chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84001631540016316CCTT3GENIChomozygous52963640
84001633440016335CCTTTTTTTTTTTTTT1GENIChomozygous53378295
84001795640017957AG15GENIChomozygous52963642
84001831140018312TA28GENIChomozygous52963643
84001840740018411AAAA----8GENICheterozygous52592035
84001840840018411AAA---8GENICheterozygous52592036
84001861040018611AT27GENIChomozygous52963644
84001864040018641TTTGCCTCTATGGG39GENIChomozygous52592037
84001909940019100CT15GENIChomozygous52963645
84001972740019728TC18GENIChomozygous52963646
84001982640019827GGTT13GENIChomozygous52963647
84002005440020055GGT18GENIChomozygous52963648
84002006940020070CCTT7GENICheterozygous52963649
84002006940020070CCTTTT7GENICheterozygous53378297
84002046040020461GA23GENIChomozygous52963650
84002086340020864CT15GENIChomozygous52963651
84002097640020977AG16GENIChomozygous52963652
84002122940021230CT22GENIChomozygous52963653
84002264840022649TTG8GENICheterozygous52592042
84002264840022649TTGG8GENICpossibly homozygous52963654
84002267640022677AG12GENIChomozygous52963655
84002283140022832GA21GENIChomozygous52963656
84002300140023002GA17GENIChomozygous52592043
84002315440023155TC15GENIChomozygous52963657
84002330740023308AG21GENIChomozygous52592044
84002348640023487TC12GENIChomozygous52963658
84002371940023720AG5GENIChomozygous52592045