Variant report

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10090043	1.00[AMR][1000 genomes]
rs13255021	1.00[AMR][1000 genomes]
rs13257182	1.00[AMR][1000 genomes]
rs2929118	1.00[AMR][1000 genomes]
rs2955894	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2955896	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2955897	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2955898	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2955899	0.95[AFR][1000 genomes]
rs2955900	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2955901	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2955904	0.90[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2955905	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2955906	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2981159	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2981160	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2981161	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2981162	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4469437	1.00[AMR][1000 genomes]
rs4559228	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4633046	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56976900	1.00[AMR][1000 genomes]
rs59381479	1.00[AMR][1000 genomes]
rs6474203	1.00[AMR][1000 genomes]
rs7011669	1.00[AMR][1000 genomes]
rs73605143	1.00[AMR][1000 genomes]
rs73605152	1.00[AMR][1000 genomes]
rs7826266	1.00[AMR][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	nsv539555	chr8:39683857-40673606	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1033371	chr8:39749437-39899540	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1020859	chr8:39857347-39877897	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv611087	chr8:39865891-39884574	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv611088	chr8:39869841-39880766	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39850600-39872800	Weak transcription	Right Atrium	heart
2	chr8:39868000-39879400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:39869400-39872200	Enhancers	Colon Smooth Muscle	Colon
4	chr8:39869600-39874400	Weak transcription	Right Ventricle	heart
5	chr8:39870200-39872800	Weak transcription	Stomach Smooth Muscle	stomach
6	chr8:39870200-39873600	Enhancers	Fetal Lung	lung
7	chr8:39870800-39872400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:39871200-39873000	Weak transcription	Fetal Muscle Leg	muscle
9	chr8:39871400-39872400	Enhancers	Rectal Smooth Muscle	rectum
10	chr8:39871800-39873000	Weak transcription	Ovary	ovary
11	chr8:39872000-39872400	Enhancers	A549	lung

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