chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	33066511	33066512	G	T	15	GENIC	heterozygous	50176153
12	33073248	33073250	CA	--	4	GENIC	heterozygous	50314022
12	33079191	33079192	C	CT	14	GENIC	heterozygous	50176155
12	33084463	33084464	G	GCGTGCACAGA	24	GENIC	homozygous	50379080
12	33099276	33099277	G	-	10	GENIC	heterozygous	50176157
12	33100307	33100308	T	-	7	GENIC	heterozygous	50314026
12	33111940	33111941	A	ACC	16	GENIC	homozygous	50176159
12	33138771	33138772	A	AGATG	10	GENIC	homozygous	50379081
12	33146405	33146406	T	-	13	GENIC	heterozygous	50176162
12	33148628	33148629	C	CAGAT	10	GENIC	homozygous	50176163
12	33155411	33155412	C	T	19	GENIC	heterozygous	50379082
12	33157454	33157455	G	-	6	GENIC	homozygous	50176164
12	33163335	33163337	TG	--	10	GENIC	heterozygous	50176165
12	33163400	33163401	T	-	6	GENIC	heterozygous	50379083
12	33164678	33164679	A	-	11	GENIC	heterozygous	50176166
12	33168869	33168871	GG	--	6	GENIC	heterozygous	50176167
12	33168870	33168871	G	GGGGA	6	GENIC	homozygous	50176168
12	33171360	33171361	G	GT	18	GENIC	heterozygous	50379084