chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 25029125 25029125 C 13 GENIC homozygous 129595696 19 25029141 25029142 G 15 GENIC homozygous 129595697 19 25029163 25029163 GGC 15 GENIC homozygous 129595698 19 25029173 25029174 G 13 GENIC homozygous 129595699 19 25029178 25029179 C 13 GENIC homozygous 129595700 19 25029182 25029183 G C 13 GENIC homozygous 109672124 19 25029204 25029204 C 14 GENIC homozygous 129595701 19 25029268 25029269 G 12 GENIC homozygous 129595702 19 25029287 25029288 A G 12 GENIC homozygous 109672126 19 25029313 25029313 G 12 GENIC homozygous 129595703 19 25029324 25029326 GT 13 GENIC homozygous 129595704 19 25029347 25029347 G 12 GENIC homozygous 129595705 19 25029380 25029380 C 12 GENIC homozygous 129595706 19 25029401 25029402 G 10 GENIC homozygous 129595707 19 25029411 25029411 G 10 GENIC homozygous 129595708 19 25029422 25029422 G 11 GENIC homozygous 129595709 19 25029445 25029445 C 12 GENIC homozygous 129595710 19 25029457 25029457 C 12 GENIC homozygous 129595711 19 25029459 25029460 G 13 GENIC homozygous 129595712 19 25066488 25066489 G 13 GENIC homozygous 129595717 19 25042632 25042633 G A 19 GENIC homozygous 133693622