Variant report

Variant	rs11732137
Chromosome Location	chr4:125998923-125998924
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10518457	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11098791	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12512605	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12512644	0.90[EUR][1000 genomes]
rs13106212	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13109844	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17009138	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2390778	0.81[EUR][1000 genomes]
rs2390780	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6845411	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6858704	0.84[EUR][1000 genomes]
rs7694289	0.83[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	nsv1001338	chr4:125708756-126103293	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region	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	chr4:125998000-126001800	Weak transcription	HUVEC	blood vessel

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

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