Variant report

Variant	rs4299178
Chromosome Location	chr16:64858529-64858530
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]
rs11647632	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12149743	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12446421	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12446430	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12446445	0.87[ASN][1000 genomes]
rs12446489	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12933211	0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6498962	0.80[ASN][1000 genomes]
rs7191517	0.96[ASN][1000 genomes]
rs8046981	0.96[ASN][1000 genomes]
rs8053269	0.91[EUR][1000 genomes]
rs9924680	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][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	nsv572899	chr16:64814244-64870659	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:64857600-64858600	Weak transcription	Aorta	Aorta

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

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