chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105527545055275460CTCTCTCTCT----------11GENICheterozygous51459315
105527545255275460CTCTCTCT--------11GENICheterozygous51459316
105527659955276600CT46GENIChomozygous51459317
105527948355279484CCT15GENIChomozygous51459318
105527949255279493TTC19GENIChomozygous51459319
105528017655280180AAGA----25GENIChomozygous51459320
105528025455280255TG31GENICheterozygous51889562
105528082455280828AAAA----1GENIChomozygous51459321
105528094255280943AG34GENIChomozygous51459322
105528104155281042TA40GENIChomozygous51652629
105528111955281120T-2GENIChomozygous51459323
105528131355281314CT39GENIChomozygous51459324
105528172155281723TT--25GENIChomozygous51459325
105528181555281816CT22GENICheterozygous51459326
105528212455282125GA54GENIChomozygous51459327
105528224355282244GGT46GENIChomozygous51459328
105528354255283549CACTATA-------15GENICheterozygous51652637
105528359455283595CT33GENIChomozygous51652639
105528392355283924GT33GENICpossibly homozygous51652641
105528400055284004AAAA----13GENIChomozygous51459329
105528402055284021AAAATGAATG7GENIChomozygous51652643
105528404455284045GA21GENICheterozygous51652645
105528404455284045GGAATGAATA18GENIChomozygous51652647
105528417855284181AAA---21GENIChomozygous51459334
105528716455287165AG54GENIChomozygous51652649
105528742455287425CT32GENICpossibly homozygous51652651
105528783155287832TC36GENIChomozygous51459337