chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	25938741	25938742	G	A	11	GENIC	possibly homozygous	50144100
12	25938836	25938837	A	ATGC	6	GENIC	heterozygous	50144102
12	25939980	25939981	C	G	16	GENIC	heterozygous	50144104
12	25940199	25940200	C	T	16	GENIC	homozygous	50144106
12	25941802	25941803	T	A	9	GENIC	heterozygous	50144110
12	25941847	25941848	A	G	2	GENIC	heterozygous	50144112
12	25941930	25941931	A	G	1	GENIC	homozygous	50589463
12	25942087	25942088	T	G	28	GENIC	homozygous	50144120
12	25942329	25942330	T	C	20	GENIC	possibly homozygous	50144122
12	25942866	25942867	T	C	16	GENIC	possibly homozygous	50144126
12	25943166	25943167	C	T	18	GENIC	possibly homozygous	50144128
12	25943518	25943519	A	G	11	GENIC	homozygous	50144132
12	25943812	25943813	C	T	29	GENIC	homozygous	50144136
12	25943826	25943827	T	A	16	GENIC	homozygous	50144138
12	25943853	25943854	C	A	7	GENIC	homozygous	50144140
12	25943857	25943858	T	C	6	GENIC	homozygous	50144142
12	25944054	25944055	G	A	10	GENIC	homozygous	50144150
12	25944886	25944887	G	-	22	GENIC	possibly homozygous	50144152
12	25945042	25945043	A	C	19	GENIC	possibly homozygous	50144154
12	25945168	25945169	C	A	15	GENIC	possibly homozygous	50144156
12	25945197	25945198	A	G	15	GENIC	possibly homozygous	50419336
12	25945438	25945439	T	A	17	GENIC	possibly homozygous	50144158
12	25945980	25945981	C	A	11	GENIC	homozygous	50144160
12	25946084	25946085	T	C	15	GENIC	homozygous	50144162
12	25946191	25946192	G	GCAGCTCCGCCCAGGCCGC	3	GENIC	heterozygous	50144164
12	25946307	25946308	C	-	13	GENIC	heterozygous	50144166
12	25946316	25946317	A	C	14	GENIC	possibly homozygous	50144168
12	25946547	25946548	T	A	16	GENIC	homozygous	50144170
12	25947085	25947086	A	T	19	GENIC	homozygous	50144172
12	25947591	25947592	C	T	18	GENIC	heterozygous	50144176
12	25948456	25948457	A	G	15	GENIC	homozygous	50144178
12	25949075	25949076	C	T	22	GENIC	possibly homozygous	50144182