chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1526788192678820T-6GENIChomozygous49024143
1526788202678821AATGGCTCAGCG6GENIChomozygous49024145
1526788222678823TTTAAGAGCA5GENIChomozygous49024148
1526788242678825CCCGACTGCTCTT5GENIChomozygous49024150
1526804122680413CCTTCGCCGGA14GENIChomozygous48222368
1526804322680433CCT6GENICheterozygous48222370
1526804392680440CT6GENIChomozygous49024156
1526804462680447AAT8GENIChomozygous48222372
1526804502680451GGT8GENIChomozygous48222373
1526805322680533AG9GENIChomozygous48222374
1526806372680638CG15GENIChomozygous48222376
1526808122680813G-24GENIChomozygous48222378
1526808142680815AAG24GENIChomozygous48222379
1526944762694478TC--17GENIChomozygous48222403
1526960602696064AAAG----4GENIChomozygous49024168
1526960652696069TACA----1GENIChomozygous49219966
1526960702696072CC--2GENIChomozygous49024170
1526960762696084ACACTAGT--------4GENIChomozygous49024172
1526986202698621AATTTTTG4GENICheterozygous49024176
1526986732698674AATTT3GENIChomozygous49078656
1527054612705465AAAG----6GENICheterozygous49413900