Variant report

Variant	rs73144774
Chromosome Location	chr3:143136625-143136626
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:65373890..65374390-chr3:143136393..143136917,2	Hela-S3	cervix:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10513200	0.96[ASN][1000 genomes]
rs10513201	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10935491	0.95[ASN][1000 genomes]
rs10935492	0.96[ASN][1000 genomes]
rs11707045	0.96[ASN][1000 genomes]
rs11707857	0.95[ASN][1000 genomes]
rs11719681	0.96[ASN][1000 genomes]
rs16846341	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16853522	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16853578	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17757146	0.96[ASN][1000 genomes]
rs17757182	0.96[ASN][1000 genomes]
rs1875459	0.96[ASN][1000 genomes]
rs2360255	0.95[ASN][1000 genomes]
rs35233571	0.95[ASN][1000 genomes]
rs35358995	0.87[ASN][1000 genomes]
rs36125349	0.96[ASN][1000 genomes]
rs3860228	0.84[EUR][1000 genomes]
rs4311209	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4521222	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56078024	0.84[EUR][1000 genomes]
rs56080141	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56152928	0.95[ASN][1000 genomes]
rs61301417	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6770293	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6782465	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73144735	0.85[EUR][1000 genomes]
rs73144736	0.85[EUR][1000 genomes]
rs73144740	0.86[ASN][1000 genomes]
rs73144743	0.92[ASN][1000 genomes]
rs73144745	0.91[ASN][1000 genomes]
rs73144749	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73144760	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73144769	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73144770	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73144771	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73144772	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73144773	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73144777	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7374585	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7617737	0.96[ASN][1000 genomes]
rs7627844	0.96[ASN][1000 genomes]
rs7652087	0.96[ASN][1000 genomes]
rs7652557	0.96[ASN][1000 genomes]
rs924576	0.84[EUR][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	nsv949288	chr3:142793323-143585882	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	esv2757894	chr3:142992697-143285979	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	esv2759184	chr3:142992697-143285979	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1011088	chr3:143135891-143163169	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region lncRNA	3 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	chr3:143100600-143142600	Weak transcription	Primary T cells from cord blood	blood
2	chr3:143129400-143140600	Weak transcription	NHDF-Ad	bronchial
3	chr3:143133200-143142800	Weak transcription	Primary B cells from cord blood	blood
4	chr3:143136000-143137200	Weak transcription	Dnd41	blood
5	chr3:143136600-143138600	Weak transcription	Aorta	Aorta

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