Variant report
Variant | rs6942125 |
---|---|
Chromosome Location | chr6:102140985-102140986 |
allele | C/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] |
---|---|
rs1415482 | 0.90[CEU][hapmap];0.90[JPT][hapmap];0.86[YRI][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1832293 | 0.86[YRI][hapmap] |
rs1856134 | 0.82[CEU][hapmap];0.92[JPT][hapmap];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs2248660 | 0.81[CEU][hapmap];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2248893 | 0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2248984 | 0.92[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2254676 | 0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs2518296 | 0.81[CEU][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs2518297 | 0.80[CEU][hapmap];1.00[JPT][hapmap] |
rs2518298 | 0.91[CEU][hapmap];0.91[JPT][hapmap] |
rs2518306 | 0.81[CEU][hapmap];0.91[JPT][hapmap];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2764234 | 0.80[CEU][hapmap];0.92[JPT][hapmap];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs2852564 | 0.91[CEU][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2852566 | 0.82[CEU][hapmap];1.00[JPT][hapmap] |
rs2852568 | 0.84[YRI][hapmap] |
rs2852569 | 0.92[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7745860 | 0.80[CEU][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs7752976 | 1.00[YRI][hapmap];0.84[AFR][1000 genomes] |
rs9399725 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs949395 | 0.81[CEU][hapmap];1.00[JPT][hapmap] |
rs9498669 | 0.85[YRI][hapmap];0.84[AFR][1000 genomes] |
rs9498670 | 0.93[YRI][hapmap];0.84[AFR][1000 genomes] |
rs9498671 | 1.00[YRI][hapmap];0.91[AFR][1000 genomes] |
rs9498672 | 1.00[YRI][hapmap];0.91[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv538392 | chr6:101938381-102148360 | Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | esv3384771 | chr6:101996253-102283808 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv1032499 | chr6:102069885-102720998 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv463993 | chr6:102084491-102165329 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | nsv604317 | chr6:102084491-102165329 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |