chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	188544068	188544069	T	C	13	GENIC	homozygous	110169345
2	188544180	188544181	A	G	21	GENIC	possibly homozygous	111344334
2	188544221	188544281	CAGCCACCAGCCCTCCAGGGGACTCCTCCAGCACTGCAGTCCCCAATGGTGCCTCTTCCT		32	GENIC	heterozygous	134184057
2	188544338	188544339	T	C	16	GENIC	homozygous	111344344
2	188544440	188544440		T	27	GENIC	possibly homozygous	134184058
2	188544443	188544444	C		27	GENIC	possibly homozygous	134184059
2	188544801	188544802	C	T	38	GENIC	homozygous	111344346
2	188544803	188544804	T	A	39	GENIC	homozygous	111344348
2	188544889	188544890	T	A	46	GENIC	homozygous	110169384
2	188545443	188545444	G	A	45	GENIC	homozygous	111344350
2	188545717	188545718	G	A	26	GENIC	homozygous	111344352
2	188546294	188546295	C	T	25	GENIC	homozygous	111344354
2	188546536	188546537	T	C	19	GENIC	homozygous	111344356
2	188546562	188546563	C	A	24	GENIC	homozygous	110169388
2	188546579	188546585	AAAAAG		24	GENIC	possibly homozygous	134184060
2	188547146	188547147	T	G	39	GENIC	homozygous	111344358
2	188547298	188547298		T	24	GENIC	homozygous	134184061