Variant report

Variant	rs7627844
Chromosome Location	chr3:143131154-143131155
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10513200	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10513201	0.95[ASN][1000 genomes]
rs10513210	1.00[CHB][hapmap]
rs10804692	1.00[CHB][hapmap]
rs10935491	0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10935492	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11707045	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11707857	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11711068	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs11717437	1.00[CHB][hapmap]
rs11718728	0.81[CEU][hapmap];1.00[CHB][hapmap]
rs11719681	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11915421	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs11915761	1.00[CHB][hapmap]
rs11927016	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13061014	1.00[CHB][hapmap]
rs13072761	1.00[CHB][hapmap]
rs13074801	1.00[CHB][hapmap]
rs13099124	1.00[CHB][hapmap]
rs1501631	1.00[CHB][hapmap]
rs1604377	1.00[CHB][hapmap]
rs1604380	1.00[CHB][hapmap]
rs1609727	1.00[CHB][hapmap]
rs1610217	1.00[CHB][hapmap]
rs16846341	0.96[ASN][1000 genomes]
rs16853522	0.96[ASN][1000 genomes]
rs16853578	0.95[ASN][1000 genomes]
rs16853767	1.00[CHB][hapmap]
rs16853866	1.00[CHB][hapmap]
rs16853903	1.00[CHB][hapmap]
rs17637392	1.00[CHB][hapmap]
rs17757146	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17757182	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1808882	1.00[CHB][hapmap]
rs1812200	1.00[CHB][hapmap]
rs1875459	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1875462	1.00[CHB][hapmap]
rs1995356	1.00[CHB][hapmap]
rs2083528	1.00[CHB][hapmap]
rs2360255	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35233571	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35358995	0.80[AFR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs36125349	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4024563	1.00[CHB][hapmap]
rs4311209	0.96[ASN][1000 genomes]
rs4521222	0.96[ASN][1000 genomes]
rs4839627	1.00[CHB][hapmap]
rs5003886	1.00[CHB][hapmap]
rs56080141	0.96[ASN][1000 genomes]
rs56152928	0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61301417	0.96[ASN][1000 genomes]
rs6770293	0.96[ASN][1000 genomes]
rs6782465	0.96[ASN][1000 genomes]
rs6784124	1.00[CHB][hapmap]
rs73144740	0.85[ASN][1000 genomes]
rs73144743	0.91[ASN][1000 genomes]
rs73144745	0.90[ASN][1000 genomes]
rs73144749	0.96[ASN][1000 genomes]
rs73144760	0.97[ASN][1000 genomes]
rs73144769	0.93[ASN][1000 genomes]
rs73144770	0.96[ASN][1000 genomes]
rs73144771	0.96[ASN][1000 genomes]
rs73144772	0.96[ASN][1000 genomes]
rs73144773	0.96[ASN][1000 genomes]
rs73144774	0.96[ASN][1000 genomes]
rs73144777	0.96[ASN][1000 genomes]
rs7374585	0.93[ASN][1000 genomes]
rs7617737	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7642361	1.00[CHB][hapmap]
rs7652087	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7652557	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs894176	1.00[CHB][hapmap]
rs9850863	1.00[CHB][hapmap]
rs9862119	1.00[CHB][hapmap]

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	nsv999000	chr3:143086325-143136128	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 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	chr3:143130600-143132400	Enhancers	GM12878-XiMat	blood
4	chr3:143130800-143134200	Enhancers	Dnd41	blood
5	chr3:143130800-143135000	Enhancers	Fetal Thymus	thymus
6	chr3:143131000-143131200	Enhancers	Primary B cells from cord blood	blood
7	chr3:143131000-143134400	Enhancers	Primary B cells from peripheral blood	blood

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