chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 55789199 55789201 TC -- 2 GENIC heterozygous 707810766 13 55789618 55789622 TCTC ---- 1 GENIC homozygous 707810769 13 55791033 55791034 G A 12 GENIC heterozygous 562160624 13 55793030 55793031 A G 7 GENIC possibly homozygous 562160625 13 55793073 55793074 T - 4 GENIC heterozygous 707810772 13 55794003 55794004 G A 2 GENIC homozygous 564887153 13 55794461 55794462 C T 19 GENIC homozygous 562160626 13 55795127 55795128 A G 25 GENIC homozygous 562160627 13 55795270 55795271 C T 4 GENIC homozygous 562160628 13 55795483 55795484 T C 19 GENIC possibly homozygous 562160629 13 55795686 55795687 G GC 19 GENIC possibly homozygous 707810773 13 55795972 55795973 G A 18 GENIC possibly homozygous 562160630 13 55798086 55798087 A G 5 GENIC homozygous 564887154 13 55798309 55798310 T TG 6 GENIC heterozygous 707810774 13 55799099 55799100 A C 18 GENIC homozygous 562160631 13 55799877 55799878 A G 9 GENIC heterozygous 562160632 13 55800623 55800624 C G 21 GENIC possibly homozygous 562160633 13 55801649 55801650 A G 27 GENIC homozygous 562160634 13 55801725 55801726 A G 18 GENIC homozygous 562160635