Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10863758	0.85[EUR][1000 genomes]
rs10863761	0.85[EUR][1000 genomes]
rs11119231	0.86[EUR][1000 genomes]
rs11119232	0.85[EUR][1000 genomes]
rs11119233	0.85[EUR][1000 genomes]
rs11581106	0.84[EUR][1000 genomes]
rs12077139	0.85[EUR][1000 genomes]
rs1933598	0.84[EUR][1000 genomes]
rs1933606	0.85[EUR][1000 genomes]
rs1933614	0.85[EUR][1000 genomes]
rs4382726	0.94[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4391667	0.86[EUR][1000 genomes]
rs4844776	0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4844779	0.86[EUR][1000 genomes]
rs4844780	0.85[EUR][1000 genomes]
rs4844781	0.83[EUR][1000 genomes]
rs6540522	0.85[EUR][1000 genomes]
rs6676230	0.84[EUR][1000 genomes]
rs6687541	0.85[EUR][1000 genomes]
rs6703480	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv873137	chr1:209301571-209338673	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv522816	chr1:209325038-209342622	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region lncRNA	2 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	chr1:209329600-209335800	Weak transcription	HSMM	muscle
2	chr1:209334000-209335000	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr1:209334200-209335600	Weak transcription	HSMMtube	muscle
4	chr1:209334200-209335800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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