chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135708360135708361CT30GENIChomozygous59635720
4135709620135709622AG--4GENICheterozygous58338648
4135711624135711625CCAG7GENICpossibly homozygous59635722
4135711662135711663CG27GENICpossibly homozygous56939073
4135712585135712586GA16GENIChomozygous57338441
4135712758135712759GT28GENIChomozygous59635724
4135713257135713258CT13GENIChomozygous56939075
4135714639135714640GA11GENIChomozygous56939078
4135714791135714792CT26GENIChomozygous56939079
4135715426135715452ACACACACACACACACACACACACAC--------------------------15GENIChomozygous59635726
4135715926135715927TC22GENIChomozygous56939081
4135716097135716098CA21GENIChomozygous56939082
4135716661135716666CAGTT-----19GENIChomozygous57338449
4135717331135717332AT20GENIChomozygous59635728
4135719827135719828G-28GENICpossibly homozygous57338453
4135719869135719870TC21GENIChomozygous57338455
4135720510135720511TTA21GENIChomozygous57338457
4135720528135720534CGATCA------28GENIChomozygous57338459
4135720895135720896TC28GENIChomozygous57338469
4135721169135721170AG22GENIChomozygous57338471