Tag | Content |
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EnhancerAtlas ID | HS073-07076 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr19:2182520-2183650 |
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) |
Zfx | MA0146.2 | chr19:2183413-2183427 | CCCGCCTCGGCCTC | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr19 | 2183443 | 2183622 | chr19 | 2182979 | 2183242 | chr19 | 2182800 | 2183595 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I002181 | chr19 | 2181002 | 2183356 |
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Enhancer Sequence | CTCAAGAAAC AAAACCCAAA CAAGAAAGAG TGCTCCAGGG CTGTGGCTTC CCGGGGCTGT 60 GACTGTGCAG GTTCTGCCAG TGCTGCCCAG ACGTGGTCTC TCTGGGTTAG GATCTCGGTG 120 CAGCAGGGGT GGAAGCCCCT CTCTGACCAG GCGCTTGCTA GTGTGTCTGG AGGTGCTCAG 180 CAGCAGGGGA GCTGCACCTG CTCCCCATGG GAAGGGGCCT GCACAGACTT CTGGGGTCAG 240 AGGAGACCCC AGGCCCCCGG ATCTCAGGCA GTGGCGGTGA GAGTGCCTCT CTGGCTGCAT 300 GCTCGCCTTC TGCAGGGCTC GGAGCTGACT GTCTTGTTTG AACCTTGTGT GTTTTCTGGG 360 GAGCGCATCT GGAGTCTGGA GCTTAAGCGT TGTAGGGAGC AGGGTCCAGG CACAGGGGCG 420 TGCACCAACA CCTGGGCATC CGCGACGTAG GCAGAGACCT CGAAACTCGA ACCCCCACCA 480 CCTGGAGAGG CTGCTTTCTC CCGTGCATCC CCAGCATGTG GCCAGGGTTC TCACGGTGTG 540 GCTGCACAGA CCTTTTCTGT CTCACTTCCT CTAGAAACAC CGACGACGTT CTTACACAGC 600 AAACACCATT CAGTCCCCAT ACGGCCAGTG TCCCAAGCAC GTCCTCCCAC AGTGGTGTTG 660 TTTTTTTGAG TCAGCGTCTG GCTCTGCTGC TCAGGCTGGG GTGCAGTGGT GCCATCTCAG 720 CTCACTGCAA CTTCCACCTC CCAGGTTCAA GCAATTCTCC TGCCTCAGCC TCCCGAGTAG 780 CAGGGATTAC AGGTGCCTGC AACCACGCCC AGCTAATTTT TGTATTTTTA GTAGAGGCGA 840 GGTTTTGCCA CCTTGGCCAG GCTGGTCTCA AACTCCTGGC CTCAAGTGAT CCACCCGCCT 900 CGGCCTCCCG AAGTGTGGGG AGGGCTGTTG TTTAAAGATG ATTGGGCTGT CCTAGGCTCT 960 CCTCGTTTGG ATGTCCGTTG AGAATCAGCC TTTCCATTTC TCCAGAAAAG CTAGCTGGGC 1020 TTTTTCTAGA AATTGGTTTG AGCCTGCAGT TCAGCTTGGG GAAAGGGGCG TTTAAACAGT 1080 GTCACTCCCA GGTATTCCTG CTTCAGTGCT TTTTTTTTTT TTTAAGGCGG 1130
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