chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 42479561 42479562 A T 25 GENIC homozygous 50209153 12 42480660 42480661 C CCA 5 GENIC heterozygous 50209156 12 42483114 42483157 AGATGGGTGCTCTTAACCGCTGAGCCATCTCTCCAGCCCCCCC ------------------------------------------- 11 GENIC heterozygous 50544349 12 42483954 42483955 T - 14 GENIC heterozygous 50563860 12 42484990 42484994 GTGT ---- 2 GENIC homozygous 50804591 12 42486270 42486271 A AC 1 INTERGENIC homozygous 50209165 12 42486435 42486436 C G 8 INTERGENIC homozygous 50804593 12 42487729 42487730 T C 17 GENIC homozygous 50209169 12 42488256 42488257 A G 16 GENIC homozygous 50804595 12 42488606 42488607 C T 23 GENIC homozygous 50563866 12 42488909 42488910 A T 19 GENIC homozygous 50563868 12 42489036 42489037 C T 23 GENIC homozygous 50563870 12 42489914 42489915 C T 34 GENIC possibly homozygous 50563872 12 42490538 42490539 A G 27 GENIC homozygous 50209176 12 42490657 42490658 C T 23 GENIC homozygous 50209180 12 42490876 42490877 A C 24 GENIC homozygous 50563880 12 42491393 42491394 C T 7 GENIC homozygous 50209181 12 42493649 42493650 T C 31 INTERGENIC possibly homozygous 50592219 12 42483953 42483955 TT -- 14 GENIC possibly homozygous 50572255 12 42490252 42490253 G - 40 GENIC homozygous 50592216 12 42490598 42490603 CACGC ----- 12 GENIC heterozygous 50885553 12 42493679 42493680 G A 29 INTERGENIC homozygous 50804597 12 42493899 42493900 C T 34 INTERGENIC homozygous 50592220 12 42494101 42494102 C A 30 INTERGENIC possibly homozygous 50209183 12 42494157 42494158 A G 25 INTERGENIC possibly homozygous 50209184