chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15149037351490374CG51GENIChomozygous61413057
15149649951496500GA50GENIChomozygous61413058
15150897551508976A-16GENIChomozygous61868225
15151277451512775GC35GENIChomozygous61413064
15151387051513874TACA----13GENICpossibly homozygous61868226
15151611351516114TC28GENICpossibly homozygous61868227
15153467851534679A-19GENICheterozygous60699946
15153556251535563CA27GENICpossibly homozygous61868228
15153614351536144GGA14GENIChomozygous61290608
15153948251539484AC--5GENIChomozygous60699947
15154726351547264TC36GENIChomozygous61413068
15155163051551631A-36GENICheterozygous61666291
15155163151551632C-30GENIChomozygous61290609
15155172651551727CT30GENICheterozygous61868229
15155176451551765TC32GENICheterozygous61868230
15155177151551772GA36GENICheterozygous61868231
15155187951551880AG35GENICpossibly homozygous61413069
15155208851552089CG19GENIChomozygous60699950
15156579851565799GC4GENIChomozygous60699951
15157285751572858GGA15GENIChomozygous61413071
15157545251575453TTGG15GENICpossibly homozygous61868232
15157566151575662AG21GENIChomozygous61413072
15157580051575801GGC12GENICheterozygous61666292
15157585451575855CT26GENIChomozygous61413074
15157678051576781GC23GENIChomozygous61868233