Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10158373	1.00[ASN][1000 genomes]
rs10737513	1.00[ASN][1000 genomes]
rs16827869	1.00[ASN][1000 genomes]
rs16846014	1.00[ASN][1000 genomes]
rs16846040	1.00[ASN][1000 genomes]
rs172258	1.00[ASN][1000 genomes]
rs172259	1.00[ASN][1000 genomes]
rs17408354	0.81[EUR][1000 genomes]
rs176231	1.00[ASN][1000 genomes]
rs2433134	1.00[ASN][1000 genomes]
rs285471	1.00[ASN][1000 genomes]
rs61804063	0.82[EUR][1000 genomes]
rs61804064	0.82[EUR][1000 genomes]
rs61804065	0.82[EUR][1000 genomes]
rs72692012	1.00[ASN][1000 genomes]
rs72692014	1.00[ASN][1000 genomes]
rs72692015	1.00[ASN][1000 genomes]
rs72692041	1.00[ASN][1000 genomes]
rs72692042	1.00[ASN][1000 genomes]
rs72693813	1.00[ASN][1000 genomes]
rs72693821	1.00[ASN][1000 genomes]
rs72693831	1.00[ASN][1000 genomes]
rs72693858	1.00[ASN][1000 genomes]
rs7355084	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429902	chr1:165531342-165574342	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165547400-165566800	Weak transcription	Psoas Muscle	Psoas

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