chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	59986643	59986644	T	C	40	GENIC	homozygous	155097606
18	59986722	59986723	G	T	40	GENIC	homozygous	140333311
18	59987168	59987169	C	G	33	GENIC	homozygous	140333312
18	59987189	59987190	T	C	34	GENIC	homozygous	140333313
18	59987220	59987221	C	G	34	GENIC	homozygous	140333314
18	59987349	59987350	T	G	41	GENIC	homozygous	140333315
18	59987414	59987415	G	A	40	GENIC	homozygous	140333316
18	59987667	59987668	G	A	28	GENIC	homozygous	140333317
18	59987689	59987690	G	A	31	GENIC	homozygous	140333318
18	59988482	59988483	T	A	49	GENIC	homozygous	140333322
18	59987700	59987701	G	T	34	GENIC	homozygous	140333319
18	59988177	59988178	G	A	49	GENIC	homozygous	140333320
18	59988338	59988339	A	G	36	GENIC	homozygous	140333321
18	59987759	59987772	ATTGGGCAATGTC		45	GENIC	homozygous	140227237
18	59988420	59988420		C	42	GENIC	homozygous	140227238
18	59988598	59988599	A	G	45	GENIC	homozygous	140333323
18	59988701	59988702	G	T	50	GENIC	homozygous	140333324
18	59989416	59989417	G	C	40	GENIC	homozygous	140333325
18	59989646	59989647	T	C	38	GENIC	homozygous	140333326
18	59989707	59989708	T	C	43	GENIC	homozygous	140333327
18	59990096	59990097	G	C	42	GENIC	homozygous	140333328