Variant report
Variant | rs11985873 |
---|---|
Chromosome Location | chr8:107041417-107041418 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10086055 | 0.81[EUR][1000 genomes] |
rs10098367 | 0.91[ASN][1000 genomes] |
rs10955408 | 0.82[EUR][1000 genomes] |
rs1429681 | 0.81[EUR][1000 genomes] |
rs1496181 | 0.82[EUR][1000 genomes] |
rs1496183 | 0.81[EUR][1000 genomes] |
rs1817939 | 0.82[EUR][1000 genomes] |
rs1835268 | 0.80[AMR][1000 genomes] |
rs2029878 | 0.81[EUR][1000 genomes] |
rs2029879 | 0.81[EUR][1000 genomes] |
rs2029880 | 0.81[EUR][1000 genomes] |
rs2163124 | 0.81[EUR][1000 genomes] |
rs28643398 | 0.91[ASN][1000 genomes] |
rs34872724 | 0.82[EUR][1000 genomes] |
rs55639043 | 0.82[EUR][1000 genomes] |
rs62527360 | 0.81[EUR][1000 genomes] |
rs62527405 | 0.82[EUR][1000 genomes] |
rs6469030 | 0.82[EUR][1000 genomes] |
rs6469032 | 0.82[EUR][1000 genomes] |
rs6999580 | 0.81[EUR][1000 genomes] |
rs7006651 | 0.83[AMR][1000 genomes] |
rs7460291 | 0.82[EUR][1000 genomes] |
rs7830426 | 0.82[EUR][1000 genomes] |
rs7846149 | 0.81[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1021369 | chr8:106493317-107243322 | Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 13 gene(s) | inside rSNPs | diseases |
2 | nsv611840 | chr8:106913294-107265915 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:107036400-107052000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |