chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 42637750 42637755 GGTTC ----- 15 GENIC heterozygous 750559709 13 42638968 42638969 C T 12 GENIC homozygous 639255502 13 42639249 42639251 AG -- 14 GENIC homozygous 750559710 13 42641093 42641094 T TTGTGTG 4 GENIC heterozygous 750559711 13 42641837 42641838 A G 21 GENIC homozygous 639255503 13 42641886 42641887 T C 24 GENIC homozygous 639255504 13 42641986 42641987 G - 15 GENIC homozygous 750559712 13 42642405 42642406 T TCTCACA 8 GENIC homozygous 750559713 13 42642578 42642579 A - 17 GENIC homozygous 750559715 13 42642619 42642620 C T 24 GENIC homozygous 639255505 13 42642706 42642707 A G 24 GENIC homozygous 639255506 13 42642823 42642824 C T 15 GENIC homozygous 639255507 13 42642885 42642886 T G 21 GENIC homozygous 639255508 13 42643220 42643228 GAAGGAAG -------- 8 GENIC homozygous 750559716 13 42644063 42644064 T C 18 GENIC possibly homozygous 639255509 13 42645354 42645355 C CCA 18 GENIC heterozygous 750559718 13 42645362 42645468 ACACACATACCACAAGCACACACACACACACACACATACCACATGAACACATACACACACACACTCAAATACACATACACACATGTACTCACACACATGCATACAT ---------------------------------------------------------------------------------------------------------- 40 GENIC heterozygous 750559719 13 42646602 42646603 T TGATA 8 GENIC homozygous 750559720 13 42648291 42648292 A AACACACACACAC 14 GENIC homozygous 750559721 13 42648307 42648308 G C 19 GENIC homozygous 639255510 13 42648691 42648692 A AGT 14 GENIC possibly homozygous 750559724 13 42649107 42649109 CG -- 13 GENIC heterozygous 750559725