chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134304772143047722AT15GENIChomozygous143579213
134304783343047833CTGCAGTTGCTA20GENIChomozygous143549548
134304833543048336AG18GENIChomozygous142366391
134304844743048448AG17GENIChomozygous143579215
134304885243048853GC17GENIChomozygous143579216
134304907443049075GA24GENIChomozygous143579218
134304924043049241GA18GENIChomozygous143579219
134304950943049629CCTGGTTCTTTTTTTTTTTTTTTTTTCTTTTTTCTTTTTTTGGAGCTGGGGACCGAACCCAGGGCCTTGTGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCTACAAT7GENICpossibly homozygous143549549
134305065843050658TACCC14GENIChomozygous143549550
134305172343051724GA20GENIChomozygous143579224
134304980543049806TC17GENIChomozygous143579220
134305037643050377CT21GENIChomozygous143579221
134305059343050594CT13GENIChomozygous143579222
134305155643051557GA15GENIChomozygous143579223
134304944343049444CT15GENIChomozygous145800841
134304992743049928GA15GENIChomozygous147024017
134305207143052072CT14GENIChomozygous143579225
134305210943052110TC15GENIChomozygous143579226
134305226443052265CT16GENIChomozygous143579228
134305229243052293CG16GENIChomozygous143579229
134305247143052472AG12GENIChomozygous143579231
134305271243052713CT22GENIChomozygous143579233
134305297143052972AT25GENIChomozygous143579234
134305299143052992TC29GENIChomozygous143579235
134305306243053063AG23GENIChomozygous143579236
134305318743053188TG16GENIChomozygous143579237
134305339743053398CT22GENIChomozygous143579238
134305345943053460TC19GENIChomozygous143579239
134305363043053631TC20GENIChomozygous143579240
134305411743054118CT15GENIChomozygous147024018
134305455643054557CT8GENIChomozygous143579241
134305458543054586AG11GENIChomozygous142366396
134305519343055194GA20GENIChomozygous142366397