Variant report
Variant | rs11951865 |
---|---|
Chromosome Location | chr5:115492280-115492281 |
allele | G/T |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs10036669 | 0.85[ASN][1000 genomes] |
rs10042177 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10043670 | 0.82[ASN][1000 genomes] |
rs10051072 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10051302 | 1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10059455 | 0.82[ASN][1000 genomes] |
rs10062347 | 0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10063312 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs10063392 | 0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs10065178 | 0.82[ASN][1000 genomes] |
rs10065554 | 0.81[ASN][1000 genomes] |
rs10066026 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs10066081 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10068479 | 0.85[ASN][1000 genomes] |
rs10073458 | 0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs10075063 | 0.85[ASN][1000 genomes] |
rs10077013 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs10078121 | 0.88[ASN][1000 genomes] |
rs10079176 | 0.85[ASN][1000 genomes] |
rs10079466 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10079691 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10079903 | 0.82[ASN][1000 genomes] |
rs10463676 | 0.84[ASN][1000 genomes] |
rs10478280 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1090077 | 0.82[EUR][1000 genomes] |
rs11241359 | 0.85[ASN][1000 genomes] |
rs11241364 | 0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11241365 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11241366 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11241367 | 0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11241371 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11241372 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs11241374 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs11241375 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1129494 | 0.81[ASN][1000 genomes] |
rs11738674 | 0.82[ASN][1000 genomes] |
rs11738775 | 0.82[ASN][1000 genomes] |
rs11739600 | 0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11742938 | 1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11746600 | 0.86[ASN][1000 genomes] |
rs11950936 | 0.85[ASN][1000 genomes] |
rs11952043 | 0.85[ASN][1000 genomes] |
rs11953135 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs11958648 | 0.85[ASN][1000 genomes] |
rs11960815 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs12054994 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12332433 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12656463 | 0.82[ASN][1000 genomes] |
rs12657249 | 0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs13159102 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs13161146 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs13161987 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs13162238 | 0.82[ASN][1000 genomes] |
rs13162293 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs13172482 | 0.85[ASN][1000 genomes] |
rs13179593 | 0.81[ASN][1000 genomes] |
rs13180407 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs13181756 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs13182605 | 0.85[ASN][1000 genomes] |
rs13184073 | 0.82[ASN][1000 genomes] |
rs13190269 | 0.81[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs1396478 | 0.85[ASN][1000 genomes] |
rs1396479 | 0.85[ASN][1000 genomes] |
rs1396481 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1396482 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1508875 | 0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs1588267 | 0.82[ASN][1000 genomes] |
rs2063250 | 0.82[ASN][1000 genomes] |
rs2063253 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2221676 | 0.84[ASN][1000 genomes] |
rs2416426 | 0.82[ASN][1000 genomes] |
rs2416427 | 0.80[ASN][1000 genomes] |
rs2416430 | 1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs253959 | 0.82[EUR][1000 genomes] |
rs4921062 | 0.85[ASN][1000 genomes] |
rs4921063 | 0.85[ASN][1000 genomes] |
rs55783029 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6594938 | 0.81[ASN][1000 genomes] |
rs6594948 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6594951 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6594952 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6865237 | 0.87[ASN][1000 genomes] |
rs6871968 | 0.84[ASN][1000 genomes] |
rs6876901 | 0.81[ASN][1000 genomes] |
rs6878596 | 0.85[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs6889212 | 0.87[ASN][1000 genomes] |
rs6894046 | 0.81[ASN][1000 genomes] |
rs6896479 | 0.81[ASN][1000 genomes] |
rs712561 | 0.82[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7703164 | 0.83[ASN][1000 genomes] |
rs7715759 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7715797 | 0.85[ASN][1000 genomes] |
rs7723358 | 0.82[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs7728838 | 0.84[ASN][1000 genomes] |
rs7729414 | 0.85[ASN][1000 genomes] |
rs7732346 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs7733128 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7735539 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7736189 | 0.99[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs809188 | 0.82[EUR][1000 genomes] |
rs9326986 | 0.81[ASN][1000 genomes] |
rs9326987 | 0.82[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949677 | chr5:115104829-115496168 | Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 40 gene(s) | inside rSNPs | diseases |
2 | nsv882736 | chr5:115254723-115552945 | Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
3 | nsv882737 | chr5:115263853-115552945 | Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
4 | 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 |
5 | nsv527320 | chr5:115382097-115573543 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
6 | nsv1027266 | chr5:115382704-115501792 | Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
7 | 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 |
8 | nsv1032199 | chr5:115384131-115525738 | Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
9 | nsv1019972 | chr5:115386860-115563533 | Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
10 | nsv537869 | chr5:115386860-115563533 | Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
11 | nsv1018861 | chr5:115397834-115563533 | Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
12 | nsv537870 | chr5:115397834-115563533 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
13 | nsv882739 | chr5:115471015-115552945 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
14 | nsv1016891 | chr5:115477740-115523778 | Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
15 | nsv537871 | chr5:115477740-115523778 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
16 | nsv882740 | chr5:115482794-115540041 | Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
17 | nsv882741 | chr5:115484252-115552945 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
18 | nsv1032531 | chr5:115489694-115583800 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
19 | nsv882742 | chr5:115489770-115584159 | ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
20 | nsv1032338 | chr5:115490345-115533527 | ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
21 | nsv537872 | chr5:115490345-115533527 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
22 | nsv1034069 | chr5:115490345-115563533 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
23 | nsv537873 | chr5:115490345-115563533 | Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:115462600-115502000 | Weak transcription | Fetal Intestine Large | intestine |
2 | chr5:115468200-115494400 | Weak transcription | Primary T cells from cord blood | blood |
3 | chr5:115468600-115501400 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
4 | chr5:115471600-115521600 | Weak transcription | Primary B cells from peripheral blood | blood |
5 | chr5:115472800-115500200 | Weak transcription | Primary B cells from cord blood | blood |
6 | chr5:115472800-115500400 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
7 | chr5:115473600-115494800 | Weak transcription | Fetal Kidney | kidney |
8 | chr5:115473600-115495200 | Weak transcription | Primary T helper naive cells from peripheral blood | blood |
9 | chr5:115481400-115536000 | Weak transcription | Primary T helper naive cells fromperipheralblood | blood |
10 | chr5:115484400-115510000 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
11 | chr5:115484400-115521400 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
12 | chr5:115488400-115501200 | Weak transcription | Psoas Muscle | Psoas |
13 | chr5:115489200-115526800 | Weak transcription | Pancreas | Pancrea |
14 | chr5:115489800-115494600 | Weak transcription | Fetal Heart | heart |
15 | chr5:115489800-115528600 | Weak transcription | Ovary | ovary |
16 | chr5:115490000-115524400 | Weak transcription | Left Ventricle | heart |
17 | chr5:115491600-115492400 | Enhancers | Primary neutrophils fromperipheralblood | blood |