Variant report
Variant | rs73214940 |
---|---|
Chromosome Location | chr4:30910125-30910126 |
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] |
---|---|
rs1447370 | 0.87[EUR][1000 genomes] |
rs16884077 | 0.87[EUR][1000 genomes] |
rs16884127 | 0.87[EUR][1000 genomes] |
rs16884144 | 0.87[EUR][1000 genomes] |
rs16884156 | 0.87[EUR][1000 genomes] |
rs73213194 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73213196 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73213199 | 0.87[EUR][1000 genomes] |
rs73213201 | 0.87[EUR][1000 genomes] |
rs73214905 | 0.87[EUR][1000 genomes] |
rs73214907 | 0.87[EUR][1000 genomes] |
rs73214910 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73214913 | 0.87[EUR][1000 genomes] |
rs73214914 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73214915 | 0.87[EUR][1000 genomes] |
rs73214920 | 0.87[EUR][1000 genomes] |
rs73214924 | 0.87[EUR][1000 genomes] |
rs73214926 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73214941 | 0.87[EUR][1000 genomes] |
rs73214946 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73214956 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73216794 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs73218825 | 1.00[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv878810 | chr4:30823157-30987395 | Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
2 | nsv998450 | chr4:30823631-31628179 | Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:30907000-30913800 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |