chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118045459080454591TTTA25GENICpossibly homozygous51022068
118045560780455608GT34GENIChomozygous50969400
118045580480455805TC32GENIChomozygous51022069
118045611080456111AG36GENIChomozygous50969401
118045635180456352GA35GENIChomozygous50969402
118045708180457082AAAAAGC8GENIChomozygous51228417
118045710280457103AAAAAAAACAAAAAC14GENICpossibly homozygous51228419
118045712280457123CCAAAA15GENIChomozygous51228421
118045732180457322TTCCCCC3GENIChomozygous51170336
118045760380457605CG--21GENIChomozygous50969406
118045799480457995CCG4GENICheterozygous51288667
118045872080458724AAAC----15GENICheterozygous50969410
118046032180460322GA28GENIChomozygous51022072
118046238580462386A-33GENIChomozygous51022073
118046283880462839GA15GENIChomozygous50969411
118046375080463751AT34GENIChomozygous50969412
118046375480463755AC31GENIChomozygous50969413
118046462080464621GA38GENIChomozygous50969414
118047149980471500TTA21GENICheterozygous51243667
118046508080465081CT45GENIChomozygous51380804
118046523080465231CG34GENIChomozygous50969418
118046534880465349AG35GENIChomozygous51022074
118046992380469928TTTTT-----15GENIChomozygous50992713
118046712580467127CA--1GENIChomozygous51190816
118047150080471501A-21GENICheterozygous50969423
118047400880474009A-22GENICpossibly homozygous51197197
118047495380474954TTACACACAC1GENIChomozygous51261452
118047607180476072CT12GENIChomozygous51022077
118047663380476634CT11GENIChomozygous51022078