chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155026493155026494CT38GENIChomozygous114063166
5155026503155026504CT37GENIChomozygous114544544
5155039085155039086TC34GENIChomozygous114063170
5155039197155039198GA33GENIChomozygous114063172
5155040316155040317TG32GENIChomozygous114544548
5155040332155040333CT30GENIChomozygous114544550
5155041528155041529AC30GENIChomozygous114063182
5155041566155041567CG26GENIChomozygous114063184
5155041889155041890GA29GENIChomozygous114544552
5155042587155042588TC41GENIChomozygous114544554
5155042841155042842AG24GENIChomozygous114063186
5155045851155045852CT18GENIChomozygous114063199
5155046757155046758AC20GENIChomozygous114063203
5155046977155046978TG37GENIChomozygous114063205
5155047411155047412CT31GENIChomozygous114544556
5155048453155048454TC35GENIChomozygous114063209
5155048911155048912GA35GENIChomozygous114544558
5155050451155050452AG35GENIChomozygous114063215
5155051183155051184CT30GENIChomozygous114544560
5155052431155052432CT44GENIChomozygous114544562
5155052828155052829AG22GENIChomozygous114544564
5155074497155074498CT37GENIChomozygous114063223
5155075099155075100AC43GENIChomozygous114063227
5155085350155085351AT36GENIChomozygous114063253
5155136470155136471GA33GENIChomozygous114063452
5155136487155136488GA34GENIChomozygous114063454
5155136499155136500GA36GENIChomozygous114063456