chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	100291857	100291858	T		12	GENIC	homozygous	137700512
6	100295567	100295568	T	G	20	GENIC	homozygous	137862686
6	100295736	100295737	C	G	29	GENIC	homozygous	137862687
6	100299867	100299867		T	12	GENIC	heterozygous	137700513
6	100302444	100302444		A	21	GENIC	homozygous	137700514
6	100303272	100303273	C	T	25	GENIC	homozygous	137862688
6	100303302	100303303	A	G	24	GENIC	homozygous	137862689
6	100305296	100305297	C	A	32	GENIC	homozygous	137862690
6	100305855	100305856	C	T	28	GENIC	homozygous	137862691
6	100305860	100305863	TCC		26	GENIC	homozygous	137700515
6	100313161	100313161		CTCCCCTCATGG	13	GENIC	homozygous	137700516
6	100318430	100318431	T		25	GENIC	homozygous	137700517
6	100318679	100318679		TGTGTA	25	GENIC	possibly homozygous	137700518
6	100320701	100320702	T	A	20	GENIC	homozygous	137862692
6	100320932	100320933	T	C	27	GENIC	homozygous	137862693
6	100321626	100321627	T	C	26	GENIC	homozygous	137862694
6	100322790	100322791	C	T	19	GENIC	homozygous	137862695
6	100323384	100323384		T	22	GENIC	possibly homozygous	137700519
6	100323731	100323732	G	A	31	GENIC	homozygous	137862696
6	100325993	100325994	A	G	27	GENIC	homozygous	137862697
6	100328257	100328258	T	G	35	GENIC	homozygous	137862698
6	100328685	100328686	G	A	19	GENIC	homozygous	137862699
6	100313835	100313836	G	C	7	GENIC	heterozygous	403181921
6	100313833	100313834	G		7	GENIC	heterozygous	403181918
6	100313833	100313834	G	C	7	GENIC	heterozygous	403181919
6	100313835	100313836	G		7	GENIC	heterozygous	403181920