Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1205578	0.86[EUR][1000 genomes]
rs151642	0.84[EUR][1000 genomes]
rs151645	0.84[EUR][1000 genomes]
rs151657	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs151660	0.89[CEU][hapmap];0.86[EUR][1000 genomes]
rs2149082	0.94[ASN][1000 genomes]
rs239497	0.84[EUR][1000 genomes]
rs239500	0.84[EUR][1000 genomes]
rs239560	0.88[CEU][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs239578	0.82[EUR][1000 genomes]
rs240213	0.81[CEU][hapmap]
rs240214	0.84[EUR][1000 genomes]
rs240217	0.88[CEU][hapmap];0.84[EUR][1000 genomes]
rs240218	0.88[CEU][hapmap];0.84[EUR][1000 genomes]
rs2757084	0.84[EUR][1000 genomes]
rs2769337	0.85[EUR][1000 genomes]
rs3828761	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3967160	0.96[ASN][1000 genomes]
rs465483	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs4706826	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs587984	0.86[EUR][1000 genomes]
rs652752	0.86[EUR][1000 genomes]
rs666040	0.89[CEU][hapmap];0.86[EUR][1000 genomes]
rs9350843	1.00[CHB][hapmap];0.93[JPT][hapmap];0.96[ASN][1000 genomes]
rs9448877	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9448880	0.96[ASN][1000 genomes]
rs9448881	0.92[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[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	nsv970144	chr6:80775545-80779779	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6923330	ELOVL4	cis	Artery Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:80764800-80784400	Weak transcription	Thymus	Thymus

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