ID | HS052-18332 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr19:9988360-9989480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU6F1 | MA0628.1 | chr19:9988525-9988535 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr19:9988525-9988535 | ATTAATTAAT | - | 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 |
GH19I009877 | chr19 | 9988581 | 9988730 |
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Enhancer Sequence | GTGGGCTATT GACAACAAGA ATGATTTTGG TCCAATTTCC TCTCTCTGTG TCACTTTTGC 60 CTTCAGCCCT TTGGCCATGG GATAACCTTT GCCAGAGGCT GGTGCTATGC CCTTGGACTT 120 CCCAGTCTCC AGAACTGGAA AAATAAATTT TTTTTTTTAA GAAAGATTAA TTAATTGATT 180 ATTTTACAGA TGAGGTCTGG TTCTGTTGCC CAGGCTGGAG TGCAATGATG CGATCCTGAC 240 TCATCACAGT CTCAACATTC CAGGCTCAGT CGATCCCCCT GCCTTAGCCT CCTGAGTAGC 300 TGGGACTACA CACGTGCCAC CACATCTGGC TAATTTAAAA AATCTGTGTA GTCATGGGGT 360 CTGGCCACAT TGCCCAGGTG GGTCTTGAAC TCCTGGGCTC AAGCAACCCT TCCACCTTGG 420 CTGCCTAGGT GCTCGGATTA CAGGCGTGAG CCACCACACC CAGCCCTTTA TAAATTACCC 480 AATCTGTGGT AGTCTGTTAT AGTAACAGCA AACAGGCCGG GACACATACG CAACGTGATA 540 TTCAAGGGAG TGTGACAGAA TTGCCTATGG AATAAAAATA AGCAAATCGG TGCTGACTGG 600 GAACACAGAA AGGTGGGCTG GACCATCTGA GCTTCAATCT TGGCTCTGTG TTACCCTGGA 660 CAAGTGACTC TCTCTGAGCC TCAGTTTCAT TTCTCTCTTT TTTTTTTTTT TTTTTTTTTT 720 TTGAGATGGA GTTTCACTCT TGTCACCCGG GCTGGAGTGC AATGGCACAA TCTCAGCTCA 780 CTGCAGCCTC CACATCCCAG GTTCAAGCAG TTCTCCTGTC TCAGCCTCCC TAGTAGCTGG 840 GATTACAGAC ATGAGCACCT GGCATCAGTT TCATTTCTCA AACAGGGAAA CTGGCAGTAG 900 GTGATGAGAT GACCCTGTCG GCATTTTGAG GCTCCAGCGA GCTAATACAA CGGAAGTGCT 960 TCAAGCCCTG GTTCAGAGAG AGTGCTCAGG AAATACCAGT GGCTGTTTTC CAGATAGGAC 1020 AGCACCCTCC ACAGCTTCCC CACATTCACA GATAAGCAAG GAAGAAAGAA AAAGGAAGAG 1080 GCAATTATAA CAGGGTGTGA TAAGTGCCAC GATGCAGGGA 1120
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