Tag | Content |
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EnhancerAtlas ID | HS044-11970 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr7:26476410-26477400 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr7:26476524-26476539 | TTATGACTCAGCATG | + | 6.48 | Nfe2l2 | MA0150.2 | chr7:26476522-26476537 | CTTTATGACTCAGCA | + | 6.32 | RARA(var.2) | MA0730.1 | chr7:26476465-26476482 | GGGTCATCTGGAGGTCA | + | 7.33 |
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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 |
GH07I026437 | chr7 | 26477083 | 26477150 |
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Enhancer Sequence | ATGATTTGTG TTTTTATTTT GATGATCATC TAAATAATTA GTAGAGGAAT ATTATGGGTC 60 ATCTGGAGGT CAGACAAAAA ACTTAGAACT GCCATGTGAT TTCGGGTCTC GACTTTATGA 120 CTCAGCATGG CTCACATGCC CCTTAAGTGA CAGAGTTTAA CTTGTAATGC ACTATTTCTC 180 AGATTGGGGT GTGTGCGCTT GTAATTTTAA GGATCTACAA GTTCTTACAT TTGGGAAACA 240 GTGATAGAAA CAAGAAATGC TTCCTCGGAG GATGGATTAG TGATATTTCA TCTGGGGAGC 300 CAAGCAAGGG AAGGCTTTCT GAGGGAGCTG GCATCTTAGA TGGCCCTCAA GGACAGACCC 360 TGTGTGCCTT CTCTTATCAA GTGTCCACTT AAAGGAACTG CTTGATAAAA ATCCCCCGCT 420 TCCAGAGGCC ATTCATTACT CCCTGGTTAT TCTTTGAGAG CCTCTGTGTG TTAGTTCTGT 480 TTAATTACAG TGTGCTGCAG ACTGAAGAAG GAATGCAAAC ATTGTGTGGA GGGAGGCATG 540 AGAAAAGAAA GTGTGGGGCT TCAAGAGGGA ACAGGAAATA GTTCAGTTTA ACTACAGGTC 600 AGGAGATGCA GGGTGTAGTG GGGCATGGGA TGCAAGGCTG GCGATGGCCT ATTGTGAAGG 660 ACAAGGCATT TTTTTTTTCT CTGTGTTTTA TCCCCTGTAA TTAGGAAGGG AGTGTTTCTG 720 CGTTGTTTTT TTTTTTTTGC TGGGGTAGTC ATTTTATACT GATGGAGATG ATTCTGACAA 780 GGCTGCAGAT ATGTCTGCAA GTCATGACAT GCTGACAAGT CATGATAATA TTGTTGAATA 840 ACTATCTTAG CATCATTTTG TTGAAGAGCT CTTGCTTACC TGTAAAGTTT CTGGGCACAT 900 GGGAAGTTTT TAATTCATGT ATCATCTTTG ATTTTTGTAG AAGACATATT TTTAATGTGT 960 GCCTTGCCTT TGCTGAAGGC TGTAGCTGGG 990
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