Variant report

Variant	rs12325022
Chromosome Location	chr16:76372629-76372630
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 105 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs1035531	0.91[CHB][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs1035532	0.91[CHB][hapmap];0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs10492885	1.00[YRI][hapmap]
rs11865494	0.89[EUR][1000 genomes]
rs12595966	0.95[EUR][1000 genomes]
rs12596487	0.89[CEU][hapmap];0.98[EUR][1000 genomes]
rs12596963	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs12597605	0.98[EUR][1000 genomes]
rs12597720	0.98[EUR][1000 genomes]
rs12600063	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs1346554	0.80[CEU][hapmap];0.81[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs1346555	1.00[CEU][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs1346556	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs1346557	1.00[YRI][hapmap]
rs1549660	0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs1549661	0.91[CHB][hapmap];0.89[ASN][1000 genomes]
rs1559329	0.91[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.89[ASN][1000 genomes]
rs16944192	0.95[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap]
rs16944208	1.00[YRI][hapmap]
rs16944222	0.82[CEU][hapmap];0.98[EUR][1000 genomes]
rs16944224	1.00[YRI][hapmap]
rs16944225	0.90[CEU][hapmap];0.95[CHB][hapmap];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16944228	0.95[CHB][hapmap];0.85[ASN][1000 genomes]
rs17362336	1.00[YRI][hapmap]
rs17698989	1.00[YRI][hapmap]
rs17699048	1.00[YRI][hapmap]
rs17699107	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs17699131	0.98[EUR][1000 genomes]
rs17699142	0.98[EUR][1000 genomes]
rs17699214	0.91[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs17699220	0.93[EUR][1000 genomes]
rs17699232	0.91[EUR][1000 genomes]
rs17766542	1.00[YRI][hapmap]
rs17766584	1.00[AFR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17766704	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs17766740	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs17766856	0.91[EUR][1000 genomes]
rs17766862	1.00[YRI][hapmap];0.93[EUR][1000 genomes]
rs17766904	0.81[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs1964297	0.91[CHB][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs2195428	0.89[CEU][hapmap];1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs2195429	0.90[CEU][hapmap];0.97[EUR][1000 genomes]
rs2216743	1.00[YRI][hapmap]
rs28417722	0.92[EUR][1000 genomes]
rs2866713	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs2866714	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs34500194	0.94[EUR][1000 genomes]
rs4448976	0.98[EUR][1000 genomes]
rs4528602	0.89[CEU][hapmap];0.97[EUR][1000 genomes]
rs4595825	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs4644883	0.91[CHB][hapmap]
rs58234937	0.91[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs58799953	0.94[ASN][1000 genomes]
rs59708157	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs61245681	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs66508951	0.95[EUR][1000 genomes]
rs7184662	1.00[YRI][hapmap]
rs7187194	1.00[YRI][hapmap]
rs7193350	0.90[EUR][1000 genomes]
rs7204781	0.91[CHB][hapmap];0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs72626199	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72628208	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs72628209	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs72628210	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs72628211	0.98[EUR][1000 genomes]
rs72628212	0.93[EUR][1000 genomes]
rs72628213	0.93[EUR][1000 genomes]
rs72628214	0.91[EUR][1000 genomes]
rs72628215	0.91[EUR][1000 genomes]
rs72628216	0.93[EUR][1000 genomes]
rs7501035	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs8043911	0.93[EUR][1000 genomes]
rs8044400	0.89[CEU][hapmap];0.91[CHB][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8044637	0.90[CEU][hapmap];0.90[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8045505	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs8045699	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs8045862	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs8046953	1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.89[ASN][1000 genomes]
rs8047690	1.00[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs8049390	0.94[ASN][1000 genomes]
rs8058722	0.89[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8059413	0.93[EUR][1000 genomes]
rs8062657	0.93[EUR][1000 genomes]
rs8062793	0.91[EUR][1000 genomes]
rs8063803	0.92[EUR][1000 genomes]
rs9921874	0.99[EUR][1000 genomes]
rs9924992	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9939553	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9939792	0.91[CHB][hapmap]

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	nsv1064607	chr16:75787129-76449101	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv1065794	chr16:75792288-76434118	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv542961	chr16:75792288-76434118	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv1059162	chr16:75929348-76730816	Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv572995	chr16:75935025-76708417	Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv572996	chr16:75935025-76735249	Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv817220	chr16:75939705-76735383	ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv1056021	chr16:75955522-76729765	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
9	nsv542962	chr16:75955522-76729765	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
10	nsv906935	chr16:76031737-76453110	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
11	nsv906936	chr16:76031737-76768178	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
12	nsv817549	chr16:76067068-76582099	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
13	nsv1065644	chr16:76166579-76475634	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
14	nsv869200	chr16:76227867-76695732	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
15	nsv833286	chr16:76243730-76444283	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	esv2763142	chr16:76271660-76461841	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76369800-76376800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr16:76370000-76378800	Weak transcription	Brain Hippocampus Middle	brain
3	chr16:76370000-76378800	Weak transcription	Brain Substantia Nigra	brain
4	chr16:76370000-76379000	Weak transcription	Brain Anterior Caudate	brain
5	chr16:76372200-76372800	Enhancers	Brain Angular Gyrus	brain

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