chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1670398207039821GGT2GENICheterozygous47257147
1670398897039890T-6GENICheterozygous47718489
1670399447039945TTTGTG7GENICpossibly homozygous47605452
1670399447039945TTTG7GENICheterozygous47784747
1670545107054512TG--10GENICheterozygous47257170
1670597927059793CCTTTT5GENICheterozygous47986599
1670757037075704TG6GENIChomozygous47257211
1670757077075708GGCTTGCCTAGCATGC6GENIChomozygous47257212
1670769487076949CCGT2GENIChomozygous47257216
1670630717063075TGTG----4GENIChomozygous47797589
1670657997065800GT12GENIChomozygous47797590
1670751717075176GGGGG-----1GENIChomozygous47901180
1670757387075739GGA4GENICheterozygous47920184
1670857507085751T-5GENICheterozygous47988446
1670889877088988AG12GENIChomozygous47257231
1670909207090921T-16GENICheterozygous47257235
1670926047092608TTGT----6GENIChomozygous47941457
1671161987116200TG--1GENIChomozygous47797591
1671162377116238GGTGTA3GENIChomozygous47257280
1671214617121462T-6GENIChomozygous47257284