Variant report
Variant | rs17008315 |
---|---|
Chromosome Location | chr2:72834955-72834956 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs10175824 | 1.00[ASN][1000 genomes] |
rs10176044 | 1.00[ASN][1000 genomes] |
rs10496183 | 1.00[ASN][1000 genomes] |
rs10496185 | 0.92[CEU][hapmap];0.89[YRI][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10496187 | 1.00[YRI][hapmap] |
rs11126367 | 1.00[ASN][1000 genomes] |
rs11126369 | 0.84[YRI][hapmap] |
rs11126378 | 0.92[CEU][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs11674508 | 1.00[ASN][1000 genomes] |
rs11681845 | 1.00[ASN][1000 genomes] |
rs11684981 | 1.00[ASN][1000 genomes] |
rs11685876 | 1.00[ASN][1000 genomes] |
rs11689339 | 0.92[CEU][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs11689707 | 0.92[CEU][hapmap];0.86[YRI][hapmap];1.00[ASN][1000 genomes] |
rs11695000 | 1.00[ASN][1000 genomes] |
rs11884162 | 1.00[ASN][1000 genomes] |
rs11884225 | 1.00[ASN][1000 genomes] |
rs11884266 | 1.00[CEU][hapmap];0.93[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs11887356 | 1.00[ASN][1000 genomes] |
rs11892598 | 0.92[CEU][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11897200 | 1.00[ASN][1000 genomes] |
rs11903908 | 1.00[ASN][1000 genomes] |
rs12619565 | 0.93[YRI][hapmap] |
rs1517179 | 1.00[ASN][1000 genomes] |
rs1562361 | 0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs17008143 | 1.00[ASN][1000 genomes] |
rs17008186 | 1.00[ASN][1000 genomes] |
rs17008188 | 1.00[ASN][1000 genomes] |
rs17008241 | 0.93[CEU][hapmap];0.85[EUR][1000 genomes] |
rs17008293 | 0.93[CEU][hapmap];0.86[YRI][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17008369 | 1.00[YRI][hapmap];0.82[AMR][1000 genomes] |
rs17008371 | 0.96[YRI][hapmap];0.82[AMR][1000 genomes] |
rs17040320 | 1.00[ASN][1000 genomes] |
rs1914339 | 1.00[ASN][1000 genomes] |
rs1949377 | 1.00[ASN][1000 genomes] |
rs2068410 | 0.93[YRI][hapmap] |
rs2901190 | 1.00[ASN][1000 genomes] |
rs4507127 | 1.00[ASN][1000 genomes] |
rs4508623 | 1.00[ASN][1000 genomes] |
rs4597553 | 0.93[YRI][hapmap] |
rs55642420 | 0.82[AMR][1000 genomes] |
rs55727931 | 1.00[ASN][1000 genomes] |
rs55728837 | 1.00[ASN][1000 genomes] |
rs55825364 | 1.00[ASN][1000 genomes] |
rs55840408 | 1.00[ASN][1000 genomes] |
rs55939880 | 1.00[ASN][1000 genomes] |
rs56058174 | 0.82[AMR][1000 genomes] |
rs56109129 | 1.00[ASN][1000 genomes] |
rs56173504 | 1.00[ASN][1000 genomes] |
rs56184446 | 1.00[ASN][1000 genomes] |
rs56718524 | 1.00[ASN][1000 genomes] |
rs56777837 | 1.00[ASN][1000 genomes] |
rs57192957 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs57286048 | 1.00[ASN][1000 genomes] |
rs58033567 | 1.00[ASN][1000 genomes] |
rs58967293 | 1.00[ASN][1000 genomes] |
rs59176504 | 1.00[ASN][1000 genomes] |
rs59216875 | 0.82[AMR][1000 genomes] |
rs59881252 | 1.00[ASN][1000 genomes] |
rs59974816 | 1.00[ASN][1000 genomes] |
rs60314340 | 0.95[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs60325013 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs60536402 | 1.00[ASN][1000 genomes] |
rs60563535 | 1.00[ASN][1000 genomes] |
rs60580301 | 1.00[ASN][1000 genomes] |
rs60806585 | 1.00[ASN][1000 genomes] |
rs6546769 | 1.00[ASN][1000 genomes] |
rs66469454 | 0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs66489235 | 1.00[ASN][1000 genomes] |
rs66539158 | 1.00[ASN][1000 genomes] |
rs66560019 | 1.00[ASN][1000 genomes] |
rs66794803 | 0.82[AMR][1000 genomes] |
rs66827358 | 1.00[ASN][1000 genomes] |
rs66920016 | 1.00[ASN][1000 genomes] |
rs67085067 | 1.00[ASN][1000 genomes] |
rs6711442 | 1.00[ASN][1000 genomes] |
rs6711701 | 0.85[EUR][1000 genomes] |
rs6712930 | 1.00[ASN][1000 genomes] |
rs6712989 | 1.00[ASN][1000 genomes] |
rs6713143 | 1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs6713712 | 0.93[CEU][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6716335 | 1.00[YRI][hapmap] |
rs67166018 | 1.00[ASN][1000 genomes] |
rs6717250 | 1.00[ASN][1000 genomes] |
rs6718052 | 1.00[ASN][1000 genomes] |
rs6731631 | 1.00[ASN][1000 genomes] |
rs6733532 | 1.00[ASN][1000 genomes] |
rs6733538 | 1.00[ASN][1000 genomes] |
rs6735400 | 1.00[ASN][1000 genomes] |
rs6736649 | 0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs6739768 | 0.93[CEU][hapmap];0.86[EUR][1000 genomes] |
rs6740390 | 0.92[CEU][hapmap] |
rs6743881 | 1.00[ASN][1000 genomes] |
rs6746583 | 1.00[ASN][1000 genomes] |
rs6746586 | 1.00[ASN][1000 genomes] |
rs67491855 | 1.00[ASN][1000 genomes] |
rs6749495 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs67535553 | 0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6755440 | 1.00[ASN][1000 genomes] |
rs6756070 | 0.92[CEU][hapmap];0.84[EUR][1000 genomes] |
rs6758689 | 1.00[ASN][1000 genomes] |
rs6761253 | 1.00[YRI][hapmap] |
rs67869181 | 0.84[EUR][1000 genomes] |
rs67970313 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72841795 | 1.00[ASN][1000 genomes] |
rs72845175 | 1.00[ASN][1000 genomes] |
rs7420583 | 1.00[ASN][1000 genomes] |
rs7424190 | 1.00[ASN][1000 genomes] |
rs7557942 | 1.00[ASN][1000 genomes] |
rs7561471 | 1.00[ASN][1000 genomes] |
rs7571517 | 1.00[ASN][1000 genomes] |
rs7573417 | 0.84[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs7575050 | 1.00[ASN][1000 genomes] |
rs7577244 | 1.00[ASN][1000 genomes] |
rs7583268 | 1.00[ASN][1000 genomes] |
rs7593084 | 1.00[YRI][hapmap] |
rs7596126 | 1.00[ASN][1000 genomes] |
rs7599755 | 1.00[ASN][1000 genomes] |
rs7600134 | 1.00[ASN][1000 genomes] |
rs7603342 | 1.00[ASN][1000 genomes] |
rs7603535 | 1.00[ASN][1000 genomes] |
rs7604083 | 0.93[CEU][hapmap];0.85[EUR][1000 genomes] |
rs7604296 | 1.00[ASN][1000 genomes] |
rs7604818 | 0.85[CEU][hapmap];0.84[EUR][1000 genomes] |
rs7607226 | 1.00[YRI][hapmap] |
rs7608054 | 1.00[ASN][1000 genomes] |
rs764766 | 0.92[CEU][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9677947 | 1.00[ASN][1000 genomes] |
rs9678682 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv874264 | chr2:72593243-72901170 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | nsv582208 | chr2:72690622-72835886 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv834257 | chr2:72701083-72853548 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv874265 | chr2:72789764-72982609 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:72830800-72837000 | Weak transcription | Fetal Heart | heart |
2 | chr2:72831000-72839800 | Weak transcription | Brain Substantia Nigra | brain |
3 | chr2:72831000-72841400 | Weak transcription | Brain Anterior Caudate | brain |
4 | chr2:72831000-72841400 | Weak transcription | Brain Inferior Temporal Lobe | brain |
5 | chr2:72831400-72840000 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
6 | chr2:72831800-72841800 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
7 | chr2:72832000-72837400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
8 | chr2:72834000-72843600 | Weak transcription | Fetal Intestine Small | intestine |