Variant report
Variant | rs6777637 |
---|---|
Chromosome Location | chr3:146054504-146054505 |
allele | C/T |
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 | chr3:146053792..146056507-chr3:146270955..146273271,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs16858173 | 1.00[EUR][1000 genomes] |
rs16858176 | 1.00[EUR][1000 genomes] |
rs16858179 | 1.00[EUR][1000 genomes] |
rs41358845 | 1.00[EUR][1000 genomes] |
rs41537446 | 1.00[EUR][1000 genomes] |
rs56364069 | 0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs56945578 | 1.00[EUR][1000 genomes] |
rs57016931 | 1.00[EUR][1000 genomes] |
rs57202132 | 1.00[EUR][1000 genomes] |
rs57555021 | 1.00[EUR][1000 genomes] |
rs57702664 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs57852021 | 1.00[EUR][1000 genomes] |
rs58284373 | 1.00[EUR][1000 genomes] |
rs58434679 | 1.00[EUR][1000 genomes] |
rs58523990 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59001257 | 1.00[EUR][1000 genomes] |
rs59060080 | 1.00[EUR][1000 genomes] |
rs59125030 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59201889 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59202860 | 1.00[EUR][1000 genomes] |
rs59652731 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60028092 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60271422 | 1.00[EUR][1000 genomes] |
rs60489907 | 1.00[EUR][1000 genomes] |
rs60843942 | 1.00[EUR][1000 genomes] |
rs60922478 | 1.00[EUR][1000 genomes] |
rs61440265 | 1.00[EUR][1000 genomes] |
rs6440427 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6765013 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6766725 | 0.90[EUR][1000 genomes] |
rs6767570 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6777974 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72991486 | 0.90[EUR][1000 genomes] |
rs72991490 | 0.90[EUR][1000 genomes] |
rs72991492 | 0.90[EUR][1000 genomes] |
rs72991494 | 0.90[EUR][1000 genomes] |
rs72992903 | 1.00[EUR][1000 genomes] |
rs72992908 | 1.00[EUR][1000 genomes] |
rs72992924 | 1.00[EUR][1000 genomes] |
rs72992931 | 1.00[EUR][1000 genomes] |
rs72992934 | 1.00[EUR][1000 genomes] |
rs72992963 | 1.00[EUR][1000 genomes] |
rs72992964 | 1.00[EUR][1000 genomes] |
rs72992966 | 1.00[EUR][1000 genomes] |
rs72992968 | 1.00[EUR][1000 genomes] |
rs72992969 | 1.00[EUR][1000 genomes] |
rs72992975 | 1.00[EUR][1000 genomes] |
rs72992981 | 1.00[EUR][1000 genomes] |
rs72992986 | 1.00[EUR][1000 genomes] |
rs72992988 | 1.00[EUR][1000 genomes] |
rs72992989 | 1.00[EUR][1000 genomes] |
rs72993002 | 1.00[EUR][1000 genomes] |
rs72995008 | 1.00[EUR][1000 genomes] |
rs72995010 | 1.00[EUR][1000 genomes] |
rs72995012 | 1.00[EUR][1000 genomes] |
rs72995014 | 1.00[EUR][1000 genomes] |
rs72995019 | 1.00[EUR][1000 genomes] |
rs72995022 | 1.00[EUR][1000 genomes] |
rs72995025 | 1.00[EUR][1000 genomes] |
rs72995029 | 1.00[EUR][1000 genomes] |
rs72995034 | 1.00[EUR][1000 genomes] |
rs72999169 | 1.00[EUR][1000 genomes] |
rs72999182 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72999189 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72999197 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73001103 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73001107 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73001112 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73001132 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73001133 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73865394 | 1.00[EUR][1000 genomes] |
rs73867504 | 1.00[EUR][1000 genomes] |
rs73867507 | 1.00[EUR][1000 genomes] |
rs73867511 | 1.00[EUR][1000 genomes] |
rs73867513 | 0.90[EUR][1000 genomes] |
rs73867518 | 1.00[EUR][1000 genomes] |
rs73867520 | 1.00[EUR][1000 genomes] |
rs73867521 | 1.00[EUR][1000 genomes] |
rs73867523 | 1.00[EUR][1000 genomes] |
rs7610563 | 1.00[EUR][1000 genomes] |
rs7629318 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7630137 | 1.00[EUR][1000 genomes] |
rs7630230 | 1.00[EUR][1000 genomes] |
rs7632298 | 1.00[EUR][1000 genomes] |
rs7642529 | 0.90[EUR][1000 genomes] |
rs7650158 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7650651 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7651598 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7651977 | 1.00[EUR][1000 genomes] |
rs7652262 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3333601 | chr3:145940702-146068210 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
2 | esv3416330 | chr3:145941029-146068457 | Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
3 | nsv998388 | chr3:145960954-146087749 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
4 | esv3410778 | chr3:146017303-146060390 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:146051600-146055400 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
2 | chr3:146053600-146063600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
3 | chr3:146054000-146063000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |