chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	108395810	108395811	A		10	GENIC	homozygous	129193941
14	108395865	108395866	A	G	16	GENIC	heterozygous	129221833
14	108395866	108395867	A	G	17	GENIC	heterozygous	113618350
14	108396281	108396282	A	C	17	GENIC	homozygous	125952189
14	108399273	108399277	AAAC		13	GENIC	homozygous	129193942
14	108399420	108399420		C	21	GENIC	homozygous	129193943
14	108396511	108396515	TTTG		11	GENIC	homozygous	131147493
14	108396672	108396673	C	T	22	GENIC	homozygous	113541154
14	108397829	108397830	G	A	20	GENIC	homozygous	113541156
14	108397982	108397983	A	G	18	GENIC	homozygous	113541158
14	108398890	108398891	G	C	14	GENIC	homozygous	113541160
14	108400566	108400567	T	A	16	GENIC	homozygous	113541168
14	108400990	108400991	A	G	16	GENIC	homozygous	113541174
14	108401086	108401087	T	G	25	GENIC	homozygous	113541176
14	108401354	108401355	T		17	GENIC	homozygous	129193944
14	108401539	108401539		TCAG	19	GENIC	homozygous	129193945
14	108401714	108401715	G	A	20	GENIC	homozygous	125952190
14	108403799	108403800	A	G	14	GENIC	homozygous	113541186
14	108404192	108404193	T	A	25	GENIC	homozygous	113541192
14	108404485	108404486	A	C	20	GENIC	homozygous	113541196
14	108405060	108405061	T	C	19	GENIC	homozygous	113541198
14	108405597	108405598	C	T	16	GENIC	homozygous	113541202
14	108406586	108406587	G	A	18	GENIC	homozygous	113541210
14	108407716	108407717	C	T	14	GENIC	homozygous	125952191
14	108408212	108408213	G	T	19	GENIC	homozygous	125952192
14	108408381	108408382	A	G	17	GENIC	homozygous	113618353
14	108407783	108407784	G	A	13	GENIC	homozygous	131153845