chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
178476676384766764TC23GENIChomozygous140200450
178476696084766960A14GENIChomozygous140041625
178476750184767502T25GENICpossibly homozygous140041626
178476921184769212AG16GENIChomozygous140200451
178477668984776690TG10GENIChomozygous140200452
178477919484779195AG21GENIChomozygous140200453
178478493584784936TC14GENIChomozygous140200456
178478633384786334CG9GENICheterozygous155051984
178478633784786338C9GENICheterozygous403425219
178478633384786334C9GENICheterozygous403425218
178478633784786338CG9GENIChomozygous403425220
178478634184786342C9GENICheterozygous403425221
178478634184786342CG9GENIChomozygous403425222
178478634584786346CG9GENIChomozygous155051985
178478634584786346C9GENICheterozygous403425223
178479352784793528AG18GENIChomozygous140200457
178479846584798466AG20GENIChomozygous140200458
178480148384801484A18GENIChomozygous140041627
178480756384807566TGT14GENIChomozygous140041628
178481069384810694GA20GENIChomozygous140200459
178481549984815500GA16GENIChomozygous140200460
178482027484820275G11GENICpossibly homozygous140041629
178482054884820549CT13GENIChomozygous140200461
178482349184823492CG17GENIChomozygous140200462