geneid | 57562 |
---|---|
ensemblid | ENSG00000110318.15 |
hgncid | 29264 |
symbol | CEP126 |
name | centrosomal protein 126 |
refseq_nuc | NM_020802.4 |
refseq_prot | NP_065853.3 |
ensembl_nuc | ENST00000263468.13 |
ensembl_prot | ENSP00000263468.8 |
mane_status | MANE Select |
chr | chr11 |
start | 101915010 |
end | 102001062 |
strand | + |
ver | v1.2 |
region | chr11:101915010-102001062 |
region5000 | chr11:101910010-102006062 |
regionname0 | CEP126_chr11_101915010_102001062 |
regionname5000 | CEP126_chr11_101910010_102006062 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1117 | 260 | 57 | 52 | 112 | 12 | 27 | 85 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0002 | 0/0 | 1117 | 40 | 0 | 5 | 29 | 0 | 6 | 20 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0003 | 0/0 | 1117 | 10 | 6 | 1 | 0 | 0 | 3 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0004 | 0/0 | 1117 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0005 | 0/0 | 1117 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0006 | 0/0 | 1117 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0007 | 0/0 | 1117 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0008 | 0/0 | 1117 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0009 | 0/0 | 1117 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0010 | 0/0 | 1117 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0011 | 0/0 | 1117 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0012 | 0/0 | 1117 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0013 | 0/0 | 1117 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0014 | 0/0 | 1117 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0015 | 0/0 | 1117 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3354 | 209 | 53 | 42 | 83 | 11 | 20 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0002 | 0/0 | 3354 | 48 | 2 | 9 | 29 | 1 | 7 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0003 | 0/0 | 3354 | 40 | 0 | 5 | 29 | 0 | 6 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0004 | 0/0 | 3354 | 10 | 6 | 1 | 0 | 0 | 3 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0005 | 0/0 | 3354 | 7 | 7 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0006 | 0/0 | 3354 | 7 | 6 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0007 | 0/0 | 3354 | 2 | 0 | 0 | 1 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0008 | 0/0 | 3354 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0009 | 0/0 | 3354 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0010 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0011 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0012 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0013 | 0/0 | 3354 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0014 | 0/0 | 3354 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0015 | 0/0 | 3354 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0016 | 0/0 | 3354 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0017 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
c0018 | 0/0 | 3354 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3705 | 64 | 13 | 13 | 26 | 3 | 9 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0002 | 0/0 | 3704 | 63 | 5 | 14 | 37 | 2 | 5 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0003 | 0/0 | 3703 | 31 | 0 | 5 | 20 | 0 | 6 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0004 | 0/0 | 3705 | 25 | 7 | 5 | 9 | 1 | 3 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0005 | 0/0 | 3706 | 23 | 10 | 3 | 9 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0006 | 0/0 | 3694 | 21 | 2 | 9 | 1 | 2 | 7 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0007 | 0/0 | 3704 | 10 | 0 | 0 | 9 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0008 | 0/0 | 3694 | 6 | 3 | 2 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0009 | 0/0 | 3703 | 6 | 4 | 2 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0010 | 0/0 | 3702 | 5 | 2 | 0 | 0 | 0 | 3 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0011 | 0/0 | 3703 | 4 | 2 | 0 | 1 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0012 | 0/0 | 3705 | 3 | 3 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0013 | 0/0 | 3700 | 3 | 3 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0014 | 0/0 | 3706 | 3 | 0 | 0 | 3 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0015 | 0/0 | 3693 | 2 | 1 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0016 | 0/0 | 3700 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0017 | 0/0 | 3705 | 2 | 0 | 1 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0018 | 0/0 | 3704 | 2 | 1 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0019 | 0/0 | 3706 | 2 | 0 | 0 | 2 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0020 | 0/0 | 3704 | 2 | 1 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0021 | 0/0 | 3702 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0022 | 0/0 | 3706 | 2 | 1 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0023 | 0/0 | 3706 | 2 | 1 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0024 | 0/0 | 3704 | 2 | 0 | 0 | 2 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0025 | 0/0 | 3705 | 2 | 0 | 0 | 2 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0026 | 0/0 | 3704 | 2 | 0 | 0 | 2 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0027 | 0/0 | 3704 | 2 | 0 | 0 | 2 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0028 | 0/0 | 3703 | 2 | 0 | 0 | 1 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0029 | 0/0 | 3705 | 2 | 0 | 0 | 2 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0030 | 0/0 | 3694 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0031 | 0/0 | 3706 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0032 | 0/0 | 3705 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0033 | 0/0 | 3694 | 2 | 0 | 0 | 0 | 1 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0034 | 0/0 | 3694 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0035 | 0/0 | 3705 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0036 | 0/0 | 3709 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0037 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0038 | 0/0 | 3702 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0039 | 0/0 | 3704 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0040 | 0/0 | 3692 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0041 | 0/0 | 3705 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0042 | 0/0 | 3707 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0043 | 0/0 | 3706 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0044 | 0/0 | 3682 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0045 | 0/0 | 3704 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0046 | 0/0 | 3705 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0047 | 0/0 | 3706 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0048 | 0/0 | 3705 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0049 | 0/0 | 3696 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0050 | 0/0 | 3695 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0051 | 0/0 | 3703 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0052 | 0/0 | 3703 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0053 | 0/0 | 3703 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0054 | 0/0 | 3707 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0055 | 0/0 | 3706 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0056 | 0/0 | 3704 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0057 | 0/0 | 3704 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0058 | 0/0 | 3701 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0059 | 0/0 | 3695 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0060 | 0/0 | 3705 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0061 | 0/0 | 3705 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0062 | 0/0 | 3706 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0063 | 0/0 | 3704 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
t0064 | 0/0 | 3708 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3354 | 209 | 53 | 42 | 83 | 11 | 20 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0002 | 0/0 | 3354 | 48 | 2 | 9 | 29 | 1 | 7 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0009 | 0/0 | 3354 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0013 | 0/0 | 3354 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0002c0003 | 0/0 | 3354 | 40 | 0 | 5 | 29 | 0 | 6 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0003c0004 | 0/0 | 3354 | 10 | 6 | 1 | 0 | 0 | 3 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0004c0005 | 0/0 | 3354 | 7 | 7 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0005c0006 | 0/0 | 3354 | 7 | 6 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0006c0008 | 0/0 | 3354 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0007c0007 | 0/0 | 3354 | 2 | 0 | 0 | 1 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0008c0010 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0009c0016 | 0/0 | 3354 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0010c0014 | 0/0 | 3354 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0011c0017 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0012c0015 | 0/0 | 3354 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0013c0018 | 0/0 | 3354 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0014c0012 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0015c0011 | 0/0 | 3354 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7058 | 33 | 11 | 5 | 12 | 2 | 3 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0002 | 0/0 | 7057 | 61 | 4 | 13 | 37 | 2 | 5 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0004 | 0/0 | 7058 | 25 | 7 | 5 | 9 | 1 | 3 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0005 | 0/0 | 7059 | 6 | 3 | 2 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0006 | 0/0 | 7047 | 20 | 2 | 9 | 1 | 2 | 6 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0008 | 0/0 | 7047 | 6 | 3 | 2 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0009 | 0/0 | 7056 | 6 | 4 | 2 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0011 | 0/0 | 7056 | 4 | 2 | 0 | 1 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0012 | 0/0 | 7058 | 3 | 3 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0015 | 0/0 | 7046 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0017 | 0/0 | 7058 | 2 | 0 | 1 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0018 | 0/0 | 7057 | 2 | 1 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0019 | 0/0 | 7059 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0020 | 0/0 | 7057 | 2 | 1 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0022 | 0/0 | 7059 | 2 | 1 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0023 | 0/0 | 7059 | 2 | 1 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0024 | 0/0 | 7057 | 2 | 0 | 0 | 2 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0025 | 0/0 | 7058 | 2 | 0 | 0 | 2 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0026 | 0/0 | 7057 | 2 | 0 | 0 | 2 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0027 | 0/0 | 7057 | 2 | 0 | 0 | 2 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0028 | 0/0 | 7056 | 2 | 0 | 0 | 1 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0031 | 0/0 | 7059 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0032 | 0/0 | 7058 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0033 | 0/0 | 7047 | 2 | 0 | 0 | 0 | 1 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0034 | 0/0 | 7047 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0036 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0037 | 0/0 | 7061 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0039 | 0/0 | 7057 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0041 | 0/0 | 7058 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0042 | 0/0 | 7060 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0043 | 0/0 | 7059 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0045 | 0/0 | 7057 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0049 | 0/0 | 7049 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0050 | 0/0 | 7048 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0054 | 0/0 | 7060 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0056 | 0/0 | 7057 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0057 | 0/0 | 7057 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0060 | 0/0 | 7058 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0061 | 0/0 | 7058 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0062 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0001t0063 | 0/0 | 7057 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0002t0001 | 0/0 | 7058 | 29 | 1 | 8 | 13 | 1 | 6 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0002t0005 | 0/0 | 7059 | 11 | 1 | 1 | 8 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0002t0014 | 0/0 | 7059 | 3 | 0 | 0 | 3 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0002t0019 | 0/0 | 7059 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0002t0044 | 0/0 | 7035 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0002t0046 | 0/0 | 7058 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0002t0047 | 0/0 | 7059 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0002t0048 | 0/0 | 7058 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0009t0055 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0009t0064 | 0/0 | 7061 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0001c0013t0002 | 0/0 | 7057 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0002c0003t0003 | 0/0 | 7056 | 29 | 0 | 5 | 19 | 0 | 5 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0002c0003t0007 | 0/0 | 7057 | 8 | 0 | 0 | 7 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0002c0003t0029 | 0/0 | 7058 | 2 | 0 | 0 | 2 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0002c0003t0059 | 0/0 | 7048 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0003c0004t0010 | 0/0 | 7055 | 5 | 2 | 0 | 0 | 0 | 3 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0003c0004t0021 | 0/0 | 7055 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0003c0004t0038 | 0/0 | 7055 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0003c0004t0052 | 0/0 | 7056 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0003c0004t0053 | 0/0 | 7056 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0004c0005t0001 | 0/0 | 7058 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0004c0005t0005 | 0/0 | 7059 | 6 | 6 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0005c0006t0013 | 0/0 | 7053 | 3 | 3 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0005c0006t0016 | 0/0 | 7053 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0005c0006t0040 | 0/0 | 7045 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0005c0006t0058 | 0/0 | 7054 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0006c0008t0030 | 0/0 | 7047 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0007c0007t0003 | 0/0 | 7056 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0007c0007t0007 | 0/0 | 7057 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0008c0010t0003 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0009c0016t0002 | 0/0 | 7057 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0010c0014t0006 | 0/0 | 7047 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0011c0017t0001 | 0/0 | 7058 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0012c0015t0035 | 0/0 | 7058 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0013c0018t0015 | 0/0 | 7046 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0014c0012t0051 | 0/0 | 7056 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
a0015c0011t0007 | 0/0 | 7057 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | copy fasta | chr11 | 101910010 | 102006062 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0008g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0008g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0008g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0009g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0009g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0009g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0009g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0009g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0011g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0011g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0011g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0011g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0012g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0012g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0012g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0015g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0017g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0017g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0018g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0018g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0019g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0020g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0020g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0022g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0022g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0023g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0023g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0024g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0024g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0025g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0025g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0026g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0026g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0027g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0027g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0028g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0028g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0031g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0031g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0032g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0032g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0033g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0033g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0034g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0036g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0037g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0039g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0041g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0042g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0043g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0045g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0049g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0050g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0054g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0056g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0057g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0060g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0061g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0062g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0001t0063g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0014g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0014g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0014g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0019g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0044g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0046g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0047g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0002t0048g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0009t0055g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0009t0064g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0001c0013t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0007g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0007g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0007g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0007g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0029g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0029g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0002c0003t0059g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0003c0004t0010g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0003c0004t0010g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0003c0004t0010g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0003c0004t0010g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0003c0004t0021g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0003c0004t0021g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0003c0004t0038g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0003c0004t0052g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0003c0004t0053g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0004c0005t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0004c0005t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0004c0005t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0004c0005t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0004c0005t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0004c0005t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0004c0005t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0005c0006t0013g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0005c0006t0013g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0005c0006t0013g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0005c0006t0016g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0005c0006t0016g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0005c0006t0040g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0005c0006t0058g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0006c0008t0030g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0006c0008t0030g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0007c0007t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0007c0007t0007g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0008c0010t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0009c0016t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0010c0014t0006g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0011c0017t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0012c0015t0035g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0013c0018t0015g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0014c0012t0051g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
a0015c0011t0007g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0041 | g0122 | EUR | FIN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0172 | EUR | FIN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00323 | hp1 | a0001 | c0001 | t0033 | g0275 | EUR | FIN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00323 | hp2 | a0001 | c0001 | t0008 | g0034 | EUR | FIN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | CHS | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00408 | hp2 | a0002 | c0003 | t0003 | g0073 | EAS | CHS | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00423 | hp1 | a0002 | c0003 | t0003 | g0019 | EAS | CHS | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | CHS | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00597 | hp1 | a0001 | c0002 | t0005 | g0176 | EAS | CHS | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00597 | hp2 | a0001 | c0001 | t0061 | g0232 | EAS | CHS | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00621 | hp1 | a0002 | c0003 | t0003 | g0076 | EAS | CHS | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00621 | hp2 | a0001 | c0001 | t0017 | g0152 | EAS | CHS | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00639 | hp1 | a0001 | c0001 | t0006 | g0120 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00642 | hp1 | a0013 | c0018 | t0015 | g0033 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00673 | hp1 | a0002 | c0003 | t0003 | g0016 | EAS | CHS | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0281 | EAS | CHS | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0206 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG00741 | hp2 | a0002 | c0003 | t0003 | g0146 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01069 | hp1 | a0001 | c0001 | t0006 | g0119 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01069 | hp2 | a0002 | c0003 | t0003 | g0145 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01081 | hp1 | a0001 | c0001 | t0006 | g0112 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01099 | hp1 | a0001 | c0001 | t0006 | g0127 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0216 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01106 | hp1 | a0002 | c0003 | t0003 | g0147 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0114 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01109 | hp1 | a0003 | c0004 | t0038 | g0314 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01175 | hp1 | a0001 | c0001 | t0017 | g0234 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0211 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0043 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0214 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01243 | hp2 | a0001 | c0001 | t0008 | g0036 | AMR | PUR | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01256 | hp1 | a0002 | c0003 | t0003 | g0143 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01256 | hp2 | a0001 | c0001 | t0006 | g0045 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01257 | hp1 | a0001 | c0001 | t0009 | g0008 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0004 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01258 | hp1 | a0001 | c0001 | t0009 | g0008 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01258 | hp2 | a0002 | c0003 | t0003 | g0144 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01346 | hp1 | a0005 | c0006 | t0058 | g0132 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0268 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0174 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01361 | hp1 | a0001 | c0001 | t0018 | g0188 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0159 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0158 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01516 | hp1 | a0001 | c0001 | t0006 | g0091 | EUR | IBS | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01516 | hp2 | a0001 | c0001 | t0028 | g0287 | EUR | IBS | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0288 | EUR | IBS | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0118 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0160 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01978 | hp1 | a0001 | c0001 | t0008 | g0030 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01978 | hp2 | a0001 | c0001 | t0049 | g0038 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01981 | hp1 | a0001 | c0001 | t0005 | g0105 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01981 | hp2 | a0001 | c0002 | t0005 | g0166 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0199 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02004 | hp2 | a0001 | c0001 | t0006 | g0093 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02027 | hp2 | a0001 | c0002 | t0005 | g0007 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02040 | hp1 | a0002 | c0003 | t0003 | g0109 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02040 | hp2 | a0001 | c0002 | t0046 | g0170 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0087 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02055 | hp2 | a0001 | c0001 | t0031 | g0141 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02071 | hp2 | a0002 | c0003 | t0059 | g0075 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02074 | hp1 | a0002 | c0003 | t0029 | g0071 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02080 | hp1 | a0001 | c0001 | t0039 | g0313 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02083 | hp1 | a0002 | c0003 | t0003 | g0028 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02129 | hp1 | a0001 | c0001 | t0026 | g0053 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0113 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02132 | hp1 | a0001 | c0001 | t0025 | g0225 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02148 | hp1 | a0001 | c0001 | t0005 | g0124 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02148 | hp2 | a0001 | c0013 | t0002 | g0250 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02155 | hp1 | a0002 | c0003 | t0003 | g0070 | EAS | CDX | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | CDX | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0270 | EAS | CDX | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02165 | hp2 | a0001 | c0002 | t0014 | g0280 | EAS | CDX | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02257 | hp1 | a0004 | c0005 | t0005 | g0325 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02257 | hp2 | a0003 | c0004 | t0010 | g0308 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02258 | hp2 | a0004 | c0005 | t0005 | g0111 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02280 | hp2 | a0001 | c0001 | t0034 | g0128 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0150 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | PEL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02451 | hp1 | a0001 | c0001 | t0037 | g0302 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02451 | hp2 | a0001 | c0001 | t0012 | g0309 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0192 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0203 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02615 | hp2 | a0003 | c0004 | t0052 | g0319 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02622 | hp1 | a0004 | c0005 | t0005 | g0121 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02622 | hp2 | a0001 | c0002 | t0005 | g0196 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02647 | hp2 | a0003 | c0004 | t0053 | g0320 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02683 | hp1 | a0002 | c0003 | t0003 | g0049 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02683 | hp2 | a0001 | c0001 | t0011 | g0290 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02698 | hp1 | a0001 | c0001 | t0033 | g0286 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02698 | hp2 | a0001 | c0001 | t0006 | g0116 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02717 | hp1 | a0004 | c0005 | t0001 | g0096 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02723 | hp1 | a0001 | c0001 | t0015 | g0035 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02723 | hp2 | a0005 | c0006 | t0013 | g0312 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02735 | hp1 | a0001 | c0001 | t0006 | g0135 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02735 | hp2 | a0010 | c0014 | t0006 | g0090 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0061 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02809 | hp2 | a0001 | c0001 | t0018 | g0272 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0044 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02818 | hp2 | a0001 | c0001 | t0011 | g0129 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02886 | hp2 | a0001 | c0001 | t0032 | g0142 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02895 | hp1 | a0005 | c0006 | t0040 | g0317 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02895 | hp2 | a0001 | c0001 | t0009 | g0298 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02897 | hp1 | a0005 | c0006 | t0016 | g0316 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02922 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | ESN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | ESN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0212 | AFR | ESN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02970 | hp1 | a0001 | c0001 | t0012 | g0310 | AFR | ESN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0003 | AFR | ESN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0326 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0283 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0213 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03098 | hp1 | a0001 | c0009 | t0064 | g0010 | AFR | MSL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03098 | hp2 | a0004 | c0005 | t0005 | g0324 | AFR | MSL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03130 | hp1 | a0001 | c0001 | t0009 | g0301 | AFR | ESN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03130 | hp2 | a0003 | c0004 | t0010 | g0322 | AFR | ESN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03195 | hp1 | a0001 | c0001 | t0023 | g0285 | AFR | ESN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03195 | hp2 | a0001 | c0001 | t0031 | g0139 | AFR | ESN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03209 | hp1 | a0001 | c0001 | t0036 | g0303 | AFR | MSL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03209 | hp2 | a0004 | c0005 | t0005 | g0115 | AFR | MSL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03225 | hp1 | a0003 | c0004 | t0021 | g0321 | AFR | MSL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03225 | hp2 | a0001 | c0001 | t0062 | g0215 | AFR | MSL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03239 | hp2 | a0002 | c0003 | t0003 | g0050 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | MSL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03453 | hp2 | a0005 | c0006 | t0016 | g0318 | AFR | MSL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03486 | hp1 | a0001 | c0001 | t0022 | g0265 | AFR | MSL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03486 | hp2 | a0006 | c0008 | t0030 | g0041 | AFR | MSL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03490 | hp1 | a0003 | c0004 | t0010 | g0009 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03490 | hp2 | a0007 | c0007 | t0003 | g0223 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03492 | hp1 | a0001 | c0001 | t0006 | g0097 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03492 | hp2 | a0003 | c0004 | t0010 | g0009 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03516 | hp1 | a0001 | c0001 | t0011 | g0130 | AFR | ESN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03540 | hp1 | a0012 | c0015 | t0035 | g0032 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | MSL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03579 | hp2 | a0005 | c0006 | t0013 | g0306 | AFR | MSL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0173 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03669 | hp1 | a0002 | c0003 | t0003 | g0126 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03688 | hp1 | a0001 | c0002 | t0005 | g0155 | SAS | STU | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03688 | hp2 | a0002 | c0003 | t0003 | g0039 | SAS | STU | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03704 | hp1 | a0002 | c0003 | t0007 | g0074 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | BEB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0193 | SAS | BEB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0291 | SAS | BEB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03942 | hp2 | a0003 | c0004 | t0010 | g0307 | SAS | BEB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0254 | SAS | STU | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG04184 | hp1 | a0001 | c0001 | t0050 | g0066 | SAS | BEB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0296 | SAS | BEB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0104 | SAS | STU | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0156 | SAS | STU | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG04228 | hp1 | a0002 | c0003 | t0003 | g0072 | SAS | STU | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0194 | SAS | STU | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | YRI | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18612 | hp2 | a0001 | c0001 | t0026 | g0259 | EAS | CHB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18942 | hp2 | a0002 | c0003 | t0003 | g0011 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18943 | hp2 | a0001 | c0002 | t0005 | g0157 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18947 | hp1 | a0002 | c0003 | t0007 | g0027 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18947 | hp2 | a0011 | c0017 | t0001 | g0095 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18951 | hp2 | a0002 | c0003 | t0003 | g0021 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18954 | hp1 | a0001 | c0002 | t0047 | g0198 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0297 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18957 | hp2 | a0001 | c0001 | t0023 | g0282 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18960 | hp2 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18965 | hp2 | a0001 | c0002 | t0005 | g0161 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18966 | hp2 | a0002 | c0003 | t0007 | g0018 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18967 | hp1 | a0001 | c0002 | t0005 | g0179 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18969 | hp1 | a0002 | c0003 | t0003 | g0069 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18969 | hp2 | a0001 | c0001 | t0011 | g0240 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18970 | hp1 | a0014 | c0012 | t0051 | g0002 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18972 | hp1 | a0001 | c0001 | t0056 | g0186 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18973 | hp1 | a0002 | c0003 | t0003 | g0023 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18973 | hp2 | a0001 | c0001 | t0045 | g0005 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18975 | hp2 | a0001 | c0001 | t0060 | g0222 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18982 | hp1 | a0002 | c0003 | t0003 | g0015 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18984 | hp1 | a0015 | c0011 | t0007 | g0068 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18985 | hp1 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18985 | hp2 | a0002 | c0003 | t0003 | g0012 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18986 | hp2 | a0001 | c0001 | t0020 | g0094 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18987 | hp1 | a0002 | c0003 | t0029 | g0026 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18991 | hp1 | a0001 | c0001 | t0042 | g0080 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18991 | hp2 | a0001 | c0001 | t0054 | g0185 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18993 | hp2 | a0001 | c0002 | t0048 | g0263 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18994 | hp1 | a0002 | c0003 | t0007 | g0029 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18995 | hp1 | a0002 | c0003 | t0003 | g0014 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18998 | hp1 | a0002 | c0003 | t0003 | g0022 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18999 | hp2 | a0002 | c0003 | t0007 | g0024 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19003 | hp2 | a0001 | c0001 | t0028 | g0238 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19004 | hp1 | a0008 | c0010 | t0003 | g0077 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19004 | hp2 | a0001 | c0001 | t0027 | g0209 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19005 | hp1 | a0001 | c0001 | t0022 | g0273 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19005 | hp2 | a0001 | c0001 | t0019 | g0047 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19007 | hp1 | a0001 | c0001 | t0057 | g0187 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19007 | hp2 | a0002 | c0003 | t0007 | g0025 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19011 | hp1 | a0001 | c0002 | t0019 | g0162 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19011 | hp2 | a0001 | c0001 | t0027 | g0236 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19030 | hp1 | a0001 | c0001 | t0032 | g0140 | AFR | LWK | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19030 | hp2 | a0004 | c0005 | t0005 | g0323 | AFR | LWK | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19057 | hp2 | a0001 | c0002 | t0014 | g0197 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19058 | hp1 | a0001 | c0001 | t0024 | g0257 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19058 | hp2 | a0002 | c0003 | t0007 | g0013 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19060 | hp1 | a0002 | c0003 | t0003 | g0017 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19062 | hp1 | a0001 | c0002 | t0014 | g0195 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19066 | hp1 | a0001 | c0001 | t0025 | g0202 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19066 | hp2 | a0001 | c0002 | t0005 | g0006 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19070 | hp2 | a0001 | c0002 | t0044 | g0264 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19076 | hp2 | a0002 | c0003 | t0007 | g0020 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19077 | hp1 | a0007 | c0007 | t0007 | g0048 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19078 | hp1 | a0001 | c0001 | t0024 | g0190 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19078 | hp2 | a0001 | c0002 | t0005 | g0178 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19084 | hp1 | a0001 | c0002 | t0005 | g0171 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19085 | hp1 | a0002 | c0003 | t0003 | g0067 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19088 | hp1 | a0002 | c0003 | t0003 | g0078 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0153 | EUR | TSI | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0060 | EUR | TSI | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0274 | EUR | TSI | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0125 | SAS | GIH | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0004 | SAS | GIH | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01123 | hp1 | a0001 | c0001 | t0043 | g0123 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | CLM | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02109 | hp1 | a0005 | c0006 | t0013 | g0305 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0300 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0175 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG02559 | hp2 | a0001 | c0001 | t0009 | g0299 | AFR | ACB | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03471 | hp1 | a0001 | c0009 | t0055 | g0304 | AFR | MSL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG03471 | hp2 | a0001 | c0001 | t0063 | g0131 | AFR | MSL | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG06807 | hp1 | a0006 | c0008 | t0030 | g0040 | AFR | USA | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
HG06807 | hp2 | a0001 | c0001 | t0012 | g0311 | AFR | USA | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA20300 | hp1 | a0003 | c0004 | t0021 | g0315 | AFR | USA | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA20300 | hp2 | a0001 | c0001 | t0020 | g0086 | AFR | USA | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA21309 | hp1 | a0009 | c0016 | t0002 | g0229 | AFR | LWK | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | LWK | CEP126_chr11_101910010_102006062 | CEP126 | chr11 | 101910010 | 102006062 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:101922698
|
G | C | 1 | a0008 | 1 | NA19004.hp1 | missense_variant | MODERATE | c.186G>C | p.Gln62His | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/11 | 461/7048 | 186/3354 | 62/1117 | chr11 | 101922698 | ||
chr11:101958193
|
G | A | 1 | a0015 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.532G>A | p.Ala178Thr | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/11 | 807/7048 | 532/3354 | 178/1117 | chr11 | 101958193 | ||
chr11:101958275
|
G | A | 1 | a0003 | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
missense_variant | MODERATE | c.614G>A | p.Arg205Lys | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/11 | 889/7048 | 614/3354 | 205/1117 | chr11 | 101958275 | ||
chr11:101961859
|
C | A | 5 | a0002a0007a0008others(2): Show | 45 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(42): Show |
missense_variant | MODERATE | c.824C>A | p.Ser275Tyr | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/11 | 1099/7048 | 824/3354 | 275/1117 | chr11 | 101961859 | ||
chr11:101961877
|
T | C | 5 | a0002a0007a0008others(2): Show | 45 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(42): Show |
missense_variant | MODERATE | c.842T>C | p.Ile281Thr | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/11 | 1117/7048 | 842/3354 | 281/1117 | chr11 | 101961877 | ||
chr11:101961939
|
G | A | 5 | a0002a0007a0008others(2): Show | 45 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(42): Show |
missense_variant | MODERATE | c.904G>A | p.Ala302Thr | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/11 | 1179/7048 | 904/3354 | 302/1117 | chr11 | 101961939 | ||
chr11:101962149
|
T | C | 1 | a0004 | 7 | HG02257.hp1 HG02258.hp2 HG02622.hp1 others(4): Show |
missense_variant | MODERATE | c.1114T>C | p.Ser372Pro | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/11 | 1389/7048 | 1114/3354 | 372/1117 | chr11 | 101962149 | ||
chr11:101962849
|
A | G | 1 | a0013 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.1814A>G | p.Lys605Arg | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/11 | 2089/7048 | 1814/3354 | 605/1117 | chr11 | 101962849 | ||
chr11:101963037
|
G | A | 1 | a0007 | 2 | HG03490.hp2 NA19077.hp1 |
missense_variant | MODERATE | c.2002G>A | p.Gly668Ser | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/11 | 2277/7048 | 2002/3354 | 668/1117 | chr11 | 101963037 | ||
chr11:101963163
|
C | T | 1 | a0005 | 7 | HG01346.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
missense_variant | MODERATE | c.2128C>T | p.Pro710Ser | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/11 | 2403/7048 | 2128/3354 | 710/1117 | chr11 | 101963163 | ||
chr11:101963244
|
C | A | 1 | a0012 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.2209C>A | p.Pro737Thr | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/11 | 2484/7048 | 2209/3354 | 737/1117 | chr11 | 101963244 | ||
chr11:101963734
|
G | A | 1 | a0009 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.2699G>A | p.Arg900Gln | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/11 | 2974/7048 | 2699/3354 | 900/1117 | chr11 | 101963734 | ||
chr11:101963769
|
C | A | 1 | a0011 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.2734C>A | p.Pro912Thr | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/11 | 3009/7048 | 2734/3354 | 912/1117 | chr11 | 101963769 | ||
chr11:101978359
|
T | C | 1 | a0014 | 1 | NA18970.hp1 | missense_variant | MODERATE | c.2858T>C | p.Met953Thr | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/11 | 3133/7048 | 2858/3354 | 953/1117 | chr11 | 101978359 | ||
chr11:101986859
|
T | C | 2 | a0006a0012 | 3 | HG03486.hp2 HG03540.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.3062T>C | p.Met1021Thr | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/11 | 3337/7048 | 3062/3354 | 1021/1117 | chr11 | 101986859 | ||
chr11:101987027
|
G | A | 14 | a0001a0002a0003others(11): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
missense_variant | MODERATE | c.3230G>A | p.Ser1077Asn | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/11 | 3505/7048 | 3230/3354 | 1077/1117 | chr11 | 101987027 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:101958339
|
C | T | 1 | a0001c0009 | 2 | HG03098.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.678C>T | p.Leu226Leu | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/11 | 953/7048 | 678/3354 | 226/1117 | chr11 | 101958339 | ||
chr11:101961977
|
A | T | 1 | a0001c0002 | 48 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(45): Show |
synonymous_variant | LOW | c.942A>T | p.Thr314Thr | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/11 | 1217/7048 | 942/3354 | 314/1117 | chr11 | 101961977 | ||
chr11:101962577
|
G | A | 1 | a0001c0013 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.1542G>A | p.Glu514Glu | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/11 | 1817/7048 | 1542/3354 | 514/1117 | chr11 | 101962577 | ||
chr11:101962913
|
C | T | 17 | a0001c0001a0001c0002a0001c0009others(14): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
synonymous_variant | LOW | c.1878C>T | p.Thr626Thr | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/11 | 2153/7048 | 1878/3354 | 626/1117 | chr11 | 101962913 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:101915016
|
T | C | 6 | a0001c0001t0008a0001c0001t0012a0001c0001t0015others(3): Show | 13 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-269T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/11 | 269 | chr11 | 101915016 | |||||
chr11:101915056
|
C | G | 1 | a0001c0001t0033 | 2 | HG00323.hp1 HG02698.hp1 |
5_prime_UTR_variant | MODIFIER | c.-229C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/11 | 229 | chr11 | 101915056 | |||||
chr11:101915069
|
G | T | 4 | a0001c0001t0031a0001c0001t0032a0001c0001t0063others(1): Show | 6 | HG02055.hp2 HG02886.hp2 HG03098.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-216G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/11 | 216 | chr11 | 101915069 | |||||
chr11:101915106
|
G | A | 8 | a0001c0001t0036a0001c0001t0037a0001c0001t0039others(5): Show | 15 | HG01109.hp1 HG02080.hp1 HG02109.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-179G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/11 | 179 | chr11 | 101915106 | |||||
chr11:101915283
|
G | A | 2 | a0001c0001t0017a0001c0001t0018 | 4 | HG00621.hp2 HG01175.hp1 HG01361.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-2G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/11 | 2 | chr11 | 101915283 | |||||
chr11:101997684
|
C | T | 52 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(49): Show | 207 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*41C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 41 | chr11 | 101997684 | |||||
chr11:101997888
|
T | C | 1 | a0001c0001t0041 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*245T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 245 | chr11 | 101997888 | |||||
chr11:101997922
|
G | A | 1 | a0014c0012t0051 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*279G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 279 | chr11 | 101997922 | |||||
chr11:101998001
|
AT | A | 5 | a0003c0004t0010a0003c0004t0021a0003c0004t0038others(2): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*359delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 359 | chr11 | 101998001 | |||||
chr11:101998089
|
AT | A | 48 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(45): Show | 201 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*453delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 453 | INFO_REALIGN_3_PRIME | chr11 | 101998089 | ||||
chr11:101998364
|
G | A | 1 | a0001c0001t0034 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*721G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 721 | chr11 | 101998364 | |||||
chr11:101998382
|
C | T | 1 | a0006c0008t0030 | 2 | HG03486.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*739C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 739 | chr11 | 101998382 | |||||
chr11:101998395
|
G | T | 1 | a0001c0001t0061 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*752G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 752 | chr11 | 101998395 | |||||
chr11:101998592
|
C | CAA | 3 | a0001c0001t0008a0001c0001t0015a0013c0018t0015 | 8 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*966_*967dupAA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 968 | INFO_REALIGN_3_PRIME | chr11 | 101998592 | ||||
chr11:101998592
|
C | CAAAAAAA others(1): Show |
7 | a0002c0003t0003a0005c0006t0013a0005c0006t0016others(4): Show | 38 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*960_*967dupAAAAAA others(2): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 968 | INFO_REALIGN_3_PRIME | chr11 | 101998592 | ||||
chr11:101998592
|
C | CAAAAAAA others(2): Show |
5 | a0001c0001t0012a0002c0003t0007a0002c0003t0029others(2): Show | 15 | HG02074.hp1 HG02451.hp2 HG02970.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*959_*967dupAAAAAA others(3): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 968 | INFO_REALIGN_3_PRIME | chr11 | 101998592 | ||||
chr11:101998592
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0011a0001c0001t0020a0001c0001t0062others(2): Show | 9 | HG02683.hp2 HG02818.hp2 HG03225.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*958_*967dupAAAAAA others(4): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 968 | INFO_REALIGN_3_PRIME | chr11 | 101998592 | ||||
chr11:101998592
|
C | CAAAAAAA others(4): Show |
33 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(30): Show | 172 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*957_*967dupAAAAAA others(5): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 968 | INFO_REALIGN_3_PRIME | chr11 | 101998592 | ||||
chr11:101998592
|
C | CAAAAAAA others(5): Show |
12 | a0001c0001t0004a0001c0001t0005a0001c0001t0017others(9): Show | 59 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*956_*967dupAAAAAA others(6): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 968 | INFO_REALIGN_3_PRIME | chr11 | 101998592 | ||||
chr11:101998592
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0022a0001c0001t0036a0001c0001t0054 | 4 | HG03209.hp1 HG03486.hp1 NA18991.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*955_*967dupAAAAAA others(7): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 968 | INFO_REALIGN_3_PRIME | chr11 | 101998592 | ||||
chr11:101998597
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0060 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*965_*966insTAAAAA others(6): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 966 | INFO_REALIGN_3_PRIME | chr11 | 101998597 | ||||
chr11:101998650
|
CAT | C | 3 | a0001c0001t0008a0001c0001t0015a0013c0018t0015 | 8 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1008_*1009delAT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 1008 | chr11 | 101998650 | |||||
chr11:101999034
|
A | G | 1 | a0001c0002t0046 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1391A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 1391 | chr11 | 101999034 | |||||
chr11:101999143
|
A | G | 1 | a0001c0001t0043 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1500A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 1500 | chr11 | 101999143 | |||||
chr11:101999219
|
TTCAATGG others(16): Show |
T | 1 | a0001c0002t0044 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1577_*1599delTCAA others(19): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 1577 | chr11 | 101999219 | |||||
chr11:101999223
|
A | G | 1 | a0001c0001t0057 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1580A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 1580 | chr11 | 101999223 | |||||
chr11:101999340
|
C | G | 2 | a0001c0001t0031a0001c0001t0032 | 4 | HG02055.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1697C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 1697 | chr11 | 101999340 | |||||
chr11:101999449
|
G | A | 1 | a0001c0001t0024 | 2 | NA19058.hp1 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1806G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 1806 | chr11 | 101999449 | |||||
chr11:101999488
|
C | CA | 12 | a0001c0001t0036a0001c0001t0037a0001c0001t0062others(9): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1864dupA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 1865 | INFO_REALIGN_3_PRIME | chr11 | 101999488 | ||||
chr11:101999488
|
C | CAA | 3 | a0001c0001t0012a0001c0009t0064a0002c0003t0029 | 6 | HG02074.hp1 HG02451.hp2 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1863_*1864dupAA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 1865 | INFO_REALIGN_3_PRIME | chr11 | 101999488 | ||||
chr11:101999488
|
CA | C | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(40): Show | 247 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*1864delA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 1864 | INFO_REALIGN_3_PRIME | chr11 | 101999488 | ||||
chr11:101999488
|
CAA | C | 7 | a0001c0001t0028a0001c0001t0045a0003c0004t0010others(4): Show | 15 | HG01109.hp1 HG01516.hp2 HG02109.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1863_*1864delAA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 1863 | INFO_REALIGN_3_PRIME | chr11 | 101999488 | ||||
chr11:101999727
|
A | G | 52 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(49): Show | 205 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(202): Show |
3_prime_UTR_variant | MODIFIER | c.*2084A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2084 | chr11 | 101999727 | |||||
chr11:101999734
|
G | C | 1 | a0012c0015t0035 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2091G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2091 | chr11 | 101999734 | |||||
chr11:101999747
|
G | A | 1 | a0001c0001t0026 | 2 | HG02129.hp1 NA18612.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2104G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2104 | chr11 | 101999747 | |||||
chr11:101999769
|
A | G | 14 | a0001c0001t0012a0002c0003t0003a0002c0003t0007others(11): Show | 55 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2126A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2126 | chr11 | 101999769 | |||||
chr11:101999834
|
C | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2191C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2191 | chr11 | 101999834 | |||||
chr11:101999836
|
A | C | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2193A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2193 | chr11 | 101999836 | |||||
chr11:101999837
|
G | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2194G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2194 | chr11 | 101999837 | |||||
chr11:101999839
|
A | C | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2196A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2196 | chr11 | 101999839 | |||||
chr11:101999840
|
G | C | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2197G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2197 | chr11 | 101999840 | |||||
chr11:101999843
|
T | G | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2200T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2200 | chr11 | 101999843 | |||||
chr11:101999845
|
A | C | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2202A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2202 | chr11 | 101999845 | |||||
chr11:101999846
|
G | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2203G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2203 | chr11 | 101999846 | |||||
chr11:101999847
|
A | C | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2204A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2204 | chr11 | 101999847 | |||||
chr11:101999849
|
C | A | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2206C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2206 | chr11 | 101999849 | |||||
chr11:101999852
|
C | G | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2209C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2209 | chr11 | 101999852 | |||||
chr11:101999855
|
G | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2212G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2212 | chr11 | 101999855 | |||||
chr11:101999868
|
A | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2225A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2225 | chr11 | 101999868 | |||||
chr11:101999871
|
C | G | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2228C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2228 | chr11 | 101999871 | |||||
chr11:101999881
|
A | G | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2238A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2238 | chr11 | 101999881 | |||||
chr11:101999884
|
T | G | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2241T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2241 | chr11 | 101999884 | |||||
chr11:101999885
|
A | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2242A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2242 | chr11 | 101999885 | |||||
chr11:101999886
|
A | C | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2243A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2243 | chr11 | 101999886 | |||||
chr11:101999887
|
A | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2244A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2244 | chr11 | 101999887 | |||||
chr11:101999888
|
A | G | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2245A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2245 | chr11 | 101999888 | |||||
chr11:101999889
|
T | G | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2246T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2246 | chr11 | 101999889 | |||||
chr11:101999890
|
A | C | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2247A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2247 | chr11 | 101999890 | |||||
chr11:101999891
|
T | C | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2248T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2248 | chr11 | 101999891 | |||||
chr11:101999901
|
G | A | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2258G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2258 | chr11 | 101999901 | |||||
chr11:101999907
|
G | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2264G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2264 | chr11 | 101999907 | |||||
chr11:101999923
|
C | G | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2280C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2280 | chr11 | 101999923 | |||||
chr11:101999928
|
A | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2285A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2285 | chr11 | 101999928 | |||||
chr11:101999933
|
A | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2290A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2290 | chr11 | 101999933 | |||||
chr11:101999934
|
G | C | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2291G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2291 | chr11 | 101999934 | |||||
chr11:101999941
|
G | A | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2298G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2298 | chr11 | 101999941 | |||||
chr11:101999942
|
G | A | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2299G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2299 | chr11 | 101999942 | |||||
chr11:101999943
|
G | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2300G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2300 | chr11 | 101999943 | |||||
chr11:101999944
|
A | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2301A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2301 | chr11 | 101999944 | |||||
chr11:101999945
|
G | C | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2302G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2302 | chr11 | 101999945 | |||||
chr11:101999946
|
G | A | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2303G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2303 | chr11 | 101999946 | |||||
chr11:101999948
|
C | A | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2305C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2305 | chr11 | 101999948 | |||||
chr11:101999965
|
G | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2322G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2322 | chr11 | 101999965 | |||||
chr11:101999967
|
G | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2324G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2324 | chr11 | 101999967 | |||||
chr11:101999975
|
G | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2332G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2332 | chr11 | 101999975 | |||||
chr11:101999988
|
C | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2345C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2345 | chr11 | 101999988 | |||||
chr11:101999990
|
G | A | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2347G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2347 | chr11 | 101999990 | |||||
chr11:101999991
|
G | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2348G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2348 | chr11 | 101999991 | |||||
chr11:101999993
|
C | A | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2350C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2350 | chr11 | 101999993 | |||||
chr11:101999994
|
A | C | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2351A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2351 | chr11 | 101999994 | |||||
chr11:101999995
|
A | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2352A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2352 | chr11 | 101999995 | |||||
chr11:101999997
|
A | T | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2354A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2354 | chr11 | 101999997 | |||||
chr11:101999999
|
G | A | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2356G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2356 | chr11 | 101999999 | |||||
chr11:102000000
|
G | A | 1 | a0001c0001t0056 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2357G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2357 | chr11 | 102000000 | |||||
chr11:102000050
|
C | T | 10 | a0001c0001t0012a0002c0003t0003a0002c0003t0007others(7): Show | 48 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2407C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2407 | chr11 | 102000050 | |||||
chr11:102000125
|
G | A | 9 | a0002c0003t0003a0002c0003t0007a0002c0003t0029others(6): Show | 45 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2482G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2482 | chr11 | 102000125 | |||||
chr11:102000141
|
T | C | 1 | a0003c0004t0038 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2498T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2498 | chr11 | 102000141 | |||||
chr11:102000142
|
G | T | 1 | a0003c0004t0038 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2499G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2499 | chr11 | 102000142 | |||||
chr11:102000155
|
A | G | 14 | a0001c0001t0012a0002c0003t0003a0002c0003t0007others(11): Show | 55 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2512A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2512 | chr11 | 102000155 | |||||
chr11:102000224
|
G | A | 50 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(47): Show | 203 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*2581G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2581 | chr11 | 102000224 | |||||
chr11:102000449
|
G | A | 14 | a0001c0001t0012a0002c0003t0003a0002c0003t0007others(11): Show | 55 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2806G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2806 | chr11 | 102000449 | |||||
chr11:102000552
|
C | T | 2 | a0001c0001t0062a0001c0009t0064 | 2 | HG03098.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2909C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 2909 | chr11 | 102000552 | |||||
chr11:102000644
|
A | G | 1 | a0001c0001t0027 | 2 | NA19004.hp2 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3001A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 3001 | chr11 | 102000644 | |||||
chr11:102000696
|
G | GA | 4 | a0001c0001t0049a0001c0002t0014a0001c0002t0047others(1): Show | 6 | HG01978.hp2 HG02165.hp2 NA18954.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3065dupA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 3066 | INFO_REALIGN_3_PRIME | chr11 | 102000696 | ||||
chr11:102000696
|
GA | G | 3 | a0001c0001t0009a0005c0006t0016a0005c0006t0040 | 9 | HG01257.hp1 HG01258.hp1 HG02109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3065delA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 3065 | INFO_REALIGN_3_PRIME | chr11 | 102000696 | ||||
chr11:102000707
|
A | G | 5 | a0003c0004t0010a0003c0004t0021a0003c0004t0038others(2): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3064A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 3064 | chr11 | 102000707 | |||||
chr11:102000828
|
T | A | 1 | a0001c0001t0049 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3185T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 3185 | chr11 | 102000828 | |||||
chr11:102000959
|
C | A | 1 | a0001c0001t0034 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3316C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 11/11 | 3316 | chr11 | 102000959 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:101915484
|
C | T | 1 | a0001c0002t0001g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.128+72C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101915484 | ||||||
chr11:101915755
|
C | T | 3 | a0004c0005t0005g0323a0004c0005t0005g0324a0004c0005t0005g0325 | 3 | HG02257.hp1 HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.128+343C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101915755 | ||||||
chr11:101915984
|
A | T | 22 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(19): Show | 23 | HG01109.hp1 HG02080.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.128+572A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101915984 | ||||||
chr11:101916294
|
G | A | 1 | a0001c0009t0064g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.128+882G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101916294 | ||||||
chr11:101916381
|
A | G | 161 | a0001c0001t0002g0151a0001c0001t0002g0153a0001c0001t0002g0180others(158): Show | 164 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.128+969A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101916381 | ||||||
chr11:101916498
|
A | G | 1 | a0003c0004t0010g0322 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.128+1086A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101916498 | ||||||
chr11:101916796
|
A | T | 5 | a0001c0001t0009g0008a0001c0001t0009g0298a0001c0001t0009g0299others(2): Show | 6 | HG01257.hp1 HG01258.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.128+1384A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101916796 | ||||||
chr11:101916857
|
A | C | 5 | a0002c0003t0003g0143a0002c0003t0003g0144a0002c0003t0003g0145others(2): Show | 5 | HG00741.hp2 HG01069.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.128+1445A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101916857 | ||||||
chr11:101916970
|
G | C | 2 | a0001c0001t0036g0303a0001c0001t0037g0302 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.128+1558G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101916970 | ||||||
chr11:101917028
|
A | ATG | 8 | a0001c0001t0002g0288a0001c0001t0002g0289a0001c0001t0002g0291others(5): Show | 8 | HG01516.hp2 HG01517.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.128+1663_128+1664d others(4): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101917028 | |||||
chr11:101917028
|
A | ATGTG | 5 | a0001c0001t0002g0294a0001c0001t0002g0295a0001c0001t0004g0296others(2): Show | 5 | HG01192.hp1 HG02109.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.128+1661_128+1664d others(6): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101917028 | |||||
chr11:101917028
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0004g0297 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.128+1655_128+1664d others(12): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101917028 | |||||
chr11:101917028
|
ATG | A | 31 | a0001c0001t0002g0117a0001c0001t0002g0266a0001c0001t0002g0268others(28): Show | 32 | HG00280.hp1 HG00639.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.128+1663_128+1664d others(4): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101917028 | |||||
chr11:101917028
|
ATGTG | A | 102 | a0001c0001t0001g0005a0001c0001t0001g0081a0001c0001t0001g0082others(99): Show | 105 | HG00408.hp1 HG00597.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.128+1661_128+1664d others(6): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101917028 | |||||
chr11:101917028
|
ATGTGTG | A | 70 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(67): Show | 70 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.128+1659_128+1664d others(8): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101917028 | |||||
chr11:101917028
|
ATGTGTGT others(1): Show |
A | 62 | a0001c0001t0001g0046a0001c0001t0001g0055a0001c0001t0001g0056others(59): Show | 62 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.128+1657_128+1664d others(10): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101917028 | |||||
chr11:101917028
|
ATGTGTGT others(3): Show |
A | 8 | a0001c0001t0049g0038a0001c0002t0001g0149a0002c0003t0003g0039others(5): Show | 9 | HG01978.hp2 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.128+1655_128+1664d others(12): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101917028 | |||||
chr11:101917028
|
ATGTGTGT others(5): Show |
A | 3 | a0001c0001t0001g0037a0001c0002t0001g0148a0001c0009t0055g0304 | 3 | HG02602.hp1 HG03471.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.128+1653_128+1664d others(14): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101917028 | |||||
chr11:101917028
|
ATGTGTGT others(7): Show |
A | 2 | a0001c0001t0036g0303a0001c0001t0037g0302 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.128+1651_128+1664d others(16): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101917028 | |||||
chr11:101917028
|
ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0008g0036 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.128+1649_128+1664d others(18): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101917028 | |||||
chr11:101917028
|
ATGTGTGT others(11): Show |
A | 7 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(4): Show | 8 | HG00323.hp2 HG00642.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.128+1647_128+1664d others(20): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101917028 | |||||
chr11:101917029
|
TGTG | T | 4 | a0001c0001t0031g0139a0001c0001t0031g0141a0001c0001t0032g0140others(1): Show | 4 | HG02055.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.128+1618_128+1620d others(5): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101917029 | ||||||
chr11:101917063
|
T | C | 21 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(18): Show | 21 | HG00423.hp1 HG00673.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.128+1651T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101917063 | ||||||
chr11:101917124
|
G | T | 1 | a0001c0001t0042g0080 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.128+1712G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101917124 | ||||||
chr11:101917125
|
T | G | 1 | a0001c0001t0042g0080 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.128+1713T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101917125 | ||||||
chr11:101917218
|
T | A | 9 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(6): Show | 10 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.128+1806T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101917218 | ||||||
chr11:101917313
|
T | G | 2 | a0001c0001t0011g0129a0001c0001t0011g0130 | 2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.128+1901T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101917313 | ||||||
chr11:101917400
|
A | C | 19 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(16): Show | 20 | HG01109.hp1 HG02080.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.128+1988A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101917400 | ||||||
chr11:101917401
|
C | A | 19 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(16): Show | 20 | HG01109.hp1 HG02080.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.128+1989C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101917401 | ||||||
chr11:101917501
|
T | C | 1 | a0001c0002t0001g0150 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.128+2089T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101917501 | ||||||
chr11:101917514
|
C | G | 1 | a0001c0001t0009g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.128+2102C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101917514 | ||||||
chr11:101917603
|
TA | T | 122 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0110others(119): Show | 123 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.128+2207delA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101917603 | |||||
chr11:101917624
|
G | C | 1 | a0001c0001t0015g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.128+2212G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101917624 | ||||||
chr11:101917694
|
T | C | 57 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(54): Show | 57 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.128+2282T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101917694 | ||||||
chr11:101917817
|
A | G | 2 | a0006c0008t0030g0040a0006c0008t0030g0041 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.128+2405A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101917817 | ||||||
chr11:101918050
|
A | G | 1 | a0001c0001t0002g0153 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.128+2638A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101918050 | ||||||
chr11:101918306
|
T | C | 3 | a0001c0001t0036g0303a0001c0001t0037g0302a0001c0009t0055g0304 | 3 | HG02451.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.128+2894T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101918306 | ||||||
chr11:101918391
|
T | G | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.128+2979T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101918391 | ||||||
chr11:101918597
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.128+3185C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101918597 | ||||||
chr11:101918644
|
T | C | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.128+3232T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101918644 | ||||||
chr11:101918762
|
G | T | 1 | a0001c0001t0002g0138 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.128+3350G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101918762 | ||||||
chr11:101918783
|
T | C | 4 | a0001c0001t0002g0266a0001c0001t0002g0294a0001c0001t0004g0267others(1): Show | 4 | HG01123.hp2 HG02280.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.128+3371T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101918783 | ||||||
chr11:101918962
|
A | G | 62 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(59): Show | 63 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.128+3550A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101918962 | ||||||
chr11:101918994
|
T | G | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.128+3582T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101918994 | ||||||
chr11:101919064
|
G | A | 3 | a0005c0006t0016g0316a0005c0006t0016g0318a0005c0006t0040g0317 | 3 | HG02895.hp1 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.129-3577G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101919064 | ||||||
chr11:101919101
|
A | G | 8 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(5): Show | 9 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.129-3540A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101919101 | ||||||
chr11:101919166
|
A | G | 1 | a0001c0009t0064g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.129-3475A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101919166 | ||||||
chr11:101919386
|
G | A | 3 | a0005c0006t0016g0316a0005c0006t0016g0318a0005c0006t0040g0317 | 3 | HG02895.hp1 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.129-3255G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101919386 | ||||||
chr11:101919498
|
TG | T | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.129-3142delG | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101919498 | ||||||
chr11:101919695
|
T | C | 6 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(3): Show | 6 | HG02109.hp1 HG02723.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-2946T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101919695 | ||||||
chr11:101919697
|
A | C | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.129-2944A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101919697 | ||||||
chr11:101919719
|
A | G | 1 | a0001c0001t0011g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.129-2922A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101919719 | ||||||
chr11:101919883
|
A | G | 1 | a0001c0002t0001g0201 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.129-2758A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101919883 | ||||||
chr11:101919940
|
T | C | 204 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(201): Show | 209 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.129-2701T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101919940 | ||||||
chr11:101920125
|
A | T | 2 | a0003c0004t0010g0009a0003c0004t0010g0308 | 3 | HG02257.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.129-2516A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101920125 | ||||||
chr11:101920207
|
A | G | 1 | a0002c0003t0003g0078 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.129-2434A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101920207 | ||||||
chr11:101920310
|
G | C | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.129-2331G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101920310 | ||||||
chr11:101920387
|
A | G | 1 | a0001c0001t0002g0255 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.129-2254A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101920387 | ||||||
chr11:101920426
|
A | C | 1 | a0001c0001t0006g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.129-2215A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101920426 | ||||||
chr11:101920496
|
TA | T | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.129-2139delA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101920496 | |||||
chr11:101920515
|
T | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084 | 3 | HG02523.hp2 NA18975.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.129-2126T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101920515 | ||||||
chr11:101920517
|
C | T | 6 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(3): Show | 6 | HG02109.hp1 HG02723.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-2124C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101920517 | ||||||
chr11:101920605
|
C | CT | 7 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0008g0036others(4): Show | 7 | HG01243.hp2 HG03471.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.129-2020dupT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101920605 | |||||
chr11:101920605
|
CT | C | 17 | a0001c0001t0001g0085a0001c0001t0001g0088a0001c0001t0002g0051others(14): Show | 18 | HG01109.hp1 HG02055.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.129-2020delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101920605 | |||||
chr11:101920658
|
T | C | 1 | a0002c0003t0003g0067 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.129-1983T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101920658 | ||||||
chr11:101920701
|
G | A | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.129-1940G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101920701 | ||||||
chr11:101920722
|
C | A | 1 | a0001c0009t0055g0304 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.129-1919C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101920722 | ||||||
chr11:101920745
|
G | A | 62 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(59): Show | 63 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.129-1896G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101920745 | ||||||
chr11:101920765
|
C | G | 1 | a0002c0003t0003g0028 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.129-1876C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101920765 | ||||||
chr11:101921012
|
G | A | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.129-1629G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101921012 | ||||||
chr11:101921425
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.129-1216G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101921425 | ||||||
chr11:101921434
|
C | T | 2 | a0006c0008t0030g0040a0006c0008t0030g0041 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.129-1207C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101921434 | ||||||
chr11:101921578
|
A | G | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.129-1063A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101921578 | ||||||
chr11:101921706
|
C | CA | 68 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0089others(65): Show | 68 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.129-916dupA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101921706 | |||||
chr11:101921706
|
CA | C | 6 | a0001c0001t0001g0088a0001c0001t0002g0252a0001c0002t0001g0177others(3): Show | 6 | HG00642.hp1 HG02897.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.129-916delA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101921706 | |||||
chr11:101921751
|
T | A | 1 | a0001c0001t0037g0302 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.129-890T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101921751 | ||||||
chr11:101921753
|
C | T | 330 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0046others(327): Show | 336 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.129-888C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101921753 | ||||||
chr11:101921755
|
CT | C | 330 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0046others(327): Show | 336 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.129-883delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101921755 | |||||
chr11:101921763
|
GA | G | 330 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0046others(327): Show | 336 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.129-876delA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101921763 | |||||
chr11:101921777
|
C | CT | 78 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(75): Show | 78 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.129-839dupT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101921777 | |||||
chr11:101921777
|
C | CTT | 11 | a0001c0001t0001g0089a0001c0001t0001g0107a0001c0001t0001g0108others(8): Show | 11 | HG02055.hp2 HG02132.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.129-840_129-839dup others(2): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101921777 | |||||
chr11:101921777
|
CT | C | 8 | a0001c0001t0002g0181a0001c0001t0012g0309a0001c0001t0012g0310others(5): Show | 8 | HG02451.hp1 HG02451.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-839delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101921777 | |||||
chr11:101921777
|
CTTTTTTT others(7): Show |
C | 2 | a0002c0003t0003g0078a0015c0011t0007g0068 | 2 | NA18984.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.129-852_129-839del others(14): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101921777 | |||||
chr11:101921777
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0002t0001g0158 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.129-853_129-839del others(15): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101921777 | |||||
chr11:101921788
|
T | C | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.129-853T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101921788 | ||||||
chr11:101921819
|
T | C | 199 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(196): Show | 204 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.129-822T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101921819 | ||||||
chr11:101921942
|
C | T | 1 | a0001c0001t0004g0283 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.129-699C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101921942 | ||||||
chr11:101921943
|
G | A | 2 | a0001c0001t0002g0268a0001c0001t0002g0284 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.129-698G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101921943 | ||||||
chr11:101921947
|
G | A | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.129-694G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101921947 | ||||||
chr11:101922008
|
C | T | 1 | a0001c0001t0002g0079 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.129-633C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101922008 | ||||||
chr11:101922013
|
G | A | 9 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(6): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.129-628G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101922013 | ||||||
chr11:101922109
|
AT | A | 61 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(58): Show | 62 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.129-524delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101922109 | |||||
chr11:101922145
|
T | G | 62 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(59): Show | 63 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.129-496T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101922145 | ||||||
chr11:101922164
|
A | AT | 128 | a0001c0001t0001g0089a0001c0001t0001g0134a0001c0001t0002g0051others(125): Show | 131 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.129-460dupT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 101922164 | |||||
chr11:101922322
|
G | A | 3 | a0001c0001t0036g0303a0001c0001t0037g0302a0001c0009t0055g0304 | 3 | HG02451.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.129-319G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101922322 | ||||||
chr11:101922353
|
C | T | 2 | a0006c0008t0030g0040a0006c0008t0030g0041 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.129-288C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101922353 | ||||||
chr11:101922378
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.129-263G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101922378 | ||||||
chr11:101922418
|
C | T | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.129-223C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101922418 | ||||||
chr11:101922543
|
C | T | 2 | a0002c0003t0003g0126a0002c0003t0007g0074 | 2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.129-98C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 1/10 | chr11 | 101922543 | ||||||
chr11:101923114
|
G | A | 2 | a0001c0001t0011g0129a0001c0001t0011g0130 | 2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.248+354G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101923114 | ||||||
chr11:101923136
|
G | T | 1 | a0001c0002t0005g0171 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.248+376G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101923136 | ||||||
chr11:101923185
|
C | T | 1 | a0001c0001t0005g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.248+425C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101923185 | ||||||
chr11:101923636
|
T | C | 1 | a0002c0003t0003g0069 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.248+876T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101923636 | ||||||
chr11:101923716
|
G | A | 1 | a0013c0018t0015g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.248+956G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101923716 | ||||||
chr11:101923719
|
G | A | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.248+959G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101923719 | ||||||
chr11:101923942
|
T | C | 2 | a0001c0001t0004g0274a0001c0001t0004g0296 | 2 | HG04184.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.248+1182T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101923942 | ||||||
chr11:101924268
|
A | T | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.248+1508A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101924268 | ||||||
chr11:101924438
|
C | CTG | 125 | a0001c0001t0001g0046a0001c0001t0001g0056a0001c0001t0001g0057others(122): Show | 128 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.248+1697_248+1698d others(4): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101924438 | |||||
chr11:101924547
|
C | A | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0005c0006t0058g0132others(2): Show | 5 | HG01346.hp1 HG02818.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.248+1787C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101924547 | ||||||
chr11:101924552
|
G | A | 1 | a0001c0001t0006g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.248+1792G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101924552 | ||||||
chr11:101924574
|
C | T | 207 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0051others(204): Show | 212 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.248+1814C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101924574 | ||||||
chr11:101924589
|
C | T | 1 | a0001c0002t0046g0170 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.248+1829C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101924589 | ||||||
chr11:101924612
|
C | T | 47 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0148others(44): Show | 47 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.248+1852C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101924612 | ||||||
chr11:101924657
|
A | G | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.248+1897A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101924657 | ||||||
chr11:101924749
|
GT | G | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.248+1993delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101924749 | |||||
chr11:101924753
|
T | G | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.248+1993T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101924753 | ||||||
chr11:101924757
|
T | G | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.248+1997T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101924757 | ||||||
chr11:101924833
|
T | C | 4 | a0001c0002t0001g0150a0001c0002t0001g0158a0001c0002t0001g0159others(1): Show | 4 | HG01361.hp2 HG01496.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.248+2073T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101924833 | ||||||
chr11:101925067
|
C | T | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.248+2307C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101925067 | ||||||
chr11:101925242
|
T | C | 32 | a0001c0001t0002g0153a0001c0001t0002g0217a0001c0001t0002g0266others(29): Show | 34 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.248+2482T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101925242 | ||||||
chr11:101925346
|
T | C | 7 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(4): Show | 8 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.248+2586T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101925346 | ||||||
chr11:101925474
|
T | C | 1 | a0001c0002t0001g0192 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.248+2714T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101925474 | ||||||
chr11:101925477
|
C | T | 1 | a0001c0002t0001g0200 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.248+2717C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101925477 | ||||||
chr11:101925638
|
G | A | 2 | a0001c0001t0008g0003a0001c0001t0008g0036 | 3 | HG01243.hp2 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.248+2878G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101925638 | ||||||
chr11:101925704
|
G | GGTGCAGT others(828): Show |
1 | a0001c0001t0024g0190 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(837): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(822): Show |
1 | a0001c0001t0024g0257 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(831): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(798): Show |
1 | a0001c0001t0012g0309 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(807): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(801): Show |
1 | a0001c0001t0012g0310 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(810): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(802): Show |
1 | a0001c0001t0012g0311 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(811): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(813): Show |
1 | a0003c0004t0010g0308 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(822): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(813): Show |
1 | a0003c0004t0010g0307 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(822): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(809): Show |
1 | a0003c0004t0010g0322 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(818): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(802): Show |
1 | a0003c0004t0021g0315 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(811): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(809): Show |
1 | a0005c0006t0013g0305 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(818): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(811): Show |
1 | a0005c0006t0013g0306 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(820): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(802): Show |
3 | a0003c0004t0021g0321a0003c0004t0052g0319a0003c0004t0053g0320 | 3 | HG02615.hp2 HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(811): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(810): Show |
1 | a0005c0006t0013g0312 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(819): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(797): Show |
1 | a0003c0004t0010g0009 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(806): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(802): Show |
1 | a0005c0006t0016g0318 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(811): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(803): Show |
2 | a0005c0006t0016g0316a0005c0006t0040g0317 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(812): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(793): Show |
1 | a0001c0001t0001g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(802): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(824): Show |
1 | a0001c0001t0002g0218 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(833): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(817): Show |
1 | a0001c0001t0004g0253 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(826): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(818): Show |
6 | a0001c0001t0002g0207a0001c0001t0002g0219a0001c0001t0002g0220others(3): Show | 6 | NA18950.hp1 NA18955.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.248+2952_248+2953i others(827): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(819): Show |
1 | a0001c0001t0060g0222 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(828): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(827): Show |
1 | a0001c0001t0031g0141 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(836): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(825): Show |
1 | a0001c0001t0008g0003 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(834): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(830): Show |
1 | a0001c0001t0034g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(839): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(821): Show |
1 | a0001c0009t0064g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(830): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(827): Show |
1 | a0013c0018t0015g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(836): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(821): Show |
1 | a0001c0001t0015g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(830): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(823): Show |
1 | a0001c0001t0008g0036 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(832): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(817): Show |
1 | a0001c0001t0032g0142 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(826): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(813): Show |
1 | a0001c0001t0031g0139 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(822): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(816): Show |
1 | a0001c0001t0032g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(825): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(819): Show |
1 | a0012c0015t0035g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(828): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(804): Show |
1 | a0001c0001t0001g0108 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(813): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(801): Show |
1 | a0001c0002t0001g0154 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(810): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(803): Show |
1 | a0001c0001t0001g0081 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(812): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(797): Show |
1 | a0001c0002t0005g0171 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(806): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(798): Show |
3 | a0001c0002t0001g0172a0001c0002t0001g0193a0001c0002t0001g0194 | 3 | HG00280.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(807): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(799): Show |
2 | a0001c0002t0001g0192a0001c0002t0048g0263 | 2 | HG02602.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(808): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(807): Show |
1 | a0001c0001t0008g0030 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(816): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(796): Show |
3 | a0001c0001t0006g0127a0001c0002t0001g0200a0001c0002t0046g0170 | 3 | HG01099.hp1 HG02040.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(805): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(797): Show |
37 | a0001c0001t0001g0037a0001c0001t0001g0055a0001c0001t0001g0092others(34): Show | 37 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.248+2952_248+2953i others(806): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(798): Show |
6 | a0001c0001t0006g0061a0001c0001t0006g0093a0001c0002t0001g0150others(3): Show | 6 | HG01361.hp2 HG01496.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.248+2952_248+2953i others(807): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(799): Show |
1 | a0001c0001t0006g0044 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(808): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(805): Show |
2 | a0001c0001t0008g0031a0001c0001t0008g0034 | 2 | HG00323.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(814): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(794): Show |
1 | a0004c0005t0005g0111 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(803): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(795): Show |
4 | a0001c0001t0001g0133a0001c0001t0006g0114a0004c0005t0005g0115others(1): Show | 4 | HG01106.hp2 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.248+2952_248+2953i others(804): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(796): Show |
20 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0058others(17): Show | 20 | HG00280.hp1 HG00597.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.248+2952_248+2953i others(805): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(797): Show |
29 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0063others(26): Show | 30 | HG01081.hp2 HG01123.hp1 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.248+2952_248+2953i others(806): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(798): Show |
4 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0042g0080others(1): Show | 4 | HG03669.hp2 NA18991.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.248+2952_248+2953i others(807): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(799): Show |
1 | a0001c0001t0005g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(808): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(795): Show |
1 | a0001c0001t0006g0104 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(804): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(796): Show |
1 | a0004c0005t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(805): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(797): Show |
2 | a0001c0001t0005g0105a0001c0001t0050g0066 | 2 | HG01981.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(806): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(817): Show |
1 | a0001c0001t0009g0301 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(826): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(836): Show |
2 | a0001c0001t0002g0288a0001c0001t0028g0287 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(845): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(842): Show |
1 | a0007c0007t0003g0223 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(851): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(831): Show |
1 | a0001c0001t0002g0294 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(840): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(836): Show |
1 | a0001c0001t0002g0051 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(845): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(839): Show |
1 | a0001c0001t0004g0052 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(848): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(842): Show |
1 | a0001c0001t0002g0248 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(851): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(831): Show |
1 | a0001c0001t0023g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(840): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(839): Show |
1 | a0001c0001t0002g0224 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(848): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(824): Show |
1 | a0001c0001t0037g0302 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(833): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(831): Show |
1 | a0001c0001t0004g0296 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(840): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(836): Show |
1 | a0001c0001t0025g0225 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(845): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(823): Show |
1 | a0001c0001t0002g0266 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(832): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(824): Show |
1 | a0001c0001t0022g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(833): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(826): Show |
1 | a0001c0001t0004g0211 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(835): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(828): Show |
1 | a0001c0001t0009g0008 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(837): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(829): Show |
1 | a0001c0009t0055g0304 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(838): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(833): Show |
3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0026g0053 | 3 | HG02129.hp1 NA18987.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(842): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(834): Show |
3 | a0001c0001t0002g0226a0001c0001t0002g0258a0001c0001t0004g0270 | 3 | HG02165.hp1 NA18960.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(843): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(836): Show |
1 | a0001c0001t0002g0227 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(845): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(819): Show |
1 | a0001c0001t0063g0131 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(828): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(825): Show |
1 | a0001c0001t0009g0298 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(834): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(831): Show |
1 | a0001c0001t0002g0184 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(840): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(834): Show |
2 | a0001c0001t0002g0249a0001c0001t0002g0256 | 2 | HG01346.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(843): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(821): Show |
1 | a0001c0001t0002g0284 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(830): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(822): Show |
2 | a0001c0001t0004g0203a0001c0001t0036g0303 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(831): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(826): Show |
1 | a0001c0001t0002g0054 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(835): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(827): Show |
2 | a0001c0001t0002g0228a0001c0001t0009g0299 | 2 | HG02559.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(836): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(828): Show |
2 | a0001c0001t0002g0208a0001c0001t0054g0185 | 2 | NA18991.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(837): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(831): Show |
1 | a0001c0001t0056g0186 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(840): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(809): Show |
1 | a0001c0001t0017g0152 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(818): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(818): Show |
1 | a0001c0001t0004g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(827): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(820): Show |
2 | a0001c0001t0002g0268a0001c0001t0004g0213 | 2 | HG01358.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(829): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(821): Show |
1 | a0001c0001t0004g0267 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(830): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(822): Show |
1 | a0001c0001t0033g0275 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(831): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(824): Show |
1 | a0001c0001t0057g0187 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(833): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(825): Show |
4 | a0001c0001t0002g0271a0001c0001t0002g0279a0001c0001t0002g0289others(1): Show | 4 | HG02647.hp1 HG03834.hp1 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.248+2952_248+2953i others(834): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(826): Show |
1 | a0001c0001t0002g0204 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(835): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(827): Show |
1 | a0001c0002t0014g0280 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(836): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(828): Show |
2 | a0001c0001t0002g0230a0001c0013t0002g0250 | 2 | HG02148.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(837): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(829): Show |
1 | a0001c0001t0004g0191 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(838): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(814): Show |
1 | a0001c0001t0039g0313 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(823): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(819): Show |
5 | a0001c0001t0004g0001a0001c0001t0004g0206a0001c0001t0004g0214others(2): Show | 7 | HG00738.hp1 HG01099.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.248+2952_248+2953i others(828): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(820): Show |
2 | a0001c0001t0004g0283a0001c0001t0011g0290 | 2 | HG02683.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(829): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(822): Show |
4 | a0001c0001t0002g0205a0001c0001t0002g0261a0001c0001t0002g0276others(1): Show | 4 | HG00408.hp1 HG02083.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.248+2952_248+2953i others(831): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(824): Show |
3 | a0001c0001t0002g0231a0001c0001t0002g0269a0001c0001t0061g0232 | 3 | HG00597.hp2 NA18942.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(833): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(825): Show |
2 | a0001c0001t0002g0233a0001c0001t0017g0234 | 2 | HG01175.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(834): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(826): Show |
1 | a0001c0001t0004g0297 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(835): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(813): Show |
1 | a0001c0001t0002g0277 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(822): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(817): Show |
1 | a0001c0001t0002g0295 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(826): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(818): Show |
1 | a0001c0001t0009g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(827): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(819): Show |
1 | a0001c0001t0033g0286 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(828): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(822): Show |
9 | a0001c0001t0002g0079a0001c0001t0002g0151a0001c0001t0002g0235others(6): Show | 9 | HG01934.hp2 HG02027.hp1 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.248+2952_248+2953i others(831): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(823): Show |
3 | a0001c0001t0004g0281a0001c0001t0004g0292a0001c0001t0027g0209 | 3 | HG00673.hp2 NA19004.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(832): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(824): Show |
5 | a0001c0001t0002g0180a0001c0001t0002g0239a0001c0001t0002g0260others(2): Show | 5 | HG02155.hp2 NA18957.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.248+2952_248+2953i others(833): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(817): Show |
1 | a0001c0001t0004g0274 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(826): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(818): Show |
1 | a0001c0001t0002g0291 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(827): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(822): Show |
3 | a0001c0001t0011g0240a0001c0001t0018g0272a0001c0001t0022g0273 | 3 | HG02809.hp2 NA18969.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(831): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(823): Show |
1 | a0001c0001t0018g0188 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(832): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(811): Show |
1 | a0001c0001t0002g0217 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(820): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(812): Show |
1 | a0001c0001t0004g0251 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(821): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(816): Show |
1 | a0001c0001t0002g0189 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(825): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(811): Show |
1 | a0001c0001t0002g0241 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(820): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(812): Show |
2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG01261.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(821): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(807): Show |
1 | a0001c0001t0002g0181 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(816): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(808): Show |
1 | a0001c0001t0002g0244 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(817): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(797): Show |
1 | a0001c0001t0002g0245 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(806): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(792): Show |
1 | a0001c0001t0002g0153 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(801): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(796): Show |
2 | a0001c0001t0001g0046a0001c0001t0001g0056 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(805): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(851): Show |
1 | a0001c0001t0002g0252 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(860): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(838): Show |
1 | a0001c0001t0002g0246 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(847): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(831): Show |
1 | a0001c0001t0004g0254 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(840): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(836): Show |
1 | a0006c0008t0030g0040 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(845): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(832): Show |
1 | a0001c0001t0011g0129 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(841): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(834): Show |
1 | a0006c0008t0030g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(843): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(816): Show |
1 | a0001c0001t0011g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(825): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(835): Show |
1 | a0005c0006t0058g0132 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(844): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(798): Show |
1 | a0001c0001t0001g0106 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(807): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(793): Show |
2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG01261.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(802): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(813): Show |
1 | a0003c0004t0038g0314 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(822): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(791): Show |
1 | a0002c0003t0003g0028 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(800): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(794): Show |
1 | a0002c0003t0007g0024 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(803): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(790): Show |
1 | a0002c0003t0003g0078 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(799): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(791): Show |
1 | a0002c0003t0003g0021 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.248+2952_248+2953i others(800): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(792): Show |
16 | a0002c0003t0003g0002a0002c0003t0003g0012a0002c0003t0003g0014others(13): Show | 16 | HG00423.hp1 HG00673.hp1 NA18947.hp1 others(13): Show |
intron_variant | MODIFIER | c.248+2952_248+2953i others(801): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(793): Show |
1 | a0002c0003t0007g0029 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(802): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(790): Show |
2 | a0007c0007t0007g0048a0015c0011t0007g0068 | 2 | NA18984.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(799): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(791): Show |
3 | a0002c0003t0003g0011a0002c0003t0003g0069a0002c0003t0007g0074 | 3 | HG03704.hp1 NA18942.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(800): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(792): Show |
8 | a0002c0003t0003g0039a0002c0003t0003g0070a0002c0003t0003g0073others(5): Show | 8 | HG00408.hp2 HG00621.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.248+2952_248+2953i others(801): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(793): Show |
1 | a0002c0003t0003g0143 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(802): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(794): Show |
6 | a0002c0003t0003g0049a0002c0003t0003g0109a0002c0003t0003g0144others(3): Show | 6 | HG00741.hp2 HG01069.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.248+2952_248+2953i others(803): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(790): Show |
1 | a0008c0010t0003g0077 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.248+2952_248+2953i others(799): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925704
|
G | GGTGCAGT others(792): Show |
2 | a0002c0003t0003g0050a0002c0003t0003g0072 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.248+2952_248+2953i others(801): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101925704 | |||||
chr11:101925781
|
A | G | 4 | a0004c0005t0001g0096a0004c0005t0005g0323a0004c0005t0005g0324others(1): Show | 4 | HG02257.hp1 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.248+3021A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101925781 | ||||||
chr11:101925814
|
C | T | 1 | a0001c0001t0004g0270 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.248+3054C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101925814 | ||||||
chr11:101925825
|
T | G | 3 | a0005c0006t0016g0316a0005c0006t0016g0318a0005c0006t0040g0317 | 3 | HG02895.hp1 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.248+3065T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101925825 | ||||||
chr11:101925846
|
G | A | 1 | a0001c0001t0034g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.248+3086G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101925846 | ||||||
chr11:101925874
|
C | T | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.248+3114C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101925874 | ||||||
chr11:101926022
|
G | A | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.248+3262G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101926022 | ||||||
chr11:101926296
|
GA | G | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.248+3537delA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101926296 | ||||||
chr11:101926461
|
C | T | 3 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312 | 3 | HG02109.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.248+3701C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101926461 | ||||||
chr11:101926499
|
A | G | 2 | a0001c0001t0012g0310a0001c0001t0012g0311 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.248+3739A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101926499 | ||||||
chr11:101926963
|
T | C | 1 | a0002c0003t0007g0013 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.248+4203T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101926963 | ||||||
chr11:101927153
|
T | C | 1 | a0001c0001t0034g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.248+4393T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101927153 | ||||||
chr11:101927228
|
G | A | 1 | a0001c0001t0015g0035 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.248+4468G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101927228 | ||||||
chr11:101927364
|
T | A | 1 | a0001c0001t0002g0051 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.248+4604T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101927364 | ||||||
chr11:101927454
|
G | T | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.248+4694G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101927454 | ||||||
chr11:101927459
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.248+4699A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101927459 | ||||||
chr11:101927489
|
A | C | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.248+4729A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101927489 | ||||||
chr11:101927687
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.248+4927G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101927687 | ||||||
chr11:101927695
|
CT | C | 3 | a0001c0001t0036g0303a0001c0001t0037g0302a0001c0009t0055g0304 | 3 | HG02451.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.248+4938delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101927695 | |||||
chr11:101927782
|
T | C | 2 | a0001c0002t0014g0195a0001c0002t0048g0263 | 2 | NA18993.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.248+5022T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101927782 | ||||||
chr11:101927812
|
T | C | 1 | a0001c0001t0006g0112 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.248+5052T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101927812 | ||||||
chr11:101928089
|
GTGGT | G | 9 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(6): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.248+5331_248+5334d others(6): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101928089 | |||||
chr11:101928170
|
T | G | 1 | a0001c0002t0005g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.248+5410T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101928170 | ||||||
chr11:101928437
|
G | A | 1 | a0001c0001t0034g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.248+5677G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101928437 | ||||||
chr11:101928768
|
C | T | 3 | a0001c0002t0001g0172a0001c0002t0001g0175a0001c0002t0005g0196 | 3 | HG00280.hp2 HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.248+6008C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101928768 | ||||||
chr11:101928976
|
A | T | 2 | a0001c0001t0011g0129a0001c0001t0011g0130 | 2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.248+6216A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101928976 | ||||||
chr11:101928980
|
C | G | 1 | a0001c0001t0001g0110 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.248+6220C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101928980 | ||||||
chr11:101929042
|
C | T | 120 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(117): Show | 123 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.248+6282C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101929042 | ||||||
chr11:101929194
|
A | T | 1 | a0002c0003t0003g0147 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.248+6434A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101929194 | ||||||
chr11:101929239
|
C | T | 1 | a0001c0001t0019g0047 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.248+6479C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101929239 | ||||||
chr11:101929748
|
G | A | 4 | a0001c0002t0014g0195a0001c0002t0014g0197a0001c0002t0047g0198others(1): Show | 4 | NA18954.hp1 NA18993.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.248+6988G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101929748 | ||||||
chr11:101929974
|
C | CT | 69 | a0001c0001t0001g0065a0001c0001t0002g0051a0001c0001t0002g0054others(66): Show | 69 | HG00597.hp2 HG00639.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.248+7232dupT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101929974 | |||||
chr11:101929974
|
C | CTTTTTTT others(2): Show |
11 | a0003c0004t0010g0307a0003c0004t0010g0322a0003c0004t0021g0315others(8): Show | 11 | HG01109.hp1 HG02109.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.248+7224_248+7232d others(11): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101929974 | |||||
chr11:101929974
|
C | CTTTTTTT others(3): Show |
41 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0014others(38): Show | 42 | HG00408.hp2 HG00423.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.248+7223_248+7232d others(12): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101929974 | |||||
chr11:101929974
|
C | CTTTTTTT others(4): Show |
6 | a0002c0003t0003g0012a0002c0003t0003g0039a0002c0003t0003g0076others(3): Show | 6 | HG00621.hp1 HG01106.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.248+7222_248+7232d others(13): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101929974 | |||||
chr11:101929974
|
C | CTTTTTTT others(7): Show |
3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.248+7219_248+7232d others(16): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101929974 | |||||
chr11:101930022
|
T | C | 40 | a0001c0001t0002g0153a0001c0001t0002g0217a0001c0001t0002g0266others(37): Show | 43 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.248+7262T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101930022 | ||||||
chr11:101930089
|
T | G | 1 | a0012c0015t0035g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.248+7329T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101930089 | ||||||
chr11:101930194
|
C | CT | 272 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0055others(269): Show | 277 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.248+7435dupT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101930194 | |||||
chr11:101930255
|
A | T | 4 | a0001c0001t0011g0129a0001c0001t0011g0130a0006c0008t0030g0040others(1): Show | 4 | HG02818.hp2 HG03486.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.248+7495A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101930255 | ||||||
chr11:101930430
|
G | C | 6 | a0001c0001t0031g0139a0001c0001t0031g0141a0001c0001t0032g0140others(3): Show | 6 | HG02055.hp2 HG02886.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.248+7670G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101930430 | ||||||
chr11:101930469
|
G | A | 3 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312 | 3 | HG02109.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.248+7709G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101930469 | ||||||
chr11:101930727
|
G | T | 198 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(195): Show | 203 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.248+7967G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101930727 | ||||||
chr11:101930903
|
A | G | 2 | a0001c0001t0002g0181a0001c0001t0057g0187 | 2 | NA18953.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.248+8143A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101930903 | ||||||
chr11:101930934
|
G | A | 3 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312 | 3 | HG02109.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.248+8174G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101930934 | ||||||
chr11:101931069
|
A | T | 1 | a0001c0001t0004g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.248+8309A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101931069 | ||||||
chr11:101931071
|
T | C | 182 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(179): Show | 186 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.248+8311T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101931071 | ||||||
chr11:101931154
|
A | T | 1 | a0005c0006t0058g0132 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.248+8394A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101931154 | ||||||
chr11:101931204
|
A | C | 1 | a0002c0003t0003g0069 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.248+8444A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101931204 | ||||||
chr11:101931246
|
A | G | 1 | a0001c0001t0002g0226 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.248+8486A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101931246 | ||||||
chr11:101931318
|
G | A | 3 | a0001c0001t0036g0303a0001c0001t0037g0302a0001c0009t0055g0304 | 3 | HG02451.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.248+8558G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101931318 | ||||||
chr11:101931402
|
C | T | 1 | a0001c0002t0001g0169 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.248+8642C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101931402 | ||||||
chr11:101931403
|
G | A | 6 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(3): Show | 6 | HG02109.hp1 HG02723.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.248+8643G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101931403 | ||||||
chr11:101931496
|
A | G | 1 | a0001c0001t0049g0038 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.248+8736A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101931496 | ||||||
chr11:101931510
|
T | C | 1 | a0001c0001t0002g0226 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.248+8750T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101931510 | ||||||
chr11:101931935
|
T | C | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0005c0006t0058g0132others(2): Show | 5 | HG01346.hp1 HG02818.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.248+9175T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101931935 | ||||||
chr11:101932037
|
C | T | 81 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(78): Show | 81 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.248+9277C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101932037 | ||||||
chr11:101932133
|
A | G | 1 | a0002c0003t0003g0078 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.248+9373A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101932133 | ||||||
chr11:101932143
|
A | C | 7 | a0001c0001t0001g0085a0001c0001t0001g0088a0001c0001t0001g0092others(4): Show | 7 | HG02055.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.248+9383A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101932143 | ||||||
chr11:101932369
|
C | T | 1 | a0001c0001t0006g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.248+9609C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101932369 | ||||||
chr11:101932431
|
G | T | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.248+9671G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101932431 | ||||||
chr11:101932519
|
G | A | 5 | a0001c0001t0002g0231a0001c0001t0002g0235a0001c0001t0002g0237others(2): Show | 5 | NA18942.hp1 NA18982.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.248+9759G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101932519 | ||||||
chr11:101932608
|
T | C | 1 | a0001c0001t0034g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.248+9848T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101932608 | ||||||
chr11:101932626
|
G | A | 121 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(118): Show | 124 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.248+9866G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101932626 | ||||||
chr11:101932661
|
A | G | 2 | a0001c0002t0001g0168a0001c0002t0005g0157 | 2 | NA18943.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.248+9901A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101932661 | ||||||
chr11:101932788
|
A | T | 1 | a0003c0004t0021g0315 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.248+10028A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101932788 | ||||||
chr11:101932850
|
C | T | 1 | a0001c0001t0025g0202 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.248+10090C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101932850 | ||||||
chr11:101932917
|
A | G | 1 | a0001c0002t0005g0176 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.248+10157A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101932917 | ||||||
chr11:101933165
|
G | T | 1 | a0001c0009t0055g0304 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.248+10405G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101933165 | ||||||
chr11:101933166
|
C | T | 1 | a0001c0009t0055g0304 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.248+10406C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101933166 | ||||||
chr11:101933279
|
T | C | 47 | a0001c0001t0002g0189a0001c0001t0004g0191a0001c0001t0056g0186others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.248+10519T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101933279 | ||||||
chr11:101933461
|
T | G | 1 | a0001c0001t0042g0080 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.248+10701T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101933461 | ||||||
chr11:101933492
|
G | T | 3 | a0001c0001t0036g0303a0001c0001t0037g0302a0001c0009t0055g0304 | 3 | HG02451.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.248+10732G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101933492 | ||||||
chr11:101933814
|
A | AC | 19 | a0001c0001t0001g0065a0001c0001t0002g0224a0001c0001t0004g0211others(16): Show | 20 | HG01109.hp1 HG01175.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.249-10441dupC | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101933814 | |||||
chr11:101933814
|
AC | A | 48 | a0001c0001t0002g0189a0001c0001t0004g0191a0001c0001t0005g0118others(45): Show | 48 | HG00423.hp1 HG00621.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.249-10441delC | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101933814 | |||||
chr11:101933817
|
C | T | 1 | a0001c0002t0014g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.249-10448C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101933817 | ||||||
chr11:101933821
|
C | T | 3 | a0002c0003t0003g0012a0002c0003t0003g0019a0002c0003t0007g0027 | 3 | HG00423.hp1 NA18947.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.249-10444C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101933821 | ||||||
chr11:101933913
|
G | A | 2 | a0001c0002t0001g0172a0001c0002t0001g0175 | 2 | HG00280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.249-10352G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101933913 | ||||||
chr11:101934216
|
A | G | 9 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(6): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-10049A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101934216 | ||||||
chr11:101934225
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.249-10040T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101934225 | ||||||
chr11:101934328
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.249-9937G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101934328 | ||||||
chr11:101934611
|
T | C | 47 | a0001c0001t0002g0189a0001c0001t0004g0191a0001c0001t0056g0186others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.249-9654T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101934611 | ||||||
chr11:101934962
|
T | C | 1 | a0002c0003t0003g0011 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.249-9303T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101934962 | ||||||
chr11:101935109
|
T | G | 62 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(59): Show | 63 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.249-9156T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101935109 | ||||||
chr11:101935522
|
G | A | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.249-8743G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101935522 | ||||||
chr11:101935562
|
A | G | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.249-8703A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101935562 | ||||||
chr11:101935662
|
T | C | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.249-8603T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101935662 | ||||||
chr11:101935892
|
C | T | 1 | a0001c0001t0002g0241 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.249-8373C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101935892 | ||||||
chr11:101935908
|
A | G | 62 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(59): Show | 63 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.249-8357A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101935908 | ||||||
chr11:101935947
|
G | A | 205 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(202): Show | 210 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.249-8318G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101935947 | ||||||
chr11:101936189
|
C | G | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.249-8076C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101936189 | ||||||
chr11:101936205
|
ATTTTGGT others(8): Show |
A | 1 | a0001c0001t0002g0271 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.249-8049_249-8035d others(17): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101936205 | |||||
chr11:101936423
|
AGAACTT | A | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.249-7840_249-7835d others(8): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101936423 | |||||
chr11:101936430
|
G | A | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.249-7835G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101936430 | ||||||
chr11:101936647
|
G | A | 1 | a0001c0001t0002g0230 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.249-7618G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101936647 | ||||||
chr11:101936725
|
A | G | 62 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(59): Show | 63 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.249-7540A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101936725 | ||||||
chr11:101936825
|
C | G | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.249-7440C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101936825 | ||||||
chr11:101936888
|
G | T | 2 | a0002c0003t0007g0018a0002c0003t0007g0020 | 2 | NA18966.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.249-7377G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101936888 | ||||||
chr11:101936895
|
T | A | 2 | a0001c0001t0036g0303a0001c0001t0037g0302 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.249-7370T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101936895 | ||||||
chr11:101936980
|
G | A | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.249-7285G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101936980 | ||||||
chr11:101937130
|
T | A | 9 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(6): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-7135T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101937130 | ||||||
chr11:101937145
|
A | G | 3 | a0001c0001t0036g0303a0001c0001t0037g0302a0001c0009t0055g0304 | 3 | HG02451.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.249-7120A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101937145 | ||||||
chr11:101937223
|
G | A | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.249-7042G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101937223 | ||||||
chr11:101937340
|
A | G | 1 | a0012c0015t0035g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.249-6925A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101937340 | ||||||
chr11:101937718
|
C | T | 6 | a0001c0001t0031g0139a0001c0001t0031g0141a0001c0001t0032g0140others(3): Show | 6 | HG01346.hp1 HG02055.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.249-6547C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101937718 | ||||||
chr11:101937831
|
G | A | 2 | a0002c0003t0003g0023a0002c0003t0007g0025 | 2 | NA18973.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.249-6434G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101937831 | ||||||
chr11:101937857
|
A | G | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.249-6408A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101937857 | ||||||
chr11:101937876
|
G | A | 2 | a0001c0001t0004g0253a0001c0002t0001g0199 | 2 | HG01993.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.249-6389G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101937876 | ||||||
chr11:101937906
|
C | G | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.249-6359C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101937906 | ||||||
chr11:101937925
|
G | A | 2 | a0001c0001t0002g0184a0001c0001t0054g0185 | 2 | NA18991.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.249-6340G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101937925 | ||||||
chr11:101938070
|
G | T | 3 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312 | 3 | HG02109.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.249-6195G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101938070 | ||||||
chr11:101938084
|
C | A | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.249-6181C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101938084 | ||||||
chr11:101938147
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0002g0277 | 2 | HG00738.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.249-6118G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101938147 | ||||||
chr11:101938159
|
C | CA | 26 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0081others(23): Show | 26 | HG00323.hp2 HG00423.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.249-6089dupA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAA | 41 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0002g0224others(38): Show | 41 | HG00408.hp2 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.249-6092_249-6089d others(6): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAA | 9 | a0001c0001t0002g0208a0001c0001t0002g0226a0001c0001t0009g0301others(6): Show | 9 | HG00423.hp1 HG02071.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.249-6093_249-6089d others(7): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(2): Show |
6 | a0001c0001t0002g0235a0001c0001t0004g0270a0001c0001t0012g0309others(3): Show | 6 | HG02165.hp1 HG02165.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.249-6097_249-6089d others(11): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(3): Show |
4 | a0001c0001t0002g0288a0001c0001t0004g0274a0001c0001t0012g0310others(1): Show | 4 | HG01517.hp1 HG02970.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.249-6098_249-6089d others(12): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(4): Show |
4 | a0001c0001t0004g0296a0001c0001t0023g0285a0001c0001t0028g0287others(1): Show | 4 | HG01516.hp2 HG03195.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.249-6099_249-6089d others(13): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0002g0266 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.249-6100_249-6089d others(14): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0004g0283 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.249-6101_249-6089d others(15): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0002g0289 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.249-6102_249-6089d others(16): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0002g0079a0001c0001t0033g0275a0001c0001t0033g0286 | 3 | HG00323.hp1 HG02698.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.249-6103_249-6089d others(17): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0063g0131 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.249-6104_249-6089d others(18): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0002g0278 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.249-6089_249-6088i others(21): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0022g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.249-6089_249-6088i others(23): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0002g0271 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.249-6089_249-6088i others(24): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0009g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.249-6089_249-6088i others(25): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(17): Show |
7 | a0001c0001t0002g0180a0001c0001t0002g0205a0001c0001t0002g0241others(4): Show | 7 | HG00408.hp1 HG00597.hp2 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.249-6089_249-6088i others(26): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(18): Show |
11 | a0001c0001t0002g0051a0001c0001t0002g0151a0001c0001t0002g0227others(8): Show | 11 | HG01261.hp1 HG02004.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.249-6089_249-6088i others(27): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(19): Show |
10 | a0001c0001t0002g0054a0001c0001t0002g0207a0001c0001t0002g0221others(7): Show | 10 | HG01993.hp1 HG02015.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.249-6089_249-6088i others(28): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(20): Show |
4 | a0001c0001t0002g0242a0001c0001t0018g0272a0001c0001t0025g0202others(1): Show | 4 | HG02129.hp1 HG02809.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.249-6089_249-6088i others(29): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(21): Show |
10 | a0001c0001t0002g0228a0001c0001t0002g0246a0001c0001t0002g0249others(7): Show | 11 | HG00673.hp2 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.249-6089_249-6088i others(30): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(22): Show |
10 | a0001c0001t0002g0181a0001c0001t0002g0184a0001c0001t0002g0189others(7): Show | 10 | HG02523.hp1 NA18953.hp1 NA18954.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-6089_249-6088i others(31): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(23): Show |
5 | a0001c0001t0002g0220a0001c0001t0002g0255a0001c0001t0004g0191others(2): Show | 5 | HG01109.hp2 HG03704.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.249-6089_249-6088i others(32): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(24): Show |
3 | a0001c0001t0002g0252a0001c0001t0004g0052a0001c0001t0017g0234 | 3 | HG01175.hp1 NA18990.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.249-6089_249-6088i others(33): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(25): Show |
2 | a0001c0001t0002g0204a0001c0001t0011g0290 | 2 | HG02074.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.249-6089_249-6088i others(34): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(27): Show |
6 | a0001c0001t0002g0268a0001c0001t0002g0284a0001c0001t0002g0291others(3): Show | 6 | HG01175.hp2 HG01255.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.249-6089_249-6088i others(36): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(30): Show |
1 | a0001c0001t0002g0153 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.249-6089_249-6088i others(39): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(31): Show |
3 | a0001c0001t0002g0277a0001c0001t0002g0294a0001c0001t0004g0267 | 3 | HG01255.hp1 HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.249-6089_249-6088i others(40): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(32): Show |
2 | a0001c0001t0002g0247a0001c0001t0002g0295 | 2 | HG01192.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.249-6089_249-6088i others(41): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(34): Show |
1 | a0001c0001t0002g0217 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.249-6089_249-6088i others(43): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938159
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0002g0279 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.249-6089_249-6088i others(25): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938159 | |||||
chr11:101938171
|
A | AAAAAAAA others(6): Show |
1 | a0001c0009t0055g0304 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.249-6089_249-6088i others(15): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938171 | |||||
chr11:101938171
|
A | AAACAAAA others(3): Show |
2 | a0001c0001t0036g0303a0001c0001t0037g0302 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.249-6092_249-6091i others(12): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938171 | |||||
chr11:101938173
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0011g0240 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.249-6089_249-6088i others(26): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938173 | |||||
chr11:101938175
|
AAT | A | 12 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(9): Show | 13 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.249-6088_249-6087d others(4): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938175 | |||||
chr11:101938176
|
AT | A | 8 | a0001c0001t0002g0218a0001c0001t0011g0129a0001c0002t0014g0195others(5): Show | 8 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.249-6088delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101938176 | ||||||
chr11:101938177
|
T | A | 309 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0046others(306): Show | 314 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.249-6088T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101938177 | ||||||
chr11:101938401
|
AT | A | 58 | a0001c0001t0001g0059a0001c0001t0006g0112a0001c0001t0012g0309others(55): Show | 58 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.249-5850delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101938401 | |||||
chr11:101938449
|
T | A | 1 | a0001c0001t0002g0258 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.249-5816T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101938449 | ||||||
chr11:101938478
|
C | T | 1 | a0001c0002t0001g0200 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.249-5787C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101938478 | ||||||
chr11:101938634
|
G | A | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.249-5631G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101938634 | ||||||
chr11:101938693
|
T | A | 1 | a0002c0003t0003g0109 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.249-5572T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101938693 | ||||||
chr11:101938924
|
G | C | 121 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(118): Show | 124 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.249-5341G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101938924 | ||||||
chr11:101938943
|
A | G | 1 | a0001c0001t0006g0135 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.249-5322A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101938943 | ||||||
chr11:101939058
|
T | C | 2 | a0001c0001t0002g0245a0001c0001t0026g0259 | 2 | HG02015.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.249-5207T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101939058 | ||||||
chr11:101939254
|
A | G | 9 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(6): Show | 10 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.249-5011A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101939254 | ||||||
chr11:101939341
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.249-4924A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101939341 | ||||||
chr11:101939592
|
T | G | 1 | a0001c0001t0034g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.249-4673T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101939592 | ||||||
chr11:101939596
|
C | T | 1 | a0002c0003t0003g0017 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.249-4669C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101939596 | ||||||
chr11:101940133
|
G | A | 3 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308 | 4 | HG02257.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.249-4132G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101940133 | ||||||
chr11:101940175
|
A | G | 1 | a0001c0001t0006g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.249-4090A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101940175 | ||||||
chr11:101940486
|
A | G | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.249-3779A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101940486 | ||||||
chr11:101940871
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.249-3394C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101940871 | ||||||
chr11:101940906
|
G | A | 4 | a0002c0003t0003g0070a0002c0003t0003g0073a0002c0003t0059g0075others(1): Show | 4 | HG00408.hp2 HG02071.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.249-3359G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101940906 | ||||||
chr11:101941157
|
C | G | 1 | a0001c0001t0002g0261 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.249-3108C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101941157 | ||||||
chr11:101941212
|
A | G | 3 | a0001c0001t0036g0303a0001c0001t0037g0302a0001c0009t0055g0304 | 3 | HG02451.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.249-3053A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101941212 | ||||||
chr11:101941218
|
G | A | 1 | a0001c0002t0014g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.249-3047G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101941218 | ||||||
chr11:101941285
|
G | A | 2 | a0001c0002t0001g0156a0001c0002t0005g0161 | 2 | HG04199.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.249-2980G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101941285 | ||||||
chr11:101941306
|
C | G | 1 | a0013c0018t0015g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.249-2959C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101941306 | ||||||
chr11:101941442
|
A | G | 1 | a0002c0003t0003g0069 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.249-2823A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101941442 | ||||||
chr11:101942107
|
C | T | 1 | a0001c0001t0002g0261 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.249-2158C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101942107 | ||||||
chr11:101942123
|
G | C | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.249-2142G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101942123 | ||||||
chr11:101942563
|
G | GT | 122 | a0001c0001t0001g0055a0001c0001t0001g0110a0001c0001t0002g0051others(119): Show | 125 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.249-1689dupT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101942563 | |||||
chr11:101942563
|
GT | G | 58 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(55): Show | 58 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.249-1689delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101942563 | |||||
chr11:101942834
|
C | T | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.249-1431C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101942834 | ||||||
chr11:101943086
|
C | CT | 59 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(56): Show | 60 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.249-1169dupT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101943086 | |||||
chr11:101943271
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.249-994A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101943271 | ||||||
chr11:101943503
|
C | CT | 8 | a0001c0001t0006g0125a0002c0003t0007g0025a0004c0005t0001g0096others(5): Show | 8 | HG02257.hp1 HG02717.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.249-749dupT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101943503 | |||||
chr11:101943503
|
CT | C | 21 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(18): Show | 23 | HG00323.hp2 HG01109.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.249-749delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101943503 | |||||
chr11:101943508
|
T | C | 1 | a0001c0002t0019g0162 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.249-757T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101943508 | ||||||
chr11:101943545
|
T | TAC | 9 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0002t0001g0154others(6): Show | 9 | HG00423.hp2 HG01346.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.249-704_249-703dup others(2): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 101943545 | |||||
chr11:101943953
|
C | G | 1 | a0001c0001t0002g0258 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.249-312C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101943953 | ||||||
chr11:101943992
|
G | A | 5 | a0001c0002t0001g0006a0001c0002t0001g0163a0001c0002t0001g0167others(2): Show | 5 | NA18955.hp2 NA18989.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.249-273G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101943992 | ||||||
chr11:101944138
|
A | T | 2 | a0001c0001t0011g0129a0001c0001t0011g0130 | 2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.249-127A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101944138 | ||||||
chr11:101944258
|
A | C | 1 | a0001c0009t0055g0304 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.249-7A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 2/10 | chr11 | 101944258 | ||||||
chr11:101944435
|
G | A | 1 | a0001c0001t0022g0273 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.394+25G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101944435 | ||||||
chr11:101944436
|
A | G | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.394+26A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101944436 | ||||||
chr11:101944564
|
G | T | 9 | a0001c0002t0001g0007a0001c0002t0001g0164a0001c0002t0001g0165others(6): Show | 9 | HG01358.hp2 HG01934.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.394+154G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101944564 | ||||||
chr11:101944690
|
G | A | 1 | a0009c0016t0002g0229 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.394+280G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101944690 | ||||||
chr11:101944750
|
T | C | 2 | a0001c0001t0036g0303a0001c0001t0037g0302 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.394+340T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101944750 | ||||||
chr11:101944828
|
C | G | 123 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0002g0051others(120): Show | 126 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.394+418C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101944828 | ||||||
chr11:101945293
|
C | T | 1 | a0001c0001t0041g0122 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.394+883C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101945293 | ||||||
chr11:101945361
|
G | A | 1 | a0001c0001t0034g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.394+951G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101945361 | ||||||
chr11:101945571
|
T | A | 2 | a0001c0001t0002g0268a0001c0001t0002g0284 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.394+1161T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101945571 | ||||||
chr11:101945576
|
G | A | 75 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(72): Show | 75 | HG00408.hp1 HG00597.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.394+1166G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101945576 | ||||||
chr11:101945709
|
C | T | 2 | a0001c0001t0036g0303a0001c0001t0037g0302 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.394+1299C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101945709 | ||||||
chr11:101945932
|
G | T | 1 | a0001c0009t0055g0304 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.394+1522G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101945932 | ||||||
chr11:101945937
|
C | G | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.394+1527C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101945937 | ||||||
chr11:101946024
|
T | G | 6 | a0001c0001t0011g0129a0001c0001t0011g0130a0001c0009t0055g0304others(3): Show | 6 | HG01346.hp1 HG02818.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.394+1614T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101946024 | ||||||
chr11:101946189
|
C | T | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.394+1779C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101946189 | ||||||
chr11:101946337
|
ATC | A | 3 | a0001c0001t0036g0303a0001c0001t0037g0302a0001c0009t0055g0304 | 3 | HG02451.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.395-1690_395-1689d others(4): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 101946337 | |||||
chr11:101946427
|
G | T | 9 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(6): Show | 10 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.395-1604G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101946427 | ||||||
chr11:101946643
|
T | C | 205 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(202): Show | 210 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.395-1388T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101946643 | ||||||
chr11:101946676
|
A | C | 1 | a0001c0002t0005g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.395-1355A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101946676 | ||||||
chr11:101946701
|
A | C | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.395-1330A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101946701 | ||||||
chr11:101946711
|
T | G | 1 | a0001c0001t0001g0056 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.395-1320T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101946711 | ||||||
chr11:101946729
|
G | A | 2 | a0001c0001t0002g0180a0001c0001t0002g0239 | 2 | NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.395-1302G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101946729 | ||||||
chr11:101946775
|
G | T | 3 | a0005c0006t0016g0316a0005c0006t0016g0318a0005c0006t0040g0317 | 3 | HG02895.hp1 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.395-1256G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101946775 | ||||||
chr11:101946841
|
G | A | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.395-1190G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101946841 | ||||||
chr11:101947272
|
G | C | 1 | a0001c0002t0001g0156 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.395-759G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101947272 | ||||||
chr11:101947280
|
T | C | 6 | a0001c0001t0031g0139a0001c0001t0031g0141a0001c0001t0032g0140others(3): Show | 6 | HG01346.hp1 HG02055.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.395-751T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101947280 | ||||||
chr11:101947408
|
G | A | 3 | a0004c0005t0005g0323a0004c0005t0005g0324a0004c0005t0005g0325 | 3 | HG02257.hp1 HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.395-623G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101947408 | ||||||
chr11:101947456
|
A | G | 1 | a0001c0002t0001g0262 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.395-575A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101947456 | ||||||
chr11:101947742
|
A | C | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.395-289A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101947742 | ||||||
chr11:101947755
|
G | A | 2 | a0001c0001t0002g0184a0001c0001t0054g0185 | 2 | NA18991.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.395-276G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101947755 | ||||||
chr11:101947997
|
A | G | 121 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(118): Show | 124 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.395-34A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 3/10 | chr11 | 101947997 | ||||||
chr11:101948624
|
G | A | 45 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.506+482G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101948624 | ||||||
chr11:101948876
|
G | A | 42 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(39): Show | 42 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.506+734G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101948876 | ||||||
chr11:101948957
|
A | T | 5 | a0001c0001t0011g0129a0001c0001t0011g0130a0005c0006t0058g0132others(2): Show | 5 | HG01346.hp1 HG02818.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.506+815A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101948957 | ||||||
chr11:101949045
|
T | C | 3 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308 | 4 | HG02257.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+903T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101949045 | ||||||
chr11:101949348
|
C | T | 3 | a0004c0005t0005g0111a0004c0005t0005g0115a0004c0005t0005g0121 | 3 | HG02258.hp2 HG02622.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.506+1206C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101949348 | ||||||
chr11:101949963
|
A | C | 1 | a0001c0001t0001g0108 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.506+1821A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101949963 | ||||||
chr11:101950067
|
G | C | 1 | a0013c0018t0015g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.506+1925G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101950067 | ||||||
chr11:101950097
|
G | A | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.506+1955G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101950097 | ||||||
chr11:101950616
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.506+2474T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101950616 | ||||||
chr11:101950713
|
C | T | 120 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(117): Show | 123 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.506+2571C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101950713 | ||||||
chr11:101950869
|
C | T | 3 | a0001c0002t0001g0193a0001c0002t0001g0194a0001c0002t0001g0326 | 3 | HG03017.hp1 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.506+2727C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101950869 | ||||||
chr11:101950895
|
G | C | 1 | a0001c0002t0046g0170 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.506+2753G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101950895 | ||||||
chr11:101951072
|
G | T | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.506+2930G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101951072 | ||||||
chr11:101951110
|
A | C | 1 | a0002c0003t0003g0067 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.506+2968A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101951110 | ||||||
chr11:101951115
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.506+2973A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101951115 | ||||||
chr11:101951348
|
C | A | 2 | a0006c0008t0030g0040a0006c0008t0030g0041 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.506+3206C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101951348 | ||||||
chr11:101951779
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.506+3637T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101951779 | ||||||
chr11:101952077
|
G | T | 1 | a0001c0001t0017g0234 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.506+3935G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101952077 | ||||||
chr11:101952098
|
G | A | 3 | a0001c0001t0036g0303a0001c0001t0037g0302a0001c0009t0055g0304 | 3 | HG02451.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.506+3956G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101952098 | ||||||
chr11:101952295
|
G | C | 1 | a0001c0001t0004g0214 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.506+4153G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101952295 | ||||||
chr11:101952334
|
G | A | 1 | a0005c0006t0058g0132 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.506+4192G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101952334 | ||||||
chr11:101952360
|
G | A | 3 | a0001c0001t0002g0151a0001c0001t0002g0204a0001c0001t0002g0233 | 3 | HG02027.hp1 HG02074.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.506+4218G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101952360 | ||||||
chr11:101952709
|
A | C | 1 | a0001c0001t0039g0313 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.506+4567A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101952709 | ||||||
chr11:101952827
|
G | A | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.506+4685G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101952827 | ||||||
chr11:101953185
|
TATC | T | 6 | a0001c0001t0002g0217a0001c0001t0002g0268a0001c0001t0002g0284others(3): Show | 6 | HG00741.hp1 HG01175.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.507-4980_507-4978d others(5): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 101953185 | |||||
chr11:101953235
|
G | T | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.507-4933G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101953235 | ||||||
chr11:101953393
|
G | T | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.507-4775G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101953393 | ||||||
chr11:101953399
|
TTTG | T | 4 | a0001c0001t0031g0139a0001c0001t0031g0141a0001c0001t0032g0140others(1): Show | 4 | HG02055.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-4766_507-4764d others(5): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 101953399 | |||||
chr11:101953690
|
G | T | 1 | a0001c0002t0001g0167 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.507-4478G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101953690 | ||||||
chr11:101953713
|
A | C | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.507-4455A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101953713 | ||||||
chr11:101953748
|
G | A | 257 | a0001c0001t0001g0055a0001c0001t0001g0083a0001c0001t0001g0084others(254): Show | 262 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.507-4420G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101953748 | ||||||
chr11:101953796
|
T | C | 202 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0002g0051others(199): Show | 207 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.507-4372T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101953796 | ||||||
chr11:101953823
|
G | A | 1 | a0001c0002t0005g0196 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.507-4345G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101953823 | ||||||
chr11:101954020
|
T | TTTTG | 69 | a0001c0001t0002g0241a0001c0001t0008g0003a0001c0001t0008g0030others(66): Show | 70 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.507-4124_507-4121d others(6): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 101954020 | |||||
chr11:101954020
|
T | TTTTGTTT others(1): Show |
119 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(116): Show | 122 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.507-4128_507-4121d others(10): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 101954020 | |||||
chr11:101954020
|
TTTTG | T | 15 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(12): Show | 16 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.507-4124_507-4121d others(6): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 101954020 | |||||
chr11:101954174
|
C | T | 121 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(118): Show | 124 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.507-3994C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101954174 | ||||||
chr11:101954176
|
T | C | 1 | a0001c0002t0001g0172 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.507-3992T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101954176 | ||||||
chr11:101954501
|
A | C | 1 | a0012c0015t0035g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.507-3667A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101954501 | ||||||
chr11:101954636
|
T | TTATATA | 9 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(6): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.507-3529_507-3524d others(8): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 101954636 | |||||
chr11:101954645
|
C | T | 204 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(201): Show | 209 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.507-3523C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101954645 | ||||||
chr11:101954688
|
G | C | 1 | a0001c0002t0044g0264 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.507-3480G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101954688 | ||||||
chr11:101954845
|
T | C | 1 | a0001c0001t0004g0052 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.507-3323T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101954845 | ||||||
chr11:101955206
|
TTAA | T | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.507-2958_507-2956d others(5): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 101955206 | |||||
chr11:101955231
|
A | G | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.507-2937A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101955231 | ||||||
chr11:101955241
|
A | G | 1 | a0001c0001t0002g0230 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.507-2927A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101955241 | ||||||
chr11:101955246
|
T | G | 1 | a0001c0001t0049g0038 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.507-2922T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101955246 | ||||||
chr11:101955571
|
TAA | T | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.507-2596_507-2595d others(4): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101955571 | ||||||
chr11:101955758
|
G | A | 62 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(59): Show | 63 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.507-2410G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101955758 | ||||||
chr11:101955859
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.507-2309C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101955859 | ||||||
chr11:101955889
|
A | G | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.507-2279A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101955889 | ||||||
chr11:101955947
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.507-2221A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101955947 | ||||||
chr11:101956218
|
T | C | 203 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(200): Show | 209 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.507-1950T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101956218 | ||||||
chr11:101956550
|
C | A | 1 | a0001c0001t0001g0103 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.507-1618C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101956550 | ||||||
chr11:101956617
|
G | T | 1 | a0001c0002t0001g0262 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.507-1551G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101956617 | ||||||
chr11:101956795
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.507-1373C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101956795 | ||||||
chr11:101956808
|
C | T | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.507-1360C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101956808 | ||||||
chr11:101956854
|
T | C | 23 | a0001c0001t0001g0046a0001c0001t0001g0056a0001c0001t0005g0118others(20): Show | 23 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.507-1314T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101956854 | ||||||
chr11:101957273
|
A | C | 1 | a0001c0001t0034g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.507-895A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101957273 | ||||||
chr11:101957274
|
A | G | 1 | a0001c0001t0034g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.507-894A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101957274 | ||||||
chr11:101957298
|
G | T | 12 | a0001c0001t0002g0266a0001c0001t0002g0294a0001c0001t0004g0001others(9): Show | 14 | HG00738.hp1 HG01099.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.507-870G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101957298 | ||||||
chr11:101957313
|
T | C | 108 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0046others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.507-855T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101957313 | ||||||
chr11:101957313
|
T | G | 199 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(196): Show | 204 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.507-855T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101957313 | ||||||
chr11:101957391
|
C | A | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.507-777C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101957391 | ||||||
chr11:101957604
|
C | CTGAAAAT others(11): Show |
44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.507-561_507-544dup others(18): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 101957604 | |||||
chr11:101957684
|
T | C | 55 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.507-484T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101957684 | ||||||
chr11:101957788
|
G | T | 3 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312 | 3 | HG02109.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.507-380G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101957788 | ||||||
chr11:101957969
|
T | C | 7 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(4): Show | 8 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.507-199T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101957969 | ||||||
chr11:101957979
|
A | G | 7 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(4): Show | 8 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.507-189A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 4/10 | chr11 | 101957979 | ||||||
chr11:101958487
|
G | T | 1 | a0001c0002t0005g0166 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.705+121G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101958487 | ||||||
chr11:101958530
|
AT | A | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.705+170delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr11 | 101958530 | |||||
chr11:101958535
|
T | C | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.705+169T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101958535 | ||||||
chr11:101958880
|
T | A | 120 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(117): Show | 123 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.705+514T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101958880 | ||||||
chr11:101958915
|
G | A | 2 | a0001c0001t0006g0060a0001c0001t0006g0113 | 2 | HG02129.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.705+549G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101958915 | ||||||
chr11:101959115
|
C | T | 2 | a0001c0001t0002g0246a0001c0001t0002g0252 | 2 | NA18966.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.705+749C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959115 | ||||||
chr11:101959197
|
A | C | 1 | a0001c0001t0002g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.705+831A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959197 | ||||||
chr11:101959206
|
G | C | 1 | a0001c0001t0002g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.705+840G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959206 | ||||||
chr11:101959210
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.705+844A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959210 | ||||||
chr11:101959217
|
T | C | 1 | a0001c0001t0002g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.705+851T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959217 | ||||||
chr11:101959220
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.705+854A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959220 | ||||||
chr11:101959234
|
G | A | 1 | a0001c0001t0002g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.705+868G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959234 | ||||||
chr11:101959238
|
C | G | 1 | a0001c0001t0002g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.705+872C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959238 | ||||||
chr11:101959257
|
A | C | 1 | a0001c0001t0002g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.705+891A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959257 | ||||||
chr11:101959258
|
G | A | 1 | a0001c0001t0002g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.705+892G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959258 | ||||||
chr11:101959260
|
A | C | 1 | a0001c0001t0002g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.705+894A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959260 | ||||||
chr11:101959261
|
G | A | 1 | a0001c0001t0002g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.705+895G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959261 | ||||||
chr11:101959274
|
A | G | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.705+908A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959274 | ||||||
chr11:101959278
|
C | G | 1 | a0001c0001t0002g0279 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.705+912C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959278 | ||||||
chr11:101959348
|
G | A | 1 | a0001c0002t0001g0200 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.705+982G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959348 | ||||||
chr11:101959391
|
G | T | 1 | a0001c0001t0063g0131 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.705+1025G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959391 | ||||||
chr11:101959395
|
C | T | 120 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(117): Show | 123 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.705+1029C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959395 | ||||||
chr11:101959400
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.705+1034G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959400 | ||||||
chr11:101959701
|
T | C | 1 | a0001c0002t0001g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.705+1335T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101959701 | ||||||
chr11:101960065
|
A | G | 1 | a0001c0001t0002g0230 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.706-1676A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101960065 | ||||||
chr11:101960142
|
A | T | 2 | a0001c0001t0008g0003a0001c0001t0008g0036 | 3 | HG01243.hp2 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.706-1599A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101960142 | ||||||
chr11:101960172
|
TA | T | 198 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(195): Show | 203 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.706-1566delA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr11 | 101960172 | |||||
chr11:101960232
|
G | A | 54 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(51): Show | 54 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.706-1509G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101960232 | ||||||
chr11:101960499
|
A | G | 2 | a0005c0006t0016g0316a0005c0006t0040g0317 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.706-1242A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101960499 | ||||||
chr11:101960533
|
T | C | 55 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.706-1208T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101960533 | ||||||
chr11:101960638
|
T | C | 1 | a0001c0002t0001g0168 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.706-1103T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101960638 | ||||||
chr11:101960771
|
T | A | 3 | a0004c0005t0005g0111a0004c0005t0005g0115a0004c0005t0005g0121 | 3 | HG02258.hp2 HG02622.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.706-970T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101960771 | ||||||
chr11:101960898
|
A | G | 9 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(6): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.706-843A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101960898 | ||||||
chr11:101961154
|
G | A | 7 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(4): Show | 7 | HG01346.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.706-587G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101961154 | ||||||
chr11:101961195
|
A | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG02970.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.706-546A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101961195 | ||||||
chr11:101961203
|
C | T | 2 | a0001c0001t0036g0303a0001c0001t0037g0302 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.706-538C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101961203 | ||||||
chr11:101961228
|
T | C | 1 | a0002c0003t0003g0069 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.706-513T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101961228 | ||||||
chr11:101961380
|
A | G | 1 | a0001c0001t0002g0284 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.706-361A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101961380 | ||||||
chr11:101961409
|
T | G | 55 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.706-332T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101961409 | ||||||
chr11:101961583
|
T | C | 45 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.706-158T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101961583 | ||||||
chr11:101961584
|
G | A | 1 | a0002c0003t0003g0039 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.706-157G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 5/10 | chr11 | 101961584 | ||||||
chr11:101963893
|
T | G | 1 | a0001c0001t0002g0235 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2845+13T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101963893 | ||||||
chr11:101964019
|
C | T | 5 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(2): Show | 5 | HG01975.hp1 NA18986.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.2845+139C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964019 | ||||||
chr11:101964173
|
C | T | 1 | a0001c0009t0064g0010 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2845+293C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964173 | ||||||
chr11:101964195
|
C | T | 3 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312 | 3 | HG02109.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2845+315C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964195 | ||||||
chr11:101964230
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2845+350G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964230 | ||||||
chr11:101964252
|
G | A | 3 | a0005c0006t0016g0316a0005c0006t0016g0318a0005c0006t0040g0317 | 3 | HG02895.hp1 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2845+372G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964252 | ||||||
chr11:101964320
|
G | A | 48 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0148others(45): Show | 48 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2845+440G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964320 | ||||||
chr11:101964368
|
C | A | 10 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(7): Show | 10 | HG01346.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2845+488C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964368 | ||||||
chr11:101964489
|
C | G | 1 | a0001c0001t0006g0093 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2845+609C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964489 | ||||||
chr11:101964489
|
C | T | 3 | a0001c0001t0006g0119a0001c0001t0006g0120a0001c0001t0006g0127 | 3 | HG00639.hp1 HG01069.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.2845+609C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964489 | ||||||
chr11:101964604
|
A | C | 1 | a0015c0011t0007g0068 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2845+724A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964604 | ||||||
chr11:101964611
|
C | T | 35 | a0001c0001t0002g0205a0001c0001t0002g0207a0001c0001t0002g0218others(32): Show | 35 | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.2845+731C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964611 | ||||||
chr11:101964637
|
T | TA | 11 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(8): Show | 11 | HG01346.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2845+769dupA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 101964637 | |||||
chr11:101964649
|
AC | A | 78 | a0001c0001t0002g0153a0001c0001t0002g0217a0001c0001t0002g0266others(75): Show | 81 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.2845+770delC | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964649 | ||||||
chr11:101964650
|
C | A | 123 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(120): Show | 125 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.2845+770C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964650 | ||||||
chr11:101964653
|
C | A | 1 | a0003c0004t0010g0307 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2845+773C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964653 | ||||||
chr11:101964667
|
C | G | 9 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(6): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2845+787C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964667 | ||||||
chr11:101964668
|
G | A | 1 | a0001c0002t0014g0197 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2845+788G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964668 | ||||||
chr11:101964779
|
A | C | 1 | a0001c0009t0055g0304 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2845+899A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101964779 | ||||||
chr11:101965044
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2845+1164G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101965044 | ||||||
chr11:101965165
|
T | TA | 5 | a0001c0001t0001g0055a0001c0001t0001g0110a0001c0001t0002g0138others(2): Show | 5 | HG02451.hp1 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2845+1288dupA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 101965165 | |||||
chr11:101965206
|
T | C | 1 | a0001c0001t0006g0127 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2845+1326T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101965206 | ||||||
chr11:101966052
|
G | A | 1 | a0001c0001t0063g0131 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2845+2172G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101966052 | ||||||
chr11:101966192
|
A | G | 1 | a0001c0001t0017g0152 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2845+2312A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101966192 | ||||||
chr11:101966323
|
T | C | 1 | a0001c0001t0002g0260 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2845+2443T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101966323 | ||||||
chr11:101966504
|
T | C | 3 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308 | 4 | HG02257.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2845+2624T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101966504 | ||||||
chr11:101966646
|
G | A | 118 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(115): Show | 121 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(118): Show |
intron_variant | MODIFIER | c.2845+2766G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101966646 | ||||||
chr11:101966989
|
T | C | 1 | a0002c0003t0003g0021 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2845+3109T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101966989 | ||||||
chr11:101967022
|
TTTC | T | 44 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.2845+3145_2845+314 others(7): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 101967022 | |||||
chr11:101967025
|
C | CT | 40 | a0001c0001t0001g0046a0001c0001t0001g0056a0001c0001t0001g0059others(37): Show | 41 | HG00673.hp2 HG00738.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.2845+3166dupT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 101967025 | |||||
chr11:101967025
|
CT | C | 8 | a0001c0001t0001g0057a0001c0001t0002g0228a0001c0001t0002g0269others(5): Show | 8 | HG01255.hp1 HG01975.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.2845+3166delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 101967025 | |||||
chr11:101967141
|
A | C | 1 | a0001c0001t0006g0116 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2845+3261A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101967141 | ||||||
chr11:101967209
|
G | T | 1 | a0001c0001t0001g0102 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2845+3329G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101967209 | ||||||
chr11:101967236
|
T | G | 10 | a0001c0001t0004g0203a0001c0001t0004g0213a0001c0001t0004g0214others(7): Show | 11 | HG00323.hp2 HG00642.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.2845+3356T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101967236 | ||||||
chr11:101967415
|
G | A | 3 | a0005c0006t0016g0316a0005c0006t0016g0318a0005c0006t0040g0317 | 3 | HG02895.hp1 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2845+3535G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101967415 | ||||||
chr11:101967418
|
A | G | 7 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(4): Show | 7 | HG01346.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2845+3538A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101967418 | ||||||
chr11:101967505
|
T | A | 1 | a0001c0009t0055g0304 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2845+3625T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101967505 | ||||||
chr11:101967765
|
A | G | 1 | a0001c0001t0002g0228 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2845+3885A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101967765 | ||||||
chr11:101967819
|
A | G | 1 | a0001c0001t0008g0003 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2845+3939A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101967819 | ||||||
chr11:101967896
|
C | T | 48 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0148others(45): Show | 48 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2845+4016C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101967896 | ||||||
chr11:101968025
|
T | G | 1 | a0001c0001t0006g0060 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2845+4145T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101968025 | ||||||
chr11:101968360
|
G | T | 7 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(4): Show | 7 | HG01346.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2845+4480G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101968360 | ||||||
chr11:101968423
|
AAATG | A | 9 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(6): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2845+4546_2845+454 others(8): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 101968423 | |||||
chr11:101968693
|
A | C | 1 | a0001c0009t0055g0304 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2845+4813A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101968693 | ||||||
chr11:101968784
|
G | A | 48 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(45): Show | 48 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.2845+4904G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101968784 | ||||||
chr11:101969193
|
A | G | 45 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.2845+5313A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101969193 | ||||||
chr11:101969240
|
T | C | 55 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.2845+5360T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101969240 | ||||||
chr11:101969312
|
C | G | 1 | a0001c0001t0001g0058 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2845+5432C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101969312 | ||||||
chr11:101969325
|
A | G | 7 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(4): Show | 8 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.2845+5445A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101969325 | ||||||
chr11:101969567
|
C | T | 2 | a0001c0001t0004g0274a0001c0001t0004g0296 | 2 | HG04184.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2845+5687C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101969567 | ||||||
chr11:101969568
|
G | A | 1 | a0001c0001t0063g0131 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2845+5688G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101969568 | ||||||
chr11:101969659
|
A | G | 199 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(196): Show | 204 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.2845+5779A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101969659 | ||||||
chr11:101969689
|
A | C | 7 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(4): Show | 7 | HG01346.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2845+5809A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101969689 | ||||||
chr11:101969719
|
C | T | 3 | a0005c0006t0016g0316a0005c0006t0016g0318a0005c0006t0040g0317 | 3 | HG02895.hp1 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2845+5839C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101969719 | ||||||
chr11:101969829
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2845+5949A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101969829 | ||||||
chr11:101969998
|
T | C | 121 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(118): Show | 124 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(121): Show |
intron_variant | MODIFIER | c.2845+6118T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101969998 | ||||||
chr11:101970111
|
C | A | 1 | a0001c0002t0001g0159 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2845+6231C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101970111 | ||||||
chr11:101970181
|
C | T | 1 | a0001c0001t0017g0234 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2845+6301C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101970181 | ||||||
chr11:101970244
|
G | A | 196 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(193): Show | 201 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.2845+6364G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101970244 | ||||||
chr11:101970340
|
T | C | 17 | a0001c0001t0002g0153a0001c0001t0002g0217a0001c0001t0002g0268others(14): Show | 17 | HG00741.hp1 HG01175.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.2845+6460T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101970340 | ||||||
chr11:101970549
|
CT | C | 6 | a0001c0001t0001g0046a0001c0001t0002g0224a0001c0001t0002g0226others(3): Show | 6 | HG00738.hp1 HG01099.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.2845+6680delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 101970549 | |||||
chr11:101970610
|
T | C | 1 | a0001c0001t0006g0135 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2845+6730T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101970610 | ||||||
chr11:101970653
|
C | T | 45 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.2845+6773C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101970653 | ||||||
chr11:101970705
|
C | A | 55 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.2845+6825C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101970705 | ||||||
chr11:101970840
|
C | T | 1 | a0001c0001t0005g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2845+6960C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101970840 | ||||||
chr11:101970997
|
C | T | 1 | a0001c0001t0034g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2845+7117C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101970997 | ||||||
chr11:101971218
|
G | A | 1 | a0003c0004t0021g0315 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2846-7129G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101971218 | ||||||
chr11:101971316
|
A | AG | 55 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.2846-7031_2846-703 others(5): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101971316 | ||||||
chr11:101971327
|
G | GA | 7 | a0001c0001t0002g0233a0001c0001t0031g0139a0001c0001t0031g0141others(4): Show | 7 | HG02055.hp2 HG02080.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.2846-7010dupA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 101971327 | |||||
chr11:101971535
|
C | T | 2 | a0001c0001t0002g0289a0001c0001t0004g0283 | 2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2846-6812C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101971535 | ||||||
chr11:101971556
|
TTTTG | T | 9 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(6): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2846-6779_2846-677 others(8): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 101971556 | |||||
chr11:101971572
|
T | G | 121 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(118): Show | 124 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(121): Show |
intron_variant | MODIFIER | c.2846-6775T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101971572 | ||||||
chr11:101971660
|
G | A | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.2846-6687G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101971660 | ||||||
chr11:101971838
|
G | T | 3 | a0001c0001t0008g0030a0001c0001t0008g0031a0001c0001t0008g0034 | 3 | HG00323.hp2 HG01891.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.2846-6509G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101971838 | ||||||
chr11:101971867
|
G | A | 1 | a0001c0002t0014g0280 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2846-6480G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101971867 | ||||||
chr11:101971925
|
A | G | 1 | a0001c0002t0001g0200 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2846-6422A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101971925 | ||||||
chr11:101972008
|
C | T | 45 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.2846-6339C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972008 | ||||||
chr11:101972091
|
G | C | 1 | a0001c0001t0004g0052 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2846-6256G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972091 | ||||||
chr11:101972276
|
A | T | 3 | a0006c0008t0030g0040a0006c0008t0030g0041a0012c0015t0035g0032 | 3 | HG03486.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2846-6071A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972276 | ||||||
chr11:101972283
|
G | A | 8 | a0001c0002t0001g0172a0005c0006t0013g0305a0005c0006t0013g0306others(5): Show | 8 | HG00280.hp2 HG01346.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2846-6064G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972283 | ||||||
chr11:101972287
|
G | A | 2 | a0001c0001t0011g0129a0001c0001t0011g0130 | 2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2846-6060G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972287 | ||||||
chr11:101972291
|
T | G | 121 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(118): Show | 124 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(121): Show |
intron_variant | MODIFIER | c.2846-6056T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972291 | ||||||
chr11:101972319
|
G | T | 1 | a0001c0002t0046g0170 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2846-6028G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972319 | ||||||
chr11:101972341
|
G | A | 1 | a0002c0003t0003g0014 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2846-6006G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972341 | ||||||
chr11:101972347
|
T | A | 201 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(198): Show | 206 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.2846-6000T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972347 | ||||||
chr11:101972381
|
G | A | 2 | a0001c0001t0002g0231a0001c0001t0002g0235 | 2 | NA18942.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.2846-5966G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972381 | ||||||
chr11:101972397
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2846-5950G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972397 | ||||||
chr11:101972442
|
A | G | 1 | a0001c0001t0034g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2846-5905A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972442 | ||||||
chr11:101972577
|
C | A | 1 | a0002c0003t0029g0071 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2846-5770C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972577 | ||||||
chr11:101972587
|
G | A | 1 | a0001c0001t0004g0274 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2846-5760G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972587 | ||||||
chr11:101972624
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2846-5723A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972624 | ||||||
chr11:101972658
|
G | A | 1 | a0001c0001t0005g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2846-5689G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972658 | ||||||
chr11:101972669
|
C | T | 6 | a0001c0001t0004g0281a0001c0001t0004g0292a0001c0001t0004g0293others(3): Show | 6 | HG00673.hp2 NA18954.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.2846-5678C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972669 | ||||||
chr11:101972855
|
G | A | 1 | a0001c0001t0009g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2846-5492G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101972855 | ||||||
chr11:101973062
|
G | A | 120 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(117): Show | 123 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.2846-5285G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101973062 | ||||||
chr11:101973089
|
C | T | 7 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(4): Show | 8 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.2846-5258C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101973089 | ||||||
chr11:101973324
|
T | C | 1 | a0006c0008t0030g0040 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2846-5023T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101973324 | ||||||
chr11:101973324
|
T | TA | 7 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(4): Show | 7 | HG01346.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2846-5022dupA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 101973324 | |||||
chr11:101973355
|
T | C | 9 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(6): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2846-4992T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101973355 | ||||||
chr11:101973685
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0100 | 2 | HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2846-4662A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101973685 | ||||||
chr11:101973726
|
A | G | 1 | a0001c0001t0009g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2846-4621A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101973726 | ||||||
chr11:101973993
|
T | C | 1 | a0003c0004t0021g0321 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2846-4354T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101973993 | ||||||
chr11:101973996
|
G | A | 45 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.2846-4351G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101973996 | ||||||
chr11:101974139
|
A | AAC | 9 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(6): Show | 9 | HG01346.hp1 HG02109.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2846-4192_2846-419 others(6): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 101974139 | |||||
chr11:101974160
|
C | CA | 120 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(117): Show | 123 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.2846-4181dupA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 101974160 | |||||
chr11:101974165
|
A | G | 7 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(4): Show | 7 | HG01346.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2846-4182A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101974165 | ||||||
chr11:101974313
|
G | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0056 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2846-4034G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101974313 | ||||||
chr11:101974371
|
A | G | 2 | a0001c0001t0002g0051a0001c0001t0026g0053 | 2 | HG02129.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.2846-3976A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101974371 | ||||||
chr11:101974380
|
A | G | 55 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.2846-3967A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101974380 | ||||||
chr11:101974604
|
A | G | 48 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(45): Show | 48 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.2846-3743A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101974604 | ||||||
chr11:101975099
|
A | C | 2 | a0001c0001t0033g0275a0001c0001t0033g0286 | 2 | HG00323.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2846-3248A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101975099 | ||||||
chr11:101975332
|
T | C | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2846-3015T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101975332 | ||||||
chr11:101975481
|
C | A | 2 | a0001c0001t0011g0129a0001c0001t0011g0130 | 2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2846-2866C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101975481 | ||||||
chr11:101975979
|
C | A | 2 | a0001c0001t0002g0246a0001c0001t0002g0252 | 2 | NA18966.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2846-2368C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101975979 | ||||||
chr11:101976117
|
G | C | 1 | a0001c0001t0009g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2846-2230G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101976117 | ||||||
chr11:101976175
|
T | C | 1 | a0012c0015t0035g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2846-2172T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101976175 | ||||||
chr11:101976230
|
C | T | 3 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312 | 3 | HG02109.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2846-2117C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101976230 | ||||||
chr11:101976576
|
A | T | 1 | a0001c0001t0001g0081 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2846-1771A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101976576 | ||||||
chr11:101976594
|
T | C | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2846-1753T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101976594 | ||||||
chr11:101976610
|
G | A | 43 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(40): Show | 43 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.2846-1737G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101976610 | ||||||
chr11:101976619
|
G | T | 16 | a0001c0001t0002g0153a0001c0001t0002g0268a0001c0001t0002g0276others(13): Show | 16 | HG01175.hp2 HG01192.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.2846-1728G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101976619 | ||||||
chr11:101977000
|
C | G | 4 | a0003c0004t0021g0315a0003c0004t0021g0321a0003c0004t0052g0319others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2846-1347C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101977000 | ||||||
chr11:101977043
|
G | A | 1 | a0001c0001t0006g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2846-1304G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101977043 | ||||||
chr11:101977328
|
TA | T | 3 | a0005c0006t0016g0316a0005c0006t0016g0318a0005c0006t0040g0317 | 3 | HG02895.hp1 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2846-1018delA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101977328 | ||||||
chr11:101977448
|
T | A | 4 | a0001c0002t0001g0150a0001c0002t0001g0158a0001c0002t0001g0159others(1): Show | 4 | HG01361.hp2 HG01496.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2846-899T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101977448 | ||||||
chr11:101977503
|
C | T | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2846-844C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101977503 | ||||||
chr11:101977549
|
T | G | 2 | a0005c0006t0016g0316a0005c0006t0040g0317 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2846-798T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101977549 | ||||||
chr11:101977630
|
C | CA | 12 | a0001c0001t0002g0228a0001c0001t0002g0247a0001c0001t0002g0269others(9): Show | 12 | HG01192.hp1 HG02451.hp2 HG02970.hp1 others(9): Show |
intron_variant | MODIFIER | c.2846-697dupA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 101977630 | |||||
chr11:101977755
|
T | G | 2 | a0006c0008t0030g0040a0006c0008t0030g0041 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2846-592T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101977755 | ||||||
chr11:101977820
|
A | G | 4 | a0001c0001t0036g0303a0001c0001t0037g0302a0001c0009t0055g0304others(1): Show | 4 | HG02451.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2846-527A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101977820 | ||||||
chr11:101977878
|
C | G | 1 | a0011c0017t0001g0095 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2846-469C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101977878 | ||||||
chr11:101978152
|
G | A | 7 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(4): Show | 7 | HG01346.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2846-195G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101978152 | ||||||
chr11:101978259
|
A | G | 204 | a0001c0001t0001g0059a0001c0001t0002g0051a0001c0001t0002g0054others(201): Show | 209 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.2846-88A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101978259 | ||||||
chr11:101978332
|
T | C | 4 | a0001c0001t0036g0303a0001c0001t0037g0302a0001c0009t0055g0304others(1): Show | 4 | HG02451.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2846-15T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 6/10 | chr11 | 101978332 | ||||||
chr11:101978621
|
G | A | 3 | a0002c0003t0003g0012a0002c0003t0003g0019a0002c0003t0007g0027 | 3 | HG00423.hp1 NA18947.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2958+162G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101978621 | ||||||
chr11:101978629
|
TC | T | 7 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(4): Show | 7 | HG01346.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2958+172delC | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 101978629 | |||||
chr11:101978653
|
C | T | 3 | a0006c0008t0030g0040a0006c0008t0030g0041a0012c0015t0035g0032 | 3 | HG03486.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2958+194C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101978653 | ||||||
chr11:101978862
|
C | G | 1 | a0001c0001t0063g0131 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2958+403C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101978862 | ||||||
chr11:101978988
|
CA | C | 8 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(5): Show | 9 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.2958+530delA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101978988 | ||||||
chr11:101978995
|
G | A | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2958+536G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101978995 | ||||||
chr11:101979072
|
C | T | 45 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.2958+613C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101979072 | ||||||
chr11:101979092
|
A | G | 2 | a0001c0001t0011g0129a0001c0001t0011g0130 | 2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2958+633A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101979092 | ||||||
chr11:101979133
|
A | G | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2958+674A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101979133 | ||||||
chr11:101979245
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2958+786G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101979245 | ||||||
chr11:101979363
|
C | T | 7 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(4): Show | 7 | HG01346.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2958+904C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101979363 | ||||||
chr11:101979451
|
C | T | 4 | a0001c0001t0031g0139a0001c0001t0031g0141a0001c0001t0032g0140others(1): Show | 4 | HG02055.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2958+992C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101979451 | ||||||
chr11:101979477
|
G | C | 7 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(4): Show | 7 | HG01346.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2958+1018G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101979477 | ||||||
chr11:101979575
|
T | C | 1 | a0003c0004t0021g0315 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2958+1116T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101979575 | ||||||
chr11:101979645
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2958+1186G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101979645 | ||||||
chr11:101979663
|
A | G | 1 | a0001c0001t0034g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2958+1204A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101979663 | ||||||
chr11:101979736
|
T | A | 3 | a0001c0001t0001g0055a0001c0001t0001g0110a0001c0001t0002g0138 | 3 | HG02886.hp1 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2958+1277T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101979736 | ||||||
chr11:101979749
|
T | C | 3 | a0006c0008t0030g0040a0006c0008t0030g0041a0012c0015t0035g0032 | 3 | HG03486.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2958+1290T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101979749 | ||||||
chr11:101979877
|
A | G | 1 | a0009c0016t0002g0229 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2958+1418A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101979877 | ||||||
chr11:101980146
|
A | G | 195 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(192): Show | 200 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.2958+1687A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101980146 | ||||||
chr11:101980149
|
T | G | 2 | a0001c0001t0002g0289a0001c0001t0004g0283 | 2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2958+1690T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101980149 | ||||||
chr11:101980294
|
A | T | 1 | a0001c0001t0006g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2959-1595A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101980294 | ||||||
chr11:101980605
|
A | T | 1 | a0001c0002t0005g0166 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2959-1284A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101980605 | ||||||
chr11:101980669
|
G | A | 3 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312 | 3 | HG02109.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2959-1220G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101980669 | ||||||
chr11:101980746
|
C | G | 118 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(115): Show | 121 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(118): Show |
intron_variant | MODIFIER | c.2959-1143C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101980746 | ||||||
chr11:101980818
|
C | T | 8 | a0001c0002t0001g0148a0001c0002t0001g0150a0001c0002t0001g0158others(5): Show | 8 | HG00597.hp1 HG01361.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959-1071C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101980818 | ||||||
chr11:101980827
|
C | T | 1 | a0001c0001t0002g0258 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2959-1062C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101980827 | ||||||
chr11:101980849
|
A | G | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2959-1040A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101980849 | ||||||
chr11:101980942
|
C | T | 1 | a0001c0001t0006g0114 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2959-947C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101980942 | ||||||
chr11:101981168
|
A | ATAAT | 48 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(45): Show | 48 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.2959-718_2959-715d others(6): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 101981168 | |||||
chr11:101981169
|
T | C | 1 | a0001c0002t0005g0176 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2959-720T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101981169 | ||||||
chr11:101981216
|
T | C | 1 | a0002c0003t0003g0039 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2959-673T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101981216 | ||||||
chr11:101981221
|
A | G | 199 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(196): Show | 204 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.2959-668A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101981221 | ||||||
chr11:101981235
|
C | A | 1 | a0001c0002t0001g0174 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2959-654C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101981235 | ||||||
chr11:101981494
|
C | T | 3 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312 | 3 | HG02109.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2959-395C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101981494 | ||||||
chr11:101981515
|
G | A | 5 | a0001c0001t0002g0231a0001c0001t0002g0235a0001c0001t0002g0237others(2): Show | 5 | NA18942.hp1 NA18982.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2959-374G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101981515 | ||||||
chr11:101981583
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2959-306G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101981583 | ||||||
chr11:101981795
|
AT | A | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2959-93delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101981795 | ||||||
chr11:101981801
|
A | G | 1 | a0003c0004t0038g0314 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2959-88A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 7/10 | chr11 | 101981801 | ||||||
chr11:101982071
|
T | C | 1 | a0009c0016t0002g0229 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3034+107T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101982071 | ||||||
chr11:101982427
|
T | C | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3034+463T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101982427 | ||||||
chr11:101982463
|
T | C | 1 | a0001c0001t0034g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3034+499T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101982463 | ||||||
chr11:101982466
|
T | C | 1 | a0001c0002t0001g0169 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3034+502T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101982466 | ||||||
chr11:101982471
|
A | G | 9 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(6): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.3034+507A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101982471 | ||||||
chr11:101982834
|
A | T | 1 | a0012c0015t0035g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3034+870A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101982834 | ||||||
chr11:101982845
|
A | G | 1 | a0009c0016t0002g0229 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3034+881A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101982845 | ||||||
chr11:101982887
|
T | C | 48 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0148others(45): Show | 48 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.3034+923T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101982887 | ||||||
chr11:101983059
|
G | A | 3 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308 | 4 | HG02257.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.3034+1095G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101983059 | ||||||
chr11:101983389
|
T | TA | 55 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.3034+1425_3034+142 others(5): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101983389 | ||||||
chr11:101983712
|
G | T | 1 | a0001c0001t0050g0066 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3034+1748G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101983712 | ||||||
chr11:101983808
|
A | G | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3034+1844A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101983808 | ||||||
chr11:101983821
|
T | A | 1 | a0001c0002t0001g0169 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3034+1857T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101983821 | ||||||
chr11:101984383
|
T | G | 1 | a0001c0001t0006g0091 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3034+2419T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101984383 | ||||||
chr11:101984426
|
A | G | 2 | a0001c0001t0001g0089a0001c0001t0005g0098 | 2 | NA18985.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.3035-2406A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101984426 | ||||||
chr11:101984857
|
A | G | 3 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312 | 3 | HG02109.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3035-1975A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101984857 | ||||||
chr11:101984903
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3035-1929T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101984903 | ||||||
chr11:101984948
|
A | G | 8 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(5): Show | 9 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.3035-1884A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101984948 | ||||||
chr11:101985099
|
GAGTCAGG others(6): Show |
G | 2 | a0001c0001t0008g0031a0001c0001t0008g0034 | 2 | HG00323.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.3035-1729_3035-171 others(17): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 101985099 | |||||
chr11:101985286
|
CT | C | 12 | a0001c0001t0001g0057a0001c0001t0001g0083a0001c0001t0001g0088others(9): Show | 12 | HG02055.hp2 HG02886.hp2 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.3035-1531delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 101985286 | |||||
chr11:101985483
|
A | G | 1 | a0001c0001t0002g0278 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3035-1349A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101985483 | ||||||
chr11:101985697
|
C | T | 199 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(196): Show | 204 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.3035-1135C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101985697 | ||||||
chr11:101985743
|
G | A | 7 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(4): Show | 8 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.3035-1089G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101985743 | ||||||
chr11:101985899
|
G | A | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3035-933G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101985899 | ||||||
chr11:101985988
|
A | AT | 22 | a0001c0001t0002g0204a0001c0001t0002g0247a0001c0001t0004g0253others(19): Show | 22 | HG00423.hp2 HG00597.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.3035-841dupT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 101985988 | |||||
chr11:101985988
|
A | ATT | 4 | a0001c0002t0005g0179a0001c0009t0055g0304a0002c0003t0003g0145others(1): Show | 4 | HG01069.hp2 HG03471.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.3035-842_3035-841d others(4): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 101985988 | |||||
chr11:101985988
|
A | ATTT | 37 | a0001c0009t0064g0010a0002c0003t0003g0002a0002c0003t0003g0011others(34): Show | 37 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.3035-843_3035-841d others(5): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 101985988 | |||||
chr11:101985988
|
A | ATTTT | 7 | a0002c0003t0003g0014a0002c0003t0003g0016a0002c0003t0007g0013others(4): Show | 7 | HG00673.hp1 NA18966.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.3035-841_3035-840i others(6): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 101985988 | |||||
chr11:101985990
|
TTC | T | 7 | a0001c0001t0002g0276a0001c0001t0002g0291a0001c0001t0004g0213others(4): Show | 7 | HG02083.hp2 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3035-840_3035-839d others(4): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 101985990 | |||||
chr11:101985991
|
TC | T | 43 | a0001c0001t0002g0153a0001c0001t0002g0217a0001c0001t0002g0233others(40): Show | 47 | HG00323.hp2 HG00642.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.3035-840delC | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101985991 | ||||||
chr11:101985992
|
C | T | 200 | a0001c0001t0001g0055a0001c0001t0002g0051a0001c0001t0002g0054others(197): Show | 201 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.3035-840C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101985992 | ||||||
chr11:101986082
|
A | G | 1 | a0001c0001t0004g0254 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3035-750A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101986082 | ||||||
chr11:101986474
|
A | G | 1 | a0013c0018t0015g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3035-358A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101986474 | ||||||
chr11:101986487
|
T | C | 1 | a0001c0001t0034g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3035-345T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101986487 | ||||||
chr11:101986611
|
G | T | 7 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(4): Show | 7 | HG01346.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3035-221G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101986611 | ||||||
chr11:101986613
|
C | T | 1 | a0001c0002t0014g0197 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3035-219C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101986613 | ||||||
chr11:101986624
|
A | G | 3 | a0001c0002t0001g0177a0001c0002t0005g0178a0001c0002t0044g0264 | 3 | NA18950.hp2 NA19070.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.3035-208A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 8/10 | chr11 | 101986624 | ||||||
chr11:101987183
|
C | T | 5 | a0001c0009t0055g0304a0001c0009t0064g0010a0006c0008t0030g0040others(2): Show | 5 | HG03098.hp1 HG03471.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3244+142C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101987183 | ||||||
chr11:101987251
|
T | C | 1 | a0001c0001t0032g0142 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3244+210T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101987251 | ||||||
chr11:101987562
|
G | A | 2 | a0006c0008t0030g0040a0006c0008t0030g0041 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3244+521G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101987562 | ||||||
chr11:101987568
|
C | A | 44 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.3244+527C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101987568 | ||||||
chr11:101987665
|
TA | T | 270 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0055others(267): Show | 275 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.3244+638delA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 101987665 | |||||
chr11:101987682
|
C | T | 1 | a0002c0003t0007g0020 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3244+641C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101987682 | ||||||
chr11:101987953
|
G | A | 1 | a0003c0004t0010g0308 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3244+912G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101987953 | ||||||
chr11:101987967
|
T | TAAAA | 51 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.3244+932_3244+935d others(6): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 101987967 | |||||
chr11:101988025
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3244+984A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101988025 | ||||||
chr11:101988176
|
A | T | 5 | a0001c0001t0001g0085a0001c0001t0001g0088a0001c0001t0005g0042others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3244+1135A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101988176 | ||||||
chr11:101988212
|
A | G | 7 | a0002c0003t0003g0069a0002c0003t0003g0070a0002c0003t0003g0073others(4): Show | 7 | HG00408.hp2 HG00621.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.3244+1171A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101988212 | ||||||
chr11:101988308
|
C | T | 4 | a0001c0001t0006g0120a0001c0001t0008g0030a0001c0001t0008g0031others(1): Show | 4 | HG00323.hp2 HG00639.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.3244+1267C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101988308 | ||||||
chr11:101988386
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3244+1345T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101988386 | ||||||
chr11:101988490
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3244+1449T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101988490 | ||||||
chr11:101988778
|
G | GTA | 117 | a0001c0001t0001g0106a0001c0001t0001g0136a0001c0001t0001g0137others(114): Show | 120 | HG00597.hp2 HG00621.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.3244+1753_3244+175 others(6): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 101988778 | |||||
chr11:101988778
|
G | GTATA | 6 | a0001c0001t0009g0300a0001c0001t0009g0301a0001c0001t0031g0139others(3): Show | 6 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.3244+1751_3244+175 others(8): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 101988778 | |||||
chr11:101988778
|
G | GTATATA | 11 | a0001c0001t0002g0205a0001c0001t0002g0258a0001c0001t0004g0281others(8): Show | 11 | HG00408.hp1 HG00673.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.3244+1749_3244+175 others(10): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 101988778 | |||||
chr11:101988778
|
GTA | G | 10 | a0001c0002t0044g0264a0003c0004t0010g0009a0003c0004t0010g0307others(7): Show | 11 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.3244+1753_3244+175 others(6): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 101988778 | |||||
chr11:101989007
|
C | G | 1 | a0001c0001t0009g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3244+1966C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101989007 | ||||||
chr11:101989035
|
G | A | 2 | a0002c0003t0003g0126a0002c0003t0007g0074 | 2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.3244+1994G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101989035 | ||||||
chr11:101989060
|
G | A | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3244+2019G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101989060 | ||||||
chr11:101989069
|
C | A | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3244+2028C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101989069 | ||||||
chr11:101989128
|
C | T | 1 | a0001c0001t0002g0138 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3244+2087C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101989128 | ||||||
chr11:101989257
|
G | T | 1 | a0001c0001t0002g0138 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3244+2216G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101989257 | ||||||
chr11:101989293
|
T | C | 204 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(201): Show | 209 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.3244+2252T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101989293 | ||||||
chr11:101989352
|
G | A | 3 | a0006c0008t0030g0040a0006c0008t0030g0041a0012c0015t0035g0032 | 3 | HG03486.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3244+2311G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101989352 | ||||||
chr11:101989502
|
A | G | 200 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(197): Show | 205 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.3244+2461A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101989502 | ||||||
chr11:101989520
|
T | C | 1 | a0001c0002t0001g0149 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3244+2479T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101989520 | ||||||
chr11:101989586
|
A | C | 1 | a0001c0001t0006g0116 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3244+2545A>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101989586 | ||||||
chr11:101989674
|
A | G | 2 | a0001c0001t0006g0044a0001c0001t0006g0061 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3244+2633A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101989674 | ||||||
chr11:101989807
|
C | A | 6 | a0003c0004t0010g0322a0003c0004t0021g0315a0003c0004t0021g0321others(3): Show | 6 | HG01109.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.3244+2766C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101989807 | ||||||
chr11:101990034
|
G | C | 3 | a0002c0003t0003g0012a0002c0003t0003g0019a0002c0003t0007g0027 | 3 | HG00423.hp1 NA18947.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.3245-2744G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101990034 | ||||||
chr11:101990039
|
A | AGGGAAAT others(28): Show |
7 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(4): Show | 7 | HG01346.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3245-2706_3245-270 others(39): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 101990039 | |||||
chr11:101990315
|
G | T | 1 | a0001c0001t0001g0057 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3245-2463G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101990315 | ||||||
chr11:101990337
|
C | G | 1 | a0001c0009t0055g0304 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3245-2441C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101990337 | ||||||
chr11:101990431
|
A | T | 9 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(6): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.3245-2347A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101990431 | ||||||
chr11:101990532
|
T | G | 1 | a0001c0001t0001g0082 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3245-2246T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101990532 | ||||||
chr11:101990658
|
C | T | 9 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(6): Show | 11 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.3245-2120C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101990658 | ||||||
chr11:101990688
|
C | G | 2 | a0001c0002t0001g0156a0001c0002t0005g0161 | 2 | HG04199.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.3245-2090C>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101990688 | ||||||
chr11:101990738
|
A | G | 62 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(59): Show | 62 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.3245-2040A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101990738 | ||||||
chr11:101990802
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3245-1976A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101990802 | ||||||
chr11:101990808
|
G | A | 198 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(195): Show | 203 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.3245-1970G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101990808 | ||||||
chr11:101991158
|
C | T | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3245-1620C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101991158 | ||||||
chr11:101991203
|
G | A | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3245-1575G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101991203 | ||||||
chr11:101991566
|
G | A | 120 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(117): Show | 123 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.3245-1212G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101991566 | ||||||
chr11:101991811
|
C | A | 4 | a0002c0003t0003g0016a0002c0003t0003g0023a0002c0003t0007g0013others(1): Show | 4 | HG00673.hp1 NA18973.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.3245-967C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101991811 | ||||||
chr11:101991819
|
G | A | 2 | a0001c0001t0036g0303a0001c0001t0037g0302 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3245-959G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101991819 | ||||||
chr11:101992055
|
T | C | 1 | a0001c0001t0031g0141 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3245-723T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101992055 | ||||||
chr11:101992153
|
T | A | 1 | a0001c0001t0023g0282 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3245-625T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101992153 | ||||||
chr11:101992153
|
T | TA | 47 | a0001c0001t0012g0309a0001c0001t0012g0310a0002c0003t0003g0002others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3245-616dupA | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 101992153 | |||||
chr11:101992167
|
AAGC | A | 120 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(117): Show | 123 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.3245-608_3245-606d others(5): Show |
CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 101992167 | |||||
chr11:101992182
|
A | G | 45 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.3245-596A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101992182 | ||||||
chr11:101992190
|
C | A | 2 | a0001c0002t0001g0165a0001c0002t0005g0166 | 2 | HG01981.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.3245-588C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101992190 | ||||||
chr11:101992295
|
T | A | 1 | a0003c0004t0010g0307 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3245-483T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101992295 | ||||||
chr11:101992504
|
G | C | 1 | a0001c0001t0001g0083 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3245-274G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101992504 | ||||||
chr11:101992529
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3245-249A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 9/10 | chr11 | 101992529 | ||||||
chr11:101992963
|
T | A | 55 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.3309+121T>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101992963 | ||||||
chr11:101992975
|
C | T | 202 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(199): Show | 207 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.3309+133C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101992975 | ||||||
chr11:101993022
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3309+180G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101993022 | ||||||
chr11:101993094
|
G | C | 2 | a0001c0001t0062g0215a0001c0009t0064g0010 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3309+252G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101993094 | ||||||
chr11:101993151
|
T | C | 48 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(45): Show | 48 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.3309+309T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101993151 | ||||||
chr11:101993251
|
G | A | 2 | a0001c0001t0002g0256a0001c0001t0006g0125 | 2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.3309+409G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101993251 | ||||||
chr11:101993356
|
C | T | 45 | a0002c0003t0003g0002a0002c0003t0003g0011a0002c0003t0003g0012others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.3309+514C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101993356 | ||||||
chr11:101993408
|
G | T | 2 | a0006c0008t0030g0040a0006c0008t0030g0041 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3309+566G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101993408 | ||||||
chr11:101993570
|
G | A | 49 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(46): Show | 49 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.3309+728G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101993570 | ||||||
chr11:101993716
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3309+874G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101993716 | ||||||
chr11:101993895
|
T | C | 1 | a0001c0001t0041g0122 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3309+1053T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101993895 | ||||||
chr11:101993991
|
T | C | 3 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311 | 3 | HG02451.hp2 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.3309+1149T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101993991 | ||||||
chr11:101994122
|
C | A | 4 | a0003c0004t0021g0315a0003c0004t0021g0321a0003c0004t0052g0319others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3309+1280C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101994122 | ||||||
chr11:101994262
|
A | G | 1 | a0001c0001t0042g0080 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3309+1420A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101994262 | ||||||
chr11:101994365
|
T | C | 2 | a0001c0001t0062g0215a0001c0009t0064g0010 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3309+1523T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101994365 | ||||||
chr11:101994506
|
C | T | 50 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.3309+1664C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101994506 | ||||||
chr11:101994535
|
A | G | 1 | a0007c0007t0007g0048 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.3309+1693A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101994535 | ||||||
chr11:101994537
|
G | T | 204 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(201): Show | 209 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.3309+1695G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101994537 | ||||||
chr11:101994629
|
C | T | 1 | a0001c0001t0050g0066 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3309+1787C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101994629 | ||||||
chr11:101994630
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3309+1788G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101994630 | ||||||
chr11:101994758
|
C | T | 2 | a0006c0008t0030g0040a0006c0008t0030g0041 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3309+1916C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101994758 | ||||||
chr11:101994852
|
A | G | 1 | a0001c0002t0001g0262 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3309+2010A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101994852 | ||||||
chr11:101994872
|
G | GT | 199 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(196): Show | 204 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(201): Show |
intron_variant | MODIFIER | c.3309+2044dupT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 101994872 | |||||
chr11:101994872
|
GT | G | 6 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(3): Show | 6 | HG01975.hp1 HG01975.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.3309+2044delT | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr11 | 101994872 | |||||
chr11:101994955
|
G | A | 48 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(45): Show | 48 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.3309+2113G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101994955 | ||||||
chr11:101995119
|
C | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0056 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3309+2277C>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101995119 | ||||||
chr11:101995312
|
T | G | 1 | a0001c0001t0060g0222 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3310-2287T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101995312 | ||||||
chr11:101995485
|
C | T | 121 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(118): Show | 124 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(121): Show |
intron_variant | MODIFIER | c.3310-2114C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101995485 | ||||||
chr11:101995537
|
C | T | 1 | a0009c0016t0002g0229 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3310-2062C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101995537 | ||||||
chr11:101995579
|
C | T | 1 | a0001c0001t0034g0128 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3310-2020C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101995579 | ||||||
chr11:101995761
|
A | G | 1 | a0001c0002t0001g0326 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3310-1838A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101995761 | ||||||
chr11:101995986
|
G | C | 2 | a0001c0002t0001g0168a0001c0002t0005g0157 | 2 | NA18943.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.3310-1613G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101995986 | ||||||
chr11:101996049
|
G | T | 4 | a0001c0001t0002g0266a0001c0001t0002g0294a0001c0001t0004g0267others(1): Show | 4 | HG01123.hp2 HG02280.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3310-1550G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101996049 | ||||||
chr11:101996053
|
G | C | 1 | a0001c0002t0001g0169 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3310-1546G>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101996053 | ||||||
chr11:101996150
|
C | T | 3 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312 | 3 | HG02109.hp1 HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3310-1449C>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101996150 | ||||||
chr11:101996257
|
T | G | 1 | a0012c0015t0035g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3310-1342T>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101996257 | ||||||
chr11:101996355
|
T | C | 9 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(6): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.3310-1244T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101996355 | ||||||
chr11:101996383
|
G | A | 4 | a0001c0001t0031g0139a0001c0001t0031g0141a0001c0001t0032g0140others(1): Show | 4 | HG02055.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3310-1216G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101996383 | ||||||
chr11:101996423
|
A | G | 7 | a0005c0006t0013g0305a0005c0006t0013g0306a0005c0006t0013g0312others(4): Show | 7 | HG01346.hp1 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3310-1176A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101996423 | ||||||
chr11:101996526
|
T | C | 2 | a0001c0001t0062g0215a0001c0009t0064g0010 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3310-1073T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101996526 | ||||||
chr11:101996531
|
T | C | 48 | a0001c0001t0012g0309a0001c0001t0012g0310a0001c0001t0012g0311others(45): Show | 48 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.3310-1068T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101996531 | ||||||
chr11:101996533
|
G | T | 120 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(117): Show | 123 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.3310-1066G>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101996533 | ||||||
chr11:101996865
|
G | A | 129 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(126): Show | 133 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(130): Show |
intron_variant | MODIFIER | c.3310-734G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101996865 | ||||||
chr11:101996927
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3310-672G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101996927 | ||||||
chr11:101997218
|
A | T | 9 | a0003c0004t0010g0009a0003c0004t0010g0307a0003c0004t0010g0308others(6): Show | 10 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.3310-381A>T | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101997218 | ||||||
chr11:101997222
|
G | A | 1 | a0001c0002t0001g0159 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3310-377G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101997222 | ||||||
chr11:101997239
|
T | C | 120 | a0001c0001t0002g0051a0001c0001t0002g0054a0001c0001t0002g0079others(117): Show | 123 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.3310-360T>C | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101997239 | ||||||
chr11:101997388
|
A | G | 8 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0031others(5): Show | 9 | HG00323.hp2 HG00642.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.3310-211A>G | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101997388 | ||||||
chr11:101997484
|
G | A | 4 | a0001c0001t0031g0139a0001c0001t0031g0141a0001c0001t0032g0140others(1): Show | 4 | HG02055.hp2 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3310-115G>A | CEP126 | ENSG00000110318.15 | transcript | ENST00000263468.13 | protein_coding | 10/10 | chr11 | 101997484 |