chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
203103592931035930CG26GENICheterozygous134760365
203103593631035937AT29GENICheterozygous134760366
203103594031035941AT29GENICheterozygous134760367
203103595231035953CG31GENICheterozygous134760368
203103647731036477TTTGCCTATCTGTAGTTTA43GENIChomozygous129679398
203103754531037546GA45GENIChomozygous109339088
203104068031040681AT25GENICpossibly homozygous109339090
203104356631043567CT45GENIChomozygous109339092