chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	110035607	110035608	G	A	18	GENIC	homozygous	114444320
13	110036970	110036971	T	C	12	GENIC	homozygous	114444328
13	110038965	110038966	A	G	11	GENIC	homozygous	114872487
13	110046490	110046491	A	G	26	GENIC	homozygous	114859511
13	110047173	110047174	T	C	15	GENIC	heterozygous	115103064
13	110051788	110051789	G	A	23	GENIC	homozygous	114859513
13	110052680	110052681	T	A	20	GENIC	homozygous	114859515
13	110052681	110052682	T	A	20	GENIC	homozygous	114859517
13	110052867	110052868	G	A	22	GENIC	homozygous	114859519
13	110052936	110052937	G	A	28	GENIC	homozygous	114859521
13	110053117	110053118	C	T	13	GENIC	homozygous	114444416
13	110053657	110053658	G	A	20	GENIC	homozygous	114835205
13	110053894	110053895	A	G	24	GENIC	homozygous	114444418
13	110054390	110054391	T	C	7	GENIC	homozygous	114444422
13	110055004	110055005	C	T	13	GENIC	homozygous	114859523
13	110055133	110055134	T	C	13	GENIC	homozygous	114444428
13	110055138	110055139	G	C	14	GENIC	homozygous	114444430
13	110055589	110055590	A	G	25	GENIC	homozygous	114859527
13	110056710	110056711	G	C	17	GENIC	homozygous	114444436
13	110057402	110057403	A	G	19	GENIC	homozygous	114859529
13	110057493	110057494	G	A	26	GENIC	homozygous	114835215
13	110057799	110057800	T	C	27	GENIC	homozygous	114701879
13	110058064	110058065	G	A	33	GENIC	homozygous	114859531
13	110058529	110058530	C	T	31	GENIC	homozygous	114835217
13	110058561	110058562	C	T	30	GENIC	homozygous	114835219
13	110058709	110058710	A	G	16	GENIC	possibly homozygous	114444440
13	110059074	110059075	C	T	5	GENIC	homozygous	114444442
13	110059200	110059201	T	A	25	GENIC	homozygous	114444446
13	110060594	110060595	C	A	14	GENIC	homozygous	114444450
13	110060645	110060646	T	C	14	GENIC	homozygous	114444452
13	110060802	110060803	C	A	13	GENIC	homozygous	114444454
13	110071120	110071121	A	C	14	GENIC	homozygous	114859533
13	110071410	110071411	T	C	5	GENIC	homozygous	114444484
13	110073552	110073553	G	A	22	GENIC	homozygous	114444494