chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118045406880454069CT21GENIChomozygous50969397
118045459180454593TA--5GENIChomozygous51296646
118045507680455077AG13GENIChomozygous50969398
118045556680455567GA34GENIChomozygous50969399
118045560780455608GT31GENIChomozygous50969400
118045611080456111AG20GENIChomozygous50969401
118045635180456352GA24GENIChomozygous50969402
118045708580457086AG11GENIChomozygous50969403
118045760380457605CG--13GENIChomozygous50969406
118045872080458724AAAC----20GENIChomozygous50969410
118046283880462839GA26GENIChomozygous50969411
118046375080463751AT40GENICpossibly homozygous50969412
118046375480463755AC38GENICpossibly homozygous50969413
118046462080464621GA25GENIChomozygous50969414
118046523080465231CG22GENIChomozygous50969418
118046684880466849TTA22GENICpossibly homozygous50969419
118046791480467915CT25GENIChomozygous50969420
118046851780468518GC29GENIChomozygous50969421
118046992580469928TTT---13GENIChomozygous50969422
118047149980471500TTA20GENICheterozygous51243667
118047150080471501A-20GENICpossibly homozygous50969423
118047233680472337GA22GENIChomozygous50969424
118047495380474954TTACAC5GENICheterozygous50969426
118047572380475724CA26GENIChomozygous50969427
118046712580467127CA--1GENIChomozygous51190816