chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79962624799626248AG17GENIChomozygous896230221
79962781099627811AG10GENIChomozygous896230222
79962932399629324CG27GENIChomozygous896230223
79963048599630486AC21GENIChomozygous896230224
79963077699630777GA23GENIChomozygous896230225
79963276699632767CT21GENIChomozygous896230226
79963354999633550CG26GENIChomozygous896230227
79963494799634948TC12GENIChomozygous896230228
79963561799635618CT17GENIChomozygous896230229
79963574199635742CG12GENIChomozygous896230230
79963580699635807TC11GENIChomozygous896230231
79963718599637186CT15GENIChomozygous896230232
79963932799639328AG21GENIChomozygous896230233
79963952299639523CG10GENIChomozygous896230234
79964003299640033TA7GENICheterozygous896230235
79964114399641144CA19GENIChomozygous896230236
79964581299645813AT17GENIChomozygous896230237
79965331599653316AG19GENIChomozygous896230238
79965548599655486AG4GENIChomozygous896230239
79965804199658042CT13GENIChomozygous896230240
79965822799658228CT16GENIChomozygous896230241
79965867699658677CT22GENIChomozygous896230242
79967021699670217AC16GENIChomozygous896230243
79967094699670947TC17GENICheterozygous896230244
79967147199671472TC32GENIChomozygous896230245
79967227699672277CT15GENIChomozygous896230246
79967241699672417GA22GENIChomozygous896230247
79967301499673015CT26GENIChomozygous896230248
79967466099674661AC6GENICheterozygous896230249
79967477899674779AC22GENICheterozygous896230250
79967486299674863CA19GENICheterozygous896230251
79967489099674891TG22GENIChomozygous896230252
79967523299675233CG24GENICheterozygous896230253
79967527799675278TC23GENICheterozygous896230254
79967533699675337GA21GENICheterozygous896230255
79967552999675530AT5GENIChomozygous896230256
79967648799676488TC19GENIChomozygous896230257