Variant report

Variant	rs9934361
Chromosome Location	chr16:76354742-76354743
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs11149893	0.95[CHB][hapmap]
rs11864692	0.89[YRI][hapmap];0.89[AFR][1000 genomes]
rs11864766	1.00[YRI][hapmap];0.94[AFR][1000 genomes]
rs11865582	0.91[CHB][hapmap];0.84[JPT][hapmap]
rs12325009	0.91[CHB][hapmap]
rs12325365	0.89[CHB][hapmap]
rs12596487	0.95[CHB][hapmap]
rs12596963	0.95[CHB][hapmap]
rs12600063	0.95[CHB][hapmap]
rs12716807	0.95[CHB][hapmap];0.83[JPT][hapmap]
rs12716808	0.95[CHB][hapmap];0.84[JPT][hapmap]
rs12924751	0.95[CHB][hapmap];0.84[JPT][hapmap]
rs12930160	0.95[CHB][hapmap];0.83[JPT][hapmap]
rs13332281	0.81[CEU][hapmap];0.86[CHB][hapmap];0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs13333980	0.91[CHB][hapmap]
rs13339408	0.91[CHB][hapmap]
rs1346555	0.95[CHB][hapmap]
rs1346556	0.91[CHB][hapmap]
rs1346557	0.95[CHB][hapmap]
rs1428753	0.95[CHB][hapmap];0.83[JPT][hapmap]
rs1549660	0.96[CEU][hapmap];0.92[YRI][hapmap];0.82[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs16944222	0.95[CHB][hapmap];0.88[ASN][1000 genomes]
rs17698989	0.95[CHB][hapmap]
rs17699048	0.91[CHB][hapmap]
rs17699214	0.95[CHB][hapmap]
rs17699220	0.90[CHB][hapmap]
rs17766542	0.95[CHB][hapmap]
rs17766704	0.95[CHB][hapmap]
rs17766740	0.91[CHB][hapmap]
rs17766862	0.95[CHB][hapmap]
rs17766904	0.86[CHB][hapmap]
rs2195428	0.94[CHB][hapmap]
rs2195429	0.95[CHB][hapmap]
rs2216743	0.91[CHB][hapmap];0.90[ASN][1000 genomes]
rs2866713	0.95[CHB][hapmap]
rs2866714	0.95[CHB][hapmap]
rs4528602	0.95[CHB][hapmap]
rs4595825	0.95[CHB][hapmap]
rs4644883	0.80[CEU][hapmap]
rs61147122	0.84[ASN][1000 genomes]
rs7184662	0.91[CHB][hapmap];0.85[ASN][1000 genomes]
rs7187266	0.95[CHB][hapmap];0.83[JPT][hapmap]
rs7193350	0.91[CHB][hapmap]
rs72626197	0.84[ASN][1000 genomes]
rs7501035	0.95[CHB][hapmap]
rs8045505	0.95[CHB][hapmap]
rs8045699	0.91[CHB][hapmap]
rs9319495	0.91[CHB][hapmap]
rs9921874	0.90[CHB][hapmap]
rs9937260	0.95[CHB][hapmap];0.88[JPT][hapmap]
rs9939792	0.81[CEU][hapmap];0.89[YRI][hapmap];0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532562	chr16:75614947-76371158	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76338400-76368600	Weak transcription	Brain Hippocampus Middle	brain
2	chr16:76342600-76368800	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr16:76344600-76368400	Weak transcription	Brain Substantia Nigra	brain

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