Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11127674	1.00[EUR][1000 genomes]
rs13318110	1.00[EUR][1000 genomes]
rs17046784	1.00[AMR][1000 genomes]
rs17046807	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17046819	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2634726	1.00[EUR][1000 genomes]
rs57076692	1.00[AMR][1000 genomes]
rs58050190	1.00[AMR][1000 genomes]
rs58257624	1.00[AMR][1000 genomes]
rs58304740	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60234547	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61554478	1.00[AMR][1000 genomes]
rs6775101	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6795974	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs72917913	1.00[EUR][1000 genomes]
rs72917922	1.00[EUR][1000 genomes]
rs9828107	1.00[EUR][1000 genomes]
rs9846683	1.00[EUR][1000 genomes]
rs9852077	1.00[EUR][1000 genomes]
rs9867357	1.00[EUR][1000 genomes]
rs9868744	1.00[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	nsv470638	chr3:67367341-67814738	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	esv3359258	chr3:67589615-67828274	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv876922	chr3:67635506-67755257	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv428739	chr3:67656829-67730379	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:67705600-67756200	Weak transcription	Aorta	Aorta
2	chr3:67705800-67776000	Weak transcription	Ovary	ovary
3	chr3:67712200-67728400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr3:67717200-67730800	Weak transcription	Gastric	stomach
5	chr3:67721200-67759200	Weak transcription	Psoas Muscle	Psoas
6	chr3:67721400-67800400	Weak transcription	Left Ventricle	heart
7	chr3:67725000-67728400	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr3:67726000-67729000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr3:67727600-67747600	Weak transcription	A549	lung
10	chr3:67727800-67729200	Enhancers	Primary T cells from cord blood	blood
11	chr3:67727800-67730000	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr3:67727800-67755000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr3:67728000-67730600	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr3:67728000-67730600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr3:67728000-67730600	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr3:67728200-67730000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr3:67728200-67730600	Enhancers	Primary T helper cells fromperipheralblood	blood

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