Variant report
Variant | rs1191700 |
---|---|
Chromosome Location | chr2:142426615-142426616 |
allele | C/T |
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] |
---|---|
rs10177354 | 0.86[YRI][hapmap] |
rs10200671 | 0.89[YRI][hapmap] |
rs11690612 | 0.86[JPT][hapmap] |
rs13019062 | 0.83[ASN][1000 genomes] |
rs13024134 | 0.82[ASN][1000 genomes] |
rs1370327 | 0.85[CEU][hapmap] |
rs1384664 | 0.94[CHB][hapmap];1.00[JPT][hapmap] |
rs1437351 | 0.89[YRI][hapmap] |
rs164975 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap] |
rs173323 | 0.90[YRI][hapmap] |
rs1821820 | 0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs2028130 | 1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap] |
rs2118276 | 1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap] |
rs354855 | 0.86[YRI][hapmap] |
rs355545 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs355547 | 0.89[YRI][hapmap] |
rs355553 | 0.89[YRI][hapmap] |
rs355556 | 0.83[YRI][hapmap] |
rs4427957 | 1.00[CEU][hapmap];0.90[CHB][hapmap];0.93[JPT][hapmap];0.93[YRI][hapmap] |
rs6712100 | 0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6733033 | 0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs6751890 | 1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7582357 | 0.83[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv834393 | chr2:142256714-142431564 | Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | n/a |
2 | nsv583214 | chr2:142299923-142458316 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
3 | nsv1011019 | chr2:142314999-142430460 | Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:142418600-142428400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |