Variant report

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs11964013	1.00[JPT][hapmap]
rs11964063	1.00[JPT][hapmap]
rs11967448	1.00[JPT][hapmap]
rs1334829	1.00[JPT][hapmap]
rs1334835	1.00[JPT][hapmap]
rs150145	0.85[EUR][1000 genomes]
rs169542	0.92[EUR][1000 genomes]
rs176168	0.85[EUR][1000 genomes]
rs2011710	1.00[JPT][hapmap]
rs205929	0.85[EUR][1000 genomes]
rs205931	0.85[EUR][1000 genomes]
rs205932	0.85[EUR][1000 genomes]
rs205934	0.85[EUR][1000 genomes]
rs205940	0.85[EUR][1000 genomes]
rs205947	0.92[EUR][1000 genomes]
rs205949	1.00[JPT][hapmap]
rs205953	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs205956	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs205960	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs205964	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs205969	1.00[JPT][hapmap]
rs205970	1.00[JPT][hapmap]
rs205973	1.00[JPT][hapmap]
rs2105019	1.00[JPT][hapmap]
rs2484144	1.00[JPT][hapmap]
rs2484145	1.00[JPT][hapmap]
rs2484148	1.00[JPT][hapmap]
rs2484149	1.00[JPT][hapmap]
rs2501519	1.00[JPT][hapmap]
rs2859146	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs2859147	1.00[JPT][hapmap]
rs441671	1.00[EUR][1000 genomes]
rs73523952	0.92[EUR][1000 genomes]
rs7763206	1.00[JPT][hapmap]
rs928597	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530526	chr6:118027339-118718476	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv428153	chr6:118430517-118586974	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1030089	chr6:118436482-118604516	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv538427	chr6:118436482-118604516	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 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	chr6:118468000-118485000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr6:118476800-118485800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:118477000-118484200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:118478400-118484800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr6:118481200-118484400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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