chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47869508178695082AT5GENIChomozygous984918011
47869628078696281TC21GENIChomozygous984918012
47869634878696349AG16GENIChomozygous984918013
47869688578696886GT20GENIChomozygous984918014
47869699078696991GC18GENIChomozygous984918015
47869726378697264TC18GENIChomozygous984918016
47869787678697877AG16GENIChomozygous984918017
47869897278698973TC19GENIChomozygous984918018
47870092978700930CT16GENIChomozygous984918019
47870324178703242AG29GENIChomozygous984918020
47870354678703547GA12GENIChomozygous984918021
47870381578703816AC25GENIChomozygous984918022
47870389678703897AC20GENIChomozygous984918023
47870389878703899AG20GENIChomozygous984918024
47870447478704475CT24GENIChomozygous984918025
47870565978705660GA27GENIChomozygous984918026
47870675378706754GA9GENIChomozygous984918027
47870702178707022GA14GENIChomozygous984918028
47870717678707177CG32GENIChomozygous984918029
47870725778707258CT27GENIChomozygous984918030
47870735978707360CT24GENIChomozygous984918031
47870759078707591GA18GENIChomozygous984918032
47870759178707592CA19GENIChomozygous984918033
47870811578708116GA14GENIChomozygous984918034
47870819578708196TC17GENIChomozygous984918035
47870901578709016AG37GENIChomozygous984918036
47870910778709108AG24GENIChomozygous984918037
47870922878709229AC21GENIChomozygous984918038
47870969678709697TC26GENIChomozygous984918039
47871022078710221CT28GENICpossibly homozygous984918040
47871034678710347GA14GENIChomozygous984918041
47871080878710809TC24GENIChomozygous984918042
47871088278710883CT30GENIChomozygous984918043
47871198178711982CT23GENIChomozygous984918044
47871400578714006CT24GENIChomozygous984918045
47871533878715339CT27GENIChomozygous984918046
47871538778715388AG31GENIChomozygous984918047
47871560278715603AG31GENIChomozygous984918048