chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4146430520146430521TA67GENICpossibly homozygous146424234
4146433501146433502GA57GENIChomozygous137226273
4146433704146433705CA54GENIChomozygous137226274
4146434658146434662ATTT50GENIChomozygous146403727
4146435299146435300TC43GENIChomozygous137226275
4146435860146435861CG44GENIChomozygous137226276
4146436080146436081TC41GENIChomozygous146424235
4146436525146436526TA52GENIChomozygous146424236
4146440003146440004TC41GENIChomozygous146424237
4146437146146437147GT46GENIChomozygous137226277
4146439509146439510AC43GENIChomozygous137226278
4146441737146441738TC63GENIChomozygous146424238
4146442699146442700TC59GENIChomozygous137226280
4146445751146445752CT65GENIChomozygous146424239
4146449067146449068A42GENIChomozygous146403729
4146450658146450659AG57GENIChomozygous137226281
4146451214146451215AG74GENIChomozygous137226282
4146451502146451503AT49GENIChomozygous146424240
4146439673146439674GA34GENIChomozygous403122326
4146439673146439674G34GENICheterozygous403122325