chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 137357344 137357345 A C 49 GENIC homozygous 114022986 5 137357457 137357458 T G 44 GENIC homozygous 114022987 5 137358071 137358072 C T 38 GENIC homozygous 114022989 5 137358221 137358222 C 38 GENIC homozygous 128244389 5 137358586 137358587 A T 38 GENIC homozygous 114022991 5 137358592 137358593 C G 39 GENIC homozygous 114022993 5 137359187 137359188 A C 33 GENIC homozygous 114022995 5 137359453 137359454 C T 44 GENIC homozygous 114022997 5 137359479 137359483 CCCT 37 GENIC homozygous 128244390 5 137359484 137359492 TCCTCAGC 37 GENIC homozygous 128244391 5 137359673 137359674 A G 39 GENIC homozygous 114022999 5 137359676 137359677 T C 38 GENIC homozygous 114023001 5 137359846 137359847 G T 37 GENIC homozygous 114023002