chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154521914154521915TTAA15GENICheterozygous57742566
3154521915154521916A-15GENICheterozygous58697264
3154532857154532858GGT29GENIChomozygous57742611
3154532866154532867GGT28GENIChomozygous57742613
3154535666154535667A-4GENICheterozygous58658319
3154532851154532852GGT29GENIChomozygous58564679
3154528096154528098GT--10GENICheterozygous58628845
3154532740154532744TGTG----8GENICheterozygous58628846
3154538890154538891TC27GENIChomozygous57742671
3154540078154540079C-51GENIChomozygous57742682
3154542616154542617TG25GENIChomozygous57742692
3154542619154542620CG25GENIChomozygous57742694
3154542644154542645AC21GENIChomozygous57742698
3154542649154542650TA20GENIChomozygous57742700
3154542650154542651AG19GENIChomozygous57742702
3154542658154542659GT16GENIChomozygous57742704
3154542670154542671GA15GENIChomozygous57742705
3154542690154542692AT--23GENIChomozygous57742707
3154542693154542694GGC23GENIChomozygous57742709
3154543796154543797GGA10GENICpossibly homozygous58953570
3154545596154545600AATG----14GENIChomozygous57742740