chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212655812212655813GA5GENICheterozygous596181504
1212658705212658706GA16GENIChomozygous596181505
1212659762212659763TG22GENIChomozygous596181506
1212659968212659969AAT2GENIChomozygous726388558
1212661571212661572GT6GENIChomozygous596181507
1212663465212663466CT21GENIChomozygous596181508
1212664831212664832CT18GENIChomozygous596181509
1212666283212666284AG12GENIChomozygous596181510
1212666736212666737CCAG3GENICheterozygous726388559
1212669279212669280TC20GENIChomozygous596181511
1212669743212669744AG26GENICpossibly homozygous596181512
1212670030212670031AG20GENIChomozygous596181513
1212670346212670347CG21GENIChomozygous596181514
1212671116212671117CT15GENICpossibly homozygous596181515
1212674420212674421GA21GENIChomozygous596181516
1212674751212674752T-6GENIChomozygous726388560
1212676526212676527GA21GENIChomozygous596181517
1212680462212680463CT36GENIChomozygous596181518
1212681105212681229AAAAACACGTGAGTCCGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA----------------------------------------------------------------------------------------------------------------------------2GENICheterozygous726388561
1212685080212685081GA33GENIChomozygous596181519
1212688791212688792TC30GENICpossibly homozygous596181520