Variant report

Variant	rs12446445
Chromosome Location	chr16:64847642-64847643
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]
rs11647632	0.95[ASN][1000 genomes]
rs12149743	0.87[ASN][1000 genomes]
rs12446421	0.90[ASN][1000 genomes]
rs12446430	0.90[ASN][1000 genomes]
rs12446489	0.90[ASN][1000 genomes]
rs12933211	0.90[ASN][1000 genomes]
rs4299178	0.87[ASN][1000 genomes]
rs7191517	0.89[ASN][1000 genomes]
rs8046981	0.89[ASN][1000 genomes]
rs9924680	0.87[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	chr16:64847600-64848800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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