chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103635855036358551AG13GENIChomozygous142232582
103635870936358710CT15GENIChomozygous142232583
103635943336359434GA11GENIChomozygous138766444
103635962936359631AC7GENIChomozygous142200040
103635967736359678GA12GENIChomozygous138766445
103635988136359881G4GENIChomozygous147457395
103636123836361239AG16GENIChomozygous142232584
103636241736362418GA21GENIChomozygous142232585
103636271736362718AG11GENIChomozygous138766447
103636291236362913CT17GENIChomozygous142232586
103636305836363059CG18GENIChomozygous142232587
103636667736366678AC14GENIChomozygous138766448
103636735936367360TA21GENIChomozygous142232588
103636768436367685AC16GENIChomozygous142232589
103635990936359909CC4GENIChomozygous143431045
103636285936362859T18GENICpossibly homozygous138678863
103636802236368023TC8GENIChomozygous142232590
103636844036368441AC9GENIChomozygous142232591
103637244936372450CT24GENIChomozygous142232592
103637323236373233AG18GENIChomozygous142232593
103637367636373677GA14GENIChomozygous142232594
103637436236374363AC19GENIChomozygous142232595
103637457136374571TGGT16GENIChomozygous142200041
103637494236374943CA9GENIChomozygous142232596
103637536436375365AT13GENIChomozygous142232597
103637583036375831CT16GENIChomozygous142232598
103637631836376318AAAAAGAAAAAAG6GENIChomozygous142200042
103637637336376374CT17GENIChomozygous142232599
103637638336376383TGC21GENICpossibly homozygous142200043
103637660336376606AAC15GENIChomozygous142200044
103636750936367510C13GENICpossibly homozygous403732897
103636750936367510CT13GENICheterozygous403732898