Variant report
Variant | rs34633836 |
---|---|
Chromosome Location | chr10:55260590-55260591 |
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] |
---|---|
rs11003643 | 0.81[AFR][1000 genomes] |
rs11003657 | 1.00[ASN][1000 genomes] |
rs11812259 | 1.00[ASN][1000 genomes] |
rs11812663 | 1.00[ASN][1000 genomes] |
rs11813997 | 1.00[ASN][1000 genomes] |
rs11814685 | 1.00[ASN][1000 genomes] |
rs11816676 | 1.00[ASN][1000 genomes] |
rs11817911 | 1.00[ASN][1000 genomes] |
rs11818534 | 1.00[ASN][1000 genomes] |
rs12762519 | 1.00[ASN][1000 genomes] |
rs12762857 | 1.00[ASN][1000 genomes] |
rs12763251 | 1.00[ASN][1000 genomes] |
rs12763853 | 1.00[ASN][1000 genomes] |
rs12764777 | 1.00[ASN][1000 genomes] |
rs12766128 | 0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12767042 | 1.00[ASN][1000 genomes] |
rs12767051 | 0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12767289 | 1.00[ASN][1000 genomes] |
rs12768602 | 0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12771089 | 1.00[ASN][1000 genomes] |
rs12771423 | 0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12771750 | 1.00[ASN][1000 genomes] |
rs12771866 | 1.00[ASN][1000 genomes] |
rs12772547 | 0.88[AFR][1000 genomes];0.88[AMR][1000 genomes] |
rs12772572 | 0.89[AFR][1000 genomes];0.80[AMR][1000 genomes] |
rs12772777 | 1.00[ASN][1000 genomes] |
rs12772990 | 0.94[AFR][1000 genomes];0.89[AMR][1000 genomes] |
rs12776740 | 1.00[ASN][1000 genomes] |
rs12778636 | 1.00[ASN][1000 genomes] |
rs12779337 | 0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs12784700 | 0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs34038423 | 1.00[ASN][1000 genomes] |
rs34071784 | 1.00[ASN][1000 genomes] |
rs34135641 | 0.87[AFR][1000 genomes];0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs34216097 | 1.00[ASN][1000 genomes] |
rs34260847 | 1.00[ASN][1000 genomes] |
rs34274587 | 1.00[ASN][1000 genomes] |
rs34284453 | 0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs34345813 | 0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs34373500 | 0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs34375821 | 1.00[ASN][1000 genomes] |
rs34433914 | 1.00[ASN][1000 genomes] |
rs34476067 | 1.00[ASN][1000 genomes] |
rs34517473 | 0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs34535347 | 0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs34640672 | 1.00[ASN][1000 genomes] |
rs34751043 | 1.00[ASN][1000 genomes] |
rs34847447 | 0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs34894185 | 0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs35066816 | 1.00[ASN][1000 genomes] |
rs35082584 | 1.00[ASN][1000 genomes] |
rs35090347 | 1.00[ASN][1000 genomes] |
rs35096407 | 1.00[ASN][1000 genomes] |
rs35160613 | 0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs351819 | 1.00[ASN][1000 genomes] |
rs351820 | 1.00[ASN][1000 genomes] |
rs35206171 | 1.00[ASN][1000 genomes] |
rs35317048 | 1.00[ASN][1000 genomes] |
rs35604248 | 1.00[ASN][1000 genomes] |
rs35609676 | 1.00[ASN][1000 genomes] |
rs35635224 | 0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs35639921 | 1.00[ASN][1000 genomes] |
rs35659760 | 1.00[ASN][1000 genomes] |
rs35662065 | 1.00[ASN][1000 genomes] |
rs35704741 | 1.00[ASN][1000 genomes] |
rs35834597 | 1.00[ASN][1000 genomes] |
rs36047711 | 1.00[ASN][1000 genomes] |
rs36068349 | 1.00[ASN][1000 genomes] |
rs58389486 | 0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs59911333 | 0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs66484271 | 1.00[ASN][1000 genomes] |
rs66624849 | 1.00[ASN][1000 genomes] |
rs66715040 | 0.82[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs66778160 | 1.00[ASN][1000 genomes] |
rs66825416 | 1.00[ASN][1000 genomes] |
rs67035493 | 1.00[ASN][1000 genomes] |
rs67254307 | 1.00[ASN][1000 genomes] |
rs67398316 | 1.00[ASN][1000 genomes] |
rs67524958 | 1.00[ASN][1000 genomes] |
rs67606828 | 0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs67671940 | 1.00[ASN][1000 genomes] |
rs67746475 | 0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs67779403 | 1.00[ASN][1000 genomes] |
rs67805701 | 0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs68120396 | 0.88[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs68130066 | 1.00[ASN][1000 genomes] |
rs7069859 | 1.00[ASN][1000 genomes] |
rs7070023 | 1.00[ASN][1000 genomes] |
rs7070911 | 1.00[ASN][1000 genomes] |
rs7072768 | 1.00[ASN][1000 genomes] |
rs7073482 | 1.00[ASN][1000 genomes] |
rs7073891 | 1.00[ASN][1000 genomes] |
rs7081932 | 1.00[ASN][1000 genomes] |
rs7082398 | 1.00[ASN][1000 genomes] |
rs7083591 | 1.00[ASN][1000 genomes] |
rs7084403 | 1.00[ASN][1000 genomes] |
rs7084882 | 1.00[ASN][1000 genomes] |
rs7085026 | 1.00[ASN][1000 genomes] |
rs7086598 | 1.00[ASN][1000 genomes] |
rs7086889 | 1.00[ASN][1000 genomes] |
rs7087312 | 1.00[ASN][1000 genomes] |
rs7090579 | 1.00[ASN][1000 genomes] |
rs7100164 | 1.00[ASN][1000 genomes] |
rs7100590 | 1.00[ASN][1000 genomes] |
rs7100956 | 1.00[ASN][1000 genomes] |
rs7101007 | 1.00[ASN][1000 genomes] |
rs7101019 | 1.00[ASN][1000 genomes] |
rs7101316 | 1.00[ASN][1000 genomes] |
rs71490957 | 0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs71490966 | 1.00[ASN][1000 genomes] |
rs71490968 | 1.00[ASN][1000 genomes] |
rs71502020 | 0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs71502021 | 1.00[ASN][1000 genomes] |
rs73231800 | 1.00[ASN][1000 genomes] |
rs73233405 | 1.00[ASN][1000 genomes] |
rs73233406 | 1.00[ASN][1000 genomes] |
rs73233409 | 1.00[ASN][1000 genomes] |
rs73233410 | 1.00[ASN][1000 genomes] |
rs73233412 | 1.00[ASN][1000 genomes] |
rs73233413 | 1.00[ASN][1000 genomes] |
rs73233414 | 1.00[ASN][1000 genomes] |
rs73233416 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73233419 | 1.00[ASN][1000 genomes] |
rs73233420 | 1.00[ASN][1000 genomes] |
rs73233421 | 1.00[ASN][1000 genomes] |
rs73237596 | 1.00[ASN][1000 genomes] |
rs73239887 | 1.00[ASN][1000 genomes] |
rs73347344 | 0.81[AFR][1000 genomes] |
rs73347346 | 0.81[AFR][1000 genomes] |
rs73347349 | 0.81[AFR][1000 genomes] |
rs73347350 | 0.81[AFR][1000 genomes] |
rs73347353 | 0.81[AFR][1000 genomes] |
rs73347357 | 0.84[AFR][1000 genomes] |
rs73347374 | 0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73356752 | 0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs7919179 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2752952 | chr10:54900994-55497594 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
2 | nsv1041908 | chr10:55003164-55283251 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv540629 | chr10:55003164-55283251 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
4 | nsv1040943 | chr10:55040577-55279797 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv540630 | chr10:55040577-55279797 | Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv1037480 | chr10:55102814-55289571 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
7 | esv2755889 | chr10:55150173-55278481 | Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
8 | nsv1048399 | chr10:55151470-55313737 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
9 | nsv1044282 | chr10:55186501-55516392 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
10 | nsv540631 | chr10:55186501-55516392 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
11 | nsv1043501 | chr10:55186701-55516253 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
12 | nsv540632 | chr10:55186701-55516253 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
13 | nsv1050323 | chr10:55190079-55546575 | Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:55259000-55261000 | ZNF genes & repeats | H9 Cell Line | embryonic stem cell |
2 | chr10:55259200-55261000 | ZNF genes & repeats | H1 Cell Line | embryonic stem cell |
3 | chr10:55259400-55261000 | ZNF genes & repeats | ES-I3 Cell Line | embryonic stem cell |
4 | chr10:55259400-55261000 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
5 | chr10:55259400-55261000 | ZNF genes & repeats | iPS-20b Cell Line | embryonic stem cell |
6 | chr10:55259400-55272600 | Weak transcription | ES-WA7 Cell Line | embryonic stem cell |
7 | chr10:55259800-55265200 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
8 | chr10:55259800-55268400 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
9 | chr10:55260000-55261000 | Strong transcription | ES-UCSF4 Cell Line | embryonic stem cell |