Variant report

Variant	rs73451832
Chromosome Location	chr6:75491771-75491772
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12526043	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2095664	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35779502	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57121615	0.88[AFR][1000 genomes]
rs61570947	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73450001	0.95[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs73451830	0.91[AFR][1000 genomes]
rs73451893	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73758083	0.89[ASN][1000 genomes]
rs73758155	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7745945	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs962008	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs962009	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv520746	chr6:75211546-75691814	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv917283	chr6:75234428-75641440	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv830695	chr6:75409656-75583115	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv886169	chr6:75432861-75610722	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv886170	chr6:75477971-75577359	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75490400-75492000	Enhancers	Ovary	ovary
2	chr6:75490600-75492000	Enhancers	Pancreas	Pancrea
3	chr6:75491600-75492000	Enhancers	Aorta	Aorta

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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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