Variant report
Variant | rs16994501 |
---|---|
Chromosome Location | chr20:14328064-14328065 |
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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No data |
rs_ID | r2[population] |
---|---|
rs1114952 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs1114953 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs1555411 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs16994428 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs16994463 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs16994493 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs16994496 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs16994499 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1998487 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs2181530 | 0.81[ASN][1000 genomes] |
rs2208457 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs2327820 | 0.93[ASN][1000 genomes] |
rs2876375 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs35253731 | 0.81[ASN][1000 genomes] |
rs4813154 | 0.81[ASN][1000 genomes] |
rs4814292 | 0.93[ASN][1000 genomes] |
rs55763358 | 0.93[ASN][1000 genomes] |
rs55985306 | 0.93[ASN][1000 genomes] |
rs6033905 | 0.93[ASN][1000 genomes] |
rs6033907 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs6033916 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs6033917 | 0.93[ASN][1000 genomes] |
rs6033946 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs6042596 | 0.81[ASN][1000 genomes] |
rs6042601 | 0.93[ASN][1000 genomes] |
rs6042606 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs6042614 | 0.93[ASN][1000 genomes] |
rs6042616 | 0.93[ASN][1000 genomes] |
rs6042623 | 1.00[CHB][hapmap] |
rs6042677 | 1.00[CHB][hapmap];0.81[ASN][1000 genomes] |
rs6042678 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs6042679 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs6074706 | 0.93[ASN][1000 genomes] |
rs6074707 | 0.93[ASN][1000 genomes] |
rs6079359 | 0.93[ASN][1000 genomes] |
rs6079360 | 0.93[ASN][1000 genomes] |
rs6079371 | 0.93[ASN][1000 genomes] |
rs73901234 | 0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs8120919 | 1.00[CHB][hapmap];0.83[YRI][hapmap];0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs912190 | 0.93[ASN][1000 genomes] |
rs9967919 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:6 , 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 |
No data |