chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1281265388126539GC22GENIChomozygous139077548
1281266278126628GT16GENIChomozygous139077549
1281270338127034CT26GENIChomozygous139077550
1281273368127336A19GENIChomozygous139039272
1281273398127345GTTTGT18GENIChomozygous139039273
1281298898129890CT18GENIChomozygous139077554
1281273378127338GC18GENIChomozygous139077551
1281274358127436TC20GENIChomozygous139077552
1281291118129112AG19GENIChomozygous139077553
1281301918130192CT23GENIChomozygous139077555
1281316018131601G7GENICheterozygous139039274
1281316328131633TA6GENIChomozygous139077556
1281319868131987A8GENICpossibly homozygous139039275
1281335148133515AT20GENICpossibly homozygous139077557
1281354218135422AG20GENIChomozygous139077558
1281359158135916AG18GENIChomozygous139077559
1281373698137370TC17GENIChomozygous139077560
1281378248137825GA25GENIChomozygous139077561
1281379148137915AG32GENIChomozygous139077562
1281388248138825CT19GENIChomozygous139077563
1281388298138830CT17GENIChomozygous139077564
1281391478139148GA17GENIChomozygous139077565
1281316908131691A5GENICheterozygous403315112
1281316908131691AC5GENIChomozygous154756957