chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 61121085 61121086 T TA 14 GENIC homozygous 821749491 4 61121169 61121170 C G 16 GENIC homozygous 821749492 4 61121180 61121181 C G 7 GENIC homozygous 821749493 4 61121181 61121182 C T 7 GENIC homozygous 821749494 4 61121186 61121187 T G 7 GENIC homozygous 821749495 4 61121187 61121188 T A 7 GENIC homozygous 821749496 4 61121188 61121189 T G 7 GENIC homozygous 821749497 4 61121190 61121191 T G 7 GENIC homozygous 821749498 4 61121196 61121197 T A 7 GENIC homozygous 821749499 4 61121198 61121199 C A 7 GENIC homozygous 821749500 4 61121211 61121212 C T 16 GENIC homozygous 821749501 4 61138572 61138573 G T 16 GENIC homozygous 821749502 4 61138575 61138576 A AT 16 GENIC homozygous 821749503 4 61138593 61138594 G - 16 GENIC homozygous 821749504 4 61138818 61138819 C A 11 GENIC homozygous 821749505 4 61138821 61138822 C A 11 GENIC homozygous 821749506 4 61138831 61138832 T A 11 GENIC homozygous 821749507 4 61138836 61138837 G C 10 GENIC homozygous 821749508 4 61138838 61138839 A C 11 GENIC homozygous 821749509 4 61138879 61138880 G A 10 GENIC homozygous 821749510 4 61138893 61138894 G A 12 GENIC homozygous 821749511