Variant report

Variant	rs479596
Chromosome Location	chr10:44760473-44760474
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs11238889	0.85[CHB][hapmap]
rs11238890	0.82[CHB][hapmap]
rs11592445	1.00[CHB][hapmap]
rs1632484	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1657344	0.80[EUR][1000 genomes]
rs1657345	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17155842	0.91[ASN][1000 genomes]
rs1746047	0.89[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs1746048	0.88[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs1746049	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1746050	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1746052	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs2146807	1.00[JPT][hapmap]
rs2576354	0.87[EUR][1000 genomes]
rs2576355	0.89[EUR][1000 genomes]
rs473501	0.89[EUR][1000 genomes]
rs474281	0.89[EUR][1000 genomes]
rs475926	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs487465	1.00[CEU][hapmap];0.97[YRI][hapmap];0.90[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs492152	0.87[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs498810	0.88[EUR][1000 genomes]
rs501120	0.92[EUR][1000 genomes]
rs504799	0.92[EUR][1000 genomes]
rs510785	0.87[EUR][1000 genomes]
rs513391	0.89[EUR][1000 genomes]
rs518594	0.87[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs522293	0.87[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs523297	0.91[ASN][1000 genomes]
rs534079	0.92[EUR][1000 genomes]
rs535176	0.89[EUR][1000 genomes]
rs535949	0.92[EUR][1000 genomes]
rs541483	0.87[EUR][1000 genomes]
rs545025	0.91[ASN][1000 genomes]
rs554565	0.92[EUR][1000 genomes]
rs556434	1.00[CHB][hapmap]
rs559469	0.92[EUR][1000 genomes]
rs559580	0.92[EUR][1000 genomes]
rs573141	1.00[CEU][hapmap];0.97[YRI][hapmap];0.91[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs579058	0.92[EUR][1000 genomes]
rs587375	0.88[EUR][1000 genomes]
rs589655	0.91[ASN][1000 genomes]
rs604674	0.87[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs605445	0.87[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs606314	0.88[ASN][1000 genomes]
rs607363	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs607592	0.89[EUR][1000 genomes]
rs607609	0.89[EUR][1000 genomes]
rs607760	0.92[EUR][1000 genomes]
rs617019	0.91[ASN][1000 genomes]
rs620356	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs620828	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs622472	0.89[EUR][1000 genomes]
rs622725	0.91[ASN][1000 genomes]
rs622956	0.92[EUR][1000 genomes]
rs629213	0.91[ASN][1000 genomes]
rs634963	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs635612	0.89[EUR][1000 genomes]
rs661697	0.91[ASN][1000 genomes]
rs665855	0.90[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs670056	0.92[EUR][1000 genomes]
rs671765	0.92[EUR][1000 genomes]
rs676966	0.91[ASN][1000 genomes]
rs677465	1.00[CHB][hapmap]
rs680091	0.91[ASN][1000 genomes]
rs683297	0.86[EUR][1000 genomes]
rs684196	0.89[EUR][1000 genomes]
rs684521	0.92[EUR][1000 genomes]
rs684666	0.89[EUR][1000 genomes]
rs687175	0.92[EUR][1000 genomes]
rs694425	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs73286667	0.91[ASN][1000 genomes]
rs915083	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038511	chr10:44596885-44870030	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv508579	chr10:44709770-44799256	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv3495951	chr10:44757085-44761391	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
4	esv3496062	chr10:44757120-44761379	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
5	esv3495840	chr10:44757152-44761335	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
6	esv3496173	chr10:44757152-44761335	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44756000-44761000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr10:44756200-44760800	Enhancers	Rectal Smooth Muscle	rectum
3	chr10:44757200-44760600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:44758400-44762200	Weak transcription	Right Ventricle	heart
5	chr10:44760200-44761000	Enhancers	GM12878-XiMat	blood

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