chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	34051573	34051574	G	T	19	GENIC	homozygous	145077475
19	34052416	34052416		TTT	19	GENIC	homozygous	145068302
19	34052708	34052709	G	A	14	GENIC	homozygous	145077476
19	34052869	34052870	G	T	7	GENIC	homozygous	145077477
19	34054314	34054315	A		20	GENIC	homozygous	145068303
19	34054330	34054330		A	23	GENIC	possibly homozygous	145068304
19	34054710	34054711	G	A	22	GENIC	homozygous	145077478
19	34056113	34056114	C	A	17	GENIC	homozygous	145077479
19	34056892	34056893	C	T	23	GENIC	homozygous	145077480
19	34057146	34057147	T	C	18	GENIC	homozygous	145077481
19	34058033	34058036	TCT		15	GENIC	homozygous	145068305
19	34059714	34059715	T	C	17	GENIC	homozygous	145077482
19	34060842	34060843	G	A	22	GENIC	homozygous	145077483
19	34061369	34061370	T	C	15	GENIC	homozygous	145077484
19	34061693	34061694	G	A	24	GENIC	homozygous	145077485
19	34062087	34062088	T	C	20	GENIC	homozygous	145077486
19	34062223	34062224	G	A	25	GENIC	homozygous	145077487
19	34062302	34062303	A	G	21	GENIC	homozygous	145077488
19	34063539	34063540	T	C	21	GENIC	homozygous	145077489
19	34063819	34063820	C	T	12	GENIC	homozygous	145077490
19	34064196	34064202	TTTGTT		6	GENIC	homozygous	145068306
19	34064353	34064353		T	10	GENIC	homozygous	145068307
19	34065143	34065144	T	G	16	GENIC	homozygous	145077491
19	34065449	34065450	C	T	14	GENIC	homozygous	145077492
19	34065575	34065576	T	C	24	GENIC	possibly homozygous	145077493
19	34058035	34058036	T	C	15	GENIC	heterozygous	403450091
19	34058035	34058036	T		15	GENIC	homozygous	403450090
19	34056054	34056055	C		13	GENIC	homozygous	403450088
19	34056054	34056055	C	A	13	GENIC	heterozygous	403450089