Variant report
Variant | rs7535845 |
---|---|
Chromosome Location | chr1:174471810-174471811 |
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] |
---|---|
rs1013769 | 0.88[ASN][1000 genomes] |
rs10489256 | 0.88[ASN][1000 genomes] |
rs10489258 | 0.88[ASN][1000 genomes] |
rs10489260 | 0.88[ASN][1000 genomes] |
rs10798310 | 0.88[ASN][1000 genomes] |
rs10798311 | 0.83[ASN][1000 genomes] |
rs10798312 | 0.88[ASN][1000 genomes] |
rs10798313 | 0.88[ASN][1000 genomes] |
rs10798314 | 0.83[ASN][1000 genomes] |
rs10798315 | 0.88[ASN][1000 genomes] |
rs10798319 | 0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10912772 | 0.88[ASN][1000 genomes] |
rs10912774 | 0.90[ASN][1000 genomes] |
rs10912775 | 0.83[ASN][1000 genomes] |
rs10912776 | 0.88[ASN][1000 genomes] |
rs10912777 | 0.85[ASN][1000 genomes] |
rs10912778 | 0.88[ASN][1000 genomes] |
rs10912779 | 0.88[ASN][1000 genomes] |
rs10912782 | 0.90[ASN][1000 genomes] |
rs10912786 | 0.88[ASN][1000 genomes] |
rs10912789 | 0.88[ASN][1000 genomes] |
rs10912791 | 0.88[ASN][1000 genomes] |
rs10912795 | 0.88[ASN][1000 genomes] |
rs10912799 | 0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10912800 | 0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs11487399 | 0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs11799535 | 0.88[ASN][1000 genomes] |
rs11799704 | 0.88[ASN][1000 genomes] |
rs12058377 | 0.88[ASN][1000 genomes] |
rs12062170 | 0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12062483 | 0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12064743 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12065326 | 0.88[ASN][1000 genomes] |
rs12065454 | 0.88[ASN][1000 genomes] |
rs12069134 | 0.88[ASN][1000 genomes] |
rs12070095 | 0.88[ASN][1000 genomes] |
rs12071794 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12073751 | 0.88[ASN][1000 genomes] |
rs12074416 | 0.83[ASN][1000 genomes] |
rs12074754 | 0.88[ASN][1000 genomes] |
rs12076548 | 0.88[ASN][1000 genomes] |
rs12077381 | 0.88[ASN][1000 genomes] |
rs12077529 | 0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12078960 | 0.88[ASN][1000 genomes] |
rs12079334 | 0.88[ASN][1000 genomes] |
rs12080407 | 0.88[ASN][1000 genomes] |
rs12080535 | 0.81[EUR][1000 genomes] |
rs12083628 | 0.81[EUR][1000 genomes] |
rs12083972 | 0.88[ASN][1000 genomes] |
rs12084291 | 0.88[ASN][1000 genomes] |
rs12086693 | 0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12090860 | 0.88[ASN][1000 genomes] |
rs12091056 | 0.88[ASN][1000 genomes] |
rs12092768 | 0.83[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs12095629 | 0.88[ASN][1000 genomes] |
rs12097931 | 0.83[ASN][1000 genomes] |
rs16828481 | 0.88[ASN][1000 genomes] |
rs16846938 | 0.90[ASN][1000 genomes] |
rs16846949 | 0.88[ASN][1000 genomes] |
rs16847012 | 0.88[ASN][1000 genomes] |
rs1806329 | 0.88[ASN][1000 genomes] |
rs1883262 | 0.88[ASN][1000 genomes] |
rs1989177 | 0.88[ASN][1000 genomes] |
rs2012558 | 0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs2072759 | 0.88[ASN][1000 genomes] |
rs2205937 | 0.88[ASN][1000 genomes] |
rs2281009 | 0.88[ASN][1000 genomes] |
rs2281010 | 0.83[ASN][1000 genomes] |
rs2281011 | 0.88[ASN][1000 genomes] |
rs2860955 | 0.88[ASN][1000 genomes] |
rs2860959 | 0.88[ASN][1000 genomes] |
rs28628056 | 0.83[ASN][1000 genomes] |
rs2901815 | 0.88[ASN][1000 genomes] |
rs2901817 | 0.88[ASN][1000 genomes] |
rs2901818 | 0.89[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs2901820 | 0.88[ASN][1000 genomes] |
rs35425383 | 0.88[ASN][1000 genomes] |
rs4233181 | 0.88[ASN][1000 genomes] |
rs4651015 | 0.88[ASN][1000 genomes] |
rs4651016 | 0.88[ASN][1000 genomes] |
rs4651019 | 0.88[ASN][1000 genomes] |
rs4652365 | 0.88[ASN][1000 genomes] |
rs4652422 | 0.88[ASN][1000 genomes] |
rs4652425 | 0.88[ASN][1000 genomes] |
rs4652460 | 0.88[ASN][1000 genomes] |
rs4652494 | 0.88[ASN][1000 genomes] |
rs4652500 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4652511 | 0.88[ASN][1000 genomes] |
rs4652512 | 0.88[ASN][1000 genomes] |
rs4652513 | 0.88[ASN][1000 genomes] |
rs5015737 | 0.81[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs56148594 | 0.88[ASN][1000 genomes] |
rs56213002 | 0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs56407387 | 0.88[ASN][1000 genomes] |
rs57512497 | 0.88[ASN][1000 genomes] |
rs57953555 | 0.88[ASN][1000 genomes] |
rs58750544 | 0.88[ASN][1000 genomes] |
rs61218633 | 0.83[ASN][1000 genomes] |
rs61624206 | 0.81[EUR][1000 genomes] |
rs6656925 | 0.88[ASN][1000 genomes] |
rs6658315 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs6668096 | 0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs6674239 | 0.88[ASN][1000 genomes] |
rs6677262 | 0.88[ASN][1000 genomes] |
rs6681970 | 0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs6682997 | 0.88[ASN][1000 genomes] |
rs6684688 | 0.88[ASN][1000 genomes] |
rs6689327 | 0.88[ASN][1000 genomes] |
rs6691118 | 0.81[EUR][1000 genomes] |
rs6692173 | 0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs6699142 | 0.83[ASN][1000 genomes] |
rs6699697 | 0.88[ASN][1000 genomes] |
rs6701534 | 0.83[ASN][1000 genomes] |
rs6701911 | 0.88[ASN][1000 genomes] |
rs72713537 | 0.88[ASN][1000 genomes] |
rs72713540 | 0.88[ASN][1000 genomes] |
rs72713583 | 0.88[ASN][1000 genomes] |
rs72713584 | 0.88[ASN][1000 genomes] |
rs72713586 | 0.88[ASN][1000 genomes] |
rs72713591 | 0.88[ASN][1000 genomes] |
rs72713601 | 0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs72713602 | 0.88[ASN][1000 genomes] |
rs72715204 | 0.88[ASN][1000 genomes] |
rs72715226 | 0.83[ASN][1000 genomes] |
rs74126805 | 0.88[ASN][1000 genomes] |
rs74128393 | 0.88[ASN][1000 genomes] |
rs7413513 | 0.88[ASN][1000 genomes] |
rs7515116 | 0.88[ASN][1000 genomes] |
rs7522253 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7530265 | 0.81[EUR][1000 genomes] |
rs7536102 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7536987 | 0.90[ASN][1000 genomes] |
rs7537823 | 0.88[ASN][1000 genomes] |
rs7542775 | 0.81[EUR][1000 genomes] |
rs7554728 | 0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7554740 | 0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs926327 | 0.88[ASN][1000 genomes] |
rs926349 | 0.88[ASN][1000 genomes] |
rs969472 | 0.88[ASN][1000 genomes] |
rs9729907 | 0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs9730220 | 0.87[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv1799250 | chr1:174119038-174484277 | Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 29 gene(s) | inside rSNPs | diseases |
2 | esv1800060 | chr1:174132703-174501836 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
3 | nsv1010069 | chr1:174215293-174539512 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
4 | nsv1014637 | chr1:174265631-174826765 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
5 | nsv535208 | chr1:174265631-174826765 | Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
6 | nsv1014753 | chr1:174271770-174694838 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
7 | nsv872555 | chr1:174343705-174565720 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
8 | nsv1003113 | chr1:174367687-174499155 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
9 | nsv535209 | chr1:174367687-174499155 | Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
10 | esv2755184 | chr1:174388343-174970343 | Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 54 gene(s) | inside rSNPs | diseases |
11 | nsv1007667 | chr1:174438778-174556953 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
12 | nsv1009056 | chr1:174457532-174549665 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
13 | nsv999295 | chr1:174457532-174596961 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
14 | nsv534381 | chr1:174468168-174656796 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
15 | nsv548195 | chr1:174469002-174519276 | Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
16 | esv2757762 | chr1:174469281-174569776 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
17 | esv2758979 | chr1:174469281-174569776 | Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:174442200-174491800 | Weak transcription | Primary B cells from cord blood | blood |
2 | chr1:174457400-174473600 | Weak transcription | Aorta | Aorta |
3 | chr1:174457600-174475400 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
4 | chr1:174461200-174474200 | Weak transcription | GM12878-XiMat | blood |
5 | chr1:174461200-174476800 | Weak transcription | Primary T cells from cord blood | blood |
6 | chr1:174466800-174474200 | Weak transcription | Fetal Intestine Small | intestine |
7 | chr1:174466800-174489800 | Weak transcription | Left Ventricle | heart |
8 | chr1:174467000-174481200 | Weak transcription | Rectal Smooth Muscle | rectum |