chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1157676912157676913AG17GENIChomozygous108326220
1157680180157680181GA18GENIChomozygous108326232
1157682328157682329GA28GENIChomozygous108326236
1157685343157685344GT18GENIChomozygous108326248
1157686788157686789AC21GENIChomozygous109154455
1157687730157687731CT20GENIChomozygous108326256
1157688031157688032TC24GENIChomozygous109154457
1157688655157688656AT22GENIChomozygous109154459
1157689678157689679CT20GENIChomozygous108326266
1157689681157689682TC21GENIChomozygous108326268
1157691380157691381TC23GENIChomozygous108326280
1157692585157692586T14GENIChomozygous127449237
1157693797157693798AG26GENIChomozygous108326290
1157694162157694163AG19GENICheterozygous132446334
1157694163157694164TC19GENICheterozygous132446335
1157694450157694451AG20GENIChomozygous108326296
1157694468157694469AG22GENIChomozygous108326298
1157694795157694796AC19GENIChomozygous108326300
1157694848157694849CT19GENIChomozygous108326302
1157695737157695738GA15GENIChomozygous108326304
1157696116157696117TG21GENIChomozygous108326306
1157696118157696119TC21GENIChomozygous108326308
1157696144157696145TC20GENIChomozygous108326310
1157696363157696364AT17GENIChomozygous108326312
1157696440157696441TC21GENIChomozygous108326314
1157696907157696908CA23GENIChomozygous108326316
1157696977157696977ACCATA18GENIChomozygous127449239
1157697277157697278CT22GENIChomozygous108326318
1157697494157697495TC17GENIChomozygous108326320
1157699841157699842GA26GENIChomozygous108326323
1157699704157699705CT30GENIChomozygous120506807
1157688026157688030TTGT24GENIChomozygous131988928
1157693661157693661G19GENIChomozygous131988929
1157698328157698328C9GENIChomozygous131988930