Variant report
Variant | rs10479344 |
---|---|
Chromosome Location | chr5:98348380-98348381 |
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 | chr5:98341705..98344564-chr5:98346126..98348724,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10038192 | 0.82[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs10040066 | 0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs10050423 | 0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs10076291 | 0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10479345 | 0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10479346 | 0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs1093794 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs1104262 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs11242567 | 0.86[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs11949103 | 0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs11950452 | 0.92[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs11950855 | 0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs11960896 | 0.92[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs12109067 | 0.86[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs12189335 | 0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs13179812 | 0.92[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs1393210 | 0.86[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs1472622 | 0.81[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs161731 | 0.82[AMR][1000 genomes] |
rs161935 | 0.84[EUR][1000 genomes] |
rs161936 | 0.84[EUR][1000 genomes] |
rs162341 | 0.84[EUR][1000 genomes] |
rs172874 | 0.81[AMR][1000 genomes] |
rs2455423 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs2927647 | 0.85[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs2927648 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs2927654 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs2937706 | 0.81[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs2937708 | 0.82[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs2937709 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs325220 | 0.81[AMR][1000 genomes] |
rs326493 | 0.84[EUR][1000 genomes] |
rs34489 | 0.84[EUR][1000 genomes] |
rs34490 | 0.82[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs34491 | 0.84[EUR][1000 genomes] |
rs34496 | 0.84[EUR][1000 genomes] |
rs34497 | 0.84[EUR][1000 genomes] |
rs34499 | 0.82[EUR][1000 genomes] |
rs363929 | 0.84[EUR][1000 genomes] |
rs366000 | 0.85[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs366353 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs370529 | 0.82[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs378089 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs380156 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs393697 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs395668 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs398436 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs40075 | 0.81[AMR][1000 genomes] |
rs407562 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs416750 | 0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs422127 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs434039 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs443726 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs4448016 | 0.86[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs447044 | 0.81[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs449204 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs451141 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs4565239 | 0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs45931 | 0.81[AMR][1000 genomes] |
rs4703049 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs4703051 | 0.90[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs4703052 | 0.90[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs4703340 | 0.90[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs539024 | 0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs559574 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs6865618 | 0.86[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs6885458 | 0.88[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs709390 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7710032 | 0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs7711061 | 0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs819232 | 0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv1826071 | chr5:98312447-98358852 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | esv1827754 | chr5:98312447-98358852 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | esv1837772 | chr5:98312447-98358852 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | esv1838335 | chr5:98312447-98358852 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | esv1845131 | chr5:98312447-98358852 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv4930 | chr5:98318768-98350644 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | esv3420271 | chr5:98343152-98349350 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
8 | esv3422141 | chr5:98343952-98348650 | Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
9 | esv3341596 | chr5:98344077-98348625 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
10 | esv3346446 | chr5:98344352-98348850 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
11 | nsv599093 | chr5:98344571-98356733 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
12 | nsv599099 | chr5:98345182-98356733 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
13 | nsv599100 | chr5:98345182-98357415 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
14 | esv1794778 | chr5:98345182-98358852 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
15 | esv1825119 | chr5:98345182-98358852 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
16 | nsv599103 | chr5:98345287-98356733 | Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Active TSS | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
17 | nsv599107 | chr5:98345400-98356733 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
18 | nsv599113 | chr5:98345632-98357415 | Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:98343600-98354800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |