Variant report

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FIBIN-4	chr11:26481341-26482905	ucscGeneNc_uc001mqu_1

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10047414	0.92[ASN][1000 genomes]
rs10047464	0.92[ASN][1000 genomes]
rs10742138	0.89[ASN][1000 genomes]
rs10742139	0.89[ASN][1000 genomes]
rs10767528	0.81[ASN][1000 genomes]
rs10767529	0.92[ASN][1000 genomes]
rs10767530	0.92[ASN][1000 genomes]
rs10767531	0.92[ASN][1000 genomes]
rs10767532	0.92[ASN][1000 genomes]
rs10767535	0.92[ASN][1000 genomes]
rs10834982	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11029555	0.91[ASN][1000 genomes]
rs11029556	0.92[ASN][1000 genomes]
rs11029557	0.92[ASN][1000 genomes]
rs11500182	0.92[ASN][1000 genomes]
rs12273739	0.91[ASN][1000 genomes]
rs12275424	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12277506	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12288668	0.92[ASN][1000 genomes]
rs12288844	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2029712	0.93[ASN][1000 genomes]
rs4032918	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4339995	0.92[ASN][1000 genomes]
rs4489698	0.92[ASN][1000 genomes]
rs4923359	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57857863	0.92[ASN][1000 genomes]
rs7107402	0.92[ASN][1000 genomes]
rs7107710	0.92[ASN][1000 genomes]
rs7107960	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7108703	0.88[ASN][1000 genomes]
rs7109872	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7111512	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7115101	0.91[ASN][1000 genomes]
rs7123118	0.88[ASN][1000 genomes]
rs7123359	0.88[ASN][1000 genomes]
rs7925575	0.92[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	nsv1051211	chr11:26473131-26604553	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr11:26472000-26503600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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