Tag | Content |
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EnhancerAtlas ID | HS193-23345 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr3:53117530-53118910 |
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) |
Znf423 | MA0116.1 | chr3:53117603-53117618 | GCACCCCTGGGGTCC | - | 7.8 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 53117674 | 53117903 | chr3 | 53118007 | 53118685 | chr3 | 53118046 | 53118214 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I053083 | chr3 | 53117568 | 53118295 |
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Enhancer Sequence | AAATAAATAA AAGACATGGT CGCAGGTGGA TTTCTCCAGT GATGGTGCAG ATGGAAGAAG 60 TGCTGAACAC AGGGCACCCC TGGGGTCCTT CCACCCAGGG CCCGGCGCTT GGCCCTGTGC 120 TTGCAGATCT GCGGCAGGCA GAGCTGAGAG CAGGCAAAGA CAAGTCACCA CTGTGCTTGG 180 GCATCCTGCC CACCAGCCCC ACCGGGCAGC CAGAGCTCCA CATGGTTTCC ATCATGGTTA 240 CAAAATAAAC AAATGCAAGT CACTCTGTCC CTTCTGTGGC CCCCCACAGC CCGACATCTG 300 CACATCTGCG AGAACATTCT CTCGTCATTA GAGAGATGCC ACTTGGGGAT CTCAGAAGCC 360 ATGTGGGGAA GACAGAAACC TTCAGCTCTA GTTCAGGAAC ATTAAACACA CCATGCTATC 420 CCAGTTTGTT CATAAAATTC TTGTGTTAAT GTCCTAGGGG AAACAAAAAG GATAGCTATT 480 TTAGCAGCAT TCTCTAGTTT GGTTGGGATT CTGTGTGGAG AAGAGCTCTG TTTTCCTTCT 540 GGCTGCAATG TCTTGATTCT CTGGGTCTTT GTGGTTCTCC CTGCATGGCC CTGCCGGGCT 600 CTGGTGAGGG AAGATAAGAG TGTGCTCCAA GGCTGGCGAG GCTGGGGTTT TCGTCTGCAC 660 CTGGTGAAAG GACTGGCTCC TACATCACCA GCTTCCCTCT GAATATTTTC AGAATTCTCC 720 TGGGAACAGT GGTGGACAAC AAAAGCCTTC TGAAAGAGGT CCTCTGGCAC CCCTTATGCC 780 ATTCCCCTGG TGTTACCTTT TGTGATTTTC AAATGAAAGG GCAAAGAAGT GAGGAGTAGA 840 TGAGCCGGGA ACAAAACTGG CGCTGCCCGC AGACAGTCAT GCTTTCATTT CAGGCTCCCC 900 CTGCTCTCCC ACCCCACATG GCCACGTGGA AGCCGCACAC TATTAGTTCC ACATAATTGG 960 AAAGGGTGTC AGGATCTCCC AGACATTAAC CAGAAACATG CTGCTCAGTT GTCACCTCCA 1020 ATGTGACTAA TGCAGCCGTG TCTTAATTAG TCACTGCTCA CTGACTGCGA TGACAGCTCC 1080 CGAGCCTGTT CCAAGGCCCC AACCTGTGAT GGGGCACTGC AGAGCAGATT AAAGGTGAGA 1140 GGCCGCTGGG AAGGAAGGAC CAGGAGTTGC CAGTTTTTCA GGTCTCTTTC CCACTGAGCA 1200 CTGTGAACCC AGGTGGCCTC TGCCAAACCC CTTTGTCAAC ATTGTGACAG TAGAGTCAAT 1260 AGGGTCATAA CATTGGGACA CATTTATTGG AGGGAGAGAA GAAATGTGAC AGGGAAATGG 1320 TCTAGAAGAT TCCTTCACAA GTCAGCTGTT ATGTCACGGG TCCCCATGCA GCTCCCTGGG 1380
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