Variant report

Variant	rs17090861
Chromosome Location	chr12:42403283-42403284
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11181296	1.00[ASN][1000 genomes]
rs11831569	1.00[ASN][1000 genomes]
rs11835443	1.00[ASN][1000 genomes]
rs12321742	1.00[ASN][1000 genomes]
rs17090831	0.90[AFR][1000 genomes]
rs17090872	1.00[ASN][1000 genomes]
rs41508147	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs57642687	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs59569493	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61457506	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs73278262	0.82[ASN][1000 genomes]
rs7959671	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9919692	0.82[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	nsv430505	chr12:42297931-42720773	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv832387	chr12:42345541-42465505	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr12:42402800-42417000	Weak transcription	Right Atrium	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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