Variant report
Variant | rs60283435 |
---|---|
Chromosome Location | chr8:69850953-69850954 |
allele | C/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] |
---|---|
rs16935048 | 1.00[ASN][1000 genomes] |
rs16935249 | 0.98[EUR][1000 genomes] |
rs34176595 | 0.98[EUR][1000 genomes] |
rs34207383 | 0.91[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs34781970 | 0.90[EUR][1000 genomes] |
rs57043258 | 1.00[ASN][1000 genomes] |
rs57996050 | 1.00[ASN][1000 genomes] |
rs58757685 | 1.00[ASN][1000 genomes] |
rs59404825 | 1.00[ASN][1000 genomes] |
rs68191047 | 1.00[ASN][1000 genomes] |
rs6999003 | 0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71517216 | 0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71517217 | 0.84[EUR][1000 genomes] |
rs72652153 | 1.00[ASN][1000 genomes] |
rs72668533 | 1.00[ASN][1000 genomes] |
rs73289410 | 1.00[ASN][1000 genomes] |
rs73683711 | 1.00[ASN][1000 genomes] |
rs73683724 | 1.00[ASN][1000 genomes] |
rs73683725 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1031633 | chr8:69766575-70322790 | Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
2 | esv33049 | chr8:69836813-69943360 | Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:69848200-69852400 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |