chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	71830154	71830155	C	CTG	38	GENIC	homozygous	48786756
14	71836923	71836924	A	AGATGCTTCCCTAGCCTTTAGTTTAGT	45	GENIC	homozygous	48786758
14	71837004	71837005	G	GA	28	GENIC	homozygous	48786760
14	71837013	71837014	G	GA	29	GENIC	homozygous	48786762
14	71837018	71837019	T	TC	30	GENIC	homozygous	48786764
14	71837706	71837707	C	-	46	GENIC	homozygous	49314256
14	71837710	71837711	G	A	46	GENIC	homozygous	49290715
14	71838284	71838285	T	TTTTGAAC	5	GENIC	homozygous	49314257
14	71838287	71838288	C	CTTGCCTCAAAGTGGCTAGGTGACTCTGGGCTGT	5	GENIC	homozygous	49314258
14	71839812	71839813	A	-	36	GENIC	homozygous	48786770
14	71839823	71839824	G	T	38	GENIC	homozygous	48786772
14	71840760	71840761	C	CTCTTAACCTCTGAGCCGACTCTCCACCCCCCTAACCACCCCTTTTTCCCCATTGTTGCTCTTATCCATTACTATAGATGCTACCTACCTCAGAGAATT	31	GENIC	homozygous	49314259
14	71842378	71842381	CAC	---	8	GENIC	heterozygous	49314260
14	71842380	71842381	C	-	8	GENIC	heterozygous	48786774