Tag | Content |
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EnhancerAtlas ID | HS007-02191 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr10:80513980-80515570 |
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 | GTGGAGACTG CTAGAGACAA GCTTGTAGAG AGAAGCAGAA ACACTTGAAT GCAAAGGAGT 60 TGGGACTTTA TTCTGTACCT GCTGGGGGCC GTTGGAGGCT GTTAAGCCTA CTGTGTAGGG 120 TGAACAAATT TGCAGTGCAG AAAGATCACT CAGGCAGCAA GAGGGGACAG AGGGCGCAGG 180 CTGGGAGCAG GGAAACAAGC AGGAAGCTAT TGCAACAGCC CCGTGAGAGA TGACAAGGGC 240 AGTGGCATGC GACGGAGAAG AAGGAGTGGA TGCAAGAGGT ATGTGAGGAG CAACCTGCAC 300 GGGGCTTGGT GACCTCACAC CAGCCAGCTT TGCTGACCTG TCTGTGGGTC ACAGAAGATA 360 ATGGATGTGA TGCACTTTGA AAGCTGCAGA GCACCTTGTC TGGGTGCCAT GGCTGGTTTT 420 GACCAGATCA TGAAATGCAG CCTCTCTCCT CCTCCCTGGC TCATCTCTGC TGCTTGCTTT 480 TGCCTGTAAG CAAGGGAGAG AGGGGAGGTG AAAAACAGAG ACATTAAGTG CCAAAGCTTA 540 TGTTAATACA GCATTAAGGT TGAAAATGTA ATCTCCTAGG AGTCAGGAAA TTCCGAACAA 600 GGGGTTTCCA TGGCAACCCA GCCACACTGC TCCTCTGTCC ATTCGGGCCC TGTTTTCCTT 660 GTTAAATATG ATCCCATCGT ATATTATATG TTATCGAGTT AAATGTGCTA CCCACAGCAT 720 GCAGAGCTCC AGCCAGCAGC CCTCAGAGCT GCAGGAAATG AGTGTGTGTG TGTGTGTGTG 780 TGTGTGTGTG TCCAGGGGTG GGAGCCTTCA GAATTCGCCT AATATAACAC AGCCACATCT 840 TAGGTCCTCG TATCTAATAA ATGAGGTGTA ATTCCATTAA GAGCAGCTCC TGTGTACACC 900 AATGAGCAAG GAGGCTGCAA GCCCTGTGTT CAGAAGGGGT CGTTCAGGGT GCCTGCCCCT 960 GCTTGGGGTG GGTAGGTGAG GGACGTGGCA GATTCCATCA CATCCCCCAC AGGAGTGCCC 1020 AGCAGCTCCG GCAGGACCAT CCCTGCCACC CGGGGCTGCC TCCTGGATGC AGTTCTGAAG 1080 AGGTGAACTG GAATTACCTG ACCCAGTGGT TCTTCTCACA TGCCAGCCGA TTGAAGATCA 1140 GCTGTCACTG TTAGTTAGCA TCCCAGGGTA CACTGGGCAC CAGCAAACAG ATGCGGAAAG 1200 GAAATTTGAT GCTTCTCCAA ACCCTGTCTC CCCACTAACA CACCACAGTG GACAAAAGAC 1260 TTCCAAAGAC TTCCTCGGTG GCAGTGGGAG TTAGAAAGAA GGGGGAAATG ACTGTCAGGG 1320 AGGGCAGCTA AGTAGTGCAG TGTGTGACGG AGAAACATCT GTAGGATAAT ACAGCGGAAA 1380 AAGCATGGAA TGTTAGAATC AGGCTGCCTG ACCTCAGCCG TCTCCCAGCC ATGCGGTCTT 1440 CAGCAAGTCC CTTAATTTCC CTTTGTCTTA GTTTTTTCAT CTGCAAAATT GGGATAAAAT 1500 TACCATTAAC CTCACACAGG CTTGTTGGAG GATTAAATGG GATAATTGAT GCAAAAGCTC 1560 ACTGTAAACT TCTAAATCCC TATACAAATG 1590
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