chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
62520715725207158CT59GENIChomozygous70172184
62521066825210669CT15GENIChomozygous70172187
62521067825210679AG13GENIChomozygous70172190
62521068325210684TC12GENIChomozygous70172193
62521083825210839GT31GENICpossibly homozygous70172195
62521088525210886AG40GENIChomozygous70172198
62521162525211626GT20GENIChomozygous70172201
62521163425211635GT20GENIChomozygous70172204
62521163625211637GT19GENIChomozygous70172207
62521208825212089CT33GENICheterozygous70172210
62521426025214261CA37GENICheterozygous70172213
62521437925214380GA49GENICheterozygous70172216
62521438125214382TC75GENICheterozygous70172219
62521438225214383CT75GENICheterozygous70172222
62521441325214414GA82GENICheterozygous70172225
62521450225214503GA56GENICheterozygous70172228
62521452125214522TC44GENICheterozygous70172231