chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143595239143595240TA10GENIChomozygous537567215
4143595754143595755AG38GENIChomozygous537567216
4143595803143595804GGCCAA27GENIChomozygous697146505
4143597231143597232AAATAT4GENIChomozygous697146506
4143598137143598138GGAA20GENICheterozygous697146507
4143598137143598138GGA20GENICpossibly homozygous697146508
4143598221143598222CA24GENIChomozygous537567217
4143599736143599737AG32GENIChomozygous537567218
4143599907143599908TC43GENIChomozygous537567219
4143604440143604441C-11GENIChomozygous697146509
4143604674143604675CT24GENIChomozygous537567220
4143604748143604754ACACCC------8GENIChomozygous697146510
4143605173143605174GA16GENIChomozygous537567221
4143605245143605246AAT4GENIChomozygous697146511
4143605468143605469GT4GENIChomozygous537567222
4143605475143605476TA5GENIChomozygous537567223
4143605713143605714TC13GENIChomozygous540889489
4143605997143605998TG8GENIChomozygous540889490
4143606027143606028AC12GENIChomozygous537567224
4143606162143606163CT13GENIChomozygous537567225
4143606292143606293T-13GENICheterozygous697146513
4143606891143606892GGCCTA17GENIChomozygous697146514
4143606956143606960CTCC----7GENIChomozygous697146515
4143606958143606961CCC---5GENIChomozygous697146516
4143607052143607053T-3GENIChomozygous697146517
4143607735143607736TG30GENICpossibly homozygous537567226
4143608290143608291GA28GENIChomozygous537567227
4143609090143609091AAAAAG36GENIChomozygous697146518
4143609308143609309AATTT3GENIChomozygous697146520
4143610355143610356AG22GENIChomozygous537567228
4143611152143611153AT11GENIChomozygous537567229
4143611621143611622A-18GENIChomozygous697146523
4143611780143611781TC19GENIChomozygous537567230
4143612095143612096GA5GENICheterozygous537567231
4143612108143612109A-3GENIChomozygous697146524
4143612121143612122CCAA3GENICheterozygous697146525
4143612444143612445GA14GENIChomozygous537567232