Tag | Content |
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EnhancerAtlas ID | HS182-08206 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr16:28987590-28988290 |
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) |
EWSR1-FLI1 | MA0149.1 | chr16:28987704-28987722 | TTTTTCTTCCTTCCATCC | - | 6.19 | EWSR1-FLI1 | MA0149.1 | chr16:28987712-28987730 | CCTTCCATCCTTCATTCA | - | 6.46 | EWSR1-FLI1 | MA0149.1 | chr16:28987708-28987726 | TCTTCCTTCCATCCTTCA | - | 6.8 |
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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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Enhancer Sequence | TCATAAATAA ATAAATAAGT AAAGGCAGGA GAGGGTGTCT GGAATGGGGA GAGGTGTGTT 60 TTACTTGTTC ACAACTTTGG GACTTGTGGG AGAGGCAAAG CTAGAGCCAA GCCCTTTTTC 120 TTCCTTCCAT CCTTCATTCA TTTCTCAACC ATTTCTGAGT ACTCATTGTG TGCCAGGCCT 180 GGAGGAAGTG ATGATTACAC CTGTAGGACT TTGCGAAGAA CTTTTATGCC CCTTGTCTTC 240 TAATCCTTCT ATCAGTCAAA AATAGGTGTT ACTGTTCCTA TTTTATAGAG GAAGTAGGTA 300 GTGATATCTA CAGCTTATAA AGAAACTGAG GCTTGGAGAA GAGTTAAGAC TTGCCCAGGG 360 TCACACCACC AGTTGGAGGC GGAACAGGAA TTTGAAACCA GGTCTTGCAG TGTTCTTTTC 420 TCTACTCCAG GCCAATGAGG AACTGGAGGT ATTTGAGGTG AAGTCTGGAG CAATGAGAAT 480 GGGATCATAG GGCAAGGTCT TCAAACCTCT GAAGAGTTGT TGAGTTAGAG CAGCAGCTCT 540 TTCTAGGCAG CCGGATTTAT TCACTCTCTT CACATGCTTA TTGAGCACCT GTTTTGCACT 600 AGGCTGTGTG TTAAGTAAGT GAAAGAAACA CAGTCATGGC CAATACAGGC AAGGACCTTG 660 CCTTGGGAGC TGATAGTACG CTATGCATGA GGCAGCAACA 700
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