Tag | Content |
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EnhancerAtlas ID | HS044-01831 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr10:80513890-80515780 |
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) |
ESR2 | MA0258.2 | chr10:80514280-80514295 | GGGGCTTGGTGACCT | - | 6.32 | RFX1 | MA0509.2 | chr10:80514582-80514598 | GGTTTCCATGGCAACC | - | 7.07 | RFX1 | MA0509.2 | chr10:80514582-80514598 | GGTTTCCATGGCAACC | + | 7.09 | RFX2 | MA0600.2 | chr10:80514582-80514598 | GGTTTCCATGGCAACC | + | 7.58 | RFX2 | MA0600.2 | chr10:80514582-80514598 | GGTTTCCATGGCAACC | - | 7.65 | RFX5 | MA0510.2 | chr10:80514582-80514598 | GGTTTCCATGGCAACC | + | 7.49 | RFX5 | MA0510.2 | chr10:80514582-80514598 | GGTTTCCATGGCAACC | - | 7.5 |
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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 |
GH10I078754 | chr10 | 80513925 | 80515352 |
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Enhancer Sequence | CCCTTGGAAG TGCAGTATGG CCCTTGGAAG TGCTCTGTGT ATTCCGAAAG GACATCATCA 60 CCTCTACGGG GTTGGAGGGT AGGGACTGTG GTGGAGACTG CTAGAGACAA GCTTGTAGAG 120 AGAAGCAGAA ACACTTGAAT GCAAAGGAGT TGGGACTTTA TTCTGTACCT GCTGGGGGCC 180 GTTGGAGGCT GTTAAGCCTA CTGTGTAGGG TGAACAAATT TGCAGTGCAG AAAGATCACT 240 CAGGCAGCAA GAGGGGACAG AGGGCGCAGG CTGGGAGCAG GGAAACAAGC AGGAAGCTAT 300 TGCAACAGCC CCGTGAGAGA TGACAAGGGC AGTGGCATGC GACGGAGAAG AAGGAGTGGA 360 TGCAAGAGGT ATGTGAGGAG CAACCTGCAC GGGGCTTGGT GACCTCACAC CAGCCAGCTT 420 TGCTGACCTG TCTGTGGGTC ACAGAAGATA ATGGATGTGA TGCACTTTGA AAGCTGCAGA 480 GCACCTTGTC TGGGTGCCAT GGCTGGTTTT GACCAGATCA TGAAATGCAG CCTCTCTCCT 540 CCTCCCTGGC TCATCTCTGC TGCTTGCTTT TGCCTGTAAG CAAGGGAGAG AGGGGAGGTG 600 AAAAACAGAG ACATTAAGTG CCAAAGCTTA TGTTAATACA GCATTAAGGT TGAAAATGTA 660 ATCTCCTAGG AGTCAGGAAA TTCCGAACAA GGGGTTTCCA TGGCAACCCA GCCACACTGC 720 TCCTCTGTCC ATTCGGGCCC TGTTTTCCTT GTTAAATATG ATCCCATCGT ATATTATATG 780 TTATCGAGTT AAATGTGCTA CCCACAGCAT GCAGAGCTCC AGCCAGCAGC CCTCAGAGCT 840 GCAGGAAATG AGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TCCAGGGGTG GGAGCCTTCA 900 GAATTCGCCT AATATAACAC AGCCACATCT TAGGTCCTCG TATCTAATAA ATGAGGTGTA 960 ATTCCATTAA GAGCAGCTCC TGTGTACACC AATGAGCAAG GAGGCTGCAA GCCCTGTGTT 1020 CAGAAGGGGT CGTTCAGGGT GCCTGCCCCT GCTTGGGGTG GGTAGGTGAG GGACGTGGCA 1080 GATTCCATCA CATCCCCCAC AGGAGTGCCC AGCAGCTCCG GCAGGACCAT CCCTGCCACC 1140 CGGGGCTGCC TCCTGGATGC AGTTCTGAAG AGGTGAACTG GAATTACCTG ACCCAGTGGT 1200 TCTTCTCACA TGCCAGCCGA TTGAAGATCA GCTGTCACTG TTAGTTAGCA TCCCAGGGTA 1260 CACTGGGCAC CAGCAAACAG ATGCGGAAAG GAAATTTGAT GCTTCTCCAA ACCCTGTCTC 1320 CCCACTAACA CACCACAGTG GACAAAAGAC TTCCAAAGAC TTCCTCGGTG GCAGTGGGAG 1380 TTAGAAAGAA GGGGGAAATG ACTGTCAGGG AGGGCAGCTA AGTAGTGCAG TGTGTGACGG 1440 AGAAACATCT GTAGGATAAT ACAGCGGAAA AAGCATGGAA TGTTAGAATC AGGCTGCCTG 1500 ACCTCAGCCG TCTCCCAGCC ATGCGGTCTT CAGCAAGTCC CTTAATTTCC CTTTGTCTTA 1560 GTTTTTTCAT CTGCAAAATT GGGATAAAAT TACCATTAAC CTCACACAGG CTTGTTGGAG 1620 GATTAAATGG GATAATTGAT GCAAAAGCTC ACTGTAAACT TCTAAATCCC TATACAAATG 1680 TCACTCTTCC AGGGAGCTCT AGAAAACCAT GCTGGATTCT GGACTACTAC AGTAGGCTGT 1740 AGAAATTTTG TGATTGGTTC TGGAATTCTG CGTTGGGTTC CAGAATTCAT GGATGGGTCT 1800 AGAACACAGA CAGACTTTTT CTGTAAAGAC TCAGATCATA AATATTTTGG GATTTGAGGG 1860 CCATGCTGTG ACTACTCAAG TTTTCTGGAG 1890
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