Variant report

Variant	rs73747466
Chromosome Location	chr5:35464984-35464985
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10472966	0.95[ASN][1000 genomes]
rs1396386	0.95[ASN][1000 genomes]
rs1605685	0.90[AFR][1000 genomes]
rs1605687	0.86[AFR][1000 genomes]
rs16902178	0.95[ASN][1000 genomes]
rs17252095	0.95[ASN][1000 genomes]
rs17252130	0.95[ASN][1000 genomes]
rs17252290	0.95[ASN][1000 genomes]
rs17318782	0.95[ASN][1000 genomes]
rs17618881	0.90[AFR][1000 genomes]
rs2113065	0.90[AFR][1000 genomes]
rs2397841	0.90[AFR][1000 genomes]
rs2397844	0.95[ASN][1000 genomes]
rs57022371	0.90[AFR][1000 genomes]
rs57133953	0.90[AFR][1000 genomes]
rs57874690	0.95[ASN][1000 genomes]
rs58024975	0.90[AFR][1000 genomes]
rs59897804	0.90[AFR][1000 genomes]
rs61548660	0.90[AFR][1000 genomes]
rs61627014	0.90[AFR][1000 genomes]
rs73747462	0.90[AFR][1000 genomes]
rs73747463	0.90[AFR][1000 genomes]
rs73747464	0.90[AFR][1000 genomes]
rs73747465	0.90[AFR][1000 genomes]
rs73747467	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs764912	0.95[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	nsv1018541	chr5:35446209-35491185	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1030395	chr5:35446516-35491185	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 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	chr5:35464400-35468000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr5:35464600-35465400	Enhancers	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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