Variant report
Variant | rs1105985 |
---|---|
Chromosome Location | chr1:71953123-71953124 |
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 |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1033268 | 0.85[EUR][1000 genomes] |
rs10889916 | 0.85[CEU][hapmap];0.82[CHB][hapmap];0.88[TSI][hapmap] |
rs10889918 | 0.85[CEU][hapmap];0.82[CHB][hapmap];0.83[EUR][1000 genomes] |
rs1112456 | 0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap] |
rs1155175 | 0.85[CEU][hapmap];0.82[CHB][hapmap];0.97[TSI][hapmap] |
rs12123319 | 0.84[CEU][hapmap];0.82[TSI][hapmap] |
rs12125823 | 0.90[CHB][hapmap];0.80[JPT][hapmap] |
rs12135145 | 0.85[CEU][hapmap];0.90[CHB][hapmap];0.80[JPT][hapmap];0.97[TSI][hapmap];0.82[EUR][1000 genomes] |
rs1506457 | 0.85[CHB][hapmap] |
rs1517760 | 0.85[CEU][hapmap];0.90[CHB][hapmap];0.80[JPT][hapmap];0.97[TSI][hapmap];0.85[EUR][1000 genomes] |
rs17091269 | 1.00[CEU][hapmap];0.94[TSI][hapmap] |
rs2056206 | 0.90[CHB][hapmap];0.80[JPT][hapmap] |
rs2222177 | 0.83[EUR][1000 genomes] |
rs2421926 | 0.82[CHB][hapmap];0.83[EUR][1000 genomes] |
rs357245 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
rs4649938 | 0.85[CEU][hapmap];0.90[CHB][hapmap];0.80[JPT][hapmap] |
rs6424429 | 0.85[CHB][hapmap];0.80[JPT][hapmap] |
rs6668512 | 0.85[CEU][hapmap];0.82[CHB][hapmap];0.81[EUR][1000 genomes] |
rs6703162 | 0.85[CEU][hapmap];0.90[CHB][hapmap];0.80[JPT][hapmap];0.97[TSI][hapmap];0.83[EUR][1000 genomes] |
rs7516999 | 0.85[CEU][hapmap];0.85[CHB][hapmap];0.80[JPT][hapmap] |
rs7552024 | 0.83[EUR][1000 genomes] |
rs908686 | 0.85[EUR][1000 genomes] |
rs975842 | 0.97[TSI][hapmap] |
rs977145 | 0.85[CEU][hapmap];0.81[CHB][hapmap] |
rs9787180 | 0.84[CEU][hapmap];0.82[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949599 | chr1:71655652-72327802 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
2 | nsv1005726 | chr1:71701840-71953242 | Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
3 | esv1848377 | chr1:71718838-71964514 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
4 | nsv531880 | chr1:71724941-71964501 | Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
5 | nsv916508 | chr1:71777392-72046388 | Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
6 | nsv546474 | chr1:71793221-72040354 | Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
7 | nsv830170 | chr1:71856447-72008758 | ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:71953000-71954000 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |