chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	2439188	2439189	C	T	30	GENIC	homozygous	46640170
18	2439282	2439283	C	A	20	GENIC	homozygous	46640172
18	2440834	2440835	G	A	23	GENIC	homozygous	46640174
18	2441079	2441080	C	CCT	11	GENIC	homozygous	46640176
18	2442203	2442204	A	G	17	GENIC	homozygous	46560686
18	2442590	2442591	A	-	28	GENIC	homozygous	46640180
18	2443263	2443264	A	AT	15	GENIC	homozygous	46640182
18	2444047	2444048	A	G	30	GENIC	homozygous	46640184
18	2444119	2444120	T	C	31	GENIC	homozygous	46640186
18	2444160	2444161	T	-	24	GENIC	possibly homozygous	46640188
18	2445100	2445101	T	TTAATC	29	GENIC	homozygous	46640190
18	2445298	2445299	C	A	25	GENIC	homozygous	46640192
18	2445777	2445778	T	C	9	GENIC	homozygous	46640194
18	2446275	2446276	A	C	32	GENIC	homozygous	46640196
18	2447054	2447055	T	-	19	GENIC	homozygous	46640198