chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 55791151 55791152 G T 19 GENIC possibly homozygous 668857276 13 55791660 55791661 C T 20 GENIC possibly homozygous 668857277 13 55792149 55792150 G A 21 GENIC homozygous 668857278 13 55793030 55793031 A G 6 GENIC homozygous 668857279 13 55793073 55793074 T - 6 GENIC homozygous 768271376 13 55794059 55794060 A AG 5 GENIC heterozygous 768271377 13 55794173 55794174 C A 10 GENIC homozygous 668857280 13 55795016 55795017 C T 13 GENIC homozygous 668857281 13 55795127 55795128 A G 21 GENIC homozygous 668857282 13 55795483 55795484 T C 14 GENIC homozygous 668857283 13 55795686 55795687 G GC 11 GENIC homozygous 768271378 13 55796399 55796400 G A 27 GENIC possibly homozygous 668857284 13 55798078 55798079 A ACCCC 2 GENIC homozygous 768271380 13 55799099 55799100 A C 12 GENIC possibly homozygous 668857285 13 55799877 55799878 A G 1 GENIC homozygous 668857286 13 55800117 55800118 A C 2 GENIC homozygous 668857287 13 55800298 55800299 C T 23 GENIC possibly homozygous 668857288 13 55800385 55800386 G A 15 GENIC possibly homozygous 668857289 13 55800623 55800624 C G 9 GENIC homozygous 668857290 13 55801310 55801311 G T 6 GENIC heterozygous 668857291 13 55801649 55801650 A G 22 GENIC possibly homozygous 668857292