Variant report
Variant | rs3981073 |
---|---|
Chromosome Location | chr2:125129080-125129081 |
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] |
---|---|
rs11884566 | 0.90[YRI][hapmap] |
rs11886998 | 1.00[CHD][hapmap] |
rs12373652 | 1.00[CEU][hapmap];1.00[YRI][hapmap] |
rs12373815 | 1.00[CEU][hapmap];1.00[YRI][hapmap] |
rs13384799 | 1.00[ASW][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[MEX][hapmap];0.80[TSI][hapmap];0.90[YRI][hapmap] |
rs1365019 | 0.81[CEU][hapmap] |
rs17011429 | 0.81[CEU][hapmap];0.82[GIH][hapmap];0.85[YRI][hapmap] |
rs17011610 | 1.00[CHD][hapmap] |
rs17392176 | 1.00[CHD][hapmap] |
rs2553625 | 0.81[CEU][hapmap];0.81[GIH][hapmap] |
rs6541961 | 1.00[CHD][hapmap] |
rs7564671 | 1.00[CEU][hapmap];1.00[YRI][hapmap] |
rs7564699 | 1.00[CEU][hapmap];1.00[YRI][hapmap] |
rs7574198 | 0.90[CEU][hapmap];0.84[GIH][hapmap];0.80[MEX][hapmap];0.90[TSI][hapmap] |
rs7581635 | 0.82[CEU][hapmap] |
rs7582767 | 0.82[CEU][hapmap];0.83[EUR][1000 genomes] |
rs7591043 | 1.00[CEU][hapmap];0.95[YRI][hapmap] |
rs7603847 | 0.90[CEU][hapmap];0.81[GIH][hapmap];0.80[MEX][hapmap];0.85[TSI][hapmap];0.90[YRI][hapmap] |
rs7609391 | 0.82[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv874989 | chr2:124892592-125176030 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | nsv1014610 | chr2:125124983-125350342 | Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv834355 | chr2:125128585-125291043 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |