chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 60393378 60393379 T G 34 GENIC homozygous 53273089 8 60393674 60393675 C T 23 GENIC homozygous 53273090 8 60393866 60393867 C T 27 GENIC homozygous 53273091 8 60394345 60394346 A T 25 GENIC homozygous 53273092 8 60394425 60394426 C T 23 GENIC homozygous 53273093 8 60394652 60394653 T C 17 GENIC homozygous 52984379 8 60394969 60394970 G - 14 GENIC possibly homozygous 53273094 8 60394971 60394975 TTTG ---- 14 GENIC possibly homozygous 53273095 8 60394972 60394975 TTG --- 14 GENIC possibly homozygous 53273096 8 60395971 60395972 C G 26 GENIC possibly homozygous 53300370 8 60396065 60396068 CCC --- 4 GENIC homozygous 53273097 8 60396277 60396278 C G 27 GENIC homozygous 53300371 8 60396568 60396569 A G 23 GENIC homozygous 53300372 8 60396611 60396612 G A 26 GENIC homozygous 53273098 8 60397085 60397086 A C 16 GENIC homozygous 53273099 8 60397836 60397838 TT -- 9 GENIC heterozygous 53300373 8 60398069 60398070 A C 17 GENIC homozygous 52984381 8 60398822 60398823 C T 13 GENIC homozygous 52984382 8 60398870 60398871 G - 16 GENIC homozygous 52984383 8 60399367 60399368 G A 25 GENIC homozygous 53273101 8 60399615 60399616 T G 18 GENIC homozygous 53273102 8 60399738 60399739 A ATTT 8 GENIC homozygous 53300374 8 60399780 60399781 T TCTTC 9 GENIC possibly homozygous 53182151 8 60400730 60400731 A T 29 GENIC homozygous 53273105 8 60401039 60401040 T A 20 GENIC homozygous 53273106 8 60397837 60397838 T - 9 GENIC heterozygous 52666440