Variant report
Variant | rs7428118 |
---|---|
Chromosome Location | chr3:162383597-162383598 |
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] |
---|---|
rs10048975 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10513588 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10513589 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1121055 | 0.93[AMR][1000 genomes] |
rs11922500 | 0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12054159 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs12330272 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs13083886 | 0.87[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1382211 | 0.93[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs1382212 | 0.93[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs1382213 | 0.87[AMR][1000 genomes] |
rs1496738 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1600099 | 0.93[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs17707153 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs17758116 | 0.93[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs1845912 | 0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs1874510 | 0.91[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1874512 | 0.91[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1904101 | 0.93[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs2029925 | 0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs28748005 | 0.87[AMR][1000 genomes] |
rs28814090 | 0.93[AMR][1000 genomes] |
rs28879757 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs3907217 | 0.90[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs56242739 | 0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6414403 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6414407 | 0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6441534 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs6441540 | 0.87[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6441541 | 0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6441543 | 0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6441545 | 0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6764576 | 0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6778765 | 0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs7427964 | 0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7427978 | 0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7433902 | 0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7620379 | 0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs7624234 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7630042 | 0.88[EUR][1000 genomes] |
rs7634217 | 0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7635263 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7646046 | 0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7647069 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs7652432 | 0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9810012 | 0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9813079 | 0.91[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9822252 | 0.81[AMR][1000 genomes] |
rs9824243 | 0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs9826812 | 0.93[AMR][1000 genomes] |
rs9828168 | 0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs9828507 | 0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs9831314 | 0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9832503 | 0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9845518 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs9850473 | 0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs9859307 | 0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9867039 | 0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs9870314 | 0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9878965 | 0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9880391 | 0.87[AMR][1000 genomes] |
rs9880875 | 0.93[AMR][1000 genomes] |
rs9882410 | 0.91[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9882755 | 0.91[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9883974 | 0.81[AMR][1000 genomes] |
rs993524 | 0.93[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1006802 | chr3:161921063-162599175 | Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv428424 | chr3:162145988-163033943 | ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | nsv1012160 | chr3:162182166-162540478 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv592201 | chr3:162188625-163142162 | Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
5 | nsv829775 | chr3:162211618-162406402 | Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | nsv470994 | chr3:162217993-162945834 | Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
7 | nsv877755 | chr3:162218849-162386891 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
8 | nsv877756 | chr3:162218849-162391801 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
9 | nsv877757 | chr3:162226534-162391801 | Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
10 | nsv1005142 | chr3:162284967-162447818 | Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
11 | nsv877758 | chr3:162287573-162521339 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
12 | nsv877759 | chr3:162303276-162521339 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
13 | nsv592207 | chr3:162310379-162391801 | Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
14 | nsv877760 | chr3:162314038-162391801 | Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
15 | nsv877761 | chr3:162346392-162521339 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
16 | nsv592208 | chr3:162369863-162437102 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' | Chromatin interactive region | n/a | inside rSNPs | diseases |
17 | nsv460957 | chr3:162370941-162399269 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
18 | nsv592209 | chr3:162370941-162399269 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
19 | nsv1005637 | chr3:162379324-162635451 | Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
20 | nsv965128 | chr3:162381250-162393381 | Enhancers Weak transcription ZNF genes & repeats | n/a | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:162383200-162384200 | Enhancers | Dnd41 | blood |
2 | chr3:162383400-162384200 | Enhancers | Stomach Smooth Muscle | stomach |