Tag | Content |
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EnhancerAtlas ID | HS187-12119 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr19:18451620-18452740 |
Target genes | Number: 14 | Name | Ensembl ID |
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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) |
ESR1 | MA0112.3 | chr19:18452266-18452283 | GGGGTCATTTTGACCTG | - | 6.51 | RREB1 | MA0073.1 | chr19:18452164-18452184 | CTCCCCCCCACCCCCAAACC | + | 6.01 | ZEB1 | MA0103.3 | chr19:18452039-18452050 | GGGCAGGTGGG | - | 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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Enhancer Sequence | TCCTCTCAGA TTTGGAAGGT GTCATCACCC GCGGGAGCCC CGCGCAGCCC AGGCTTCCTG 60 GAAAGTGGAG GAGGAGGAGC CTTGGGGGTC CCAGGGTCGG GAGTCAGGGC AGTCGGGCGC 120 GGGGCTTGGG GGGCCGGGCA AAAGCCCGGC GCTGCGCAGG CCCCCCTGGC GTCCTTTCCT 180 CCCAAGGTGG GGATGGTGAC CCTCCTGGCA CCTGCCTCCT CTGTCTGGCC TGCGGGCTGG 240 ACTGGACCCT TCCTCCCTGC CCCTTCCGAG GTCCAGCCTG TCCCCACACC GCTCCCCCAA 300 CCCCTGGCCC CAGGGGACAA AGGCCGATTT GCGGGCAGGA AGTGTCCCAG TGACAAATGA 360 ACCTCCCAGT CACTGCTCGC CGCGCCCTGC GCTCCTGGGG GGCTACTCTC CCAAGGCAGG 420 GGCAGGTGGG GGTCCGGGGA CCTCGGGCTC TCCCAGCTGT CCCAGGGACT GTCTTCAGCG 480 GAAACCTTTT TGTGTTTTGT GCCAGGGCTG TTTGTTGGTG AGTCAGGGCC CCTGCTGTCA 540 CCGACTCCCC CCCACCCCCA AACCAACTGT TTCTCCTCCC TGAGACTCCG CCTCGGGGCC 600 ACGTGGGGCG CCAACTTCCG CTGGGGCCTC AGAGTCAAGG AGTGGGGGGG TCATTTTGAC 660 CTGCTGTCTG GAGGGGTCAG AGTGGGAAAT CCAGCAAAGG TGCACACAGG TGTTTTGTGG 720 CTGTTGAAGG GAGATTGAGG CTGATCCAGG AGATTCAGGG AAGAAGGAAG AAACAAGGCA 780 CCTGCTTAAC AGGTGTGTAT AATTGGGAGG AGGGTCACTG CCCCCATCCC TTCCAGCCTT 840 CCTTTATCTG GTTATTTATT CCAGCACTTT TTGCATGAGC TGATTACATC TTTACTGTCT 900 CCATTTTGCA GAAAGGGAAA CTGAGGCTCA CAGAGGTCAT CCAGTTTGTA AGGGGCTGAG 960 CTGAGACTCA AACTTTGGCT GTACAGAAGG ATAGAGTTAG GAGGTCCCCT CCTGAGCCAC 1020 AGCCCCTACC TGCTATCCCA GGCTACAGCA TCTCTGCATA GCATTCATAT CCTGTGGGAT 1080 CACTGGCCCA GATGGACCGT ATTTTTTTTT TTTTGAGACG 1120
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