Variant report

Variant	rs212045
Chromosome Location	chr3:60036883-60036884
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11130751	0.92[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11711227	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs11716199	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11718208	0.80[CEU][hapmap];0.81[AMR][1000 genomes]
rs11718957	0.88[CEU][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11718994	0.85[EUR][1000 genomes]
rs11720431	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13058814	0.85[YRI][hapmap]
rs13062399	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13063836	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13075738	0.87[CEU][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13081934	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13088111	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs169841	0.80[CHB][hapmap];0.87[JPT][hapmap];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs212042	0.81[CHB][hapmap];0.88[JPT][hapmap];0.87[ASN][1000 genomes]
rs212043	0.81[CHB][hapmap];0.80[JPT][hapmap];0.86[ASN][1000 genomes]
rs212044	0.81[CHB][hapmap];0.88[JPT][hapmap];0.89[ASN][1000 genomes]
rs212058	0.81[CHB][hapmap]
rs34476175	0.89[EUR][1000 genomes]
rs35122656	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35138137	0.84[EUR][1000 genomes]
rs3845972	0.87[CHB][hapmap]
rs3845973	0.88[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3856663	0.86[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3856664	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3856665	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3912495	0.81[CHB][hapmap];0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs4083381	0.81[CHB][hapmap]
rs60458864	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62238444	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6801817	0.81[CHB][hapmap]
rs9311746	0.84[CEU][hapmap];0.81[CHB][hapmap];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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	nsv834707	chr3:60005679-60184046	Weak transcription Enhancers Flanking Active TSS 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	1 gene(s)	inside rSNPs	diseases
5	nsv876839	chr3:60024084-60039488	Flanking Active TSS Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60034600-60044400	Enhancers	Primary T helper cells fromperipheralblood	blood
2	chr3:60034800-60037600	Enhancers	Dnd41	blood
3	chr3:60034800-60038000	Weak transcription	Thymus	Thymus
4	chr3:60034800-60041400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr3:60035000-60038200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr3:60035000-60038200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr3:60035000-60039000	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr3:60035000-60041200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr3:60035000-60043200	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr3:60035000-60043200	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr3:60035200-60038200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr3:60035400-60041400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr3:60036200-60037200	Enhancers	Fetal Thymus	thymus
14	chr3:60036400-60037200	Enhancers	Primary T cells fromperipheralblood	blood
15	chr3:60036600-60038000	Weak transcription	Primary T cells from cord blood	blood
16	chr3:60036800-60041200	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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