Variant report

Variant	rs34784852
Chromosome Location	chr2:142090288-142090289
allele	-/TT
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs1003130	0.94[ASN][1000 genomes]
rs1033309	0.90[ASN][1000 genomes]
rs13406676	0.90[ASN][1000 genomes]
rs13406775	0.89[ASN][1000 genomes]
rs1357026	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1357027	0.97[ASN][1000 genomes]
rs1357028	0.97[ASN][1000 genomes]
rs1357029	0.97[ASN][1000 genomes]
rs1402473	0.90[ASN][1000 genomes]
rs1402475	0.96[ASN][1000 genomes]
rs1402476	0.93[ASN][1000 genomes]
rs1402477	0.96[ASN][1000 genomes]
rs1521105	0.89[ASN][1000 genomes]
rs1521106	0.89[ASN][1000 genomes]
rs1521107	0.88[ASN][1000 genomes]
rs1521109	0.90[ASN][1000 genomes]
rs1521110	0.90[ASN][1000 genomes]
rs1521111	0.90[ASN][1000 genomes]
rs1521112	0.90[ASN][1000 genomes]
rs1533737	0.97[ASN][1000 genomes]
rs2049154	0.90[ASN][1000 genomes]
rs2244402	0.94[ASN][1000 genomes]
rs2248431	0.90[ASN][1000 genomes]
rs2248439	0.90[ASN][1000 genomes]
rs2683821	0.89[ASN][1000 genomes]
rs2683838	0.90[ASN][1000 genomes]
rs2683839	0.90[ASN][1000 genomes]
rs2683840	0.89[ASN][1000 genomes]
rs2683841	0.90[ASN][1000 genomes]
rs2683848	0.94[ASN][1000 genomes]
rs2683849	0.94[ASN][1000 genomes]
rs2683850	0.94[ASN][1000 genomes]
rs2683851	0.96[ASN][1000 genomes]
rs2683852	0.97[ASN][1000 genomes]
rs2683853	0.97[ASN][1000 genomes]
rs2683854	0.97[ASN][1000 genomes]
rs2683855	0.96[ASN][1000 genomes]
rs2683856	0.96[ASN][1000 genomes]
rs2683857	0.97[ASN][1000 genomes]
rs2683861	0.90[ASN][1000 genomes]
rs2683862	0.90[ASN][1000 genomes]
rs2683863	0.94[ASN][1000 genomes]
rs2683864	0.94[ASN][1000 genomes]
rs2714176	0.87[ASN][1000 genomes]
rs2714180	0.94[ASN][1000 genomes]
rs2714182	0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2714183	0.94[ASN][1000 genomes]
rs2714184	0.94[ASN][1000 genomes]
rs2714185	0.96[ASN][1000 genomes]
rs2714186	0.96[ASN][1000 genomes]
rs2714187	0.96[ASN][1000 genomes]
rs2714188	0.97[ASN][1000 genomes]
rs2714189	0.97[ASN][1000 genomes]
rs2714190	0.97[ASN][1000 genomes]
rs2714191	0.97[ASN][1000 genomes]
rs2714192	0.97[ASN][1000 genomes]
rs2714193	0.97[ASN][1000 genomes]
rs2714194	0.94[ASN][1000 genomes]
rs2714195	0.94[ASN][1000 genomes]
rs2714196	0.97[ASN][1000 genomes]
rs2714197	0.96[ASN][1000 genomes]
rs2714198	0.96[ASN][1000 genomes]
rs2714199	0.97[ASN][1000 genomes]
rs2714223	0.84[ASN][1000 genomes]
rs2714224	0.90[ASN][1000 genomes]
rs2714225	0.90[ASN][1000 genomes]
rs2714226	0.90[ASN][1000 genomes]
rs2714227	0.90[ASN][1000 genomes]
rs2714228	0.90[ASN][1000 genomes]
rs3107479	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3109348	0.91[ASN][1000 genomes]
rs3109350	0.90[ASN][1000 genomes]
rs3109351	0.90[ASN][1000 genomes]
rs3109352	0.90[ASN][1000 genomes]
rs4245854	0.83[ASN][1000 genomes]
rs4536594	0.89[ASN][1000 genomes]
rs4622648	0.89[ASN][1000 genomes]
rs4954902	0.83[ASN][1000 genomes]
rs57189720	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv583198	chr2:141510791-142150620	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv817518	chr2:141714174-142287302	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1009434	chr2:141832339-142156180	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv2830111	chr2:142047759-142164422	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3693337	chr2:142047759-142164422	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv875230	chr2:142055133-142119323	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	nsv583203	chr2:142055133-142378975	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv2757835	chr2:142071391-142217569	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv2759095	chr2:142071391-142245947	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	esv2204134	chr2:142090288-142090290	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:142089200-142093400	Weak transcription	Dnd41	blood

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