Tag | Content |
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EnhancerAtlas ID | HS044-12526 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr8:11499080-11500710 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF14 | MA0740.1 | chr8:11500516-11500530 | GGACACGCCCACTC | + | 6.43 | SP4 | MA0685.1 | chr8:11500514-11500531 | CAGGACACGCCCACTCC | + | 6.46 | SP8 | MA0747.1 | chr8:11500517-11500529 | GACACGCCCACT | + | 6.37 | ZNF740 | MA0753.2 | chr8:11500218-11500231 | CCGCCCCCCCCCC | + | 6.64 |
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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 |
GH08I011640 | chr8 | 11498236 | 11501093 |
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Enhancer Sequence | CCTTTGCTTC CCTTGAGGGT CCCTGTCCCC AGCTGAATGC TATTTCTTGT CCAAAAACCA 60 TTGCTTCATA TACTGGTTTT GAGTGTTTAA GGTGAGAGTG AACATGGCCT TTCACTCCAT 120 GTTGGCTGGA GCTGGAGGTC AGTCCTGCTT AAACTTTTAG AGCAGAGAGC TCTTCTTCTT 180 CCCTGGGCCT GGACCTTAGA GGACGCCAGG GATCCGAGTG GCTCTTGCCA TTTTACCTCT 240 TCAAGGAGCC TGAATCTAAA GCCAACACAG CAAAAGGCAG ACCCAGGAGG TGGAGAGAGA 300 TCAGCTGCAG GTGACATCCT TGCAGCCCTG AATCAAGCTT GTTCACTAGA TTCTTAACTA 360 CAAGAGACAG AGAGGAAAAC AAAATCCCTT TGCTCAGGTC AGTTGGAGTC AGGGTTTTCT 420 AACATTTTTG CAAGCGAACA AGTCTCAAGT GATTCGCTCT ACTGTTTAAA AATGCATATG 480 ATGACGGCAT GTGTGTACCG AGCTGGGGCA GAGGTTAGAG AAATTTAAAA ATGCGTATGA 540 ATAACAGCAT GTCTCTACAG AGCTGGGGCA AAGGTTAGAG AAAGCGATCT ATGTAAACGA 600 GCTGCCAGGC CCGTACACAG TAGGTGCTCC GTGAAGGCTG TCTCCCTGCC CCGTCCTCAA 660 ATATCTGCTT CTTGATCTGG GCTTCAAAGC TGATCCCATT CTCTCTCCAG TCACCTCTCA 720 AACTCCTCCT TCTTTTCTGT TAAGTAGCAA GTCTGGTCTT TCCTTCTTTC CGAGCAGAAC 780 CCAGGCTTTA CAGTTAATAT CCTGCCGCCT CTGATTGCAG CTTTAAGAGG TGTAACATTT 840 GATAAGCTCC ATTTAGCTTG GCTGAGCTGC ATTGTTTAAA TTATTCGAAG ACAGATTGCT 900 CCCTCCCCCT ACCCTGAGGA TTTCTGCTCT ACTGAGCTTG CCCACAGCAA GTTACCAGGA 960 AACACGGCAG GGAAGTCAGC AGGGCAGTTT GTCACCGTGA GGCTGAAAGT CAGTTCCAGC 1020 CGCTGTTCTG CAGCCATCAC ACCCCATTAT TCCCTGCTAA TTGCAAGCCT GGTATGCAGG 1080 CTAACTCTTT GAGAACAATG CCAGCTTTGA TTGCTGAAGA GGCTTATTCC TCTCCGCACC 1140 GCCCCCCCCC CCCGCCCCCG CCCTCTTCTC CCACCGTCCT CAGCTGACTC TGCCTGTCTG 1200 GGATTCCAAG CATCTCACAC TGGGGAAGAA GAGTCTGGGT TGGGAAGGAA TCTGAAGTGA 1260 AGCCCGTTCC CCAGGCATTC CGATTGGGGG AGGGAAGGAG GGCACTGAGG GGAAGGCTGG 1320 GTGGGTCCCA GCCCCCTGAG ACGTGAGCAG CCTCCATTCT AAATGATGTG GAAGAGCCGG 1380 CAACCCAGAC ACAGCTGCTC TGCAAGCCCA TCTGCCCAGC TCAGGGCTCA ACCTCAGGAC 1440 ACGCCCACTC CTCCTGGTCC AAACGAGGAT GGAGCCCCTC GAGCCTGTGC TCATGGGCAC 1500 TGTCTCACTC CATCCGAGCA CTGCTTAAAA CACACTGGAT AAATGCGGAT GGCTGTCAGA 1560 CGCTTTTAAT GAGGAAATAT TAGAGGAATA TTAGAGGAAT AATGAGGAAA TGATAGAAAA 1620 ATCAGAGACT 1630
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