Tag | Content |
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EnhancerAtlas ID | HS044-13613 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr9:116800150-116801580 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr9:116800279-116800290 | GCTTCCCGCCC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH09I114037 | chr9 | 116800107 | 116801028 |
| Enhancer Sequence | AGTGGCAGCC AAGGCACTTG CCTCGGAGAC CTGCTCTAAC TGGTGTGTCT GGGTGCTGTG 60 TGACCTCCTG CAGGAAGCTG TGTCTCCATC TCTAAAGCAA GGGCCTGAAA ATCCCCTTCC 120 CCACACCACG CTTCCCGCCC CCTGCTTTCC TTTGCTGTCA GCTGTGCCTC ACCAGGGAAG 180 GCCTTGAATG CCAGCTCAAG GTGTTTAGAC CCCATGGGGA AGCAGGATCC TCGGGCTAGG 240 GACAGCAGTT GGCAGGCTGC TTGGGAACCA CTGCCTGAAC ATATCGCTTG GTCCTGAGAC 300 TCCCACAGCA CAGCCTTCTG CACTCCTCCT CTGAATCCTC GGCACTCTGC CTGCGCCCTG 360 CCAGCTTCTG GAAGCTGAGC TGTGATTAGG GAAGAGCCTG GGTGCCAGTG CTTTCCCATC 420 CCTGGAGGCC ATTAAAATGC AAATCAGGTC TGAGCTTTGA GGTGGCCCCA CCTCTCCCAA 480 GCATCTTGAC TTGTTTTCGG AGTGGAGCCG TGGGCTGCTT TGTTCTGGTT CAGCGCAGCC 540 AGAGAATGCC TGGCCGGCCA TCCAGCGCAA AGCCAGGCTG AATCCCAGCC ACACTGAATC 600 GGGATTAAAG GCTTGGCTCC ATAGAGAGAA ATTAAGCATC ATGAGCTGCG CAGTTCACAG 660 CGCCGACGAT AAGGAGGATC AGCCTTGAAT AACACCAATC TCATTATGGA GCTGCTGAAT 720 GGCACAGGGT AATTCCCGCT AATAAACTTC CTTTCTGTGC TGTAGGAAAA CCTGGCGTGC 780 CTTGGTGACG TTGGAGAAGC ATGCTTTGGC AGTAATAATA CCAAAGATAG CTACAATTTT 840 GTGAGTGCTT TCTATGCGTC ACTTGTGGCA CTGAGAGCTT TACGCAGGTT ATTTCATCAG 900 ATCTTCCTGA TTAGGTAGTT GACGTTTTCA TCCCCATTAT GCAGATGATG AAACCGAGGC 960 TCAGAGAACA TAATCACTGG CCCAAAGTTG CACAGCTCCT AAAAAAAGTA TCCAATAGCA 1020 TTTGAGCTTT TACGTGGCGC CAGGCCTTGT TCTAAGACTT TTACATATAT TCACTTATTT 1080 AATTCTCGGA ACAACCCTCA GAGTTAAGTG CCCATAACAG TTCCACTTCA TAGCTAACGA 1140 AACGGAGGCA CAAACTGGTT AAGTAACTTG TCCAAGGCTA TGCAGTCACT GTGGCAGGCT 1200 ATAGATAGGA TTCCAGTTCT CGCAGTGAAC TCCAGAGCCC ATGCTCTCAA CATCCACCCT 1260 GTGCAGCCTC AGGTAGACCC TGATGGAAGG TTAGCAGAGA TGGAAGCCCT CTCAGAGGTC 1320 ATCTCTTTCA GCCTCCGCGT TAAAGTACAG CCAGGAGGAC CGCAGCTAAG AGGGATTGGG 1380 AGACTTTCCA GACAGCAAGC AAGCTGGCAG CTCATGGGTT TAGGATTTTG 1430
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