Tag | Content |
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EnhancerAtlas ID | HS187-25543 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr9:139860090-139860990 |
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) |
KLF16 | MA0741.1 | chr9:139860596-139860607 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr9:139860596-139860606 | GCCCCGCCCC | + | 6.02 | SP1 | MA0079.4 | chr9:139860593-139860608 | GAAGCCCCGCCCCCA | + | 6.6 | SP2 | MA0516.2 | chr9:139860592-139860609 | GGAAGCCCCGCCCCCAT | + | 6.67 | SP4 | MA0685.1 | chr9:139860593-139860610 | GAAGCCCCGCCCCCATT | + | 7.22 | SPDEF | MA0686.1 | chr9:139860278-139860289 | AACCGGATGTG | + | 6.02 |
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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 |
GH09I136965 | chr9 | 139859834 | 139861061 |
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Enhancer Sequence | AGGAGAATCA CTTGAACCCA GGAGGCGGAG GTTGCGGTGA GCCCAGATCC CACCACTGCA 60 CTCCAGCCTG GCGACAAGAG CAAAACTCCA TCTCAAAAAA AAAAAAAAAA AAACCATTTC 120 GCAGAGAAGG ACGCAGAAGC CAATGGAAAA GCTGCCAGTA GCTGCAGCTG GCCTGATGTG 180 AGCCACAAAA CCGGATGTGA CAGTAGGGTG TGAGCCAAAG TGTAAAACAC CTGAGGTCCA 240 CACGGATGTC AGTGAAGGGC TGTGCCCACC CATGGGAGAG CAGAGACAAA TGATCTCGGT 300 GCAGCAAAGT TGCAAATGTG TGTGGATTCC CCTTCCGGGG GAGGTGAGGG CCACACACAG 360 GGACTTCATC CAGAGAGGAC AGTTCAAAAA GAAAAAGACG GAGAGGTGCA GGGTTAGGGT 420 GGGGGAACCT CAGCCAGGTG ACCAAGGTCA ACATGGGCAG TGAAGGTCGC GCTGATGGTG 480 TCCCCCATGT GATGTGGTGG GAGGAAGCCC CGCCCCCATT CTCTTCCTCC CGACCATCAC 540 CGGATTCAGC GTGAGAAACT CAGCAGACGG AGCCCAACTG AGGGACGCCC CACAAACACC 600 CGAGCAGCGC CCCTCAAGGC TGCTGAGGTC ATCAAGGACC GGGAAAAGCT GAGAAACGTC 660 ACTCAGGAGG AGCCCGTGGA AGAGAGACAG AATGTCACGT GGTGTCCTGG AGAGAAAGGG 720 ACCTTCAGTA ACTAAGGGAA TCTGGAGAAA GCCTGGATGT CAGCTGACTC GACGTCCCAA 780 CACTGGCTCA CTGATTGTGA CAAAGGGACC ATGAGAATTA GGACGCCAGC GAGAGGGAAA 840 CTGGGGGAGG GGCACGCAGG AACTCCCTGA TCTGTCTTCA CATTTTTTTT CTGTAAATAT 900
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