chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	43519065	43519066	G	T	15	GENIC	homozygous	111053222
17	43520078	43520079	C	T	26	GENIC	homozygous	111053223
17	43521071	43521072	G	A	26	GENIC	homozygous	111053225
17	43522593	43522594	A	G	39	GENIC	homozygous	111053227
17	43522799	43522800	A	G	40	GENIC	homozygous	111053229
17	43523177	43523178	T	C	28	GENIC	homozygous	111053231
17	43523749	43523750	A	G	34	GENIC	homozygous	111053235
17	43524789	43524790	C	T	40	GENIC	homozygous	111053237
17	43528814	43528815	G	T	22	GENIC	homozygous	111053239
17	43530232	43530233	T	C	31	GENIC	homozygous	111053241
17	43530952	43530953	G	T	27	GENIC	homozygous	111053243
17	43531337	43531338	A	G	29	GENIC	homozygous	111053245
17	43535005	43535006	A	G	20	GENIC	homozygous	111053247
17	43535196	43535197	G	A	20	GENIC	homozygous	111053249
17	43535683	43535684	C	T	14	GENIC	homozygous	111053251
17	43537206	43537207	C	T	20	GENIC	homozygous	111053253
17	43537877	43537878	T	C	17	GENIC	homozygous	111053255
17	43538132	43538133	G	A	29	GENIC	homozygous	111053257
17	43538495	43538496	G	A	30	GENIC	possibly homozygous	111053259
17	43540327	43540328	A	T	30	GENIC	homozygous	111244671
17	43542436	43542437	C	T	19	GENIC	homozygous	111053261
17	43543669	43543670	T	A	14	GENIC	homozygous	111053263