chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 90559591 90559592 C G 30 GENIC homozygous 538678265 10 90559688 90559689 C - 30 GENIC homozygous 697702360 10 90560123 90560124 G T 44 GENIC homozygous 538678266 10 90560514 90560515 C T 45 GENIC homozygous 541217378 10 90560916 90560917 C T 43 GENIC homozygous 541217379 10 90560928 90560929 C T 38 GENIC possibly homozygous 538678267 10 90561411 90561412 A - 13 GENIC homozygous 697702362 10 90561444 90561445 T TTGTGTG 5 GENIC heterozygous 697702364 10 90561444 90561445 T TTGTG 5 GENIC heterozygous 697702365 10 90561996 90561997 A G 30 GENIC homozygous 538678268 10 90562174 90562175 G A 22 GENIC homozygous 538678269 10 90562239 90562240 G T 28 GENIC homozygous 538678270 10 90562346 90562347 T - 13 GENIC homozygous 697702366 10 90563153 90563154 A C 26 GENIC possibly homozygous 538678271 10 90564601 90564602 A G 28 GENIC homozygous 541217380 10 90564617 90564618 A C 27 GENIC homozygous 541217381 10 90564647 90564648 C T 26 GENIC homozygous 541217382 10 90564681 90564682 A G 27 GENIC homozygous 541217383 10 90564747 90564748 T C 27 GENIC homozygous 541217384 10 90565116 90565117 A G 22 GENIC homozygous 541217385 10 90565125 90565129 GCTG ---- 13 GENIC homozygous 697702367 10 90565198 90565199 G A 32 GENIC homozygous 541217386 10 90565243 90565244 T C 34 GENIC homozygous 541217387 10 90565277 90565278 C T 30 GENIC homozygous 541217388 10 90565426 90565427 A T 26 GENIC homozygous 541217389 10 90565464 90565465 G A 34 GENIC homozygous 541217390 10 90565475 90565476 C T 32 GENIC homozygous 541217391 10 90565841 90565842 T A 11 GENIC homozygous 541217392 10 90565869 90565870 G A 19 GENIC homozygous 541217393