Variant report

Variant	rs4472974
Chromosome Location	chr12:57269643-57269644
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10735869	0.91[ASN][1000 genomes]
rs10876941	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10876943	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11172025	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11172033	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2888106	0.81[EUR][1000 genomes]
rs2888107	0.81[EUR][1000 genomes]
rs2888108	0.81[EUR][1000 genomes]
rs4254104	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4477473	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4759036	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4759041	0.82[EUR][1000 genomes]
rs55812315	0.85[EUR][1000 genomes]
rs61939604	0.82[EUR][1000 genomes]
rs7303219	0.95[ASN][1000 genomes]
rs7305700	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7306442	0.95[ASN][1000 genomes]
rs7314652	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7955918	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7956391	0.85[EUR][1000 genomes]
rs7959253	0.81[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs7959654	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7959725	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7960137	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7960618	0.83[EUR][1000 genomes]
rs7961602	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7967940	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7972591	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7979655	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9668259	0.82[AMR][1000 genomes];0.92[EUR][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	nsv1040850	chr12:57055011-57679209	Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 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	chr12:57265400-57270000	Weak transcription	Liver	Liver
2	chr12:57267400-57274200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr12:57268400-57274200	Weak transcription	Fetal Kidney	kidney
4	chr12:57269200-57270200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr12:57269400-57271000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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