chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1816973861697387AT49GENIChomozygous147159414
1816978961697897AG38GENIChomozygous144190857
1816984971698500CAT56GENIChomozygous147155421
1816988191698820TG40GENIChomozygous142637675
1816990811699082TC53GENIChomozygous142637679
1816996451699646GT47GENIChomozygous142637686
1817002061700207AG48GENIChomozygous147159415
1817002281700229CT51GENIChomozygous142637691
1817006101700611CT36GENIChomozygous142637692
1816981371698137AGG54GENIChomozygous142627470
1816982231698224A42GENIChomozygous142627471
1817009771700979AT29GENIChomozygous147155422
1817020251702061ACACTTACCATTGAGTCGTGTCTCTGGCCCCTGAAA51GENIChomozygous147155423
1817025151702516TC36GENIChomozygous142637699
1817027671702768TC28GENIChomozygous142637701
1817027801702781GA29GENIChomozygous144190860
1817033141703315GA37GENIChomozygous142637705
1817040711704072GA42GENIChomozygous147159416
1817040931704094TG41GENIChomozygous142637710
1817041671704168TC38GENIChomozygous142637711
1817050451705046G34GENIChomozygous142627475
1817056371705639GT29GENIChomozygous144185247
1817059211705922AG26GENIChomozygous142637722
1817062161706217CT33GENIChomozygous147159417
1817072361707237CG50GENIChomozygous142637724
1817014071701408TA51GENIChomozygous148790411