chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	53190150	53190151	G	C	18	GENIC	homozygous	75957590
2	53191301	53191302	C	A	5	GENIC	homozygous	78677212
2	53194262	53194263	A	G	30	GENIC	homozygous	74716323
2	53194766	53194767	C	T	20	GENIC	homozygous	74716325
2	53196121	53196122	G	A	28	GENIC	homozygous	74716335
2	53193717	53193718	C	T	14	GENIC	heterozygous	78695093
2	53195111	53195112	G	A	28	GENIC	homozygous	74716327
2	53195281	53195282	C	T	23	GENIC	possibly homozygous	74716329
2	53195756	53195757	C	T	26	GENIC	homozygous	74716331
2	53195796	53195797	T	A	17	GENIC	homozygous	74716333
2	53196798	53196799	A	G	35	GENIC	homozygous	74716337
2	53196980	53196981	C	G	26	GENIC	homozygous	74716339
2	53196997	53196998	G	A	20	GENIC	homozygous	74716341
2	53197338	53197339	A	G	8	GENIC	homozygous	74716343
2	53197363	53197364	A	G	10	GENIC	homozygous	74716345
2	53197432	53197433	T	A	20	GENIC	homozygous	74716347
2	53210245	53210246	C	T	22	GENIC	possibly homozygous	74716353
2	53210266	53210267	T	C	19	GENIC	possibly homozygous	74716355
2	53211183	53211184	T	C	13	GENIC	heterozygous	74716361
2	53211382	53211383	G	C	9	GENIC	heterozygous	74716363
2	53211415	53211416	G	T	4	GENIC	homozygous	74716365
2	53211421	53211422	T	C	3	GENIC	homozygous	74716367
2	53211542	53211543	T	G	12	GENIC	heterozygous	74716369
2	53211647	53211648	C	G	16	GENIC	possibly homozygous	76485678
2	53212307	53212308	C	T	24	GENIC	homozygous	74716373
2	53213552	53213553	T	A	35	GENIC	homozygous	75504421
2	53213818	53213819	G	T	28	GENIC	homozygous	74716375
2	53213937	53213938	A	G	16	GENIC	homozygous	74716379
2	53215197	53215198	G	A	18	GENIC	homozygous	75957602
2	53210001	53210002	C	A	7	GENIC	homozygous	73604006
2	53215020	53215021	C	T	13	GENIC	homozygous	75611782
2	53216470	53216471	G	A	34	GENIC	homozygous	74716385
2	53217473	53217474	A	G	34	GENIC	homozygous	74716387