Variant report
Variant | rs2892408 |
---|---|
Chromosome Location | chr20:25576481-25576482 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
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No data |
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Variant related genes | Relation type |
---|---|
ENSG00000213742 | Chromatin interaction |
ENSG00000101004 | Chromatin interaction |
ENSG00000170191 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1569617 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs16987934 | 0.82[ASN][1000 genomes] |
rs1883528 | 0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2006249 | 0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs2103661 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2388026 | 0.81[AFR][1000 genomes] |
rs242130 | 0.80[ASN][1000 genomes] |
rs242133 | 0.98[AFR][1000 genomes];0.91[ASN][1000 genomes] |
rs35516971 | 0.95[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs402120 | 0.84[AFR][1000 genomes] |
rs409322 | 0.84[AFR][1000 genomes] |
rs4098823 | 0.82[AFR][1000 genomes] |
rs41308623 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs4280527 | 0.80[ASN][1000 genomes] |
rs4343537 | 0.82[AFR][1000 genomes] |
rs4813572 | 0.83[AFR][1000 genomes] |
rs4815436 | 0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs58877578 | 0.94[ASN][1000 genomes] |
rs6037159 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6037161 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6037164 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6037166 | 0.94[AFR][1000 genomes];0.83[ASN][1000 genomes] |
rs6037167 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6037168 | 0.85[ASN][1000 genomes] |
rs6037179 | 0.94[AFR][1000 genomes] |
rs6037180 | 0.94[AFR][1000 genomes] |
rs6037192 | 0.91[AFR][1000 genomes] |
rs6037193 | 0.95[AFR][1000 genomes] |
rs6037198 | 0.84[AFR][1000 genomes] |
rs6037199 | 0.82[AFR][1000 genomes] |
rs6037220 | 0.80[AFR][1000 genomes] |
rs6037223 | 0.82[AFR][1000 genomes] |
rs60394570 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6050692 | 0.92[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs6050707 | 0.95[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050709 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050710 | 0.96[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050712 | 0.96[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050714 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050717 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050720 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050723 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050724 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050725 | 0.95[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050726 | 0.92[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050727 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050729 | 0.92[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050730 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050732 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050733 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050737 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs6050743 | 0.91[AFR][1000 genomes] |
rs6050745 | 0.92[AFR][1000 genomes] |
rs6050749 | 0.89[AFR][1000 genomes] |
rs6050753 | 0.90[AFR][1000 genomes] |
rs6050754 | 0.89[AFR][1000 genomes] |
rs6050758 | 0.94[AFR][1000 genomes] |
rs6050768 | 0.92[AFR][1000 genomes] |
rs6050788 | 0.95[AFR][1000 genomes] |
rs6050795 | 0.84[AFR][1000 genomes] |
rs6050804 | 0.82[AFR][1000 genomes] |
rs6050807 | 0.83[ASN][1000 genomes] |
rs6050809 | 0.82[AFR][1000 genomes] |
rs6050834 | 0.82[AFR][1000 genomes] |
rs6050853 | 0.82[AFR][1000 genomes] |
rs6076372 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6083886 | 0.85[AFR][1000 genomes];0.97[ASN][1000 genomes] |
rs6083896 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6083897 | 0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6083899 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6083902 | 0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs6115214 | 0.80[ASN][1000 genomes] |
rs6115215 | 0.80[ASN][1000 genomes] |
rs6115220 | 0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6115224 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6132848 | 0.80[ASN][1000 genomes] |
rs6132850 | 0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6138608 | 0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6138612 | 0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6138613 | 0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7261537 | 0.82[ASN][1000 genomes] |
rs7261902 | 0.94[ASN][1000 genomes] |
rs7266592 | 0.94[ASN][1000 genomes] |
rs7274550 | 0.94[ASN][1000 genomes] |
rs73337355 | 0.94[ASN][1000 genomes] |
rs73337356 | 0.94[ASN][1000 genomes] |
rs73337364 | 0.94[ASN][1000 genomes] |
rs73337366 | 0.94[ASN][1000 genomes] |
rs73337369 | 0.94[ASN][1000 genomes] |
rs73337372 | 0.94[ASN][1000 genomes] |
rs73337394 | 0.94[ASN][1000 genomes] |
rs73337401 | 0.94[ASN][1000 genomes] |
rs73339323 | 0.94[ASN][1000 genomes] |
rs73339335 | 0.94[ASN][1000 genomes] |
rs73339360 | 0.88[ASN][1000 genomes] |
rs73339379 | 0.82[ASN][1000 genomes] |
rs73339383 | 0.82[ASN][1000 genomes] |
rs73339387 | 0.82[ASN][1000 genomes] |
rs73341305 | 0.82[ASN][1000 genomes] |
rs73341314 | 0.82[ASN][1000 genomes] |
rs73341328 | 0.82[ASN][1000 genomes] |
rs7346687 | 0.90[AFR][1000 genomes] |
rs8120065 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs8120594 | 0.96[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs8120972 | 0.94[ASN][1000 genomes] |
rs8121013 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs8125002 | 0.82[ASN][1000 genomes] |
rs8126111 | 0.88[ASN][1000 genomes] |
rs8126236 | 0.94[AFR][1000 genomes];0.85[ASN][1000 genomes] |
rs981441 | 0.95[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1067379 | chr20:25355484-25593240 | Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 24 gene(s) | inside rSNPs | diseases |
2 | nsv1060591 | chr20:25388781-25628750 | ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
3 | nsv544223 | chr20:25388781-25628750 | ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
4 | nsv1067441 | chr20:25397566-25615439 | Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
5 | nsv912828 | chr20:25433015-25595175 | Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
6 | nsv1062452 | chr20:25438025-25590278 | Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
7 | nsv1066066 | chr20:25439367-25588016 | Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
8 | nsv544224 | chr20:25439367-25588016 | Genic enhancers ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
9 | nsv912829 | chr20:25444242-25595175 | Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
10 | nsv912830 | chr20:25449945-25595175 | Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
11 | nsv912831 | chr20:25449945-25595868 | Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
12 | nsv994976 | chr20:25466406-25593286 | Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
13 | nsv534623 | chr20:25466406-25593296 | Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
14 | esv2762069 | chr20:25506582-25619528 | Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
15 | nsv912832 | chr20:25527984-25595175 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 8 gene(s) | inside rSNPs | diseases |
16 | nsv912833 | chr20:25539486-25595175 | Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr20:25573800-25581000 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
2 | chr20:25573800-25590400 | Weak transcription | Thymus | Thymus |
3 | chr20:25576000-25576800 | Enhancers | HepG2 | liver |
4 | chr20:25576000-25585800 | Weak transcription | Fetal Stomach | stomach |
5 | chr20:25576400-25576600 | Enhancers | iPS DF 6.9 Cell Line | embryonic stem cell |