chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	253689916	253689917	T	C	24	GENIC	homozygous	110395602
2	253690129	253690130	C	T	28	GENIC	homozygous	110395604
2	253690369	253690370	A	G	29	GENIC	homozygous	110395606
2	253690557	253690558	C	T	29	GENIC	homozygous	110395608
2	253690682	253690683	A	C	32	GENIC	homozygous	110395610
2	253690693	253690694	C	T	29	GENIC	homozygous	110395612
2	253691569	253691570	T	A	28	GENIC	homozygous	110395622
2	253691714	253691715	A	G	28	GENIC	homozygous	110395624
2	253694021	253694022	A	C	34	GENIC	homozygous	110395626
2	253694158	253694159	A	G	29	GENIC	homozygous	110395628
2	253694519	253694520	G	T	22	GENIC	homozygous	110395630
2	253695126	253695127	A	G	42	GENIC	homozygous	110395632
2	253695504	253695505	A	G	26	GENIC	homozygous	110395634
2	253695694	253695695	G	A	26	GENIC	homozygous	110395636
2	253696247	253696248	G	A	33	GENIC	homozygous	110395640
2	253696413	253696414	T	A	23	GENIC	homozygous	110395642
2	253698219	253698220	T	A	21	GENIC	homozygous	110395648
2	253698266	253698267	A	C	26	GENIC	homozygous	120132252