Variant report

Variant	rs10450344
Chromosome Location	chr10:50781073-50781074
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:50780517..50784653-chr10:50786786..50789571,3	K562	blood:

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs4253045	1.00[EUR][1000 genomes]
rs4253094	1.00[EUR][1000 genomes]
rs4253104	1.00[EUR][1000 genomes]
rs4253129	1.00[EUR][1000 genomes]
rs4253186	1.00[EUR][1000 genomes]
rs57865789	0.89[AMR][1000 genomes]
rs58788269	1.00[EUR][1000 genomes]
rs59862996	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60749172	0.89[AMR][1000 genomes]
rs73311046	0.89[AMR][1000 genomes]
rs73315042	0.89[AMR][1000 genomes]
rs73315047	0.89[AMR][1000 genomes]
rs73315061	0.89[AMR][1000 genomes]
rs73315065	0.89[AMR][1000 genomes]
rs73315070	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73315072	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73315075	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73315077	0.89[AMR][1000 genomes]
rs73315079	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73315083	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73315085	0.89[AMR][1000 genomes]
rs73315096	0.89[AMR][1000 genomes]
rs73316905	0.89[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	nsv895375	chr10:50306386-51028871	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv534410	chr10:50317458-50826916	Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	nsv831867	chr10:50607857-50788751	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	esv3346476	chr10:50610853-50987802	Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
5	esv3385048	chr10:50610942-50988537	Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50777800-50781200	Enhancers	Placenta Amnion	Placenta Amnion
2	chr10:50778000-50782600	Enhancers	Hela-S3	cervix
3	chr10:50779000-50782000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr10:50779400-50782200	Enhancers	Muscle Satellite Cultured Cells	--
5	chr10:50779400-50782400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr10:50779400-50782400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr10:50779800-50781400	Weak transcription	Osteobl	bone
8	chr10:50780000-50787400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr10:50780200-50782200	Enhancers	Placenta	Placenta
10	chr10:50780600-50782200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr10:50781000-50781200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
12	chr10:50781000-50781600	Active TSS	HepG2	liver

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