chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
16593341065933411GT20GENIChomozygous144243609
16593825365938254A5GENIChomozygous135410281
16593604465936045AC38GENIChomozygous148661240
16593685065936858CTCCCTCC10GENIChomozygous148655667
16594033965940339T40GENIChomozygous147891173
16594260965942610CA21GENIChomozygous148661241
16594393065943931GA36GENIChomozygous148661242
16594679865946799GA28GENIChomozygous144243635
16594946665949467CA8GENICheterozygous147860638
16595673565956736TC33GENIChomozygous148661243
16595674065956741AG37GENIChomozygous144243643
16595813365958134AC38GENIChomozygous144243646
16595813465958135AC38GENIChomozygous144243647
16596139465961402AGATGGCC32GENIChomozygous148655668
16596312565963126GA51GENIChomozygous148661244
16596382265963823GA38GENIChomozygous148661245
16596403365964034TC43GENIChomozygous148661246
16596493865964938CTC30GENIChomozygous144226979
16596588465965885CT13GENICpossibly homozygous148661247
16596691565966916CT37GENIChomozygous148661248
16596968865969703CCGACAGTGTAGCAT43GENIChomozygous148655669
16596878265968783GA28GENIChomozygous147913652
16596920665969207CT49GENIChomozygous148661249