chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	69444339	69444340	A	T	28	GENIC	homozygous	113031329
4	69444458	69444459	T	G	32	GENIC	homozygous	113031330
4	69444542	69444543	C	T	28	GENIC	homozygous	112695779
4	69444736	69444737	T	C	33	GENIC	homozygous	113031331
4	69444860	69444861	A	C	33	GENIC	homozygous	113031332
4	69445057	69445058	A	T	23	GENIC	homozygous	112695781
4	69445176	69445177	T	C	21	GENIC	homozygous	113031333
4	69445285	69445286	A	G	24	GENIC	homozygous	113031334
4	69445404	69445405	G	A	26	GENIC	homozygous	113031335
4	69445451	69445452	T	C	26	GENIC	homozygous	113031336
4	69445586	69445587	T	A	29	GENIC	homozygous	113031337
4	69445677	69445678	G	A	22	GENIC	homozygous	113031338
4	69445753	69445754	T	C	24	GENIC	homozygous	113031339
4	69445805	69445806	G	C	27	GENIC	homozygous	113031340
4	69445887	69445888	C	T	22	GENIC	homozygous	113031341
4	69445930	69445931	A	G	24	GENIC	homozygous	113031342
4	69446179	69446180	G	A	22	GENIC	homozygous	112695783
4	69446217	69446218	T	C	20	GENIC	homozygous	113031343
4	69446408	69446409	G	A	22	GENIC	homozygous	112695785
4	69447560	69447561	G	A	24	GENIC	homozygous	113031344
4	69447988	69447989	G	C	28	GENIC	homozygous	112695790
4	69448971	69448972	G	A	24	GENIC	homozygous	113031345
4	69451674	69451675	T	C	32	GENIC	homozygous	112695794
4	69449165	69449166	C	T	15	GENIC	homozygous	113031346
4	69449772	69449773	A	G	34	GENIC	homozygous	113031347
4	69449986	69449987	A	G	25	GENIC	homozygous	112695792
4	69450595	69450596	A	G	29	GENIC	homozygous	113031348
4	69451412	69451413	G	A	20	GENIC	homozygous	113031349
4	69451990	69451991	C	T	36	GENIC	homozygous	112695796
4	69452210	69452211	G	T	37	GENIC	homozygous	112695798
4	69452233	69452234	T	C	34	GENIC	homozygous	112695800