chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	14310031	14310032	A	G	25	GENIC	homozygous	58412636
3	14310074	14310075	T	C	29	GENIC	homozygous	58412637
3	14310495	14310496	T	C	23	GENIC	homozygous	58412638
3	14311376	14311377	T	G	22	GENIC	homozygous	58412639
3	14311424	14311425	T	C	19	GENIC	homozygous	57163819
3	14312029	14312030	G	T	31	GENIC	possibly homozygous	57163823
3	14312284	14312288	CCAT	----	18	GENIC	homozygous	58412640
3	14313276	14313277	C	A	20	GENIC	homozygous	57163825
3	14313697	14313698	G	-	23	GENIC	homozygous	58276692
3	14313888	14313889	A	T	26	GENIC	homozygous	58412641
3	14313907	14313908	T	C	30	GENIC	homozygous	57163827
3	14314791	14314792	T	C	37	GENIC	homozygous	57163833
3	14315100	14315101	T	C	24	GENIC	homozygous	57163837
3	14315259	14315264	TTTTT	-----	7	GENIC	heterozygous	58276694
3	14315260	14315264	TTTT	----	7	GENIC	possibly homozygous	58276696
3	14315277	14315282	GGTTC	-----	16	GENIC	heterozygous	57163841
3	14316007	14316008	C	T	35	GENIC	homozygous	58276700
3	14318324	14318325	C	T	23	GENIC	homozygous	57163851
3	14318550	14318551	G	A	20	GENIC	homozygous	58276711
3	14318571	14318572	C	T	23	GENIC	homozygous	58276713
3	14318888	14318889	G	C	45	GENIC	homozygous	58412642