Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1130656	0.92[ASN][1000 genomes]
rs1321201	0.89[ASN][1000 genomes]
rs14224	0.92[ASN][1000 genomes]
rs1465620	0.89[ASN][1000 genomes]
rs1652508	0.89[ASW][hapmap];0.91[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.90[MKK][hapmap];0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1830519	0.91[CHB][hapmap];0.91[CHD][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes]
rs2295368	0.92[ASN][1000 genomes]
rs2465836	0.89[ASW][hapmap];0.89[GIH][hapmap]
rs3757019	0.86[ASN][1000 genomes]
rs3778217	0.83[ASN][1000 genomes]
rs3798903	0.88[ASN][1000 genomes]
rs3823055	0.92[ASN][1000 genomes]
rs4252075	0.86[ASN][1000 genomes]
rs4252092	0.88[ASN][1000 genomes]
rs4252105	0.89[ASN][1000 genomes]
rs4252108	0.92[ASN][1000 genomes]
rs783147	1.00[ASN][1000 genomes]
rs783176	0.89[ASW][hapmap];0.89[GIH][hapmap]
rs783185	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs813641	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9295131	0.89[ASN][1000 genomes]

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	esv2758089	chr6:160372244-161234665	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	esv2759484	chr6:160372244-161234665	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv605005	chr6:161069941-161152449	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1019113	chr6:161127584-161197558	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs783146	IGF2R	cis	cerebellum	SCAN
rs783146	PACRG	cis	parietal	SCAN

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161138600-161139000	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr6:161138800-161140000	Strong transcription	Liver	Liver

Quick Search: