chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	25853524	25853525	C	A	1	GENIC	homozygous	50467243
12	25854834	25854835	C	G	7	GENIC	homozygous	50143425
12	25854991	25854992	A	G	2	GENIC	homozygous	50467249
12	25856638	25856639	G	T	5	GENIC	homozygous	50467251
12	25857351	25857352	C	G	3	GENIC	homozygous	50143445
12	25858943	25858945	GG	--	4	GENIC	homozygous	50297483
12	25861436	25861437	G	A	6	GENIC	heterozygous	50297498
12	25862020	25862021	C	T	28	GENIC	homozygous	50467261
12	25862507	25862508	T	C	14	GENIC	possibly homozygous	50419305
12	25863180	25863181	A	G	23	GENIC	possibly homozygous	50143492
12	25863223	25863226	TTT	---	4	GENIC	homozygous	50297508
12	25863248	25863249	G	A	14	GENIC	possibly homozygous	50467263
12	25863374	25863375	G	A	16	GENIC	possibly homozygous	50297512
12	25863753	25863754	G	GCCC	1	GENIC	homozygous	50372433
12	25863836	25863837	A	-	5	GENIC	homozygous	50143500
12	25866095	25866096	T	C	15	GENIC	homozygous	50143516
12	25866376	25866377	A	G	7	GENIC	heterozygous	50143519
12	25866444	25866445	G	T	7	GENIC	possibly homozygous	50143522
12	25866591	25866592	G	T	7	GENIC	possibly homozygous	50143528
12	25867064	25867065	A	G	4	GENIC	homozygous	50143530
12	25867066	25867067	A	G	4	GENIC	homozygous	50467265
12	25867122	25867123	C	CT	3	GENIC	homozygous	50372437
12	25868200	25868201	A	AAC	7	GENIC	heterozygous	50404335
12	25881399	25881400	T	TAC	9	GENIC	homozygous	50143597
12	25887522	25887523	C	G	3	GENIC	heterozygous	50143653
12	25895261	25895262	G	GTC	2	GENIC	homozygous	50143740
12	25897948	25897949	A	-	1	GENIC	homozygous	50143744
12	25911187	25911188	A	G	7	GENIC	heterozygous	50143881