chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 30284704 30284705 A ACTGGG 27 GENIC homozygous 55270009 5 30285647 30285648 C T 25 GENIC homozygous 57223299 5 30286729 30286730 C T 29 GENIC homozygous 57223301 5 30286913 30286914 A C 33 GENIC homozygous 55270015 5 30286984 30286985 T C 23 GENIC homozygous 55270018 5 30287351 30287353 AA -- 23 GENIC homozygous 55270021 5 30287434 30287435 C A 29 GENIC homozygous 55270024 5 30288510 30288511 T TC 8 GENIC homozygous 55270027 5 30288869 30288870 T - 21 GENIC homozygous 57223303 5 30289074 30289075 A C 19 GENIC homozygous 55270033 5 30289260 30289261 C CTTT 11 GENIC homozygous 56571691 5 30289311 30289312 C G 23 GENIC homozygous 55270039 5 30289708 30289709 C T 26 GENIC homozygous 55270042 5 30289846 30289847 C T 17 GENIC homozygous 55270045 5 30289927 30289928 T C 19 GENIC homozygous 55270048 5 30290282 30290283 A T 3 GENIC homozygous 55270054 5 30290624 30290625 G A 6 GENIC homozygous 55270066 5 30290483 30290484 C CTG 3 GENIC homozygous 55270057 5 30290576 30290577 C A 6 GENIC homozygous 55270060 5 30290593 30290594 T C 8 GENIC homozygous 55270063