chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 29980212 29980213 C T 21 GENIC homozygous 110859011 18 30015890 30015891 C T 15 GENIC homozygous 110319239 18 30068000 30068001 G A 9 GENIC heterozygous 131547759 18 30068033 30068034 G A 12 GENIC heterozygous 131547760 18 30068034 30068035 T G 13 GENIC heterozygous 131547761 18 30080766 30080767 C T 16 GENIC heterozygous 131547762 18 30071454 30071456 TG 8 GENIC heterozygous 131542073 18 30080728 30080729 C G 15 GENIC heterozygous 130711987 18 30080729 30080730 G A 15 GENIC heterozygous 130475676 18 30080855 30080856 G A 18 GENIC heterozygous 130475679 18 30081156 30081157 G A 17 GENIC heterozygous 129570026 18 30081277 30081278 C G 22 GENIC heterozygous 131547763 18 30081614 30081615 G T 10 GENIC heterozygous 130604305 18 30081676 30081677 C T 14 GENIC heterozygous 130475688 18 30097227 30097228 T A 14 GENIC heterozygous 130604310 18 30097230 30097231 A T 14 GENIC heterozygous 130475692 18 30097241 30097242 T A 14 GENIC heterozygous 130604311 18 30140211 30140212 T C 16 GENIC homozygous 110319712 18 30184510 30184511 C T 26 GENIC homozygous 110859013