chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	19054772	19054773	G	A	33	GENIC	homozygous	111176105
17	19054784	19054785	A	G	36	GENIC	homozygous	111176107
17	19055359	19055360	A	G	31	GENIC	homozygous	111176109
17	19055523	19055524	G	A	23	GENIC	homozygous	111176111
17	19056312	19056313	G	A	29	GENIC	homozygous	111176113
17	19056646	19056647	A	G	21	GENIC	homozygous	111176115
17	19057508	19057509	A	G	23	GENIC	homozygous	111176117
17	19058558	19058559	G	A	28	GENIC	homozygous	111176119
17	19058564	19058565	G	T	28	GENIC	homozygous	111176121
17	19059491	19059492	C	T	6	GENIC	homozygous	111413233
17	19059513	19059514	T	G	5	GENIC	homozygous	111315607
17	19059652	19059653	C	T	16	GENIC	homozygous	111176123
17	19060173	19060174	T	A	18	GENIC	homozygous	111176125
17	19060792	19060793	C	T	22	GENIC	homozygous	111176127
17	19061249	19061250	A	G	18	GENIC	homozygous	111176129
17	19061290	19061291	T	G	15	GENIC	homozygous	111176131
17	19061302	19061303	G	A	15	GENIC	homozygous	111176133