Variant report
Variant | rs74102126 |
---|---|
Chromosome Location | chr13:86461654-86461655 |
allele | C/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] |
---|---|
rs10450864 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11841292 | 0.87[EUR][1000 genomes] |
rs1576453 | 0.97[EUR][1000 genomes] |
rs1576454 | 1.00[EUR][1000 genomes] |
rs4402443 | 0.84[EUR][1000 genomes] |
rs4432164 | 0.84[EUR][1000 genomes] |
rs55659080 | 0.86[ASN][1000 genomes] |
rs55865303 | 0.86[ASN][1000 genomes] |
rs55980796 | 0.86[ASN][1000 genomes] |
rs56313870 | 0.86[ASN][1000 genomes] |
rs57018101 | 0.84[EUR][1000 genomes] |
rs61969481 | 0.86[ASN][1000 genomes] |
rs61969503 | 0.86[ASN][1000 genomes] |
rs61969511 | 0.86[ASN][1000 genomes] |
rs61969522 | 0.86[ASN][1000 genomes] |
rs61969525 | 0.93[ASN][1000 genomes] |
rs61969530 | 0.96[ASN][1000 genomes] |
rs61969532 | 0.93[ASN][1000 genomes] |
rs61969536 | 0.85[ASN][1000 genomes] |
rs61971063 | 0.81[ASN][1000 genomes] |
rs61971066 | 0.86[ASN][1000 genomes] |
rs61971074 | 0.82[ASN][1000 genomes] |
rs61971075 | 0.86[ASN][1000 genomes] |
rs61971076 | 0.86[ASN][1000 genomes] |
rs61971078 | 0.86[ASN][1000 genomes] |
rs72632783 | 0.82[ASN][1000 genomes] |
rs72632788 | 0.86[ASN][1000 genomes] |
rs72632789 | 0.86[ASN][1000 genomes] |
rs72632794 | 0.86[ASN][1000 genomes] |
rs72632795 | 0.86[ASN][1000 genomes] |
rs72632797 | 0.86[ASN][1000 genomes] |
rs72632799 | 0.93[ASN][1000 genomes] |
rs7318134 | 0.87[EUR][1000 genomes] |
rs73541869 | 0.87[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs73541886 | 0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs73541889 | 0.80[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs73545703 | 0.87[EUR][1000 genomes] |
rs7990625 | 0.84[EUR][1000 genomes] |
rs7998102 | 0.84[EUR][1000 genomes] |
rs7998674 | 0.84[EUR][1000 genomes] |
rs7998922 | 0.81[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv900734 | chr13:86415632-86911159 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv900735 | chr13:86426757-86545903 | Enhancers ZNF genes & repeats Weak transcription | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | nsv900736 | chr13:86429834-86529275 | Enhancers ZNF genes & repeats Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv900737 | chr13:86429834-86639464 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv456053 | chr13:86448054-86551371 | Enhancers ZNF genes & repeats Weak transcription Active TSS | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | nsv562610 | chr13:86448054-86551371 | Enhancers Weak transcription ZNF genes & repeats Active TSS | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
7 | nsv1050020 | chr13:86449037-86499673 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | inside rSNPs | diseases |
8 | nsv900738 | chr13:86449302-86628241 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
9 | nsv900739 | chr13:86449302-86736910 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
10 | nsv900740 | chr13:86449302-86911159 | Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
11 | nsv900741 | chr13:86461429-86959695 | Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr13:86461400-86462000 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
2 | chr13:86461400-86462400 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |