chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 109641053 109641054 C T 5 GENIC homozygous 51599570 10 109641084 109641085 C T 10 GENIC homozygous 51599571 10 109641097 109641098 G A 15 GENIC homozygous 51599572 10 109642746 109642747 T TA 23 GENIC homozygous 51599573 10 109643497 109643498 T - 4 GENIC heterozygous 52410061 10 109645822 109645823 G T 25 GENIC homozygous 51599576 10 109653139 109653140 C CA 2 GENIC heterozygous 52605554 10 109664126 109664127 T TC 9 GENIC homozygous 51599593 10 109664265 109664266 A AACTTATTACAAGCCAAAG 26 GENIC possibly homozygous 51599594 10 109664535 109664536 C G 19 GENIC homozygous 51599602 10 109664571 109664572 A T 24 GENIC homozygous 51599603 10 109664577 109664578 A T 22 GENIC homozygous 51599604 10 109664579 109664580 A T 23 GENIC homozygous 51599605 10 109664580 109664581 A T 24 GENIC homozygous 51599606 10 109664589 109664590 C - 27 GENIC homozygous 51599607 10 109664592 109664593 C CA 28 GENIC homozygous 51599608 10 109664595 109664596 C G 28 GENIC homozygous 51599609 10 109669029 109669030 A AT 4 GENIC heterozygous 52447947 10 109670208 109670209 C CTTTTT 1 GENIC homozygous 52331829 10 109678059 109678060 C CA 6 GENIC homozygous 51599623