chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
35605784456057845GT30GENIChomozygous111577718
35605977756059778TC25GENIChomozygous111577719
35605986456059865AG28GENIChomozygous111577720
35606007156060072CA35GENIChomozygous111577721
35606031556060316CT49GENIChomozygous111577722
35606031856060319GA49GENIChomozygous111577723
35606033056060331CT50GENIChomozygous111577724
35606059256060593GA25GENIChomozygous111577725
35606233256062333CG28GENIChomozygous111577726
35606280556062806TC32GENIChomozygous111577727
35606396656063967CG28GENIChomozygous111577728
35606419356064194GA26GENIChomozygous111577729
35606491656064917AG46GENIChomozygous111577730
35606532756065328CT21GENICheterozygous111909921
35606533156065332CT22GENICpossibly homozygous111577731
35606538556065386GA25GENIChomozygous111909922
35606549356065494CT28GENIChomozygous111577732
35606557356065574GA30GENIChomozygous111577733
35606697756066978TC36GENIChomozygous111577734
35606790256067903GA26GENIChomozygous111577735
35606870156068702AG21GENIChomozygous111577736
35606894156068942TC39GENIChomozygous111577737
35606912356069124GA30GENIChomozygous111577738
35606960956069610TC34GENIChomozygous111577739
35607013156070132GA42GENIChomozygous111577740
35607025756070258GT43GENIChomozygous111577741