Variant report
Variant | rs16849957 |
---|---|
Chromosome Location | chr3:139857978-139857979 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
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rs_ID | r2[population] |
---|---|
rs12494072 | 1.00[CHB][hapmap] |
rs16849961 | 1.00[MEX][hapmap];0.83[YRI][hapmap] |
rs16849965 | 1.00[MEX][hapmap] |
rs16849992 | 1.00[MEX][hapmap] |
rs4428137 | 1.00[CHB][hapmap] |
rs4462908 | 1.00[CHB][hapmap] |
rs56009777 | 1.00[ASN][1000 genomes] |
rs56047746 | 1.00[ASN][1000 genomes] |
rs56910077 | 1.00[ASN][1000 genomes] |
rs58796461 | 1.00[ASN][1000 genomes] |
rs59850626 | 1.00[ASN][1000 genomes] |
rs6439896 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6439901 | 1.00[MEX][hapmap] |
rs6767558 | 1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6767879 | 1.00[ASN][1000 genomes] |
rs6799894 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6807785 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs72986148 | 1.00[ASN][1000 genomes] |
rs72986195 | 1.00[ASN][1000 genomes] |
rs73868789 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs7617224 | 1.00[MEX][hapmap] |
rs7645419 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs922565 | 1.00[MEX][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv998423 | chr3:139526446-139947336 | Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv829739 | chr3:139797496-140002685 | Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:139835800-139862800 | Weak transcription | HSMMtube | muscle |