chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101891144418911462ATCATCATCATCATCATC------------------12GENIChomozygous51630215
101891148218911483CG26GENICheterozygous51630216
101891274718912748CT3GENICheterozygous51337776
101891278318912784CT5GENICheterozygous51630217
101891279518912796TC8GENICheterozygous52030550
101891280118912802CT9GENICheterozygous51630218
101891280718912808TC8GENICheterozygous51816850
101891284918912850TC10GENICheterozygous52030552
101891297318912974TC14GENICheterozygous51630219
101891299718912998CT14GENICheterozygous51816860
101891302118913022TC16GENICheterozygous51337779
101891302718913028TC20GENICheterozygous51337780
101891303318913034CT18GENICheterozygous51337781
101891382918913831AA--17GENICheterozygous51630222
101891383018913831A-17GENICpossibly homozygous51630223
101891435018914351TA52GENIChomozygous51630224
101891467418914675GA35GENIChomozygous51630225
101891488318914884AG26GENIChomozygous51337789
101891494218914946GAAT----25GENIChomozygous51630226
101891496818914970AT--39GENICheterozygous51337792
101891497118914977AATGAA------38GENICheterozygous51337793
101891514518915146AAAG39GENIChomozygous51337795
101891599818915999TC33GENIChomozygous51337802
101891634818916349CT52GENIChomozygous51630227
101891704418917045GA47GENIChomozygous51630228
101891868918918690GA45GENICheterozygous51337817
101891869218918693GA49GENICheterozygous51337818
101891893118918932AG29GENIChomozygous51337821
101891903118919032GT46GENIChomozygous51630229
101891904218919043AG46GENIChomozygous51630230
101892025318920254GA39GENIChomozygous51630231
101892058618920587CT56GENIChomozygous51630232
101892107118921072CT36GENIChomozygous51337831
101892111318921117ACAC----14GENICheterozygous51630233
101892111518921117AC--14GENICpossibly homozygous51630234
101892114118921143GC--15GENICheterozygous51337834
101892157118921572TC31GENIChomozygous51337837
101892275218922753GA43INTERGENIChomozygous51630235