Tag | Content |
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EnhancerAtlas ID | HS184-17821 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr20:17908850-17910350 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr20:17910164-17910179 | TGACCCCTCACCTCC | - | 6.06 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH20I017927 | chr20 | 17908501 | 17910920 |
| Enhancer Sequence | TGTTTGGCAG AAAAAATGTC CAGTGACCTG TCCGAGGGCC AGTCACACAT TTATCAGGAG 60 TATTAGCAGC TCCGCATTCC CAGTGCAGGT CTCCCAGGTC CACGCCCTAG CCTCAGCCCA 120 GGACAGGCTC TGATTTCTCC GAAAATGATG TGCAAATCTG TTTCAAACCA CATGACCTTT 180 TGCCACAACC TCTTTGTGGC TTGTTCTATT GGATCAGAAG CCAGGAGTAT TTTCGGAACA 240 TTGCTAATGC TCTGAGCATC TCAGTTCTAG GCCTGTAGGC CACATATGAT GTGCGTTGGG 300 CCAGAGGCCC AGGTCAAGGT GTCTCGAGGG AAATTGGAGT CAATGGTGAA GTGAGAAAGC 360 TCTTGTGAGG CCTTTGGCCC CAGTGGGAGG GCCAGGGACA GAGGTGGGCC TGCCTGGTGA 420 GCCCACCTGC AGGCAAGAGG CACCCTGGGG AGGTGCCAGG AAGCAGGGCG CAAGGCAAGG 480 AGGCAGGAAC AGCCACGTCT GCTCCTGCCC TTTAAACAAA TACCAGGCTG TTCGAGTCCA 540 GAGAAGAAAT AAATATTGAC AAAGGTGCGG AGCGGCAGGA AGGCCAGGTG GCCGAGGCCC 600 CAGAAGGAAC ATGGCCTAGA TAGGGTCTCC TGGGATGACT GCGAGGAAGC CTCAGCCCCG 660 AGCCACCCTC CCCAGGGGCC CTTGGCGAGG CTGCCTCTAC GGAGGTCCTT CCCCCGTCTC 720 GGCAGGTGCT TCGGCACCTT GAGGGCTTGG ACTCAGGCTG TCAGGATGAG GAGCCTATCC 780 ACGGGATCAG TTGCTGGTGT TTGCCAAAGG TGTGTCCCAG AGGGGCCACC CGTAGCCTCT 840 GACGGTGCCA CGGCTGGAAG GCCCTGGCCA AACACCTGTC CCACTTCAAC AGCGCGTTCA 900 GTGGATCCCC CAAACCAAAG GGCCTGCTGG CGTTCTTCAG TGAGCTTCTC AAAGTGTGGG 960 TGCAGGGCTC TCAATAGAGG CCCCTGGGCG CTGGGTAAGA GGCACATTCC TGAGCCCACA 1020 CCTACCCCTC CAGGACACTG CAGGTCGAAG CTCAGGAATG TGCATTTTCA CCACCTTCCC 1080 TAGTGATTTT AGGCAGAGGG CTCATTAGAG CCAAGTAACA GAAGAGGAAG CGAAGTCTCA 1140 GAGAGGGAGC AGCACTCTTT GGCAGCACAG GGAGTGAGGG GCAGCGAGGG AGGAGGGTCC 1200 AGGGCAGAGT GAAGTGGCCA CACCTGCTCT GTCCCTTGGC TGGAAACAGC CTAATGGTCC 1260 AGACGACCCC CTGGGCTATG GGAGCTCAAA TCACTTCCCG CCAGAAGGCT TCTCTGACCC 1320 CTCACCTCCA GCCCAGGGAG ATGCCCCTGC CTGTCCCCTG GGCTCCGCGG CCCCTGGGCT 1380 TCCTGCTCCC CTGGCACTGG GCACACTGGA ATGCAAATAA CCACCGACCC TTGAATGTCC 1440 CCACCAGCAT GGTGCCTGGC GTGTAGTGGA TACGGCCGGG ATGCAGGTGC TTGAGCCATG 1500
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