chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10539532	10539532		G	18	GENIC	heterozygous	129421608
17	10539576	10539577	A	G	32	GENIC	homozygous	110954320
17	10542421	10542422	A	G	62	GENIC	homozygous	110954322
17	10542745	10542746	T	C	53	GENIC	homozygous	110954324
17	10543058	10543059	T	C	49	GENIC	homozygous	110954326
17	10543406	10543407	C	T	45	GENIC	homozygous	110954328
17	10543603	10543604	A	G	44	GENIC	homozygous	110954330
17	10543768	10543769	C	G	34	GENIC	homozygous	110954332
17	10544550	10544551	T	C	38	GENIC	homozygous	110954334
17	10544948	10544948		A	31	GENIC	homozygous	129421609
17	10544985	10544994	CGAAAAAAA		32	GENIC	homozygous	129421610
17	10544995	10544996	A	G	32	GENIC	homozygous	124297743
17	10545003	10545004	A	G	30	GENIC	homozygous	124297744
17	10545009	10545010	A	C	31	GENIC	homozygous	124297745
17	10545017	10545018	A	C	35	GENIC	homozygous	124297746
17	10545067	10545068	A	G	35	GENIC	homozygous	110954336
17	10545861	10545862	C	T	38	GENIC	homozygous	110954338
17	10546825	10546826	A	G	44	GENIC	homozygous	110954340
17	10546960	10546961	T	C	60	GENIC	homozygous	110954342
17	10547488	10547489	G	A	48	GENIC	homozygous	110954344
17	10550473	10550477	TCCC		14	GENIC	heterozygous	129421611