chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	78806621	78806622	G	GA	1	GENIC	homozygous	50552629
13	78807045	78807046	G	GA	7	GENIC	homozygous	50435930
13	78807890	78807891	T	C	32	GENIC	homozygous	49829915
13	78808806	78808807	C	T	31	GENIC	homozygous	49829932
13	78808906	78808907	A	AGTAC	25	GENIC	homozygous	49829934
13	78809580	78809581	C	T	25	GENIC	homozygous	49829940
13	78810407	78810408	C	T	21	GENIC	homozygous	50435932
13	78810569	78810570	A	G	16	GENIC	homozygous	49829960
13	78810646	78810647	G	C	23	GENIC	homozygous	49829964
13	78811236	78811237	A	T	17	GENIC	homozygous	49829977
13	78812303	78812307	ACAC	----	31	GENIC	homozygous	49829996
13	78812406	78812407	C	T	41	GENIC	homozygous	50435934
13	78812778	78812779	G	A	28	GENIC	homozygous	50435936
13	78813371	78813372	T	TAGACAAGATGGATGAAGCAAAGAAGTGCAGACC	7	GENIC	homozygous	50524375
13	78813475	78813476	T	TA	4	GENIC	homozygous	49830011
13	78814043	78814044	G	A	18	GENIC	homozygous	50435938
13	78814122	78814142	TCTTTCTTTCTTTCTTTCTC	--------------------	4	GENIC	homozygous	50524376
13	78814670	78814671	A	G	19	GENIC	homozygous	49830028
13	78815126	78815127	T	A	35	GENIC	homozygous	49830033
13	78815507	78815508	T	TA	9	GENIC	homozygous	50435944
13	78816808	78816809	T	C	16	GENIC	homozygous	50435946
13	78817010	78817016	ACGCTG	------	22	GENIC	homozygous	49830060
13	78817102	78817103	T	C	26	GENIC	homozygous	50435950
13	78817105	78817106	A	G	27	GENIC	homozygous	50435952
13	78817296	78817297	T	C	41	GENIC	homozygous	49830061
13	78818227	78818228	C	T	29	GENIC	possibly homozygous	50435955
13	78818370	78818371	A	G	23	GENIC	homozygous	50435957
13	78818790	78818791	T	C	22	GENIC	homozygous	50435959
13	78819874	78819875	T	C	18	GENIC	heterozygous	49830096
13	78820041	78820042	C	T	15	GENIC	homozygous	50435961
13	78820224	78820225	T	A	15	GENIC	homozygous	49830098