Variant report
Variant | rs34949438 |
---|---|
Chromosome Location | chr6:118744959-118744960 |
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] |
---|---|
rs10509681 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11188124 | 1.00[ASN][1000 genomes] |
rs11188148 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11188153 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11188154 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11572064 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11572080 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11572082 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11572094 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11572107 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11572116 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11572128 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11572150 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11572168 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11572169 | 1.00[ASN][1000 genomes] |
rs11572174 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11591385 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11593816 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11598823 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs12761249 | 1.00[ASN][1000 genomes] |
rs12761315 | 1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12762602 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12762652 | 1.00[ASN][1000 genomes] |
rs12763201 | 1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12763939 | 1.00[ASN][1000 genomes] |
rs12766965 | 1.00[ASN][1000 genomes] |
rs12774244 | 1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12777852 | 1.00[ASN][1000 genomes] |
rs12778481 | 1.00[ASN][1000 genomes] |
rs12779007 | 1.00[ASN][1000 genomes] |
rs12779339 | 1.00[ASN][1000 genomes] |
rs12780333 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12784371 | 1.00[ASN][1000 genomes] |
rs17443251 | 1.00[ASN][1000 genomes] |
rs17452671 | 1.00[ASN][1000 genomes] |
rs17452714 | 1.00[ASN][1000 genomes] |
rs17453533 | 1.00[ASN][1000 genomes] |
rs17523627 | 1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17524348 | 1.00[ASN][1000 genomes] |
rs17525659 | 1.00[ASN][1000 genomes] |
rs1799853 | 1.00[ASN][1000 genomes] |
rs1934954 | 1.00[ASN][1000 genomes] |
rs1934966 | 1.00[ASN][1000 genomes] |
rs2153629 | 1.00[ASN][1000 genomes] |
rs2185570 | 1.00[ASN][1000 genomes] |
rs2860968 | 1.00[ASN][1000 genomes] |
rs34031095 | 1.00[ASN][1000 genomes] |
rs34119978 | 1.00[ASN][1000 genomes] |
rs34246390 | 1.00[ASN][1000 genomes] |
rs34254643 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34320910 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34409900 | 1.00[ASN][1000 genomes] |
rs34462937 | 1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34729632 | 1.00[ASN][1000 genomes] |
rs34883883 | 1.00[ASN][1000 genomes] |
rs35203700 | 1.00[ASN][1000 genomes] |
rs35213500 | 1.00[ASN][1000 genomes] |
rs35238981 | 1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35432490 | 1.00[ASN][1000 genomes] |
rs35461306 | 1.00[ASN][1000 genomes] |
rs35598837 | 1.00[ASN][1000 genomes] |
rs35883122 | 1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35955220 | 1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35998772 | 1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs36037322 | 1.00[ASN][1000 genomes] |
rs36042065 | 1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs36168663 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3980257 | 1.00[ASN][1000 genomes] |
rs41291560 | 1.00[ASN][1000 genomes] |
rs4351748 | 1.00[ASN][1000 genomes] |
rs45457395 | 1.00[ASN][1000 genomes] |
rs45523137 | 1.00[ASN][1000 genomes] |
rs45535939 | 1.00[ASN][1000 genomes] |
rs45546031 | 1.00[ASN][1000 genomes] |
rs45601238 | 1.00[ASN][1000 genomes] |
rs4607998 | 1.00[ASN][1000 genomes] |
rs483239 | 1.00[ASN][1000 genomes] |
rs4917636 | 1.00[ASN][1000 genomes] |
rs4918746 | 1.00[ASN][1000 genomes] |
rs4918795 | 1.00[ASN][1000 genomes] |
rs507728 | 1.00[ASN][1000 genomes] |
rs55753924 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs56028148 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs56044736 | 1.00[ASN][1000 genomes] |
rs56090603 | 1.00[ASN][1000 genomes] |
rs56380192 | 1.00[ASN][1000 genomes] |
rs56408997 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs570849 | 1.00[ASN][1000 genomes] |
rs595924 | 1.00[ASN][1000 genomes] |
rs601746 | 1.00[ASN][1000 genomes] |
rs61886771 | 1.00[ASN][1000 genomes] |
rs61886773 | 1.00[ASN][1000 genomes] |
rs61886796 | 1.00[ASN][1000 genomes] |
rs61886797 | 1.00[ASN][1000 genomes] |
rs61886802 | 1.00[ASN][1000 genomes] |
rs623544 | 1.00[ASN][1000 genomes] |
rs639937 | 1.00[ASN][1000 genomes] |
rs659309 | 1.00[ASN][1000 genomes] |
rs66648066 | 1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs66816038 | 1.00[ASN][1000 genomes] |
rs670565 | 1.00[ASN][1000 genomes] |
rs67403627 | 1.00[ASN][1000 genomes] |
rs67728892 | 1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs67737822 | 1.00[ASN][1000 genomes] |
rs67851687 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs67918795 | 1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs682349 | 1.00[ASN][1000 genomes] |
rs684203 | 1.00[ASN][1000 genomes] |
rs686705 | 1.00[ASN][1000 genomes] |
rs701889 | 1.00[ASN][1000 genomes] |
rs7082506 | 1.00[ASN][1000 genomes] |
rs7099702 | 1.00[ASN][1000 genomes] |
rs71482344 | 1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71505737 | 1.00[ASN][1000 genomes] |
rs72818618 | 1.00[ASN][1000 genomes] |
rs72818651 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs72818652 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs72818673 | 1.00[ASN][1000 genomes] |
rs72818680 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs72818681 | 1.00[ASN][1000 genomes] |
rs72820645 | 1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9332100 | 1.00[ASN][1000 genomes] |
rs9332101 | 1.00[ASN][1000 genomes] |
rs9332102 | 1.00[ASN][1000 genomes] |
rs9332119 | 1.00[ASN][1000 genomes] |
rs9332155 | 1.00[ASN][1000 genomes] |
rs9332163 | 1.00[ASN][1000 genomes] |
rs9332179 | 1.00[ASN][1000 genomes] |
rs9332216 | 1.00[ASN][1000 genomes] |
rs9332222 | 1.00[ASN][1000 genomes] |
rs9332242 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv532051 | chr6:118551027-119044197 | Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
2 | nsv1020463 | chr6:118593028-119146363 | Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
3 | nsv830787 | chr6:118631902-118805106 | Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | nsv1025403 | chr6:118635123-119122551 | Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
5 | nsv1025456 | chr6:118669672-119058789 | Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
6 | nsv1027444 | chr6:118687556-119121660 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
7 | nsv538428 | chr6:118687556-119121660 | Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
8 | nsv949321 | chr6:118692304-119137658 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
9 | nsv432958 | chr6:118692307-119010307 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
10 | nsv604555 | chr6:118695049-118856822 | Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
11 | nsv1034448 | chr6:118698169-119016383 | Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
12 | nsv1025097 | chr6:118699752-119058789 | Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
13 | nsv1020586 | chr6:118711098-118900012 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 7 gene(s) | inside rSNPs | diseases |
14 | nsv532052 | chr6:118711850-119057295 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
15 | nsv432959 | chr6:118716318-119010307 | Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
16 | nsv604556 | chr6:118722589-119065365 | Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
17 | nsv432960 | chr6:118723307-118826307 | Strong transcription ZNF genes & repeats Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 2 gene(s) | inside rSNPs | diseases |
18 | nsv525179 | chr6:118726243-118876092 | Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 6 gene(s) | inside rSNPs | diseases |
19 | nsv1019357 | chr6:118731468-118860705 | Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:118730400-118745000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr6:118737800-118748000 | Weak transcription | Aorta | Aorta |