chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 160735121 160735125 TGTG ---- 13 GENIC homozygous 57540572 4 160737395 160737396 T TTCAC 22 GENIC homozygous 57540573 4 160739729 160739731 GT -- 17 GENIC possibly homozygous 57540575 4 160741034 160741054 GGTTAGGGATTTAGCTCAGT -------------------- 11 GENIC homozygous 57540577 4 160741118 160741119 C CA 5 GENIC heterozygous 57003247 4 160744607 160744623 AGAGAGAGAGAGAGAG ---------------- 2 GENIC homozygous 57540579 4 160745299 160745300 A G 22 GENIC homozygous 57540581 4 160746495 160746496 A G 28 GENIC homozygous 57540583 4 160747094 160747095 G GC 25 GENIC homozygous 57540585 4 160747151 160747152 A C 12 GENIC homozygous 57540587 4 160748311 160748312 T A 27 GENIC homozygous 57540589 4 160748489 160748490 G T 22 GENIC homozygous 57540591 4 160749273 160749274 C CA 3 GENIC homozygous 57003248 4 160749289 160749290 A - 3 GENIC homozygous 57540595 4 160749335 160749336 G A 17 GENIC possibly homozygous 57540597 4 160749863 160749864 A C 19 GENIC homozygous 57540599 4 160750465 160750466 T C 6 GENIC homozygous 57540601 4 160752684 160752685 C G 26 GENIC heterozygous 57540603 4 160753419 160753420 A G 21 GENIC homozygous 57540605 4 160753820 160753821 T - 4 GENIC heterozygous 57540607 4 160754762 160754763 C A 17 GENIC homozygous 57540609 4 160741119 160741123 AAAA ---- 5 GENIC heterozygous 57351099 4 160756881 160756882 C CT 19 GENIC homozygous 57540611 4 160758201 160758202 A AACAC 8 GENIC homozygous 57540615