Variant report

Variant	rs12333631
Chromosome Location	chr7:83847574-83847575
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1006795	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10224865	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10256270	0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs10258884	0.83[ASN][1000 genomes]
rs10264700	0.92[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs1356804	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17158818	0.83[ASN][1000 genomes]
rs17158848	0.83[ASN][1000 genomes]
rs28397702	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28884542	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58835109	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6949774	0.83[ASN][1000 genomes]
rs6953184	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6972377	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6978737	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73179400	0.89[ASN][1000 genomes]
rs73181306	0.91[ASN][1000 genomes]
rs73181369	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73181375	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73181392	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73183125	0.91[EUR][1000 genomes]
rs73185111	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73185120	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73185127	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73185135	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73189024	0.81[ASN][1000 genomes]
rs73189039	0.83[ASN][1000 genomes]
rs7802925	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9642178	0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs977752	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529344	chr7:83714286-84592857	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv888629	chr7:83722691-83896025	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1017884	chr7:83724138-83972995	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv538995	chr7:83724138-83972995	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:83846200-83848600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr7:83846600-83848000	Weak transcription	Fetal Heart	heart
3	chr7:83846800-83849000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr7:83847000-83849600	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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