Variant report
Variant | rs73072063 |
---|---|
Chromosome Location | chr1:185794182-185794183 |
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 | chr1:185793023..185794662-chr1:185796349..185798124,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10489716 | 1.00[EUR][1000 genomes] |
rs12079734 | 1.00[EUR][1000 genomes] |
rs12097100 | 1.00[EUR][1000 genomes] |
rs1407428 | 1.00[EUR][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] |
rs2170858 | 1.00[EUR][1000 genomes] |
rs28477118 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28510615 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55731570 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55887884 | 1.00[EUR][1000 genomes] |
rs56100961 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56331179 | 1.00[EUR][1000 genomes] |
rs56347630 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56881574 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];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] |
rs58375153 | 0.84[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs58433773 | 1.00[EUR][1000 genomes] |
rs58610741 | 1.00[EUR][1000 genomes] |
rs59024653 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs59175860 | 1.00[EUR][1000 genomes] |
rs59660733 | 0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59967839 | 1.00[EUR][1000 genomes] |
rs60307030 | 0.84[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs60308365 | 1.00[EUR][1000 genomes] |
rs60458315 | 1.00[EUR][1000 genomes] |
rs60735946 | 1.00[EUR][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 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];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 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];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 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];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 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73072023 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73072049 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73072067 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73072075 | 0.84[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs74134207 | 1.00[EUR][1000 genomes] |
rs74134210 | 1.00[EUR][1000 genomes] |
rs74134216 | 1.00[EUR][1000 genomes] |
rs74134265 | 1.00[EUR][1000 genomes] |
rs74134306 | 1.00[EUR][1000 genomes] |
rs74135337 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74135346 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74135350 | 1.00[EUR][1000 genomes] |
rs74135351 | 1.00[EUR][1000 genomes] |
rs74135359 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74135362 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs74135365 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7517811 | 1.00[EUR][1000 genomes] |
rs7520805 | 0.84[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs7540727 | 1.00[EUR][1000 genomes] |
rs7540773 | 1.00[EUR][1000 genomes] |
rs7544162 | 1.00[EUR][1000 genomes] |
rs7544394 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7544808 | 1.00[EUR][1000 genomes] |
rs7554996 | 0.84[AFR][1000 genomes];0.87[AMR][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 | chr1:185791600-185795800 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
2 | chr1:185792200-185795600 | Enhancers | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
3 | chr1:185792400-185795600 | Enhancers | NHDF-Ad | bronchial |
4 | chr1:185792400-185795800 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
5 | chr1:185793800-185794800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |