chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106562151065621511CT6INTERGENIChomozygous51478023
106562159465621595AT8INTERGENICheterozygous51478024
106562202165622022CT1INTERGENIChomozygous51906658
106562203565622036A-1INTERGENIChomozygous51478027
106562203665622037AG1INTERGENIChomozygous52382293
106562206565622067AA--2INTERGENIChomozygous51906660
106562227765622278TA6INTERGENICheterozygous51478029
106562345465623455GC9GENICpossibly homozygous51478035
106562531365625314GA17INTERGENIChomozygous51478037
106562655765626558AG12INTERGENIChomozygous51906666
106562665365626657TGTT----5INTERGENIChomozygous51906668
106562951565629516GC6INTERGENIChomozygous51906672
106562974265629743TC10INTERGENIChomozygous51478055
106562975465629755TTC7INTERGENIChomozygous51478056
106563014465630145AAGAAAGAGGTGGGAGAGGAGGGAAGCC2INTERGENICheterozygous51478058
106563039465630395GA10INTERGENIChomozygous51478062
106563055865630559GT16INTERGENICheterozygous51906674
106563149065631491GA8INTERGENIChomozygous51906676
106563177765631779GG--1INTERGENIChomozygous51478068
106563178665631787GT4INTERGENICheterozygous52320269
106563235065632351TC7INTERGENIChomozygous51478072
106563244865632449CT12INTERGENICpossibly homozygous51906678
106563293265632933A-3INTERGENIChomozygous51678580
106563324565633246TC2INTERGENIChomozygous51478075
106563329965633300GA5INTERGENICheterozygous51906682
106563455165634552GA11INTERGENIChomozygous51906688