chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55742392257423923TC16GENIChomozygous113815253
55742411957424120AG22GENIChomozygous113815255
55742445757424458TC20GENIChomozygous113815259
55742457957424580GT13GENIChomozygous113815263
55742458157424582AG13GENIChomozygous113815265
55742465157424652AG16GENIChomozygous113815267
55742566557425666GT28GENICpossibly homozygous113815269
55742582957425830CT22GENICpossibly homozygous113815271
55742612357426124TC33GENICpossibly homozygous113815274
55742616757426168CT30GENIChomozygous113815276
55742658457426585TC33GENIChomozygous113815278
55742672257426723AG37GENIChomozygous113815280
55742680057426801CT36GENICheterozygous114205618
55742706657427067CT28GENIChomozygous113815282
55742717457427175AC24GENIChomozygous113815284
55742747057427471TG21GENICpossibly homozygous118842916
55742769357427694GT36GENIChomozygous113815286
55742785857427859TC27GENIChomozygous113815288
55742800257428003TC21GENIChomozygous113815290
55742814657428147GA16GENIChomozygous118842917
55742867357428674CG23GENIChomozygous113815292
55742873257428733CT27GENIChomozygous113815294
55742887157428872CT26GENIChomozygous113815296
55742888857428889TA26GENIChomozygous113815298