chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	13875110	13875111	C	G	42	GENIC	homozygous	116736508
10	13880062	13880063	T	C	35	GENIC	homozygous	116736509
10	13881214	13881215	G	A	41	GENIC	homozygous	116736510
10	13881757	13881758	T	C	31	GENIC	homozygous	116736511
10	13883457	13883458	T	C	26	GENIC	possibly homozygous	116736512
10	13883603	13883604	A	G	17	GENIC	homozygous	116736513
10	13884958	13884959	G	A	21	GENIC	homozygous	116736514
10	13885665	13885666	C	T	29	GENIC	homozygous	116736515
10	13885782	13885783	A	G	33	GENIC	homozygous	116736516
10	13887287	13887288	A	G	9	GENIC	homozygous	116736517
10	13889281	13889282	G	A	30	GENIC	homozygous	116736518
10	13889570	13889571	A	G	41	GENIC	heterozygous	118030546
10	13889575	13889576	G	C	37	GENIC	possibly homozygous	118093447
10	13889581	13889582	G	C	36	GENIC	heterozygous	118030548
10	13889715	13889716	G	C	27	GENIC	homozygous	116736519
10	13891933	13891934	A	G	35	GENIC	homozygous	116736520
10	13892155	13892156	C	T	28	GENIC	possibly homozygous	116736521