Variant report

Variant	rs73286667
Chromosome Location	chr10:44761477-44761478
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:16)

rs_ID	r²[population]
rs1632484	0.91[ASN][1000 genomes]
rs1657345	1.00[ASN][1000 genomes]
rs17155842	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17155988	1.00[EUR][1000 genomes]
rs479596	0.91[ASN][1000 genomes]
rs523297	1.00[ASN][1000 genomes]
rs545025	1.00[ASN][1000 genomes]
rs589655	1.00[ASN][1000 genomes]
rs606314	0.97[ASN][1000 genomes]
rs617019	1.00[ASN][1000 genomes]
rs622725	1.00[ASN][1000 genomes]
rs629213	1.00[ASN][1000 genomes]
rs661697	1.00[ASN][1000 genomes]
rs676966	1.00[ASN][1000 genomes]
rs680091	1.00[ASN][1000 genomes]
rs800314	0.83[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	nsv1038511	chr10:44596885-44870030	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv508579	chr10:44709770-44799256	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44758400-44762200	Weak transcription	Right Ventricle	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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