Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10165672	0.83[AMR][1000 genomes]
rs10166050	0.83[AMR][1000 genomes]
rs10202374	0.83[AMR][1000 genomes]
rs13389257	1.00[EUR][1000 genomes]
rs13396099	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13398499	1.00[EUR][1000 genomes]
rs13401849	0.83[AMR][1000 genomes]
rs13408350	0.83[AMR][1000 genomes]
rs13421608	0.83[AMR][1000 genomes]
rs13424203	1.00[EUR][1000 genomes]
rs13427586	1.00[EUR][1000 genomes]
rs13428678	1.00[EUR][1000 genomes]
rs17047868	1.00[EUR][1000 genomes]
rs28530709	1.00[EUR][1000 genomes]
rs28723570	1.00[EUR][1000 genomes]
rs4287805	1.00[EUR][1000 genomes]
rs56274428	1.00[EUR][1000 genomes]
rs57138748	1.00[EUR][1000 genomes]
rs6736677	1.00[EUR][1000 genomes]
rs7355401	1.00[EUR][1000 genomes]
rs73940673	1.00[EUR][1000 genomes]
rs73940701	1.00[EUR][1000 genomes]
rs73940702	1.00[EUR][1000 genomes]
rs7570781	0.85[AMR][1000 genomes]
rs7576776	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530516	chr2:56447922-56633505	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv834093	chr2:56538097-56708677	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1004449	chr2:56538460-56715861	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv874171	chr2:56545845-56727178	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv522944	chr2:56603985-56676997	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv1806915	chr2:56607397-56633217	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3426994	chr2:56615848-56617796	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:56612200-56617200	Weak transcription	Muscle Satellite Cultured Cells	--

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