Variant report
Variant | rs6437608 |
---|---|
Chromosome Location | chr3:94777000-94777001 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr3:94776805..94778652-chr3:94799142..94801105,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1039646 | 0.85[AMR][1000 genomes] |
rs11915767 | 1.00[CEU][hapmap] |
rs11919076 | 0.85[AMR][1000 genomes] |
rs11927923 | 0.90[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs16853213 | 0.89[EUR][1000 genomes] |
rs34490494 | 0.84[EUR][1000 genomes] |
rs4407407 | 0.85[AMR][1000 genomes] |
rs56767894 | 0.85[AMR][1000 genomes] |
rs60964852 | 0.85[AMR][1000 genomes] |
rs6779933 | 0.82[AMR][1000 genomes] |
rs73172320 | 0.85[AMR][1000 genomes] |
rs7625700 | 1.00[CEU][hapmap] |
rs9821870 | 0.82[AMR][1000 genomes] |
rs9836994 | 0.80[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs9839723 | 0.85[AMR][1000 genomes] |
rs9867698 | 0.82[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv877169 | chr3:94675697-94840854 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv590993 | chr3:94759504-94841342 | Enhancers Weak transcription | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
3 | nsv1012191 | chr3:94769139-94854973 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
4 | nsv536652 | chr3:94769139-94854973 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:94774400-94777200 | Weak transcription | Fetal Heart | heart |