Variant report

Variant	rs8015994
Chromosome Location	chr14:84518756-84518757
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1462344	1.00[EUR][1000 genomes]
rs1462345	1.00[EUR][1000 genomes]
rs1462357	1.00[EUR][1000 genomes]
rs1676056	1.00[EUR][1000 genomes]
rs1676059	1.00[EUR][1000 genomes]
rs17094350	1.00[EUR][1000 genomes]
rs17119377	1.00[EUR][1000 genomes]
rs17119387	1.00[EUR][1000 genomes]
rs17119437	1.00[EUR][1000 genomes]
rs17119458	1.00[EUR][1000 genomes]
rs17119468	1.00[EUR][1000 genomes]
rs17119485	1.00[EUR][1000 genomes]
rs17119497	1.00[EUR][1000 genomes]
rs17119501	1.00[EUR][1000 genomes]
rs1779560	1.00[EUR][1000 genomes]
rs1779571	1.00[EUR][1000 genomes]
rs1779572	1.00[EUR][1000 genomes]
rs2372556	1.00[EUR][1000 genomes]
rs6574765	1.00[EUR][1000 genomes]
rs6574766	1.00[EUR][1000 genomes]
rs7144926	1.00[EUR][1000 genomes]
rs7150612	1.00[EUR][1000 genomes]
rs7152811	1.00[EUR][1000 genomes]
rs8005774	1.00[EUR][1000 genomes]
rs8010331	1.00[EUR][1000 genomes]
rs8014313	1.00[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	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	chr14:84518600-84519400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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