Variant report
Variant | rs35802620 |
---|---|
Chromosome Location | chr6:81361863-81361864 |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs10455372 | 0.88[ASN][1000 genomes] |
rs12213889 | 0.88[ASN][1000 genomes] |
rs12214028 | 0.88[ASN][1000 genomes] |
rs12214145 | 0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs13193169 | 0.81[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs13207200 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1454453 | 0.88[ASN][1000 genomes] |
rs16892045 | 0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs28643369 | 0.84[EUR][1000 genomes] |
rs34538775 | 0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs36018197 | 0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4380719 | 0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs56049233 | 0.82[EUR][1000 genomes] |
rs9294177 | 0.81[EUR][1000 genomes] |
rs9294179 | 0.80[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9341821 | 0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9344028 | 0.91[ASN][1000 genomes] |
rs9344033 | 0.86[AFR][1000 genomes] |
rs9344037 | 0.81[EUR][1000 genomes] |
rs9352848 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs9352849 | 0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs9359425 | 0.81[EUR][1000 genomes] |
rs9361632 | 0.93[ASN][1000 genomes] |
rs9361634 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9361636 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs9361637 | 0.91[ASN][1000 genomes] |
rs9361638 | 0.91[ASN][1000 genomes] |
rs9361644 | 0.81[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531333 | chr6:81042427-81836484 | Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
2 | nsv1019670 | chr6:81086504-81569984 | ZNF genes & repeats Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
3 | nsv915714 | chr6:81134888-81366749 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
4 | nsv1020533 | chr6:81288890-81406533 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv538340 | chr6:81288890-81406533 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv604085 | chr6:81297890-81439973 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
7 | nsv1015520 | chr6:81309213-81374699 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
8 | nsv886314 | chr6:81341175-81379791 | Weak transcription Enhancers Flanking Active TSS Active TSS | n/a | n/a | inside rSNPs | diseases |
9 | nsv886315 | chr6:81352515-81946866 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:81359600-81364200 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |