chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 49282272 49282273 T C 28 GENIC homozygous 980562985 16 49285438 49285439 T C 7 GENIC homozygous 980562986 16 49287269 49287270 C T 30 GENIC possibly homozygous 980562987 16 49297039 49297040 C G 24 GENIC homozygous 980562988 16 49297880 49297881 C G 43 GENIC homozygous 980562989 16 49297949 49297950 G A 38 GENIC homozygous 980562990 16 49298498 49298499 C G 28 GENIC homozygous 980562991 16 49305126 49305127 G C 36 GENIC homozygous 980562992 16 49310356 49310357 A G 18 GENIC homozygous 980562993 16 49313593 49313594 G A 28 GENIC homozygous 980562994 16 49315881 49315882 G T 4 GENIC homozygous 980562995 16 49316463 49316464 T C 11 GENIC homozygous 980562996 16 49319233 49319234 C T 38 GENIC homozygous 980562997 16 49321001 49321002 T C 21 GENIC homozygous 980562998 16 49321028 49321029 C T 21 GENIC homozygous 980562999 16 49322929 49322930 C T 21 GENIC homozygous 980563000 16 49323114 49323115 G A 28 GENIC homozygous 980563001 16 49323222 49323223 A T 21 GENIC homozygous 980563002 16 49323305 49323306 C T 26 GENIC homozygous 980563003 16 49325269 49325270 T C 27 GENIC homozygous 980563004 16 49325950 49325951 A G 24 GENIC homozygous 980563005 16 49326197 49326198 T C 46 GENIC homozygous 980563006 16 49328078 49328079 T C 33 GENIC homozygous 980563007 16 49328440 49328441 A C 29 GENIC homozygous 980563008