chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	74099620	74099621	C	CT	10	GENIC	possibly homozygous	58374293
3	74099621	74099622	T	-	10	GENIC	heterozygous	58157117
3	74104695	74104696	C	CA	12	GENIC	homozygous	57453460
3	74105396	74105397	G	A	24	GENIC	homozygous	57453470
3	74106180	74106181	A	G	22	GENIC	homozygous	57453478
3	74106276	74106277	T	C	30	GENIC	homozygous	57898853
3	74106739	74106740	T	C	30	GENIC	heterozygous	58421913
3	74106996	74106997	C	A	14	GENIC	homozygous	57453482
3	74107551	74107552	G	A	16	GENIC	homozygous	57453484
3	74108827	74108828	C	CTTCCTT	11	GENIC	homozygous	57453490
3	74113278	74113279	T	C	15	GENIC	homozygous	57453530
3	74118378	74118379	T	C	28	GENIC	homozygous	57453573
3	74118388	74118389	C	T	29	GENIC	homozygous	58421914
3	74118486	74118487	T	C	38	GENIC	homozygous	58421915
3	74120659	74120660	C	T	21	GENIC	homozygous	57453601
3	74121006	74121007	C	G	30	GENIC	homozygous	58421916
3	74127319	74127320	C	CA	15	GENIC	possibly homozygous	58421917
3	74127413	74127414	C	T	18	GENIC	homozygous	58421918
3	74131805	74131806	C	T	14	GENIC	homozygous	58421919
3	74133001	74133002	G	GT	12	GENIC	homozygous	58292044
3	74135538	74135539	C	T	19	GENIC	homozygous	58421920
3	74136551	74136552	A	G	21	GENIC	homozygous	57453653
3	74137443	74137444	C	A	31	GENIC	homozygous	57453655
3	74137576	74137579	TTG	---	21	GENIC	homozygous	57453661
3	74138094	74138095	C	A	26	GENIC	homozygous	57453665