chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	53189589	53189590	C	T	39	GENIC	homozygous	74716313
2	53191752	53191753	C	T	18	GENIC	homozygous	74716315
2	53192128	53192129	G	T	23	GENIC	homozygous	74716317
2	53192532	53192533	T	C	31	GENIC	homozygous	74716319
2	53193798	53193799	A	T	10	GENIC	homozygous	74716321
2	53194262	53194263	A	G	24	GENIC	possibly homozygous	74716323
2	53194697	53194698	A	G	18	GENIC	heterozygous	75755172
2	53194766	53194767	C	T	28	GENIC	homozygous	74716325
2	53195111	53195112	G	A	21	GENIC	possibly homozygous	74716327
2	53195281	53195282	C	T	31	GENIC	possibly homozygous	74716329
2	53195756	53195757	C	T	23	GENIC	possibly homozygous	74716331
2	53195796	53195797	T	A	23	GENIC	homozygous	74716333
2	53196121	53196122	G	A	24	GENIC	homozygous	74716335
2	53196387	53196388	T	A	3	GENIC	homozygous	75755173
2	53196798	53196799	A	G	19	GENIC	homozygous	74716337
2	53196980	53196981	C	G	28	GENIC	homozygous	74716339
2	53196997	53196998	G	A	34	GENIC	homozygous	74716341
2	53197338	53197339	A	G	24	GENIC	homozygous	74716343
2	53197363	53197364	A	G	25	GENIC	homozygous	74716345
2	53197432	53197433	T	A	12	GENIC	homozygous	74716347
2	53211683	53211684	T	A	6	GENIC	heterozygous	75755174
2	53212307	53212308	C	T	25	GENIC	homozygous	74716373
2	53213818	53213819	G	T	32	GENIC	homozygous	74716375
2	53213825	53213826	C	T	27	GENIC	homozygous	74716377
2	53213937	53213938	A	G	10	GENIC	homozygous	74716379
2	53214535	53214536	T	G	22	GENIC	homozygous	74716383
2	53216470	53216471	G	A	24	GENIC	homozygous	74716385
2	53217473	53217474	A	G	22	GENIC	homozygous	74716387
2	53217800	53217801	A	T	7	GENIC	heterozygous	75755175
2	53215018	53215019	C	T	6	GENIC	homozygous	75611781
2	53215020	53215021	C	T	7	GENIC	homozygous	75611782