Variant report
Variant | rs638198 |
---|---|
Chromosome Location | chr2:141070883-141070884 |
allele | C/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] |
---|---|
rs10469558 | 0.81[YRI][hapmap] |
rs12477489 | 0.93[YRI][hapmap] |
rs12612910 | 0.90[YRI][hapmap] |
rs12692048 | 0.85[AMR][1000 genomes] |
rs12992137 | 0.83[AMR][1000 genomes] |
rs13002228 | 0.82[AMR][1000 genomes] |
rs1388809 | 0.81[YRI][hapmap] |
rs1486963 | 0.83[YRI][hapmap] |
rs2046563 | 0.84[AMR][1000 genomes] |
rs2945572 | 0.92[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.83[YRI][hapmap];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs595789 | 0.93[ASN][1000 genomes] |
rs597222 | 0.87[AMR][1000 genomes] |
rs598786 | 0.96[YRI][hapmap] |
rs634115 | 0.90[CHB][hapmap];0.90[JPT][hapmap] |
rs639195 | 0.87[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs649284 | 0.88[CEU][hapmap] |
rs650706 | 0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs651125 | 0.92[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap] |
rs654051 | 0.83[YRI][hapmap] |
rs655308 | 0.96[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap] |
rs667446 | 0.92[CEU][hapmap] |
rs6755087 | 0.84[CEU][hapmap];0.95[CHB][hapmap];0.92[YRI][hapmap] |
rs825429 | 0.81[AMR][1000 genomes] |
rs982233 | 0.90[YRI][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv834392 | chr2:140920900-141086613 | Flanking Active TSS Weak transcription Enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
2 | nsv431757 | chr2:140931289-141098020 | Enhancers Flanking Active TSS Weak transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
3 | esv2754266 | chr2:141023643-141270786 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv875185 | chr2:141055080-141179257 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
5 | nsv1002168 | chr2:141056296-141157971 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
No data |