Variant report
Variant | rs2339486 |
---|---|
Chromosome Location | chr1:152983513-152983514 |
allele | A/G |
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 |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1015995 | 0.87[AMR][1000 genomes] |
rs1015996 | 0.87[AMR][1000 genomes] |
rs10399896 | 0.91[AMR][1000 genomes] |
rs10494285 | 0.87[AMR][1000 genomes] |
rs1055935 | 0.91[AMR][1000 genomes] |
rs10788850 | 0.84[AMR][1000 genomes] |
rs10788853 | 0.80[AMR][1000 genomes] |
rs11205149 | 0.81[AMR][1000 genomes] |
rs11205151 | 0.83[AMR][1000 genomes] |
rs11205160 | 0.84[AMR][1000 genomes] |
rs11205174 | 0.80[AMR][1000 genomes] |
rs11205175 | 0.80[AMR][1000 genomes] |
rs11205176 | 0.80[AMR][1000 genomes] |
rs11205177 | 0.80[AMR][1000 genomes] |
rs1129654 | 0.83[AMR][1000 genomes] |
rs1129655 | 0.82[AMR][1000 genomes] |
rs1134220 | 0.87[AMR][1000 genomes] |
rs12029168 | 0.80[AMR][1000 genomes] |
rs12046286 | 0.81[AMR][1000 genomes] |
rs1338178 | 0.87[AMR][1000 genomes] |
rs1338180 | 0.87[AMR][1000 genomes] |
rs1413848 | 0.88[AMR][1000 genomes] |
rs1413849 | 0.88[AMR][1000 genomes] |
rs1415959 | 0.87[AMR][1000 genomes] |
rs1415960 | 0.87[AMR][1000 genomes] |
rs1415961 | 0.91[AMR][1000 genomes] |
rs1415962 | 0.83[AMR][1000 genomes] |
rs1415965 | 0.80[AMR][1000 genomes] |
rs1415966 | 0.80[AMR][1000 genomes] |
rs1415967 | 0.81[AMR][1000 genomes] |
rs1415968 | 0.88[AMR][1000 genomes] |
rs1415970 | 0.81[AMR][1000 genomes] |
rs1415971 | 0.81[AMR][1000 genomes] |
rs1577962 | 0.83[AMR][1000 genomes] |
rs1577963 | 0.81[AMR][1000 genomes] |
rs1577964 | 0.82[AMR][1000 genomes] |
rs1577965 | 0.87[AMR][1000 genomes] |
rs1591736 | 0.80[AMR][1000 genomes] |
rs1611753 | 0.81[AMR][1000 genomes] |
rs1611754 | 0.81[AMR][1000 genomes] |
rs1611755 | 0.83[AMR][1000 genomes] |
rs1611759 | 0.82[AMR][1000 genomes] |
rs1611760 | 0.84[AMR][1000 genomes] |
rs1611764 | 0.81[AMR][1000 genomes] |
rs1933383 | 0.84[AMR][1000 genomes] |
rs1933384 | 0.81[AMR][1000 genomes] |
rs1970328 | 0.87[AMR][1000 genomes] |
rs1977734 | 0.84[AMR][1000 genomes] |
rs1984197 | 0.81[AMR][1000 genomes] |
rs1984198 | 0.84[AMR][1000 genomes] |
rs1999886 | 0.84[AMR][1000 genomes] |
rs2075739 | 0.87[AMR][1000 genomes] |
rs2225919 | 0.87[AMR][1000 genomes] |
rs2339487 | 0.86[AMR][1000 genomes];0.80[ASN][1000 genomes] |
rs2339488 | 0.81[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs2339489 | 0.86[AMR][1000 genomes] |
rs2339490 | 0.91[AMR][1000 genomes] |
rs2339491 | 0.86[AMR][1000 genomes] |
rs2339493 | 0.87[AMR][1000 genomes] |
rs2339494 | 0.91[AMR][1000 genomes] |
rs2339495 | 0.87[AMR][1000 genomes] |
rs2339496 | 0.87[AMR][1000 genomes] |
rs2879488 | 0.87[AMR][1000 genomes] |
rs2879489 | 0.88[AMR][1000 genomes] |
rs3737867 | 0.91[AMR][1000 genomes] |
rs3753454 | 0.90[AMR][1000 genomes] |
rs3806219 | 0.87[AMR][1000 genomes] |
rs3806221 | 0.80[AMR][1000 genomes] |
rs3806222 | 0.80[AMR][1000 genomes] |
rs3806223 | 0.80[AMR][1000 genomes] |
rs3964619 | 0.91[AMR][1000 genomes] |
rs407448 | 0.80[AMR][1000 genomes] |
rs4240866 | 0.84[AMR][1000 genomes] |
rs4240867 | 0.81[AMR][1000 genomes] |
rs4240868 | 0.87[AMR][1000 genomes] |
rs4255332 | 0.84[AMR][1000 genomes] |
rs4314835 | 0.87[AMR][1000 genomes] |
rs4319267 | 0.91[AMR][1000 genomes] |
rs4323653 | 0.87[AMR][1000 genomes] |
rs4388644 | 0.87[AMR][1000 genomes] |
rs4478766 | 0.87[AMR][1000 genomes] |
rs4568784 | 0.87[AMR][1000 genomes] |
rs4845329 | 0.87[AMR][1000 genomes] |
rs4845331 | 0.87[AMR][1000 genomes] |
rs4845332 | 0.87[AMR][1000 genomes] |
rs4845333 | 0.87[AMR][1000 genomes] |
rs4845334 | 0.87[AMR][1000 genomes] |
rs4845504 | 0.83[AMR][1000 genomes] |
rs4845506 | 0.85[AMR][1000 genomes] |
rs4845507 | 0.85[AMR][1000 genomes] |
rs4845508 | 0.84[AMR][1000 genomes] |
rs4845509 | 0.87[AMR][1000 genomes] |
rs4845514 | 0.80[AMR][1000 genomes] |
rs61811863 | 0.80[AMR][1000 genomes] |
rs6587716 | 0.84[AMR][1000 genomes] |
rs6587717 | 0.87[AMR][1000 genomes] |
rs6665527 | 0.84[AMR][1000 genomes] |
rs6665575 | 0.84[AMR][1000 genomes] |
rs6668215 | 0.81[AMR][1000 genomes] |
rs6668311 | 0.83[AMR][1000 genomes] |
rs6668696 | 0.81[AMR][1000 genomes] |
rs6670614 | 0.81[AMR][1000 genomes] |
rs6671414 | 0.87[AMR][1000 genomes] |
rs6671524 | 0.87[AMR][1000 genomes] |
rs6672735 | 0.87[AMR][1000 genomes] |
rs6678107 | 0.81[AMR][1000 genomes] |
rs6679201 | 0.87[AMR][1000 genomes] |
rs6680624 | 0.87[AMR][1000 genomes] |
rs6684188 | 0.87[AMR][1000 genomes] |
rs6686286 | 0.83[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs6689609 | 0.81[AMR][1000 genomes] |
rs6698820 | 0.88[AMR][1000 genomes] |
rs6704105 | 0.81[AMR][1000 genomes] |
rs6704498 | 0.81[AMR][1000 genomes] |
rs71582278 | 0.85[AMR][1000 genomes] |
rs7521181 | 0.81[AMR][1000 genomes] |
rs885096 | 0.91[AMR][1000 genomes] |
rs9325996 | 0.81[AMR][1000 genomes] |
rs946097 | 0.91[AMR][1000 genomes] |
rs946098 | 0.91[AMR][1000 genomes] |
rs946099 | 0.87[AMR][1000 genomes] |
rs946100 | 0.91[AMR][1000 genomes] |
rs946101 | 0.87[AMR][1000 genomes] |
rs9659389 | 0.80[AMR][1000 genomes] |
rs9659623 | 0.81[AMR][1000 genomes] |
rs9919227 | 0.90[AMR][1000 genomes] |
rs9919276 | 0.90[AMR][1000 genomes] |
rs9919333 | 0.91[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1013433 | chr1:152619305-153262215 | Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 46 gene(s) | inside rSNPs | diseases |
2 | nsv535170 | chr1:152619305-153262215 | Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 46 gene(s) | inside rSNPs | diseases |
3 | nsv1001834 | chr1:152648853-153279143 | Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 44 gene(s) | inside rSNPs | diseases |
4 | nsv547899 | chr1:152672005-153245082 | Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 42 gene(s) | inside rSNPs | diseases |
5 | nsv831592 | chr1:152815054-152997162 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
6 | nsv1010488 | chr1:152901263-153670972 | Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 236 gene(s) | inside rSNPs | diseases |
7 | nsv535171 | chr1:152901263-153670972 | Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 236 gene(s) | inside rSNPs | diseases |
8 | nsv533877 | chr1:152923645-153468131 | Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 56 gene(s) | inside rSNPs | diseases |
9 | nsv1003756 | chr1:152944201-153044621 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
10 | esv3416199 | chr1:152957887-153005113 | Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:152981600-152983600 | Weak transcription | Esophagus | oesophagus |