Variant report
Variant | rs72806930 |
---|---|
Chromosome Location | chr5:115592439-115592440 |
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 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10073557 | 0.85[ASN][1000 genomes] |
rs1031365 | 0.86[ASN][1000 genomes] |
rs10519452 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1422498 | 0.85[ASN][1000 genomes] |
rs17138924 | 0.83[AMR][1000 genomes] |
rs17139210 | 0.85[ASN][1000 genomes] |
rs17139251 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs17139353 | 0.93[ASN][1000 genomes] |
rs2271225 | 0.83[AMR][1000 genomes] |
rs2900096 | 1.00[ASN][1000 genomes] |
rs4308513 | 0.96[ASN][1000 genomes] |
rs4605830 | 0.85[ASN][1000 genomes] |
rs55742067 | 0.92[EUR][1000 genomes] |
rs56168251 | 1.00[AFR][1000 genomes] |
rs57526524 | 1.00[AFR][1000 genomes] |
rs57659470 | 0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs58291729 | 1.00[AFR][1000 genomes] |
rs58424191 | 0.87[ASN][1000 genomes] |
rs58776100 | 1.00[AFR][1000 genomes] |
rs6594958 | 0.86[ASN][1000 genomes] |
rs66783056 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs67139169 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs67339497 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs67412230 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs72804829 | 0.83[AMR][1000 genomes] |
rs72804830 | 0.83[AMR][1000 genomes] |
rs72804832 | 0.83[AMR][1000 genomes] |
rs72804839 | 0.83[AMR][1000 genomes] |
rs72804843 | 1.00[AMR][1000 genomes] |
rs72804844 | 1.00[AMR][1000 genomes] |
rs72804845 | 1.00[AMR][1000 genomes] |
rs72804850 | 0.92[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs72804862 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs72804864 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs72804867 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs72804869 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs72804873 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs72804875 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs72804877 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs72804882 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs72804884 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs72804885 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs72804889 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs72804891 | 0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs72804892 | 0.83[ASN][1000 genomes] |
rs72804893 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs72804896 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs72804898 | 0.85[ASN][1000 genomes] |
rs72804899 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs72804900 | 1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs72804901 | 0.85[ASN][1000 genomes] |
rs72806907 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs72806908 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs72806910 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs72806917 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs72806919 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs72806920 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs72806923 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs72806926 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs72806927 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs72806931 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72806933 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72806937 | 0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72806941 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs72806944 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs72808904 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs72808909 | 0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs72808912 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs72808916 | 0.93[ASN][1000 genomes] |
rs72808917 | 0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs72808922 | 0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs72808927 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs72808928 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs72808929 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs72808930 | 0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs72808931 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs72808932 | 1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs72808934 | 0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs72808943 | 0.92[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs72808945 | 0.92[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs72808949 | 1.00[AFR][1000 genomes];0.95[EUR][1000 genomes] |
rs72808952 | 0.95[EUR][1000 genomes] |
rs72808958 | 0.92[EUR][1000 genomes] |
rs72808959 | 0.92[EUR][1000 genomes] |
rs72808960 | 0.92[EUR][1000 genomes] |
rs72808961 | 0.95[EUR][1000 genomes] |
rs72808964 | 0.95[EUR][1000 genomes] |
rs72808976 | 1.00[AFR][1000 genomes] |
rs72808979 | 1.00[AFR][1000 genomes] |
rs72808985 | 1.00[AFR][1000 genomes] |
rs72808987 | 1.00[AFR][1000 genomes] |
rs72808992 | 1.00[AFR][1000 genomes] |
rs7715621 | 0.99[ASN][1000 genomes] |
rs7729344 | 0.87[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv34146 | chr5:115315944-115729919 | Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 29 gene(s) | inside rSNPs | diseases |
2 | esv2755349 | chr5:115384101-115733101 | Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 24 gene(s) | inside rSNPs | diseases |
3 | nsv882743 | chr5:115501792-115634127 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
4 | nsv1019540 | chr5:115526349-115610020 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | esv2752058 | chr5:115533065-115605198 | Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv1016585 | chr5:115533065-115605455 | Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | nsv1032799 | chr5:115533065-115609552 | Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
8 | nsv1016924 | chr5:115533065-115610020 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
9 | nsv599481 | chr5:115540041-115609552 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
10 | nsv1024670 | chr5:115540586-115615459 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
11 | nsv462401 | chr5:115541563-115609552 | Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
12 | nsv599482 | chr5:115541563-115609552 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
13 | nsv521050 | chr5:115541563-115617297 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
14 | nsv599483 | chr5:115561128-115609552 | Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
15 | nsv882744 | chr5:115561128-115609552 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
16 | nsv882745 | chr5:115561128-115616288 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
17 | nsv882746 | chr5:115566026-115704566 | Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
18 | nsv882747 | chr5:115566636-115662510 | Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
19 | esv34428 | chr5:115575513-115626966 | Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
20 | esv2753795 | chr5:115576026-115626966 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
21 | esv2755740 | chr5:115576139-115633474 | ZNF genes & repeats Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
22 | nsv1017983 | chr5:115578765-115713688 | Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
23 | esv2757134 | chr5:115578810-115633474 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
24 | esv2759372 | chr5:115578810-115633474 | Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
25 | esv2760969 | chr5:115583627-115630890 | Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
26 | nsv882748 | chr5:115584159-115669950 | ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
27 | nsv1018714 | chr5:115586834-115625245 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:115560400-115610600 | Weak transcription | Left Ventricle | heart |
2 | chr5:115579600-115610600 | Weak transcription | Primary B cells from cord blood | blood |
3 | chr5:115582600-115594600 | Weak transcription | Fetal Intestine Large | intestine |
4 | chr5:115584800-115603600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
5 | chr5:115585800-115601200 | Weak transcription | Primary T helper memory cells from peripheral blood 1 | blood |
6 | chr5:115586600-115595600 | Weak transcription | Aorta | Aorta |
7 | chr5:115586600-115603000 | Weak transcription | Dnd41 | blood |
8 | chr5:115586800-115597000 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
9 | chr5:115586800-115608000 | Weak transcription | Adipose Nuclei | Adipose |
10 | chr5:115586800-115609800 | Weak transcription | Duodenum Smooth Muscle | Duodenum |
11 | chr5:115586800-115610800 | Weak transcription | Primary hematopoietic stem cells | blood |
12 | chr5:115587000-115599800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
13 | chr5:115590800-115610200 | Weak transcription | Primary B cells from peripheral blood | blood |
14 | chr5:115591000-115607200 | Weak transcription | Primary T killer naive cells fromperipheralblood | blood |
15 | chr5:115592000-115599600 | Weak transcription | Primary T cells from cord blood | blood |
16 | chr5:115592000-115607800 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
17 | chr5:115592200-115593400 | Weak transcription | Sigmoid Colon | Sigmoid Colon |