chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5161242393161242394AG9GENIChomozygous55817793
5161242404161242405TC7GENIChomozygous55817794
5161242407161242408CCCCCCT9GENIChomozygous55817795
5161242415161242416TA10GENIChomozygous55817796
5161242464161242465GA7GENIChomozygous55817797
5161244398161244399T-7GENIChomozygous55817798
5161244508161244509TTAGATAGATAGATAGAG5GENIChomozygous56463319
5161244798161244799AG8GENIChomozygous55817804
5161244970161244971CT17GENIChomozygous55817805
5161245201161245202TC21GENIChomozygous55817807
5161245274161245279AAATC-----14GENIChomozygous55817809
5161245280161245281AT14GENIChomozygous56463320
5161245286161245287TTA14GENIChomozygous55817810
5161245598161245606CTCACGAG--------10GENIChomozygous55817811
5161245635161245636AG11GENIChomozygous55817812
5161246109161246110T-20GENIChomozygous55817813
5161246730161246731AG16GENIChomozygous55817814
5161246785161246794AAAAAAAAA---------5GENIChomozygous56463321
5161247319161247320CG21GENIChomozygous55817817
5161248844161248845CT10GENIChomozygous55817818
5161248996161248997CT7GENIChomozygous55817819
5161249100161249101AG15GENIChomozygous55817820
5161249268161249269TA9GENIChomozygous55817821
5161249591161249592CT14GENIChomozygous55817822
5161249650161249651CT9GENIChomozygous55817823
5161249695161249696GA11GENIChomozygous55817824
5161249697161249698CT10GENIChomozygous55817825
5161249861161249862GA9GENIChomozygous55817826
5161249876161249877GC9GENIChomozygous55817827
5161249906161249907GA16GENIChomozygous55817828
5161249943161249944CT10GENIChomozygous55817829
5161250142161250143GT17GENIChomozygous55817830
5161251163161251164CCA9GENIChomozygous55817831
5161251291161251292AAAAAT1GENIChomozygous55817832
5161252935161252936CCGAT3GENIChomozygous55817833
5161253178161253190AATAATAATAAT------------1GENIChomozygous56496129
5161253814161253826AAAGAAAGAAAG------------12GENIChomozygous56619350
5161254104161254105CCTGTGTGTGTGTGTGTGTGTGTG2GENIChomozygous56463324