Variant report
Variant | rs354853 |
---|---|
Chromosome Location | chr2:142429315-142429316 |
allele | 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] |
---|---|
rs10177354 | 0.82[YRI][hapmap] |
rs10177919 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs10177925 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs10200671 | 0.86[YRI][hapmap] |
rs11885120 | 0.86[CHB][hapmap] |
rs1347659 | 0.86[CHB][hapmap] |
rs1370330 | 1.00[CHB][hapmap];0.89[ASN][1000 genomes] |
rs1437351 | 0.86[YRI][hapmap] |
rs164978 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap] |
rs164979 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap] |
rs16846700 | 1.00[CHB][hapmap] |
rs16846719 | 0.86[CHB][hapmap];1.00[JPT][hapmap] |
rs16846817 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs16846884 | 1.00[CHB][hapmap];0.89[ASN][1000 genomes] |
rs16846918 | 0.86[CHB][hapmap];0.81[ASN][1000 genomes] |
rs16846922 | 0.86[CHB][hapmap];0.81[ASN][1000 genomes] |
rs16846935 | 1.00[CHB][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes] |
rs16846937 | 0.85[CHB][hapmap];0.81[ASN][1000 genomes] |
rs16846962 | 1.00[CHB][hapmap];0.83[ASN][1000 genomes] |
rs16846974 | 1.00[CHB][hapmap] |
rs173323 | 0.84[YRI][hapmap] |
rs354855 | 0.80[YRI][hapmap] |
rs354856 | 0.86[CHB][hapmap];1.00[JPT][hapmap] |
rs355547 | 0.83[YRI][hapmap] |
rs355553 | 0.83[YRI][hapmap] |
rs355556 | 0.83[YRI][hapmap] |
rs355558 | 0.93[ASN][1000 genomes] |
rs355559 | 0.93[ASN][1000 genomes] |
rs355583 | 0.86[CHB][hapmap] |
rs355591 | 0.85[JPT][hapmap] |
rs41320547 | 0.86[CHB][hapmap] |
rs58328208 | 1.00[ASN][1000 genomes] |
rs6736591 | 1.00[CHB][hapmap];0.85[JPT][hapmap] |
rs72980183 | 0.82[ASN][1000 genomes] |
rs7560183 | 1.00[JPT][hapmap] |
rs7560557 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv834393 | chr2:142256714-142431564 | Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | n/a |
2 | nsv583214 | chr2:142299923-142458316 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
3 | nsv1011019 | chr2:142314999-142430460 | Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
No data |