Variant report
Variant | rs8106936 |
---|---|
Chromosome Location | chr19:21570206-21570207 |
allele | C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
(count:1 , 50 per page) page:
1
No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-ZNF738-1 | chr19:21560191-21571384 | NR_027130 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10405716 | 0.97[ASN][1000 genomes] |
rs1055753 | 0.97[ASN][1000 genomes] |
rs10854043 | 0.92[ASN][1000 genomes] |
rs11085443 | 0.86[ASN][1000 genomes] |
rs11085447 | 0.95[AFR][1000 genomes];0.98[ASN][1000 genomes] |
rs1142653 | 0.91[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs11667770 | 0.97[ASN][1000 genomes] |
rs11668691 | 0.96[ASN][1000 genomes] |
rs11669043 | 0.86[ASN][1000 genomes] |
rs11669588 | 0.91[ASN][1000 genomes] |
rs11673304 | 0.92[ASN][1000 genomes] |
rs11673406 | 0.83[ASN][1000 genomes] |
rs11882553 | 0.81[ASN][1000 genomes] |
rs12459702 | 0.87[ASN][1000 genomes] |
rs12461384 | 0.90[ASN][1000 genomes] |
rs12462022 | 0.88[ASN][1000 genomes] |
rs12610331 | 0.83[ASN][1000 genomes] |
rs12971736 | 0.93[AFR][1000 genomes];0.94[ASN][1000 genomes] |
rs12972339 | 0.89[ASN][1000 genomes] |
rs12972580 | 0.93[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs12972601 | 0.80[ASN][1000 genomes] |
rs12974735 | 0.91[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs12975081 | 0.91[AFR][1000 genomes];0.96[ASN][1000 genomes] |
rs12975464 | 0.91[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs12978116 | 0.90[ASN][1000 genomes] |
rs12979646 | 0.94[ASN][1000 genomes] |
rs12980097 | 0.90[ASN][1000 genomes] |
rs12981564 | 0.91[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs12981735 | 0.91[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs12981775 | 0.91[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs12981777 | 0.91[ASN][1000 genomes] |
rs12982162 | 0.91[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs12982282 | 0.91[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs12982346 | 0.82[ASN][1000 genomes] |
rs12983426 | 0.91[ASN][1000 genomes] |
rs12983787 | 0.97[ASN][1000 genomes] |
rs12984300 | 0.83[ASN][1000 genomes] |
rs12984871 | 0.94[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs1781863 | 0.81[ASN][1000 genomes] |
rs1813234 | 0.86[ASN][1000 genomes] |
rs1932088 | 0.91[ASN][1000 genomes] |
rs1963531 | 0.91[AFR][1000 genomes];0.94[ASN][1000 genomes] |
rs1963532 | 0.85[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs1976384 | 0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2012013 | 0.91[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs2012038 | 0.91[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs2061917 | 0.92[ASN][1000 genomes] |
rs2061918 | 0.88[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs2061919 | 0.88[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs2086317 | 0.89[AFR][1000 genomes];0.92[ASN][1000 genomes] |
rs2086318 | 0.91[AFR][1000 genomes];0.94[ASN][1000 genomes] |
rs2086320 | 0.95[ASN][1000 genomes] |
rs2088762 | 0.96[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs2102072 | 0.95[ASN][1000 genomes] |
rs2127404 | 0.91[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs2127405 | 0.89[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs2127406 | 0.87[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs2127407 | 0.94[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs2127408 | 0.94[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs2133819 | 0.87[ASN][1000 genomes] |
rs2170024 | 0.95[ASN][1000 genomes] |
rs2170025 | 0.95[ASN][1000 genomes] |
rs2173728 | 0.83[ASN][1000 genomes] |
rs2219840 | 0.91[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs2358982 | 0.90[AFR][1000 genomes];0.93[ASN][1000 genomes] |
rs2358983 | 0.91[AFR][1000 genomes];0.93[ASN][1000 genomes] |
rs2358984 | 0.89[ASN][1000 genomes] |
rs2358985 | 0.91[AFR][1000 genomes];0.94[ASN][1000 genomes] |
rs2358986 | 0.93[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs2358988 | 0.86[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs2358989 | 0.95[ASN][1000 genomes] |
rs2358990 | 0.93[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs2358991 | 0.95[ASN][1000 genomes] |
rs2358992 | 0.95[ASN][1000 genomes] |
rs2434997 | 0.95[ASN][1000 genomes] |
rs2650774 | 0.87[ASN][1000 genomes] |
rs2650810 | 0.84[ASN][1000 genomes] |
rs2650845 | 0.84[ASN][1000 genomes] |
rs2650847 | 0.84[ASN][1000 genomes] |
rs2884601 | 0.84[AFR][1000 genomes];0.94[ASN][1000 genomes] |
rs2914629 | 0.83[ASN][1000 genomes] |
rs2914638 | 0.95[ASN][1000 genomes] |
rs2928208 | 0.89[ASN][1000 genomes] |
rs2968025 | 0.81[ASN][1000 genomes] |
rs35580411 | 0.89[ASN][1000 genomes] |
rs35773446 | 0.97[ASN][1000 genomes] |
rs4315457 | 0.89[AFR][1000 genomes];0.96[ASN][1000 genomes] |
rs4341872 | 0.84[ASN][1000 genomes] |
rs4398213 | 0.80[AFR][1000 genomes];0.80[ASN][1000 genomes] |
rs4438422 | 0.91[AFR][1000 genomes];0.96[ASN][1000 genomes] |
rs4461198 | 0.84[ASN][1000 genomes] |
rs4525621 | 0.87[AFR][1000 genomes];0.83[ASN][1000 genomes] |
rs4566304 | 0.91[AFR][1000 genomes];0.92[ASN][1000 genomes] |
rs4621113 | 0.88[ASN][1000 genomes] |
rs6511222 | 0.83[ASN][1000 genomes] |
rs6511228 | 0.88[ASN][1000 genomes] |
rs6511229 | 0.91[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs6511231 | 0.93[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs6511232 | 0.92[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs6511233 | 0.94[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs6511237 | 0.95[ASN][1000 genomes] |
rs6511238 | 0.97[ASN][1000 genomes] |
rs6511239 | 0.97[ASN][1000 genomes] |
rs6511242 | 0.97[ASN][1000 genomes] |
rs6511245 | 0.96[ASN][1000 genomes] |
rs6511246 | 0.96[ASN][1000 genomes] |
rs7245920 | 0.93[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs7247411 | 0.96[AFR][1000 genomes];0.98[ASN][1000 genomes] |
rs7248601 | 0.97[ASN][1000 genomes] |
rs7248989 | 0.86[ASN][1000 genomes] |
rs7249412 | 0.97[ASN][1000 genomes] |
rs7252261 | 0.91[AFR][1000 genomes];0.93[ASN][1000 genomes] |
rs7252873 | 0.88[ASN][1000 genomes] |
rs7253178 | 0.91[ASN][1000 genomes] |
rs7253886 | 0.86[ASN][1000 genomes] |
rs7254059 | 0.97[ASN][1000 genomes] |
rs7256361 | 0.90[ASN][1000 genomes] |
rs7257580 | 0.96[AFR][1000 genomes];0.98[ASN][1000 genomes] |
rs7257857 | 0.98[ASN][1000 genomes] |
rs7258086 | 0.89[ASN][1000 genomes] |
rs7258335 | 0.93[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs7259311 | 0.96[ASN][1000 genomes] |
rs7260369 | 0.90[ASN][1000 genomes] |
rs7508030 | 0.82[AFR][1000 genomes];0.94[ASN][1000 genomes] |
rs7508092 | 0.87[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs7508104 | 0.87[AFR][1000 genomes];0.91[ASN][1000 genomes] |
rs7508671 | 0.91[AFR][1000 genomes];0.96[ASN][1000 genomes] |
rs8099940 | 0.94[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs8102328 | 0.89[ASN][1000 genomes] |
rs8102342 | 0.95[ASN][1000 genomes] |
rs8103325 | 0.93[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs8103459 | 0.93[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs8103908 | 0.93[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs8104017 | 0.91[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs8110690 | 0.97[ASN][1000 genomes] |
rs8110842 | 0.85[AFR][1000 genomes];0.87[ASN][1000 genomes] |
rs8110967 | 0.91[AFR][1000 genomes];0.94[ASN][1000 genomes] |
rs8111549 | 0.89[ASN][1000 genomes] |
rs8112059 | 0.89[ASN][1000 genomes] |
rs8112583 | 0.93[AFR][1000 genomes];0.97[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3518033 | chr19:21278465-21747567 | Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 41 gene(s) | inside rSNPs | diseases |
2 | esv3518034 | chr19:21278465-21747567 | ZNF genes & repeats Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 41 gene(s) | inside rSNPs | diseases |
3 | esv3414204 | chr19:21301761-21839451 | ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 44 gene(s) | inside rSNPs | diseases |
4 | esv3325271 | chr19:21445407-21792817 | Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 35 gene(s) | inside rSNPs | diseases |
5 | nsv911420 | chr19:21454672-21613397 | ZNF genes & repeats Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 15 gene(s) | inside rSNPs | diseases |
6 | esv2751783 | chr19:21465822-21726337 | Strong transcription ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 31 gene(s) | inside rSNPs | diseases |
7 | esv3363678 | chr19:21483148-21756908 | Strong transcription Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 31 gene(s) | inside rSNPs | diseases |
8 | nsv963023 | chr19:21491992-21570395 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
9 | nsv578952 | chr19:21535707-21868584 | Genic enhancers Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 34 gene(s) | inside rSNPs | diseases |
10 | esv1793996 | chr19:21544242-21609607 | Active TSS Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
11 | esv1801985 | chr19:21544242-21609607 | ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
12 | esv1844586 | chr19:21544242-21609607 | Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
13 | esv1834499 | chr19:21557835-21609607 | Active TSS Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
14 | esv1834993 | chr19:21557835-21609607 | Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
SNP | Gene | Cis/trans | Tissue | Source |
---|---|---|---|---|
rs8106936 | ZNF429 | cis | Whole Blood | GTEx |
rs8106936 | RP11-678G14.3 | cis | Adipose Subcutaneous | GTEx |
rs8106936 | CTD-2561J22.5 | cis | lung | GTEx |
rs8106936 | ZNF738 | Cis_1M | lymphoblastoid | RTeQTL |
rs8106936 | CTD-2561J22.5 | cis | Skin Sun Exposed Lower leg | GTEx |
rs8106936 | CTD-2561J22.5 | cis | Artery Tibial | GTEx |
rs8106936 | RP11-420K14.2 | cis | Heart Left Ventricle | GTEx |
rs8106936 | CTD-2561J22.5 | cis | Adipose Subcutaneous | GTEx |
rs8106936 | RP11-678G14.2 | cis | Muscle Skeletal | GTEx |
rs8106936 | RP11-678G14.2 | cis | Adipose Subcutaneous | GTEx |
rs8106936 | CTD-2561J22.5 | cis | Esophagus Muscularis | GTEx |
rs8106936 | RP11-678G14.2 | cis | lung | GTEx |
rs8106936 | ZNF493 | Cis_1M | lymphoblastoid | RTeQTL |
rs8106936 | CTD-2561J22.5 | cis | Nerve Tibial | GTEx |
rs8106936 | CTD-2561J22.5 | cis | Thyroid | GTEx |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr19:21543400-21570600 | ZNF genes & repeats | Monocytes-CD14+_RO01746 | blood |
2 | chr19:21547800-21571000 | ZNF genes & repeats | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
3 | chr19:21551000-21570800 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
4 | chr19:21552000-21570800 | ZNF genes & repeats | iPS-20b Cell Line | embryonic stem cell |
5 | chr19:21565600-21570400 | ZNF genes & repeats | Adipose Nuclei | Adipose |
6 | chr19:21567400-21579800 | Weak transcription | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |