chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170262372170262373AC25GENIChomozygous108375500
1170262418170262419AC23GENIChomozygous108375502
1170262757170262758AG13GENIChomozygous108375504
1170262979170262980CT24GENIChomozygous108375506
1170263862170263863AG25GENIChomozygous108375508
1170264182170264183TC28GENIChomozygous108375510
1170264224170264225AG28GENIChomozygous108375512
1170264473170264474AG32GENIChomozygous108375514
1170264622170264623AG27GENICpossibly homozygous108375516
1170265005170265006GA27GENIChomozygous108375518
1170265015170265016AG27GENIChomozygous108375520
1170265119170265120T25GENIChomozygous127455468
1170265193170265198GACTA24GENIChomozygous127455469
1170265503170265504TC37GENIChomozygous108375522
1170265683170265684TC19GENIChomozygous108375524
1170266684170266686CA12GENIChomozygous127455470
1170266750170266751CT11GENIChomozygous108375526
1170266986170266987CT17GENIChomozygous108375528
1170267002170267003GA16GENIChomozygous108375530
1170267220170267221CT13GENIChomozygous108375532
1170267279170267280GA6GENICheterozygous108755101
1170267548170267549TA3GENIChomozygous109523819
1170267551170267552AT3GENIChomozygous120474632
1170267553170267554GA3GENIChomozygous120474633
1170267561170267562GA5GENIChomozygous108958554
1170267572170267573TA4GENIChomozygous108958555
1170267581170267582AT2GENIChomozygous109437508
1170267885170267886GA31GENIChomozygous108375536
1170267919170267920AG37GENIChomozygous108375538
1170269227170269228TC28GENIChomozygous108375540
1170269278170269279TG15GENIChomozygous108375542
1170269659170269660GA24GENIChomozygous108375544
1170270944170270945TC25GENIChomozygous108375546
1170271310170271311CG15GENIChomozygous108375548
1170271689170271690AG30GENIChomozygous108375550
1170272010170272011GA10GENIChomozygous108375552