chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	127229651	127229652	C	CT	19	GENIC	possibly homozygous	52882519
8	127230372	127230373	C	T	11	GENIC	homozygous	52882520
8	127230405	127230406	C	A	15	GENIC	homozygous	52882521
8	127230785	127230786	T	TC	13	GENIC	homozygous	52882523
8	127231174	127231175	T	C	26	GENIC	homozygous	53231911
8	127231666	127231667	C	T	21	GENIC	homozygous	52882524
8	127231980	127231981	T	C	11	GENIC	homozygous	52882525
8	127231996	127231997	A	G	9	GENIC	homozygous	52882526
8	127232263	127232264	G	A	17	GENIC	homozygous	52882527
8	127232284	127232285	T	C	14	GENIC	homozygous	52882528
8	127233589	127233590	T	C	17	GENIC	homozygous	52882529
8	127233661	127233662	A	T	14	GENIC	homozygous	52882530
8	127233694	127233695	T	C	16	GENIC	homozygous	52882531