Variant report

Variant	rs11050994
Chromosome Location	chr12:30765133-30765134
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11519114	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2083251	0.92[EUR][1000 genomes]
rs7134692	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs7135640	1.00[ASW][hapmap];1.00[CEU][hapmap];0.89[LWK][hapmap];0.89[MKK][hapmap];0.85[TSI][hapmap];0.88[YRI][hapmap];0.89[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs7295175	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7311711	1.00[EUR][1000 genomes]
rs7977562	1.00[CEU][hapmap];1.00[YRI][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3343291	chr12:30455597-30992837	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11050994	OAZ2	trans	brain	seeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30764800-30766000	Weak transcription	Placenta	Placenta

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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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