chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5156391348156391349CCT10GENIChomozygous56462075
5156391351156391352TTCC10GENIChomozygous56462076
5156391361156391362AAC8GENIChomozygous55804300
5156391372156391373AAC8GENIChomozygous55804301
5156391406156391407AG11GENIChomozygous55804302
5156391407156391408AT11GENIChomozygous55804303
5156391420156391421AT10GENIChomozygous55804304
5156391482156391483AT13GENIChomozygous55804305
5156391505156391506C-3GENIChomozygous55804306
5156395099156395101AA--6GENICheterozygous56495238
5156395100156395101A-6GENICheterozygous56462077
5156395931156395933GT--4GENICheterozygous56462078
5156398733156398734CCTTTTTTTTTTT10GENICpossibly homozygous56462079
5156400089156400090CCTGTGTG17GENICheterozygous56580349
5156400090156400092TG--17GENICheterozygous56495240
5156407566156407567CCAT16GENICheterozygous55804309
5156407566156407567CCATATATAT16GENICheterozygous56619195