chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183098084030980841TC33GENIChomozygous110321597
183099954130999542TA9GENIChomozygous110321605
183100092531000926AC16GENIChomozygous110321611
183100031031000311TA9GENIChomozygous119487747
183100034731000348TG16GENIChomozygous119487748
183100518131005182AG5GENICheterozygous119545133
183100583431005835TC22GENIChomozygous110321619
183101665031016651TC20GENIChomozygous110321632
183102675731026758TG10GENIChomozygous119487753
183105267431052675GC21GENIChomozygous110321705
183105730831057309TG13GENIChomozygous119487756
183105754731057548CG11GENIChomozygous119487757
183106267431062675AT22GENIChomozygous110321719
183106332631063327GA20GENIChomozygous110321721
183106334431063345CT17GENIChomozygous110321723
183106351231063513CT14GENIChomozygous110321725
183106387531063876AG27GENIChomozygous110321727
183106398131063982AC21GENIChomozygous110321731
183106440631064407TC25GENIChomozygous110457577
183106501331065014CA19GENIChomozygous110321735
183106570631065707TC9GENIChomozygous110321739
183106636531066366TG17GENIChomozygous110321741
183106643931066440AG14GENIChomozygous110321743
183106718431067185CT15GENIChomozygous110321746
183106736931067370TC26GENIChomozygous110321748
183106804431068045AC28GENIChomozygous110532848
183101103531011036GT51GENICheterozygous119553584
183101508331015084GA25GENIChomozygous110532834
183106296631062967TC26GENIChomozygous110532836
183106299231062993GC33GENIChomozygous110532838
183106336231063363TC14GENIChomozygous110532840
183106469831064699CT10GENIChomozygous110532842
183106687731066878CT23GENIChomozygous110532844
183106745131067452CA23GENIChomozygous110532846
183106864731068648TC23GENIChomozygous110321756
183106958531069586AG17GENIChomozygous110321758
183106994031069941GA19GENIChomozygous110321760
183107012631070127CG18GENICpossibly homozygous110630449
183107080131070802CT22GENIChomozygous110321762
183107127431071275GC26GENIChomozygous110321764
183107001631070017AG20GENIChomozygous110680712