chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 55789159 55789170 CTGTCTCTCTC ----------- 4 GENIC homozygous 769596339 13 55789173 55789176 TTC --- 2 GENIC homozygous 769596340 13 55789227 55789228 T TC 3 GENIC homozygous 769596341 13 55789236 55789237 G GTC 3 GENIC homozygous 769596342 13 55789270 55789271 T TTCTCTCTCTGTCTTCTCTCTGTCTCTGTCTCTCTCTCTTTC 2 GENIC homozygous 769596343 13 55789617 55789618 G GTC 25 GENIC homozygous 769596345 13 55789724 55789725 T TC 11 GENIC heterozygous 769596346 13 55789731 55789732 C CTCT 10 GENIC possibly homozygous 769596347 13 55791151 55791152 G T 28 GENIC homozygous 672410701 13 55791660 55791661 C T 35 GENIC homozygous 672410702 13 55792009 55792010 G GCA 16 GENIC heterozygous 769596348 13 55792009 55792010 G GCACA 16 GENIC heterozygous 769596349 13 55792009 55792010 G GCACACA 16 GENIC heterozygous 769596350 13 55792149 55792150 G A 34 GENIC homozygous 672410703 13 55793030 55793031 A G 21 GENIC homozygous 672410704 13 55793073 55793074 T - 24 GENIC homozygous 769596351 13 55794059 55794060 A AG 11 GENIC homozygous 769596352 13 55794173 55794174 C A 13 GENIC homozygous 672410705 13 55795016 55795017 C T 25 GENIC possibly homozygous 672410706 13 55795127 55795128 A G 27 GENIC homozygous 672410707 13 55795483 55795484 T C 18 GENIC homozygous 672410708 13 55795686 55795687 G GC 19 GENIC homozygous 769596353 13 55796399 55796400 G A 32 GENIC possibly homozygous 672410709 13 55798078 55798079 A ACACCC 1 GENIC homozygous 769596356 13 55798086 55798087 A G 9 GENIC heterozygous 672410710 13 55799099 55799100 A C 37 GENIC homozygous 672410711 13 55799877 55799878 A G 23 GENIC homozygous 672410712 13 55800117 55800118 A C 25 GENIC possibly homozygous 672410713 13 55800298 55800299 C T 30 GENIC possibly homozygous 672410714 13 55800385 55800386 G A 29 GENIC homozygous 672410715 13 55800623 55800624 C G 24 GENIC homozygous 672410716 13 55801310 55801311 G T 23 GENIC possibly homozygous 672410717 13 55801649 55801650 A G 21 GENIC homozygous 672410718