Tag | Content |
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EnhancerAtlas ID | HS062-10802 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr22:37177540-37178940 |
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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I036781 | chr22 | 37177595 | 37178790 |
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Enhancer Sequence | TTATGGGGGC TGTCCTGAGC AATATAGACA GCATCTCTGT CCTCTGCCCA CTAGATGCCA 60 GAGCAAGCTC CCTTGCTGAG ACCACCAAAA ATGTCCCTGG ACATTGCCAA ATGTCCCCTG 120 GGGGGCAAAA TCTTCCACGG ATGAGAAGCA CTGATTTAGA TGTATGAACC CACTGAATAA 180 AGGATATTGA TTTTGCACTT GCAATCTACA AGGCCTTGGG CCTCGGGCTT CCTGGGCTTG 240 AATCTTTGTC TTGCCACCTC TCCTCTGTGT CTCAGTCTCC TCCCACCTGC TCCAGTAGGC 300 GCTTTGAGGC TCAGAAGAGT GGCCACATGC AAGGGGTCCC CAGCACGCCT GACACGTGGT 360 AAGACTCAGT GAGCACCAGT TCTGATGAAC AGCCACTGGG GTGGCCATGA GTCCCTGGAG 420 GAGGATTTAT AATGCGGTGG TACAGTTCTG TTTTACAATT TCCTATAACG CACTGTCACA 480 TCTGGTGCAC TGCCTTCTCT CGGTAATGAC CTTTGCTGTT CTTTTTTCCA CTGTTCACGT 540 GGGCCCGGTT GTTTATGTCT CCGCTGATGC AGTACTTGGC GGTGGCCATC TCAATAAAGG 600 GCAGAGGAAA TGGAACTGAC TCACCTTCTG TGCGCCCGGA ATGCAAAGTG GAGGCCTGAG 660 CTGTGGCCTC GGCGGGGCAC GGAGGCCGCG ATGTCCTGAT TCTGTCAGCA GGGGGCAGCA 720 GCAGCCGGGA AATTGTCTGC TGCAGGAGGG CAGAAGGGCT GCCGCCTTTT GACTTATTTG 780 CTGCCGCCTT TATTTAAAGT TGAGCAAATC ATCCCTCCAG AGCCACCCGG AGGCCCCCTT 840 TAACAGCCCG AGATACTCCA TCTGCAGAAG CCAAGAGCCG CTTTTCCAGA ACGTTCCACA 900 TTAGTGCATC TCTGTCCGTT TGCTCGCCAA CTGAGAATGA GAGGCTGAGA CATCACCTGG 960 GCGCCTCTCT TTGAGGCGCG GTGCTTTGAT TTACATCCCA GAGCCAAGGG CTCCTGAGTC 1020 CTGCTGGAGA GTTCTTCTCG CACCTGCCGC CTTCCCTCAC TGCCCCCTTT CCACACTCCA 1080 CGCATAAAGC CTGGGTGGTT GTGTTCAAGG AGGGCCAAGG AATTCTGGGT GCCCCAGGCT 1140 GAAGCTATGT CAAATTCTGC TAGAGGCAAA GTTGAGTGGG TCCCTGACAC TCTACCCTTT 1200 TTTCCCTTCC CCGGCCCCCA CTCCATATAA CACCCTGCAG CTGCGCGACA CAGTGCCCTT 1260 CCCAGAACAG CCCTCCCCCG GCAGCTGCAC CCACCACACT CAGGGCCCAT CTTAGTTGAT 1320 TCCTCACCTC ATGCACTTGG AAACTTAATA GCCCAGTTTC ATTCTCGCAT CATACCTTGG 1380 AATACGCCGT AGACATCCTG 1400
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