chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4232665984232665988GTGT----2GENIChomozygous687345663
4232666879232666880TG26GENICheterozygous514743650
4232671250232671251T-12GENICheterozygous687345664
4232679980232679981T-14GENICheterozygous687345665
4232699094232699098TGTG----7GENICheterozygous687345666
4232699096232699098TG--7GENICpossibly homozygous687345667
4232712797232712798CCAA18GENIChomozygous687345668
4232712799232712800CCGGACTTTTATTTAA12GENIChomozygous687345669
4232722869232722870TG29GENICheterozygous514743651
4232725449232725450G-18GENIChomozygous687345670
4232725452232725453A-18GENICpossibly homozygous687345671
4232725454232725455AT18GENIChomozygous514743652
4232725455232725456GGTC18GENIChomozygous687345672
4232727292232727293T-13GENICheterozygous687345673
4232728011232728012AAC10GENICpossibly homozygous687345674
4232728013232728014T-8GENICheterozygous687345676
4232747081232747082AG26GENIChomozygous514743653