Variant report

Variant	rs7650825
Chromosome Location	chr3:35012263-35012264
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11925888	0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12632359	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs17032340	0.82[EUR][1000 genomes]
rs4549234	0.84[EUR][1000 genomes]
rs4678716	0.94[JPT][hapmap];0.86[EUR][1000 genomes]
rs4678724	0.80[ASN][1000 genomes]
rs73061969	0.89[EUR][1000 genomes]
rs73063843	0.84[ASN][1000 genomes]
rs73063864	0.92[ASN][1000 genomes]
rs7653203	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876686	chr3:34967346-35075355	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv834656	chr3:35006198-35156132	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:35011000-35013800	Weak transcription	Fetal Heart	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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