Variant report

Variant	rs590424
Chromosome Location	chr5:41597714-41597715
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10078011	1.00[CEU][hapmap]
rs1027348	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs11744826	0.92[EUR][1000 genomes]
rs11747941	0.92[EUR][1000 genomes]
rs12109887	0.92[EUR][1000 genomes]
rs1423242	0.92[EUR][1000 genomes]
rs1423243	0.92[EUR][1000 genomes]
rs167583	0.92[EUR][1000 genomes]
rs170299	0.92[EUR][1000 genomes]
rs188818	0.92[EUR][1000 genomes]
rs222224	0.92[EUR][1000 genomes]
rs2453241	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2656967	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs316710	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs316711	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs316712	0.92[EUR][1000 genomes]
rs316713	0.92[EUR][1000 genomes]
rs316714	0.92[EUR][1000 genomes]
rs316715	0.92[EUR][1000 genomes]
rs316729	0.92[EUR][1000 genomes]
rs316731	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs316732	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs316733	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs316734	0.92[EUR][1000 genomes]
rs316743	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs316746	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs316747	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs316748	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs316749	0.92[EUR][1000 genomes]
rs316750	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs316752	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs316754	0.92[EUR][1000 genomes]
rs316756	0.92[EUR][1000 genomes]
rs316757	0.92[EUR][1000 genomes]
rs316758	0.92[EUR][1000 genomes]
rs582920	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs583090	0.82[EUR][1000 genomes]
rs584067	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs590851	0.85[EUR][1000 genomes]
rs591384	1.00[CEU][hapmap]
rs602274	0.85[EUR][1000 genomes]
rs605064	0.89[EUR][1000 genomes]
rs607620	0.92[EUR][1000 genomes]
rs609410	0.92[EUR][1000 genomes]
rs61058110	0.85[EUR][1000 genomes]
rs614952	0.92[EUR][1000 genomes]
rs614990	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs620185	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs620501	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs621944	0.92[EUR][1000 genomes]
rs627476	0.92[EUR][1000 genomes]
rs636461	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs636905	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs641270	0.92[EUR][1000 genomes]
rs654400	0.92[EUR][1000 genomes]
rs660692	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67041756	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs67152480	0.85[EUR][1000 genomes]
rs675785	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs675812	0.92[EUR][1000 genomes]
rs676512	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs678061	0.87[EUR][1000 genomes]
rs679399	0.92[EUR][1000 genomes]
rs679548	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs694212	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72746926	0.85[EUR][1000 genomes]
rs72746928	0.85[EUR][1000 genomes]
rs72746930	0.85[EUR][1000 genomes]
rs72746932	0.85[EUR][1000 genomes]
rs72746933	0.83[EUR][1000 genomes]
rs72758378	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72760304	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72761834	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7706652	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv881563	chr5:41560079-41616100	Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv2753438	chr5:41571309-41600812	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv881628	chr5:41585079-41600651	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41597400-41598000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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