Variant report
Variant | rs73063148 |
---|---|
Chromosome Location | chr2:213337252-213337253 |
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] |
---|---|
rs10191941 | 0.98[AFR][1000 genomes] |
rs10497974 | 1.00[EUR][1000 genomes] |
rs13389646 | 1.00[AFR][1000 genomes] |
rs1384288 | 1.00[AFR][1000 genomes] |
rs1384289 | 1.00[EUR][1000 genomes] |
rs16848640 | 1.00[EUR][1000 genomes] |
rs16848646 | 1.00[EUR][1000 genomes] |
rs16848661 | 1.00[EUR][1000 genomes] |
rs59744201 | 1.00[EUR][1000 genomes] |
rs60588961 | 0.95[AFR][1000 genomes] |
rs73062337 | 1.00[EUR][1000 genomes] |
rs73062343 | 1.00[EUR][1000 genomes] |
rs73063113 | 0.95[AFR][1000 genomes] |
rs73063156 | 1.00[EUR][1000 genomes] |
rs73063158 | 1.00[EUR][1000 genomes] |
rs73063161 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1004573 | chr2:213186537-213365252 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionmiRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv875811 | chr2:213200920-213347104 | Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionmiRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv432024 | chr2:213314899-213446726 | Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:213335200-213342400 | Weak transcription | Fetal Heart | heart |