chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	107212279	107212280	T	C	80	GENIC	heterozygous	118012680
10	107220675	107220676	T	A	41	GENIC	homozygous	116714151
10	107254973	107254974	T	C	40	GENIC	homozygous	116714153
10	107256540	107256541	G	T	10	GENIC	heterozygous	118109153
10	107256548	107256549	G	T	12	GENIC	heterozygous	118012683
10	107258144	107258145	G	A	25	GENIC	possibly homozygous	116714155
10	107258918	107258919	A	T	36	GENIC	homozygous	116714157
10	107259752	107259753	A	G	24	GENIC	homozygous	116714159
10	107263430	107263431	A	T	40	GENIC	homozygous	116714161
10	107264393	107264394	T	C	23	GENIC	homozygous	116714163
10	107267144	107267145	G	A	19	GENIC	homozygous	116714165
10	107270467	107270468	C	T	34	GENIC	homozygous	116714167
10	107270496	107270497	G	A	31	GENIC	homozygous	116714169
10	107270708	107270709	C	G	42	GENIC	homozygous	116714171
10	107271461	107271462	G	A	33	GENIC	homozygous	116714173
10	107274389	107274390	G	T	5	GENIC	heterozygous	118012684
10	107275118	107275119	C	A	42	GENIC	homozygous	116714175
10	107276559	107276560	A	C	32	GENIC	homozygous	116714177
10	107277181	107277182	A	G	28	GENIC	homozygous	116714179
10	107277840	107277841	G	A	28	GENIC	homozygous	116714181
10	107280664	107280665	C	A	27	GENIC	homozygous	116714183