chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	50502395	50502396	C	-	22	GENIC	homozygous	46154309
19	50502468	50502469	A	T	28	GENIC	homozygous	46154310
19	50502757	50502758	C	T	34	GENIC	homozygous	46154311
19	50502761	50502762	C	T	30	GENIC	homozygous	46154312
19	50502884	50502885	C	T	16	GENIC	homozygous	46154313
19	50503157	50503158	G	C	37	GENIC	homozygous	46154314
19	50503198	50503199	G	T	22	GENIC	homozygous	46154315
19	50503243	50503244	G	GAAAAAAAAAA	16	GENIC	homozygous	46566263
19	50503344	50503345	T	C	24	GENIC	homozygous	46154317
19	50503554	50503555	C	CT	39	GENIC	homozygous	46154318
19	50503701	50503702	A	T	29	GENIC	homozygous	46154319
19	50504714	50504715	A	-	23	GENIC	homozygous	46154320
19	50504718	50504719	A	-	24	GENIC	homozygous	46154322
19	50505292	50505293	A	G	28	GENIC	homozygous	46154323
19	50505620	50505621	G	GT	19	GENIC	homozygous	46154324
19	50505625	50505626	G	GT	20	GENIC	homozygous	46154325
19	50505717	50505718	C	T	30	GENIC	homozygous	46154326
19	50505726	50505727	A	AAC	12	GENIC	homozygous	46154327
19	50505973	50505974	C	T	31	GENIC	homozygous	46154328
19	50506424	50506425	C	T	33	GENIC	homozygous	46154329
19	50506504	50506505	T	C	29	GENIC	homozygous	46154330
19	50506751	50506752	G	A	32	GENIC	homozygous	46154331
19	50508376	50508377	C	T	12	GENIC	homozygous	46154332