Variant report

Variant	rs59528535
Chromosome Location	chr12:40004868-40004869
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10877173	0.91[ASN][1000 genomes]
rs10877201	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11172366	0.81[ASN][1000 genomes]
rs11172616	0.92[ASN][1000 genomes]
rs11172645	0.92[ASN][1000 genomes]
rs11172646	0.85[ASN][1000 genomes]
rs11172647	0.92[ASN][1000 genomes]
rs11172687	0.92[ASN][1000 genomes]
rs11172692	0.92[ASN][1000 genomes]
rs11172697	0.92[ASN][1000 genomes]
rs11172713	0.81[ASN][1000 genomes]
rs11172722	0.80[ASN][1000 genomes]
rs11172794	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11172848	0.91[ASN][1000 genomes]
rs11172896	0.97[ASN][1000 genomes]
rs11172897	0.97[ASN][1000 genomes]
rs12227286	0.85[ASN][1000 genomes]
rs12227668	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12228617	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12229370	0.89[ASN][1000 genomes]
rs12230055	0.89[ASN][1000 genomes]
rs12231004	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35790935	0.89[ASN][1000 genomes]
rs35858791	0.89[ASN][1000 genomes]
rs4072006	0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4285917	0.81[ASN][1000 genomes]
rs4294600	0.92[ASN][1000 genomes]
rs4298947	0.94[ASN][1000 genomes]
rs57847223	0.92[ASN][1000 genomes]
rs58036566	0.92[ASN][1000 genomes]
rs59518553	0.85[ASN][1000 genomes]
rs6581228	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7133599	0.92[ASN][1000 genomes]
rs7134015	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7307784	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7309234	0.86[ASN][1000 genomes]
rs73094488	0.81[ASN][1000 genomes]
rs7310178	0.92[ASN][1000 genomes]
rs7310871	0.92[ASN][1000 genomes]
rs73268358	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73268359	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531527	chr12:39680812-40182822	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv1037457	chr12:39898349-40245401	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv541480	chr12:39898349-40245401	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv1039645	chr12:39903123-40022029	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv469359	chr12:39946354-40034699	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv558591	chr12:39946354-40034699	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv469361	chr12:39946354-40042220	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS 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
8	nsv558592	chr12:39946354-40042220	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv899014	chr12:39946354-40068896	Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv899015	chr12:39946354-40118249	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
11	nsv899016	chr12:39949147-40004906	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv899017	chr12:39949147-40081619	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
13	nsv899018	chr12:39949147-40111761	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
14	nsv899019	chr12:39955802-40004906	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv899020	chr12:39985206-40040331	Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv899021	chr12:39989172-40053423	Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:39963800-40010200	Weak transcription	Left Ventricle	heart
2	chr12:39966800-40009400	Weak transcription	Primary T cells from cord blood	blood
3	chr12:39980200-40006000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr12:39980200-40009200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr12:39993800-40005600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr12:39996400-40007800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr12:39996800-40009400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr12:39997800-40005800	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr12:39999600-40009800	Weak transcription	Brain Anterior Caudate	brain
10	chr12:40000200-40009400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr12:40000200-40010200	Weak transcription	Brain Substantia Nigra	brain
12	chr12:40001000-40005600	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr12:40001200-40010000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr12:40002000-40009800	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr12:40002200-40005200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr12:40003400-40006400	Active TSS	GM12878-XiMat	blood
17	chr12:40003600-40005800	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr12:40003800-40005800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr12:40004200-40005600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr12:40004400-40009200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr12:40004600-40005400	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr12:40004600-40006400	Weak transcription	Adipose Nuclei	Adipose
23	chr12:40004600-40007400	Weak transcription	Fetal Brain Female	brain
24	chr12:40004800-40005000	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
25	chr12:40004800-40005600	Weak transcription	Fetal Brain Male	brain
26	chr12:40004800-40006600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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