chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13105760024105760025TC15GENICheterozygous49976659
13105760417105760418TC9GENICheterozygous49976660
13105761149105761150GA12GENICheterozygous49976661
13105763722105763723TTAACC8GENICheterozygous49976664
13105764557105764558GGCAGA9GENICheterozygous49976666
13105764979105764980TG27GENICheterozygous49976667
13105767280105767281TA19GENIChomozygous49873882
13105767282105767283TC18GENIChomozygous49873883
13105768177105768179AC--10GENICheterozygous49873885
13105768857105768858TTGTCACAGCGGCGTCACGGGG12GENICheterozygous50597873
13105769147105769148TTC7GENICheterozygous49976670
13105769165105769166CCA10GENICheterozygous49976671
13105769169105769170CT10GENICheterozygous49976672
13105770143105770144CT14GENICheterozygous49976684
13105770947105770948GA11GENICheterozygous49976685
13105771043105771044CG8GENICheterozygous49976686
13105771383105771384AC11GENICheterozygous49976687
13105771550105771551CT12GENICheterozygous49976688
13105774338105774339AC10GENICheterozygous49976689
13105776006105776007CT16GENICheterozygous49976690
13105776190105776191TC15GENICheterozygous49976691
13105776328105776329AG17GENICheterozygous49976692
13105785531105785532CT14GENICheterozygous49976694
13105785887105785888AG16GENICheterozygous49976695
13105788585105788586T-7GENICheterozygous49976696
13105790610105790611GA18GENICheterozygous49976702
13105793358105793359AG17GENICheterozygous49976703
13105794181105794182CT10GENICheterozygous49976704
13105769299105769300T-10GENICheterozygous51257271
13105769301105769309ATCATCAT--------12GENICheterozygous51257273
13105787331105787332GA11GENICheterozygous51282079
13105807083105807084CT12GENICheterozygous49976726
13105807804105807805GGAGAGAGAGAA8GENICheterozygous50813631
13105808361105808362A-7GENICheterozygous51269798