Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10487183	1.00[YRI][hapmap]
rs11982003	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs11984388	0.82[CEU][hapmap]
rs12705177	0.81[CEU][hapmap]
rs17324209	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs194836	0.81[CEU][hapmap]
rs194840	0.82[CEU][hapmap]
rs194842	0.81[CEU][hapmap]
rs194850	0.82[CEU][hapmap]
rs194853	0.82[CEU][hapmap]
rs194854	0.82[CEU][hapmap]
rs2299407	0.81[CEU][hapmap]
rs3808011	0.82[CEU][hapmap]
rs3808012	0.81[CEU][hapmap]
rs3808013	0.81[CEU][hapmap]
rs4305831	1.00[YRI][hapmap]
rs4729960	0.86[CEU][hapmap]
rs55848	0.82[CEU][hapmap]
rs62485872	0.88[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs62485875	0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs62485876	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6944360	0.82[CEU][hapmap]
rs6952639	0.80[CEU][hapmap]
rs6979022	0.82[CEU][hapmap]
rs6979695	0.82[CEU][hapmap]
rs9641322	0.85[CEU][hapmap]

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	nsv888924	chr7:103637906-103706936	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1018253	chr7:103669491-103731850	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103679600-103688600	Weak transcription	HepG2	liver
2	chr7:103680000-103689200	Weak transcription	K562	blood

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