Variant report
Variant | rs61818779 |
---|---|
Chromosome Location | chr1:190319316-190319317 |
allele | A/G |
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] |
---|---|
rs10047048 | 0.81[AMR][1000 genomes] |
rs10800937 | 0.81[AMR][1000 genomes] |
rs10920680 | 0.81[AMR][1000 genomes] |
rs1143860 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs1148610 | 0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs1148612 | 0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs1148614 | 0.87[ASN][1000 genomes] |
rs1148615 | 0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs1171044 | 0.85[EUR][1000 genomes] |
rs1171045 | 0.81[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1171046 | 0.81[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1171338 | 0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1185689 | 0.81[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs12072689 | 0.81[AMR][1000 genomes] |
rs12072690 | 0.81[AMR][1000 genomes] |
rs12093349 | 0.83[AMR][1000 genomes] |
rs12406050 | 0.81[AMR][1000 genomes] |
rs12407537 | 0.81[AMR][1000 genomes] |
rs3849278 | 0.90[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs4399162 | 0.81[AMR][1000 genomes] |
rs60812740 | 0.81[AMR][1000 genomes] |
rs6665930 | 0.81[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv548532 | chr1:189758772-190371671 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv932040 | chr1:190005334-190914580 | Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
3 | nsv1013402 | chr1:190197674-190332464 | Enhancers ZNF genes & repeats Active TSS Weak transcription | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | n/a |
4 | nsv535246 | chr1:190197674-190332464 | Enhancers Weak transcription Active TSS ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | n/a |
5 | nsv430013 | chr1:190288297-190351677 | Enhancers Active TSS Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:190319000-190319400 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |