Tag | Content |
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EnhancerAtlas ID | HS187-16280 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr22:37177420-37178720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr22:37178241-37178260 | CTGTCAGCAGGGGGCAGCA | + | 6.24 | HSF1 | MA0486.2 | chr22:37178423-37178436 | TTCCAGAACGTTC | + | 6.87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 37177462 | 37177720 | chr22 | 37177639 | 37178200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I036781 | chr22 | 37177595 | 37178790 |
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Enhancer Sequence | CCCTCATGTC AGAGGCAATG CCAAAAAGAG AGTGCTAATA GATTTGTAGA AATTTTATGT 60 ATTTAGATCA GGGTTTCCCT ACCTCGGCAC TATTGACATT TGGGGGTGAA GGGTTCTTAG 120 TTATGGGGGC TGTCCTGAGC AATATAGACA GCATCTCTGT CCTCTGCCCA CTAGATGCCA 180 GAGCAAGCTC CCTTGCTGAG ACCACCAAAA ATGTCCCTGG ACATTGCCAA ATGTCCCCTG 240 GGGGGCAAAA TCTTCCACGG ATGAGAAGCA CTGATTTAGA TGTATGAACC CACTGAATAA 300 AGGATATTGA TTTTGCACTT GCAATCTACA AGGCCTTGGG CCTCGGGCTT CCTGGGCTTG 360 AATCTTTGTC TTGCCACCTC TCCTCTGTGT CTCAGTCTCC TCCCACCTGC TCCAGTAGGC 420 GCTTTGAGGC TCAGAAGAGT GGCCACATGC AAGGGGTCCC CAGCACGCCT GACACGTGGT 480 AAGACTCAGT GAGCACCAGT TCTGATGAAC AGCCACTGGG GTGGCCATGA GTCCCTGGAG 540 GAGGATTTAT AATGCGGTGG TACAGTTCTG TTTTACAATT TCCTATAACG CACTGTCACA 600 TCTGGTGCAC TGCCTTCTCT CGGTAATGAC CTTTGCTGTT CTTTTTTCCA CTGTTCACGT 660 GGGCCCGGTT GTTTATGTCT CCGCTGATGC AGTACTTGGC GGTGGCCATC TCAATAAAGG 720 GCAGAGGAAA TGGAACTGAC TCACCTTCTG TGCGCCCGGA ATGCAAAGTG GAGGCCTGAG 780 CTGTGGCCTC GGCGGGGCAC GGAGGCCGCG ATGTCCTGAT TCTGTCAGCA GGGGGCAGCA 840 GCAGCCGGGA AATTGTCTGC TGCAGGAGGG CAGAAGGGCT GCCGCCTTTT GACTTATTTG 900 CTGCCGCCTT TATTTAAAGT TGAGCAAATC ATCCCTCCAG AGCCACCCGG AGGCCCCCTT 960 TAACAGCCCG AGATACTCCA TCTGCAGAAG CCAAGAGCCG CTTTTCCAGA ACGTTCCACA 1020 TTAGTGCATC TCTGTCCGTT TGCTCGCCAA CTGAGAATGA GAGGCTGAGA CATCACCTGG 1080 GCGCCTCTCT TTGAGGCGCG GTGCTTTGAT TTACATCCCA GAGCCAAGGG CTCCTGAGTC 1140 CTGCTGGAGA GTTCTTCTCG CACCTGCCGC CTTCCCTCAC TGCCCCCTTT CCACACTCCA 1200 CGCATAAAGC CTGGGTGGTT GTGTTCAAGG AGGGCCAAGG AATTCTGGGT GCCCCAGGCT 1260 GAAGCTATGT CAAATTCTGC TAGAGGCAAA GTTGAGTGGG 1300
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