chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	93343081	93343085	AAAT		20	GENIC	homozygous	138699683
10	93344380	93344381	T	C	22	GENIC	homozygous	138852431
10	93344784	93344785	A	G	17	GENIC	homozygous	138852432
10	93345248	93345249	A	G	21	GENIC	homozygous	138852433
10	93345495	93345496	G	A	24	GENIC	homozygous	138852434
10	93345890	93345891	A	C	25	GENIC	homozygous	138852435
10	93346135	93346141	TTCTTT		7	GENIC	homozygous	138699684
10	93347701	93347702	T	C	13	GENIC	homozygous	138852437
10	93348078	93348079	T	C	20	GENIC	homozygous	138852438
10	93349600	93349601	G	C	19	GENIC	homozygous	138852439
10	93349907	93349908	G	C	18	GENIC	homozygous	138852440
10	93350591	93350592	A	G	24	GENIC	homozygous	138852441
10	93351306	93351310	TTTG		14	GENIC	homozygous	138699686
10	93351314	93351315	T	G	16	GENIC	homozygous	138852442
10	93351398	93351399	T	A	17	GENIC	homozygous	138852443
10	93352379	93352380	T	C	12	GENIC	homozygous	138852444
10	93352519	93352520	G	A	18	GENIC	possibly homozygous	138852445
10	93352523	93352524	G	A	19	GENIC	possibly homozygous	138852446
10	93352790	93352791	T	C	15	GENIC	homozygous	138852447
10	93353397	93353398	T	C	11	GENIC	homozygous	138852448
10	93353570	93353571	G	A	27	GENIC	homozygous	138852449
10	93353695	93353696	C	T	23	GENIC	homozygous	138852450
10	93354008	93354009	C	T	22	GENIC	homozygous	138852451
10	93354066	93354067	A	G	26	GENIC	homozygous	138852452
10	93354121	93354122	C	T	25	GENIC	homozygous	138852453
10	93354322	93354323	C	A	19	GENIC	homozygous	138852454
10	93354622	93354623	G	A	21	GENIC	homozygous	138852455
10	93354816	93354817	C	T	20	GENIC	homozygous	138852456
10	93355614	93355615	C	T	15	GENIC	homozygous	138852457
10	93355688	93355689	G	A	18	GENIC	homozygous	138852458
10	93356017	93356018	T		21	GENIC	homozygous	138699690
10	93351342	93351343	A		19	GENIC	homozygous	138699687
10	93352521	93352521		A	18	GENIC	possibly homozygous	138699688
10	93353389	93353391	TG		10	GENIC	homozygous	138699689