Variant report
Variant | rs2744420 |
---|---|
Chromosome Location | chr6:163792821-163792822 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr6:163787459..163789359-chr6:163790484..163793224,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1016501 | 1.00[ASN][1000 genomes] |
rs1016502 | 1.00[ASN][1000 genomes] |
rs1040514 | 1.00[ASN][1000 genomes] |
rs11752044 | 1.00[ASN][1000 genomes] |
rs12194023 | 1.00[ASN][1000 genomes] |
rs1230321 | 1.00[ASN][1000 genomes] |
rs1234603 | 1.00[ASN][1000 genomes] |
rs1234604 | 1.00[ASN][1000 genomes] |
rs1234976 | 1.00[ASN][1000 genomes] |
rs1614795 | 1.00[ASN][1000 genomes] |
rs1619076 | 1.00[ASN][1000 genomes] |
rs1619863 | 1.00[ASN][1000 genomes] |
rs1629251 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1737329 | 1.00[ASN][1000 genomes] |
rs1737333 | 1.00[ASN][1000 genomes] |
rs1737600 | 1.00[ASN][1000 genomes] |
rs1737601 | 1.00[ASN][1000 genomes] |
rs1737603 | 1.00[ASN][1000 genomes] |
rs1737604 | 1.00[ASN][1000 genomes] |
rs1737606 | 1.00[ASN][1000 genomes] |
rs1737607 | 1.00[ASN][1000 genomes] |
rs1737609 | 1.00[ASN][1000 genomes] |
rs1737611 | 1.00[ASN][1000 genomes] |
rs1737612 | 1.00[ASN][1000 genomes] |
rs1744924 | 1.00[ASN][1000 genomes] |
rs1744925 | 1.00[ASN][1000 genomes] |
rs1744926 | 1.00[ASN][1000 genomes] |
rs1744927 | 1.00[ASN][1000 genomes] |
rs1744928 | 1.00[ASN][1000 genomes] |
rs1744933 | 1.00[ASN][1000 genomes] |
rs1745094 | 1.00[ASN][1000 genomes] |
rs2038146 | 1.00[ASN][1000 genomes] |
rs2038147 | 1.00[ASN][1000 genomes] |
rs2057003 | 1.00[ASN][1000 genomes] |
rs2092406 | 1.00[ASN][1000 genomes] |
rs2092407 | 1.00[ASN][1000 genomes] |
rs2179523 | 1.00[ASN][1000 genomes] |
rs2179524 | 1.00[ASN][1000 genomes] |
rs2321698 | 1.00[ASN][1000 genomes] |
rs2321700 | 1.00[ASN][1000 genomes] |
rs2321701 | 1.00[ASN][1000 genomes] |
rs2321702 | 1.00[ASN][1000 genomes] |
rs2484877 | 1.00[ASN][1000 genomes] |
rs2744421 | 0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2745364 | 1.00[ASN][1000 genomes] |
rs2745365 | 1.00[ASN][1000 genomes] |
rs2757579 | 1.00[ASN][1000 genomes] |
rs2757580 | 1.00[ASN][1000 genomes] |
rs2757581 | 1.00[ASN][1000 genomes] |
rs2757582 | 1.00[ASN][1000 genomes] |
rs2757583 | 1.00[ASN][1000 genomes] |
rs2757586 | 1.00[ASN][1000 genomes] |
rs2757587 | 1.00[ASN][1000 genomes] |
rs2757589 | 1.00[ASN][1000 genomes] |
rs2759381 | 1.00[ASN][1000 genomes] |
rs2759383 | 1.00[ASN][1000 genomes] |
rs2759384 | 1.00[ASN][1000 genomes] |
rs2759385 | 1.00[ASN][1000 genomes] |
rs2759387 | 1.00[ASN][1000 genomes] |
rs2759388 | 1.00[ASN][1000 genomes] |
rs2759389 | 1.00[ASN][1000 genomes] |
rs2759390 | 1.00[ASN][1000 genomes] |
rs2759391 | 1.00[ASN][1000 genomes] |
rs2759392 | 1.00[ASN][1000 genomes] |
rs2759393 | 1.00[ASN][1000 genomes] |
rs2759395 | 1.00[ASN][1000 genomes] |
rs2759398 | 1.00[ASN][1000 genomes] |
rs2759399 | 1.00[ASN][1000 genomes] |
rs2784865 | 1.00[ASN][1000 genomes] |
rs2784867 | 1.00[ASN][1000 genomes] |
rs2784873 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2874602 | 1.00[ASN][1000 genomes] |
rs4708996 | 1.00[ASN][1000 genomes] |
rs4708997 | 1.00[ASN][1000 genomes] |
rs56721804 | 1.00[ASN][1000 genomes] |
rs6455900 | 1.00[ASN][1000 genomes] |
rs6455902 | 1.00[ASN][1000 genomes] |
rs6455903 | 1.00[ASN][1000 genomes] |
rs6455904 | 1.00[ASN][1000 genomes] |
rs6913113 | 1.00[ASN][1000 genomes] |
rs6914387 | 1.00[ASN][1000 genomes] |
rs6915247 | 1.00[ASN][1000 genomes] |
rs6924130 | 1.00[ASN][1000 genomes] |
rs6926584 | 1.00[ASN][1000 genomes] |
rs6927417 | 1.00[ASN][1000 genomes] |
rs721190 | 1.00[ASN][1000 genomes] |
rs721191 | 1.00[ASN][1000 genomes] |
rs7746116 | 1.00[ASN][1000 genomes] |
rs7749189 | 1.00[ASN][1000 genomes] |
rs7761088 | 1.00[ASN][1000 genomes] |
rs7768051 | 1.00[ASN][1000 genomes] |
rs7769145 | 1.00[ASN][1000 genomes] |
rs7775850 | 1.00[ASN][1000 genomes] |
rs783136 | 1.00[ASN][1000 genomes] |
rs783138 | 1.00[ASN][1000 genomes] |
rs783140 | 1.00[ASN][1000 genomes] |
rs803613 | 1.00[ASN][1000 genomes] |
rs809155 | 1.00[ASN][1000 genomes] |
rs813640 | 1.00[ASN][1000 genomes] |
rs814143 | 1.00[ASN][1000 genomes] |
rs9295222 | 1.00[ASN][1000 genomes] |
rs9295223 | 1.00[ASN][1000 genomes] |
rs9295224 | 1.00[ASN][1000 genomes] |
rs9347754 | 1.00[ASN][1000 genomes] |
rs9347755 | 1.00[ASN][1000 genomes] |
rs9347756 | 1.00[ASN][1000 genomes] |
rs9347759 | 1.00[ASN][1000 genomes] |
rs9347763 | 1.00[ASN][1000 genomes] |
rs9356117 | 1.00[ASN][1000 genomes] |
rs9365572 | 1.00[ASN][1000 genomes] |
rs9365573 | 1.00[ASN][1000 genomes] |
rs9365574 | 1.00[ASN][1000 genomes] |
rs9456866 | 1.00[ASN][1000 genomes] |
rs9456869 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv932127 | chr6:163000261-163950870 | Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
2 | nsv1022610 | chr6:163591786-163814041 | Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
3 | nsv534621 | chr6:163731741-163950870 | Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
4 | nsv970668 | chr6:163792636-163802489 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:163791000-163794200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr6:163791000-163794200 | Weak transcription | Left Ventricle | heart |
3 | chr6:163791000-163813000 | Weak transcription | Right Atrium | heart |
4 | chr6:163791200-163793800 | Weak transcription | Spleen | Spleen |
5 | chr6:163791200-163794200 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
6 | chr6:163791600-163793800 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
7 | chr6:163792200-163794200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
8 | chr6:163792400-163793200 | Weak transcription | Fetal Heart | heart |
9 | chr6:163792400-163796200 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
10 | chr6:163792400-163796400 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
11 | chr6:163792800-163794000 | Weak transcription | Brain Substantia Nigra | brain |