chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 52935614 52935617 AAT --- 1 GENIC homozygous 745217245 2 52935899 52935900 T C 15 GENIC homozygous 630072539 2 52935932 52935933 C G 23 GENIC heterozygous 630072540 2 52937534 52937535 A C 12 GENIC heterozygous 630072541 2 52937567 52937569 AC -- 4 GENIC homozygous 745217246 2 52938464 52938468 CTTC ---- 8 GENIC homozygous 745217247 2 52938880 52938881 T - 1 GENIC homozygous 745217248 2 52941192 52941193 A G 22 GENIC possibly homozygous 630072542 2 52944103 52944104 A G 31 GENIC possibly homozygous 630072543 2 52944630 52944631 A G 29 GENIC heterozygous 630072544 2 52945834 52945835 C G 2 GENIC homozygous 630072545 2 52946070 52946071 G GGTGTTTCA 4 GENIC homozygous 745217249 2 52950037 52950038 T C 19 GENIC possibly homozygous 630072546 2 52951325 52951326 A T 19 GENIC homozygous 630072547 2 52951466 52951467 C T 16 GENIC possibly homozygous 630072548 2 52951787 52951788 A - 13 GENIC homozygous 745217250 2 52952281 52952282 C T 24 GENIC possibly homozygous 630072549 2 52952338 52952339 A G 20 GENIC homozygous 630072550 2 52958511 52958512 A - 5 GENIC heterozygous 745217251 2 52960190 52960191 G GT 22 GENIC possibly homozygous 745217252 2 52960768 52960769 G - 11 GENIC possibly homozygous 745217253 2 52965392 52965393 T C 21 GENIC homozygous 630072551 2 52966524 52966525 G A 18 GENIC possibly homozygous 630072552 2 52967981 52967982 A G 13 GENIC homozygous 630072553 2 52968565 52968566 T C 26 GENIC possibly homozygous 630072554