chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887210140887211TG12GENIChomozygous784949372
4140887405140887406GC21GENIChomozygous784949373
4140887526140887527AG23GENIChomozygous784949374
4140887695140887696GA24GENIChomozygous784949375
4140888161140888162GT20GENIChomozygous784949376
4140894149140894150GA18GENIChomozygous784949377
4140896329140896330TC21GENICheterozygous784949378
4140896988140896989GA20GENIChomozygous784949379
4140897414140897415CT22GENIChomozygous784949380
4140902715140902716TC24GENIChomozygous784949381
4140902957140902958AG30GENIChomozygous784949382
4140903807140903808CT25GENIChomozygous784949383
4140906350140906351AG27GENIChomozygous784949384
4140906395140906396AG26GENIChomozygous784949385
4140908274140908275TG25GENIChomozygous784949386
4140908798140908799AG21GENIChomozygous784949387
4140908994140908995GC25GENIChomozygous784949388
4140909196140909197CT26GENIChomozygous784949389
4140909244140909245GT29GENIChomozygous784949390
4140909248140909249TA31GENIChomozygous784949391
4140916630140916631TG22GENIChomozygous784949392
4140916631140916632CA22GENIChomozygous784949393
4140916796140916797CG14GENIChomozygous784949394