chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 80547343 80547344 A AT 14 GENIC homozygous 762190357 17 80547353 80547354 G GT 15 GENIC homozygous 762190358 17 80547408 80547410 AA -- 5 GENIC heterozygous 762190359 17 80547409 80547410 A - 5 GENIC heterozygous 762190360 17 80547826 80547827 G T 13 GENIC homozygous 658554305 17 80548223 80548224 T C 31 GENIC homozygous 658554306 17 80548517 80548518 C T 26 GENIC homozygous 658554307 17 80549169 80549170 A G 4 GENIC homozygous 658554308 17 80549172 80549173 G A 6 GENIC homozygous 658554309 17 80549272 80549273 T C 33 GENIC homozygous 658554310 17 80549406 80549407 G A 6 GENIC homozygous 658554311 17 80550117 80550120 TTT --- 3 GENIC heterozygous 762190361 17 80550118 80550120 TT -- 3 GENIC heterozygous 762190362 17 80550138 80550139 G T 7 GENIC homozygous 658554312 17 80552120 80552121 G C 35 GENIC homozygous 658554313 17 80552129 80552130 G T 38 GENIC homozygous 658554314 17 80552169 80552170 C CCT 27 GENIC homozygous 762190364 17 80552276 80552277 A G 37 GENIC homozygous 658554315 17 80552311 80552312 C A 42 GENIC homozygous 658554316 17 80552457 80552458 C T 48 GENIC homozygous 658554317 17 80552701 80552702 G GCTCGTCA 23 GENIC homozygous 762190365 17 80552859 80552860 C - 48 GENIC homozygous 762190366 17 80552866 80552867 C T 49 GENIC homozygous 658554318 17 80553570 80553571 C CAA 6 GENIC homozygous 762190368 17 80553906 80553907 A G 20 GENIC homozygous 658554319 17 80554086 80554087 C CT 36 GENIC possibly homozygous 762190370 17 80554094 80554095 C G 36 GENIC possibly homozygous 658554320 17 80554103 80554104 C A 35 GENIC possibly homozygous 658554321 17 80554288 80554289 A G 13 GENIC homozygous 658554322 17 80554347 80554348 T TA 7 GENIC homozygous 762190371 17 80554424 80554425 G GA 6 GENIC homozygous 762190372 17 80554444 80554445 A C 7 GENIC homozygous 658554323