chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1673861816738619TC11GENIChomozygous108371310
X1673861916738620CT11GENIChomozygous108371312
X1673874816738749GC12GENIChomozygous108371314
X1673875816738759CA14GENIChomozygous108371316
X1673877216738773CA16GENIChomozygous108371318
X1674125216741253TG15GENIChomozygous108233663
X1674125616741257CA14GENIChomozygous108233665
X1674125716741258CG13GENIChomozygous108233667
X1674154116741542GA11GENIChomozygous108233669
X1674433616744337CT10GENIChomozygous108233671
X1674455916744560CT7GENIChomozygous108233673
X1674464616744647CG9GENIChomozygous108371320
X1675465316754654AC3GENIChomozygous108233681
X1675466516754666GC5GENIChomozygous108233683
X1677260416772605GA11GENIChomozygous108233689
X1688969916889700CT7GENIChomozygous108371322
X1691464816914649CT9GENIChomozygous108233693