chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2260110312260110313AG19GENIChomozygous110425813
2260110418260110419GA17GENIChomozygous110425815
2260110449260110450TC25GENIChomozygous110425817
2260110514260110515CT33GENIChomozygous110425823
2260110675260110676CT20GENIChomozygous110425827
2260110681260110682GT21GENICpossibly homozygous110425829
2260110786260110787AG22GENIChomozygous110425831
2260110894260110895TC19GENIChomozygous110425833
2260110898260110899CA18GENIChomozygous110425835
2260110942260110943TC27GENIChomozygous110425837
2260111002260111003CT13GENIChomozygous110425839
2260111010260111011CT14GENIChomozygous110425841
2260111017260111018AT12GENIChomozygous110425843
2260111034260111035CG6GENIChomozygous110425845
2260111442260111443CT21GENIChomozygous110425851
2260111467260111468AC20GENIChomozygous110425853
2260111643260111644TG23GENIChomozygous110425857
2260111647260111648TC24GENIChomozygous110425859
2260111685260111686CT26GENIChomozygous110425861
2260111690260111691TC24GENIChomozygous110425863
2260111754260111755CG26GENIChomozygous110425865
2260111768260111769GA24GENIChomozygous110425867
2260111791260111792AC26GENIChomozygous110425869
2260111912260111913CA19GENIChomozygous110425871
2260111980260111981CA21GENIChomozygous110425873
2260111983260111984GA20GENIChomozygous110425875
2260112111260112112AG16GENIChomozygous110425881
2260112503260112504CT22GENIChomozygous110425893
2260112568260112569CT17GENIChomozygous110425895
2260112724260112725GA22GENIChomozygous110425897
2260112806260112807GA14GENIChomozygous110425899
2260112869260112870AG9GENIChomozygous110425901
2260112911260112912AG15GENIChomozygous110425903
2260112614260112615GA21GENIChomozygous111047636