chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 140845519 140845520 G A 42 GENIC homozygous 108259022 1 140847799 140847800 G A 33 GENIC homozygous 108259024 1 140848283 140848284 G A 38 GENIC possibly homozygous 108259026 1 140849398 140849399 T C 49 GENIC homozygous 108259032 1 140849499 140849500 G A 55 GENIC homozygous 108259034 1 140850550 140850551 G T 54 GENIC homozygous 108259035 1 140850659 140850660 G A 54 GENIC homozygous 108259037 1 140851129 140851130 C T 47 GENIC homozygous 108259039 1 140851141 140851142 A T 52 GENIC homozygous 108259041 1 140851469 140851470 T C 26 GENIC homozygous 108259043 1 140851904 140851905 C T 34 GENIC homozygous 108259045 1 140855002 140855003 A G 66 GENIC homozygous 108259049 1 140855711 140855712 C T 61 GENIC homozygous 108259051 1 140857565 140857566 T C 46 GENIC homozygous 108259053 1 140858263 140858264 G C 47 GENIC homozygous 108259055 1 140858312 140858313 A C 53 GENIC homozygous 108259057 1 140848084 140848084 TG 50 GENIC homozygous 127438686 1 140854126 140854126 T 55 GENIC homozygous 127438687 1 140858624 140858628 TGTC 38 GENIC homozygous 127438688