chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	110109790	110109791	A	AGTCTTT	13	GENIC	homozygous	51601013
10	110111122	110111123	C	CTGAG	16	GENIC	homozygous	52273060
10	110112201	110112202	G	A	19	GENIC	homozygous	52273062
10	110112210	110112211	A	T	17	GENIC	homozygous	51601022
10	110113054	110113055	A	ACCCAG	15	GENIC	homozygous	51601024
10	110113511	110113512	T	G	24	GENIC	homozygous	52273064
10	110117288	110117289	G	T	20	GENIC	homozygous	52273066
10	110118333	110118334	C	T	23	GENIC	homozygous	52273068
10	110118483	110118484	A	G	24	GENIC	possibly homozygous	52273070
10	110123186	110123187	A	C	12	GENIC	homozygous	51601038
10	110123943	110123944	C	T	18	GENIC	homozygous	52273074
10	110125186	110125187	C	T	27	GENIC	homozygous	52273076
10	110125484	110125485	A	G	17	GENIC	homozygous	52273078
10	110126512	110126513	C	A	19	GENIC	homozygous	52273080
10	110126650	110126651	G	A	14	GENIC	homozygous	52273082
10	110127506	110127507	G	T	24	GENIC	homozygous	51601044
10	110127566	110127567	T	C	30	GENIC	homozygous	52273084
10	110128590	110128591	T	C	21	GENIC	homozygous	52273086
10	110130809	110130810	T	C	15	GENIC	homozygous	51601049
10	110131727	110131728	G	GC	12	GENIC	homozygous	51601050
10	110133807	110133808	T	C	24	GENIC	homozygous	51601051
10	110133842	110133843	C	G	25	GENIC	homozygous	51601052
10	110136504	110136505	G	A	17	GENIC	homozygous	51958632
10	110137289	110137290	A	G	15	GENIC	homozygous	51601054
10	110137471	110137472	G	A	18	GENIC	homozygous	52273094
10	110137952	110137953	G	A	24	GENIC	possibly homozygous	52273096
10	110138168	110138169	A	G	22	GENIC	homozygous	51601057
10	110140015	110140019	AAAT	----	13	GENIC	homozygous	51601061
10	110140024	110140025	C	T	20	GENIC	homozygous	51958641
10	110140048	110140049	A	T	23	GENIC	homozygous	52273098
10	110140154	110140155	A	G	13	GENIC	homozygous	51601062
10	110140346	110140347	A	-	13	GENIC	homozygous	51601063
10	110140635	110140636	A	G	11	GENIC	homozygous	51601064