chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	51577590	51577591	T	C	24	GENIC	possibly homozygous	115246263
6	51577697	51577698	C	T	34	GENIC	homozygous	115246265
6	51578317	51578318	T	C	26	GENIC	homozygous	115246267
6	51578339	51578340	C	T	22	GENIC	homozygous	115246269
6	51578511	51578512	T	C	39	GENIC	possibly homozygous	115246271
6	51578757	51578758	T	C	33	GENIC	homozygous	115246273
6	51578776	51578777	T	C	31	GENIC	homozygous	115246275
6	51578783	51578784	A	G	28	GENIC	homozygous	115246277
6	51578982	51578983	A	G	41	GENIC	homozygous	115246279
6	51578997	51578998	C	T	36	GENIC	homozygous	115246281
6	51579107	51579108	G	A	31	GENIC	homozygous	115246283
6	51579402	51579403	T	C	24	GENIC	homozygous	115246285
6	51579432	51579433	A	T	26	GENIC	homozygous	115246287
6	51579692	51579693	T	C	32	GENIC	homozygous	115246289
6	51579832	51579833	G	A	29	GENIC	homozygous	115246291
6	51580247	51580248	C	T	33	GENIC	homozygous	115246293
6	51580642	51580643	G	A	28	GENIC	possibly homozygous	115246295