Tag | Content |
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EnhancerAtlas ID | HS044-09252 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr3:129248330-129249710 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr3:129248421-129248431 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr3:129248421-129248431 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr3:129248421-129248431 | ATTTTCCATT | + | 6.02 | RREB1 | MA0073.1 | chr3:129249371-129249391 | ACACAACACACACACACACA | + | 6.19 | ZNF263 | MA0528.1 | chr3:129249548-129249569 | TCTGCCCCTTCCCCCTCCTCC | - | 6.07 | ZNF263 | MA0528.1 | chr3:129248685-129248706 | GAGGCAGGGAGAGGGGAAGAG | + | 6.12 |
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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 |
GH03I129530 | chr3 | 129248844 | 129249644 |
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Enhancer Sequence | GTGCTGAGTC AGACCCAGGC TGGGCACTGA GGGAGAGCTG GGCAAGCCAG ACCCCTCCTC 60 TCTGGGGGCC CAAGCTCAGG GTGGGAAGTG GATTTTCCAT TCTCCAGTCA TTGGGTCTTC 120 CCTGTGCTGG GCAATGGGCT CGGTCCCCTC TGGCATCCTC TGCCTCCCCT CTCAGCCCCT 180 GTCCTCAGGT GCCCCTCCAG CCTCCCTGCC GCGTTCCAAG TCTCCTGGTG TTGAGAACCG 240 CAAGCAGCCG CTCTGAAGCA GTTCCTTTTT GCTTTAGAAT AATGTCTTGC ATTTAACAGG 300 AAAACAGATG GGGTGCTGCA GGGATAACAG ATCCCACTTA ACAGAGAGGA AAACTGAGGC 360 AGGGAGAGGG GAAGAGACTC ATTTAGGGAT GTGGCCAGGC AGCAACAAGA GCCTAGGTCT 420 CCTGGCTGTG ATCCAGGAAT ATCTCTGCTG AGATGCAGGA GGAGACGCTA GAAGCAGCCA 480 TTGCAAAGCT GGGTGACGGG GAGAGCTTAC CGCCAGCCAC AAGCGTCTCT CTGCCAGCCT 540 TGCCCTGTCT CCCCCATGTC CAGGCTGCTG CCTCGGTCCC ATTCTCAGGG AATCTCTGGC 600 CATTGTTGGG TGTTTGTTGC ATTCAATAAT CACAGATCAC TCAGTTCTGG CCAGAAGGTG 660 GGTGTGCCAC TTACGGGTGG TTGTTCTCTG CAGGGTCAGT CCCAGTTTAC AAATATTGTC 720 CCTTTCACTG TTAGGAATGT CCCAGTTTGG TTGATTAACT ATATGGCCAC TCTCCCTATG 780 GAACTTCATG GGGTGGTGAG CAGGACAGAT GTCTGAATTC CATCATTTCC TTCTTCTTCC 840 TCTGGGCAAA ACATTGCACA TTGCTTCATG GCTCCTAGGA GAGGCCCCCA CATGTCCGGG 900 TTATTTCATT TCCCGAGAAG GGAGAGGGAG GAAGGACTGC CAATTCTGGG TTTCCACCAC 960 CTCTGCATTC CTTCCCAACA AGGAACTCTG CCCCACATTA GGATGCATTC TTCTGCTAAA 1020 CACACACACA CACACACACA CACACAACAC ACACACACAC ACACACACAC ACACACACAC 1080 AAAACTCCCT ACCGGGTTCC CAGTTCAATC CTGACCCCCT GATCTGATTC GTGTCCCTTA 1140 TGGGCCCAGA GCGCTAAGCA AATAACTTCC CCCATTCCCT GGAATTTCTT TGCCCAGCTC 1200 TCCTCAGCGT GTGGTCCCTC TGCCCCTTCC CCCTCCTCCC AGCACCAAGC TCTCTCCTTC 1260 CCCAAGGCCT CCTCAAATCC CTCTCCCACT CCTGGTTGCC TTCCTAGCTA CCCTCTCCCT 1320 GTCTAGGGGG GAGTGCACCC TCCTTAGGCA GTGGGGTCTG TGCTGACCGC CTGCTGACTG 1380
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