chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4232665984232665988GTGT----1GENIChomozygous695547388
4232666879232666880TG29GENICheterozygous536611205
4232671250232671251T-22GENICheterozygous695547389
4232684545232684546CG41GENICheterozygous536611206
4232699096232699098TG--19GENICheterozygous695547391
4232712797232712798CCAA34GENIChomozygous695547392
4232712799232712800CCGGACTTTTATTTAA18GENICpossibly homozygous695547393
4232722869232722870TG51GENICheterozygous536611207
4232725449232725450G-22GENIChomozygous695547394
4232725452232725453A-19GENIChomozygous695547395
4232725454232725455AT19GENIChomozygous536611208
4232725455232725456GGTC19GENIChomozygous695547396
4232728011232728012A-20GENICheterozygous695547397
4232728011232728012AAC19GENICpossibly homozygous695547398
4232728013232728014T-9GENIChomozygous695547400
4232747081232747082AG45GENIChomozygous536611209