Variant report
Variant | rs62188290 |
---|---|
Chromosome Location | chr2:183316693-183316694 |
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] |
---|---|
rs10178586 | 0.89[ASN][1000 genomes] |
rs10207132 | 0.82[EUR][1000 genomes] |
rs10497600 | 0.87[EUR][1000 genomes] |
rs10497601 | 0.83[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs10497602 | 0.84[ASN][1000 genomes] |
rs10497603 | 0.81[ASN][1000 genomes] |
rs1125184 | 0.95[ASN][1000 genomes] |
rs12465662 | 0.89[ASN][1000 genomes] |
rs12465755 | 0.89[ASN][1000 genomes] |
rs12466618 | 0.83[ASN][1000 genomes] |
rs12466937 | 0.89[ASN][1000 genomes] |
rs12468232 | 0.83[ASN][1000 genomes] |
rs12468346 | 0.83[ASN][1000 genomes] |
rs12470124 | 0.86[ASN][1000 genomes] |
rs12473820 | 0.86[AFR][1000 genomes];0.91[ASN][1000 genomes] |
rs12474820 | 0.83[ASN][1000 genomes] |
rs12475048 | 0.83[ASN][1000 genomes] |
rs12478132 | 0.83[ASN][1000 genomes] |
rs12479259 | 0.83[ASN][1000 genomes] |
rs13407156 | 0.92[EUR][1000 genomes] |
rs1346775 | 0.83[ASN][1000 genomes] |
rs1367203 | 0.91[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs1367204 | 0.89[ASN][1000 genomes] |
rs1430160 | 0.87[ASN][1000 genomes] |
rs1583112 | 0.82[ASN][1000 genomes] |
rs1583114 | 0.81[EUR][1000 genomes] |
rs16823233 | 0.89[EUR][1000 genomes] |
rs16823254 | 0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs16823257 | 0.83[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs16823275 | 0.84[ASN][1000 genomes] |
rs17265027 | 0.90[EUR][1000 genomes] |
rs17265061 | 0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs17265166 | 0.83[ASN][1000 genomes] |
rs17265189 | 0.83[ASN][1000 genomes] |
rs17356166 | 0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs17356207 | 0.91[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs17356214 | 0.91[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs17356296 | 0.83[ASN][1000 genomes] |
rs17356303 | 0.83[ASN][1000 genomes] |
rs28569979 | 0.83[EUR][1000 genomes] |
rs34103461 | 0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs34744930 | 0.89[ASN][1000 genomes] |
rs35809203 | 0.89[ASN][1000 genomes] |
rs4318355 | 0.85[AFR][1000 genomes] |
rs4496292 | 0.84[ASN][1000 genomes] |
rs4572561 | 0.96[ASN][1000 genomes] |
rs4666582 | 0.89[ASN][1000 genomes] |
rs4666585 | 0.89[ASN][1000 genomes] |
rs4666835 | 0.89[ASN][1000 genomes] |
rs4666837 | 0.83[ASN][1000 genomes] |
rs4666840 | 0.82[ASN][1000 genomes] |
rs4666841 | 0.82[ASN][1000 genomes] |
rs62187662 | 0.83[ASN][1000 genomes] |
rs62187664 | 0.82[ASN][1000 genomes] |
rs62187665 | 0.82[ASN][1000 genomes] |
rs62188260 | 0.82[EUR][1000 genomes] |
rs62188266 | 0.82[EUR][1000 genomes] |
rs62188267 | 0.85[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs62188268 | 0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs62188269 | 0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs62188270 | 0.91[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs62188283 | 0.91[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs62188284 | 0.91[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs62188286 | 0.91[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62188287 | 0.91[AFR][1000 genomes];0.83[EUR][1000 genomes] |
rs62188288 | 0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs62188289 | 0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs62188294 | 0.93[ASN][1000 genomes] |
rs62188295 | 0.95[ASN][1000 genomes] |
rs62188296 | 0.95[ASN][1000 genomes] |
rs62188297 | 0.95[ASN][1000 genomes] |
rs62189024 | 0.95[ASN][1000 genomes] |
rs62189025 | 0.87[ASN][1000 genomes] |
rs62189027 | 0.89[ASN][1000 genomes] |
rs62190201 | 0.84[EUR][1000 genomes] |
rs62190676 | 0.83[ASN][1000 genomes] |
rs62190677 | 0.84[ASN][1000 genomes] |
rs62190678 | 0.83[ASN][1000 genomes] |
rs62190679 | 0.83[ASN][1000 genomes] |
rs62190680 | 0.83[ASN][1000 genomes] |
rs62190681 | 0.83[ASN][1000 genomes] |
rs62190682 | 0.83[ASN][1000 genomes] |
rs62190684 | 0.84[ASN][1000 genomes] |
rs6760364 | 0.83[AFR][1000 genomes];0.89[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv533782 | chr2:183059730-183500040 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv834481 | chr2:183189758-183339577 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv1009882 | chr2:183213152-184171519 | Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 35 gene(s) | inside rSNPs | diseases |
4 | esv2830429 | chr2:183300759-183545378 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | esv3323574 | chr2:183315057-183317155 | Weak transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
6 | esv2479479 | chr2:183315368-183316896 | Weak transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:183298800-183320800 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
2 | chr2:183313000-183321400 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
3 | chr2:183313000-183342600 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
4 | chr2:183313800-183320800 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |