Variant report
Variant | rs7422793 |
---|---|
Chromosome Location | chr2:212603778-212603779 |
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] |
---|---|
rs10932401 | 0.82[JPT][hapmap] |
rs12622176 | 0.85[CEU][hapmap];0.88[EUR][1000 genomes] |
rs35444377 | 0.90[EUR][1000 genomes] |
rs4130781 | 0.88[CEU][hapmap];0.88[EUR][1000 genomes] |
rs4130782 | 0.88[CEU][hapmap];0.88[EUR][1000 genomes] |
rs4132462 | 0.85[CEU][hapmap];0.82[EUR][1000 genomes] |
rs55897719 | 0.90[EUR][1000 genomes] |
rs56405287 | 0.82[EUR][1000 genomes] |
rs61079605 | 0.85[EUR][1000 genomes] |
rs62182986 | 0.83[EUR][1000 genomes] |
rs62182989 | 0.88[EUR][1000 genomes] |
rs62182991 | 0.88[EUR][1000 genomes] |
rs62182999 | 0.90[EUR][1000 genomes] |
rs62183021 | 0.86[EUR][1000 genomes] |
rs62183023 | 0.82[EUR][1000 genomes] |
rs62183024 | 0.83[EUR][1000 genomes] |
rs62183031 | 0.80[EUR][1000 genomes] |
rs6749448 | 0.88[CEU][hapmap];0.90[EUR][1000 genomes] |
rs72946582 | 0.88[EUR][1000 genomes] |
rs72948506 | 0.85[EUR][1000 genomes] |
rs7556896 | 0.82[EUR][1000 genomes] |
rs7583068 | 0.81[EUR][1000 genomes] |
rs7588431 | 0.82[JPT][hapmap] |
rs7600261 | 0.85[CEU][hapmap];0.88[EUR][1000 genomes] |
rs7601502 | 0.84[CEU][hapmap];0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv34128 | chr2:212581485-212857122 | Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:212602400-212606200 | Weak transcription | Fetal Heart | heart |