chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 23960800 23960801 T A 5 GENIC homozygous 111953319 16 23961159 23961160 C T 13 GENIC homozygous 111953321 16 23961162 23961163 T G 13 GENIC homozygous 111953323 16 23961168 23961169 G A 15 GENIC homozygous 111953325 16 23962698 23962699 C T 28 GENIC homozygous 111953327 16 23962828 23962829 A G 26 GENIC homozygous 111953329 16 23962931 23962932 G T 26 GENIC homozygous 111761457 16 23962914 23962915 C A 27 GENIC homozygous 111761455 16 23963233 23963234 A C 22 GENIC homozygous 111761461 16 23965643 23965644 A T 15 GENIC homozygous 111761467 16 23965888 23965889 G T 26 GENIC homozygous 111761469 16 23969052 23969053 A G 31 GENIC homozygous 111761473 16 23969229 23969230 C T 31 GENIC homozygous 112220481 16 23964014 23964015 C G 26 GENIC homozygous 112220475 16 23965734 23965735 A C 17 GENIC homozygous 112220476 16 23966266 23966267 G A 18 GENIC homozygous 112220477 16 23967243 23967244 T C 22 GENIC homozygous 112220478 16 23968458 23968459 G A 22 GENIC homozygous 112220479 16 23968750 23968751 C A 20 GENIC homozygous 112220480 16 23980207 23980208 A G 34 GENIC homozygous 112220482 16 23980253 23980254 A C 27 GENIC homozygous 112220483 16 23985729 23985730 A G 14 GENIC homozygous 111761489 16 23990609 23990610 G A 23 GENIC homozygous 111761515 16 23990999 23991000 G T 22 GENIC homozygous 111761521 16 23991516 23991517 G A 13 GENIC homozygous 111761523