chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139840228898402292ACAC----16GENICheterozygous49865852
139840229098402292AC--16GENICpossibly homozygous50416031
139840273998402740GGTT5GENIChomozygous50532411
139840291398402914CT21GENIChomozygous50444019
139840619398406194TTTTTG18GENIChomozygous50444021
139840632598406326TC14GENIChomozygous49971388
139840655398406554TC18GENIChomozygous49865857
139840693198406932G-3GENIChomozygous49865858
139840693898406939C-3GENIChomozygous49865859
139840787298407873AG19GENIChomozygous50444023
139840791798407918CT14GENIChomozygous49865861
139840792998407930TC11GENIChomozygous49865862
139840800798408008G-16GENIChomozygous49865863
139840924698409247AG28GENIChomozygous49865867
139840972298409723CT17GENIChomozygous49865868
139841027898410279AG28GENIChomozygous49865870
139841201398412018TTAAC-----26GENIChomozygous50444025
139841227698412277CCTTT5GENICheterozygous49865874
139841242598412426CCT13GENICheterozygous50444027
139841329198413292AG11GENIChomozygous49865878
139841379498413795TG33GENIChomozygous50444029
139841427898414279A-2GENIChomozygous49971391
139841472398414724AATTTTTT6GENICheterozygous50532416
139841534898415349CT17GENIChomozygous50444031
139841708498417085AAT4GENIChomozygous50532418
139841708598417086AATATTT4GENIChomozygous50532420
139841709398417094TTATATATA4GENIChomozygous50532422
139841771198417712GC17GENIChomozygous49865884
139841855398418554T-17GENIChomozygous49865888
139841858998418590CG23GENIChomozygous49865889
139841887098418871GA36GENIChomozygous49971396
139842142698421427GC22GENIChomozygous50444033
139842193698421937GC27GENIChomozygous49865897
139842735298427353GT16GENIChomozygous49865907