chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1212658705212658706GA10GENIChomozygous668383595
1212659762212659763TG19GENIChomozygous668383596
1212659968212659969AAT3GENIChomozygous768126726
1212661571212661572GT12GENICpossibly homozygous668383597
1212663465212663466CT22GENIChomozygous668383598
1212664831212664832CT11GENIChomozygous668383599
1212666283212666284AG14GENIChomozygous668383600
1212666736212666737CCAG3GENICheterozygous768126727
1212669279212669280TC19GENIChomozygous668383601
1212669743212669744AG29GENIChomozygous668383602
1212670030212670031AG33GENIChomozygous668383603
1212670346212670347CG12GENIChomozygous668383604
1212671116212671117CT16GENICpossibly homozygous668383605
1212674420212674421GA21GENICpossibly homozygous668383606
1212674751212674752T-3GENIChomozygous768126728
1212676526212676527GA16GENIChomozygous668383607
1212680462212680463CT24GENICpossibly homozygous668383608
1212681105212681229AAAAACACGTGAGTCCGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA----------------------------------------------------------------------------------------------------------------------------1GENIChomozygous768126729
1212685080212685081GA26GENICheterozygous668383609
1212688791212688792TC19GENICpossibly homozygous668383610