chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 110741872 110741873 T C 26 GENIC homozygous 930204295 13 110742696 110742697 A G 58 GENIC homozygous 930204296 13 110743778 110743779 C T 35 GENIC homozygous 930204297 13 110743788 110743789 C T 40 GENIC homozygous 930204298 13 110743858 110743859 G A 35 GENIC homozygous 930204299 13 110743981 110743982 T C 42 GENIC homozygous 930204300 13 110744513 110744514 A G 43 GENIC homozygous 930204301 13 110744526 110744527 C T 34 GENIC homozygous 930204302 13 110745556 110745557 A G 44 GENIC homozygous 930204303 13 110745588 110745589 A G 35 GENIC homozygous 930204304 13 110745907 110745908 T A 45 GENIC homozygous 930204305 13 110746430 110746431 C T 56 GENIC homozygous 930204306 13 110746508 110746509 C T 34 GENIC homozygous 930204307 13 110747171 110747172 T C 32 GENIC homozygous 930204308 13 110748032 110748033 A C 56 GENIC homozygous 930204309 13 110748585 110748586 C T 33 GENIC homozygous 930204310 13 110748713 110748714 T C 58 GENIC homozygous 930204311 13 110748723 110748724 T C 58 GENIC homozygous 930204312 13 110748906 110748907 A G 46 GENIC homozygous 930204313