Variant report
Variant | rs17090955 |
---|---|
Chromosome Location | chr1:71670281-71670282 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:71654729..71657445-chr1:71668068..71670402,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10493482 | 0.83[AFR][1000 genomes];0.97[AMR][1000 genomes] |
rs10493484 | 0.94[AFR][1000 genomes];0.97[EUR][1000 genomes] |
rs11578414 | 0.83[AMR][1000 genomes] |
rs11800532 | 0.90[AMR][1000 genomes] |
rs11801478 | 0.90[AMR][1000 genomes] |
rs11808123 | 0.90[AMR][1000 genomes] |
rs12402425 | 0.83[GIH][hapmap];0.85[MEX][hapmap];0.83[AMR][1000 genomes] |
rs12409826 | 0.83[GIH][hapmap];0.85[MEX][hapmap];0.83[AMR][1000 genomes] |
rs1418448 | 0.90[AMR][1000 genomes] |
rs17090804 | 0.91[ASW][hapmap];0.83[GIH][hapmap];0.86[LWK][hapmap];0.85[MEX][hapmap];0.87[TSI][hapmap];0.90[AMR][1000 genomes] |
rs17091031 | 0.94[AFR][1000 genomes];0.97[EUR][1000 genomes] |
rs1891417 | 0.97[AFR][1000 genomes];0.97[EUR][1000 genomes] |
rs2744901 | 0.83[GIH][hapmap];0.87[TSI][hapmap];0.81[AMR][1000 genomes] |
rs2744909 | 0.83[GIH][hapmap];0.83[TSI][hapmap];0.81[AMR][1000 genomes] |
rs2796200 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2817867 | 0.81[AMR][1000 genomes] |
rs57667850 | 0.87[AMR][1000 genomes] |
rs59019236 | 0.83[AMR][1000 genomes] |
rs6699719 | 0.97[AMR][1000 genomes] |
rs72942304 | 0.90[AMR][1000 genomes] |
rs7528792 | 0.87[AMR][1000 genomes] |
rs7545836 | 0.90[AMR][1000 genomes] |
rs7554527 | 0.81[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949599 | chr1:71655652-72327802 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:71665600-71672400 | Weak transcription | Pancreas | Pancrea |