| Tag | Content |
|---|
EnhancerAtlas ID | HS101-26763 | Organism | Homo sapiens | Tissue/cell | HT29 | Coordinate | chr20:17908700-17910560 | 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 | GTGTTGATGT GAGCAGTACT CAAAACTGAG GCAACAGATC TCAAAATATT TTGGCATGTG 60
GGAGTGGGGA GGTAAAGGCT GAAGCCTCCT CTGTCCGAAG CATGCCCCCG AGGCTGGGAG 120
GAGGCAAAAA TGACAAATCA CATCTGAATC TGTTTGGCAG AAAAAATGTC CAGTGACCTG 180
TCCGAGGGCC AGTCACACAT TTATCAGGAG TATTAGCAGC TCCGCATTCC CAGTGCAGGT 240
CTCCCAGGTC CACGCCCTAG CCTCAGCCCA GGACAGGCTC TGATTTCTCC GAAAATGATG 300
TGCAAATCTG TTTCAAACCA CATGACCTTT TGCCACAACC TCTTTGTGGC TTGTTCTATT 360
GGATCAGAAG CCAGGAGTAT TTTCGGAACA TTGCTAATGC TCTGAGCATC TCAGTTCTAG 420
GCCTGTAGGC CACATATGAT GTGCGTTGGG CCAGAGGCCC AGGTCAAGGT GTCTCGAGGG 480
AAATTGGAGT CAATGGTGAA GTGAGAAAGC TCTTGTGAGG CCTTTGGCCC CAGTGGGAGG 540
GCCAGGGACA GAGGTGGGCC TGCCTGGTGA GCCCACCTGC AGGCAAGAGG CACCCTGGGG 600
AGGTGCCAGG AAGCAGGGCG CAAGGCAAGG AGGCAGGAAC AGCCACGTCT GCTCCTGCCC 660
TTTAAACAAA TACCAGGCTG TTCGAGTCCA GAGAAGAAAT AAATATTGAC AAAGGTGCGG 720
AGCGGCAGGA AGGCCAGGTG GCCGAGGCCC CAGAAGGAAC ATGGCCTAGA TAGGGTCTCC 780
TGGGATGACT GCGAGGAAGC CTCAGCCCCG AGCCACCCTC CCCAGGGGCC CTTGGCGAGG 840
CTGCCTCTAC GGAGGTCCTT CCCCCGTCTC GGCAGGTGCT TCGGCACCTT GAGGGCTTGG 900
ACTCAGGCTG TCAGGATGAG GAGCCTATCC ACGGGATCAG TTGCTGGTGT TTGCCAAAGG 960
TGTGTCCCAG AGGGGCCACC CGTAGCCTCT GACGGTGCCA CGGCTGGAAG GCCCTGGCCA 1020
AACACCTGTC CCACTTCAAC AGCGCGTTCA GTGGATCCCC CAAACCAAAG GGCCTGCTGG 1080
CGTTCTTCAG TGAGCTTCTC AAAGTGTGGG TGCAGGGCTC TCAATAGAGG CCCCTGGGCG 1140
CTGGGTAAGA GGCACATTCC TGAGCCCACA CCTACCCCTC CAGGACACTG CAGGTCGAAG 1200
CTCAGGAATG TGCATTTTCA CCACCTTCCC TAGTGATTTT AGGCAGAGGG CTCATTAGAG 1260
CCAAGTAACA GAAGAGGAAG CGAAGTCTCA GAGAGGGAGC AGCACTCTTT GGCAGCACAG 1320
GGAGTGAGGG GCAGCGAGGG AGGAGGGTCC AGGGCAGAGT GAAGTGGCCA CACCTGCTCT 1380
GTCCCTTGGC TGGAAACAGC CTAATGGTCC AGACGACCCC CTGGGCTATG GGAGCTCAAA 1440
TCACTTCCCG CCAGAAGGCT TCTCTGACCC CTCACCTCCA GCCCAGGGAG ATGCCCCTGC 1500
CTGTCCCCTG GGCTCCGCGG CCCCTGGGCT TCCTGCTCCC CTGGCACTGG GCACACTGGA 1560
ATGCAAATAA CCACCGACCC TTGAATGTCC CCACCAGCAT GGTGCCTGGC GTGTAGTGGA 1620
TACGGCCGGG ATGCAGGTGC TTGAGCCATG CCATCAGGAA TCTCTCCCAT CATCTCAGTC 1680
CTGCCTTCCC TTCTATGGCC CCCTGCAGTC CCCACTAACC CCAGCTTGCC CTGCAGCTCC 1740
AACAGAATGG GAGTGCATCC CCAACTATCA GCCCGGCCAC AGTCCCGGGG CTCCCTGTCC 1800
TTGGACTGCC AGGGGTCAGG TGCCAGTGTG TGAGCCAGTA TCTGTGGCTG GATGCAAGGA 1860
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