chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157613853157613854GT24GENIChomozygous112906744
4157614185157614186TG22GENIChomozygous112906746
4157614654157614655CA24GENIChomozygous119317695
4157614774157614775AT33GENIChomozygous112906748
4157616535157616536CA35GENIChomozygous112906752
4157620744157620745TC41GENIChomozygous112906756
4157623083157623084GA39GENIChomozygous112906760
4157625710157625711CT36GENIChomozygous112906762
4157627043157627044TC35GENIChomozygous112906766
4157627242157627243CT32GENIChomozygous119317696
4157629525157629526TC32GENIChomozygous112906768
4157630918157630919GT20GENIChomozygous112906770
4157631950157631951AG27GENIChomozygous112906772
4157632657157632658TC24GENIChomozygous112906774
4157633311157633312CT24GENIChomozygous119317698
4157633500157633501AG34GENIChomozygous112906776
4157634098157634099TC36GENIChomozygous112906778
4157635239157635240AC29GENIChomozygous112906780
4157635295157635296CT27GENIChomozygous112906782
4157638495157638496TC28GENIChomozygous112906784
4157639657157639658GC24GENIChomozygous112906786
4157644216157644217CG21GENIChomozygous112906788
4157644340157644341TC28GENIChomozygous112906790