Tag | Content |
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EnhancerAtlas ID | HS187-25784 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chrX:53217530-53219010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RORA(var.2) | MA0072.1 | chrX:53217553-53217567 | CTGACCTACTTTTT | - | 6.8 | STAT3 | MA0144.2 | chrX:53218741-53218752 | CTTCTGGGAAG | + | 6.14 |
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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 |
GH0XI053188 | chrX | 53218041 | 53218190 |
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Enhancer Sequence | TGAGTGTGGC CTGGACCTAG TAACTGACCT ACTTTTTTTT TTTTTGAGAC GGAGTTTGCA 60 CTTGTTGCCC AGACTGGAGT GCAATGGCGC GATCTTGGCT CACCGCAACC TCTGCCTCCC 120 GGGTTCAAGC AATTCTCCTG CCTCAGCCTC CTGAGTAGCT GGAATTACAG GCACCCGCGA 180 CGACACCCAG CTAATTTTGT ACTTTTAGTA GAGATGGGGT TTCTCCATGT TGGTCAGGTT 240 GGTCTCGAAC TCCTGACCTC AGGTGATCCG CCCGTCTCAG CTTCCCAAAG TGCTGGGATT 300 ACAGGTGTGA GCCACTGTGC CCGGCAGTAA CTGACTTACT TCTAACGAAT AGAATATTGC 360 AAAAGTGATG GGATCTCACA TCTGAAATTA AGTTATAAAG ACTATGAGTT CTGTCTGGCA 420 TGTGGGCACT CTCCTTCTAT CTCTAGCTCA TCTTACTTGT TTGCTGTGAT GAAGCAAGCT 480 GCCATATTAT GAGCCACCCT ATGAAAGGGT GCACATGGCA AGGAACCTGA GAGTGACCCC 540 CAGCCAACAG CCAGCAAGAC TGAATATGCC AACAGCCACA TGAGTCAGCT TGAAAGCAGA 600 TCTTTCCCCA GTCAAGCCTT GAGATGACTG TAGCCCCAGC TCACACCTTG CTGGCTGTGA 660 GACCCTGAAA CAGAAACTCA GCTAAGTTGT GCCCAGATTC CTAACCACAG GGACTGTGAG 720 ATAAAATGTT GTTTTAAGCC ACTGTTTTTG AGATAATTTG TTATGTAGCA AATATATAAC 780 CAATAGAGAT AGGCGTGGAG GTTATGTACC TCGGCAATAT GAACTTCTAA CCTACCAAGG 840 CCACTGTGGC CCTAGCACTG CTGAATTCCC AACCTACCAA CAGCAGAGAT CAACACTGAG 900 CTCCCACTGT GAACTATTTC CGGATTGCAG GCTGATTACT TTGGACCCCT TCTGTCTAGC 960 ACAGGCCTTA GGGTCACAGA GATTTGGTGA AAATCCCAGC TCTGCCAGGC TGATATGCTT 1020 AGGTGAGGCC TGTTTTCCTA GGGGTCTGTT TCCTGTGTCT GTTGGGGACT TTGTGAAATA 1080 CCTCACATGG AGCTGAGCAC CCAGGTGGAG GTTCACAAGG GGCTGTTCCC CTTCCTTTCA 1140 TGTGAGTGCC CAGGGGCAAG AACCCTGTTC CTCTGCTTCC TAACCCCTCT TCTCCCATCA 1200 CAATTTCAGG TCTTCTGGGA AGCATGGTTA GTGTCTGCCC CTTCAAGGAC CCACTGACCA 1260 TGTACCTCAG ACCCCAGGCG CCACTCCCAA GGGGTGGTAT CCTGTACCAC TGGACTCTGC 1320 AATGCAAAGG AAACAGAGTC ATATGCACAG TGTGGAGCCC CAACTGATGC TCCTACCTCC 1380 TTCTAAGCTA GATTGCGGGC CCTTGGCCTG GAAGTGGAGA CAGACTGAGG CCTGGGCCTT 1440 GCCTTCCCTC CAGAAGCTCC AGAGCTTGGG GGTGGGAGGA 1480
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