Variant report

Variant	rs59427889
Chromosome Location	chr14:63187587-63187588
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]
rs12589213	0.90[EUR][1000 genomes]
rs17100282	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17100325	0.90[EUR][1000 genomes]
rs4533187	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs66531558	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs67434559	0.87[EUR][1000 genomes]
rs67701746	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7147349	0.82[EUR][1000 genomes]
rs72625622	0.87[EUR][1000 genomes]
rs72625624	0.82[EUR][1000 genomes]
rs8020611	0.87[EUR][1000 genomes]
rs8022441	0.90[EUR][1000 genomes];0.92[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	nsv527675	chr14:63168547-63211280	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	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	chr14:63178600-63193000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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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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