chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 78853346 78853347 C G 48 GENIC homozygous 510047947 13 78853536 78853537 A T 36 GENIC homozygous 506214372 13 78854501 78854502 T TTTCCTCAG 18 GENIC homozygous 686315210 13 78854567 78854568 G T 36 GENIC homozygous 510047948 13 78855773 78855774 G T 59 GENIC possibly homozygous 510047949 13 78856250 78856251 G A 55 GENIC homozygous 510047950 13 78856251 78856252 A T 56 GENIC homozygous 510047951 13 78856361 78856362 A ATGTTT 31 GENIC possibly homozygous 686315211 13 78857717 78857718 T A 75 GENIC homozygous 510047952 13 78857846 78857847 C CG 13 GENIC homozygous 686315213 13 78858682 78858683 T C 59 GENIC homozygous 510047953 13 78859393 78859395 CA -- 21 GENIC heterozygous 686315215 13 78859410 78859411 G GCA 24 GENIC heterozygous 686315216 13 78859412 78859413 G GCGCA 26 GENIC homozygous 686315217 13 78859430 78859431 G GCTCTCTCT 14 GENIC possibly homozygous 686315218 13 78859556 78859557 T C 32 GENIC homozygous 510047954 13 78859573 78859575 GA -- 30 GENIC homozygous 686315220 13 78860238 78860239 T - 50 GENIC homozygous 686315221 13 78860640 78860641 T C 38 GENIC homozygous 506214373 13 78861943 78861944 A - 40 GENIC homozygous 686315222 13 78862255 78862256 T C 66 GENIC homozygous 510047955 13 78862266 78862267 T C 66 GENIC homozygous 506214374 13 78862677 78862678 A G 64 GENIC possibly homozygous 510047956 13 78862748 78862749 C T 66 GENIC homozygous 510047957 13 78863800 78863801 T C 62 GENIC homozygous 506214375 13 78864020 78864021 A G 51 GENIC homozygous 506214376 13 78864042 78864043 T A 54 GENIC homozygous 506214377 13 78865124 78865125 C T 61 GENIC homozygous 510047958 13 78865377 78865378 G A 55 GENIC possibly homozygous 510047959 13 78865497 78865498 C T 64 GENIC homozygous 510047960