Tag | Content |
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EnhancerAtlas ID | HS044-11808 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr6:166062520-166063870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr6:166062666-166062681 | GAGGTTTAAAGGTCA | + | 6.2 | Rxra | MA0512.2 | chr6:166062667-166062681 | AGGTTTAAAGGTCA | + | 6.39 | ZNF263 | MA0528.1 | chr6:166063849-166063870 | CCCCTTCTCCCCTCCACCTCC | - | 6.5 |
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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 |
GH06I165648 | chr6 | 166062296 | 166063929 |
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Enhancer Sequence | GGGTGCCCTG CAGAAAGAGA ACTAGGTGAG TGCACACTGA CAGGCCCGTA CCTTTCAGAG 60 ACTTGGGTGT GCTCCACGGG TTACCTGAAG AGATCTCACG AGGAGCTTGC AGCTCCAAGG 120 AGAAGCTTGC AAGGGGAGTG AAGATGGAGG TTTAAAGGTC AGGAAAGGGT TCTCATAAAA 180 TCCAGTAACT TGGAAGGAAG TAGCAGCTAA AATAAAACCA AGCAGCGGAC TAGAAGGAAA 240 TAATATTAAG TGATAAGACA AAGAAAGCTG TCACCACTAG AAGCAGAGCA CAGGAAAATA 300 AGCAGGATGA TATCCAAACC AAGGGGGAAG AGTCAGTGAG GGGACAGCAA AGAGGCCCAC 360 TGAGACACTC CCAGAGACAG CATGAGCTCT AAACCCCAAG GAAAACCAGG GCGGAGGGCA 420 AACACGGGAA TCTAAATAAT TCAAGTGTCC CCATGAAGGC CCAGCCAGAG GGAAGGCTTT 480 GTCCCTCTGG CCCTGGGCAG AAAGCTCTCC CAGGGCAGAG TTCTGGTCAG CCTAGACCCC 540 TAGCCCCGGT ATACAGCAGC TCCCACTCTG CCCTGCAAAG CTGCTGAGGA AGAGGTGCAG 600 GGGTGCCCAC TGCCCCTGCT GTCCAGTCAA CTAATCAAAT CCCTGTCACA ACAGAATAAC 660 TTGTAATAAA TTGCTGGGGC CCCCTTTAGT GGTGTCATTA AATGTCAATG TCACTTGAGG 720 CTACATTTGC ACTCACTGGA GAAGCGCTAG TATCTAAAGC TCATGTTTCT ACAACAAGGC 780 ATCTGGTTTC TTTCTAAAAA GTAGTGATTT CTACCAGATG AAACTGGCTG GGCAGCTCTC 840 CAGTGGTTTA AACGATAGTT CACATCTTAA GCATGAAACC ATCAATTGCA TCAGTCAGAA 900 ACTGTATTAA AATAGAAGTG ATGCTTTCCA CGTTCAAATC TGTGCATGAC GTCAGAAAAG 960 AGCTGATAAG ATAACCACAA GGGGTAGTGA TGCGTGCAAT TTTTTTAATA TTCATCGTTT 1020 GACATTTTGG GATCTTGTGT AGGAGAAGTG GGAGGCCAGA GGAAGACAGA AATCGATCAA 1080 ATTTTAGGGG CTGACAAATG AAACCATGAT CCCAGGAGGA AGACCATAAA AACATGACCC 1140 CCTAATGAAC ACGTGAACAG CAAAGTAAGG CAATTCACCG TTAATTCAAT GCCACTTCGG 1200 TACCTTCTTG CTAATTCTGA AATTTAATTT TTGAATGGGA GATAAGTTAT ATTATTCAAA 1260 AATCAAAATG TATAAAACGG GGTAACACTG AAAAGTCTCC CCACAACTCT GGTTTTCCAT 1320 CCCCCAGGAC CCCTTCTCCC CTCCACCTCC 1350
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