chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4152502401152502402TC75GENICheterozygous56986210
4152502450152502451GT31GENICheterozygous57349540
4152502453152502454AT37GENICheterozygous57349542
4152502462152502463AG36GENICheterozygous57349544
4152502463152502464AG34GENICheterozygous57349546
4152502474152502475AG29GENICheterozygous57349548
4152502476152502477AG32GENICheterozygous57349550
4152502477152502478AT32GENICheterozygous57349552
4152502512152502513GA65GENICheterozygous57349554
4152503058152503059GA245GENICheterozygous56986211
4152504514152504515A-2GENIChomozygous56986212
4152506598152506599GT36GENICheterozygous56986213
4152506605152506606GC34GENICheterozygous56986214
4152506663152506664CCA26GENICpossibly homozygous56986215
4152506692152506693TA33GENIChomozygous56986216
4152506723152506724GGTT35GENIChomozygous56986217
4152506867152506868TC49GENIChomozygous56986218
4152506962152506963AG56GENIChomozygous56986219
4152507171152507172GT60GENIChomozygous56986220