chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117215131117215132AG47GENIChomozygous112818305
4117216867117216868GA73GENIChomozygous112818307
4117217476117217477CT56GENIChomozygous112818309
4117217548117217565CACCGGATAAAGCCTAG67GENIChomozygous128072510
4117217832117217833TC48GENIChomozygous112818311
4117219725117219726TG44GENIChomozygous112818315
4117220593117220595GT41GENIChomozygous128072511
4117221254117221255TC61GENIChomozygous112818317
4117222794117222795AG47GENIChomozygous112818319
4117220604117220605TC40GENIChomozygous113048274
4117226184117226185AG37GENIChomozygous112818321
4117227533117227534TC54GENIChomozygous112818323
4117227666117227667GA31GENIChomozygous112818325
4117228158117228159GA49GENIChomozygous112818327
4117228447117228448T49GENIChomozygous128072512