chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15149037351490374CG20GENIChomozygous61413057
15149649951496500GA27GENIChomozygous61413058
15150897551508976A-3GENIChomozygous61868225
15151277451512775GC20GENIChomozygous61413064
15151387051513874TACA----18GENIChomozygous61868226
15151611351516114TC14GENIChomozygous61868227
15152210251522104AC--3GENICheterozygous62226440
15153614351536144GGA14GENIChomozygous61290608
15154337251543373CCA6GENICheterozygous62226442
15154726351547264TC7GENIChomozygous61413068
15153948251539484AC--4GENIChomozygous60699947
15154337351543374A-6GENICheterozygous60699948
15152210151522102AAAC3GENICheterozygous62127247
15153334551533346TTGA4GENICheterozygous62127248
15155187951551880AG9GENIChomozygous61413069
15155208851552089CG26GENIChomozygous60699950
15157285751572858GGA19GENIChomozygous61413071
15157545251575453TTGG2GENIChomozygous61868232
15157566151575662AG17GENIChomozygous61413072
15157580051575801GGCC3GENICheterozygous61413073
15157580051575801GGC3GENICheterozygous61666292
15157585451575855CT21GENIChomozygous61413074
15157678051576781GC5GENIChomozygous61868233