chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106645853766458538TC17GENIChomozygous51908217
106645960166459602GGA11GENIChomozygous51908219
106645983266459833A-15GENIChomozygous51908221
106646045866460459CT23GENIChomozygous51479799
106646065966460660C-16GENIChomozygous51678751
106646104666461047CCTTTT7GENIChomozygous51908223
106646129566461296GA21GENIChomozygous51908225
106646209866462099T-8GENIChomozygous51987873
106646248866462490TT--4GENICheterozygous51908227
106646454466464545G-30GENIChomozygous51479801
106646464066464641CT22GENIChomozygous51908228
106646475866464759TTA11GENIChomozygous51479802
106646536266465363TA12GENIChomozygous51908232
106646548166465482AAGT5GENIChomozygous51908234
106646628666466287AAC1GENIChomozygous51479804
106646902666469027TTATTC6GENIChomozygous51908236
106646919266469193GGT10GENIChomozygous51479810
106646930166469302TA1GENIChomozygous52320389
106646479766464798CCAG15GENIChomozygous52382704
106646628866466289AC1GENIChomozygous52382706