chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1218419369218419370AT14GENIChomozygous61967106
1218420290218420291CT30GENICpossibly homozygous61967107
1218420400218420401AT32GENIChomozygous61592504
1218421196218421197TG32GENIChomozygous61592505
1218421615218421616GA24GENICpossibly homozygous61967108
1218422728218422729GGATTA29GENIChomozygous61087819
1218422941218422942CT27GENIChomozygous61967109
1218422950218422951GA24GENIChomozygous61967110
1218425800218425804AAAT----12GENIChomozygous61087822
1218427629218427630TTCA7GENICpossibly homozygous61087830
1218427901218427902GA15GENICheterozygous61087832
1218432431218432432C-7GENICheterozygous61087862
1218435137218435139AC--18GENICpossibly homozygous61592522
1218437268218437269CCA13GENIChomozygous61087889
1218442122218442123C-4GENICheterozygous61592529
1218442129218442130CCT2GENICheterozygous61087898
1218442227218442228AC36GENICheterozygous61087900
1218442233218442235CA--28GENICheterozygous61087901
1218445280218445293TTGGTTGGTTGGT-------------15GENICheterozygous61592537
1218445805218445806T-2GENICheterozygous61087919
1218445891218445892CG18GENICheterozygous61087920
1218447378218447379TTGGGG6INTERGENIChomozygous61320849