chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 101556444 101556445 T C 23 GENIC homozygous 113941749 5 101558635 101558636 A G 6 GENIC homozygous 113941753 5 101557922 101557922 A 12 GENIC homozygous 132077699 5 101565195 101565196 T C 13 GENIC homozygous 118908920 5 101566101 101566102 C T 18 GENIC homozygous 118908922 5 101567327 101567328 G C 19 GENIC homozygous 118908924 5 101565326 101565326 G 14 GENIC homozygous 128218257 5 101568795 101568796 C G 21 GENIC homozygous 118908926 5 101571929 101571930 T C 19 GENIC homozygous 118908928 5 101573394 101573395 A 15 GENIC homozygous 132077700 5 101573855 101573856 T 24 GENIC heterozygous 130551768 5 101574332 101574336 TCAG 12 GENIC homozygous 128218259 5 101577594 101577594 A 19 GENIC homozygous 130551769 5 101579850 101579851 A T 21 GENIC homozygous 118908930 5 101579878 101579879 G A 21 GENIC homozygous 118908932 5 101582595 101582596 G A 12 GENIC homozygous 118908934 5 101583391 101583391 AT 12 GENIC homozygous 132077701 5 101584519 101584520 T A 17 GENIC homozygous 114233904 5 101585232 101585233 A G 13 GENIC homozygous 113941763 5 101587363 101587365 TC 12 GENIC homozygous 128218262 5 101583595 101583596 G A 5 GENIC homozygous 132088249 5 101583831 101583832 A T 14 GENIC homozygous 132088250 5 101585228 101585229 A T 13 GENIC homozygous 132088251