chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 145079966 145079966 T 40 GENIC homozygous 128250436 5 145079991 145079991 C 43 GENIC homozygous 128250437 5 145080004 145080005 G 40 GENIC homozygous 128250438 5 145080009 145080009 C 38 GENIC homozygous 128250439 5 145080019 145080020 A 37 GENIC homozygous 128250440 5 145080039 145080040 T G 37 GENIC homozygous 114152464 5 145080042 145080044 AA 37 GENIC homozygous 128250441 5 145080048 145080048 C 35 GENIC homozygous 128250442 5 145080056 145080057 G 36 GENIC homozygous 128250443 5 145080068 145080069 T 39 GENIC homozygous 128250444 5 145080086 145080090 ATTT 39 GENIC homozygous 128250445 5 145080091 145080094 TTG 39 GENIC homozygous 128250446 5 145080095 145080096 T C 38 GENIC homozygous 122410289 5 145080103 145080103 G 36 GENIC homozygous 128250447 5 145080117 145080118 G 36 GENIC homozygous 128250448 5 145080164 145080165 A C 40 GENIC homozygous 114152465 5 145080167 145080168 C 39 GENIC homozygous 128250449 5 145080256 145080257 G C 33 GENIC possibly homozygous 114038190 5 145080277 145080278 A C 27 GENIC heterozygous 132636895 5 145080269 145080270 G C 29 GENIC heterozygous 132636892 5 145080273 145080274 G C 27 GENIC heterozygous 132636893 5 145080276 145080277 A C 27 GENIC heterozygous 132636894 5 145080296 145080297 T C 27 GENIC homozygous 114038191 5 145082327 145082328 C G 40 GENIC homozygous 114038192 5 145088376 145088377 G A 54 GENIC homozygous 114038193