chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10538418	10538418		TTTC	34	GENIC	heterozygous	131750782
17	10539532	10539532		G	22	GENIC	heterozygous	129421608
17	10539576	10539577	A	G	36	GENIC	homozygous	110954320
17	10542421	10542422	A	G	70	GENIC	homozygous	110954322
17	10542745	10542746	T	C	59	GENIC	homozygous	110954324
17	10543058	10543059	T	C	54	GENIC	homozygous	110954326
17	10543406	10543407	C	T	36	GENIC	homozygous	110954328
17	10543603	10543604	A	G	61	GENIC	homozygous	110954330
17	10543768	10543769	C	G	46	GENIC	homozygous	110954332
17	10544550	10544551	T	C	67	GENIC	homozygous	110954334
17	10544948	10544948		A	48	GENIC	homozygous	129421609
17	10544985	10544994	CGAAAAAAA		48	GENIC	homozygous	129421610
17	10544995	10544996	A	G	48	GENIC	homozygous	124297743
17	10545003	10545004	A	G	54	GENIC	homozygous	124297744
17	10545009	10545010	A	C	57	GENIC	homozygous	124297745
17	10545017	10545018	A	C	57	GENIC	homozygous	124297746
17	10545067	10545068	A	G	57	GENIC	homozygous	110954336
17	10545861	10545862	C	T	46	GENIC	possibly homozygous	110954338
17	10546825	10546826	A	G	67	GENIC	homozygous	110954340
17	10546960	10546961	T	C	63	GENIC	homozygous	110954342
17	10547488	10547489	G	A	63	GENIC	homozygous	110954344