Variant report
Variant | rs73122844 |
---|---|
Chromosome Location | chr12:41689910-41689911 |
allele | A/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] |
---|---|
rs11180661 | 0.83[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs12297169 | 0.81[AFR][1000 genomes];0.84[ASN][1000 genomes] |
rs1560448 | 0.83[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17129215 | 0.85[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs17129216 | 0.85[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs55917050 | 0.95[AFR][1000 genomes] |
rs60683724 | 0.95[AFR][1000 genomes] |
rs61587111 | 0.88[EUR][1000 genomes] |
rs6582304 | 1.00[AFR][1000 genomes] |
rs6582305 | 1.00[AFR][1000 genomes] |
rs7298753 | 0.83[AFR][1000 genomes];0.92[ASN][1000 genomes] |
rs73117077 | 0.88[EUR][1000 genomes] |
rs73117080 | 0.88[EUR][1000 genomes] |
rs73122828 | 0.83[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73122829 | 0.83[AFR][1000 genomes] |
rs73122830 | 0.96[ASN][1000 genomes] |
rs73122831 | 0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs73122836 | 0.82[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73122838 | 0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs73122851 | 1.00[AFR][1000 genomes] |
rs7958277 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7958391 | 0.98[AFR][1000 genomes] |
rs7958538 | 1.00[AFR][1000 genomes] |
rs7959120 | 0.83[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs7961153 | 1.00[AFR][1000 genomes] |
rs7961270 | 1.00[AFR][1000 genomes] |
rs7962171 | 0.81[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs7971709 | 1.00[AFR][1000 genomes] |
rs7979212 | 1.00[AFR][1000 genomes] |
rs7980336 | 0.95[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv497867 | chr12:41286305-41728650 | Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
2 | nsv899034 | chr12:41515090-41698342 | Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv899035 | chr12:41548545-41710912 | Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv469364 | chr12:41631105-41710912 | Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
5 | nsv558699 | chr12:41631105-41710912 | Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers | Chromatin interactive region | n/a | inside rSNPs | n/a |
6 | nsv558700 | chr12:41665279-41710912 | Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:41686600-41692600 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |