chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	48718987	48718988	G	T	35	GENIC	possibly homozygous	50229013
12	48718991	48718992	A	G	31	GENIC	homozygous	50229015
12	48720342	48720343	A	G	41	GENIC	homozygous	50229017
12	48720661	48720662	A	G	32	GENIC	possibly homozygous	50229019
12	48720661	48720662	A	AAAGAAAGAAAG	27	GENIC	heterozygous	50229021
12	48721335	48721336	C	T	15	GENIC	heterozygous	50343550
12	48721343	48721344	C	T	15	GENIC	heterozygous	50229023
12	48722154	48722155	T	C	42	GENIC	homozygous	50229025
12	48722566	48722567	A	T	38	GENIC	homozygous	50229027
12	48722709	48722710	C	T	30	GENIC	homozygous	50229029
12	48723786	48723787	A	AACACAC	14	GENIC	heterozygous	50229031
12	48723786	48723787	A	AACACACAC	14	GENIC	heterozygous	50229033
12	48724479	48724480	T	TA	43	GENIC	homozygous	50229035
12	48724660	48724661	A	G	35	GENIC	homozygous	50229037
12	48724758	48724762	AGGG	----	8	GENIC	homozygous	50229039
12	48724880	48724881	C	T	16	GENIC	homozygous	50229041
12	48725390	48725391	T	C	32	GENIC	homozygous	50229043
12	48725874	48725875	T	A	12	GENIC	heterozygous	50343552
12	48726205	48726206	A	C	40	GENIC	homozygous	50229045
12	48726214	48726215	A	G	41	GENIC	homozygous	50229047
12	48726323	48726324	A	G	54	GENIC	homozygous	50229049
12	48726719	48726720	A	G	27	GENIC	homozygous	50229051
12	48726975	48726976	C	T	29	GENIC	homozygous	50229053
12	48726998	48726999	G	A	24	GENIC	homozygous	50229055
12	48727036	48727037	T	C	28	GENIC	homozygous	50229057