chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	22726689	22726690	C	T	20	GENIC	homozygous	115282658
12	22727040	22727041	G	A	15	GENIC	homozygous	115282660
12	22727154	22727155	T	A	11	GENIC	homozygous	115282662
12	22727184	22727185	G	C	12	GENIC	homozygous	115421854
12	22727720	22727721	C	T	15	GENIC	homozygous	115282664
12	22728227	22728227		G	15	GENIC	possibly homozygous	132892179
12	22728003	22728004	G	A	14	GENIC	homozygous	115367034
12	22729031	22729032	G	A	37	GENIC	homozygous	115484240
12	22729064	22729065	G	T	35	GENIC	homozygous	115484241
12	22729638	22729639	A	G	26	GENIC	homozygous	115484242
12	22729959	22729960	T	G	27	GENIC	homozygous	115484243
12	22729973	22729974	A	T	22	GENIC	homozygous	115484244
12	22730293	22730294	A	T	21	GENIC	homozygous	123609744
12	22730294	22730295	A	T	21	GENIC	homozygous	123609745
12	22731093	22731093		TTTTC	13	GENIC	homozygous	131490570
12	22731312	22731313	A	G	26	GENIC	homozygous	115484245
12	22731388	22731389	G	A	16	GENIC	possibly homozygous	132893839
12	22731541	22731542	C	T	15	GENIC	homozygous	115484246
12	22731551	22731552	G	A	15	GENIC	homozygous	115484247
12	22731680	22731681	G	A	15	GENIC	homozygous	115484248
12	22731756	22731757	T	C	14	GENIC	homozygous	115484249
12	22730295	22730296	A	T	21	GENIC	homozygous	115581421
12	22731399	22731400	T	C	15	GENIC	homozygous	115664557