Variant report
Variant | rs62384186 |
---|---|
Chromosome Location | chr5:115506021-115506022 |
allele | C/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 |
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No data |
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rs_ID | r2[population] |
---|---|
rs10035646 | 0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10036292 | 0.87[EUR][1000 genomes] |
rs10040345 | 0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10042278 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10043228 | 0.87[EUR][1000 genomes] |
rs10051240 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10051697 | 0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10052306 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10054248 | 0.85[EUR][1000 genomes] |
rs10055868 | 0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10056936 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10063296 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10073364 | 0.87[EUR][1000 genomes] |
rs10079089 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10079394 | 0.87[EUR][1000 genomes] |
rs10478281 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10478288 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10519448 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12152964 | 0.86[AFR][1000 genomes];0.87[EUR][1000 genomes] |
rs12153717 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12332489 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12332585 | 0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12332658 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12514600 | 0.86[AFR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12514785 | 0.86[AFR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12515251 | 0.87[EUR][1000 genomes] |
rs12515466 | 0.87[EUR][1000 genomes] |
rs12519989 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12520568 | 0.86[AFR][1000 genomes];0.87[EUR][1000 genomes] |
rs12520613 | 0.86[AFR][1000 genomes];0.87[EUR][1000 genomes] |
rs12520632 | 1.00[AFR][1000 genomes];0.87[EUR][1000 genomes] |
rs12520838 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12521612 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12522027 | 0.85[EUR][1000 genomes] |
rs12522441 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12523347 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13362043 | 0.85[EUR][1000 genomes] |
rs1382339 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1422500 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1592917 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17138907 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs17138917 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs17139192 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17139193 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17139224 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17139265 | 0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs17139314 | 1.00[AFR][1000 genomes];0.85[EUR][1000 genomes] |
rs17139457 | 0.85[EUR][1000 genomes] |
rs2136208 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35696109 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4283834 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4398671 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs59447169 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62383956 | 0.86[AFR][1000 genomes] |
rs62383957 | 0.86[AFR][1000 genomes] |
rs62384181 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62384184 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62384187 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs62384189 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62384212 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62384213 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62384215 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62384229 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62384230 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62384231 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62384233 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62384235 | 0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62384236 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62384237 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs62384238 | 0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62384250 | 0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs62384253 | 0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62384461 | 0.87[EUR][1000 genomes] |
rs62384468 | 0.87[EUR][1000 genomes] |
rs62385177 | 0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs62385178 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs62385179 | 0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs62385215 | 0.89[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs62385219 | 0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62385975 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs62385980 | 1.00[AFR][1000 genomes];0.87[EUR][1000 genomes] |
rs62385993 | 1.00[AFR][1000 genomes];0.87[EUR][1000 genomes] |
rs6876972 | 0.85[EUR][1000 genomes] |
rs6880880 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7443669 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7727882 | 0.87[EUR][1000 genomes] |
rs9326989 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9326990 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9326994 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | 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 |
2 | 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 |
3 | 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 |
4 | 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 |
5 | 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 |
6 | 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 |
7 | 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 |
8 | 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 |
9 | 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 |
10 | 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 |
11 | 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 |
12 | 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 |
13 | 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 |
14 | 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 |
15 | 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 |
16 | 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 |
17 | 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 |
18 | 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 |
19 | 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 |
20 | 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 |
21 | 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 |
22 | nsv10744 | chr5:115498687-115509358 | Weak transcription ZNF genes & repeats Enhancers Strong transcription | n/a | n/a | inside rSNPs | diseases |
23 | nsv968852 | chr5:115498928-115509249 | Weak transcription Strong transcription ZNF genes & repeats Enhancers | n/a | n/a | inside rSNPs | diseases |
24 | 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 |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:115471600-115521600 | Weak transcription | Primary B cells from peripheral blood | blood |
2 | chr5:115481400-115536000 | Weak transcription | Primary T helper naive cells fromperipheralblood | blood |
3 | chr5:115484400-115510000 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
4 | chr5:115484400-115521400 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
5 | chr5:115489200-115526800 | Weak transcription | Pancreas | Pancrea |
6 | chr5:115489800-115528600 | Weak transcription | Ovary | ovary |
7 | chr5:115490000-115524400 | Weak transcription | Left Ventricle | heart |
8 | chr5:115494600-115522200 | Weak transcription | Primary T helper memory cells from peripheral blood 1 | blood |
9 | chr5:115495200-115521600 | Weak transcription | Adipose Nuclei | Adipose |
10 | chr5:115495200-115524400 | Weak transcription | Primary mononuclear cells fromperipheralblood | Blood |
11 | chr5:115497400-115528800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
12 | chr5:115499200-115527400 | Weak transcription | Primary T helper cells PMA-I stimulated | -- |
13 | chr5:115501200-115511600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
14 | chr5:115502200-115508800 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
15 | chr5:115502400-115524400 | Weak transcription | Fetal Intestine Large | intestine |
16 | chr5:115502400-115526400 | Weak transcription | Lung | lung |
17 | chr5:115502800-115521600 | Weak transcription | Primary T cells from cord blood | blood |
18 | chr5:115503000-115509200 | Weak transcription | Primary B cells from cord blood | blood |