chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116755929967559300TC41GENIChomozygous50809228
116756112467561125GGTC4GENICheterozygous50809230
116756546267565463GT9GENICheterozygous50883628
116756675167566752G-27GENIChomozygous50809232
116756783367567834G-17GENIChomozygous50809235
116757029767570298TC31GENIChomozygous50809237
116757088967570890AAGG26GENIChomozygous50809241
116757124167571242TA37GENIChomozygous50809242
116757396067573961TC24GENIChomozygous50809244
116758118167581183CA--20GENIChomozygous50809246
116758199867581999T-20GENIChomozygous50809247
116758311967583120A-19GENICheterozygous50883694
116758350067583501AT36GENIChomozygous50809249
116758362967583633GTGT----17GENICheterozygous50809251
116758363167583633GT--17GENICheterozygous50809253
116758463967584645AGAGAG------13GENICheterozygous50809255
116758464167584645AGAG----13GENICheterozygous50809257
116758496867584969CCAA7GENICheterozygous50809259
116758554767585548A-11GENICheterozygous50809261
116758591467585915TC32GENIChomozygous50809262
116758601267586013TC22GENIChomozygous50809264
116758619167586192TC31GENIChomozygous50809266
116758622667586227CT29GENIChomozygous50809268
116758628767586288CT26GENIChomozygous50809270
116758643567586436CT30GENIChomozygous50809272