Variant report
Variant | rs6548943 |
---|---|
Chromosome Location | chr3:68094829-68094830 |
allele | A/G |
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] |
---|---|
rs10865603 | 0.97[EUR][1000 genomes] |
rs11920675 | 1.00[MEX][hapmap] |
rs13078759 | 1.00[CEU][hapmap] |
rs1447756 | 1.00[MEX][hapmap] |
rs1595489 | 1.00[CEU][hapmap];0.83[GIH][hapmap] |
rs17140932 | 0.87[ASN][1000 genomes] |
rs4302389 | 1.00[CEU][hapmap];0.85[GIH][hapmap] |
rs4419383 | 1.00[CEU][hapmap] |
rs4508789 | 1.00[CEU][hapmap] |
rs4602395 | 1.00[CEU][hapmap] |
rs6548957 | 0.97[EUR][1000 genomes] |
rs6548958 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.85[GIH][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes] |
rs6548964 | 1.00[CEU][hapmap];0.94[CHD][hapmap];0.85[GIH][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes] |
rs6548970 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.85[GIH][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes] |
rs6548977 | 1.00[CEU][hapmap];0.88[CHB][hapmap] |
rs6548978 | 1.00[CEU][hapmap];0.88[CHB][hapmap];0.80[EUR][1000 genomes] |
rs6548979 | 1.00[CEU][hapmap];0.88[CHB][hapmap];0.80[EUR][1000 genomes] |
rs6549006 | 1.00[CEU][hapmap];0.85[GIH][hapmap] |
rs6771439 | 1.00[CEU][hapmap];0.81[CHD][hapmap];0.85[GIH][hapmap] |
rs6777162 | 1.00[CEU][hapmap];0.88[CHB][hapmap];0.88[CHD][hapmap];0.85[GIH][hapmap] |
rs6781199 | 1.00[CEU][hapmap] |
rs6786795 | 0.97[EUR][1000 genomes] |
rs6792628 | 1.00[CEU][hapmap];0.81[CHD][hapmap];0.85[GIH][hapmap] |
rs6809593 | 1.00[CEU][hapmap] |
rs73837230 | 0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs7630992 | 1.00[CEU][hapmap] |
rs7634100 | 1.00[CEU][hapmap] |
rs961915 | 1.00[CEU][hapmap];0.81[CHD][hapmap];0.85[GIH][hapmap] |
rs9867112 | 1.00[EUR][1000 genomes] |
rs9874375 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1002010 | chr3:67785913-68312064 | Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv1009871 | chr3:67862617-68312064 | Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | nsv536583 | chr3:67862617-68312064 | Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
4 | nsv1010231 | chr3:67894825-68117879 | Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv999747 | chr3:68066423-68188180 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv536584 | chr3:68066423-68188180 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | esv2752014 | chr3:68091879-68416989 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
8 | nsv1007450 | chr3:68094416-68346546 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:68094800-68098800 | Weak transcription | Fetal Intestine Small | intestine |