Variant report

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11621233	0.88[EUR][1000 genomes]
rs11622454	0.81[EUR][1000 genomes]
rs11623231	0.85[EUR][1000 genomes]
rs11623788	0.80[EUR][1000 genomes]
rs11626919	0.84[EUR][1000 genomes]
rs11628786	0.81[EUR][1000 genomes]
rs12588653	1.00[ASN][1000 genomes]
rs12590427	0.96[ASN][1000 genomes]
rs1364966	0.84[AFR][1000 genomes]
rs1593376	0.81[AFR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2296918	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4899340	0.98[ASN][1000 genomes]
rs4902794	0.88[AFR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55692830	0.84[EUR][1000 genomes]
rs56113470	0.84[EUR][1000 genomes]
rs59398189	1.00[ASN][1000 genomes]
rs61654805	0.96[ASN][1000 genomes]
rs61740021	1.00[ASN][1000 genomes]
rs61745654	0.96[ASN][1000 genomes]
rs7149733	1.00[ASN][1000 genomes]
rs7153452	0.88[AFR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72731878	0.84[EUR][1000 genomes]
rs72731882	0.85[EUR][1000 genomes]
rs72731883	0.85[EUR][1000 genomes]
rs72731885	0.85[EUR][1000 genomes]
rs72731887	0.85[EUR][1000 genomes]
rs72731896	0.88[EUR][1000 genomes]
rs72731898	0.88[EUR][1000 genomes]
rs72733703	0.88[EUR][1000 genomes]
rs72733705	0.88[EUR][1000 genomes]
rs72733709	0.80[EUR][1000 genomes]
rs72733718	0.80[EUR][1000 genomes]
rs73280734	1.00[ASN][1000 genomes]
rs73280744	0.96[ASN][1000 genomes]

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	nsv832826	chr14:70559589-70723464	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh 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 lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv902075	chr14:70612618-70919016	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv983840	chr14:70696676-70714926	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70691000-70703400	Weak transcription	K562	blood
2	chr14:70697400-70719400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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