chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 119055128 119055129 G GTTC 4 GENIC homozygous 768960121 7 119056013 119056014 A C 16 GENIC homozygous 671187125 7 119058660 119058661 C T 40 GENIC homozygous 671187126 7 119060332 119060333 C CT 3 GENIC heterozygous 768960122 7 119060638 119060639 T G 14 GENIC possibly homozygous 671187127 7 119060676 119060680 CCCT ---- 8 GENIC homozygous 768960123 7 119060988 119060989 C T 17 GENIC homozygous 671187128 7 119061805 119061806 C T 16 GENIC possibly homozygous 671187129 7 119062366 119062367 A G 18 GENIC possibly homozygous 671187130 7 119062556 119062557 A G 18 GENIC homozygous 671187131 7 119063659 119063660 T G 6 GENIC homozygous 671187132 7 119065285 119065286 C T 18 GENIC possibly homozygous 671187133 7 119066563 119066564 A G 1 GENIC homozygous 671187134 7 119067033 119067034 C A 2 GENIC homozygous 671187135