chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	253689660	253689661	T	C	13	GENIC	homozygous	111293179
2	253689916	253689917	T	C	22	GENIC	homozygous	110395602
2	253690129	253690130	C	T	25	GENIC	homozygous	110395604
2	253690369	253690370	A	G	23	GENIC	homozygous	110395606
2	253690682	253690683	A	C	25	GENIC	homozygous	110395610
2	253690693	253690694	C	T	27	GENIC	homozygous	110395612
2	253691112	253691113	G	A	16	GENIC	homozygous	111293180
2	253691285	253691286	G	A	25	GENIC	homozygous	111293181
2	253691569	253691570	T	A	18	GENIC	homozygous	110395622
2	253691714	253691715	A	G	26	GENIC	homozygous	110395624
2	253693615	253693616	G	A	14	GENIC	homozygous	111293182
2	253694158	253694159	A	G	11	GENIC	homozygous	110395628
2	253694266	253694267	G	A	14	GENIC	homozygous	111293183
2	253695126	253695127	A	G	8	GENIC	homozygous	110395632
2	253695504	253695505	A	G	15	GENIC	homozygous	110395634
2	253695694	253695695	G	A	22	GENIC	homozygous	110395636
2	253696247	253696248	G	A	20	GENIC	homozygous	110395640
2	253696413	253696414	T	A	9	GENIC	homozygous	110395642
2	253697943	253697944	G	A	16	GENIC	homozygous	110395646
2	253698219	253698220	T	A	18	GENIC	homozygous	110395648
2	253698266	253698267	A	C	14	GENIC	homozygous	120132252