Variant report

Variant	rs72931064
Chromosome Location	chr3:97959884-97959885
allele	C/T
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:63)

rs_ID	r²[population]
rs1497536	1.00[EUR][1000 genomes]
rs1497543	1.00[EUR][1000 genomes]
rs35724172	1.00[EUR][1000 genomes]
rs56274587	1.00[EUR][1000 genomes]
rs56695531	1.00[AMR][1000 genomes]
rs56741748	0.83[AMR][1000 genomes]
rs57153638	1.00[EUR][1000 genomes]
rs57210707	1.00[AMR][1000 genomes]
rs57263843	1.00[EUR][1000 genomes]
rs57431594	1.00[EUR][1000 genomes]
rs57521928	1.00[AMR][1000 genomes]
rs57711450	1.00[AMR][1000 genomes]
rs57870129	1.00[EUR][1000 genomes]
rs58044901	1.00[EUR][1000 genomes]
rs58134115	1.00[AMR][1000 genomes]
rs58224654	1.00[EUR][1000 genomes]
rs58323070	1.00[AMR][1000 genomes]
rs58952611	1.00[AMR][1000 genomes]
rs58974727	1.00[AMR][1000 genomes]
rs59111149	1.00[EUR][1000 genomes]
rs59291702	1.00[AMR][1000 genomes]
rs59330240	1.00[AMR][1000 genomes]
rs59403104	1.00[AMR][1000 genomes]
rs59461359	1.00[AMR][1000 genomes]
rs59576981	1.00[EUR][1000 genomes]
rs59605835	1.00[AMR][1000 genomes]
rs59878229	1.00[AMR][1000 genomes]
rs59886059	1.00[AMR][1000 genomes]
rs60039150	1.00[EUR][1000 genomes]
rs60427156	1.00[AMR][1000 genomes]
rs60567919	1.00[AMR][1000 genomes]
rs61483585	1.00[EUR][1000 genomes]
rs61583728	1.00[EUR][1000 genomes]
rs6775472	1.00[EUR][1000 genomes]
rs6779299	1.00[EUR][1000 genomes]
rs6792579	1.00[EUR][1000 genomes]
rs72929044	0.83[AMR][1000 genomes]
rs72929064	0.83[AMR][1000 genomes]
rs72931068	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72931070	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72931073	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72931074	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72931078	1.00[EUR][1000 genomes]
rs72931079	1.00[EUR][1000 genomes]
rs72931081	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72931088	1.00[EUR][1000 genomes]
rs72931090	1.00[EUR][1000 genomes]
rs72931092	1.00[EUR][1000 genomes]
rs72932841	1.00[EUR][1000 genomes]
rs73853773	1.00[EUR][1000 genomes]
rs73853774	1.00[EUR][1000 genomes]
rs73853775	1.00[EUR][1000 genomes]
rs73854545	1.00[EUR][1000 genomes]
rs73854549	1.00[EUR][1000 genomes]
rs73855904	1.00[EUR][1000 genomes]
rs7609946	1.00[EUR][1000 genomes]
rs7615266	1.00[EUR][1000 genomes]
rs7620005	1.00[EUR][1000 genomes]
rs7621627	1.00[EUR][1000 genomes]
rs7624999	1.00[EUR][1000 genomes]
rs7625339	1.00[EUR][1000 genomes]
rs7632822	1.00[EUR][1000 genomes]
rs7652703	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869347	chr3:97742604-98051633	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv877209	chr3:97806616-98049409	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv963576	chr3:97825434-98041343	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1004820	chr3:97852875-98169488	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv834773	chr3:97855362-98043888	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1000834	chr3:97859880-98095473	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv877210	chr3:97866177-97992964	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
8	nsv432462	chr3:97918267-98001710	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv877212	chr3:97931105-98033400	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	esv1842860	chr3:97934241-98075543	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv1004762	chr3:97935701-98000227	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
12	nsv1008569	chr3:97937168-97983117	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv1009918	chr3:97946030-98155450	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
14	nsv965340	chr3:97957002-97980365	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
15	esv3444875	chr3:97957818-97983549	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:97959000-97961600	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr3:97959200-97960600	Enhancers	H9 Cell Line	embryonic stem cell
3	chr3:97959200-97961400	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr3:97959200-97961400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr3:97959200-97961800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr3:97959400-97961400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr3:97959600-97960000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr3:97959800-97960400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr3:97959800-97960600	Enhancers	H1 Cell Line	embryonic stem cell
10	chr3:97959800-97962000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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