Variant report
Variant | rs13034561 |
---|---|
Chromosome Location | chr2:148541447-148541448 |
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 |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1014064 | 0.89[EUR][1000 genomes] |
rs10460259 | 0.81[EUR][1000 genomes] |
rs10497024 | 0.88[EUR][1000 genomes] |
rs10803523 | 0.87[EUR][1000 genomes] |
rs1128919 | 0.86[EUR][1000 genomes] |
rs11884013 | 0.95[EUR][1000 genomes] |
rs11889608 | 0.91[EUR][1000 genomes] |
rs11904758 | 0.88[EUR][1000 genomes] |
rs12053113 | 0.87[EUR][1000 genomes] |
rs12464617 | 0.91[EUR][1000 genomes] |
rs12469504 | 0.83[EUR][1000 genomes] |
rs12469939 | 0.81[EUR][1000 genomes] |
rs12472058 | 0.95[EUR][1000 genomes] |
rs12475399 | 0.95[EUR][1000 genomes] |
rs12479193 | 0.95[EUR][1000 genomes] |
rs12987286 | 0.85[EUR][1000 genomes] |
rs12989596 | 0.89[EUR][1000 genomes] |
rs12990959 | 0.92[EUR][1000 genomes] |
rs12997065 | 0.89[AFR][1000 genomes];0.97[EUR][1000 genomes] |
rs12998729 | 0.89[EUR][1000 genomes] |
rs13000597 | 0.87[EUR][1000 genomes] |
rs13004041 | 0.81[EUR][1000 genomes] |
rs13004451 | 0.90[EUR][1000 genomes] |
rs13005423 | 0.94[EUR][1000 genomes] |
rs13006184 | 0.81[EUR][1000 genomes] |
rs13008497 | 0.85[EUR][1000 genomes] |
rs13013743 | 0.92[EUR][1000 genomes] |
rs13013867 | 0.91[EUR][1000 genomes] |
rs13014904 | 0.92[EUR][1000 genomes] |
rs13014926 | 0.95[AFR][1000 genomes];0.98[EUR][1000 genomes] |
rs13016083 | 0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs13017754 | 0.92[EUR][1000 genomes] |
rs13019386 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs13019809 | 0.84[EUR][1000 genomes] |
rs13022319 | 0.85[AFR][1000 genomes];0.97[EUR][1000 genomes] |
rs13025219 | 0.90[EUR][1000 genomes] |
rs13025589 | 0.91[EUR][1000 genomes] |
rs13025701 | 0.96[EUR][1000 genomes] |
rs13026220 | 0.92[EUR][1000 genomes] |
rs13026650 | 0.86[EUR][1000 genomes] |
rs13027200 | 0.81[EUR][1000 genomes] |
rs13027706 | 0.81[EUR][1000 genomes] |
rs13028411 | 0.88[EUR][1000 genomes] |
rs13031064 | 0.81[EUR][1000 genomes] |
rs13033696 | 0.88[EUR][1000 genomes] |
rs13034494 | 0.89[EUR][1000 genomes] |
rs1345994 | 0.82[EUR][1000 genomes] |
rs1364658 | 0.89[EUR][1000 genomes] |
rs1364660 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs1424944 | 0.91[EUR][1000 genomes] |
rs1424946 | 0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1424949 | 0.96[EUR][1000 genomes] |
rs1424954 | 0.90[EUR][1000 genomes] |
rs1469210 | 0.87[EUR][1000 genomes] |
rs1531032 | 0.81[EUR][1000 genomes] |
rs16855486 | 0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1863152 | 0.95[EUR][1000 genomes] |
rs1863153 | 0.95[EUR][1000 genomes] |
rs1895693 | 0.87[EUR][1000 genomes] |
rs1991169 | 0.95[EUR][1000 genomes] |
rs2059422 | 0.80[EUR][1000 genomes] |
rs2161983 | 0.85[EUR][1000 genomes] |
rs2161985 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs2303392 | 0.83[EUR][1000 genomes] |
rs2307394 | 0.81[EUR][1000 genomes] |
rs34005843 | 0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs34539489 | 0.81[EUR][1000 genomes] |
rs35370215 | 0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs3764955 | 0.86[EUR][1000 genomes] |
rs3768687 | 0.86[EUR][1000 genomes] |
rs3768689 | 0.86[EUR][1000 genomes] |
rs3926960 | 0.83[EUR][1000 genomes] |
rs4972272 | 0.95[EUR][1000 genomes] |
rs4972316 | 0.95[AFR][1000 genomes];0.99[EUR][1000 genomes] |
rs4972356 | 0.92[EUR][1000 genomes] |
rs4972357 | 0.89[EUR][1000 genomes] |
rs57679331 | 0.81[EUR][1000 genomes] |
rs6430241 | 0.96[EUR][1000 genomes] |
rs6430242 | 0.96[EUR][1000 genomes] |
rs6711673 | 0.87[EUR][1000 genomes] |
rs6729465 | 0.81[EUR][1000 genomes] |
rs6729997 | 0.86[EUR][1000 genomes] |
rs6734998 | 0.95[EUR][1000 genomes] |
rs6760703 | 0.89[EUR][1000 genomes] |
rs723681 | 0.86[EUR][1000 genomes] |
rs7559714 | 0.88[EUR][1000 genomes] |
rs7559925 | 0.89[EUR][1000 genomes] |
rs7594075 | 0.81[EUR][1000 genomes] |
rs7600869 | 0.96[EUR][1000 genomes] |
rs929939 | 0.87[EUR][1000 genomes] |
rs9679427 | 0.96[EUR][1000 genomes] |
rs987122 | 0.95[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv875275 | chr2:148166428-148711242 | Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 14 gene(s) | inside rSNPs | diseases |
2 | nsv916286 | chr2:148438001-148977722 | Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
3 | nsv529388 | chr2:148471340-148934846 | Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
4 | esv3392562 | chr2:148476961-148843061 | Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 15 gene(s) | inside rSNPs | diseases |
5 | esv1842822 | chr2:148505544-148542682 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:148540600-148550200 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
2 | chr2:148541000-148547000 | Weak transcription | HSMMtube | muscle |
3 | chr2:148541200-148546800 | Weak transcription | NH-A | brain |