chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3103727017103727018GC44GENIChomozygous111663128
3103727083103727084GA59GENIChomozygous111990407
3103727365103727366AG25GENICpossibly homozygous111663129
3103728491103728492GA53GENIChomozygous111990409
3103729625103729626A12GENIChomozygous127913496
3103731099103731100CA67GENIChomozygous111663133
3103731364103731365GA51GENICheterozygous111663135
3103731379103731380AT55GENICpossibly homozygous111990411
3103731466103731467TC52GENIChomozygous111990413
3103731611103731612TC46GENIChomozygous111990415
3103731718103731719AC54GENIChomozygous111990417
3103732464103732465TA58GENIChomozygous111663141
3103732540103732541CG59GENIChomozygous111663142
3103733671103733671GA43GENIChomozygous133474630
3103731279103731280G44GENIChomozygous133474629