chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 58690977 58690978 C T 19 GENIC possibly homozygous 563442954 10 58691500 58691501 G A 11 GENIC homozygous 563442955 10 58691509 58691510 A G 13 GENIC possibly homozygous 563442956 10 58692070 58692071 T C 8 GENIC homozygous 563442957 10 58692721 58692722 G T 14 GENIC possibly homozygous 563442958 10 58692860 58692861 G A 21 GENIC homozygous 563442959 10 58693324 58693325 C T 20 GENIC possibly homozygous 563442960 10 58693447 58693448 A G 13 GENIC homozygous 563442961 10 58693535 58693540 ACAAA ----- 9 GENIC homozygous 707722760 10 58695565 58695566 T A 20 GENIC heterozygous 563442962 10 58695832 58695833 A G 27 GENIC possibly homozygous 563442963 10 58696001 58696002 C CAA 14 GENIC possibly homozygous 707722761 10 58697107 58697108 A G 18 GENIC possibly homozygous 563442964 10 58697229 58697230 G T 16 GENIC possibly homozygous 563442965 10 58698305 58698306 T A 17 GENIC heterozygous 563442966 10 58698569 58698573 GGTA ---- 4 GENIC heterozygous 707722762 10 58698612 58698613 C T 21 GENIC homozygous 563442967 10 58698898 58698899 T C 19 GENIC possibly homozygous 563442968 10 58700173 58700174 G A 28 GENIC possibly homozygous 563442969 10 58700484 58700485 C T 28 GENIC homozygous 563442970 10 58700662 58700663 T G 21 GENIC homozygous 563442971 10 58700817 58700818 G A 11 GENIC possibly homozygous 563442972 10 58700872 58700873 G A 15 GENIC possibly homozygous 563442973 10 58701374 58701375 G A 23 GENIC possibly homozygous 563442974 10 58701552 58701553 G A 19 GENIC possibly homozygous 563442975 10 58704065 58704066 G A 9 GENIC possibly homozygous 563442976 10 58706707 58706708 A G 16 GENIC homozygous 563442977 10 58707048 58707049 A G 16 GENIC homozygous 563442978 10 58708287 58708288 C T 13 GENIC homozygous 563442979 10 58708704 58708705 G A 10 GENIC heterozygous 563442980 10 58709240 58709241 A T 23 GENIC possibly homozygous 563442981 10 58709875 58709876 C T 22 GENIC possibly homozygous 563442982