Variant report
Variant | rs73940723 |
---|---|
Chromosome Location | chr2:56801072-56801073 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10165672 | 1.00[EUR][1000 genomes] |
rs10165892 | 1.00[EUR][1000 genomes] |
rs10166050 | 1.00[EUR][1000 genomes] |
rs10171224 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10176983 | 1.00[EUR][1000 genomes] |
rs10178661 | 1.00[EUR][1000 genomes] |
rs10180194 | 1.00[EUR][1000 genomes] |
rs10181815 | 1.00[EUR][1000 genomes] |
rs10181900 | 1.00[EUR][1000 genomes] |
rs10183259 | 1.00[EUR][1000 genomes] |
rs10193624 | 1.00[EUR][1000 genomes] |
rs10193747 | 1.00[EUR][1000 genomes] |
rs10195595 | 1.00[EUR][1000 genomes] |
rs10198440 | 1.00[EUR][1000 genomes] |
rs10200031 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10202374 | 1.00[EUR][1000 genomes] |
rs10202443 | 1.00[EUR][1000 genomes] |
rs10208606 | 1.00[EUR][1000 genomes] |
rs11887424 | 1.00[EUR][1000 genomes] |
rs11896577 | 1.00[EUR][1000 genomes] |
rs11897129 | 1.00[EUR][1000 genomes] |
rs12328751 | 1.00[EUR][1000 genomes] |
rs13382467 | 1.00[EUR][1000 genomes] |
rs13384170 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13384989 | 1.00[EUR][1000 genomes] |
rs13385548 | 1.00[EUR][1000 genomes] |
rs13386206 | 1.00[EUR][1000 genomes] |
rs13386727 | 1.00[EUR][1000 genomes] |
rs13387143 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13392858 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13396144 | 1.00[EUR][1000 genomes] |
rs13398609 | 1.00[EUR][1000 genomes] |
rs13398719 | 1.00[EUR][1000 genomes] |
rs13401849 | 1.00[EUR][1000 genomes] |
rs13407080 | 1.00[EUR][1000 genomes] |
rs13407738 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13408350 | 1.00[EUR][1000 genomes] |
rs13411174 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13412157 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13417902 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13418673 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs13421608 | 1.00[EUR][1000 genomes] |
rs13431398 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17047938 | 1.00[EUR][1000 genomes] |
rs17047945 | 1.00[EUR][1000 genomes] |
rs17048166 | 1.00[EUR][1000 genomes] |
rs17048167 | 1.00[EUR][1000 genomes] |
rs17048189 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17048223 | 1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2067828 | 1.00[EUR][1000 genomes] |
rs2081427 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2193483 | 1.00[EUR][1000 genomes] |
rs2194793 | 1.00[EUR][1000 genomes] |
rs2216493 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28654487 | 1.00[EUR][1000 genomes] |
rs28673216 | 1.00[EUR][1000 genomes] |
rs28678883 | 1.00[EUR][1000 genomes] |
rs2904312 | 1.00[EUR][1000 genomes] |
rs55923854 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59211909 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59956872 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6740161 | 1.00[EUR][1000 genomes] |
rs6741874 | 1.00[EUR][1000 genomes] |
rs73940724 | 1.00[EUR][1000 genomes] |
rs73940726 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73940728 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73940730 | 0.81[AMR][1000 genomes] |
rs7556872 | 1.00[EUR][1000 genomes] |
rs7559732 | 1.00[EUR][1000 genomes] |
rs7570781 | 1.00[EUR][1000 genomes] |
rs7586424 | 1.00[EUR][1000 genomes] |
rs7595192 | 1.00[EUR][1000 genomes] |
rs7599191 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv874172 | chr2:56638856-56811749 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | esv2757800 | chr2:56659685-56851198 | Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | esv2759052 | chr2:56659685-56851198 | Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv582050 | chr2:56702495-56854346 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | esv2756921 | chr2:56706672-56811290 | Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | nsv582051 | chr2:56706758-56902709 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
7 | nsv874175 | chr2:56731966-56821883 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
8 | nsv874176 | chr2:56736097-56821883 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
9 | nsv874177 | chr2:56739650-56821883 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
10 | nsv874178 | chr2:56739650-56839139 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
11 | esv35146 | chr2:56741749-56811290 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
12 | nsv817973 | chr2:56743435-56817927 | Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
13 | nsv1005547 | chr2:56751574-56887287 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
14 | nsv1012596 | chr2:56761303-56916336 | Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
15 | nsv535725 | chr2:56761303-56916336 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
16 | nsv1008859 | chr2:56767452-57126026 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
17 | nsv535726 | chr2:56767452-57126026 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
18 | nsv1009860 | chr2:56768276-56896971 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
19 | nsv582056 | chr2:56785785-56822558 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:56792600-56803000 | Weak transcription | HSMM | muscle |