chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3103727017103727018GC37GENIChomozygous111663128
3103727083103727084GA37GENIChomozygous111990407
3103727365103727366AG23GENIChomozygous111663129
3103728491103728492GA40GENIChomozygous111990409
3103731099103731100CA43GENICpossibly homozygous111663133
3103731379103731380AT41GENICheterozygous111990411
3103731466103731467TC43GENIChomozygous111990413
3103731611103731612TC27GENIChomozygous111990415
3103731718103731719AC27GENIChomozygous111990417
3103732464103732465TA35GENIChomozygous111663141
3103732540103732541CG44GENIChomozygous111663142