Variant report

Variant	rs11627572
Chromosome Location	chr14:84618923-84618924
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11628862	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12895378	0.96[ASN][1000 genomes]
rs17624404	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17697962	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1971243	0.83[ASN][1000 genomes]
rs4369583	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4551972	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs55912304	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs67901677	0.96[ASN][1000 genomes]
rs72701082	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72701083	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72701092	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72703208	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72703211	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84618600-84619200	Enhancers	Spleen	Spleen
2	chr14:84618800-84619000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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

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