chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	53189589	53189590	C	T	27	GENIC	homozygous	74716313
2	53190642	53190643	C		13	GENIC	homozygous	76220645
2	53191752	53191753	C	T	26	GENIC	possibly homozygous	74716315
2	53192128	53192129	G	T	13	GENIC	homozygous	74716317
2	53192532	53192533	T	C	18	GENIC	homozygous	74716319
2	53193798	53193799	A	T	19	GENIC	homozygous	74716321
2	53194262	53194263	A	G	20	GENIC	homozygous	74716323
2	53194766	53194767	C	T	22	GENIC	homozygous	74716325
2	53195111	53195112	G	A	8	GENIC	homozygous	74716327
2	53195281	53195282	C	T	26	GENIC	homozygous	74716329
2	53196386	53196388	AT		13	GENIC	homozygous	75957596
2	53196798	53196799	A	G	16	GENIC	homozygous	74716337
2	53195756	53195757	C	T	23	GENIC	homozygous	74716331
2	53195796	53195797	T	A	13	GENIC	homozygous	74716333
2	53196121	53196122	G	A	16	GENIC	homozygous	74716335
2	53196980	53196981	C	G	16	GENIC	homozygous	74716339
2	53196997	53196998	G	A	17	GENIC	homozygous	74716341
2	53197338	53197339	A	G	10	GENIC	homozygous	74716343
2	53197363	53197364	A	G	6	GENIC	homozygous	74716345
2	53197432	53197433	T	A	6	GENIC	homozygous	74716347
2	53210245	53210246	C	T	4	GENIC	homozygous	74716353
2	53210879	53210880	C	T	10	GENIC	homozygous	74716359
2	53212307	53212308	C	T	7	GENIC	homozygous	74716373
2	53213818	53213819	G	T	13	GENIC	homozygous	74716375
2	53213825	53213826	C	T	10	GENIC	homozygous	74716377
2	53213937	53213938	A	G	5	GENIC	homozygous	74716379
2	53214175	53214176	C		17	GENIC	homozygous	75957598
2	53214312	53214313	G	A	4	GENIC	homozygous	74716381
2	53214535	53214536	T	G	17	GENIC	homozygous	74716383
2	53216470	53216471	G	A	18	GENIC	homozygous	74716385
2	53216564	53216564		T	23	GENIC	heterozygous	76220646
2	53217473	53217474	A	G	19	GENIC	homozygous	74716387
2	53209024	53209025	G	C	5	GENIC	homozygous	75806007