chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	53190150	53190151	G	C	9	GENIC	homozygous	75957590
2	53191364	53191365	G	C	5	GENIC	homozygous	75957592
2	53194262	53194263	A	G	16	GENIC	homozygous	74716323
2	53194746	53194746		T	14	GENIC	heterozygous	75957594
2	53194766	53194767	C	T	13	GENIC	homozygous	74716325
2	53195111	53195112	G	A	13	GENIC	homozygous	74716327
2	53195281	53195282	C	T	25	GENIC	homozygous	74716329
2	53195756	53195757	C	T	15	GENIC	homozygous	74716331
2	53195796	53195797	T	A	9	GENIC	homozygous	74716333
2	53196121	53196122	G	A	8	GENIC	homozygous	74716335
2	53196386	53196388	AT		15	GENIC	homozygous	75957596
2	53196798	53196799	A	G	18	GENIC	homozygous	74716337
2	53196980	53196981	C	G	17	GENIC	homozygous	74716339
2	53196997	53196998	G	A	16	GENIC	homozygous	74716341
2	53197338	53197339	A	G	4	GENIC	homozygous	74716343
2	53197363	53197364	A	G	7	GENIC	homozygous	74716345
2	53197432	53197433	T	A	8	GENIC	homozygous	74716347
2	53210245	53210246	C	T	11	GENIC	homozygous	74716353
2	53213552	53213553	T	A	5	GENIC	homozygous	75504421
2	53213818	53213819	G	T	17	GENIC	homozygous	74716375
2	53214175	53214176	C		23	GENIC	possibly homozygous	75957598
2	53214316	53214317	A	G	5	GENIC	homozygous	75957600
2	53215197	53215198	G	A	7	GENIC	homozygous	75957602
2	53215206	53215209	TCT		8	GENIC	heterozygous	75957604
2	53216470	53216471	G	A	19	GENIC	homozygous	74716385
2	53216564	53216564		T	25	GENIC	heterozygous	75957606
2	53217473	53217474	A	G	15	GENIC	homozygous	74716387
2	53215018	53215019	C	T	6	GENIC	homozygous	75611781