chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137969741079697411CCATTTATTTATTT1GENIChomozygous50657837
137970331079703311AAAACCAACCAACC7GENIChomozygous50657839
137970492579704926CCTGTG12GENIChomozygous49832462
137970772179707722GT29GENIChomozygous49832463
137970772379707727TAAC----29GENIChomozygous49832464
137970930479709305CT11GENIChomozygous49832465
137971127079711272AC--7GENIChomozygous50617970
137971130379711304CG9GENIChomozygous49832466
137971500979715010AATGTG10GENICpossibly homozygous50657841
137971664679716647C-4GENICheterozygous49832468