chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	104726270	104726271	A	G	18	GENIC	homozygous	116836225
10	104726669	104726670	G	A	16	GENIC	homozygous	117031194
10	104729206	104729207	G	A	22	GENIC	homozygous	117031196
10	104729449	104729450	G	T	21	GENIC	homozygous	117031198
10	104731144	104731145	A	G	22	GENIC	homozygous	116836235
10	104731636	104731637	G	A	23	GENIC	homozygous	117031200
10	104732023	104732024	A	G	22	GENIC	homozygous	116836237
10	104732083	104732084	T	G	25	GENIC	possibly homozygous	117031202
10	104734926	104734927	A	G	22	GENIC	homozygous	116836239
10	104735823	104735824	A	G	12	GENIC	homozygous	117031204
10	104736231	104736232	A	T	6	GENIC	homozygous	116836243
10	104736256	104736257	G		8	GENIC	heterozygous	131710633
10	104737457	104737458	T	C	18	GENIC	homozygous	116836245
10	104738783	104738784	T	G	17	GENIC	homozygous	116836247
10	104738899	104738900	C	G	18	GENIC	homozygous	117031212
10	104740556	104740557	A	C	3	GENIC	homozygous	126489760
10	104739128	104739129	T	A	13	GENIC	homozygous	117260749
10	104737920	104737920		ATCCTACTCCACTCG	25	GENIC	homozygous	131470379
10	104741868	104741868		AGG	11	GENIC	homozygous	131470380
10	104738156	104738156		G	13	GENIC	homozygous	128855766
10	104743057	104743057		T	19	GENIC	homozygous	128855767
10	104743120	104743120		G	20	GENIC	homozygous	128855768
10	104739145	104739146	A	G	13	GENIC	homozygous	117279725
10	104739743	104739744	G	A	11	GENIC	homozygous	118012183
10	104739757	104739758	G	C	11	GENIC	homozygous	118012184
10	104740603	104740604	C	T	2	GENIC	homozygous	133494786
10	104743130	104743131	A		25	GENIC	homozygous	128855769
10	104743706	104743707	G	C	4	GENIC	homozygous	126489762
10	104743771	104743772	A	G	3	GENIC	homozygous	126489763
10	104747471	104747471		A	6	GENIC	homozygous	128855770
10	104743644	104743644		GGAGGAAGAGGAGGAAGAAGAG	7	GENIC	homozygous	133233570
10	104743616	104743617	A	G	6	GENIC	homozygous	133241396
10	104743643	104743643		GG	7	GENIC	homozygous	133233569