Variant report
Variant | rs73582176 |
---|---|
Chromosome Location | chr6:146306770-146306771 |
allele | C/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 | chr6:146284099..146286146-chr6:146302656..146306896,3 | K562 | blood: |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000146414 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs12332892 | 1.00[EUR][1000 genomes] |
rs28738876 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55671343 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55879513 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56954340 | 1.00[EUR][1000 genomes] |
rs57057101 | 1.00[EUR][1000 genomes] |
rs57776904 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57889864 | 1.00[EUR][1000 genomes] |
rs58290238 | 1.00[EUR][1000 genomes] |
rs58702332 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59951042 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60430705 | 1.00[EUR][1000 genomes] |
rs60698481 | 1.00[EUR][1000 genomes] |
rs60885622 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60899243 | 1.00[EUR][1000 genomes] |
rs6570725 | 1.00[EUR][1000 genomes] |
rs6570727 | 1.00[EUR][1000 genomes] |
rs6570730 | 1.00[EUR][1000 genomes] |
rs6900565 | 1.00[EUR][1000 genomes] |
rs6900607 | 1.00[EUR][1000 genomes] |
rs6904612 | 1.00[EUR][1000 genomes] |
rs6918314 | 1.00[EUR][1000 genomes] |
rs6920565 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6924714 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6927890 | 1.00[EUR][1000 genomes] |
rs6928607 | 1.00[EUR][1000 genomes] |
rs6935019 | 1.00[EUR][1000 genomes] |
rs6936647 | 1.00[EUR][1000 genomes] |
rs6936879 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6938895 | 1.00[EUR][1000 genomes] |
rs6940256 | 1.00[EUR][1000 genomes] |
rs73570006 | 1.00[EUR][1000 genomes] |
rs73570010 | 1.00[EUR][1000 genomes] |
rs73570033 | 1.00[EUR][1000 genomes] |
rs73570037 | 1.00[EUR][1000 genomes] |
rs73570042 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73572161 | 1.00[EUR][1000 genomes] |
rs73572189 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73573176 | 1.00[EUR][1000 genomes] |
rs73573178 | 1.00[EUR][1000 genomes] |
rs73573193 | 1.00[EUR][1000 genomes] |
rs73574105 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73576133 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73576161 | 1.00[EUR][1000 genomes] |
rs73576173 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73576180 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73576928 | 1.00[EUR][1000 genomes] |
rs73578805 | 1.00[EUR][1000 genomes] |
rs73578807 | 1.00[EUR][1000 genomes] |
rs73578811 | 1.00[EUR][1000 genomes] |
rs73578812 | 1.00[EUR][1000 genomes] |
rs73578814 | 1.00[EUR][1000 genomes] |
rs73578823 | 1.00[EUR][1000 genomes] |
rs73578827 | 1.00[EUR][1000 genomes] |
rs73578832 | 1.00[EUR][1000 genomes] |
rs73578833 | 1.00[EUR][1000 genomes] |
rs73580158 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73580169 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73580174 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73580180 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73580202 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73582109 | 1.00[EUR][1000 genomes] |
rs73582112 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73582116 | 1.00[EUR][1000 genomes] |
rs73582125 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73582139 | 1.00[EUR][1000 genomes] |
rs73582149 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73582189 | 1.00[EUR][1000 genomes] |
rs73584226 | 1.00[EUR][1000 genomes] |
rs7739858 | 1.00[EUR][1000 genomes] |
rs7740567 | 1.00[EUR][1000 genomes] |
rs7748102 | 0.85[AMR][1000 genomes] |
rs7757974 | 1.00[EUR][1000 genomes] |
rs7762880 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9322040 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9497422 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9497423 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9497430 | 1.00[EUR][1000 genomes] |
rs9497449 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1034226 | chr6:146071068-146306942 | Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
2 | nsv604839 | chr6:146305810-146828922 | Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
No data |