Tag | Content |
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EnhancerAtlas ID | HS044-05747 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr17:46948840-46949830 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr17:46949122-46949137 | TGACCTTTGGACCTG | - | 6.27 | Nr2f6(var.2) | MA0728.1 | chr17:46949122-46949137 | TGACCTTTGGACCTG | - | 6.86 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 46948946 | 46949741 | chr17 | 46949057 | 46949324 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I048869 | chr17 | 46946510 | 46951625 |
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Enhancer Sequence | GGCTTGAACT GGCCTCAAGT GATCCTCCTG CCTTGGCTTC CCATAGTGCT GGAATTATAA 60 GTGTGAGCCA CCATGCCTGG CCTAGGTGAG TGTTCTTTTT TTTTTTTTTA ACACAAACAG 120 AACTAGGTGA GCCTTCAAGG AAAGAAAAAA GACTGTGTGC ATGTGTGCGT GCATGCCCGT 180 GAATGCCTGC CTTGATTTCC AACACACGCG TCCTCCTTTA AATCCTCCCT GAGCTGGAGA 240 CTGACTTGTG GGCCCTGGGA GAGTGTGTGG GAGTGTGGAG AGTGACCTTT GGACCTGGGT 300 ACTTTCCGGC CCCTCCTCCC ATGGAAGTTG CTGCACTGAT TTGGCCTGTG CAAACACCAG 360 GCACTTTTCG CTGGGTCAAT ATTTCACATC CGTTGTCAGG GTCTAATCCA TCTTCAACAT 420 CTGTTCCCTG GGATGTTGTG CACTGCTCTG CCACCTATGA CCCCTCATGG TCTTTGTCCC 480 CAGAAGAGGA TCTCTACAAG GTCCCCAGGG CTTTCTCCAG CTTGAGGCTG CTCGGTTCTT 540 CTCTTTTTTT CCTCTTTAAA CCCTCTCACC TTTGCCTGAG CCAATAATCT CCCTCAAATT 600 ACAGGGAGAA GCCCCTTCTG TCTGGAAGCC TTCCCTGGCT CCAGAACACA GGGACGTGGT 660 AGCTGCTGTT GTGTAGAATT CAGCAAACCT CACCTGCCAG TGGGTCCAGA ACACGTTCTG 720 ACCCAGTGTC CTGCTTGCCA CCTTGTACTT CCTGACTGCT GCTTCCTGCT GTGAGCCTGC 780 TGGAGCCCTG GGGACACACA TTTACTTGAA TAACATCTCA AAATAGACTG GGAAGACAAA 840 ATGTACTACA AGGGGCCAGG CACCGTGGCT CATGCCTGTA ATCCTAGCAC TTTGAGGGGC 900 TGAAGCAGGC GGATTGCCTG AACTCAGGAG TTCAAGACCA GCCTGGGCAA CAGGGTGAAA 960 CCCCATCTCT ACTAAAATAC AAAAAATTAG 990
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