Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10001112	0.89[AMR][1000 genomes]
rs10012964	0.89[AMR][1000 genomes]
rs10021127	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11932874	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs11934590	1.00[CEU][hapmap]
rs1495144	1.00[CEU][hapmap]
rs17008673	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17008681	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17008689	0.94[ASN][1000 genomes]
rs17008692	0.94[ASN][1000 genomes]
rs28372645	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28451675	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28532917	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28718327	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs437295	1.00[CEU][hapmap]
rs6535533	0.82[ASN][1000 genomes]
rs6857631	0.94[ASN][1000 genomes]
rs72955986	1.00[EUR][1000 genomes]
rs72955991	1.00[EUR][1000 genomes]
rs72961914	0.94[ASN][1000 genomes]
rs72961932	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72961933	1.00[ASN][1000 genomes]
rs72962002	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7654197	0.82[ASN][1000 genomes]
rs7660492	0.82[ASN][1000 genomes]
rs7668852	1.00[CEU][hapmap]
rs7699309	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829997	chr4:85244076-85409405	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:85286400-85287200	Bivalent Enhancer	Brain Germinal Matrix	brain
2	chr4:85286400-85289400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:85286800-85287000	Bivalent Enhancer	Fetal Brain Male	brain
4	chr4:85286800-85288800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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