Variant report
Variant | rs7920241 |
---|---|
Chromosome Location | chr10:25449748-25449749 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:2)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
(count:2 , 50 per page) page:
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-GPR158-1 | chr10:25448580-25450165 | ENSG00000231422.2 |
2 | lnc-GPR158-1 | chr10:25448580-25450162 | NONHSAT011799 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10828760 | 0.90[ASN][1000 genomes] |
rs10828763 | 0.87[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes] |
rs11014431 | 0.87[CEU][hapmap];0.94[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes] |
rs11014435 | 1.00[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs11818773 | 0.87[CEU][hapmap];0.81[JPT][hapmap];0.82[AMR][1000 genomes] |
rs12411980 | 0.87[CEU][hapmap];0.81[CHD][hapmap];0.81[JPT][hapmap] |
rs12411993 | 0.82[CEU][hapmap] |
rs1339996 | 0.85[JPT][hapmap] |
rs16925456 | 0.83[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes] |
rs16925458 | 0.83[CHB][hapmap];0.90[JPT][hapmap] |
rs2765697 | 1.00[CEU][hapmap];0.81[CHD][hapmap];0.81[JPT][hapmap];0.91[MEX][hapmap];0.86[AMR][1000 genomes] |
rs2765699 | 1.00[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap] |
rs2765710 | 0.81[MEX][hapmap] |
rs7081232 | 0.83[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes] |
rs7921132 | 0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs7923288 | 0.85[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv894970 | chr10:25385858-25522280 | Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv894971 | chr10:25403234-25522280 | Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |