Tag | Content |
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EnhancerAtlas ID | HS044-09046 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr3:72355800-72357290 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr3:72357266-72357287 | AGATACTTTCTTTTTTTTTTT | + | 6.11 | ZBTB18 | MA0698.1 | chr3:72356511-72356524 | CTTCCAGATGTTC | + | 6.48 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGAGAAGACC AGAGGTTCTT ACAGTTTGAG AACTTTGGGT TTCACTCTGT CATTAGAAGC 60 CATTGGGGGT TCTGAGCTGG GAATCTGGTG GTCCAATTTA CATGTTTTAA AGATTATTCA 120 TTTGCAGAGC AGCATAACGG TTGCTGGATT CCGGGGCCTT GATTCAAATC CCAGCAGAGT 180 CTACATGCCT AGCTATGTGA CTGCAGCAAG CTGTATAATC TTTGGGGGCC TCAGTTTCTC 240 AACCATAAAA TGGGATGATC ATAGCATCTC CCTTCTAGGG AGGCTTAACT GAGTGAATAT 300 TCATGAAGCA TTTGGAAGAG TGCCTGGTAC ATAGGCAATG ATCCATGAAA GTTAGGTAAC 360 TTAAGTCAAT AAGAAAGTAC TCACTGGATA GTCCCTGTCT TCCTGGGGAG AAAGCGCTGC 420 CAGCCAGGGG CTGCTTTCCG CTTTGCAAAG CTCTAGCCCC TCGCCTGGCT CAATCCAACA 480 AGTAATTGCT CCGAGGCCTC CTTCCAAATG GGCCATAAAT CAGAGGCCAG GGTCTCCTGT 540 TACCAGCGGC TGGTGGTGAA GTCCCTCCCC CGGGTAATGG GAAGCAGATG TTGGCAGCCC 600 CTTCTGGCCT CCAGAGGACT GTGTACCTGG GCTGCTCACG TCACAGCAGT TGGAGCAAGA 660 ATTTCCATGA GCTTTTAAAT CGAAGGTTGT CAAAGAAACG GCCTCCTAGG GCTTCCAGAT 720 GTTCTGCGGC GTGTTTCAAG CAGGAGGTGG GCAGCTAATG GGGGCCTTCA GGGGCTGAGA 780 GAGGAAGAGC AGGGTCAGGG ATAACACTAG GTTCCTTCCA AGGGGCCTGA CCAGCAGGCA 840 AGGTGTGGGG CCTGAGAGGT GGCAAGCTGT CAAGAAAGCA GCACAGGCTT TGCAGCCAGG 900 AGGACCTGGT TCAAATTCTG TTTCTCATTT TCTCAGCCTG TGCCCTGAAG TCAAGGGTAA 960 GTCACCTTTC CAGACCCCAG TTTTCTCGCC TGTGAAATGG GTGTGATGTT ACTTATCTCA 1020 CACATATTTG AAGGTGGGAA GTAGTTTAAG TTAAAGCACA GTGTCTCAGG CATGGTAAAT 1080 GCTCAAAAAA TGAAGGTAGT TATTAGAAGC GAGCTATGCA CAGAGCCTTG TTACCCATTA 1140 AGTCTTTATT GTCGCTGGAC GCTGAGCACT GTGACGGGCA AGGAAGTGTA GTCACCTCAC 1200 AAGACTTTCT ACGTTTCCTA AGGCCAAGGC CTTGATGAGG TCCAGAAAAT TCCTTAACAA 1260 TCTTTCAGCT ACAAGTCCAT GCACAGTTTG GCTTTAGGTA CAATTCAGGG CTCACATGAT 1320 GTCACCAAGA GGCAGCTCCT CTTTAGCTTC CACTGACTGG TTGTCAGATT TAAGCAAATA 1380 AAAATATAAA ACGTCAGTTA AACTTTAATT TCAGATAAAC AAGAAGTACT TTTCTTAGTA 1440 TAAGTATGTC CCACTAAATA TCTGGAAGAT ACTTTCTTTT TTTTTTTTTT 1490
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