chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 35644604 35644605 C A 37 GENIC homozygous 51408523 10 35644877 35644878 G A 33 GENIC homozygous 51408525 10 35645595 35645596 A G 22 GENIC homozygous 51408527 10 35645648 35645649 G A 19 GENIC homozygous 51408529 10 35645753 35645754 C CT 15 GENIC homozygous 51408531 10 35646249 35646250 T TA 24 GENIC homozygous 51408533 10 35646456 35646457 C A 15 GENIC homozygous 51408535 10 35646465 35646466 C A 18 GENIC homozygous 51408537 10 35646626 35646627 C CT 9 GENIC possibly homozygous 51408539 10 35646862 35646863 C CT 19 GENIC heterozygous 51408541 10 35647810 35647811 C T 33 GENIC homozygous 51408543 10 35647960 35647961 C CATCA 27 GENIC homozygous 51408545 10 35648059 35648060 A C 25 GENIC homozygous 51408549 10 35648144 35648147 TTA --- 28 GENIC homozygous 51408551 10 35648149 35648150 A - 29 GENIC homozygous 51408553 10 35648364 35648368 CAAA ---- 22 GENIC homozygous 52435365 10 35648368 35648369 C CGTTT 22 GENIC homozygous 52435367 10 35648391 35648392 T C 28 GENIC homozygous 51408555 10 35648422 35648423 A G 28 GENIC homozygous 51408557 10 35649061 35649062 C T 17 GENIC homozygous 51408559 10 35649071 35649072 C T 18 GENIC homozygous 51408561 10 35649108 35649109 T C 21 GENIC homozygous 51408563 10 35649202 35649203 C A 22 GENIC homozygous 51408565 10 35649915 35649916 G GT 20 GENIC homozygous 51408567 10 35650183 35650184 C CTT 25 GENIC homozygous 51408569 10 35650199 35650200 C CT 26 GENIC homozygous 51408571 10 35650512 35650513 A G 24 GENIC homozygous 51408575