Variant report

Variant	rs2447161
Chromosome Location	chr8:120373636-120373637
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs1551785	0.94[AMR][1000 genomes]
rs1599476	0.90[AMR][1000 genomes]
rs2447153	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs2447154	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs2447155	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs2447157	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs2447158	0.96[AMR][1000 genomes]
rs2447159	0.96[AMR][1000 genomes]
rs2447160	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs2447162	0.92[AMR][1000 genomes]
rs2447163	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs2447164	0.94[AMR][1000 genomes]
rs2447165	0.94[AMR][1000 genomes]
rs2447167	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs2447168	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs2447169	0.94[AMR][1000 genomes]
rs2447170	0.94[AMR][1000 genomes]
rs2447171	0.94[AMR][1000 genomes]
rs2447172	0.94[AMR][1000 genomes]
rs2447173	0.94[AMR][1000 genomes]
rs2447174	0.94[AMR][1000 genomes]
rs2447175	0.90[AMR][1000 genomes]
rs2447176	0.94[AMR][1000 genomes]
rs2447177	0.94[AMR][1000 genomes]
rs2447178	0.94[AMR][1000 genomes]
rs2447179	0.94[AMR][1000 genomes]
rs2447180	0.94[AMR][1000 genomes]
rs2447181	0.94[AMR][1000 genomes]
rs2447182	0.94[AMR][1000 genomes]
rs2447183	0.94[AMR][1000 genomes]
rs2469996	0.94[AMR][1000 genomes]
rs2469997	0.94[AMR][1000 genomes]
rs2469998	0.94[AMR][1000 genomes]
rs2469999	0.94[AMR][1000 genomes]
rs2470001	0.94[AMR][1000 genomes]
rs2470002	0.94[AMR][1000 genomes]
rs2470003	0.94[AMR][1000 genomes]
rs2470004	0.86[AMR][1000 genomes]
rs2470005	0.94[AMR][1000 genomes]
rs2470006	0.94[AMR][1000 genomes]
rs2470007	0.94[AMR][1000 genomes]
rs2470009	0.94[AMR][1000 genomes]
rs2470010	0.94[AMR][1000 genomes]
rs2470011	0.94[AMR][1000 genomes]
rs2470012	0.94[AMR][1000 genomes]
rs2470013	0.94[AMR][1000 genomes]
rs2470014	0.94[AMR][1000 genomes]
rs2470015	0.94[AMR][1000 genomes]
rs2470016	0.94[AMR][1000 genomes]
rs2470017	0.94[AMR][1000 genomes]
rs2470018	0.94[AMR][1000 genomes]
rs2470019	0.92[AMR][1000 genomes]
rs2470021	0.94[AMR][1000 genomes]
rs2470023	0.92[AMR][1000 genomes]
rs2470024	0.94[AMR][1000 genomes]
rs2470025	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs2470026	0.94[AMR][1000 genomes]
rs2470028	0.94[AMR][1000 genomes]
rs2470030	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs2470031	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs2470032	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs2470033	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs2470034	0.96[AMR][1000 genomes]
rs2470035	0.96[AMR][1000 genomes]
rs2470037	0.92[AMR][1000 genomes]
rs2470038	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs2470040	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs2957356	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs2957357	0.96[AMR][1000 genomes]
rs3110337	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes]
rs5019665	0.90[AFR][1000 genomes];0.96[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	nsv868916	chr8:119911943-120762250	Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1026655	chr8:120282929-120522329	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1032293	chr8:120311108-120389573	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region miRNA	n/a	inside rSNPs	diseases
4	nsv1019832	chr8:120327991-120380580	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region miRNA	n/a	inside rSNPs	diseases
5	nsv534028	chr8:120348940-120906079	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:120349600-120375000	Weak transcription	Aorta	Aorta
2	chr8:120368800-120373800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr8:120372400-120374200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:120373200-120376200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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