Variant report
Variant | rs8105629 |
---|---|
Chromosome Location | chr19:21609556-21609557 |
allele | A/T |
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-ZNF708-1 | chr19:21608886-21610284 | ENSG00000196686 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1012040 | 1.00[JPT][hapmap] |
rs10406824 | 1.00[JPT][hapmap] |
rs11085455 | 1.00[JPT][hapmap] |
rs12150996 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12151067 | 0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12151068 | 0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12151222 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12971724 | 0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12975330 | 0.83[ASN][1000 genomes] |
rs12975981 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.88[AFR][1000 genomes];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12976011 | 0.83[ASN][1000 genomes] |
rs12981869 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.88[AFR][1000 genomes];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12984238 | 0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1500400 | 1.00[JPT][hapmap] |
rs1500401 | 1.00[JPT][hapmap] |
rs1520073 | 1.00[JPT][hapmap] |
rs1533675 | 1.00[JPT][hapmap] |
rs1566474 | 0.83[ASN][1000 genomes] |
rs1566476 | 0.83[ASN][1000 genomes] |
rs1566477 | 0.83[ASN][1000 genomes] |
rs1607664 | 1.00[JPT][hapmap] |
rs1678822 | 0.87[CEU][hapmap];1.00[JPT][hapmap] |
rs16997924 | 0.83[ASN][1000 genomes] |
rs17618715 | 0.82[CHB][hapmap];1.00[JPT][hapmap] |
rs17618778 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs17680671 | 0.82[CHB][hapmap];0.83[YRI][hapmap] |
rs1813234 | 0.86[CEU][hapmap] |
rs1984771 | 1.00[JPT][hapmap] |
rs2133816 | 1.00[JPT][hapmap] |
rs2133820 | 1.00[JPT][hapmap] |
rs2173724 | 1.00[JPT][hapmap] |
rs2246914 | 1.00[JPT][hapmap] |
rs2262897 | 0.83[ASN][1000 genomes] |
rs2358984 | 0.87[CEU][hapmap] |
rs2562399 | 1.00[JPT][hapmap] |
rs2562448 | 1.00[JPT][hapmap] |
rs2562457 | 1.00[JPT][hapmap];0.83[ASN][1000 genomes] |
rs2562458 | 1.00[JPT][hapmap];0.83[ASN][1000 genomes] |
rs2562459 | 0.83[ASN][1000 genomes] |
rs2650778 | 0.83[ASN][1000 genomes] |
rs2650779 | 1.00[JPT][hapmap] |
rs2650780 | 1.00[JPT][hapmap];0.83[ASN][1000 genomes] |
rs2650781 | 1.00[JPT][hapmap];0.83[ASN][1000 genomes] |
rs2650782 | 0.83[ASN][1000 genomes] |
rs2650783 | 1.00[JPT][hapmap];0.83[ASN][1000 genomes] |
rs2650785 | 0.83[ASN][1000 genomes] |
rs2650786 | 0.83[ASN][1000 genomes] |
rs2650791 | 1.00[JPT][hapmap] |
rs2650794 | 1.00[JPT][hapmap] |
rs2650799 | 1.00[JPT][hapmap] |
rs2650808 | 0.83[ASN][1000 genomes] |
rs2650845 | 1.00[CEU][hapmap] |
rs2681371 | 1.00[JPT][hapmap] |
rs2681372 | 1.00[JPT][hapmap] |
rs28839521 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2914636 | 0.87[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap] |
rs2914647 | 0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2937161 | 0.80[EUR][1000 genomes] |
rs2968081 | 0.83[ASN][1000 genomes] |
rs34560125 | 0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs34875588 | 0.88[EUR][1000 genomes] |
rs35148123 | 0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs35245030 | 0.83[ASN][1000 genomes] |
rs35578515 | 0.87[AFR][1000 genomes];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs35860067 | 0.83[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs4332859 | 0.83[ASN][1000 genomes] |
rs4341872 | 1.00[CEU][hapmap] |
rs488125 | 0.86[CEU][hapmap] |
rs501647 | 0.87[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap] |
rs504280 | 0.82[CEU][hapmap] |
rs509540 | 0.86[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap] |
rs56152627 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs566230 | 0.86[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap] |
rs57841525 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs62110379 | 0.80[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs62111469 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs62111470 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs62111476 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs629548 | 1.00[JPT][hapmap] |
rs6511247 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs669046 | 1.00[JPT][hapmap] |
rs67723811 | 0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs685844 | 0.87[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap] |
rs7246684 | 0.80[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7249636 | 0.86[CEU][hapmap] |
rs7254436 | 0.82[CHB][hapmap];0.83[YRI][hapmap] |
rs7254762 | 0.82[CHB][hapmap];0.83[YRI][hapmap] |
rs7257584 | 0.83[ASN][1000 genomes] |
rs7258211 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7258523 | 0.80[ASN][1000 genomes] |
rs7259178 | 0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs8100318 | 1.00[JPT][hapmap] |
rs8101077 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs8101442 | 0.83[ASN][1000 genomes] |
rs8102655 | 0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs8102854 | 1.00[JPT][hapmap] |
rs8103151 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs8105404 | 0.80[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs8107042 | 0.84[EUR][1000 genomes] |
rs8107940 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs8107999 | 1.00[CHB][hapmap];0.80[YRI][hapmap] |
rs8111189 | 0.87[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap] |
rs8112359 | 0.80[ASN][1000 genomes] |
rs8113558 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[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 | 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 |
9 | 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 |
10 | 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 |
11 | 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 |
12 | 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 |
13 | 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 |
14 | nsv911421 | chr19:21579718-21613397 | Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | n/a |
15 | nsv578953 | chr19:21586797-21609607 | Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | n/a |
SNP | Gene | Cis/trans | Tissue | Source |
---|---|---|---|---|
rs8105629 | ZNF738 | cis | Thyroid | GTEx |
rs8105629 | ZNF738 | Cis_1M | lymphoblastoid | RTeQTL |
rs8105629 | ZNF429 | cis | Artery Aorta | GTEx |
rs8105629 | ZNF493 | Cis_1M | lymphoblastoid | RTeQTL |
rs8105629 | ZNF738 | cis | Adipose Subcutaneous | GTEx |
rs8105629 | ZNF429 | cis | Whole Blood | GTEx |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr19:21585000-21614000 | ZNF genes & repeats | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
2 | chr19:21593400-21610200 | ZNF genes & repeats | Liver | Liver |
3 | chr19:21599600-21611000 | ZNF genes & repeats | Adipose Nuclei | Adipose |
4 | chr19:21600000-21613000 | ZNF genes & repeats | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
5 | chr19:21604400-21610400 | ZNF genes & repeats | iPS-20b Cell Line | embryonic stem cell |
6 | chr19:21605600-21610800 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
7 | chr19:21605600-21610800 | Weak transcription | Ovary | ovary |
8 | chr19:21607600-21630200 | Weak transcription | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
9 | chr19:21609000-21610000 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |