Variant report
Variant | rs2219791 |
---|---|
Chromosome Location | chr12:21476113-21476114 |
allele | A/G/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] |
---|---|
rs10431251 | 0.94[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10459074 | 0.99[ASN][1000 genomes] |
rs10459075 | 0.99[ASN][1000 genomes] |
rs10743411 | 0.98[ASN][1000 genomes] |
rs10743412 | 0.98[ASN][1000 genomes] |
rs10770795 | 0.92[ASN][1000 genomes] |
rs10770796 | 0.98[ASN][1000 genomes] |
rs10770797 | 0.99[ASN][1000 genomes] |
rs10841777 | 0.89[ASN][1000 genomes] |
rs10841778 | 0.87[ASN][1000 genomes] |
rs10841779 | 0.89[ASN][1000 genomes] |
rs10841780 | 0.89[ASN][1000 genomes] |
rs10841781 | 0.87[ASN][1000 genomes] |
rs10841782 | 0.87[ASN][1000 genomes] |
rs10841786 | 0.89[ASN][1000 genomes] |
rs10841787 | 0.89[ASN][1000 genomes] |
rs10841790 | 0.97[ASN][1000 genomes] |
rs10841791 | 0.99[ASN][1000 genomes] |
rs10841794 | 0.99[ASN][1000 genomes] |
rs11045922 | 0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs11045923 | 0.86[ASN][1000 genomes] |
rs11045924 | 0.89[ASN][1000 genomes] |
rs11045925 | 0.89[ASN][1000 genomes] |
rs11045929 | 0.89[ASN][1000 genomes] |
rs11045941 | 0.90[ASN][1000 genomes] |
rs11045944 | 0.92[ASN][1000 genomes] |
rs11045948 | 0.94[ASN][1000 genomes] |
rs11045954 | 0.93[ASN][1000 genomes] |
rs11045955 | 0.94[ASN][1000 genomes] |
rs11045962 | 0.93[ASN][1000 genomes] |
rs11045965 | 0.96[ASN][1000 genomes] |
rs11045966 | 0.95[ASN][1000 genomes] |
rs11045967 | 1.00[ASN][1000 genomes] |
rs11045968 | 1.00[ASN][1000 genomes] |
rs11045969 | 0.99[ASN][1000 genomes] |
rs11045970 | 1.00[ASN][1000 genomes] |
rs11045971 | 1.00[ASN][1000 genomes] |
rs11045974 | 0.99[ASN][1000 genomes] |
rs11045975 | 0.99[ASN][1000 genomes] |
rs11045976 | 0.99[ASN][1000 genomes] |
rs11045980 | 0.99[ASN][1000 genomes] |
rs11533477 | 0.89[ASN][1000 genomes] |
rs11535998 | 0.90[ASN][1000 genomes] |
rs11536000 | 0.89[ASN][1000 genomes] |
rs11537394 | 0.89[ASN][1000 genomes] |
rs11561152 | 0.90[ASN][1000 genomes] |
rs12227319 | 1.00[ASN][1000 genomes] |
rs12228765 | 1.00[ASN][1000 genomes] |
rs12230113 | 0.87[ASN][1000 genomes] |
rs12230350 | 0.88[ASN][1000 genomes] |
rs12230401 | 0.88[ASN][1000 genomes] |
rs12231212 | 0.98[ASN][1000 genomes] |
rs12231484 | 0.99[ASN][1000 genomes] |
rs12231738 | 0.89[ASN][1000 genomes] |
rs12311809 | 0.86[ASN][1000 genomes] |
rs12581287 | 1.00[ASN][1000 genomes] |
rs12581327 | 0.89[ASN][1000 genomes] |
rs16923597 | 0.82[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2127117 | 0.99[ASN][1000 genomes] |
rs2127118 | 0.98[ASN][1000 genomes] |
rs2169883 | 0.99[ASN][1000 genomes] |
rs2219793 | 0.99[ASN][1000 genomes] |
rs2306226 | 0.99[ASN][1000 genomes] |
rs2306227 | 0.99[ASN][1000 genomes] |
rs2306229 | 0.96[ASN][1000 genomes] |
rs2306231 | 0.98[ASN][1000 genomes] |
rs2417971 | 0.84[ASN][1000 genomes] |
rs2417974 | 0.95[ASN][1000 genomes] |
rs36089711 | 0.88[ASN][1000 genomes] |
rs3736080 | 0.88[ASN][1000 genomes] |
rs3736081 | 0.89[ASN][1000 genomes] |
rs3751270 | 0.93[ASN][1000 genomes] |
rs3764041 | 0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3764042 | 0.99[ASN][1000 genomes] |
rs3764044 | 0.89[ASN][1000 genomes] |
rs3764045 | 0.90[ASN][1000 genomes] |
rs3794319 | 0.93[ASN][1000 genomes] |
rs4115170 | 0.99[ASN][1000 genomes] |
rs4140389 | 0.93[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4148977 | 0.98[ASN][1000 genomes] |
rs4148978 | 0.98[ASN][1000 genomes] |
rs4148981 | 0.98[ASN][1000 genomes] |
rs4148982 | 0.99[ASN][1000 genomes] |
rs4148983 | 0.99[ASN][1000 genomes] |
rs4148984 | 0.99[ASN][1000 genomes] |
rs4148985 | 0.99[ASN][1000 genomes] |
rs4148986 | 0.99[ASN][1000 genomes] |
rs4148987 | 0.98[ASN][1000 genomes] |
rs4148988 | 0.98[ASN][1000 genomes] |
rs4148989 | 0.99[ASN][1000 genomes] |
rs4148990 | 0.99[ASN][1000 genomes] |
rs4148991 | 0.99[ASN][1000 genomes] |
rs4148992 | 0.98[ASN][1000 genomes] |
rs4148993 | 0.93[ASN][1000 genomes] |
rs4148994 | 0.94[ASN][1000 genomes] |
rs4148995 | 0.94[ASN][1000 genomes] |
rs4148996 | 0.94[ASN][1000 genomes] |
rs4148997 | 0.94[ASN][1000 genomes] |
rs4148998 | 0.93[ASN][1000 genomes] |
rs4148999 | 0.93[ASN][1000 genomes] |
rs4149001 | 0.94[ASN][1000 genomes] |
rs4149002 | 0.92[ASN][1000 genomes] |
rs4149003 | 0.92[ASN][1000 genomes] |
rs4149004 | 0.88[ASN][1000 genomes] |
rs4149005 | 0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4149006 | 0.86[ASN][1000 genomes] |
rs4149007 | 0.86[ASN][1000 genomes] |
rs4149008 | 0.94[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs4149009 | 0.84[ASN][1000 genomes] |
rs57899519 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs6487216 | 0.98[ASN][1000 genomes] |
rs6487217 | 0.98[ASN][1000 genomes] |
rs7296472 | 0.99[ASN][1000 genomes] |
rs7300346 | 0.99[ASN][1000 genomes] |
rs7300463 | 0.99[ASN][1000 genomes] |
rs7305911 | 0.92[ASN][1000 genomes] |
rs7313671 | 0.99[ASN][1000 genomes] |
rs7315667 | 0.99[ASN][1000 genomes] |
rs7955581 | 0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs7957203 | 0.99[ASN][1000 genomes] |
rs7963398 | 0.98[ASN][1000 genomes] |
rs7967354 | 0.94[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs7967935 | 0.99[ASN][1000 genomes] |
rs7968331 | 0.99[ASN][1000 genomes] |
rs7968842 | 0.99[ASN][1000 genomes] |
rs7977517 | 0.98[ASN][1000 genomes] |
rs7977652 | 0.98[ASN][1000 genomes] |
rs7978981 | 0.98[ASN][1000 genomes] |
rs7980842 | 0.88[ASN][1000 genomes] |
rs875234 | 0.93[EUR][1000 genomes];0.87[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv557735 | chr12:21443282-21538957 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:21473800-21477800 | Active TSS | Brain Angular Gyrus | brain |
2 | chr12:21473800-21477800 | Active TSS | Brain Cingulate Gyrus | brain |
3 | chr12:21473800-21478200 | Active TSS | Brain Anterior Caudate | brain |
4 | chr12:21474600-21477800 | Active TSS | Brain Hippocampus Middle | brain |
5 | chr12:21474800-21478000 | Active TSS | Brain Substantia Nigra | brain |
6 | chr12:21475400-21478000 | Active TSS | Brain Inferior Temporal Lobe | brain |
7 | chr12:21475600-21477400 | Active TSS | Brain Dorsolateral Prefrontal Cortex | brain |
8 | chr12:21475800-21476600 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
9 | chr12:21476000-21476200 | Weak transcription | H1 Cell Line | embryonic stem cell |
10 | chr12:21476000-21476400 | Weak transcription | HUES64 Cell Line | embryonic stem cell |