chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1259079643259079644G-27GENICheterozygous62655794
1259094923259094925AC--15GENICheterozygous62212255
1259110136259110138CA--8GENICheterozygous62251198
1259116823259116827CTGT----12GENIChomozygous62212257
1259133374259133375TTAC11GENICheterozygous62596395
1259133377259133379AC--11GENICheterozygous62241724
1259096133259096134CCATTT15GENICpossibly homozygous61930190
1259103768259103769C-28GENICheterozygous62110923
1259123380259123384AAAT----8GENIChomozygous62356347
1259152159259152161CA--15GENICheterozygous62212261
1259158448259158449AG29GENIChomozygous61174943
1259163045259163046CCT19GENICpossibly homozygous61329441
1259178853259178854AAGGGCAGCACCCCGCGAG2GENICheterozygous62241725
1259184396259184397GA16GENIChomozygous61175120
1259199513259199515GT--14GENICheterozygous62212263
1259224898259224900TG--16GENICheterozygous62241727
1259231117259231118CCG20GENICheterozygous62557987
1259231123259231124CCA20GENICheterozygous62557988
1259240257259240258GGT4GENIChomozygous62212265
1259240258259240259GGCTTGCT5GENIChomozygous62212267
1259240261259240262AG5GENIChomozygous62212269
1259240265259240266AG5GENIChomozygous62212271
1259240270259240271TC4GENIChomozygous62212273
1259240271259240272TTACCAC4GENIChomozygous62212275
1259250787259250789CA--27GENICheterozygous62251200
1259281589259281590TC30GENICheterozygous61175396
1259286781259286782TC25GENIChomozygous61175419
1259294664259294665CCCAA6GENICheterozygous61175444
1259310404259310406AC--7GENICheterozygous61329612