chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 2439099 2439100 A G 24 GENIC possibly homozygous 46753033 18 2439168 2439169 A G 28 GENIC homozygous 46753034 18 2439177 2439178 G A 29 GENIC homozygous 46753035 18 2439188 2439189 C T 25 GENIC homozygous 46640170 18 2439214 2439215 C T 17 GENIC possibly homozygous 46753036 18 2439428 2439429 T TAA 5 GENIC homozygous 46753037 18 2439556 2439557 A T 11 GENIC homozygous 46753038 18 2440181 2440182 G A 16 GENIC homozygous 46753039 18 2440278 2440279 G A 13 GENIC homozygous 46753040 18 2440402 2440403 C T 17 GENIC homozygous 46753041 18 2440547 2440548 G GA 13 GENIC homozygous 46753042 18 2440570 2440571 A AAGAG 18 GENIC homozygous 46753043 18 2440726 2440727 C CGA 13 GENIC homozygous 46753044 18 2440804 2440805 C T 13 GENIC homozygous 46753045 18 2440834 2440835 G A 14 GENIC homozygous 46640174 18 2440988 2440989 T C 18 GENIC homozygous 46753046 18 2441057 2441058 T G 20 GENIC homozygous 46753047 18 2441079 2441080 C CCT 24 GENIC homozygous 46640176 18 2441127 2441128 G A 33 GENIC homozygous 46753048 18 2441414 2441415 C CA 14 GENIC homozygous 46753049 18 2441906 2441907 G - 16 GENIC homozygous 46874387 18 2442203 2442204 A G 29 GENIC homozygous 46560686 18 2442590 2442591 A - 18 GENIC homozygous 46640180 18 2444047 2444048 A G 22 GENIC homozygous 46640184 18 2444119 2444120 T C 21 GENIC homozygous 46640186 18 2444160 2444161 T - 18 GENIC homozygous 46640188 18 2445100 2445101 T TTAATC 19 GENIC homozygous 46640190 18 2445298 2445299 C A 25 GENIC homozygous 46640192 18 2445777 2445778 T C 10 GENIC homozygous 46640194 18 2446275 2446276 A C 19 GENIC homozygous 46640196 18 2447054 2447055 T - 14 GENIC homozygous 46640198