chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	253689916	253689917	T	C	12	GENIC	homozygous	110395602
2	253690129	253690130	C	T	29	GENIC	homozygous	110395604
2	253690369	253690370	A	G	31	GENIC	homozygous	110395606
2	253690557	253690558	C	T	25	GENIC	homozygous	110395608
2	253690682	253690683	A	C	27	GENIC	homozygous	110395610
2	253690693	253690694	C	T	30	GENIC	homozygous	110395612
2	253690827	253690828	C	T	40	GENIC	homozygous	110395614
2	253690864	253690865	G	A	41	GENIC	homozygous	110395618
2	253690868	253690869	G	A	42	GENIC	possibly homozygous	110395620
2	253691569	253691570	T	A	23	GENIC	homozygous	110395622
2	253691714	253691715	A	G	13	GENIC	homozygous	110395624
2	253692080	253692081	A	G	45	GENIC	homozygous	111424387
2	253694021	253694022	A	C	21	GENIC	homozygous	110395626
2	253694158	253694159	A	G	17	GENIC	homozygous	110395628
2	253694519	253694520	G	T	11	GENIC	homozygous	110395630
2	253695126	253695127	A	G	34	GENIC	homozygous	110395632
2	253695504	253695505	A	G	12	GENIC	homozygous	110395634
2	253695694	253695695	G	A	30	GENIC	homozygous	110395636
2	253695964	253695965	A	T	24	GENIC	possibly homozygous	110395638
2	253696247	253696248	G	A	22	GENIC	homozygous	110395640
2	253696413	253696414	T	A	20	GENIC	homozygous	110395642
2	253697943	253697944	G	A	28	GENIC	homozygous	110395646
2	253698219	253698220	T	A	16	GENIC	homozygous	110395648