Variant report
Variant | rs74100382 |
---|---|
Chromosome Location | chr1:90701687-90701688 |
allele | A/C |
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] |
---|---|
rs10922811 | 1.00[EUR][1000 genomes] |
rs11487633 | 1.00[EUR][1000 genomes] |
rs12057810 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs12058169 | 1.00[EUR][1000 genomes] |
rs12062997 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs12063919 | 1.00[EUR][1000 genomes] |
rs12065814 | 0.92[EUR][1000 genomes] |
rs12066835 | 0.97[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs12074198 | 1.00[EUR][1000 genomes] |
rs12074419 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs12076670 | 1.00[EUR][1000 genomes] |
rs12076765 | 1.00[EUR][1000 genomes] |
rs12080222 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12085161 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12086859 | 0.92[EUR][1000 genomes] |
rs4514225 | 1.00[EUR][1000 genomes] |
rs4514226 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs60343921 | 1.00[EUR][1000 genomes] |
rs6665059 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6665162 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74099405 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74099418 | 1.00[AMR][1000 genomes] |
rs74099427 | 1.00[AMR][1000 genomes] |
rs74100374 | 1.00[EUR][1000 genomes] |
rs74100375 | 1.00[EUR][1000 genomes] |
rs74100377 | 1.00[EUR][1000 genomes] |
rs74100378 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv546803 | chr1:90679734-90777717 | Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:90692000-90706200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |