Tag | Content |
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EnhancerAtlas ID | HS105-48232 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:232347360-232348820 |
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) |
CTCF | MA0139.1 | chr2:232347612-232347631 | TGGCCAGCAGGTGGCAGCG | + | 8.24 | STAT3 | MA0144.2 | chr2:232347939-232347950 | CTTCCCAGAAA | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 232347864 | 232348336 | chr2 | 232348515 | 232348679 |
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Enhancer Sequence | CCCGGCCAGA AAACTCCAAT TCTTAATTCC TTACCTGTAG TGGGGGGTCA TCATCTCTAC 60 CTTACTGATG TAAGGCACAG GACAGTTCAA GAGCGACAGT AACGTGCTGC CACCGTCACT 120 GGGGTGCTGT AGCCGATGTG AACTCCCTCC CCGGCTAGCT TCTCTTCTGT GAAGGTGAGG 180 TCCGGGCCAC CAAGCCGCTT GCCCACTCCA CACAAGGTCC TTCTCTCCGA GGGACGCGGC 240 AGGGGCCCGA GGTGGCCAGC AGGTGGCAGC GCCGCGGCAG CCCGGGTTTG GCATAGCTCG 300 GGAGCGGCCT CCGGGAAAGG AAGGGGTCAG GCCTCTCCAG GCAGCCCCCA GAGCCCCTCG 360 CCTCCCTGGG CGCCCCACTC GCAGATGCAG CAGGGCGGGT TCGCGGGTGT GCGGCCTGCA 420 CCTGGCGGGG CTCCGGGCTT GGGTGGAAGC TCTGCTGTCG CCATCTTGAC GTCTGAGTTA 480 CTGCTGAGCA GGAGCCCTGC ATTTTCATTT TGCGCCAGGC CTCTCAAACT GTGGTCCTGG 540 GTGCCAGGAC TCCTGCTGCC TCGGGATCCC GCCACTTTAC TTCCCAGAAA TGCGCTGAGC 600 CCGTCCCTTT CCTGCCGTTG CTCAGCCTTC CCGGGGCTCC CTGACCATGC TTGTCTCCAG 660 CTCACCGGCC TTCCAGAAGC CTGGAGAGGG CCGGGACCCC ACATGGGGAG GACGAAGAAC 720 CCACGCAAGG AAAACGGGGA CCCTACATGG GCATGGGGCA GCCATGGGGA GGAGGGGGAC 780 CACGTGGGGA TAATGGGGCC ATACGTGGAG AGGAGGGGAC CCTACAGAAG GCCTGGGTTG 840 GGCAGTGCTG GGCTCTCGTC GGAGGGTCAG GTGGCGCTGG CGGCCGGCAG GAAGCCCTGG 900 GTAGCGGGTG GCGGGCAGCA GGTCCCGGGC TGCAGGCCCC GTGGAGAGCG GAAGGCGCGC 960 GGCGAGGCCC GGGCGGGAAC CCAAGGCTGG AGGCCGGCCC TAAGAGTGCT TCCCTAGCAG 1020 CCCCGGCGGG AAAAGAAGAG AACAAAGTCT AGGAGTTCCG GGACTTCCCC GCGGTGGCAG 1080 AGGAGGGGGC TGCCATTGTC AAGGCGGCAC AGAAGCCTCG GGTTCGGGGA CCTTTGCTGG 1140 AGGAGCTGGG GCAGGGTAGG ACGGGGGCCG CAGGGGCCTC GAGAGCGAAC GGGGAAAGGC 1200 CGCGGCGCCT GCAGAGCACA GTCCATGCAG TTTGCCCGGG GCGCGGGCCT CTCGAGTGTG 1260 CTCAGGAAGC CGTGGCTCCT CGGGGCGTCT GCAGGCCTCC CAGCATCCGT CGTGCAGACC 1320 TGACGCCACC TGCCACCCGC AGACGCTGAG ACCCGGAGCC CCTCTGCCCC TGGGCTGGCC 1380 GCGGAGGCTG CCTCTGGGGT GCGGTTTCCC AGGCTGTGTC TTTTCAGCGG GTGCGCAGGT 1440 TCCCGCCCTC CCAGTGTCCC 1460
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