Variant report

Variant	rs2759451
Chromosome Location	chr6:82325874-82325875
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs1145876	0.89[EUR][1000 genomes]
rs1145882	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1145883	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1145885	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1145886	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1145888	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1276878	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1341224	1.00[ASN][1000 genomes]
rs1361548	1.00[ASN][1000 genomes]
rs1592044	1.00[ASN][1000 genomes]
rs16893194	1.00[ASN][1000 genomes]
rs16893209	1.00[ASN][1000 genomes]
rs1917064	0.90[EUR][1000 genomes]
rs1923149	1.00[ASN][1000 genomes]
rs1935003	1.00[ASN][1000 genomes]
rs2153645	1.00[ASN][1000 genomes]
rs2185588	1.00[ASN][1000 genomes]
rs2211283	1.00[ASN][1000 genomes]
rs2226075	1.00[ASN][1000 genomes]
rs2753426	1.00[ASN][1000 genomes]
rs2793331	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2793333	1.00[ASN][1000 genomes]
rs4142950	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4623287	1.00[ASN][1000 genomes]
rs4706143	1.00[ASN][1000 genomes]
rs4706899	1.00[ASN][1000 genomes]
rs4706900	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6454227	1.00[ASN][1000 genomes]
rs6454232	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6899579	1.00[ASN][1000 genomes]
rs6900544	1.00[ASN][1000 genomes]
rs725762	1.00[ASN][1000 genomes]
rs7739492	1.00[ASN][1000 genomes]
rs7755160	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9344198	1.00[ASN][1000 genomes]
rs9344200	1.00[ASN][1000 genomes]
rs9344206	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9353019	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	nsv604087	chr6:81792413-82326091	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82318000-82356600	Weak transcription	Aorta	Aorta
2	chr6:82324400-82328000	Weak transcription	Left Ventricle	heart

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