Variant report

Variant	rs7372695
Chromosome Location	chr3:54434291-54434292
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs13327625	0.80[EUR][1000 genomes]
rs1449327	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1449328	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1449329	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1449330	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1473345	0.96[ASN][1000 genomes]
rs1473346	0.96[ASN][1000 genomes]
rs1473347	0.96[ASN][1000 genomes]
rs1868497	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1868502	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1868506	0.88[EUR][1000 genomes]
rs1868507	0.88[EUR][1000 genomes]
rs1868508	0.80[EUR][1000 genomes]
rs1975611	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1992963	0.92[ASN][1000 genomes]
rs2359790	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2359792	0.81[EUR][1000 genomes]
rs2359793	0.81[EUR][1000 genomes]
rs4025912	0.80[EUR][1000 genomes]
rs731507	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7372444	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9311528	0.93[ASN][1000 genomes]
rs9827201	0.80[EUR][1000 genomes]
rs9830682	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9836159	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs9841318	0.96[ASN][1000 genomes]
rs9841979	0.93[ASN][1000 genomes]
rs9855860	0.89[ASN][1000 genomes]
rs9861155	0.89[ASN][1000 genomes]
rs9862712	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9862718	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9870407	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014595	chr3:53944473-54846754	Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv817210	chr3:54365684-54511164	Enhancers Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv428084	chr3:54404258-54742756	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	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	chr3:54428200-54434400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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