chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112044915112044916GA39GENIChomozygous57990891
3112045592112045593TTAAAA6GENIChomozygous57990893
3112045593112045594TA16GENIChomozygous57990896
3112045942112045943TG15INTERGENIChomozygous57990899
3112046063112046064TC25INTERGENIChomozygous57990902
3112046687112046688AG37INTERGENIChomozygous57990908
3112051630112051631G-21GENIChomozygous57990948
3112051631112051632TA22GENIChomozygous58424387
3112052084112052085GA40GENIChomozygous58424388
3112052686112052687CT29GENIChomozygous57990954
3112053590112053594GATT----6GENIChomozygous58424389
3112054603112054604TTACAC5GENICheterozygous57603003
3112054604112054608ACAC----5GENICheterozygous57603005
3112055939112055940GA34GENIChomozygous58424390
3112056266112056267CT34GENIChomozygous58424391
3112056359112056360TTG22GENIChomozygous58424392
3112056912112056913AG33GENIChomozygous57990969
3112056939112056940TC33GENIChomozygous57990971
3112057803112057804GA33GENIChomozygous58424393
3112057965112057966CA14GENICpossibly homozygous58424394
3112061639112061640CA24GENIChomozygous58424395
3112061809112061810TC25GENIChomozygous58424396