chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4220863861220863862GT7GENIChomozygous608770584
4220865688220865689GGTGTGTGTGTGTA9GENICheterozygous733142517
4220865950220865951TC40GENIChomozygous608770585
4220866163220866164AAACAGTCTC32GENIChomozygous733142518
4220866308220866309CT23GENIChomozygous608770586
4220867182220867183CT22GENIChomozygous608770587
4220867457220867458GT10GENIChomozygous608770588
4220867545220867546AT15GENIChomozygous608770589
4220868317220868318T-12GENICheterozygous733142519
4220869858220869859T-4GENIChomozygous733142520
4220870021220870022TC23GENIChomozygous608770590
4220870972220870973AATTTT14GENIChomozygous733142522
4220872787220872788TA9GENIChomozygous608770591
4220873146220873147TC17GENIChomozygous608770592
4220873722220873728ACACAC------4GENIChomozygous733142523
4220873953220873954TC16GENIChomozygous608770593
4220875508220875509CCTTT6GENIChomozygous733142525
4220875728220875729TTA17GENIChomozygous733142526
4220877048220877049GGGTGTGTGT9GENIChomozygous733142527
4220877136220877137GGTCTCTC16GENIChomozygous733142528
4220877271220877272CG35GENICpossibly homozygous608770594
4220877449220877450CCTGTG20GENIChomozygous733142532
4220877514220877516TC--9GENIChomozygous733142533
4220877584220877586TC--16GENICheterozygous733142534
4220877696220877697GT6GENIChomozygous608770595
4220877700220877701GT8GENICheterozygous608770596
4220879291220879292GA25GENIChomozygous608770597
4220880183220880184CT24GENIChomozygous608770598
4220880485220880486GA21GENIChomozygous608770599
4220880567220880568AG18GENIChomozygous608770600
4220880591220880592AC21GENIChomozygous608770601