chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	34336188	34336189	A	C	26	GENIC	homozygous	112847493
15	34336273	34336274	T	C	17	GENIC	homozygous	112847495
15	34336325	34336326	C	G	18	GENIC	homozygous	112847497
15	34336416	34336417	G	C	21	GENIC	homozygous	112847499
15	34336637	34336638	A	C	28	GENIC	homozygous	118995329
15	34336745	34336746	C	T	26	GENIC	homozygous	112847501
15	34336808	34336809	G	C	28	GENIC	homozygous	112847503
15	34336891	34336892	A	G	29	GENIC	homozygous	112847505
15	34336996	34336997	C	G	24	GENIC	homozygous	112847507
15	34337123	34337124	A	G	29	GENIC	homozygous	118995330
15	34337128	34337129	G	A	30	GENIC	possibly homozygous	118995331
15	34337273	34337274	C	T	27	GENIC	homozygous	112847513
15	34337334	34337335	C	T	28	GENIC	homozygous	112847515
15	34337358	34337359	T	C	30	GENIC	homozygous	112847517
15	34338767	34338768	A	G	16	GENIC	homozygous	112847519
15	34339017	34339018	C	T	19	GENIC	homozygous	112847521
15	34339058	34339059	C	T	21	GENIC	homozygous	112847523
15	34339335	34339336	A	G	12	GENIC	homozygous	112847525
15	34339414	34339415	G	A	23	GENIC	homozygous	112847527