chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 250219498 250219499 C T 28 GENIC homozygous 110850067 2 250220264 250220265 C T 26 GENIC homozygous 110850071 2 250220998 250220999 A G 33 GENIC homozygous 110850073 2 250221403 250221404 G A 32 GENIC homozygous 110850075 2 250226766 250226767 G A 26 GENIC homozygous 110850078 2 250226983 250226984 G A 26 GENIC homozygous 110850080 2 250227831 250227832 G A 36 GENIC homozygous 110850082 2 250227885 250227886 C T 20 GENIC homozygous 110850083 2 250228000 250228001 C T 31 GENIC possibly homozygous 110850085 2 250228803 250228804 G T 13 GENIC homozygous 110850087 2 250230182 250230183 C T 33 GENIC homozygous 110850089 2 250230539 250230540 A C 14 GENIC homozygous 110850090 2 250231273 250231274 C A 31 GENIC possibly homozygous 110850092 2 250227699 250227700 G T 22 GENIC homozygous 110377652 2 250229531 250229532 A C 21 GENIC homozygous 110377656 2 250230871 250230872 A C 27 GENIC homozygous 110377658