Variant report
Variant | rs74134306 |
---|---|
Chromosome Location | chr1:185836882-185836883 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10489716 | 1.00[EUR][1000 genomes] |
rs11801425 | 1.00[AMR][1000 genomes] |
rs12079734 | 1.00[EUR][1000 genomes] |
rs1321667 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs1407428 | 1.00[EUR][1000 genomes] |
rs1407432 | 1.00[AMR][1000 genomes] |
rs16824455 | 1.00[EUR][1000 genomes] |
rs16824458 | 1.00[EUR][1000 genomes] |
rs16824488 | 1.00[EUR][1000 genomes] |
rs16824497 | 1.00[EUR][1000 genomes] |
rs1830622 | 1.00[EUR][1000 genomes] |
rs1830623 | 1.00[EUR][1000 genomes] |
rs1853247 | 1.00[EUR][1000 genomes] |
rs1951514 | 1.00[AMR][1000 genomes] |
rs2170858 | 1.00[EUR][1000 genomes] |
rs28477118 | 1.00[EUR][1000 genomes] |
rs28510615 | 1.00[EUR][1000 genomes] |
rs55661579 | 1.00[AMR][1000 genomes] |
rs55731570 | 1.00[EUR][1000 genomes] |
rs55887884 | 1.00[EUR][1000 genomes] |
rs56100961 | 1.00[EUR][1000 genomes] |
rs56151138 | 1.00[AMR][1000 genomes] |
rs56331179 | 1.00[EUR][1000 genomes] |
rs56347630 | 1.00[EUR][1000 genomes] |
rs56881574 | 1.00[EUR][1000 genomes] |
rs57036166 | 1.00[EUR][1000 genomes] |
rs57107751 | 1.00[EUR][1000 genomes] |
rs57162167 | 1.00[EUR][1000 genomes] |
rs57215320 | 1.00[EUR][1000 genomes] |
rs57246058 | 1.00[EUR][1000 genomes] |
rs57257586 | 1.00[EUR][1000 genomes] |
rs57646829 | 1.00[EUR][1000 genomes] |
rs57782754 | 1.00[EUR][1000 genomes] |
rs58433773 | 1.00[EUR][1000 genomes] |
rs58610741 | 1.00[EUR][1000 genomes] |
rs59054107 | 1.00[AMR][1000 genomes] |
rs59175860 | 1.00[EUR][1000 genomes] |
rs59244411 | 1.00[AMR][1000 genomes] |
rs59660733 | 1.00[EUR][1000 genomes] |
rs59691709 | 1.00[AMR][1000 genomes] |
rs59967839 | 1.00[EUR][1000 genomes] |
rs59987592 | 1.00[AMR][1000 genomes] |
rs60308365 | 1.00[EUR][1000 genomes] |
rs60458315 | 1.00[EUR][1000 genomes] |
rs60735946 | 1.00[EUR][1000 genomes] |
rs61580019 | 1.00[AMR][1000 genomes] |
rs61679640 | 1.00[EUR][1000 genomes] |
rs61689983 | 1.00[EUR][1000 genomes] |
rs6425004 | 1.00[EUR][1000 genomes] |
rs6425005 | 1.00[EUR][1000 genomes] |
rs6671094 | 1.00[EUR][1000 genomes] |
rs6675691 | 1.00[EUR][1000 genomes] |
rs6676349 | 1.00[EUR][1000 genomes] |
rs6676522 | 1.00[EUR][1000 genomes] |
rs6677183 | 1.00[EUR][1000 genomes] |
rs6688298 | 1.00[EUR][1000 genomes] |
rs6689228 | 1.00[EUR][1000 genomes] |
rs6689359 | 1.00[EUR][1000 genomes] |
rs6690475 | 1.00[EUR][1000 genomes] |
rs6690559 | 1.00[EUR][1000 genomes] |
rs6690714 | 1.00[EUR][1000 genomes] |
rs6700856 | 1.00[EUR][1000 genomes] |
rs6703750 | 1.00[EUR][1000 genomes] |
rs73054432 | 1.00[EUR][1000 genomes] |
rs73054448 | 1.00[EUR][1000 genomes] |
rs73060487 | 1.00[EUR][1000 genomes] |
rs73062512 | 1.00[EUR][1000 genomes] |
rs73062516 | 1.00[EUR][1000 genomes] |
rs73070519 | 1.00[EUR][1000 genomes] |
rs73070522 | 1.00[EUR][1000 genomes] |
rs73070527 | 1.00[EUR][1000 genomes] |
rs73070547 | 1.00[EUR][1000 genomes] |
rs73070548 | 1.00[EUR][1000 genomes] |
rs73070567 | 1.00[EUR][1000 genomes] |
rs73070598 | 1.00[EUR][1000 genomes] |
rs73072012 | 1.00[EUR][1000 genomes] |
rs73072023 | 1.00[EUR][1000 genomes] |
rs73072049 | 1.00[EUR][1000 genomes] |
rs73072063 | 1.00[EUR][1000 genomes] |
rs73072067 | 1.00[EUR][1000 genomes] |
rs74133675 | 0.89[AFR][1000 genomes] |
rs74133687 | 1.00[AMR][1000 genomes] |
rs74133690 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74133691 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74134206 | 1.00[AMR][1000 genomes] |
rs74134207 | 1.00[EUR][1000 genomes] |
rs74134209 | 1.00[AMR][1000 genomes] |
rs74134210 | 1.00[EUR][1000 genomes] |
rs74134216 | 1.00[EUR][1000 genomes] |
rs74134265 | 1.00[EUR][1000 genomes] |
rs74134303 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74134304 | 0.89[AFR][1000 genomes] |
rs74134310 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74134313 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74134314 | 1.00[AMR][1000 genomes] |
rs74134349 | 1.00[AMR][1000 genomes] |
rs74134350 | 1.00[AMR][1000 genomes] |
rs74134353 | 1.00[AMR][1000 genomes] |
rs74134354 | 1.00[AMR][1000 genomes] |
rs74134355 | 1.00[AMR][1000 genomes] |
rs74134357 | 1.00[AMR][1000 genomes] |
rs74134358 | 1.00[AMR][1000 genomes] |
rs74134359 | 1.00[AMR][1000 genomes] |
rs74134360 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74134378 | 1.00[AMR][1000 genomes] |
rs74134384 | 1.00[AMR][1000 genomes] |
rs74134388 | 1.00[AMR][1000 genomes] |
rs74134390 | 1.00[AMR][1000 genomes] |
rs74135308 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs74135337 | 1.00[EUR][1000 genomes] |
rs74135346 | 1.00[EUR][1000 genomes] |
rs74135350 | 1.00[EUR][1000 genomes] |
rs74135351 | 1.00[EUR][1000 genomes] |
rs74135359 | 1.00[EUR][1000 genomes] |
rs74135362 | 1.00[EUR][1000 genomes] |
rs74135365 | 1.00[EUR][1000 genomes] |
rs7517811 | 1.00[EUR][1000 genomes] |
rs7540727 | 1.00[EUR][1000 genomes] |
rs7540773 | 1.00[EUR][1000 genomes] |
rs7544162 | 1.00[EUR][1000 genomes] |
rs7544394 | 1.00[EUR][1000 genomes] |
rs7544808 | 1.00[EUR][1000 genomes] |
rs959689 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv548398 | chr1:185136458-186003094 | Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 69 gene(s) | inside rSNPs | diseases |
2 | esv3424090 | chr1:185679718-186270877 | Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 12 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:185803200-185850000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr1:185813400-185839000 | Weak transcription | Fetal Lung | lung |
3 | chr1:185827200-185841200 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
4 | chr1:185834400-185837800 | Weak transcription | Esophagus | oesophagus |
5 | chr1:185834400-185839000 | Weak transcription | Left Ventricle | heart |
6 | chr1:185834600-185848200 | Weak transcription | Aorta | Aorta |
7 | chr1:185834800-185838800 | Weak transcription | NHDF-Ad | bronchial |
8 | chr1:185835000-185837600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
9 | chr1:185835000-185838400 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
10 | chr1:185835400-185841200 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
11 | chr1:185836200-185837400 | Strong transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
12 | chr1:185836600-185841000 | Weak transcription | Placenta Amnion | Placenta Amnion |