chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172798020927980210CT42GENIChomozygous111302240
172798056927980570AG23GENIChomozygous111014154
172798147827981479TC32GENIChomozygous111302241
172798166327981664CT25GENIChomozygous111302242
172798495427984955TC17GENIChomozygous111014158
172798804727988048CT31GENIChomozygous111014164
172798913027989131AC19GENIChomozygous111014170
172798915827989159GA19GENIChomozygous111343196
172798932327989324GA24GENIChomozygous111302244
172798954127989542CA15GENIChomozygous111014176
172798954427989545AG16GENIChomozygous111014178
172799099827990999TC25GENICpossibly homozygous111185558
172799127327991274GA29GENIChomozygous111185560
172799151127991512TA26GENICpossibly homozygous111185562
172799160427991605GA32GENIChomozygous111185564
172799190027991901CG23GENIChomozygous111014181
172799190827991909AT22GENIChomozygous111014183
172799345027993451GA21GENICpossibly homozygous111343198
172799394427993945AG37GENIChomozygous111014187
172799493227994933AG11GENIChomozygous111638045