Variant report
Variant | rs11903271 |
---|---|
Chromosome Location | chr2:187702364-187702365 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr2:187700922..187703123-chr2:187703577..187706331,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10164815 | 1.00[ASN][1000 genomes] |
rs10166117 | 0.81[ASN][1000 genomes] |
rs10169570 | 1.00[ASN][1000 genomes] |
rs10169582 | 1.00[ASN][1000 genomes] |
rs10169671 | 1.00[ASN][1000 genomes] |
rs10172225 | 1.00[ASN][1000 genomes] |
rs10175178 | 1.00[ASN][1000 genomes] |
rs10178860 | 1.00[ASN][1000 genomes] |
rs10179175 | 1.00[ASN][1000 genomes] |
rs10181270 | 1.00[ASN][1000 genomes] |
rs10183672 | 1.00[ASN][1000 genomes] |
rs10187599 | 1.00[ASN][1000 genomes] |
rs10188450 | 1.00[ASN][1000 genomes] |
rs10188850 | 1.00[ASN][1000 genomes] |
rs10188869 | 1.00[ASN][1000 genomes] |
rs10189037 | 1.00[ASN][1000 genomes] |
rs10191094 | 1.00[ASN][1000 genomes] |
rs10191209 | 1.00[ASN][1000 genomes] |
rs10195632 | 1.00[ASN][1000 genomes] |
rs10195758 | 1.00[ASN][1000 genomes] |
rs10200056 | 1.00[ASN][1000 genomes] |
rs10200250 | 1.00[ASN][1000 genomes] |
rs10201183 | 1.00[ASN][1000 genomes] |
rs10201512 | 0.83[ASN][1000 genomes] |
rs10204903 | 1.00[ASN][1000 genomes] |
rs10207244 | 1.00[ASN][1000 genomes] |
rs10207487 | 1.00[ASN][1000 genomes] |
rs10210233 | 1.00[ASN][1000 genomes] |
rs10210806 | 1.00[ASN][1000 genomes] |
rs10211050 | 0.83[ASN][1000 genomes] |
rs11885224 | 0.81[ASN][1000 genomes] |
rs11892669 | 1.00[ASN][1000 genomes] |
rs11894819 | 1.00[ASN][1000 genomes] |
rs11898022 | 1.00[ASN][1000 genomes] |
rs11898112 | 1.00[ASN][1000 genomes] |
rs11898665 | 0.83[ASN][1000 genomes] |
rs11898741 | 1.00[ASN][1000 genomes] |
rs13399866 | 1.00[ASN][1000 genomes] |
rs13400804 | 1.00[ASN][1000 genomes] |
rs13401173 | 0.83[ASN][1000 genomes] |
rs13401579 | 1.00[ASN][1000 genomes] |
rs13407429 | 0.81[ASN][1000 genomes] |
rs13414169 | 1.00[ASN][1000 genomes] |
rs13426438 | 1.00[ASN][1000 genomes] |
rs13431108 | 0.81[ASN][1000 genomes] |
rs13431163 | 0.81[ASN][1000 genomes] |
rs1451556 | 0.81[ASN][1000 genomes] |
rs17852915 | 1.00[ASN][1000 genomes] |
rs17852916 | 1.00[ASN][1000 genomes] |
rs17856918 | 1.00[ASN][1000 genomes] |
rs2084752 | 0.81[ASN][1000 genomes] |
rs2084753 | 0.81[ASN][1000 genomes] |
rs2084754 | 0.81[ASN][1000 genomes] |
rs28475061 | 0.83[ASN][1000 genomes] |
rs28740839 | 1.00[ASN][1000 genomes] |
rs35121986 | 1.00[ASN][1000 genomes] |
rs4429438 | 1.00[ASN][1000 genomes] |
rs4545967 | 1.00[ASN][1000 genomes] |
rs61626504 | 0.81[ASN][1000 genomes] |
rs62171870 | 0.91[ASN][1000 genomes] |
rs62171892 | 1.00[ASN][1000 genomes] |
rs6434197 | 1.00[ASN][1000 genomes] |
rs6708289 | 1.00[ASN][1000 genomes] |
rs6711860 | 0.83[ASN][1000 genomes] |
rs6722473 | 1.00[ASN][1000 genomes] |
rs6725956 | 0.81[ASN][1000 genomes] |
rs6726153 | 0.81[ASN][1000 genomes] |
rs6733279 | 1.00[ASN][1000 genomes] |
rs6736846 | 0.83[ASN][1000 genomes] |
rs6738033 | 0.81[ASN][1000 genomes] |
rs6744956 | 1.00[ASN][1000 genomes] |
rs6745065 | 1.00[ASN][1000 genomes] |
rs6745572 | 1.00[ASN][1000 genomes] |
rs6745642 | 1.00[ASN][1000 genomes] |
rs6750961 | 1.00[ASN][1000 genomes] |
rs6751828 | 1.00[ASN][1000 genomes] |
rs6752200 | 1.00[ASN][1000 genomes] |
rs6760362 | 1.00[ASN][1000 genomes] |
rs72895306 | 1.00[ASN][1000 genomes] |
rs7581809 | 1.00[ASN][1000 genomes] |
rs7595459 | 1.00[ASN][1000 genomes] |
rs7598838 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv428069 | chr2:187575692-187766209 | ZNF genes & repeats Weak transcription Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:187701000-187706800 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
2 | chr2:187701600-187705800 | Weak transcription | Osteobl | bone |