Variant report
Variant | rs10456349 |
---|---|
Chromosome Location | chr6:26975459-26975460 |
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 |
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No data |
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rs_ID | r2[population] |
---|---|
rs10946896 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10946900 | 0.94[ASN][1000 genomes] |
rs1102557 | 0.85[ASN][1000 genomes] |
rs11961179 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11961181 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11961960 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs11962196 | 0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11966939 | 0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11969887 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12153912 | 0.85[ASN][1000 genomes] |
rs12190201 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12192049 | 0.80[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12192320 | 0.94[ASN][1000 genomes] |
rs12192446 | 0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12192502 | 0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12192766 | 0.84[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12192793 | 0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12193463 | 1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12193511 | 0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12193820 | 0.94[ASN][1000 genomes] |
rs12195041 | 1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12195144 | 0.82[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12196889 | 0.88[ASN][1000 genomes] |
rs12199218 | 0.88[ASN][1000 genomes] |
rs12200482 | 0.80[EUR][1000 genomes] |
rs12200985 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12201498 | 0.82[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12201774 | 0.94[ASN][1000 genomes] |
rs12203145 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12203454 | 0.88[ASN][1000 genomes] |
rs12203728 | 0.80[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12204280 | 0.88[ASN][1000 genomes] |
rs12205921 | 0.94[ASN][1000 genomes] |
rs12206996 | 0.94[ASN][1000 genomes] |
rs12207614 | 0.82[ASN][1000 genomes] |
rs12208039 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12208534 | 0.94[ASN][1000 genomes] |
rs12209393 | 0.94[ASN][1000 genomes] |
rs12209429 | 0.80[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12209456 | 0.94[ASN][1000 genomes] |
rs12210905 | 0.85[ASN][1000 genomes] |
rs12212317 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12213361 | 0.91[ASN][1000 genomes] |
rs12214848 | 0.94[ASN][1000 genomes] |
rs12214930 | 0.94[ASN][1000 genomes] |
rs12215241 | 0.91[ASN][1000 genomes] |
rs12215773 | 0.91[ASN][1000 genomes] |
rs13207365 | 0.88[ASN][1000 genomes] |
rs17345718 | 1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3531 | 0.94[ASN][1000 genomes] |
rs36048693 | 0.88[ASN][1000 genomes] |
rs3922717 | 0.88[ASN][1000 genomes] |
rs3999221 | 0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs41269245 | 0.94[ASN][1000 genomes] |
rs4541737 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4636015 | 0.94[ASN][1000 genomes] |
rs6911234 | 0.94[ASN][1000 genomes] |
rs6920115 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6931711 | 0.85[ASN][1000 genomes] |
rs6937764 | 0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6937955 | 0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6940638 | 0.91[ASN][1000 genomes] |
rs72838236 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72838238 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72838243 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72838245 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72838249 | 0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72838258 | 0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72838260 | 0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72838262 | 0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72838263 | 0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72838266 | 0.85[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs72838268 | 0.91[ASN][1000 genomes] |
rs72842200 | 0.94[ASN][1000 genomes] |
rs72843607 | 0.94[ASN][1000 genomes] |
rs72843608 | 0.94[ASN][1000 genomes] |
rs72843609 | 0.91[ASN][1000 genomes] |
rs72843611 | 0.91[ASN][1000 genomes] |
rs72843613 | 0.91[ASN][1000 genomes] |
rs72843615 | 0.85[ASN][1000 genomes] |
rs72843619 | 0.88[ASN][1000 genomes] |
rs72843629 | 0.85[ASN][1000 genomes] |
rs72843633 | 0.85[ASN][1000 genomes] |
rs7740207 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7753123 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7753284 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7756481 | 0.94[ASN][1000 genomes] |
rs7757680 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs7773336 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs858995 | 0.85[ASN][1000 genomes] |
rs9461316 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9467939 | 0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9467940 | 0.90[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9467942 | 0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9467948 | 0.91[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs9467965 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9467971 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv948921 | chr6:26556890-27443957 | Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 472 gene(s) | inside rSNPs | diseases |
2 | esv2758038 | chr6:26695219-27095714 | Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 67 gene(s) | inside rSNPs | diseases |
3 | esv2759410 | chr6:26695219-27095714 | Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 67 gene(s) | inside rSNPs | diseases |
4 | nsv1029124 | chr6:26825468-27109774 | Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 244 gene(s) | inside rSNPs | diseases |
5 | nsv469610 | chr6:26841083-26999230 | Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
6 | nsv482509 | chr6:26841083-26999230 | Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
7 | nsv471636 | chr6:26841084-27038175 | Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 27 gene(s) | inside rSNPs | diseases |
8 | esv19090 | chr6:26843813-26983456 | Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
9 | nsv469675 | chr6:26848950-27015598 | Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
10 | nsv482429 | chr6:26848950-27015598 | Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
11 | nsv830616 | chr6:26859097-27030476 | ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
12 | esv1793267 | chr6:26864376-26987405 | Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
13 | esv1811325 | chr6:26869783-26987405 | Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
14 | esv1795502 | chr6:26873947-26983005 | Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
15 | esv1795223 | chr6:26877074-26987205 | Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
16 | esv1809024 | chr6:26877074-26987205 | Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
17 | esv1810582 | chr6:26889428-26990246 | Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 22 gene(s) | inside rSNPs | diseases |
18 | nsv469625 | chr6:26893739-27038175 | Flanking Active TSS Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 26 gene(s) | inside rSNPs | diseases |
19 | nsv482537 | chr6:26893739-27038175 | Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 26 gene(s) | inside rSNPs | diseases |
20 | esv15177 | chr6:26916403-26987915 | Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 21 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:26972600-26979200 | Weak transcription | Brain Substantia Nigra | brain |
2 | chr6:26973400-26983800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr6:26973600-26976200 | Weak transcription | Liver | Liver |
4 | chr6:26974400-26986400 | Weak transcription | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
5 | chr6:26974800-26975800 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
6 | chr6:26975000-26976200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
7 | chr6:26975200-26976200 | Weak transcription | Ovary | ovary |
8 | chr6:26975200-26986600 | Weak transcription | Stomach Smooth Muscle | stomach |