Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs13200447	0.91[EUR][1000 genomes]
rs17334264	0.91[EUR][1000 genomes]
rs2476202	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2760227	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2760230	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2760236	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2760237	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2760238	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2760248	0.88[EUR][1000 genomes]
rs2788994	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2788995	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2788997	0.91[EUR][1000 genomes]
rs2788998	0.91[EUR][1000 genomes]
rs34965495	0.87[EUR][1000 genomes]
rs35106048	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs553592	0.91[EUR][1000 genomes]
rs555789	0.91[EUR][1000 genomes]
rs6905222	0.91[EUR][1000 genomes]
rs71570870	0.91[EUR][1000 genomes]
rs7745854	0.81[EUR][1000 genomes]
rs7765524	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9654611	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 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	nsv522455	chr6:118228527-118240685	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island 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	chr6:118229800-118241400	Weak transcription	Gastric	stomach
2	chr6:118230800-118236400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:118230800-118238000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr6:118230800-118239400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr6:118232000-118238000	Weak transcription	Cortex derived primary cultured neurospheres	brain

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