Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10165220	0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10172167	0.86[CHB][hapmap]
rs10178186	0.83[YRI][hapmap]
rs10874467	0.81[ASN][1000 genomes]
rs11164111	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11164112	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11883879	0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs12612789	0.84[ASN][1000 genomes]
rs13414018	0.85[ASN][1000 genomes]
rs2004626	0.83[ASN][1000 genomes]
rs2077443	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs28680439	0.81[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs34087291	0.83[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs4555374	0.86[CHB][hapmap]
rs4564804	0.81[CHB][hapmap]
rs4854232	0.87[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs4854233	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4854234	0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4854235	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62146933	0.80[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs62146942	0.90[ASN][1000 genomes]
rs6708474	0.87[CHB][hapmap]
rs9324212	0.87[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1000661	chr2:95327875-95739468	Bivalent Enhancer Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	nsv1005016	chr2:95327875-95914467	Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Flanking 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 miRNA target site	43 gene(s)	inside rSNPs	diseases
3	esv2759075	chr2:95358799-95620108	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10180591	CYP4F32P	cis	Esophagus Mucosa	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:95534200-95549400	Weak transcription	Right Atrium	heart
2	chr2:95537200-95538400	Bivalent/Poised TSS	Brain Anterior Caudate	brain
3	chr2:95537800-95539600	Weak transcription	Gastric	stomach
4	chr2:95538200-95539800	Weak transcription	Lung	lung

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