chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 2501196 2501197 A T 14 GENIC possibly homozygous 63136026 X 2503955 2503956 T A 19 GENIC homozygous 62898564 X 2504248 2504249 A G 13 GENIC homozygous 62898565 X 2506663 2506664 A C 17 GENIC homozygous 62898567 X 2507322 2507323 C T 10 GENIC homozygous 62898568