Variant report

Variant	rs675804
Chromosome Location	chr6:150719710-150719711
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs627147	0.82[YRI][hapmap]
rs633945	0.97[GIH][hapmap];0.85[YRI][hapmap]
rs652042	0.88[CEU][hapmap];0.84[JPT][hapmap]
rs655745	0.84[YRI][hapmap]
rs670292	0.97[GIH][hapmap];0.85[YRI][hapmap]
rs672766	0.92[YRI][hapmap]
rs805989	0.88[YRI][hapmap]
rs805992	0.84[YRI][hapmap]
rs9322260	0.84[JPT][hapmap];0.85[AMR][1000 genomes]
rs9480340	0.81[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	esv2763602	chr6:150581193-150720666	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs675804	ULBP2	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150718200-150721800	Strong transcription	Liver	Liver
2	chr6:150719200-150720600	Strong transcription	Fetal Intestine Small	intestine
3	chr6:150719600-150723800	Weak transcription	Fetal Heart	heart

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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