Variant report

Variant	rs10097933
Chromosome Location	chr8:3263500-3263501
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10101928	0.82[JPT][hapmap]
rs1161520	0.90[JPT][hapmap]
rs1161522	0.90[JPT][hapmap]
rs1161523	0.89[JPT][hapmap]
rs1161526	0.83[AFR][1000 genomes]
rs1161530	0.88[JPT][hapmap]
rs1161532	0.81[JPT][hapmap]
rs1161534	0.90[JPT][hapmap];0.91[LWK][hapmap]
rs1161536	0.90[JPT][hapmap]
rs1161537	0.90[JPT][hapmap];0.91[LWK][hapmap]
rs1161543	0.89[JPT][hapmap]
rs1182739	0.90[JPT][hapmap];0.91[LWK][hapmap]
rs12544811	0.86[CHB][hapmap];0.89[JPT][hapmap]
rs12546510	0.87[EUR][1000 genomes]
rs12546535	0.87[EUR][1000 genomes]
rs12548247	1.00[CEU][hapmap]
rs13281086	0.87[EUR][1000 genomes]
rs17065861	0.82[CEU][hapmap];0.89[JPT][hapmap]
rs17065962	0.82[CEU][hapmap];1.00[JPT][hapmap]
rs17066021	0.90[JPT][hapmap]
rs17066034	0.85[CEU][hapmap];0.91[GIH][hapmap];0.88[TSI][hapmap];0.87[EUR][1000 genomes]
rs17066035	0.87[EUR][1000 genomes]
rs17066037	0.87[EUR][1000 genomes]
rs17066040	0.87[EUR][1000 genomes]
rs17066044	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17066046	0.87[EUR][1000 genomes]
rs17066051	0.87[EUR][1000 genomes]
rs17066055	0.82[CEU][hapmap];0.92[CHB][hapmap];0.88[JPT][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17066062	1.00[CEU][hapmap];0.84[CHB][hapmap];0.86[CHD][hapmap];0.81[GIH][hapmap];0.89[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17066072	0.85[CEU][hapmap];0.84[CHB][hapmap];0.89[JPT][hapmap];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17066077	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17080030	0.89[JPT][hapmap]
rs2406297	1.00[CEU][hapmap]
rs2406298	1.00[CEU][hapmap];0.86[CHB][hapmap];0.88[JPT][hapmap]
rs2406299	0.86[CHD][hapmap];0.81[GIH][hapmap];0.89[JPT][hapmap];0.87[TSI][hapmap]
rs28667319	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2897375	1.00[CEU][hapmap];0.86[CHB][hapmap];0.89[JPT][hapmap]
rs4461920	1.00[CEU][hapmap];0.86[CHB][hapmap];0.90[CHD][hapmap];0.81[GIH][hapmap];0.89[JPT][hapmap];0.87[TSI][hapmap]
rs4875710	0.84[CHB][hapmap]
rs4875715	0.82[CHB][hapmap]
rs55642600	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55748924	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56284885	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56372721	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58454178	0.87[EUR][1000 genomes]
rs58959537	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61267782	0.87[EUR][1000 genomes]
rs6990027	0.86[CHB][hapmap];0.84[JPT][hapmap]
rs73657843	0.87[EUR][1000 genomes]
rs73657844	0.87[EUR][1000 genomes]
rs73657847	0.84[EUR][1000 genomes]
rs73657848	0.87[EUR][1000 genomes]
rs73657849	0.87[EUR][1000 genomes]
rs73657850	0.87[EUR][1000 genomes]
rs73657851	0.87[EUR][1000 genomes]
rs73657852	0.87[EUR][1000 genomes]
rs73657853	0.87[EUR][1000 genomes]
rs73657855	0.94[EUR][1000 genomes]
rs73657856	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73657857	0.87[EUR][1000 genomes]
rs73657858	0.87[EUR][1000 genomes]
rs73657862	0.85[EUR][1000 genomes]
rs9644270	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033589	chr8:2498609-3305100	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1018407	chr8:2724294-3305100	Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv915568	chr8:2725834-3291312	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1025408	chr8:2733604-3302447	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1025209	chr8:3067655-3754882	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1026643	chr8:3077210-3277827	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1026998	chr8:3102679-3593264	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv1034076	chr8:3168033-3989947	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv539351	chr8:3168033-3989947	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv1017164	chr8:3174168-4026811	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv539352	chr8:3174168-4026811	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
12	nsv1018218	chr8:3180287-4089011	Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:3255200-3269800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr8:3255400-3269800	Weak transcription	Brain Anterior Caudate	brain
3	chr8:3255600-3264600	Weak transcription	Brain Angular Gyrus	brain
4	chr8:3255600-3269800	Weak transcription	Brain Hippocampus Middle	brain
5	chr8:3255600-3269800	Weak transcription	Brain Substantia Nigra	brain
6	chr8:3257000-3270000	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr8:3262600-3266600	Weak transcription	Fetal Heart	heart

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