chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10104690272104690273CT14GENICheterozygous828577013
10104690382104690383CT9GENICheterozygous828577014
10104690434104690435GC11GENICheterozygous828577015
10104690694104690695AG10GENICheterozygous828577016
10104690707104690708AT9GENICheterozygous828577017
10104690806104690807GA15GENICheterozygous828577018
10104690958104690959AG10GENICheterozygous828577019
10104691059104691060TC10GENIChomozygous828577020
10104691279104691280AAAC14GENICheterozygous828577021
10104691319104691321CA--10GENIChomozygous828577022
10104691681104691682CA17GENICheterozygous828577023
10104691775104691776AT12GENICheterozygous828577024
10104691980104691981GA14GENICheterozygous828577025
10104692097104692098CT20GENICheterozygous828577026
10104692126104692127GA20GENICheterozygous828577027
10104692195104692196TC14GENICheterozygous828577028