chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	53191168	53191169	A	T	18	GENIC	homozygous	76127776
2	53191301	53191302	C	A	13	GENIC	possibly homozygous	78677212
2	53192958	53192959	T	G	20	GENIC	homozygous	76127781
2	53193717	53193718	C	T	10	GENIC	heterozygous	78695093
2	53194262	53194263	A	G	16	GENIC	homozygous	74716323
2	53195464	53195465	G	A	21	GENIC	homozygous	76127783
2	53195796	53195797	T	A	25	GENIC	homozygous	74716333
2	53195949	53195950	T	C	26	GENIC	homozygous	76127785
2	53196121	53196122	G	A	30	GENIC	homozygous	74716335
2	53196980	53196981	C	G	14	GENIC	homozygous	74716339
2	53196997	53196998	G	A	16	GENIC	homozygous	74716341
2	53197338	53197339	A	G	16	GENIC	homozygous	74716343
2	53197363	53197364	A	G	15	GENIC	homozygous	74716345
2	53197432	53197433	T	A	9	GENIC	homozygous	74716347
2	53199989	53199990	G	C	9	GENIC	heterozygous	74716351
2	53210245	53210246	C	T	16	GENIC	homozygous	74716353
2	53210266	53210267	T	C	10	GENIC	homozygous	74716355
2	53211382	53211383	G	C	5	GENIC	homozygous	74716363
2	53211415	53211416	G	T	7	GENIC	homozygous	74716365
2	53211421	53211422	T	C	9	GENIC	homozygous	74716367
2	53211542	53211543	T	G	7	GENIC	homozygous	74716369
2	53211568	53211569	A	G	6	GENIC	homozygous	74716371
2	53212307	53212308	C	T	30	GENIC	homozygous	74716373
2	53213457	53213458	C	T	28	GENIC	homozygous	76127787
2	53213604	53213605	C	T	30	GENIC	homozygous	76127789
2	53217756	53217757	A	G	16	GENIC	homozygous	76127791
2	53217788	53217789	T	C	17	GENIC	homozygous	76127793
2	53200244	53200245	G	A	23	GENIC	heterozygous	73604002
2	53210001	53210002	C	A	4	GENIC	heterozygous	73604006