chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107078075370780754CCT18GENIChomozygous51489241
107078077670780777AAC21GENIChomozygous52384089
107078078770780788TTTC22GENIChomozygous52384091
107078079270780793TTA26GENIChomozygous51489242
107078080270780803GGA23GENIChomozygous51489243
107078081470780817AAC---23GENIChomozygous52384093
107078081670780817CCTG23GENIChomozygous52384095
107078082070780821A-24GENIChomozygous51489245
107078082370780824CG23GENIChomozygous51689426
107078259870782599A-10GENICheterozygous51489250
107078287570782876A-19GENIChomozygous51489253
107078528670785287TTA26GENIChomozygous51489266
107078529770785298C-29GENIChomozygous51489267
107079042670790427C-28GENIChomozygous51489294
107079347570793477TG--6GENICheterozygous52504087
107081202270812023T-14GENICheterozygous52461236
107082609770826098TC17GENICpossibly homozygous51689446
107082613170826132C-18GENIChomozygous51489396