Variant report

Variant	rs4767591
Chromosome Location	chr12:118072395-118072396
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10850859	0.94[ASN][1000 genomes]
rs10850875	0.85[EUR][1000 genomes]
rs10850880	0.82[EUR][1000 genomes]
rs11068571	0.95[ASN][1000 genomes]
rs1400591	0.83[ASN][1000 genomes]
rs2393237	0.81[ASN][1000 genomes]
rs4492895	0.84[EUR][1000 genomes]
rs4766866	0.83[EUR][1000 genomes]
rs4766867	0.80[EUR][1000 genomes]
rs7305116	0.84[EUR][1000 genomes]

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	nsv832527	chr12:117974007-118110244	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 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	chr12:118061000-118075000	Weak transcription	HUVEC	blood vessel
2	chr12:118065400-118072400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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

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