chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13110741872110741873TC19GENIChomozygous791104453
13110742696110742697AG27GENIChomozygous791104454
13110743778110743779CT26GENIChomozygous791104455
13110743788110743789CT30GENIChomozygous791104456
13110743858110743859GA38GENIChomozygous791104457
13110743981110743982TC36GENIChomozygous791104458
13110744513110744514AG32GENIChomozygous791104459
13110744526110744527CT37GENIChomozygous791104460
13110744864110744865CT36GENIChomozygous791104461
13110745556110745557AG34GENIChomozygous791104462
13110745588110745589AG34GENIChomozygous791104463
13110745907110745908TA38GENICpossibly homozygous791104464
13110746430110746431CT22GENIChomozygous791104465
13110746508110746509CT23GENIChomozygous791104466
13110746797110746798CT26GENIChomozygous791104467
13110747171110747172TC38GENIChomozygous791104468
13110748032110748033AC33GENIChomozygous791104469
13110748585110748586CT35GENIChomozygous791104470
13110748713110748714TC32GENIChomozygous791104471
13110748723110748724TC34GENIChomozygous791104472
13110748906110748907AG32GENIChomozygous791104473