Variant report
| Variant | rs42181 |
|---|---|
| Chromosome Location | chr7:104073443-104073444 |
| 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] |
|---|---|
| rs10233854 | 0.81[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap] |
| rs10239251 | 0.81[CHD][hapmap];0.81[YRI][hapmap] |
| rs10243493 | 0.80[EUR][1000 genomes];0.96[ASN][1000 genomes] |
| rs11763095 | 0.81[CHD][hapmap] |
| rs1557693 | 0.81[CEU][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.82[ASN][1000 genomes] |
| rs17137518 | 0.81[CEU][hapmap];0.82[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.86[TSI][hapmap];0.81[YRI][hapmap];0.82[ASN][1000 genomes] |
| rs17137665 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap] |
| rs2106501 | 0.81[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap] |
| rs36109662 | 0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs41389845 | 0.81[CEU][hapmap];0.82[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.86[TSI][hapmap];0.81[YRI][hapmap] |
| rs6976167 | 0.81[CEU][hapmap];0.86[TSI][hapmap];0.81[YRI][hapmap] |
| rs6980365 | 0.89[CEU][hapmap];0.81[YRI][hapmap] |
| rs727927 | 1.00[CEU][hapmap];0.93[GIH][hapmap];0.81[TSI][hapmap];0.86[EUR][1000 genomes] |
| rs739506 | 0.81[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv888925 | chr7:104047599-104170560 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |





