chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3103727017103727018GC14GENIChomozygous111663128
3103727083103727084GA21GENIChomozygous111990407
3103727365103727366AG19GENIChomozygous111663129
3103728491103728492GA24GENIChomozygous111990409
3103729625103729626A4GENIChomozygous127913496
3103731099103731100CA23GENIChomozygous111663133
3103731379103731380AT19GENIChomozygous111990411
3103731466103731467TC28GENIChomozygous111990413
3103731611103731612TC22GENIChomozygous111990415
3103731718103731719AC21GENIChomozygous111990417
3103732464103732465TA30GENIChomozygous111663141
3103732540103732541CG23GENIChomozygous111663142
3103733671103733671GA27GENIChomozygous133474630
3103731279103731280G16GENIChomozygous133474629