Variant report
Variant | rs8192983 |
---|---|
Chromosome Location | chr9:13682269-13682270 |
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] |
---|---|
rs10491761 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10961209 | 0.84[EUR][1000 genomes] |
rs10961212 | 0.83[EUR][1000 genomes] |
rs12000174 | 0.92[EUR][1000 genomes] |
rs12002484 | 0.92[EUR][1000 genomes] |
rs16923099 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs16930577 | 0.92[EUR][1000 genomes] |
rs16930626 | 1.00[EUR][1000 genomes] |
rs16930665 | 1.00[EUR][1000 genomes] |
rs16930668 | 1.00[EUR][1000 genomes] |
rs16930694 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs16930712 | 0.92[EUR][1000 genomes] |
rs16930740 | 0.84[EUR][1000 genomes] |
rs60961071 | 1.00[EUR][1000 genomes] |
rs61472956 | 0.92[EUR][1000 genomes] |
rs7032707 | 0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7032959 | 0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73647695 | 0.92[EUR][1000 genomes] |
rs73647696 | 0.92[EUR][1000 genomes] |
rs73647697 | 0.92[EUR][1000 genomes] |
rs73650811 | 0.92[EUR][1000 genomes] |
rs8192959 | 1.00[EUR][1000 genomes] |
rs8192961 | 1.00[EUR][1000 genomes] |
rs8192966 | 1.00[EUR][1000 genomes] |
rs8192967 | 1.00[EUR][1000 genomes] |
rs8192968 | 1.00[EUR][1000 genomes] |
rs8192969 | 1.00[EUR][1000 genomes] |
rs8192972 | 1.00[EUR][1000 genomes] |
rs8192974 | 1.00[EUR][1000 genomes] |
rs8192976 | 1.00[EUR][1000 genomes] |
rs8192978 | 1.00[EUR][1000 genomes] |
rs8192979 | 0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs8192980 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs8192985 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs8192992 | 0.92[EUR][1000 genomes] |
rs8192997 | 0.92[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1023684 | chr9:13529680-13744602 | Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | nsv540067 | chr9:13529680-13744602 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv892587 | chr9:13601074-13732363 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | esv1843958 | chr9:13631992-13706651 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | nsv892588 | chr9:13667639-13715063 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
6 | nsv1018933 | chr9:13669862-13756710 | Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:13675800-13684800 | Weak transcription | Right Atrium | heart |
2 | chr9:13677400-13684800 | Weak transcription | Fetal Heart | heart |