Variant report

Variant	rs527652
Chromosome Location	chr20:41531759-41531760
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11905939	0.85[AMR][1000 genomes]
rs11906028	0.85[AMR][1000 genomes]
rs11908022	0.85[AMR][1000 genomes]
rs11908420	0.85[AMR][1000 genomes]
rs206677	0.85[AMR][1000 genomes]
rs208202	0.85[AMR][1000 genomes]
rs208206	0.85[AMR][1000 genomes]
rs208212	0.85[AMR][1000 genomes]
rs208213	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2750074	0.85[AMR][1000 genomes]
rs488232	0.87[YRI][hapmap];0.91[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs511805	1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs535000	0.89[YRI][hapmap];0.89[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs56050355	0.85[AMR][1000 genomes]
rs56137824	0.85[AMR][1000 genomes]
rs58589364	0.85[AMR][1000 genomes]
rs58770909	0.85[AMR][1000 genomes]
rs58920280	0.85[AMR][1000 genomes]
rs60468658	0.85[AMR][1000 genomes]
rs6103098	0.98[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73907405	0.85[AMR][1000 genomes]
rs73907407	0.85[AMR][1000 genomes]
rs73910609	0.85[AMR][1000 genomes]
rs73910612	0.85[AMR][1000 genomes]
rs73910613	0.85[AMR][1000 genomes]
rs73910614	0.85[AMR][1000 genomes]
rs73910615	0.85[AMR][1000 genomes]
rs73910616	0.85[AMR][1000 genomes]
rs73910620	0.85[AMR][1000 genomes]
rs73910623	0.85[AMR][1000 genomes]
rs73910624	0.85[AMR][1000 genomes]
rs73910625	0.85[AMR][1000 genomes]
rs73910627	0.85[AMR][1000 genomes]
rs73910629	0.85[AMR][1000 genomes]
rs73910630	0.85[AMR][1000 genomes]
rs73910631	0.85[AMR][1000 genomes]
rs73910632	0.85[AMR][1000 genomes]
rs8115133	0.85[AMR][1000 genomes]
rs8115220	0.85[AMR][1000 genomes]
rs8121056	0.85[AMR][1000 genomes]
rs965018	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1058990	chr20:41289969-41543912	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv544277	chr20:41289969-41543912	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1063450	chr20:41409901-41880620	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1060690	chr20:41413369-41851935	Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1066088	chr20:41417205-42060036	Enhancers Bivalent Enhancer Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv1060468	chr20:41518010-41700012	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1061053	chr20:41521471-41704874	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:41529000-41531800	Enhancers	Pancreas	Pancrea
2	chr20:41529600-41533400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr20:41530000-41543800	Weak transcription	Spleen	Spleen
4	chr20:41530800-41532800	Enhancers	Fetal Stomach	stomach
5	chr20:41531200-41532800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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