Variant report
Variant | rs3863256 |
---|---|
Chromosome Location | chr3:162239725-162239726 |
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] |
---|---|
rs10084695 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs1026691 | 0.92[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1026693 | 0.92[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10460867 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs10936280 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs10936281 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs10936282 | 0.83[AMR][1000 genomes] |
rs10936283 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs11712285 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11927487 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12696149 | 0.83[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs1382204 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1471415 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1478142 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1478145 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1478147 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2061735 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2199604 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2318455 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs2405505 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs2405506 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs2405750 | 0.82[AMR][1000 genomes] |
rs2405753 | 0.85[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs2405754 | 0.85[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs28567923 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28667121 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs2897152 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs3853161 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs3853162 | 0.80[AMR][1000 genomes] |
rs3907216 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs3912100 | 0.85[AMR][1000 genomes] |
rs4263305 | 0.85[AMR][1000 genomes] |
rs4296607 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs4296608 | 0.81[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs4296609 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs4449332 | 0.85[AMR][1000 genomes] |
rs4621344 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs4856629 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs4856630 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs4856631 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs4856632 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs4856633 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs4856682 | 0.83[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs6441452 | 0.85[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs6441454 | 0.83[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs6441459 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6441460 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6441461 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6441462 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6441463 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6764843 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6765996 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6766883 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6766973 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6770434 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6775708 | 0.85[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs6776864 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6776986 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6777189 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6789202 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6791605 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6795724 | 0.85[AMR][1000 genomes] |
rs6798305 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6799150 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6801086 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6801492 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs6801686 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs7633312 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs7648533 | 0.83[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs9290119 | 1.00[ASN][1000 genomes] |
rs9813453 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9813595 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9813898 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9817021 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9819929 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9827825 | 0.86[EUR][1000 genomes] |
rs9839765 | 1.00[CHB][hapmap] |
rs9859293 | 1.00[CHB][hapmap] |
rs9868667 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9875471 | 0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9879717 | 0.85[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9883974 | 1.00[CHB][hapmap] |
rs993391 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs993392 | 0.94[AMR][1000 genomes];0.90[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv877721 | chr3:161878713-162303276 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | 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 |
3 | nsv877735 | chr3:162123179-162380954 | Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv592178 | chr3:162130691-162251934 | Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv877737 | chr3:162132155-162242541 | Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | 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 |
7 | 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 |
8 | nsv1000912 | chr3:162186601-162311128 | Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
9 | 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 |
10 | nsv877752 | chr3:162208062-162242541 | Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
11 | 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 |
12 | nsv877754 | chr3:162216666-162242541 | Enhancers Flanking Active TSS Genic enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
13 | 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 |
14 | nsv592205 | chr3:162217994-162263832 | Enhancers Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
15 | 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 |
16 | 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 |
17 | 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 |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:162237800-162248200 | Weak transcription | Dnd41 | blood |
2 | chr3:162238600-162245600 | Weak transcription | Aorta | Aorta |