chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10739273	10739274	C	T	23	GENIC	homozygous	111525184
17	10739799	10739800	A	T	21	GENIC	homozygous	111637380
17	10741444	10741445	T	C	15	GENIC	homozygous	111231080
17	10741502	10741503	A	G	20	GENIC	homozygous	111231082
17	10746605	10746606	C	G	23	GENIC	homozygous	111525186
17	10746614	10746615	T	C	23	GENIC	homozygous	111525188
17	10750313	10750314	A	G	19	GENIC	homozygous	111525190
17	10751186	10751187	A	G	20	GENIC	homozygous	111525192
17	10752551	10752552	T	C	25	GENIC	homozygous	111525194
17	10752621	10752622	A	C	17	GENIC	homozygous	111525196
17	10752891	10752892	C	T	14	GENIC	homozygous	111525198
17	10753607	10753608	G	A	12	GENIC	homozygous	111525200
17	10754337	10754338	T	G	16	GENIC	homozygous	111525202
17	10760680	10760681	T	C	14	GENIC	homozygous	110955061
17	10761275	10761276	A	T	29	GENIC	homozygous	110955063
17	10763062	10763063	T	C	13	GENIC	homozygous	111525204
17	10764190	10764191	C	T	35	GENIC	homozygous	111525206
17	10764929	10764930	C	T	14	GENIC	homozygous	111637382
17	10764980	10764981	A	C	14	GENIC	homozygous	111525208
17	10767457	10767458	C	T	9	GENIC	homozygous	111637385
17	10767474	10767475	A	G	10	GENIC	heterozygous	111655087
17	10768640	10768641	A	G	22	GENIC	homozygous	111525210
17	10768956	10768957	A	G	27	GENIC	homozygous	111525212
17	10769187	10769188	T	G	26	GENIC	homozygous	111167716
17	10770984	10770985	A	G	21	GENIC	homozygous	111525214
17	10771157	10771158	C	T	21	GENIC	homozygous	111525216
17	10772251	10772252	T	C	19	GENIC	homozygous	111525218
17	10772389	10772390	C	T	15	GENIC	homozygous	111525220