chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	98119505	98119506	C	T	32	GENIC	homozygous	117760545
9	98120065	98120066	C	T	30	GENIC	homozygous	117760546
9	98120202	98120203	T	C	32	GENIC	homozygous	117760547
9	98120209	98120210	T	C	34	GENIC	homozygous	117760548
9	98120319	98120320	T	G	31	GENIC	homozygous	117760549
9	98121203	98121204	G	C	21	GENIC	homozygous	117760550
9	98122359	98122360	C	T	25	GENIC	homozygous	117760551
9	98122513	98122514	A	C	15	GENIC	homozygous	117760552
9	98122882	98122883	C	T	13	GENIC	homozygous	117760553
9	98122904	98122905	C	T	18	GENIC	possibly homozygous	117760554
9	98123267	98123268	T	C	30	GENIC	homozygous	117760555
9	98123279	98123280	A	G	32	GENIC	homozygous	117794855
9	98123280	98123281	T	A	33	GENIC	homozygous	117794857
9	98123286	98123287	C	T	34	GENIC	homozygous	117760556
9	98123292	98123293	C	T	36	GENIC	homozygous	117760557
9	98128373	98128374	G	A	27	GENIC	homozygous	117760558
9	98129405	98129406	C	T	15	GENIC	homozygous	117760560
9	98129464	98129465	G	A	17	GENIC	homozygous	117760561
9	98130510	98130511	A	G	18	GENIC	homozygous	117760562
9	98130689	98130690	A	C	15	GENIC	homozygous	117760563
9	98130706	98130707	C	T	17	GENIC	homozygous	117760564
9	98130816	98130817	G	A	41	GENIC	homozygous	117760565