Tag | Content |
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EnhancerAtlas ID | HS187-16542 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr22:50431450-50432330 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr22:50431967-50431986 | CACTGCCGCCTGGTGGCAG | - | 6.19 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH22I049993 | chr22 | 50431531 | 50432447 |
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Enhancer Sequence | TTGGCTCTGG TTGTCTCTCT CATGCAAAGG TCAGCTCCAT GATCCCAGTT TGCCTGGGAC 60 TGTCCTGGTG TCAGCACTGA CACTCTGACC CAAGACCCTC CTTAGTGCCA GGCAGCCCCA 120 GACTTGGTCC CCCAGCTGCA GGGCCCGGGA TCTTTGCCAG TGTTGTTTGT TCCCGGTGCT 180 GGGTCGGGGC CCAGGGCCCA AGGCCTGCTC AGCTGTGTGT CATGAGTGAA TGAGGCAGGC 240 GGGCGTCCAA GGCTCACCCG TGTTATACTG TGGCCCAGAT GTGAGCAGGG CTGTGCACCC 300 CAGTACAGGT GCTCCTGCCC GCCCCTACCG CACCCCCCTT TCTGGGGCCC GGGGTCCTCA 360 GCACTTTTCT CCTGGCAGGT GTGGGGGTGG GTTTCCGGCG GTGGTGGTGG AGGGAGGGCA 420 GCGTCCCTGG CCAAGGAGGC GGTGGGTGCA CTGGGCTGTG GGCGCTCCGT GTTGGGTGCT 480 GGGGCGGCTG ATCCGGCTCA GCACCAGCAC TAAGAGCCAC TGCCGCCTGG TGGCAGCACG 540 CGTGTGTCCT CCAGCAGGTT CCTCCCTTGT CTGGGAGGGA CAGTAGGACA GCTGAGATCT 600 GAACACAGCC TCTTAACAGT CCCCAAAGAC TCAGTTTCCC CCATCTGCAG AAGAAAAGAC 660 TCAGTTTCCC CCATCTGTGG AAGGCTTGAG GGAGCCCACA CCCGTCAGGC AGGAGCTCAG 720 CTCTGTGACC CTGGTCTGGC CAATCCTCCC CAGCCCCACC TCCACGGTGG CCAGGATTCC 780 CGGAGTAGCC CTGGGTCAGA GCAGGGGTCT TTGTGCACCA CAGGGAGCAC CCCTGGCTGG 840 TCCAGGAGGC AGGAGCAGGA ACCTGGGGCG GGGACTGCCC 880
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