Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12100815	0.83[ASN][1000 genomes]
rs12100819	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1381614	0.86[ASN][1000 genomes]
rs1462348	0.87[ASN][1000 genomes]
rs1564057	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1766153	0.80[ASN][1000 genomes]
rs1766155	0.81[ASN][1000 genomes]
rs1766157	0.84[ASN][1000 genomes]
rs1779555	0.80[ASN][1000 genomes]
rs1779558	0.80[ASN][1000 genomes]
rs1779559	0.84[ASN][1000 genomes]
rs1779561	0.84[ASN][1000 genomes]
rs1779562	0.84[ASN][1000 genomes]
rs1779567	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1779568	0.86[ASN][1000 genomes]
rs2249653	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2787459	0.84[ASN][1000 genomes]
rs4899847	0.83[ASN][1000 genomes]
rs4904165	0.82[ASN][1000 genomes]
rs6574775	0.81[ASN][1000 genomes]
rs7146928	0.87[ASN][1000 genomes]
rs7160548	0.81[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	chr14:84615800-84618600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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