chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	32433631	32433632	G	GCTTAT	12	GENIC	heterozygous	50563027
12	32433718	32433719	C	CA	20	GENIC	heterozygous	50443527
12	32433768	32433769	A	AAT	17	GENIC	heterozygous	50175724
12	32434112	32434113	C	T	27	GENIC	homozygous	50443528
12	32434494	32434495	T	-	17	GENIC	homozygous	50443530
12	32434775	32434776	C	CATTATTATT	19	GENIC	homozygous	50443532
12	32434830	32434832	TC	--	15	GENIC	possibly homozygous	50443535
12	32435208	32435209	A	T	15	GENIC	homozygous	50443537
12	32435233	32435234	G	A	13	GENIC	homozygous	50443539
12	32435553	32435554	A	G	18	GENIC	homozygous	50443540
12	32435580	32435581	T	C	20	GENIC	homozygous	50443542
12	32435599	32435600	T	-	21	GENIC	homozygous	50443544
12	32435785	32435786	A	G	15	GENIC	homozygous	50443546
12	32435889	32435890	T	-	13	GENIC	heterozygous	50600728
12	32433833	32433834	C	CAAAAAA	9	GENIC	heterozygous	50541074
12	32433833	32433834	C	CAAAAAAAAAA	9	GENIC	heterozygous	50510248
12	32433836	32433837	C	CAAAAAACAAAAAACAAAAAACAA	9	GENIC	heterozygous	50510250
12	32436564	32436565	A	T	16	GENIC	homozygous	50443548
12	32437441	32437442	C	T	16	GENIC	homozygous	50443550
12	32438129	32438130	C	A	19	GENIC	homozygous	50443552
12	32438271	32438272	C	CAGAG	23	GENIC	homozygous	50443554
12	32438996	32438997	A	G	24	GENIC	homozygous	50443556
12	32439251	32439252	G	T	20	GENIC	homozygous	50443558
12	32439323	32439324	A	-	11	GENIC	homozygous	50443560
12	32439823	32439824	T	C	18	GENIC	homozygous	50443562
12	32439934	32439935	A	G	21	GENIC	homozygous	50443564
12	32440461	32440462	T	C	17	GENIC	homozygous	50443566
12	32441227	32441228	T	C	26	GENIC	homozygous	50443568
12	32442271	32442272	A	T	14	GENIC	homozygous	50443570
12	32443416	32443417	A	G	27	GENIC	homozygous	50443572
12	32439522	32439599	CCTGCATAGAAACAAACATTCTTCAATCGCTGTCACCTTAAAAGTAAGTGAGACTCATTCATAATTTTAAGTTCTTA	-----------------------------------------------------------------------------	23	GENIC	heterozygous	50598204
12	32439665	32439666	T	-	20	GENIC	heterozygous	50570135