chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2366907623669077GA30GENIChomozygous108701291
X2367077923670780GA24GENICheterozygous120066069
X2367075823670759TC24GENICheterozygous119990491
X2367072923670730GA26GENICheterozygous119910804
X2367073923670740GA23GENICheterozygous119910805
X2367076823670769AG23GENICheterozygous120066067
X2367077023670771CT23GENICheterozygous120066068
X2367078523670786TG24GENICheterozygous120548367
X2367079323670794CT24GENICheterozygous120788695
X2367079423670795AG24GENICheterozygous120788696
X2367079823670799TA23GENICheterozygous120788697
X2367080123670802CG23GENICheterozygous120788698
X2367080223670803CT22GENICheterozygous120788699
X2367764423677645TC28GENIChomozygous108240494
X2367786123677862AG34GENIChomozygous108701294
X2368292523682926AG32GENIChomozygous108240502
X2368801423688015AC24GENIChomozygous108240507
X2368848023688481CG9GENIChomozygous108701296
X2368463223684633A24GENICpossibly homozygous129728245
X2367899923678999AT22GENICpossibly homozygous133453221
X2368719523687196T23GENIChomozygous133453222
X2369170123691702TC25GENIChomozygous108701298