Variant report
Variant | rs204636 |
---|---|
Chromosome Location | chr20:14347737-14347738 |
allele | G/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 |
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rs_ID | r2[population] |
---|---|
rs11087084 | 0.88[CEU][hapmap];0.83[CHB][hapmap];0.86[JPT][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs12329405 | 0.81[CEU][hapmap];0.94[CHB][hapmap];0.83[CHD][hapmap];0.92[JPT][hapmap] |
rs204629 | 0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs204637 | 0.93[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];1.00[MKK][hapmap];0.84[YRI][hapmap] |
rs204645 | 1.00[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap];0.88[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2145560 | 0.81[CEU][hapmap];0.94[CHB][hapmap];0.85[JPT][hapmap];0.88[ASN][1000 genomes] |
rs2208456 | 0.80[CEU][hapmap];0.82[CHB][hapmap];0.89[CHD][hapmap];0.85[GIH][hapmap];0.92[JPT][hapmap] |
rs2327847 | 0.83[EUR][1000 genomes] |
rs3789335 | 0.81[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap];0.86[ASN][1000 genomes] |
rs6033952 | 0.93[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6042672 | 0.81[GIH][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs6042695 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs6105236 | 0.85[JPT][hapmap] |
rs6105243 | 0.80[CEU][hapmap];0.84[CHB][hapmap];0.87[GIH][hapmap];0.92[JPT][hapmap] |
rs6105246 | 0.89[CEU][hapmap];0.84[CHB][hapmap];0.93[JPT][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs6105247 | 0.87[CEU][hapmap];0.82[CHB][hapmap];0.92[CHD][hapmap];0.85[GIH][hapmap];0.92[JPT][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs6105250 | 0.86[ASN][1000 genomes] |
rs6110220 | 0.85[JPT][hapmap] |
rs6110242 | 0.85[JPT][hapmap] |
rs6110247 | 0.83[CEU][hapmap];0.86[JPT][hapmap] |
rs6110251 | 0.88[ASN][1000 genomes] |
rs6110252 | 0.81[CEU][hapmap];0.94[CHB][hapmap];0.84[CHD][hapmap];0.92[JPT][hapmap];0.88[ASN][1000 genomes] |
rs6110255 | 0.83[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap] |
rs6110259 | 0.81[CEU][hapmap];0.94[CHB][hapmap];0.81[CHD][hapmap];0.92[JPT][hapmap] |
rs6110263 | 0.81[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6110264 | 0.82[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap];0.89[ASN][1000 genomes] |
rs6135124 | 0.88[ASN][1000 genomes] |
rs6135125 | 0.81[CEU][hapmap];0.94[CHB][hapmap];0.81[CHD][hapmap];0.92[JPT][hapmap];0.86[ASN][1000 genomes] |
rs6135127 | 0.94[CHB][hapmap];0.81[CHD][hapmap];0.85[JPT][hapmap];0.88[ASN][1000 genomes] |
rs6135128 | 0.81[CEU][hapmap];0.94[CHB][hapmap];0.86[CHD][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs743216 | 0.81[CEU][hapmap];0.94[CHB][hapmap];0.81[CHD][hapmap];0.92[JPT][hapmap];0.86[ASN][1000 genomes] |
rs8126410 | 0.80[CHD][hapmap];0.85[JPT][hapmap] |
Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1066810 | chr20:13451869-14432454 | Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
2 | nsv531479 | chr20:13632491-14434432 | Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
3 | nsv1057486 | chr20:14077828-14469129 | ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv1066235 | chr20:14173771-14389050 | Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv1055499 | chr20:14224873-14848061 | Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
6 | nsv432101 | chr20:14294196-14353346 | Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | nsv1061705 | chr20:14330029-14430604 | Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
8 | nsv1062079 | chr20:14334350-14429820 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
9 | nsv1063787 | chr20:14341199-14408090 | Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |