Variant report

Variant	rs73803312
Chromosome Location	chr4:22746451-22746452
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10020177	1.00[EUR][1000 genomes]
rs10030119	1.00[EUR][1000 genomes]
rs10030375	1.00[EUR][1000 genomes]
rs10033886	1.00[EUR][1000 genomes]
rs10516412	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10516996	0.98[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs10517005	1.00[EUR][1000 genomes]
rs11935737	1.00[EUR][1000 genomes]
rs11935776	1.00[EUR][1000 genomes]
rs11935840	1.00[EUR][1000 genomes]
rs11943842	1.00[EUR][1000 genomes]
rs1564932	0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16873090	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16873092	1.00[EUR][1000 genomes]
rs16873095	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16873108	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16873110	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16873118	1.00[EUR][1000 genomes]
rs16873127	1.00[EUR][1000 genomes]
rs16873134	1.00[EUR][1000 genomes]
rs28410729	1.00[EUR][1000 genomes]
rs28414388	1.00[EUR][1000 genomes]
rs28463277	1.00[EUR][1000 genomes]
rs28592887	1.00[EUR][1000 genomes]
rs36090352	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4582135	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4697024	1.00[EUR][1000 genomes]
rs4697334	1.00[EUR][1000 genomes]
rs55815743	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs57088167	1.00[EUR][1000 genomes]
rs57398192	1.00[EUR][1000 genomes]
rs57472271	1.00[EUR][1000 genomes]
rs58082212	1.00[EUR][1000 genomes]
rs58772986	1.00[EUR][1000 genomes]
rs60669573	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61233864	1.00[EUR][1000 genomes]
rs61534097	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73111623	1.00[EUR][1000 genomes]
rs73801159	0.95[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73801171	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73801174	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73801175	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73801176	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73801177	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73801178	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73801179	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73801182	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73801184	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73803308	1.00[EUR][1000 genomes]
rs73803310	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73803311	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73803314	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73803315	0.98[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73803316	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7688368	1.00[EUR][1000 genomes]
rs9997684	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3349061	chr4:22379581-22887563	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv821634	chr4:22427074-22865948	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv829883	chr4:22666326-22842517	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:22702600-22752600	Weak transcription	Fetal Intestine Small	intestine
2	chr4:22717800-22753800	Weak transcription	Fetal Intestine Large	intestine
3	chr4:22739400-22750600	Weak transcription	Duodenum Mucosa	Duodenum
4	chr4:22746200-22747000	Strong transcription	Liver	Liver

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