Variant report
Variant | rs7589309 |
---|---|
Chromosome Location | chr2:40941054-40941055 |
allele | C/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 |
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No data |
rs_ID | r2[population] |
---|---|
rs1003616 | 0.80[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1003617 | 0.80[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1012304 | 0.80[EUR][1000 genomes] |
rs10172403 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10177047 | 0.84[AMR][1000 genomes] |
rs10197146 | 0.81[EUR][1000 genomes] |
rs10201594 | 0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10204982 | 0.85[ASN][1000 genomes] |
rs10206098 | 0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10209336 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10211572 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10445883 | 0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10490262 | 0.98[AFR][1000 genomes];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs10490263 | 0.90[ASW][hapmap];0.86[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap];0.88[LWK][hapmap];0.86[MEX][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs10490266 | 0.81[AFR][1000 genomes] |
rs11124752 | 0.81[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11124757 | 0.98[AFR][1000 genomes];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11124759 | 0.87[ASN][1000 genomes] |
rs11680340 | 0.82[ASN][1000 genomes] |
rs11682329 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs11682367 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs11689342 | 0.85[JPT][hapmap] |
rs11885458 | 0.91[ASN][1000 genomes] |
rs11891229 | 0.91[ASN][1000 genomes] |
rs11891709 | 0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11903731 | 0.82[AMR][1000 genomes] |
rs12469284 | 0.81[ASN][1000 genomes] |
rs12469493 | 0.87[ASN][1000 genomes] |
rs12474038 | 0.81[ASN][1000 genomes] |
rs12477533 | 0.80[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs12615804 | 0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs12712699 | 0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs12712700 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12712708 | 0.90[ASW][hapmap];0.93[CHB][hapmap];0.97[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12986905 | 0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12995661 | 0.81[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs13004542 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs13010274 | 0.81[ASN][1000 genomes] |
rs13016866 | 0.85[JPT][hapmap];0.91[YRI][hapmap];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs13022083 | 0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs13023675 | 0.87[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs13023757 | 0.87[ASN][1000 genomes] |
rs13031824 | 0.87[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs17026357 | 0.86[CHB][hapmap];0.80[JPT][hapmap] |
rs1861305 | 0.98[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1861306 | 0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1869988 | 0.81[EUR][1000 genomes] |
rs1869989 | 0.80[EUR][1000 genomes] |
rs2024436 | 0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs2024437 | 0.87[CHB][hapmap];0.81[CHD][hapmap];0.82[TSI][hapmap] |
rs2075195 | 0.98[AFR][1000 genomes];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs2080341 | 0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs2098360 | 0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2110786 | 0.81[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs2216041 | 0.86[CHB][hapmap];0.86[CHD][hapmap];0.85[JPT][hapmap] |
rs2216044 | 0.81[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs2373903 | 0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2888698 | 0.82[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs36081778 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs3851317 | 0.81[ASW][hapmap];0.89[CEU][hapmap];0.84[CHD][hapmap];0.85[JPT][hapmap];0.80[TSI][hapmap];0.80[EUR][1000 genomes] |
rs4101520 | 0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs4383382 | 0.81[ASN][1000 genomes] |
rs4528809 | 0.91[ASN][1000 genomes] |
rs4952649 | 0.80[EUR][1000 genomes] |
rs57950795 | 0.81[ASN][1000 genomes] |
rs6544350 | 0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs6710038 | 0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6713004 | 0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs67918843 | 0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs68168524 | 0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs74177099 | 0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7557413 | 0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7562117 | 0.85[AMR][1000 genomes];0.80[ASN][1000 genomes] |
rs7563703 | 0.88[CEU][hapmap];0.87[CHB][hapmap];0.86[CHD][hapmap];0.84[JPT][hapmap];0.86[MEX][hapmap];0.98[TSI][hapmap] |
rs767636 | 0.85[ASN][1000 genomes] |
rs918013 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs9309057 | 0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs9309058 | 0.86[ASN][1000 genomes] |
rs9677294 | 0.81[AFR][1000 genomes];0.80[ASN][1000 genomes] |
rs9808252 | 0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv873911 | chr2:40423454-41161464 | ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv873917 | chr2:40710953-41015998 | Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv528865 | chr2:40805427-41218810 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv873925 | chr2:40835285-40966719 | Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | n/a |
5 | nsv873926 | chr2:40835285-40986860 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv873927 | chr2:40835285-41034225 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | nsv470455 | chr2:40835285-41059164 | Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
8 | nsv873928 | chr2:40835285-41075134 | Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
9 | nsv873929 | chr2:40835285-41180690 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
10 | nsv873931 | chr2:40869165-40966719 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
11 | nsv456441 | chr2:40882402-41064824 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
12 | nsv581514 | chr2:40882402-41064824 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
13 | nsv456452 | chr2:40890416-40989061 | Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
14 | nsv581515 | chr2:40890416-40989061 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
15 | esv3584751 | chr2:40916853-40952073 | Enhancers Active TSS Weak transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
16 | esv2754698 | chr2:40922098-40949606 | Flanking Active TSS Active TSS Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | n/a |
17 | esv34871 | chr2:40922098-40951667 | Weak transcription Enhancers Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
18 | esv2755242 | chr2:40922098-40951667 | Weak transcription Enhancers Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
19 | esv3584750 | chr2:40926091-40949606 | Enhancers Flanking Active TSS Weak transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
20 | esv3457577 | chr2:40926899-40949434 | Enhancers Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
21 | esv3457576 | chr2:40926923-40949434 | Weak transcription Enhancers Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
22 | esv3457575 | chr2:40926941-40949439 | Enhancers Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
23 | nsv829008 | chr2:40927002-40949224 | Enhancers Flanking Active TSS Weak transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
24 | nsv829019 | chr2:40927002-40949304 | Enhancers Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
25 | esv3457578 | chr2:40927064-40949267 | Enhancers Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
26 | nsv1004050 | chr2:40927363-40949606 | Enhancers Active TSS Weak transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
27 | nsv441754 | chr2:40927375-40949602 | Enhancers Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
28 | esv3584749 | chr2:40927375-40949606 | Flanking Active TSS Enhancers Active TSS Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
29 | nsv514064 | chr2:40929032-40949156 | Weak transcription Enhancers Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
30 | nsv961752 | chr2:40929037-40950223 | Enhancers Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
31 | esv2756918 | chr2:40930721-40966719 | Enhancers Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
32 | esv2759045 | chr2:40930721-40966719 | Enhancers Weak transcription Flanking Active TSS Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:40940000-40944200 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |