chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 62168855 62168856 T C 46 GENIC homozygous 660564527 8 62170191 62170192 G GTTTGT 18 GENIC homozygous 763362072 8 62171469 62171470 G GCC 13 GENIC homozygous 763362074 8 62172226 62172227 T TGGG 3 GENIC homozygous 763362075 8 62172235 62172236 T TTAGCTCAGTGGTA 3 GENIC homozygous 763362076 8 62172237 62172238 A AGCG 3 GENIC homozygous 763362077 8 62172241 62172242 G GCCTAGCAAGC 3 GENIC homozygous 763362078 8 62172281 62172282 A - 5 GENIC heterozygous 763362079 8 62173572 62173573 C T 41 GENIC homozygous 660564528 8 62174054 62174055 C T 23 GENIC homozygous 660564529 8 62174120 62174121 A G 13 GENIC homozygous 660564530 8 62174305 62174306 C T 20 GENIC homozygous 660564531 8 62174491 62174492 C T 24 GENIC homozygous 660564532 8 62174521 62174522 C T 32 GENIC homozygous 660564533 8 62175018 62175019 G C 48 GENIC homozygous 660564534 8 62175211 62175212 T C 41 GENIC homozygous 660564535 8 62175226 62175227 A G 39 GENIC homozygous 660564536 8 62175237 62175238 T TGTGTGCGTGCATGC 6 GENIC homozygous 763362080 8 62175268 62175269 G GTGTGTGTGTC 34 GENIC possibly homozygous 763362081 8 62175417 62175418 A G 28 GENIC homozygous 660564537 8 62176229 62176230 T - 29 GENIC homozygous 763362082 8 62176233 62176239 TTTGTT ------ 29 GENIC homozygous 763362083 8 62176608 62176610 AA -- 20 GENIC heterozygous 763362084 8 62176609 62176610 A - 20 GENIC heterozygous 763362085 8 62177132 62177133 T C 63 GENIC homozygous 660564538