Tag | Content |
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EnhancerAtlas ID | HS044-13370 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr9:80077690-80079420 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr9:80078641-80078656 | AGGTTCAATAGGTCA | + | 6.27 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCTCGATCCC TGACTCTGTC ATCTCCCTCA CCACCATCCC TGCCTCACCT TTTCGGGTTC 60 AGGGAGAACT GGCAGCTTTA AACTTCTCCC CAGGGTCCCC AGATGCCCAG TCACCAAGTT 120 CCTCCACTAG ATCTGCTGCA CTTAGTCTTC CCTGTGGGGC TCCGTGCCTC TCCAGCAGAG 180 GAGTAACCCA CTGGAGTTCT CTCTTCTAAG ATGTCTCCAA CCCAAGGGTA ATAAACAACT 240 CGAGGGTAAT AAACAACTTG GGTTGGCAGC ACAGATTAGG AGAGGGGGTG TCAGATCACT 300 AAGCTCTGAT CTTGATCCTC TGCTGCGAAT GCGAAGGGCA CCATTTCCAA ATACAGAGTC 360 CTACTGCATC CCCATTGGAT TTCAGAGCAA AAGTGACAGT GGAATGTGGG ACTGTAAAAA 420 CTCCCACACC AGTAAGTAGA CCTCCTTTGC TCTCTGGATG AGGAAAGATA CTAGGAGTCG 480 CCATCACAAT CAGATGCGGC AACAGTGCAT CTCAAACAGC TGACACACTT CAGGCAATGC 540 CAATAATAAT TCTCTACTCA AGACAGCCAA GAACCAGAGC TGCTCATAAA AAGCTTGGAA 600 TCAGTGGATG TCACTTAAAA AAAGAAAAAA ACCAATGTTG TATTATATGT GGACCAGTCA 660 GTTCTCAGAC AGATGCTAAC CTTTGCTTTT AAAAATCTCC CAGCCCGGGG TAGGACCAAG 720 GCCAAGGGGA TTAAATCTAA GAAAATGGAC CTTTATCCTT AACCTTTAGT TTTTAACTTC 780 AGCCAAACAT TTCTGTCATT TAGAAAGTGT GATTAACTTT CAGATAAGTG TTTTTGTTTC 840 TTCAGCAAAG AACACATGTA GTTTCTCAAC CAGTATCAGC AGCAATGAGA AATGCCTCAA 900 AAATAATTAT TTGGCTTCCA TTTCAGGAGT GGCTGGTGGC AGAATCATGC CAGGTTCAAT 960 AGGTCAATAC CCCAGGAACC CCCACCAAGG ACAGGAAATA TTGGGATAGG AGAGCAGCTT 1020 GGAAGTTGGA CAGAACCAGG CTGATGGCTG AAATTTAGAA AGAATCCTGG GGCTGTCTGG 1080 CTTTATGTGG GTAAAAGTGC ATGTATGGAT TCCTCTCTCT TATGTAATTG CTTTTTATAT 1140 CAGCAAAGAA AAGAAAGAGA AATATATAGT TATACTGCCT TTTATCATTA CTTACATAAT 1200 TACCTTAGCT GGAACTGGTT TGTTGTTGTT GTTTTTGTTT TTTTGAGACA GGGTCTCGCT 1260 TTGTTGCCCA GGTTGGAGTG GAGTGGTGTA ATCTCAGGTC ACTGCAACCT CAGCCTCCTG 1320 GGCTCAAGTC ATTGCCCTAC CTCAGCCTCC AGAACAGCTG GGACTATAGG TCCTTGCCAC 1380 CAAGTCCGGC TAATTTTTAT ATGTTTTGTA GAGATGGGGT CTTGCCATGT TGTCCAAGCT 1440 GGTCTTGAAC TCCTGGCCTC AGGCAATCCA CCCACCTCAG GCTCCCAAAG TCCTGGGATT 1500 ACAGGCATGA GCCACCATGC CCGGCCATGT GTGTATGTGA GAGTGTGTGT ATATATATGT 1560 GTGTGTGTGT GTGTATATGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTTT 1620 AAATGTGGAT TTGAATTACC TTTTAGCGTC ACTAACTTTT AACGTGAAGA CCATCTTTAA 1680 GTATTTCTTT TTAAGATGGG CTTCTAGCCA CAAAGTCCAT TTTTTTCTTT 1730
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