chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121351511121351512AC24GENIChomozygous790188403
7121351659121351660AG20GENIChomozygous790188404
7121351666121351667GA20GENIChomozygous790188405
7121352112121352113AG26GENIChomozygous790188406
7121352821121352822AG23GENIChomozygous790188407
7121353851121353852AT20GENIChomozygous790188408
7121355445121355446TA18GENICpossibly homozygous790188409
7121357005121357006TG40GENIChomozygous790188410
7121357109121357110GA27GENICpossibly homozygous790188411
7121357662121357663CT31GENIChomozygous790188412
7121361246121361247GA18GENICheterozygous790188413
7121361280121361281CT10GENICpossibly homozygous790188414
7121364262121364263TC10GENIChomozygous790188415
7121370431121370432TC34GENIChomozygous790188416
7121370670121370671GA20GENIChomozygous790188417
7121372869121372870TC28GENIChomozygous790188418
7121374131121374132AG44GENIChomozygous790188419
7121376034121376035GA39GENIChomozygous790188420
7121376233121376234TC22GENIChomozygous790188421
7121377012121377013GA26GENIChomozygous790188422
7121377413121377414AG26GENIChomozygous790188423
7121378332121378333TC28GENIChomozygous790188424
7121378486121378487GA39GENIChomozygous790188425
7121378756121378757TC28GENIChomozygous790188426
7121380634121380635TC42GENIChomozygous790188427
7121381943121381944TC46GENIChomozygous790188428