Variant report
Variant | rs10052169 |
---|---|
Chromosome Location | chr5:144997358-144997359 |
allele | A/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] |
---|---|
rs10036664 | 1.00[AMR][1000 genomes] |
rs10040204 | 1.00[AMR][1000 genomes] |
rs10043538 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10043961 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10052024 | 0.80[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10054314 | 1.00[AMR][1000 genomes] |
rs10073313 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs10077242 | 1.00[AMR][1000 genomes] |
rs10476875 | 1.00[AMR][1000 genomes] |
rs13354398 | 1.00[AMR][1000 genomes] |
rs13356403 | 1.00[AMR][1000 genomes] |
rs13436791 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs13436850 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs2217647 | 1.00[AMR][1000 genomes] |
rs28507009 | 1.00[AMR][1000 genomes] |
rs4345360 | 1.00[AMR][1000 genomes] |
rs59384625 | 1.00[ASN][1000 genomes] |
rs73302023 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs868778 | 1.00[AMR][1000 genomes] |
rs9285664 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv883004 | chr5:144945649-145068001 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | nsv883005 | chr5:144945649-145107586 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:144997200-144998200 | Weak transcription | H1 Cell Line | embryonic stem cell |