chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	45199099	45199100	A	C	30	GENIC	homozygous	115339448
12	45204581	45204582	A	G	31	GENIC	homozygous	115339454
12	45206285	45206286	C	T	31	GENIC	homozygous	115392162
12	45206434	45206435	G	C	38	GENIC	homozygous	115392164
12	45207150	45207151	G	C	26	GENIC	homozygous	115392166
12	45207310	45207311	G	A	34	GENIC	homozygous	115392168
12	45207356	45207357	A	G	45	GENIC	homozygous	115392170
12	45207389	45207390	G	C	52	GENIC	homozygous	115392172
12	45207757	45207758	A	G	36	GENIC	homozygous	115392174
12	45208250	45208251	C	T	31	GENIC	homozygous	115392176
12	45208352	45208353	A	G	28	GENIC	homozygous	115339458
12	45208380	45208381	T	C	29	GENIC	homozygous	115392178
12	45208389	45208390	C	T	31	GENIC	homozygous	115392180
12	45208461	45208462	G	A	22	GENIC	homozygous	115392182
12	45208523	45208524	A	G	30	GENIC	homozygous	115392184
12	45208555	45208556	C	T	27	GENIC	homozygous	115392186
12	45208582	45208583	A	C	26	GENIC	homozygous	115392188
12	45209924	45209925	T	C	23	GENIC	homozygous	115392190
12	45210177	45210178	T	C	34	GENIC	homozygous	115339460
12	45211924	45211925	C	T	46	GENIC	homozygous	115392192
12	45212166	45212167	A	G	30	GENIC	homozygous	115339462
12	45213488	45213489	A	G	19	GENIC	homozygous	115339464
12	45215612	45215613	A	G	20	GENIC	homozygous	115392194
12	45215835	45215836	T	C	29	GENIC	homozygous	115392196
12	45216659	45216660	G	C	38	GENIC	homozygous	115339468
12	45217048	45217049	A	C	13	GENIC	homozygous	115392198
12	45217484	45217485	T	C	15	GENIC	homozygous	115392200
12	45217952	45217953	G	A	25	GENIC	homozygous	115392202
12	45218843	45218844	G	A	27	GENIC	homozygous	115392204
12	45218888	45218889	T	C	15	GENIC	homozygous	115392206
12	45219400	45219401	G	A	28	GENIC	homozygous	115392208
12	45220124	45220125	T	C	31	GENIC	homozygous	115339470
12	45221336	45221337	C	A	21	GENIC	homozygous	115392210
12	45208152	45208153	G	T	20	GENIC	homozygous	115430319
12	45208500	45208501	C	T	27	GENIC	homozygous	115430321