Variant report
Variant | rs6761835 |
---|---|
Chromosome Location | chr2:205782713-205782714 |
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 |
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(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs10187682 | 1.00[ASN][1000 genomes] |
rs10198599 | 1.00[ASN][1000 genomes] |
rs10205931 | 1.00[ASN][1000 genomes] |
rs10207227 | 1.00[ASN][1000 genomes] |
rs11677135 | 1.00[ASN][1000 genomes] |
rs13389161 | 1.00[ASN][1000 genomes] |
rs13389502 | 1.00[ASN][1000 genomes] |
rs13395282 | 1.00[ASN][1000 genomes] |
rs13414808 | 1.00[ASN][1000 genomes] |
rs13417895 | 1.00[ASN][1000 genomes] |
rs13418029 | 1.00[ASN][1000 genomes] |
rs13419302 | 1.00[ASN][1000 genomes] |
rs1355342 | 1.00[ASN][1000 genomes] |
rs1434157 | 1.00[ASN][1000 genomes] |
rs2060399 | 1.00[ASN][1000 genomes] |
rs28474701 | 1.00[ASN][1000 genomes] |
rs6716363 | 1.00[ASN][1000 genomes] |
rs6731783 | 1.00[ASN][1000 genomes] |
rs73053146 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7566341 | 1.00[ASN][1000 genomes] |
rs985164 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv998485 | chr2:205407813-206184006 | Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
2 | nsv536122 | chr2:205407813-206184006 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
3 | nsv1010210 | chr2:205489653-206076013 | Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
4 | esv2757846 | chr2:205539832-205841174 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | esv2759111 | chr2:205539832-205841174 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:205782000-205783800 | Active TSS | K562 | blood |
2 | chr2:205782200-205794200 | Weak transcription | Aorta | Aorta |