| Tag | Content |
|---|
EnhancerAtlas ID | HS101-17944 | Organism | Homo sapiens | Tissue/cell | HT29 | Coordinate | chr17:9337540-9338740 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA(var.2) | MA0730.1 | chr17:9338288-9338305 | AGGGCAACTGGAGGTCA | + | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 9337712 | 9337793 | | chr17 | 9337981 | 9338433 |
| Enhancer Sequence | CGATCTCTGG ACCTCGTGAT CCGCCGGCCT CAGCCTCCCA AAGTGCTGGG ATTACAGGCG 60
TGAGCCACTG CGCCCAGCCA GTATGTCAGG ATCTTAAAGT TGCTATTTCA TCCTCAATGT 120
GACAAGAAGC CACTAGAGGA TTTTAGCATG AAAACAACAC AATCAGATTT GTTTTTAAGA 180
AACTAATTGC GTTAGCAGAG GGGAAGACAG AGTGGAACAC TAAAGGACTT GTGGCAGGAA 240
ACCCAGCTAG GTATAGCCAT AGTTCCAAGG CAGAGAAGAC AGGGTCTGGG ATCAAAGCAA 300
ATTAAGGCAG CAGAGGTGGG AAGAAAAATG TGAGAGACAG TTTCAGAGGT GAAATCAACT 360
GAATTCAGTG ACTGGCTGCA GATGTCTAAC TGATATAGGG CAGGCAGGCT TAGCCTGGGA 420
GGGTTCTTGG CTTCACCCAG GAAAGAATTC AAGGGTGAGC CAGAGGTGAG CGGCAGTGTG 480
CAGCAGAGGT ACTGTTCCTT GTAGAGCAGG GCTAACTCAT AGGCAGTGTG TCCAGAGCAG 540
CAGCATATGG GCTGTTGGCT AGCTGTATTT ATATCTACTT TTAGTTGCAT GCAAATGAAG 600
AGGTGGGTTA TTTAGACCTT TTAGAAAAGG GGTGGGGCAT TTCTAGATGC ATAGAAGATA 660
ACTTTCAGGT CATTCCCATG GCATGTTGCC ACGGCATTTG TAAACTGCCA TGGCACTGCT 720
GGGAGTGCCT TTATGTTAAT GAGCAGTGAG GGCAACTGGA GGTCACTTTC ATCACCATTT 780
GCTGGTTTCA GCTGGCTTCT TCACTGCACG CCCTGTTTTG ACCACATCTT TCTCCAATCA 840
GTGGGTTGTG ACTGGTGCTC AGAAAACAAG TCCTGCTGAT CTCCTACCTC ATAACCTTGA 900
AAATAAGTTG GAGGGTGACA CTAATAACCA AGATAAAGAA CAAAAGGAAT GGAACAGGTT 960
TGTGGGGAAA GATACTGAGC CGTGTTTTAG ACATGTTGCA TTTGAAGGAC CGTTCAGGTG 1020
AAGATGCTGA GTAAAGTTGG AAATATGGAT CTAGGAATGT AGAAAAGTAC AGATTGAAAC 1080
GTTAACATCT AAAAAAGGCT AGAGCACAGG AGATTAGGAT AAGCATTAGC CATTATGAAC 1140
AGGAGAGGAC CCCAATAAGA GCATGCAGAG TGAGAGAGAC CCAAAGACAG AACCCTGAAG 1200
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