chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	50382477	50382478	T	C	53	GENIC	homozygous	111815375
16	50419224	50419225	A	C	23	GENIC	homozygous	111815469
16	50424585	50424585		T	34	GENIC	homozygous	129363553
16	50424586	50424587	C	A	34	GENIC	homozygous	124278934
16	50424588	50424588		GTAA	34	GENIC	homozygous	129363554
16	50424589	50424590	G	A	36	GENIC	homozygous	124278936
16	50424592	50424593	G	A	39	GENIC	homozygous	124278938
16	50424594	50424595	G	A	38	GENIC	homozygous	124278939
16	50433261	50433261		C	61	GENIC	homozygous	129363556
16	50441173	50441176	CGT		44	GENIC	homozygous	129363560
16	50441185	50441186	T		46	GENIC	homozygous	129363561
16	50441203	50441204	C		45	GENIC	homozygous	129363562
16	50441211	50441212	G	T	46	GENIC	homozygous	111815489
16	50441212	50441213	T	C	46	GENIC	homozygous	111815491
16	50441247	50441248	C		45	GENIC	homozygous	129363563
16	50441304	50441305	A		44	GENIC	homozygous	129363564
16	50441322	50441322		G	44	GENIC	homozygous	129363565
16	50441362	50441362		C	35	GENIC	homozygous	129363566
16	50441383	50441383		C	25	GENIC	homozygous	129363567
16	50441477	50441477		T	3	GENIC	homozygous	130703541
16	50465771	50465772	A	G	46	GENIC	homozygous	111815499
16	50465797	50465798	G	C	39	GENIC	homozygous	112220822
16	50465797	50465797		A	40	GENIC	homozygous	129363571
16	50465801	50465802	A	C	36	GENIC	homozygous	112111658
16	50465802	50465803	C	T	36	GENIC	homozygous	112111660
16	50465869	50465870	T	G	23	GENIC	homozygous	112398265
16	50467438	50467438		TTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGCAAGCA	9	GENIC	homozygous	129363573
16	50468971	50468971		C	50	GENIC	homozygous	129363574
16	50472495	50472495		G	9	GENIC	homozygous	129363577
16	50499306	50499307	C	A	13	GENIC	homozygous	111815649
16	50489410	50489412	TG		23	GENIC	heterozygous	130454150