Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10485388	0.87[ASN][1000 genomes]
rs11751061	0.87[ASN][1000 genomes]
rs11751771	0.85[ASN][1000 genomes]
rs11754164	0.85[ASN][1000 genomes]
rs12191462	0.87[ASN][1000 genomes]
rs12193999	0.85[ASN][1000 genomes]
rs12198091	0.83[ASN][1000 genomes]
rs12202104	0.90[ASN][1000 genomes]
rs12202674	0.85[ASN][1000 genomes]
rs12209571	0.85[ASN][1000 genomes]
rs3923228	0.87[ASN][1000 genomes]
rs4501395	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs4537105	0.87[ASN][1000 genomes]
rs4546447	0.87[ASN][1000 genomes]
rs55784940	1.00[AFR][1000 genomes]
rs56004196	0.92[AMR][1000 genomes]
rs56138029	0.87[ASN][1000 genomes]
rs56343698	1.00[AFR][1000 genomes]
rs56362119	0.87[ASN][1000 genomes]
rs72952344	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72952371	0.87[ASN][1000 genomes]
rs72952395	0.87[ASN][1000 genomes]
rs72952398	0.87[ASN][1000 genomes]
rs72955114	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs72955123	0.98[EUR][1000 genomes]
rs72962230	0.85[ASN][1000 genomes]
rs72964214	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3394316	chr6:74630005-74935625	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv603733	chr6:74666559-74944460	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv3327625	chr6:74716120-74971605	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1017333	chr6:74776830-74907758	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv538307	chr6:74776830-74907758	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	esv1834914	chr6:74811585-74833405	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
7	esv1839627	chr6:74811585-74833405	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74823400-74827800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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