chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 88381187 88381188 T C 33 GENIC homozygous 61458555 1 88382187 88382188 G A 13 GENIC homozygous 61458556 1 88382191 88382192 G A 13 GENIC homozygous 61458557 1 88382205 88382206 G A 21 GENIC homozygous 61458558 1 88382215 88382216 A G 24 GENIC homozygous 61458559 1 88385276 88385277 G T 29 GENIC heterozygous 61458560 1 88385279 88385280 C CT 24 GENIC heterozygous 61458561 1 88385280 88385281 G T 29 GENIC possibly homozygous 61458562 1 88385280 88385281 G GTCT 26 GENIC possibly homozygous 61458563 1 88386161 88386164 GAA --- 26 GENIC homozygous 61458564 1 88386637 88386638 C A 27 GENIC homozygous 61458565 1 88386691 88386692 A G 24 GENIC homozygous 61458566 1 88388573 88388574 A G 20 GENIC homozygous 61458567 1 88389584 88389585 C - 19 GENIC homozygous 61458568 1 88389660 88389661 T C 17 GENIC possibly homozygous 61458569 1 88391300 88391302 TT -- 20 GENIC homozygous 61458570 1 88391841 88391845 GAGA ---- 17 GENIC homozygous 61458571 1 88392545 88392546 C T 25 GENIC homozygous 61458572 1 88393145 88393146 C A 20 GENIC homozygous 61458573 1 88393279 88393280 C - 20 GENIC homozygous 61458574 1 88394528 88394529 A AG 28 GENIC homozygous 61458575 1 88397703 88397704 G A 38 GENIC homozygous 61458576 1 88397888 88397889 G A 21 GENIC homozygous 61458577 1 88398927 88398928 C CTT 3 GENIC homozygous 61458578 1 88399232 88399233 T C 29 GENIC homozygous 61458579 1 88399579 88399583 AACC ---- 8 GENIC homozygous 61458580 1 88399585 88399586 C A 8 GENIC heterozygous 61458581 1 88400127 88400144 TCACTGCCCACCATCTG ----------------- 11 GENIC homozygous 61458582 1 88400137 88400138 C CA 11 GENIC heterozygous 61458583 1 88400561 88400562 C T 26 GENIC homozygous 61458584 1 88400932 88400933 C CTGGTTTATACAACAG 12 GENIC homozygous 61458585 1 88400966 88400967 C T 20 GENIC homozygous 61458586 1 88401592 88401593 T C 32 GENIC homozygous 61458587 1 88402237 88402238 C CA 30 GENIC homozygous 60758387