Variant report
Variant | rs17025209 |
---|---|
Chromosome Location | chr4:97161412-97161413 |
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 |
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No data |
No data |
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No data |
rs_ID | r2[population] |
---|---|
rs11932384 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12642471 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs12644982 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs17025493 | 0.86[AMR][1000 genomes] |
rs1847964 | 0.88[AFR][1000 genomes];0.97[AMR][1000 genomes] |
rs1847966 | 0.94[AFR][1000 genomes];0.97[AMR][1000 genomes] |
rs1948912 | 0.85[AFR][1000 genomes];0.90[AMR][1000 genomes] |
rs2113973 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs4146410 | 0.88[AFR][1000 genomes];0.97[AMR][1000 genomes] |
rs4146411 | 0.88[AFR][1000 genomes];0.97[AMR][1000 genomes] |
rs4293790 | 1.00[YRI][hapmap] |
rs4343731 | 0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs4699503 | 0.83[AFR][1000 genomes];0.88[AMR][1000 genomes] |
rs55680326 | 0.89[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs55847611 | 0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs60275360 | 0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs6820075 | 0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs72880179 | 0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs72880182 | 0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs72883800 | 0.85[AFR][1000 genomes];0.93[AMR][1000 genomes] |
rs72885446 | 0.86[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv830013 | chr4:97033125-97204291 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv1003868 | chr4:97068155-97222544 | Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv470057 | chr4:97104880-97311657 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv461589 | chr4:97104881-97311657 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv594916 | chr4:97104881-97311657 | Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
6 | nsv879631 | chr4:97114706-97263153 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | nsv879632 | chr4:97118539-97308914 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
8 | nsv879633 | chr4:97125086-97263153 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
9 | esv2763381 | chr4:97140746-97193871 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:97161200-97161600 | Enhancers | Fetal Lung | lung |