Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10231405	0.85[EUR][1000 genomes]
rs10245317	0.85[EUR][1000 genomes]
rs10272697	0.85[EUR][1000 genomes]
rs10274911	0.85[EUR][1000 genomes]
rs12670967	0.83[EUR][1000 genomes]
rs1476927	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1476928	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17157216	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17157337	0.85[EUR][1000 genomes]
rs17269500	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2058503	0.86[EUR][1000 genomes]
rs2058504	0.85[EUR][1000 genomes]
rs2299401	0.84[EUR][1000 genomes]
rs2299403	0.85[EUR][1000 genomes]
rs41434053	0.88[EUR][1000 genomes]
rs56406130	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59078884	0.86[EUR][1000 genomes]
rs6465945	0.87[EUR][1000 genomes]
rs73183745	0.84[EUR][1000 genomes]
rs73183749	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73183755	0.85[EUR][1000 genomes]
rs7797395	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	esv1843940	chr7:103421702-103590285	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv523466	chr7:103547135-103567525	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103548400-103549600	Strong transcription	K562	blood
2	chr7:103548400-103549800	Strong transcription	HepG2	liver

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