Variant report

Variant	rs59508686
Chromosome Location	chr12:20853509-20853510
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs12578492	0.97[ASN][1000 genomes]
rs12580616	0.81[EUR][1000 genomes]
rs12580628	0.81[EUR][1000 genomes]
rs12581970	0.81[EUR][1000 genomes]
rs1399937	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1399938	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3794270	0.85[ASN][1000 genomes]
rs3809208	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55661764	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56174957	0.81[EUR][1000 genomes]
rs57238599	0.91[ASN][1000 genomes]
rs57312777	0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60480171	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61579575	0.85[ASN][1000 genomes]
rs61623220	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6487131	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6487132	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs67017312	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67028347	0.97[ASN][1000 genomes]
rs72658756	0.81[EUR][1000 genomes]
rs72658759	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72658760	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72658761	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7296571	0.81[EUR][1000 genomes]
rs7303066	0.85[ASN][1000 genomes]
rs7310399	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7314545	0.81[EUR][1000 genomes]
rs7316120	0.81[EUR][1000 genomes]
rs73240436	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73240439	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73240441	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74065151	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs74065172	0.85[ASN][1000 genomes]
rs74065173	0.85[ASN][1000 genomes]
rs74066232	0.81[EUR][1000 genomes]
rs74066238	0.81[EUR][1000 genomes]
rs74066258	0.81[EUR][1000 genomes]
rs7956705	0.81[EUR][1000 genomes]
rs7960786	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7970439	0.81[EUR][1000 genomes]
rs7970863	0.81[EUR][1000 genomes]
rs7975280	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7975334	0.97[ASN][1000 genomes]
rs7978760	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048067	chr12:20363755-20874845	Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv541408	chr12:20363755-20874845	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1043890	chr12:20659151-21309993	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv541410	chr12:20659151-21309993	Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv1054997	chr12:20682009-21292602	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
6	nsv557704	chr12:20842041-20893980	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	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	chr12:20849800-20855200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr12:20853000-20854000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr12:20853200-20863200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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