chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108236008108236009CA12GENICheterozygous52271378
10108236930108236931TC10GENICheterozygous51953274
10108237345108237346CT14GENICheterozygous52271380
10108237588108237589TC9GENICheterozygous51953280
10108238118108238119GA15GENICheterozygous51953283
10108238334108238335GA12GENICheterozygous51953286
10108239007108239008CT15GENICheterozygous51953293
10108240233108240234AAG12GENICheterozygous51953299
10108240637108240638GA15GENICheterozygous51953305
10108240787108240788GA12GENICheterozygous51953308
10108240909108240910AG13GENIChomozygous51595337
10108241442108241443GA13GENICheterozygous51953311
10108241598108241599TC11GENICheterozygous51953314
10108241604108241605TC10GENIChomozygous51595339
10108241614108241615GA10GENICheterozygous52271384
10108242408108242409GC13GENICheterozygous51953320
10108245738108245739GA11GENICheterozygous51953323
10108246353108246354GA12GENICheterozygous51953326
10108246885108246886AC10GENIChomozygous51595343
10108248787108248788GA13GENICheterozygous51953329
10108249366108249367AG10GENIChomozygous51595347
10108249539108249540CA16GENIChomozygous51595350
10108249637108249638AG16GENICheterozygous51953332
10108249640108249641AG15GENICheterozygous51953335
10108249701108249702CCCGAT10GENICheterozygous51953338
10108250758108250762AACA----11GENICheterozygous52331681
10108250761108250762AATGTT11GENICheterozygous52331683
10108250781108250782GA16GENICheterozygous51953355