Variant report

Variant	rs12895378
Chromosome Location	chr14:84621257-84621258
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:12)

rs_ID	r²[population]
rs11627572	0.96[ASN][1000 genomes]
rs11628862	1.00[AFR][1000 genomes]
rs1381621	0.84[EUR][1000 genomes]
rs1564058	0.85[EUR][1000 genomes]
rs17624404	0.84[ASN][1000 genomes]
rs17697962	1.00[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1971243	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4904160	0.85[EUR][1000 genomes]
rs4904161	0.84[EUR][1000 genomes]
rs67901677	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72703208	1.00[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs72703211	0.84[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	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	chr14:84620400-84621400	Weak transcription	Fetal Heart	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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