chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 243702436 243702437 C T 7 GENIC possibly homozygous 61359304 2 243703703 243703704 G C 11 GENIC heterozygous 61359306 2 243703891 243703892 A G 6 GENIC heterozygous 59472311 2 243704226 243704227 G T 3 GENIC heterozygous 60462656 2 243704677 243704678 G A 13 GENIC homozygous 59472315 2 243706074 243706075 A G 9 GENIC possibly homozygous 59472322 2 243706468 243706469 A G 12 GENIC homozygous 59472323 2 243706622 243706623 C T 23 GENIC possibly homozygous 59472324 2 243708087 243708088 G C 9 GENIC homozygous 59472327 2 243708210 243708211 A AT 5 GENIC heterozygous 61359308 2 243709874 243709875 G A 14 GENIC possibly homozygous 61359310 2 243711897 243711898 T C 1 GENIC homozygous 59472330 2 243713151 243713152 C A 12 GENIC homozygous 59472332 2 243713323 243713324 C - 17 GENIC heterozygous 59472333 2 243713389 243713390 C - 6 GENIC homozygous 59472334 2 243713410 243713411 A C 9 GENIC possibly homozygous 59472335 2 243713988 243713989 G A 19 GENIC possibly homozygous 59472336 2 243716541 243716542 G A 19 GENIC possibly homozygous 61359312 2 243717654 243717655 G GA 12 GENIC homozygous 61359314 2 243718212 243718213 C T 13 GENIC heterozygous 61359316 2 243718985 243718986 C T 7 GENIC homozygous 61359318 2 243719311 243719312 A C 9 GENIC homozygous 59472345 2 243720001 243720002 A G 14 GENIC homozygous 59472346