Variant report

Variant	rs7916329
Chromosome Location	chr10:21738006-21738007
allele	A/G
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:13)

rs_ID	r²[population]
rs10082426	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10466076	1.00[EUR][1000 genomes]
rs10466077	1.00[EUR][1000 genomes]
rs10466079	1.00[EUR][1000 genomes]
rs11012685	1.00[EUR][1000 genomes]
rs11012696	1.00[EUR][1000 genomes]
rs11012700	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11012706	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12247076	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12260708	0.86[YRI][hapmap];0.85[AFR][1000 genomes]
rs7071159	1.00[EUR][1000 genomes]
rs7093106	1.00[EUR][1000 genomes]
rs7915114	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21738000-21738400	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr10:21738000-21738400	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr10:21738000-21738600	Enhancers	HUES64 Cell Line	embryonic stem cell

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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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