chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 86320073 86320074 G T 25 GENIC homozygous 979898197 10 86321176 86321177 A G 51 GENIC homozygous 979898198 10 86321662 86321663 G A 64 GENIC homozygous 979898199 10 86322234 86322235 C T 53 GENIC homozygous 979898200 10 86322271 86322272 G A 71 GENIC homozygous 979898201 10 86322328 86322329 C T 76 GENIC homozygous 979898202 10 86322333 86322334 A G 75 GENIC homozygous 979898203 10 86323296 86323297 G A 57 GENIC homozygous 979898204 10 86323303 86323304 A G 56 GENIC homozygous 979898205 10 86323534 86323535 A T 28 GENIC homozygous 979898206 10 86323576 86323577 G A 32 GENIC homozygous 979898207 10 86323592 86323593 C T 41 GENIC homozygous 979898208 10 86324536 86324537 C T 38 GENIC homozygous 979898209 10 86325290 86325291 C T 38 GENIC homozygous 979898210 10 86325728 86325729 A G 54 GENIC homozygous 979898211 10 86326349 86326350 T G 51 GENIC homozygous 979898212 10 86326367 86326368 T C 39 GENIC homozygous 979898213 10 86327454 86327455 A G 38 GENIC homozygous 979898214 10 86327696 86327697 T G 37 GENIC homozygous 979898215 10 86327954 86327955 A G 53 GENIC homozygous 979898216 10 86329055 86329056 G A 31 GENIC homozygous 979898217 10 86329305 86329306 G A 34 GENIC homozygous 979898218 10 86329394 86329395 G A 51 GENIC homozygous 979898219 10 86329670 86329671 C T 57 GENIC homozygous 979898220 10 86330924 86330925 G A 56 GENIC homozygous 979898221 10 86331050 86331051 A G 50 GENIC homozygous 979898222 10 86331508 86331509 A G 46 GENIC homozygous 979898223 10 86332171 86332172 T C 68 GENIC homozygous 979898224 10 86332411 86332412 T C 53 GENIC homozygous 979898225 10 86332578 86332579 G T 60 GENIC homozygous 979898226 10 86332793 86332794 C T 63 GENIC homozygous 979898227 10 86334054 86334055 T C 47 GENIC homozygous 979898228 10 86334640 86334641 A G 61 GENIC possibly homozygous 979898229 10 86334880 86334881 A G 40 GENIC homozygous 979898230 10 86335348 86335349 C T 32 GENIC homozygous 979898231