chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 25113351 25113352 C A 80 GENIC possibly homozygous 781899968 13 25113373 25113374 C T 77 GENIC homozygous 781899969 13 25113412 25113413 C T 63 GENIC possibly homozygous 781899970 13 25113585 25113586 C T 79 GENIC possibly homozygous 781899971 13 25113651 25113652 C G 78 GENIC possibly homozygous 781899972 13 25113685 25113686 C T 67 GENIC homozygous 781899973 13 25113687 25113688 C T 66 GENIC homozygous 781899974 13 25113712 25113713 A G 52 GENIC homozygous 781899975 13 25114040 25114041 C A 56 GENIC homozygous 781899976 13 25114058 25114059 A T 56 GENIC homozygous 781899977 13 25114249 25114250 T C 53 GENIC homozygous 781899978 13 25114387 25114388 A T 71 GENIC homozygous 781899979 13 25114453 25114454 C G 59 GENIC homozygous 781899980 13 25115055 25115056 C T 58 GENIC homozygous 781899981 13 25115155 25115156 G A 56 GENIC homozygous 781899982 13 25115166 25115167 C T 59 GENIC homozygous 781899983 13 25115292 25115293 G T 76 GENIC homozygous 781899984 13 25115317 25115318 C T 77 GENIC possibly homozygous 781899985 13 25115352 25115353 C T 70 GENIC homozygous 781899986 13 25115435 25115436 G C 106 GENIC possibly homozygous 781899987 13 25115818 25115819 T G 46 GENIC possibly homozygous 781899988 13 25115954 25115955 G T 67 GENIC possibly homozygous 781899989