Variant report
Variant | rs16906211 |
---|---|
Chromosome Location | chr12:30488911-30488912 |
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] |
---|---|
rs10082751 | 0.93[CEU][hapmap] |
rs10082827 | 0.86[EUR][1000 genomes] |
rs10082936 | 0.86[EUR][1000 genomes] |
rs10083054 | 0.87[CEU][hapmap];0.86[EUR][1000 genomes] |
rs10506066 | 1.00[CEU][hapmap] |
rs10771701 | 0.87[EUR][1000 genomes] |
rs10771702 | 0.88[EUR][1000 genomes] |
rs10843721 | 0.87[EUR][1000 genomes] |
rs10843722 | 0.88[EUR][1000 genomes] |
rs10843729 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs11050819 | 0.93[CEU][hapmap];0.86[EUR][1000 genomes] |
rs11050824 | 0.87[EUR][1000 genomes] |
rs11050825 | 0.87[EUR][1000 genomes] |
rs11050839 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs11050841 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs11050842 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs11050843 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs11050844 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs11050845 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs11050846 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs11050855 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs11050856 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs11050857 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs11050861 | 0.82[AMR][1000 genomes] |
rs11050862 | 0.82[AMR][1000 genomes] |
rs11050863 | 0.82[AMR][1000 genomes] |
rs11050865 | 0.82[AMR][1000 genomes] |
rs11834249 | 0.86[EUR][1000 genomes] |
rs11835626 | 0.87[EUR][1000 genomes] |
rs11836218 | 0.82[AMR][1000 genomes] |
rs12313162 | 0.86[EUR][1000 genomes] |
rs12322792 | 0.87[EUR][1000 genomes] |
rs12322860 | 0.87[EUR][1000 genomes] |
rs12578380 | 0.87[EUR][1000 genomes] |
rs12578733 | 0.82[AMR][1000 genomes] |
rs12578937 | 0.82[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs12579164 | 0.82[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs12579212 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs12579259 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs12579283 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs12579317 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs12579379 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs12579517 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs12580125 | 0.82[AMR][1000 genomes] |
rs12580134 | 0.82[AMR][1000 genomes] |
rs12580148 | 0.82[AMR][1000 genomes] |
rs12580195 | 0.82[AMR][1000 genomes] |
rs12580203 | 0.82[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs12580204 | 0.82[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs12580209 | 0.82[AMR][1000 genomes] |
rs12580501 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs12580598 | 0.87[EUR][1000 genomes] |
rs12580879 | 0.87[EUR][1000 genomes] |
rs12581209 | 0.82[AMR][1000 genomes] |
rs12581410 | 0.82[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs12582064 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs12582654 | 0.82[AMR][1000 genomes] |
rs12582684 | 0.82[AMR][1000 genomes] |
rs1320922 | 0.93[CEU][hapmap] |
rs1320923 | 0.93[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes] |
rs1320925 | 0.87[CEU][hapmap] |
rs1429622 | 1.00[CEU][hapmap];0.87[EUR][1000 genomes] |
rs1429636 | 0.87[ASN][1000 genomes] |
rs1506373 | 0.87[EUR][1000 genomes] |
rs1506374 | 0.87[EUR][1000 genomes] |
rs1506375 | 0.87[EUR][1000 genomes] |
rs1612581 | 0.90[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes] |
rs1612791 | 0.87[ASN][1000 genomes] |
rs1612949 | 0.87[ASN][1000 genomes] |
rs1652138 | 0.86[CEU][hapmap];0.88[EUR][1000 genomes] |
rs1652184 | 0.86[CEU][hapmap] |
rs1652186 | 0.94[CHB][hapmap];0.85[JPT][hapmap];0.87[ASN][1000 genomes] |
rs1652187 | 0.85[ASN][1000 genomes] |
rs1652188 | 0.87[ASN][1000 genomes] |
rs1652191 | 0.87[ASN][1000 genomes] |
rs1652193 | 0.87[ASN][1000 genomes] |
rs16906208 | 0.91[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs16906270 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs16906272 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs16906285 | 0.82[AMR][1000 genomes] |
rs16906287 | 0.82[AMR][1000 genomes] |
rs16906288 | 0.82[AMR][1000 genomes] |
rs16906306 | 0.82[AMR][1000 genomes] |
rs1731490 | 0.87[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes] |
rs1731491 | 0.93[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.85[ASN][1000 genomes] |
rs1731492 | 0.87[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes] |
rs1731493 | 0.87[ASN][1000 genomes] |
rs1731500 | 0.87[ASN][1000 genomes] |
rs17464127 | 1.00[CEU][hapmap];0.81[YRI][hapmap];0.86[AFR][1000 genomes];0.88[EUR][1000 genomes] |
rs17525182 | 0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs1827905 | 0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs1827906 | 0.82[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs1881930 | 0.82[AMR][1000 genomes] |
rs2115689 | 0.86[EUR][1000 genomes] |
rs2115690 | 0.86[EUR][1000 genomes] |
rs2163114 | 0.86[EUR][1000 genomes] |
rs2163115 | 0.87[EUR][1000 genomes] |
rs2564526 | 0.87[ASN][1000 genomes] |
rs2564527 | 0.87[ASN][1000 genomes] |
rs2700023 | 1.00[CEU][hapmap] |
rs2700026 | 0.87[ASN][1000 genomes] |
rs2703363 | 0.87[ASN][1000 genomes] |
rs354128 | 0.81[EUR][1000 genomes] |
rs35751841 | 0.82[AMR][1000 genomes] |
rs4032076 | 0.87[EUR][1000 genomes] |
rs4032077 | 0.86[EUR][1000 genomes] |
rs4032078 | 0.86[EUR][1000 genomes] |
rs4032081 | 0.87[EUR][1000 genomes] |
rs4032082 | 0.86[EUR][1000 genomes] |
rs4032092 | 0.87[EUR][1000 genomes] |
rs4304873 | 0.87[EUR][1000 genomes] |
rs4304874 | 0.87[EUR][1000 genomes] |
rs4426203 | 0.86[EUR][1000 genomes] |
rs4444166 | 0.87[EUR][1000 genomes] |
rs4536303 | 0.82[AMR][1000 genomes] |
rs4562911 | 0.84[EUR][1000 genomes] |
rs4564417 | 0.86[EUR][1000 genomes] |
rs58747169 | 0.87[EUR][1000 genomes] |
rs6487902 | 0.80[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs7138814 | 0.80[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs7139058 | 0.80[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs7139191 | 0.80[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs7139306 | 0.80[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs7299777 | 0.82[AMR][1000 genomes] |
rs73287069 | 0.87[EUR][1000 genomes] |
rs7358618 | 0.87[EUR][1000 genomes] |
rs7358619 | 0.87[EUR][1000 genomes] |
rs7358666 | 0.87[EUR][1000 genomes] |
rs7485854 | 0.85[EUR][1000 genomes] |
rs7962895 | 0.80[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs7977589 | 0.87[EUR][1000 genomes] |
rs906114 | 0.87[EUR][1000 genomes] |
rs906115 | 0.87[EUR][1000 genomes] |
rs9804786 | 0.87[EUR][1000 genomes] |
rs9804787 | 0.87[EUR][1000 genomes] |
rs9805027 | 0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv832360 | chr12:30393329-30555693 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | esv3343291 | chr12:30455597-30992837 | Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 48 gene(s) | inside rSNPs | diseases |
3 | nsv558013 | chr12:30478371-30491382 | Enhancers Weak transcription ZNF genes & repeats | n/a | n/a | inside rSNPs | diseases |
4 | nsv558014 | chr12:30478371-30492671 | Enhancers Weak transcription ZNF genes & repeats | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:30484600-30490400 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |