Variant report
Variant | rs10199461 |
---|---|
Chromosome Location | chr2:184816518-184816519 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:32)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:32 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
ENSG00000238306 | TF binding region |
rs_ID | r2[population] |
---|---|
rs10205814 | 1.00[CHB][hapmap];0.88[ASN][1000 genomes] |
rs34942554 | 0.82[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs34974614 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4296393 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs4303682 | 0.91[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs4322806 | 0.91[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs4350706 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4458173 | 1.00[CEU][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4505484 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs4560074 | 0.94[ASN][1000 genomes] |
rs4597475 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4666646 | 0.84[EUR][1000 genomes] |
rs4666952 | 0.91[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6714564 | 0.80[EUR][1000 genomes] |
rs6743413 | 0.91[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6755058 | 0.89[EUR][1000 genomes] |
rs704864 | 0.82[EUR][1000 genomes] |
rs7601296 | 0.83[ASN][1000 genomes] |
rs826128 | 0.82[EUR][1000 genomes] |
rs826129 | 0.84[EUR][1000 genomes] |
rs826146 | 0.84[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1002074 | chr2:184697897-184955330 | ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv875487 | chr2:184737282-185186670 | Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv522576 | chr2:184797402-184826437 | Enhancers Weak transcription ZNF genes & repeats | TF binding regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:184815400-184817000 | Enhancers | Hela-S3 | cervix |
2 | chr2:184816400-184817000 | Enhancers | Muscle Satellite Cultured Cells | -- |
3 | chr2:184816400-184817800 | Enhancers | Fetal Lung | lung |