chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10085369	10085370	G	A	27	GENIC	homozygous	109632245
19	10085944	10085945	C	T	32	GENIC	homozygous	109632249
19	10086972	10086973	A	C	23	GENIC	homozygous	109912447
19	10087913	10087914	G	A	17	GENIC	possibly homozygous	109912449
19	10089568	10089569	G	A	21	GENIC	homozygous	109912451
19	10090183	10090184	A	G	21	GENIC	possibly homozygous	109912453
19	10090314	10090315	T	A	27	GENIC	possibly homozygous	109912455
19	10090678	10090679	C	T	25	GENIC	possibly homozygous	109912457
19	10090736	10090737	G	A	29	GENIC	homozygous	109912459
19	10091073	10091074	T	A	36	GENIC	homozygous	109912461
19	10092033	10092034	A	G	21	GENIC	possibly homozygous	109912463
19	10092660	10092661	A	C	25	GENIC	homozygous	109912465
19	10092691	10092692	G	A	21	GENIC	homozygous	109912467
19	10093358	10093359	T	C	21	GENIC	homozygous	109632261
19	10093529	10093530	C	T	28	GENIC	homozygous	109632263
19	10093967	10093968	T	C	26	GENIC	homozygous	109632267
19	10094436	10094437	A	G	24	GENIC	homozygous	109632271
19	10094477	10094478	T	C	17	GENIC	homozygous	109632273
19	10094734	10094735	C	T	11	GENIC	homozygous	109632275
19	10095061	10095062	A	G	23	GENIC	homozygous	109632277
19	10095092	10095093	T	G	22	GENIC	homozygous	109632279
19	10095338	10095339	A	G	33	GENIC	homozygous	109632282
19	10096725	10096726	G	C	30	GENIC	possibly homozygous	109912471
19	10096755	10096756	A	G	27	GENIC	homozygous	109632284
19	10097089	10097090	C	T	21	GENIC	homozygous	109632286
19	10097641	10097642	C	T	23	GENIC	homozygous	109632288
19	10099811	10099812	T	C	22	GENIC	homozygous	109632290
19	10100646	10100647	G	T	19	GENIC	homozygous	109632292
19	10100858	10100859	C	T	14	GENIC	homozygous	109632294
19	10098975	10098976	G	C	13	GENIC	homozygous	109764440
19	10096338	10096339	A	G	13	GENIC	homozygous	109764438