Variant report

Variant	rs57561694
Chromosome Location	chr3:59962849-59962850
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10510826	1.00[ASN][1000 genomes]
rs12152244	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12487051	1.00[ASN][1000 genomes]
rs12495052	1.00[ASN][1000 genomes]
rs12495662	1.00[ASN][1000 genomes]
rs12497400	1.00[ASN][1000 genomes]
rs13314734	1.00[ASN][1000 genomes]
rs17061573	0.84[AFR][1000 genomes]
rs17061678	0.88[AMR][1000 genomes]
rs17061683	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17061684	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17061689	0.88[AMR][1000 genomes]
rs17254065	1.00[ASN][1000 genomes]
rs17254231	1.00[ASN][1000 genomes]
rs17254574	1.00[ASN][1000 genomes]
rs17255191	1.00[ASN][1000 genomes]
rs17310854	1.00[ASN][1000 genomes]
rs17311592	1.00[ASN][1000 genomes]
rs17312006	1.00[ASN][1000 genomes]
rs17319929	1.00[ASN][1000 genomes]
rs17320006	1.00[ASN][1000 genomes]
rs17376950	1.00[ASN][1000 genomes]
rs17377293	1.00[ASN][1000 genomes]
rs3772489	0.84[AFR][1000 genomes]
rs3772503	0.85[AMR][1000 genomes]
rs3821484	0.86[AMR][1000 genomes]
rs41276483	0.84[AFR][1000 genomes]
rs55804635	0.90[AFR][1000 genomes]
rs57249968	1.00[ASN][1000 genomes]
rs58526463	1.00[ASN][1000 genomes]
rs58731594	0.84[AMR][1000 genomes]
rs59871933	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60287158	1.00[ASN][1000 genomes]
rs60590275	0.90[AFR][1000 genomes]
rs62238355	1.00[ASN][1000 genomes]
rs62238356	1.00[ASN][1000 genomes]
rs62238357	1.00[ASN][1000 genomes]
rs62238368	1.00[ASN][1000 genomes]
rs62238369	1.00[ASN][1000 genomes]
rs62238370	1.00[ASN][1000 genomes]
rs62238371	1.00[ASN][1000 genomes]
rs62240079	1.00[ASN][1000 genomes]
rs62240080	1.00[ASN][1000 genomes]
rs62240081	1.00[ASN][1000 genomes]
rs62240082	1.00[ASN][1000 genomes]
rs62240083	1.00[ASN][1000 genomes]
rs62240086	1.00[ASN][1000 genomes]
rs62240087	1.00[ASN][1000 genomes]
rs62240088	1.00[ASN][1000 genomes]
rs62240089	1.00[ASN][1000 genomes]
rs62240090	1.00[ASN][1000 genomes]
rs62240091	1.00[ASN][1000 genomes]
rs62240113	1.00[ASN][1000 genomes]
rs62240114	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62240115	1.00[ASN][1000 genomes]
rs62240117	1.00[ASN][1000 genomes]
rs62240119	1.00[ASN][1000 genomes]
rs6767115	1.00[ASN][1000 genomes]
rs6797938	1.00[ASN][1000 genomes]
rs6798364	1.00[ASN][1000 genomes]
rs6800973	1.00[ASN][1000 genomes]
rs72877026	0.82[AFR][1000 genomes]
rs72877030	0.84[AFR][1000 genomes]
rs72877033	0.84[AFR][1000 genomes]
rs72877036	0.84[AFR][1000 genomes]
rs72877063	1.00[ASN][1000 genomes]
rs802773	1.00[ASN][1000 genomes]
rs9815985	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428085	chr3:59782509-60070116	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1014983	chr3:59884024-60558331	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv590387	chr3:59890976-60481459	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv876838	chr3:59952152-59999690	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv590388	chr3:59957252-60018326	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv528597	chr3:59961514-59963131	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:59943200-59964400	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr3:59952000-59964400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr3:59956200-59964200	Weak transcription	Fetal Thymus	thymus
4	chr3:59960800-59963000	Weak transcription	Primary T cells from cord blood	blood
5	chr3:59961600-59969000	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr3:59962000-59963000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr3:59962000-59964600	Weak transcription	Dnd41	blood
8	chr3:59962200-59963200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr3:59962800-59964600	Weak transcription	Primary T helper cells fromperipheralblood	blood

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