Variant report
Variant | rs17026547 |
---|---|
Chromosome Location | chr2:40948260-40948261 |
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] |
---|---|
rs1003616 | 0.86[EUR][1000 genomes] |
rs1003617 | 0.86[EUR][1000 genomes] |
rs10048831 | 0.90[EUR][1000 genomes] |
rs1009356 | 1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10490260 | 0.90[AFR][1000 genomes];0.90[EUR][1000 genomes] |
rs10490261 | 0.90[AFR][1000 genomes];0.90[EUR][1000 genomes] |
rs10490265 | 0.92[ASN][1000 genomes] |
rs1107932 | 0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11124753 | 0.83[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs1116005 | 0.82[AFR][1000 genomes] |
rs12105490 | 0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12463635 | 0.82[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs12463684 | 0.81[CHB][hapmap];0.83[JPT][hapmap];0.83[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs12466363 | 0.97[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12466428 | 0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12466466 | 0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12466571 | 0.83[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12469295 | 0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12470937 | 0.92[ASN][1000 genomes] |
rs12474457 | 0.81[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs12474560 | 0.81[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs12474649 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12477533 | 0.83[EUR][1000 genomes] |
rs13414829 | 0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs13422403 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs17026449 | 0.84[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs17026478 | 0.83[AFR][1000 genomes];0.90[EUR][1000 genomes] |
rs17026493 | 0.91[AFR][1000 genomes];0.91[EUR][1000 genomes] |
rs17026498 | 0.93[EUR][1000 genomes] |
rs17039019 | 0.91[EUR][1000 genomes] |
rs17479653 | 0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs1861302 | 0.86[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs2110791 | 0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2192816 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2192819 | 0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2192820 | 0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2216044 | 0.88[EUR][1000 genomes] |
rs2216045 | 0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs28418485 | 0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs28704849 | 0.82[ASN][1000 genomes] |
rs2888698 | 0.88[EUR][1000 genomes] |
rs34359856 | 0.81[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs3851315 | 0.82[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs3851316 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs3851317 | 0.89[CEU][hapmap];0.87[EUR][1000 genomes] |
rs3862989 | 0.83[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4384832 | 0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4952640 | 0.85[AFR][1000 genomes] |
rs4952645 | 0.84[ASN][1000 genomes] |
rs55670471 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs55690670 | 0.86[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs55772101 | 0.93[ASN][1000 genomes] |
rs55814013 | 0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs55878022 | 0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs56121667 | 0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs56321003 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs56336113 | 0.81[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs56342806 | 0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs57243979 | 0.89[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs57950795 | 0.81[EUR][1000 genomes] |
rs60819615 | 0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs62139477 | 0.89[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs62139540 | 0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs62139545 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs62139546 | 0.82[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs62141367 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs62141369 | 0.92[ASN][1000 genomes] |
rs62141370 | 0.92[ASN][1000 genomes] |
rs62141371 | 0.82[AMR][1000 genomes];0.92[ASN][1000 genomes] |
rs62141372 | 0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6708921 | 0.82[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6712874 | 0.83[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6714526 | 0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6720960 | 0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs6721900 | 0.91[EUR][1000 genomes] |
rs6733936 | 0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6734048 | 0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs6755751 | 0.83[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs7563807 | 0.91[EUR][1000 genomes] |
rs7573722 | 0.85[ASN][1000 genomes] |
rs7584710 | 0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs881189 | 0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs888021 | 0.88[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs983123 | 0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[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 data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:40944600-40948600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
2 | chr2:40944600-40948800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr2:40944600-40949000 | Weak transcription | Osteobl | bone |
4 | chr2:40944600-40949600 | Weak transcription | Esophagus | oesophagus |
5 | chr2:40944800-40948400 | Weak transcription | NHEK | skin |
6 | chr2:40944800-40948600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
7 | chr2:40944800-40948600 | Weak transcription | HMEC | breast |
8 | chr2:40945200-40948600 | Weak transcription | NHDF-Ad | bronchial |
9 | chr2:40945600-40948600 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
10 | chr2:40946000-40948600 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
11 | chr2:40946600-40948800 | Weak transcription | HSMM | muscle |
12 | chr2:40946800-40948600 | Weak transcription | HSMMtube | muscle |
13 | chr2:40947000-40951200 | Weak transcription | Colon Smooth Muscle | Colon |
14 | chr2:40947000-40952400 | Weak transcription | Rectal Smooth Muscle | rectum |
15 | chr2:40947400-40948400 | Weak transcription | Muscle Satellite Cultured Cells | -- |