Variant report
Variant | rs6074678 |
---|---|
Chromosome Location | chr20:14031392-14031393 |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs12162441 | 0.95[JPT][hapmap] |
rs1321242 | 0.95[JPT][hapmap] |
rs1475205 | 0.80[JPT][hapmap] |
rs1570484 | 0.80[JPT][hapmap] |
rs1890221 | 0.95[JPT][hapmap] |
rs2224738 | 0.80[JPT][hapmap] |
rs2263683 | 0.95[JPT][hapmap];0.81[AFR][1000 genomes] |
rs3842812 | 0.95[JPT][hapmap] |
rs3848778 | 0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs3859621 | 0.83[ASW][hapmap];0.83[GIH][hapmap];0.95[JPT][hapmap] |
rs4052974 | 0.95[JPT][hapmap] |
rs4334554 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4405821 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6042438 | 0.82[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes] |
rs6042449 | 0.95[JPT][hapmap] |
rs6074702 | 0.80[JPT][hapmap] |
rs6074704 | 0.80[JPT][hapmap] |
rs6079226 | 0.95[JPT][hapmap] |
rs6079243 | 0.95[JPT][hapmap] |
rs6079337 | 0.80[JPT][hapmap] |
rs6105196 | 0.95[JPT][hapmap] |
rs6105222 | 0.80[JPT][hapmap] |
rs6110114 | 0.95[JPT][hapmap] |
rs6110115 | 0.83[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];0.98[TSI][hapmap];0.93[YRI][hapmap] |
rs914764 | 0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs994868 | 0.80[JPT][hapmap] |
Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv916202 | chr20:13421724-14043615 | Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
2 | 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 |
3 | nsv912689 | chr20:13570331-14155881 | Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
4 | 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 |
5 | nsv526954 | chr20:13995214-14055947 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |