Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10754075	0.86[AMR][1000 genomes]
rs10801250	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10921423	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11806873	0.86[AMR][1000 genomes]
rs1328180	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1328181	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1328184	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1410388	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1410391	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1410392	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1547207	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1887188	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2370522	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2370523	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35567573	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4622046	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6428191	0.81[EUR][1000 genomes]
rs6661798	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6695340	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7516941	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7527967	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7538028	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7543536	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008266	chr1:193550185-194481053	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv3372415	chr1:193612172-193988265	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv872832	chr1:193661626-193850407	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv872833	chr1:193681625-193774083	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv548662	chr1:193721143-193804209	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:193743000-193743600	Enhancers	Primary T helper cells PMA-I stimulated	--
2	chr1:193743000-193743800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
3	chr1:193743200-193743800	Enhancers	HUVEC	blood vessel

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