Variant report

Variant	rs73180381
Chromosome Location	chr13:47999718-47999719
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:47998849..48000404-chr13:48002509..48005061,2	K562	blood:

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs1359664	0.95[EUR][1000 genomes]
rs1359666	0.83[EUR][1000 genomes]
rs1547654	0.95[EUR][1000 genomes]
rs1571064	0.91[EUR][1000 genomes]
rs1575895	0.95[EUR][1000 genomes]
rs2478317	0.95[EUR][1000 genomes]
rs2478334	1.00[EUR][1000 genomes]
rs2478335	1.00[EUR][1000 genomes]
rs2478336	1.00[EUR][1000 genomes]
rs2503428	0.91[EUR][1000 genomes]
rs2503429	0.91[EUR][1000 genomes]
rs2503430	0.91[EUR][1000 genomes]
rs2503443	0.95[EUR][1000 genomes]
rs2503451	1.00[EUR][1000 genomes]
rs2503452	1.00[EUR][1000 genomes]
rs2503453	1.00[EUR][1000 genomes]
rs55857069	1.00[EUR][1000 genomes]
rs56088519	0.96[EUR][1000 genomes]
rs56234161	0.96[EUR][1000 genomes]
rs73180366	0.83[AFR][1000 genomes]
rs73180389	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73182280	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73182288	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73182301	1.00[EUR][1000 genomes]
rs73183803	1.00[EUR][1000 genomes]
rs73183804	1.00[EUR][1000 genomes]
rs73183808	1.00[EUR][1000 genomes]
rs73183809	1.00[EUR][1000 genomes]
rs73183810	1.00[EUR][1000 genomes]
rs73183814	1.00[EUR][1000 genomes]
rs73183816	1.00[EUR][1000 genomes]
rs73183821	1.00[EUR][1000 genomes]
rs73183822	1.00[EUR][1000 genomes]
rs73183824	1.00[EUR][1000 genomes]
rs73183826	1.00[EUR][1000 genomes]
rs73183827	1.00[EUR][1000 genomes]
rs73183828	1.00[EUR][1000 genomes]
rs73183829	1.00[EUR][1000 genomes]
rs73183830	1.00[EUR][1000 genomes]
rs73183831	1.00[EUR][1000 genomes]
rs73183832	1.00[EUR][1000 genomes]
rs73183833	1.00[EUR][1000 genomes]
rs73183834	1.00[EUR][1000 genomes]
rs73183835	1.00[EUR][1000 genomes]
rs73183836	1.00[EUR][1000 genomes]
rs73183837	1.00[EUR][1000 genomes]
rs73183838	1.00[EUR][1000 genomes]
rs73183840	1.00[EUR][1000 genomes]
rs73183841	1.00[EUR][1000 genomes]
rs73183844	0.88[EUR][1000 genomes]
rs73183846	1.00[EUR][1000 genomes]
rs73183848	1.00[EUR][1000 genomes]
rs73183849	1.00[EUR][1000 genomes]
rs73183850	1.00[EUR][1000 genomes]
rs73183851	0.95[EUR][1000 genomes]
rs73183852	1.00[EUR][1000 genomes]
rs73183853	1.00[EUR][1000 genomes]
rs73183854	0.91[EUR][1000 genomes]
rs73183856	1.00[EUR][1000 genomes]
rs73183857	0.84[EUR][1000 genomes]
rs73183859	1.00[EUR][1000 genomes]
rs73183860	1.00[EUR][1000 genomes]
rs73183862	1.00[EUR][1000 genomes]
rs73183864	1.00[EUR][1000 genomes]
rs7993497	1.00[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	esv2763019	chr13:47348229-48123447	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv3394678	chr13:47678184-48039379	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv3450125	chr13:47919050-48236684	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv455879	chr13:47919611-48190106	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv561588	chr13:47943829-48190106	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:47995000-48000200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr13:47995000-48000400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr13:47995800-48000200	Weak transcription	Adipose Nuclei	Adipose
4	chr13:47995800-48000400	Weak transcription	Liver	Liver
5	chr13:47996400-48000200	Weak transcription	NHDF-Ad	bronchial
6	chr13:47996400-48000400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr13:47997000-47999800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr13:47998800-47999800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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