chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40341047	40341048	T	C	32	GENIC	homozygous	50203281
12	40341058	40341059	G	A	32	GENIC	homozygous	50203282
12	40341213	40341214	A	C	28	GENIC	homozygous	50422620
12	40341986	40341987	T	-	29	GENIC	homozygous	50203283
12	40342338	40342339	G	A	61	GENIC	homozygous	50203284
12	40342426	40342427	A	G	43	GENIC	homozygous	50203285
12	40342760	40342761	A	G	33	GENIC	homozygous	50203286
12	40343107	40343108	G	GT	16	GENIC	homozygous	50203287
12	40349984	40349985	G	GCACACACA	3	GENIC	heterozygous	50203304
12	40354386	40354387	G	A	39	GENIC	homozygous	50422621
12	40357415	40357419	GCGT	----	3	GENIC	homozygous	50203357
12	40357417	40357425	GTGCGCGG	--------	3	GENIC	homozygous	50203358
12	40357423	40357425	GG	--	2	GENIC	homozygous	50203359
12	40357445	40357449	TCTG	----	1	GENIC	homozygous	50203363
12	40357477	40357478	A	C	3	GENIC	homozygous	50203367
12	40357479	40357480	T	A	3	GENIC	homozygous	50203368
12	40357496	40357497	G	A	3	GENIC	homozygous	50203369
12	40357502	40357503	A	T	2	GENIC	homozygous	50203370
12	40357505	40357506	C	A	2	GENIC	homozygous	50203371
12	40357507	40357508	G	C	2	GENIC	homozygous	50203372
12	40357509	40357510	A	T	2	GENIC	homozygous	50203373
12	40357513	40357514	G	C	2	GENIC	homozygous	50203374
12	40357517	40357518	T	A	2	GENIC	homozygous	50203375
12	40357521	40357522	A	T	2	GENIC	homozygous	50203376
12	40358199	40358200	T	TC	13	GENIC	homozygous	50203380
12	40358206	40358207	T	TC	14	GENIC	homozygous	50203381
12	40358210	40358211	G	GC	14	GENIC	homozygous	50203382
12	40358443	40358444	C	G	15	GENIC	possibly homozygous	50203387
12	40358445	40358446	C	G	13	GENIC	homozygous	50203388
12	40358935	40358936	A	G	39	GENIC	heterozygous	50203390
12	40358973	40358974	A	G	50	GENIC	heterozygous	50203391
12	40359055	40359056	G	C	51	GENIC	heterozygous	50203392
12	40364121	40364122	A	-	17	GENIC	homozygous	50203393
12	40349984	40349985	G	GCACACA	3	GENIC	heterozygous	50323268
12	40364774	40364775	C	T	43	GENIC	homozygous	50203396
12	40364782	40364783	A	C	38	GENIC	homozygous	50203397