chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	74098849	74098850	T	G	26	GENIC	possibly homozygous	112031397
16	74100587	74100588	A	T	16	GENIC	homozygous	111860619
16	74101723	74101724	A	G	17	GENIC	homozygous	111860620
16	74101895	74101896	G	A	27	GENIC	homozygous	112031399
16	74102191	74102192	G	A	19	GENIC	homozygous	112031401
16	74102237	74102238	G	A	23	GENIC	homozygous	112031403
16	74099758	74099759	G	A	7	GENIC	homozygous	119199608
16	74099852	74099853	A	C	11	GENIC	homozygous	112252746
16	74100125	74100126	C	G	10	GENIC	homozygous	112259706
16	74100677	74100678	C	T	17	GENIC	homozygous	112115080
16	74101245	74101246	A	G	16	GENIC	homozygous	112115082
16	74102610	74102610		A	15	GENIC	homozygous	129381529
16	74102643	74102644	A	G	19	GENIC	homozygous	119199609
16	74102756	74102757	A	G	16	GENIC	homozygous	112361287
16	74102770	74102771	T	C	17	GENIC	homozygous	119199610
16	74102880	74102881	C	A	13	GENIC	possibly homozygous	119199611
16	74102895	74102896	A	G	14	GENIC	homozygous	119129199
16	74103124	74103125	T	C	17	GENIC	homozygous	112031405
16	74103400	74103401	C	A	19	GENIC	homozygous	112115084
16	74103651	74103652	G	A	10	GENIC	homozygous	112031407
16	74103662	74103663	A	G	11	GENIC	homozygous	111860621
16	74103745	74103746	G	A	8	GENIC	homozygous	112031410
16	74103847	74103848	A	G	9	GENIC	homozygous	112031412
16	74103943	74103944	A	G	11	GENIC	homozygous	112031414
16	74103968	74103969	T	C	13	GENIC	homozygous	111860622
16	74104507	74104508	A	G	17	GENIC	homozygous	111860624
16	74104510	74104511	C	T	17	GENIC	homozygous	111860625
16	74104512	74104513	A	C	17	GENIC	homozygous	111860626
16	74104605	74104606	G	A	15	GENIC	homozygous	112031416
16	74104672	74104673	G	A	16	GENIC	homozygous	111860628
16	74104790	74104791	G	T	18	GENIC	homozygous	112031418
16	74104904	74104905	C	G	15	GENIC	homozygous	111860630
16	74103189	74103189		TGATGTGCTGTCCTCCCTCCTG	16	GENIC	homozygous	131181780
16	74103233	74103233		TGATGTGCCGTCCTCCCTCTCG	14	GENIC	homozygous	131181781