Variant report
Variant | rs554965 |
---|---|
Chromosome Location | chr2:142584472-142584473 |
allele | G/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] |
---|---|
rs11899153 | 0.83[CEU][hapmap];0.84[JPT][hapmap] |
rs12620682 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12623036 | 0.81[CEU][hapmap] |
rs12993061 | 0.87[CEU][hapmap];0.83[JPT][hapmap] |
rs13004344 | 0.87[CEU][hapmap];0.84[CHB][hapmap];0.91[JPT][hapmap] |
rs13009181 | 0.81[ASN][1000 genomes] |
rs13016459 | 0.81[CEU][hapmap] |
rs13018903 | 0.87[CEU][hapmap];0.91[JPT][hapmap];0.81[ASN][1000 genomes] |
rs13019219 | 0.94[CEU][hapmap];0.91[JPT][hapmap] |
rs13024611 | 0.88[CEU][hapmap] |
rs13031421 | 0.93[CEU][hapmap];0.90[JPT][hapmap];0.81[ASN][1000 genomes] |
rs13031743 | 0.87[CEU][hapmap] |
rs1435595 | 0.94[CEU][hapmap];0.85[CHB][hapmap];0.84[JPT][hapmap] |
rs16847378 | 0.93[CEU][hapmap];0.85[EUR][1000 genomes] |
rs352973 | 0.94[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs352974 | 0.91[ASN][1000 genomes] |
rs352975 | 0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs352976 | 0.85[CHB][hapmap];0.95[JPT][hapmap] |
rs352978 | 0.80[CHB][hapmap];0.87[JPT][hapmap] |
rs352982 | 0.91[CHB][hapmap];0.84[JPT][hapmap] |
rs352986 | 0.88[CEU][hapmap];0.85[CHB][hapmap];0.91[JPT][hapmap] |
rs352994 | 0.87[CEU][hapmap] |
rs4662271 | 0.88[CEU][hapmap] |
rs4662468 | 0.88[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv834394 | chr2:142430225-142593264 | Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | nsv530398 | chr2:142474842-142843839 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv875249 | chr2:142527100-142614345 | Enhancers Weak transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
4 | nsv875250 | chr2:142540240-142614345 | Enhancers Weak transcription | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
5 | nsv1010008 | chr2:142574406-142606021 | Enhancers Weak transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
No data |