chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107078075370780754CCT18GENIChomozygous51489241
107078077670780777AAC14GENIChomozygous52384089
107078078770780788TTTC16GENIChomozygous52384091
107078079270780793TTA15GENIChomozygous51489242
107078080270780803GGA15GENIChomozygous51489243
107078081470780817AAC---13GENIChomozygous52384093
107078081670780817CCTG12GENIChomozygous52384095
107078082070780821A-11GENIChomozygous51489245
107078082370780824CG11GENIChomozygous51689426
107078287570782876A-19GENIChomozygous51489253
107078528670785287TTA35GENIChomozygous51489266
107078529770785298C-38GENIChomozygous51489267
107078927270789273AAAC5GENICheterozygous51489287
107079042670790427C-29GENIChomozygous51489294
107078579170785792T-13GENICheterozygous52846563
107079347570793477TG--13GENICheterozygous52504087
107081202170812023TT--14GENICheterozygous51489361
107081202270812023T-14GENICheterozygous52461236
107082609770826098TC15GENIChomozygous51689446
107082613170826132C-13GENIChomozygous51489396