Variant report

Variant	rs2787452
Chromosome Location	chr14:84530365-84530366
allele	G/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]
rs17657042	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17730419	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1779566	0.84[ASN][1000 genomes]
rs2615462	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4369583	0.86[ASN][1000 genomes]
rs4551972	0.86[ASN][1000 genomes]
rs55645564	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55912304	0.86[ASN][1000 genomes]
rs72701082	0.86[ASN][1000 genomes]
rs72701083	0.90[ASN][1000 genomes]
rs72701092	0.86[ASN][1000 genomes]
rs7494031	0.86[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	nsv1382	chr14:84487547-84532237	Enhancers Weak transcription Flanking 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	chr14:84526400-84531000	Weak transcription	HUES48 Cell Line	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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