Variant report

Variant	rs1676065
Chromosome Location	chr14:84629749-84629750
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10145113	0.93[EUR][1000 genomes]
rs11159634	1.00[EUR][1000 genomes]
rs11159635	1.00[EUR][1000 genomes]
rs12590599	1.00[EUR][1000 genomes]
rs12590626	1.00[EUR][1000 genomes]
rs12590652	1.00[EUR][1000 genomes]
rs12590669	1.00[EUR][1000 genomes]
rs1779579	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2045739	1.00[EUR][1000 genomes]
rs2045740	1.00[EUR][1000 genomes]
rs58632727	1.00[EUR][1000 genomes]
rs67304290	1.00[EUR][1000 genomes]
rs7157123	1.00[EUR][1000 genomes]
rs7157150	1.00[EUR][1000 genomes]
rs72629343	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72629346	1.00[EUR][1000 genomes]
rs72629347	1.00[EUR][1000 genomes]
rs72629348	1.00[EUR][1000 genomes]
rs72629351	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	nsv565376	chr14:84612088-84644822	Enhancers Weak transcription	TF binding region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84628400-84630200	Enhancers	Fetal Heart	heart

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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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