geneid | 9731 |
---|---|
ensemblid | ENSG00000116198.14 |
hgncid | 24866 |
symbol | CEP104 |
name | centrosomal protein 104 |
refseq_nuc | NM_014704.4 |
refseq_prot | NP_055519.1 |
ensembl_nuc | ENST00000378230.8 |
ensembl_prot | ENSP00000367476.3 |
mane_status | MANE Select |
chr | chr1 |
start | 3812086 |
end | 3857211 |
strand | - |
ver | v1.2 |
region | chr1:3812086-3857211 |
region5000 | chr1:3807086-3862211 |
regionname0 | CEP104_chr1_3812086_3857211 |
regionname5000 | CEP104_chr1_3807086_3862211 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 925 | 137 | 67 | 26 | 20 | 8 | 14 | 16 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0002 | 0/0 | 925 | 130 | 6 | 37 | 66 | 4 | 17 | 48 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0003 | 0/0 | 925 | 96 | 6 | 14 | 61 | 1 | 14 | 48 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0004 | 0/0 | 925 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0005 | 0/0 | 925 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0006 | 0/0 | 925 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0007 | 0/0 | 925 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0008 | 0/0 | 925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0009 | 0/0 | 925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0010 | 0/0 | 925 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0011 | 0/0 | 925 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0012 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0013 | 0/0 | 925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0014 | 0/0 | 925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0015 | 0/0 | 925 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0016 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0017 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0018 | 0/0 | 925 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2778 | 126 | 57 | 26 | 20 | 8 | 14 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0002 | 0/0 | 2778 | 113 | 6 | 26 | 60 | 4 | 17 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0003 | 0/0 | 2778 | 76 | 6 | 14 | 41 | 1 | 14 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0004 | 0/0 | 2778 | 20 | 0 | 0 | 20 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0005 | 0/0 | 2778 | 16 | 0 | 10 | 6 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0006 | 0/0 | 2778 | 10 | 10 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0007 | 0/0 | 2778 | 3 | 3 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0008 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0009 | 0/0 | 2778 | 2 | 0 | 0 | 2 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0010 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0011 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0012 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0013 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0014 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0015 | 1/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0016 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0017 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0018 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0019 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0020 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0021 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0022 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
c0023 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3654 | 125 | 6 | 36 | 60 | 5 | 18 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0002 | 0/0 | 3656 | 86 | 2 | 12 | 58 | 1 | 13 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0003 | 0/0 | 3656 | 42 | 23 | 11 | 0 | 1 | 7 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0004 | 0/1 | 3656 | 27 | 10 | 8 | 0 | 2 | 6 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0005 | 0/0 | 3656 | 16 | 0 | 2 | 14 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0006 | 0/0 | 3657 | 10 | 10 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0007 | 0/0 | 3656 | 9 | 9 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0008 | 0/0 | 3652 | 9 | 5 | 1 | 3 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0009 | 0/0 | 3656 | 9 | 8 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0010 | 0/0 | 3656 | 7 | 0 | 2 | 2 | 3 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0011 | 0/0 | 3654 | 3 | 0 | 0 | 3 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0012 | 0/0 | 3656 | 3 | 0 | 0 | 1 | 0 | 2 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0013 | 0/0 | 3656 | 2 | 2 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0014 | 0/0 | 3656 | 2 | 1 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0015 | 0/0 | 3658 | 2 | 2 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0016 | 0/0 | 3656 | 2 | 2 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0017 | 0/0 | 3655 | 2 | 0 | 0 | 2 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0018 | 0/0 | 3656 | 2 | 0 | 0 | 2 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0019 | 0/0 | 3656 | 2 | 0 | 0 | 2 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0020 | 0/0 | 3658 | 2 | 0 | 2 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0021 | 0/0 | 3656 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0022 | 0/0 | 3654 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0023 | 0/0 | 3654 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0024 | 0/0 | 3654 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0025 | 0/0 | 3654 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0026 | 0/0 | 3656 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0027 | 0/0 | 3657 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0028 | 0/0 | 3656 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0029 | 0/0 | 3656 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0030 | 0/0 | 3656 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0031 | 1/0 | 3654 | 1 | 0 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0032 | 0/0 | 3656 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0033 | 0/0 | 3655 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0034 | 0/0 | 3656 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0035 | 0/0 | 3656 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0036 | 0/0 | 3656 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0037 | 0/0 | 3656 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0038 | 0/0 | 3656 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0039 | 0/0 | 3656 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
t0040 | 0/0 | 3656 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0002 | 0/1 | 6 | 1 | 2 | 0 | 0 | 2 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0004 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0005 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0010 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0219 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2778 | 126 | 57 | 26 | 20 | 8 | 14 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0006 | 0/0 | 2778 | 10 | 10 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0015 | 1/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0002c0002 | 0/0 | 2778 | 113 | 6 | 26 | 60 | 4 | 17 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0002c0005 | 0/0 | 2778 | 16 | 0 | 10 | 6 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0002c0012 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0003c0003 | 0/0 | 2778 | 76 | 6 | 14 | 41 | 1 | 14 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0003c0004 | 0/0 | 2778 | 20 | 0 | 0 | 20 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0004c0007 | 0/0 | 2778 | 3 | 3 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0005c0008 | 0/0 | 2778 | 2 | 2 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0006c0009 | 0/0 | 2778 | 2 | 0 | 0 | 2 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0007c0011 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0008c0013 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0009c0014 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0010c0020 | 0/0 | 2778 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0011c0018 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0012c0019 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0013c0016 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0014c0017 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0015c0021 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0016c0022 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0017c0023 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0018c0010 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003 | 0/0 | 6433 | 40 | 23 | 10 | 0 | 1 | 6 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0004 | 0/1 | 6433 | 26 | 9 | 8 | 0 | 2 | 6 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0005 | 0/0 | 6433 | 16 | 0 | 2 | 14 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0007 | 0/0 | 6433 | 9 | 9 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0008 | 0/0 | 6429 | 9 | 5 | 1 | 3 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0009 | 0/0 | 6433 | 6 | 5 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0010 | 0/0 | 6433 | 6 | 0 | 2 | 1 | 3 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0013 | 0/0 | 6433 | 2 | 2 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0020 | 0/0 | 6435 | 2 | 0 | 2 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0026 | 0/0 | 6433 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0027 | 0/0 | 6434 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0028 | 0/0 | 6433 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0033 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0035 | 0/0 | 6433 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0036 | 0/0 | 6433 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0037 | 0/0 | 6433 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0038 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0039 | 0/0 | 6433 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0001t0040 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0006t0006 | 0/0 | 6434 | 9 | 9 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0006t0021 | 0/0 | 6433 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0001c0015t0031 | 1/0 | 6431 | 1 | 0 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0002c0002t0001 | 0/0 | 6431 | 106 | 6 | 25 | 54 | 4 | 17 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0002c0002t0011 | 0/0 | 6431 | 3 | 0 | 0 | 3 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0002c0002t0022 | 0/0 | 6431 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0002c0002t0023 | 0/0 | 6431 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0002c0002t0024 | 0/0 | 6431 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0002c0002t0025 | 0/0 | 6431 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0002c0005t0001 | 0/0 | 6431 | 16 | 0 | 10 | 6 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0002c0012t0001 | 0/0 | 6431 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0003c0003t0002 | 0/0 | 6433 | 64 | 2 | 12 | 37 | 1 | 12 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0003c0003t0012 | 0/0 | 6433 | 2 | 0 | 0 | 0 | 0 | 2 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0003c0003t0014 | 0/0 | 6433 | 2 | 1 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0003c0003t0016 | 0/0 | 6433 | 2 | 2 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0003c0003t0017 | 0/0 | 6432 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0003c0003t0018 | 0/0 | 6433 | 2 | 0 | 0 | 2 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0003c0003t0019 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0003c0003t0029 | 0/0 | 6433 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0003c0003t0030 | 0/0 | 6433 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0003c0004t0002 | 0/0 | 6433 | 19 | 0 | 0 | 19 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0003c0004t0017 | 0/0 | 6432 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0004c0007t0009 | 0/0 | 6433 | 3 | 3 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0005c0008t0015 | 0/0 | 6435 | 2 | 2 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0006c0009t0002 | 0/0 | 6433 | 2 | 0 | 0 | 2 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0007c0011t0001 | 0/0 | 6431 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0008c0013t0001 | 0/0 | 6431 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0009c0014t0002 | 0/0 | 6433 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0010c0020t0003 | 0/0 | 6433 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0011c0018t0003 | 0/0 | 6433 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0012c0019t0032 | 0/0 | 6433 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0013c0016t0019 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0014c0017t0010 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0015c0021t0012 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0016c0022t0034 | 0/0 | 6433 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0017c0023t0004 | 0/0 | 6433 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
a0018c0010t0006 | 0/0 | 6434 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | copy fasta | chr1 | 3807086 | 3862211 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0002 | 0/1 | 6 | 1 | 2 | 0 | 0 | 2 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0005g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0005g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0005g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0007g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0007g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0007g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0008g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0008g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0008g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0008g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0009g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0009g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0009g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0010g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0010g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0010g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0010g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0010g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0010g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0013g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0020g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0020g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0026g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0027g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0028g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0033g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0035g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0036g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0037g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0038g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0039g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0001t0040g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0006t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0006t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0006t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0006t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0006t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0006t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0006t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0006t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0006t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0006t0021g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0001c0015t0031g0219 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0001 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0010 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0011g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0011g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0011g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0022g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0023g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0024g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0002t0025g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0005t0001g0005 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0005t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0005t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0005t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0005t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0005t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0005t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0005t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0005t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0005t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0002c0012t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0004 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0012g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0012g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0014g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0014g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0016g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0016g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0017g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0018g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0018g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0019g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0029g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0003t0030g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0004t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0004t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0004t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0004t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0004t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0004t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0004t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0004t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0004t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0004t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0004t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0004t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0004t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0004t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0003c0004t0017g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0004c0007t0009g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0004c0007t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0004c0007t0009g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0005c0008t0015g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0005c0008t0015g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0006c0009t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0006c0009t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0007c0011t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0008c0013t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0009c0014t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0010c0020t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0011c0018t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0012c0019t0032g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0013c0016t0019g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0014c0017t0010g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0015c0021t0012g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0016c0022t0034g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0017c0023t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
a0018c0010t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0003 | g0306 | EUR | GBR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00140 | hp2 | a0001 | c0001 | t0010 | g0235 | EUR | GBR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0075 | EUR | FIN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00280 | hp2 | a0001 | c0001 | t0036 | g0305 | EUR | FIN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0157 | EUR | FIN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00323 | hp2 | a0003 | c0003 | t0002 | g0166 | EUR | FIN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | CHS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0295 | EAS | CHS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | CHS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | CHS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00558 | hp1 | a0003 | c0004 | t0002 | g0008 | EAS | CHS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | CHS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00597 | hp1 | a0006 | c0009 | t0002 | g0177 | EAS | CHS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | CHS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | CHS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00609 | hp2 | a0001 | c0001 | t0005 | g0301 | EAS | CHS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0146 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00642 | hp1 | a0002 | c0005 | t0001 | g0107 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0253 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00673 | hp2 | a0003 | c0003 | t0018 | g0215 | EAS | CHS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00733 | hp1 | a0001 | c0001 | t0035 | g0266 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0063 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00735 | hp1 | a0002 | c0012 | t0001 | g0043 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0164 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01069 | hp1 | a0003 | c0003 | t0002 | g0182 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0147 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01070 | hp1 | a0003 | c0003 | t0002 | g0227 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01074 | hp1 | a0001 | c0001 | t0010 | g0244 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0054 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0103 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01081 | hp2 | a0003 | c0003 | t0002 | g0193 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0155 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01109 | hp1 | a0003 | c0003 | t0014 | g0137 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0163 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01167 | hp2 | a0003 | c0003 | t0002 | g0228 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01168 | hp1 | a0003 | c0003 | t0002 | g0192 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01169 | hp1 | a0003 | c0003 | t0002 | g0205 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01169 | hp2 | a0003 | c0003 | t0002 | g0220 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01175 | hp1 | a0001 | c0001 | t0020 | g0286 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0119 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0122 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0025 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01255 | hp1 | a0002 | c0005 | t0001 | g0005 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0058 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01257 | hp1 | a0003 | c0003 | t0002 | g0023 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0120 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01258 | hp2 | a0003 | c0003 | t0002 | g0023 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01346 | hp1 | a0001 | c0001 | t0020 | g0287 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01346 | hp2 | a0002 | c0005 | t0001 | g0005 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01361 | hp1 | a0002 | c0005 | t0001 | g0018 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01361 | hp2 | a0001 | c0001 | t0010 | g0249 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0104 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0307 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01496 | hp1 | a0002 | c0005 | t0001 | g0005 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01496 | hp2 | a0010 | c0020 | t0003 | g0313 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01515 | hp1 | a0001 | c0001 | t0010 | g0260 | EUR | IBS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0080 | EUR | IBS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0152 | EUR | IBS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01517 | hp2 | a0001 | c0001 | t0010 | g0247 | EUR | IBS | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0096 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01934 | hp1 | a0002 | c0002 | t0025 | g0076 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01934 | hp2 | a0003 | c0003 | t0002 | g0203 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0029 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0037 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01978 | hp1 | a0002 | c0005 | t0001 | g0069 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01978 | hp2 | a0003 | c0003 | t0002 | g0180 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01981 | hp1 | a0002 | c0005 | t0001 | g0045 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0041 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01993 | hp1 | a0003 | c0003 | t0002 | g0200 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0142 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0079 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02015 | hp1 | a0003 | c0003 | t0018 | g0204 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02015 | hp2 | a0002 | c0005 | t0001 | g0070 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02040 | hp1 | a0003 | c0003 | t0002 | g0173 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02056 | hp1 | a0003 | c0003 | t0002 | g0176 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02056 | hp2 | a0002 | c0002 | t0023 | g0091 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02071 | hp2 | a0003 | c0003 | t0002 | g0233 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02074 | hp2 | a0001 | c0001 | t0008 | g0248 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02080 | hp2 | a0003 | c0003 | t0002 | g0218 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02129 | hp1 | a0003 | c0003 | t0002 | g0022 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02129 | hp2 | a0001 | c0001 | t0005 | g0297 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02132 | hp2 | a0002 | c0002 | t0022 | g0084 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02135 | hp2 | a0003 | c0003 | t0002 | g0196 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02145 | hp1 | a0004 | c0007 | t0009 | g0250 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02145 | hp2 | a0001 | c0006 | t0006 | g0127 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02148 | hp1 | a0001 | c0001 | t0005 | g0291 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02148 | hp2 | a0002 | c0005 | t0001 | g0040 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02165 | hp1 | a0003 | c0003 | t0002 | g0206 | EAS | CDX | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02165 | hp2 | a0002 | c0002 | t0024 | g0115 | EAS | CDX | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02257 | hp1 | a0001 | c0006 | t0006 | g0124 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0097 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0024 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0263 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0105 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02273 | hp2 | a0003 | c0003 | t0030 | g0202 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02280 | hp1 | a0003 | c0003 | t0014 | g0138 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0280 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0053 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02300 | hp2 | a0002 | c0005 | t0001 | g0033 | AMR | PEL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02451 | hp2 | a0005 | c0008 | t0015 | g0140 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02523 | hp1 | a0003 | c0003 | t0002 | g0212 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02523 | hp2 | a0003 | c0003 | t0002 | g0185 | EAS | KHV | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02572 | hp2 | a0004 | c0007 | t0009 | g0245 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02602 | hp1 | a0003 | c0003 | t0002 | g0223 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02602 | hp2 | a0011 | c0018 | t0003 | g0265 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02622 | hp2 | a0001 | c0006 | t0006 | g0133 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02647 | hp2 | a0016 | c0022 | t0034 | g0269 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0310 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0116 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02698 | hp2 | a0003 | c0003 | t0002 | g0213 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0272 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02717 | hp2 | a0001 | c0001 | t0008 | g0270 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02723 | hp1 | a0001 | c0006 | t0006 | g0129 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02723 | hp2 | a0001 | c0006 | t0021 | g0117 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02735 | hp1 | a0003 | c0003 | t0002 | g0181 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0151 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02738 | hp2 | a0003 | c0003 | t0012 | g0290 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02818 | hp1 | a0001 | c0001 | t0027 | g0145 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0282 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02895 | hp2 | a0001 | c0001 | t0009 | g0259 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02896 | hp1 | a0001 | c0001 | t0028 | g0161 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0281 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02922 | hp2 | a0001 | c0001 | t0013 | g0031 | AFR | ESN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | ESN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02970 | hp2 | a0012 | c0019 | t0032 | g0234 | AFR | ESN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | ESN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | ESN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0123 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0267 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03041 | hp1 | a0003 | c0003 | t0016 | g0231 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03041 | hp2 | a0001 | c0006 | t0006 | g0131 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | MSL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | MSL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | ESN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | ESN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | ESN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0284 | AFR | ESN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0239 | AFR | ESN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0273 | AFR | ESN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | MSL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03209 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | MSL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03225 | hp1 | a0004 | c0007 | t0009 | g0241 | AFR | MSL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03225 | hp2 | a0001 | c0001 | t0013 | g0032 | AFR | MSL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0078 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0113 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0277 | AFR | MSL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0308 | AFR | MSL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03491 | hp1 | a0003 | c0003 | t0002 | g0195 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0020 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0059 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0020 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03516 | hp1 | a0001 | c0006 | t0006 | g0132 | AFR | ESN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0285 | AFR | ESN | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03540 | hp2 | a0003 | c0003 | t0002 | g0170 | AFR | GWD | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0254 | AFR | MSL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03579 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | MSL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0264 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03654 | hp2 | a0008 | c0013 | t0001 | g0055 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0072 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03669 | hp2 | a0003 | c0003 | t0002 | g0004 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03688 | hp1 | a0003 | c0003 | t0002 | g0174 | SAS | STU | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0083 | SAS | STU | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03704 | hp1 | a0003 | c0003 | t0002 | g0187 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0068 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03710 | hp1 | a0003 | c0003 | t0012 | g0289 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0081 | SAS | PJL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0309 | SAS | BEB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0156 | SAS | BEB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0050 | SAS | BEB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03834 | hp2 | a0003 | c0003 | t0002 | g0207 | SAS | BEB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03927 | hp1 | a0009 | c0014 | t0002 | g0183 | SAS | BEB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0311 | SAS | BEB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0101 | SAS | BEB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03942 | hp2 | a0003 | c0003 | t0002 | g0188 | SAS | BEB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0060 | SAS | STU | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0314 | SAS | STU | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG04184 | hp1 | a0001 | c0001 | t0009 | g0242 | SAS | BEB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG04184 | hp2 | a0003 | c0003 | t0002 | g0222 | SAS | BEB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0071 | SAS | STU | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | STU | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0160 | SAS | STU | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0153 | SAS | STU | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG04228 | hp1 | a0003 | c0003 | t0002 | g0022 | SAS | STU | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0114 | SAS | STU | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0278 | AFR | YRI | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18522 | hp2 | a0001 | c0006 | t0006 | g0130 | AFR | YRI | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | CHB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18747 | hp2 | a0003 | c0003 | t0017 | g0208 | EAS | CHB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18906 | hp1 | a0001 | c0006 | t0006 | g0126 | AFR | YRI | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18906 | hp2 | a0001 | c0001 | t0039 | g0238 | AFR | YRI | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18939 | hp2 | a0003 | c0004 | t0002 | g0214 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18940 | hp1 | a0002 | c0005 | t0001 | g0038 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18940 | hp2 | a0003 | c0004 | t0002 | g0178 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18941 | hp1 | a0003 | c0003 | t0002 | g0179 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18941 | hp2 | a0001 | c0001 | t0005 | g0292 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18943 | hp1 | a0003 | c0003 | t0002 | g0171 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18943 | hp2 | a0014 | c0017 | t0010 | g0236 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18945 | hp1 | a0002 | c0005 | t0001 | g0005 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18945 | hp2 | a0003 | c0003 | t0002 | g0011 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18946 | hp2 | a0001 | c0001 | t0005 | g0298 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18950 | hp2 | a0003 | c0004 | t0002 | g0191 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18951 | hp1 | a0003 | c0003 | t0002 | g0216 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18954 | hp1 | a0003 | c0003 | t0002 | g0189 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18956 | hp1 | a0001 | c0001 | t0005 | g0303 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18956 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18957 | hp1 | a0003 | c0004 | t0002 | g0012 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18959 | hp2 | a0003 | c0003 | t0002 | g0165 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18962 | hp2 | a0003 | c0003 | t0002 | g0232 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18964 | hp2 | a0003 | c0003 | t0002 | g0011 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18965 | hp1 | a0001 | c0001 | t0008 | g0262 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18965 | hp2 | a0003 | c0004 | t0017 | g0167 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18966 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18967 | hp1 | a0003 | c0003 | t0002 | g0021 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18968 | hp1 | a0003 | c0003 | t0002 | g0225 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18968 | hp2 | a0001 | c0001 | t0005 | g0293 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18970 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18971 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18973 | hp2 | a0003 | c0004 | t0002 | g0008 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18974 | hp1 | a0002 | c0002 | t0011 | g0134 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18974 | hp2 | a0001 | c0001 | t0005 | g0302 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18975 | hp1 | a0003 | c0004 | t0002 | g0012 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18977 | hp2 | a0003 | c0004 | t0002 | g0201 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18979 | hp2 | a0003 | c0003 | t0002 | g0221 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18980 | hp2 | a0001 | c0001 | t0005 | g0296 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18981 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18983 | hp1 | a0003 | c0004 | t0002 | g0008 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18983 | hp2 | a0003 | c0003 | t0002 | g0186 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18985 | hp1 | a0015 | c0021 | t0012 | g0255 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18986 | hp1 | a0003 | c0003 | t0019 | g0211 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0304 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18990 | hp1 | a0001 | c0001 | t0040 | g0315 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18993 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18997 | hp1 | a0002 | c0005 | t0001 | g0018 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18997 | hp2 | a0003 | c0004 | t0002 | g0229 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18998 | hp2 | a0003 | c0003 | t0002 | g0224 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19000 | hp1 | a0003 | c0004 | t0002 | g0168 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19001 | hp1 | a0002 | c0005 | t0001 | g0034 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19001 | hp2 | a0003 | c0004 | t0002 | g0197 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19003 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0299 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19004 | hp2 | a0002 | c0005 | t0001 | g0111 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19005 | hp1 | a0002 | c0002 | t0011 | g0135 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19005 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19011 | hp1 | a0003 | c0004 | t0002 | g0190 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19012 | hp1 | a0003 | c0004 | t0002 | g0012 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19012 | hp2 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19030 | hp1 | a0003 | c0003 | t0002 | g0172 | AFR | LWK | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | LWK | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | LWK | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19043 | hp2 | a0018 | c0010 | t0006 | g0125 | AFR | LWK | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19054 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19055 | hp2 | a0001 | c0001 | t0005 | g0294 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19058 | hp1 | a0001 | c0001 | t0038 | g0288 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19060 | hp1 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19062 | hp1 | a0003 | c0003 | t0002 | g0021 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19062 | hp2 | a0001 | c0001 | t0008 | g0261 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19064 | hp2 | a0013 | c0016 | t0019 | g0210 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19066 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19067 | hp2 | a0003 | c0004 | t0002 | g0175 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19070 | hp2 | a0003 | c0004 | t0002 | g0008 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19079 | hp2 | a0003 | c0004 | t0002 | g0198 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19081 | hp2 | a0003 | c0003 | t0002 | g0011 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19083 | hp1 | a0003 | c0004 | t0002 | g0199 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19086 | hp1 | a0002 | c0002 | t0011 | g0136 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19086 | hp2 | a0003 | c0004 | t0002 | g0226 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19087 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19088 | hp1 | a0003 | c0003 | t0002 | g0217 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19088 | hp2 | a0001 | c0001 | t0010 | g0246 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19090 | hp1 | a0006 | c0009 | t0002 | g0194 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19240 | hp1 | a0001 | c0006 | t0006 | g0128 | AFR | YRI | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | YRI | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0276 | AFR | ASW | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | ASW | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA20752 | hp1 | a0001 | c0001 | t0026 | g0154 | EUR | TSI | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0089 | EUR | TSI | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0087 | EUR | TSI | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA20805 | hp2 | a0007 | c0011 | t0001 | g0049 | EUR | TSI | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA20905 | hp1 | a0003 | c0003 | t0002 | g0184 | SAS | GIH | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA20905 | hp2 | a0001 | c0001 | t0037 | g0312 | SAS | GIH | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01123 | hp1 | a0001 | c0001 | t0008 | g0024 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG01123 | hp2 | a0002 | c0005 | t0001 | g0005 | AMR | CLM | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0275 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0243 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02559 | hp1 | a0005 | c0008 | t0015 | g0139 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0283 | AFR | ACB | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03471 | hp1 | a0001 | c0001 | t0009 | g0240 | AFR | MSL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0077 | AFR | MSL | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG06807 | hp1 | a0001 | c0001 | t0033 | g0274 | AFR | USA | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
HG06807 | hp2 | a0003 | c0003 | t0016 | g0230 | AFR | USA | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA18955 | hp2 | a0003 | c0003 | t0002 | g0169 | EAS | JPT | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA20300 | hp1 | a0017 | c0023 | t0004 | g0150 | AFR | USA | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA20300 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | USA | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA21309 | hp1 | a0001 | c0001 | t0009 | g0268 | AFR | LWK | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
NA21309 | hp2 | a0003 | c0003 | t0029 | g0209 | AFR | LWK | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0002 | REF | REF | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
homoSapiens_grch38 | hp1 | a0001 | c0015 | t0031 | g0219 | REF | REF | CEP104_chr1_3807086_3862211 | CEP104 | chr1 | 3807086 | 3862211 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:3815406
|
C | T | 1 | a0013 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.2774G>A | p.Arg925His | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 3111/6431 | 2774/2778 | 925/925 | chr1 | 3815406 | ||
chr1:3816298
|
C | A | 1 | a0007 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.2644G>T | p.Ala882Ser | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/22 | 2981/6431 | 2644/2778 | 882/925 | chr1 | 3816298 | ||
chr1:3823176
|
C | T | 1 | a0004 | 3 | HG02145.hp1 HG02572.hp2 HG03225.hp1 |
missense_variant&splice_region_variant | MODERATE | c.2569G>A | p.Glu857Lys | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/22 | 2906/6431 | 2569/2778 | 857/925 | chr1 | 3823176 | ||
chr1:3823181
|
C | T | 1 | a0006 | 2 | HG00597.hp1 NA19090.hp1 |
missense_variant | MODERATE | c.2564G>A | p.Gly855Glu | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/22 | 2901/6431 | 2564/2778 | 855/925 | chr1 | 3823181 | ||
chr1:3829306
|
C | T | 1 | a0012 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.2111G>A | p.Gly704Glu | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/22 | 2448/6431 | 2111/2778 | 704/925 | chr1 | 3829306 | ||
chr1:3829360
|
G | A | 5 | a0003a0006a0009others(2): Show | 101 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(98): Show |
missense_variant | MODERATE | c.2057C>T | p.Ala686Val | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/22 | 2394/6431 | 2057/2778 | 686/925 | chr1 | 3829360 | ||
chr1:3829369
|
C | T | 1 | a0011 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.2048G>A | p.Arg683Gln | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/22 | 2385/6431 | 2048/2778 | 683/925 | chr1 | 3829369 | ||
chr1:3829868
|
G | A | 1 | a0010 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1966C>T | p.Arg656Cys | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 14/22 | 2303/6431 | 1966/2778 | 656/925 | chr1 | 3829868 | ||
chr1:3833885
|
C | T | 1 | a0009 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.1636G>A | p.Val546Ile | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/22 | 1973/6431 | 1636/2778 | 546/925 | chr1 | 3833885 | ||
chr1:3833933
|
T | C | 1 | a0008 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.1588A>G | p.Ile530Val | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/22 | 1925/6431 | 1588/2778 | 530/925 | chr1 | 3833933 | ||
chr1:3836572
|
A | T | 3 | a0002a0007a0008 | 132 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
missense_variant | MODERATE | c.1240T>A | p.Leu414Ile | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/22 | 1577/6431 | 1240/2778 | 414/925 | chr1 | 3836572 | ||
chr1:3839011
|
C | T | 1 | a0014 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.844G>A | p.Glu282Lys | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 8/22 | 1181/6431 | 844/2778 | 282/925 | chr1 | 3839011 | ||
chr1:3839642
|
T | C | 1 | a0015 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.701A>G | p.Lys234Arg | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 7/22 | 1038/6431 | 701/2778 | 234/925 | chr1 | 3839642 | ||
chr1:3839679
|
G | A | 1 | a0016 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.664C>T | p.Arg222Trp | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 7/22 | 1001/6431 | 664/2778 | 222/925 | chr1 | 3839679 | ||
chr1:3844921
|
T | A | 1 | a0005 | 2 | HG02451.hp2 HG02559.hp1 |
missense_variant | MODERATE | c.552A>T | p.Glu184Asp | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/22 | 889/6431 | 552/2778 | 184/925 | chr1 | 3844921 | ||
chr1:3844983
|
C | A | 1 | a0017 | 1 | NA20300.hp1 | missense_variant&splice_region_variant | MODERATE | c.490G>T | p.Ala164Ser | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/22 | 827/6431 | 490/2778 | 164/925 | chr1 | 3844983 | ||
chr1:3847485
|
A | G | 1 | a0018 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.416T>C | p.Ile139Thr | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/22 | 753/6431 | 416/2778 | 139/925 | chr1 | 3847485 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:3829881
|
G | A | 1 | a0002c0012 | 1 | HG00735.hp1 | synonymous_variant | LOW | c.1953C>T | p.Asp651Asp | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 14/22 | 2290/6431 | 1953/2778 | 651/925 | chr1 | 3829881 | ||
chr1:3829920
|
T | C | 1 | a0003c0004 | 20 | HG00558.hp1 NA18939.hp2 NA18940.hp2 others(17): Show |
synonymous_variant | LOW | c.1914A>G | p.Arg638Arg | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 14/22 | 2251/6431 | 1914/2778 | 638/925 | chr1 | 3829920 | ||
chr1:3834925
|
G | A | 1 | a0008c0013 | 1 | HG03654.hp2 | splice_region_variant&synonymous_variant | LOW | c.1485C>T | p.Ser495Ser | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/22 | 1822/6431 | 1485/2778 | 495/925 | chr1 | 3834925 | ||
chr1:3835024
|
T | C | 1 | a0005c0008 | 2 | HG02451.hp2 HG02559.hp1 |
synonymous_variant | LOW | c.1386A>G | p.Leu462Leu | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/22 | 1723/6431 | 1386/2778 | 462/925 | chr1 | 3835024 | ||
chr1:3835047
|
G | A | 1 | a0005c0008 | 2 | HG02451.hp2 HG02559.hp1 |
synonymous_variant | LOW | c.1363C>T | p.Leu455Leu | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/22 | 1700/6431 | 1363/2778 | 455/925 | chr1 | 3835047 | ||
chr1:3839111
|
T | C | 16 | a0001c0001a0001c0006a0002c0002others(13): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
synonymous_variant | LOW | c.744A>G | p.Glu248Glu | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 8/22 | 1081/6431 | 744/2778 | 248/925 | chr1 | 3839111 | ||
chr1:3839662
|
C | T | 1 | a0002c0005 | 16 | HG00642.hp1 HG01123.hp2 HG01255.hp1 others(13): Show |
synonymous_variant | LOW | c.681G>A | p.Lys227Lys | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 7/22 | 1018/6431 | 681/2778 | 227/925 | chr1 | 3839662 | ||
chr1:3844915
|
C | T | 7 | a0001c0006a0002c0002a0002c0005others(4): Show | 143 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
synonymous_variant | LOW | c.558G>A | p.Thr186Thr | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/22 | 895/6431 | 558/2778 | 186/925 | chr1 | 3844915 | ||
chr1:3848718
|
C | T | 1 | a0005c0008 | 2 | HG02451.hp2 HG02559.hp1 |
synonymous_variant | LOW | c.177G>A | p.Leu59Leu | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/22 | 514/6431 | 177/2778 | 59/925 | chr1 | 3848718 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:3812183
|
C | T | 3 | a0001c0001t0005a0001c0001t0038a0001c0001t0040 | 18 | HG00423.hp2 HG00609.hp2 HG01952.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3219G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 3219 | chr1 | 3812183 | |||||
chr1:3812580
|
C | T | 1 | a0001c0001t0026 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2822G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2822 | chr1 | 3812580 | |||||
chr1:3812605
|
C | G | 26 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(23): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*2797G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2797 | chr1 | 3812605 | |||||
chr1:3812713
|
G | A | 1 | a0001c0001t0036 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2689C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2689 | chr1 | 3812713 | |||||
chr1:3812899
|
GTAAC | G | 1 | a0001c0001t0008 | 9 | HG01123.hp1 HG02074.hp2 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2499_*2502delGTTA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2499 | chr1 | 3812899 | |||||
chr1:3813003
|
A | C | 4 | a0001c0001t0005a0001c0001t0020a0001c0001t0038others(1): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2399T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2399 | chr1 | 3813003 | |||||
chr1:3813011
|
G | A | 1 | a0001c0001t0037 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2391C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2391 | chr1 | 3813011 | |||||
chr1:3813021
|
G | GTA | 2 | a0001c0001t0020a0005c0008t0015 | 4 | HG01175.hp1 HG01346.hp1 HG02451.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2379_*2380dupTA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2380 | chr1 | 3813021 | |||||
chr1:3813023
|
A | G | 39 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(36): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*2379T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2379 | chr1 | 3813023 | |||||
chr1:3813025
|
A | G | 1 | a0001c0001t0035 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2377T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2377 | chr1 | 3813025 | |||||
chr1:3813030
|
T | C | 1 | a0001c0001t0039 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2372A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2372 | chr1 | 3813030 | |||||
chr1:3813073
|
T | C | 10 | a0001c0001t0007a0001c0001t0008a0001c0001t0009others(7): Show | 38 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2329A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2329 | chr1 | 3813073 | |||||
chr1:3813232
|
T | C | 4 | a0001c0001t0005a0001c0001t0020a0001c0001t0038others(1): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2170A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2170 | chr1 | 3813232 | |||||
chr1:3813254
|
C | CT | 30 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(27): Show | 198 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*2147dupA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2147 | chr1 | 3813254 | |||||
chr1:3813254
|
C | CTT | 3 | a0001c0001t0027a0001c0006t0006a0018c0010t0006 | 11 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2146_*2147dupAA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2147 | chr1 | 3813254 | |||||
chr1:3813267
|
T | C | 1 | a0001c0001t0033 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2135A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2135 | chr1 | 3813267 | |||||
chr1:3813267
|
T | TC | 9 | a0001c0001t0007a0001c0001t0008a0001c0001t0009others(6): Show | 37 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2134dupG | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2134 | chr1 | 3813267 | |||||
chr1:3813281
|
C | T | 1 | a0012c0019t0032 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2121G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2121 | chr1 | 3813281 | |||||
chr1:3813282
|
G | A | 1 | a0002c0002t0011 | 3 | NA18974.hp1 NA19005.hp1 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2120C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2120 | chr1 | 3813282 | |||||
chr1:3813295
|
G | A | 1 | a0003c0003t0029 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2107C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2107 | chr1 | 3813295 | |||||
chr1:3813402
|
G | A | 1 | a0016c0022t0034 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2000C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 2000 | chr1 | 3813402 | |||||
chr1:3813417
|
G | C | 1 | a0003c0003t0018 | 2 | HG00673.hp2 HG02015.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1985C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 1985 | chr1 | 3813417 | |||||
chr1:3813488
|
G | A | 2 | a0003c0003t0019a0013c0016t0019 | 2 | NA18986.hp1 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1914C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 1914 | chr1 | 3813488 | |||||
chr1:3813492
|
G | A | 2 | a0001c0001t0027a0001c0001t0028 | 2 | HG02818.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1910C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 1910 | chr1 | 3813492 | |||||
chr1:3813536
|
G | C | 1 | a0005c0008t0015 | 2 | HG02451.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1866C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 1866 | chr1 | 3813536 | |||||
chr1:3813576
|
C | T | 10 | a0001c0001t0007a0001c0001t0008a0001c0001t0009others(7): Show | 38 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1826G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 1826 | chr1 | 3813576 | |||||
chr1:3813577
|
G | A | 1 | a0002c0002t0024 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1825C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 1825 | chr1 | 3813577 | |||||
chr1:3813588
|
C | T | 1 | a0002c0002t0023 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1814G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 1814 | chr1 | 3813588 | |||||
chr1:3813640
|
C | T | 1 | a0002c0002t0022 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1762G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 1762 | chr1 | 3813640 | |||||
chr1:3813871
|
T | C | 39 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(36): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*1531A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 1531 | chr1 | 3813871 | |||||
chr1:3814423
|
G | C | 1 | a0002c0002t0025 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*979C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 979 | chr1 | 3814423 | |||||
chr1:3814456
|
G | C | 4 | a0001c0001t0005a0001c0001t0020a0001c0001t0038others(1): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*946C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 946 | chr1 | 3814456 | |||||
chr1:3814711
|
C | T | 1 | a0001c0001t0038 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*691G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 691 | chr1 | 3814711 | |||||
chr1:3815053
|
G | C | 4 | a0001c0001t0005a0001c0001t0020a0001c0001t0038others(1): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*349C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 349 | chr1 | 3815053 | |||||
chr1:3815077
|
C | A | 1 | a0003c0003t0030 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*325G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 325 | chr1 | 3815077 | |||||
chr1:3815090
|
C | CT | 45 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(42): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*311_*312insA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 311 | chr1 | 3815090 | |||||
chr1:3815093
|
C | T | 10 | a0001c0001t0007a0001c0001t0008a0001c0001t0009others(7): Show | 38 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*309G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 309 | chr1 | 3815093 | |||||
chr1:3815195
|
G | A | 1 | a0001c0001t0040 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*207C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 207 | chr1 | 3815195 | |||||
chr1:3815395
|
C | T | 2 | a0001c0001t0010a0014c0017t0010 | 7 | HG00140.hp2 HG01074.hp1 HG01361.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 7 | chr1 | 3815395 | |||||
chr1:3815401
|
G | A | 6 | a0001c0001t0008a0001c0001t0009a0001c0001t0010others(3): Show | 26 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 22/22 | 1 | chr1 | 3815401 | |||||
chr1:3856937
|
G | A | 1 | a0001c0001t0040 | 1 | NA18990.hp1 | 5_prime_UTR_variant | MODIFIER | c.-63C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/22 | 4530 | chr1 | 3856937 | |||||
chr1:3856947
|
G | A | 5 | a0001c0001t0004a0001c0001t0026a0001c0001t0027others(2): Show | 30 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(27): Show |
5_prime_UTR_variant | MODIFIER | c.-73C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/22 | 4540 | chr1 | 3856947 | |||||
chr1:3856967
|
C | A | 1 | a0002c0002t0011 | 3 | NA18974.hp1 NA19005.hp1 NA19086.hp1 |
5_prime_UTR_variant | MODIFIER | c.-93G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/22 | 4560 | chr1 | 3856967 | |||||
chr1:3856982
|
A | C | 23 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(20): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
5_prime_UTR_variant | MODIFIER | c.-108T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/22 | 4575 | chr1 | 3856982 | |||||
chr1:3857024
|
C | G | 13 | a0001c0006t0006a0001c0006t0021a0002c0002t0001others(10): Show | 143 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
5_prime_UTR_variant | MODIFIER | c.-150G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/22 | 4617 | chr1 | 3857024 | |||||
chr1:3857037
|
C | G | 1 | a0001c0001t0013 | 2 | HG02922.hp2 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-163G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/22 | 4630 | chr1 | 3857037 | |||||
chr1:3857154
|
A | G | 42 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(39): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
5_prime_UTR_variant | MODIFIER | c.-280T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/22 | 4747 | chr1 | 3857154 | |||||
chr1:3857169
|
C | A | 22 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(19): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
5_prime_UTR_variant | MODIFIER | c.-295G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/22 | 4762 | chr1 | 3857169 | |||||
chr1:3857199
|
C | G | 1 | a0001c0001t0013 | 2 | HG02922.hp2 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-325G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/22 | 4792 | chr1 | 3857199 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:3815539
|
T | C | 189 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(186): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.2663-22A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3815539 | ||||||
chr1:3815608
|
C | T | 189 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(186): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.2663-91G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3815608 | ||||||
chr1:3815631
|
C | T | 17 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(14): Show | 18 | HG00423.hp2 HG00609.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.2663-114G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3815631 | ||||||
chr1:3815638
|
C | T | 1 | a0002c0005t0001g0070 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2663-121G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3815638 | ||||||
chr1:3815689
|
AT | A | 184 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(181): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.2663-173delA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3815689 | ||||||
chr1:3815849
|
G | T | 1 | a0002c0002t0001g0097 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2663-332C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3815849 | ||||||
chr1:3815888
|
C | G | 188 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(185): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.2663-371G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3815888 | ||||||
chr1:3815932
|
C | T | 33 | a0001c0001t0007g0014a0001c0001t0007g0272a0001c0001t0007g0273others(30): Show | 38 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.2662+348G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3815932 | ||||||
chr1:3816023
|
C | T | 1 | a0002c0002t0001g0121 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2662+257G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3816023 | ||||||
chr1:3816032
|
G | T | 111 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(108): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.2662+248C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3816032 | ||||||
chr1:3816059
|
G | A | 1 | a0002c0005t0001g0069 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2662+221C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3816059 | ||||||
chr1:3816067
|
C | T | 1 | a0002c0002t0001g0087 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2662+213G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3816067 | ||||||
chr1:3816075
|
T | A | 188 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(185): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.2662+205A>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3816075 | ||||||
chr1:3816086
|
G | A | 1 | a0001c0001t0003g0278 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2662+194C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3816086 | ||||||
chr1:3816143
|
T | C | 188 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(185): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.2662+137A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3816143 | ||||||
chr1:3816148
|
A | G | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2662+132T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3816148 | ||||||
chr1:3816165
|
A | G | 3 | a0001c0001t0010g0244a0001c0001t0010g0247a0001c0001t0010g0260 | 3 | HG01074.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2662+115T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3816165 | ||||||
chr1:3816218
|
T | C | 207 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(204): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.2662+62A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 21/21 | chr1 | 3816218 | ||||||
chr1:3816406
|
C | T | 2 | a0002c0002t0001g0051a0002c0002t0001g0077 | 2 | HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2572-36G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3816406 | ||||||
chr1:3816499
|
C | T | 1 | a0001c0001t0007g0273 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2572-129G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3816499 | ||||||
chr1:3816597
|
C | G | 27 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0036others(24): Show | 30 | HG00280.hp1 HG00639.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.2572-227G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3816597 | ||||||
chr1:3816653
|
C | A | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2572-283G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3816653 | ||||||
chr1:3816736
|
C | T | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2572-366G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3816736 | ||||||
chr1:3816738
|
C | T | 2 | a0003c0003t0016g0230a0003c0003t0016g0231 | 2 | HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2572-368G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3816738 | ||||||
chr1:3816751
|
G | A | 4 | a0001c0006t0006g0129a0001c0006t0006g0130a0001c0006t0006g0131others(1): Show | 4 | HG02723.hp1 HG03041.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2572-381C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3816751 | ||||||
chr1:3816827
|
G | A | 33 | a0001c0001t0007g0014a0001c0001t0007g0272a0001c0001t0007g0273others(30): Show | 38 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.2572-457C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3816827 | ||||||
chr1:3816902
|
C | T | 188 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(185): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.2572-532G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3816902 | ||||||
chr1:3816913
|
G | C | 1 | a0012c0019t0032g0234 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2572-543C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3816913 | ||||||
chr1:3817046
|
C | G | 1 | a0001c0001t0036g0305 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2572-676G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3817046 | ||||||
chr1:3817046
|
C | T | 1 | a0002c0002t0022g0084 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2572-676G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3817046 | ||||||
chr1:3817050
|
G | C | 2 | a0003c0003t0019g0211a0013c0016t0019g0210 | 2 | NA18986.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2572-680C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3817050 | ||||||
chr1:3817059
|
G | A | 1 | a0001c0001t0003g0311 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2572-689C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3817059 | ||||||
chr1:3817160
|
G | A | 1 | a0002c0005t0001g0070 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2572-790C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3817160 | ||||||
chr1:3817250
|
G | A | 1 | a0001c0001t0003g0306 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2572-880C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3817250 | ||||||
chr1:3817457
|
C | A | 1 | a0001c0001t0004g0159 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2572-1087G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3817457 | ||||||
chr1:3817459
|
G | A | 1 | a0002c0002t0001g0054 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2572-1089C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3817459 | ||||||
chr1:3817507
|
C | T | 1 | a0002c0002t0001g0046 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2572-1137G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3817507 | ||||||
chr1:3817555
|
C | T | 1 | a0001c0001t0005g0297 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2572-1185G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3817555 | ||||||
chr1:3817643
|
C | T | 1 | a0003c0003t0002g0207 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2572-1273G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3817643 | ||||||
chr1:3817807
|
G | C | 188 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(185): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.2572-1437C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3817807 | ||||||
chr1:3817813
|
G | A | 1 | a0001c0001t0004g0152 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2572-1443C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3817813 | ||||||
chr1:3817834
|
C | T | 1 | a0001c0001t0004g0149 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2572-1464G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3817834 | ||||||
chr1:3817883
|
G | A | 207 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(204): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.2572-1513C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3817883 | ||||||
chr1:3818072
|
G | C | 2 | a0002c0002t0001g0019a0002c0002t0001g0092 | 3 | NA18967.hp2 NA18998.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.2572-1702C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3818072 | ||||||
chr1:3818294
|
C | T | 1 | a0003c0003t0002g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2572-1924G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3818294 | ||||||
chr1:3818589
|
C | T | 188 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(185): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.2572-2219G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3818589 | ||||||
chr1:3818699
|
T | C | 1 | a0001c0001t0004g0146 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2572-2329A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3818699 | ||||||
chr1:3818716
|
G | T | 2 | a0003c0003t0002g0220a0003c0003t0002g0228 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2572-2346C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3818716 | ||||||
chr1:3818795
|
T | C | 1 | a0001c0006t0006g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2572-2425A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3818795 | ||||||
chr1:3819032
|
G | A | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2572-2662C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3819032 | ||||||
chr1:3819132
|
G | C | 4 | a0003c0003t0014g0137a0003c0003t0014g0138a0003c0003t0016g0230others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2572-2762C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3819132 | ||||||
chr1:3819755
|
A | G | 207 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(204): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.2572-3385T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3819755 | ||||||
chr1:3819772
|
T | C | 207 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(204): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.2571+3402A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3819772 | ||||||
chr1:3819776
|
C | T | 181 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(178): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.2571+3398G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3819776 | ||||||
chr1:3819920
|
G | A | 1 | a0016c0022t0034g0269 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2571+3254C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3819920 | ||||||
chr1:3820022
|
C | T | 1 | a0001c0001t0004g0156 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2571+3152G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820022 | ||||||
chr1:3820118
|
C | G | 17 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(14): Show | 18 | HG00423.hp2 HG00609.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.2571+3056G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820118 | ||||||
chr1:3820127
|
C | A | 33 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(30): Show | 41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.2571+3047G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820127 | ||||||
chr1:3820286
|
G | T | 3 | a0001c0001t0010g0244a0001c0001t0010g0247a0001c0001t0010g0260 | 3 | HG01074.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2571+2888C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820286 | ||||||
chr1:3820359
|
T | C | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2571+2815A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820359 | ||||||
chr1:3820472
|
G | A | 77 | a0003c0003t0002g0003a0003c0003t0002g0004a0003c0003t0002g0011others(74): Show | 97 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.2571+2702C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820472 | ||||||
chr1:3820494
|
C | CGCCTCTG others(42): Show |
22 | a0001c0001t0004g0002a0001c0001t0004g0142a0001c0001t0004g0143others(19): Show | 27 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.2571+2679_2571+268 others(53): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820494 | ||||||
chr1:3820494
|
C | CGCCTCTG others(42): Show |
166 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(163): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.2571+2679_2571+268 others(53): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820494 | ||||||
chr1:3820717
|
C | T | 2 | a0003c0004t0002g0168a0003c0004t0002g0201 | 2 | NA18977.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2571+2457G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820717 | ||||||
chr1:3820730
|
G | A | 1 | a0001c0001t0004g0160 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2571+2444C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820730 | ||||||
chr1:3820759
|
G | T | 1 | a0003c0003t0002g0206 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2571+2415C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820759 | ||||||
chr1:3820831
|
G | C | 188 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(185): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.2571+2343C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820831 | ||||||
chr1:3820835
|
G | A | 2 | a0001c0001t0020g0286a0001c0001t0020g0287 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2571+2339C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820835 | ||||||
chr1:3820863
|
G | A | 1 | a0003c0003t0018g0215 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2571+2311C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820863 | ||||||
chr1:3820906
|
G | A | 1 | a0002c0002t0001g0123 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2571+2268C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820906 | ||||||
chr1:3820976
|
A | G | 207 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(204): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.2571+2198T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3820976 | ||||||
chr1:3821079
|
C | A | 1 | a0001c0001t0003g0278 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2571+2095G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3821079 | ||||||
chr1:3821119
|
T | C | 1 | a0003c0003t0002g0212 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2571+2055A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3821119 | ||||||
chr1:3821175
|
A | C | 207 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(204): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.2571+1999T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3821175 | ||||||
chr1:3821280
|
C | T | 1 | a0001c0001t0003g0309 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2571+1894G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3821280 | ||||||
chr1:3821486
|
G | A | 1 | a0001c0001t0004g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2571+1688C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3821486 | ||||||
chr1:3821650
|
T | C | 178 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(175): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.2571+1524A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3821650 | ||||||
chr1:3821684
|
T | C | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2571+1490A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3821684 | ||||||
chr1:3821756
|
C | T | 17 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(14): Show | 18 | HG00423.hp2 HG00609.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.2571+1418G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3821756 | ||||||
chr1:3821768
|
A | G | 210 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(207): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.2571+1406T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3821768 | ||||||
chr1:3821839
|
A | G | 1 | a0016c0022t0034g0269 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2571+1335T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3821839 | ||||||
chr1:3821904
|
T | C | 1 | a0001c0001t0008g0262 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2571+1270A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3821904 | ||||||
chr1:3822019
|
C | T | 78 | a0002c0002t0001g0041a0002c0002t0001g0105a0003c0003t0002g0003others(75): Show | 98 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.2571+1155G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822019 | ||||||
chr1:3822076
|
A | C | 210 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(207): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.2571+1098T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822076 | ||||||
chr1:3822133
|
G | A | 13 | a0001c0001t0003g0028a0001c0001t0003g0030a0001c0001t0003g0264others(10): Show | 15 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.2571+1041C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822133 | ||||||
chr1:3822148
|
G | A | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2571+1026C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822148 | ||||||
chr1:3822214
|
TGA | T | 206 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(203): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.2571+958_2571+959d others(4): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822214 | ||||||
chr1:3822230
|
TGACAGAC others(9): Show |
T | 197 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(194): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.2571+928_2571+943d others(18): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822230 | ||||||
chr1:3822386
|
T | C | 9 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(6): Show | 15 | HG00642.hp2 HG00741.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2571+788A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822386 | ||||||
chr1:3822390
|
G | A | 5 | a0001c0001t0007g0272a0001c0001t0007g0283a0001c0001t0007g0284others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2571+784C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822390 | ||||||
chr1:3822553
|
A | G | 1 | a0001c0001t0003g0306 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2571+621T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822553 | ||||||
chr1:3822565
|
G | A | 20 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(17): Show | 21 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.2571+609C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822565 | ||||||
chr1:3822596
|
A | C | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2571+578T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822596 | ||||||
chr1:3822625
|
C | T | 178 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(175): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.2571+549G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822625 | ||||||
chr1:3822707
|
T | TA | 210 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(207): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.2571+466_2571+467i others(3): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822707 | ||||||
chr1:3822708
|
T | A | 210 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(207): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.2571+466A>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822708 | ||||||
chr1:3822723
|
T | C | 1 | a0001c0001t0020g0286 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2571+451A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822723 | ||||||
chr1:3822726
|
G | A | 178 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(175): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.2571+448C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822726 | ||||||
chr1:3822736
|
G | A | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2571+438C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822736 | ||||||
chr1:3822770
|
A | T | 5 | a0001c0001t0007g0272a0001c0001t0007g0283a0001c0001t0007g0284others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2571+404T>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822770 | ||||||
chr1:3822818
|
C | T | 6 | a0001c0001t0008g0013a0001c0001t0008g0024a0001c0001t0008g0248others(3): Show | 9 | HG01123.hp1 HG02074.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2571+356G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822818 | ||||||
chr1:3822948
|
G | A | 77 | a0003c0003t0002g0003a0003c0003t0002g0004a0003c0003t0002g0011others(74): Show | 97 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.2571+226C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3822948 | ||||||
chr1:3823047
|
C | A | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2571+127G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3823047 | ||||||
chr1:3823061
|
C | T | 1 | a0001c0001t0005g0301 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2571+113G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3823061 | ||||||
chr1:3823100
|
C | T | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2571+74G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 20/21 | chr1 | 3823100 | ||||||
chr1:3823383
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2503+41A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 19/21 | chr1 | 3823383 | ||||||
chr1:3823638
|
G | A | 1 | a0003c0003t0012g0290 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2365-76C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3823638 | ||||||
chr1:3823670
|
G | A | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2365-108C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3823670 | ||||||
chr1:3823706
|
G | A | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2365-144C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3823706 | ||||||
chr1:3823720
|
G | A | 1 | a0001c0001t0003g0314 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2365-158C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3823720 | ||||||
chr1:3823862
|
T | C | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2365-300A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3823862 | ||||||
chr1:3823898
|
T | C | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2365-336A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3823898 | ||||||
chr1:3823909
|
A | G | 210 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(207): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.2365-347T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3823909 | ||||||
chr1:3823989
|
C | G | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2365-427G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3823989 | ||||||
chr1:3824076
|
C | T | 22 | a0001c0001t0004g0002a0001c0001t0004g0142a0001c0001t0004g0143others(19): Show | 27 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.2365-514G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824076 | ||||||
chr1:3824084
|
T | C | 1 | a0001c0001t0005g0298 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2365-522A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824084 | ||||||
chr1:3824155
|
C | T | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2365-593G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824155 | ||||||
chr1:3824180
|
G | A | 178 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(175): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.2365-618C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824180 | ||||||
chr1:3824237
|
C | A | 33 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(30): Show | 41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.2365-675G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824237 | ||||||
chr1:3824274
|
C | T | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2365-712G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824274 | ||||||
chr1:3824341
|
C | T | 2 | a0001c0001t0003g0263a0001c0001t0003g0271 | 2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2365-779G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824341 | ||||||
chr1:3824515
|
C | T | 4 | a0003c0003t0002g0184a0003c0003t0002g0185a0003c0003t0002g0187others(1): Show | 4 | HG02523.hp2 HG03704.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.2365-953G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824515 | ||||||
chr1:3824540
|
C | T | 1 | a0001c0001t0004g0144 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2365-978G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824540 | ||||||
chr1:3824647
|
T | C | 209 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(206): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.2365-1085A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824647 | ||||||
chr1:3824648
|
G | C | 1 | a0001c0001t0008g0262 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2365-1086C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824648 | ||||||
chr1:3824666
|
C | T | 1 | a0003c0003t0002g0217 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2364+1092G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824666 | ||||||
chr1:3824761
|
A | T | 2 | a0001c0001t0027g0145a0001c0001t0028g0161 | 2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2364+997T>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824761 | ||||||
chr1:3824821
|
G | T | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2364+937C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824821 | ||||||
chr1:3824854
|
A | C | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2364+904T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824854 | ||||||
chr1:3824854
|
A | T | 4 | a0001c0001t0007g0014a0001c0001t0007g0273a0001c0001t0007g0275others(1): Show | 6 | HG02109.hp1 HG03195.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2364+904T>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824854 | ||||||
chr1:3824854
|
AGGCAGTG others(16): Show |
A | 1 | a0002c0002t0001g0081 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2364+881_2364+903d others(25): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824854 | ||||||
chr1:3824876
|
GC | G | 4 | a0001c0001t0007g0014a0001c0001t0007g0273a0001c0001t0007g0275others(1): Show | 6 | HG02109.hp1 HG03195.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2364+881delG | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824876 | ||||||
chr1:3824877
|
C | T | 174 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(171): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.2364+881G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824877 | ||||||
chr1:3824889
|
C | T | 4 | a0001c0001t0007g0014a0001c0001t0007g0273a0001c0001t0007g0275others(1): Show | 6 | HG02109.hp1 HG03195.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2364+869G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824889 | ||||||
chr1:3824896
|
A | AG | 6 | a0001c0001t0004g0151a0001c0001t0007g0014a0001c0001t0007g0273others(3): Show | 8 | HG02109.hp1 HG02738.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.2364+861dupC | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824896 | ||||||
chr1:3824901
|
G | A | 1 | a0001c0001t0003g0280 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2364+857C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824901 | ||||||
chr1:3824911
|
T | C | 13 | a0001c0001t0027g0145a0001c0001t0028g0161a0001c0006t0006g0124others(10): Show | 13 | HG02145.hp2 HG02257.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.2364+847A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824911 | ||||||
chr1:3824918
|
AG | A | 4 | a0001c0001t0007g0014a0001c0001t0007g0273a0001c0001t0007g0275others(1): Show | 6 | HG02109.hp1 HG03195.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2364+839delC | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824918 | ||||||
chr1:3824946
|
G | GA | 4 | a0001c0001t0007g0014a0001c0001t0007g0273a0001c0001t0007g0275others(1): Show | 6 | HG02109.hp1 HG03195.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2364+811_2364+812i others(3): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824946 | ||||||
chr1:3824968
|
GA | G | 4 | a0001c0001t0007g0014a0001c0001t0007g0273a0001c0001t0007g0275others(1): Show | 6 | HG02109.hp1 HG03195.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2364+789delT | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824968 | ||||||
chr1:3824978
|
C | T | 4 | a0001c0001t0007g0014a0001c0001t0007g0273a0001c0001t0007g0275others(1): Show | 6 | HG02109.hp1 HG03195.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2364+780G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3824978 | ||||||
chr1:3825000
|
C | T | 160 | a0001c0001t0003g0028a0001c0001t0003g0030a0001c0001t0003g0237others(157): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.2364+758G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825000 | ||||||
chr1:3825008
|
A | AG | 5 | a0001c0001t0007g0014a0001c0001t0007g0273a0001c0001t0007g0275others(2): Show | 7 | HG02109.hp1 HG03195.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.2364+749dupC | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825008 | ||||||
chr1:3825008
|
A | AGGGGGGC others(17): Show |
1 | a0001c0001t0004g0151 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2364+749_2364+750i others(26): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825008 | ||||||
chr1:3825012
|
GGCAGTGG others(60): Show |
G | 9 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(6): Show | 15 | HG00642.hp2 HG00741.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.2364+679_2364+745d others(69): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825012 | ||||||
chr1:3825030
|
AG | A | 4 | a0001c0001t0007g0014a0001c0001t0007g0273a0001c0001t0007g0275others(1): Show | 6 | HG02109.hp1 HG03195.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2364+727delC | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825030 | ||||||
chr1:3825031
|
G | GGGGGGGC others(16): Show |
3 | a0001c0001t0004g0143a0003c0003t0012g0290a0004c0007t0009g0250 | 3 | HG02145.hp1 HG02738.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2364+726_2364+727i others(25): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825031 | ||||||
chr1:3825035
|
G | GGCAGTGG others(15): Show |
2 | a0001c0001t0005g0294a0001c0001t0040g0315 | 2 | NA18990.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2364+722_2364+723i others(24): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825035 | ||||||
chr1:3825053
|
A | AG | 10 | a0001c0001t0004g0143a0001c0001t0004g0151a0001c0001t0007g0014others(7): Show | 12 | HG01168.hp1 HG01169.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2364+704dupC | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825053 | ||||||
chr1:3825053
|
A | AGGGGGCA others(16): Show |
1 | a0003c0003t0002g0213 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2364+704_2364+705i others(25): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825053 | ||||||
chr1:3825053
|
A | AGGGGGCA others(16): Show |
154 | a0001c0001t0003g0028a0001c0001t0003g0030a0001c0001t0003g0237others(151): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.2364+682_2364+704d others(25): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825053 | ||||||
chr1:3825053
|
A | AGGGGGCA others(17): Show |
2 | a0001c0001t0003g0311a0001c0001t0008g0248 | 2 | HG02074.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2364+681_2364+704d others(26): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825053 | ||||||
chr1:3825053
|
A | AGGGGGGC others(17): Show |
2 | a0001c0001t0004g0141a0001c0001t0008g0262 | 2 | HG03098.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.2364+704_2364+705i others(26): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825053 | ||||||
chr1:3825057
|
G | A | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2364+701C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825057 | ||||||
chr1:3825057
|
G | GGCAGTGG others(149): Show |
8 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(5): Show | 8 | HG02145.hp2 HG02257.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.2364+700_2364+701i others(158): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825057 | ||||||
chr1:3825057
|
G | GGCAGTGG others(127): Show |
2 | a0001c0006t0006g0129a0001c0006t0006g0133 | 2 | HG02622.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2364+700_2364+701i others(136): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825057 | ||||||
chr1:3825079
|
A | G | 169 | a0001c0001t0003g0028a0001c0001t0003g0030a0001c0001t0003g0237others(166): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.2364+679T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825079 | ||||||
chr1:3825080
|
G | A | 3 | a0001c0001t0005g0299a0001c0001t0005g0303a0001c0001t0038g0288 | 3 | NA18956.hp1 NA19004.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2364+678C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825080 | ||||||
chr1:3825145
|
G | A | 178 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(175): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.2364+613C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825145 | ||||||
chr1:3825218
|
C | T | 178 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(175): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.2364+540G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825218 | ||||||
chr1:3825289
|
G | A | 17 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(14): Show | 18 | HG00423.hp2 HG00609.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.2364+469C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825289 | ||||||
chr1:3825421
|
T | C | 33 | a0001c0001t0007g0014a0001c0001t0007g0272a0001c0001t0007g0273others(30): Show | 38 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.2364+337A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825421 | ||||||
chr1:3825445
|
C | T | 94 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(91): Show | 115 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.2364+313G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825445 | ||||||
chr1:3825539
|
C | T | 106 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(103): Show | 127 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.2364+219G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825539 | ||||||
chr1:3825548
|
G | A | 1 | a0001c0001t0003g0253 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2364+210C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825548 | ||||||
chr1:3825615
|
G | A | 207 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(204): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.2364+143C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825615 | ||||||
chr1:3825693
|
C | T | 35 | a0001c0001t0007g0014a0001c0001t0007g0272a0001c0001t0007g0273others(32): Show | 40 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.2364+65G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 18/21 | chr1 | 3825693 | ||||||
chr1:3825934
|
C | T | 4 | a0003c0003t0014g0137a0003c0003t0014g0138a0003c0003t0016g0230others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2256-68G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 17/21 | chr1 | 3825934 | ||||||
chr1:3825942
|
G | T | 1 | a0001c0001t0004g0157 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2256-76C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 17/21 | chr1 | 3825942 | ||||||
chr1:3825996
|
G | A | 87 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(84): Show | 107 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.2256-130C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 17/21 | chr1 | 3825996 | ||||||
chr1:3826126
|
G | A | 1 | a0001c0001t0003g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2255+244C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 17/21 | chr1 | 3826126 | ||||||
chr1:3826251
|
T | G | 1 | a0002c0002t0001g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2255+119A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 17/21 | chr1 | 3826251 | ||||||
chr1:3826260
|
TTA | T | 6 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311others(3): Show | 6 | HG01496.hp2 HG02683.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.2255+108_2255+109d others(4): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 17/21 | chr1 | 3826260 | ||||||
chr1:3826545
|
A | G | 210 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(207): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.2189-109T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 16/21 | chr1 | 3826545 | ||||||
chr1:3826568
|
T | C | 104 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(101): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.2189-132A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 16/21 | chr1 | 3826568 | ||||||
chr1:3826587
|
G | A | 23 | a0001c0001t0008g0013a0001c0001t0008g0024a0001c0001t0008g0248others(20): Show | 26 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.2188+121C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 16/21 | chr1 | 3826587 | ||||||
chr1:3826622
|
C | T | 20 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(17): Show | 21 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.2188+86G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 16/21 | chr1 | 3826622 | ||||||
chr1:3826755
|
G | A | 151 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(148): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.2152-11C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3826755 | ||||||
chr1:3826786
|
G | C | 23 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.2152-42C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3826786 | ||||||
chr1:3826827
|
C | T | 102 | a0001c0001t0004g0002a0001c0001t0004g0142a0001c0001t0004g0143others(99): Show | 127 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.2152-83G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3826827 | ||||||
chr1:3826869
|
T | TG | 241 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(238): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.2152-126dupC | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3826869 | ||||||
chr1:3826989
|
C | CA | 23 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(20): Show | 28 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.2152-246dupT | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3826989 | ||||||
chr1:3827021
|
C | T | 1 | a0001c0001t0005g0295 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2152-277G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827021 | ||||||
chr1:3827022
|
G | A | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2152-278C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827022 | ||||||
chr1:3827139
|
T | G | 4 | a0003c0003t0014g0137a0003c0003t0014g0138a0003c0003t0016g0230others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2152-395A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827139 | ||||||
chr1:3827277
|
C | T | 4 | a0003c0003t0014g0137a0003c0003t0014g0138a0003c0003t0016g0230others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2152-533G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827277 | ||||||
chr1:3827431
|
G | A | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.2152-687C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827431 | ||||||
chr1:3827478
|
C | T | 2 | a0003c0003t0018g0204a0003c0003t0018g0215 | 2 | HG00673.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.2152-734G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827478 | ||||||
chr1:3827483
|
G | C | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2152-739C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827483 | ||||||
chr1:3827520
|
G | A | 186 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(183): Show | 220 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.2152-776C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827520 | ||||||
chr1:3827562
|
T | C | 21 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(18): Show | 22 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.2152-818A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827562 | ||||||
chr1:3827572
|
T | G | 1 | a0001c0001t0004g0155 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2152-828A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827572 | ||||||
chr1:3827607
|
T | C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2152-863A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827607 | ||||||
chr1:3827685
|
A | G | 23 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(20): Show | 28 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.2152-941T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827685 | ||||||
chr1:3827697
|
C | A | 22 | a0001c0001t0004g0002a0001c0001t0004g0142a0001c0001t0004g0143others(19): Show | 27 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.2152-953G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827697 | ||||||
chr1:3827709
|
G | A | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2152-965C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827709 | ||||||
chr1:3827718
|
C | T | 4 | a0003c0003t0002g0023a0003c0003t0002g0180a0003c0003t0002g0220others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2152-974G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827718 | ||||||
chr1:3827742
|
T | C | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.2152-998A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827742 | ||||||
chr1:3827770
|
C | T | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2152-1026G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827770 | ||||||
chr1:3827804
|
G | A | 33 | a0001c0001t0007g0014a0001c0001t0007g0272a0001c0001t0007g0273others(30): Show | 38 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.2152-1060C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827804 | ||||||
chr1:3827874
|
T | C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2152-1130A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827874 | ||||||
chr1:3827935
|
C | T | 1 | a0003c0003t0002g0232 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2152-1191G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827935 | ||||||
chr1:3827984
|
A | G | 199 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(196): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2152-1240T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3827984 | ||||||
chr1:3828006
|
C | T | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2151+1260G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828006 | ||||||
chr1:3828010
|
C | T | 4 | a0001c0001t0003g0028a0001c0001t0003g0279a0001c0001t0003g0281others(1): Show | 5 | HG01168.hp2 HG01192.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2151+1256G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828010 | ||||||
chr1:3828077
|
G | A | 44 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(41): Show | 50 | HG00323.hp1 HG00423.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.2151+1189C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828077 | ||||||
chr1:3828153
|
G | A | 1 | a0004c0007t0009g0245 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2151+1113C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828153 | ||||||
chr1:3828185
|
A | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2151+1081T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828185 | ||||||
chr1:3828188
|
C | T | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2151+1078G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828188 | ||||||
chr1:3828296
|
G | A | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2151+970C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828296 | ||||||
chr1:3828429
|
G | A | 1 | a0001c0001t0009g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2151+837C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828429 | ||||||
chr1:3828451
|
T | G | 33 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(30): Show | 41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.2151+815A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828451 | ||||||
chr1:3828541
|
G | C | 2 | a0001c0001t0004g0142a0001c0001t0004g0157 | 2 | HG00323.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.2151+725C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828541 | ||||||
chr1:3828568
|
C | T | 21 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(18): Show | 22 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.2151+698G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828568 | ||||||
chr1:3828569
|
A | G | 118 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(115): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.2151+697T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828569 | ||||||
chr1:3828629
|
T | C | 118 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(115): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.2151+637A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828629 | ||||||
chr1:3828749
|
A | G | 1 | a0001c0001t0003g0278 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2151+517T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828749 | ||||||
chr1:3828810
|
A | G | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.2151+456T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828810 | ||||||
chr1:3828852
|
T | TAA | 118 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(115): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.2151+413_2151+414i others(4): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828852 | ||||||
chr1:3828907
|
C | T | 10 | a0001c0001t0007g0014a0001c0001t0007g0272a0001c0001t0007g0273others(7): Show | 12 | HG02109.hp1 HG02559.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.2151+359G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828907 | ||||||
chr1:3828993
|
G | T | 199 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(196): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.2151+273C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3828993 | ||||||
chr1:3829118
|
C | T | 1 | a0001c0006t0021g0117 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2151+148G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3829118 | ||||||
chr1:3829157
|
C | T | 44 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(41): Show | 50 | HG00323.hp1 HG00423.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.2151+109G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3829157 | ||||||
chr1:3829223
|
T | C | 210 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(207): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.2151+43A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 15/21 | chr1 | 3829223 | ||||||
chr1:3829537
|
T | C | 2 | a0003c0003t0016g0230a0003c0003t0016g0231 | 2 | HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2044-164A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 14/21 | chr1 | 3829537 | ||||||
chr1:3829552
|
A | G | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.2044-179T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 14/21 | chr1 | 3829552 | ||||||
chr1:3829564
|
C | T | 1 | a0003c0003t0030g0202 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2044-191G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 14/21 | chr1 | 3829564 | ||||||
chr1:3829620
|
T | C | 1 | a0002c0002t0001g0099 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2043+171A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 14/21 | chr1 | 3829620 | ||||||
chr1:3829671
|
C | T | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2043+120G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 14/21 | chr1 | 3829671 | ||||||
chr1:3829690
|
T | C | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.2043+101A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 14/21 | chr1 | 3829690 | ||||||
chr1:3829709
|
A | G | 1 | a0001c0001t0004g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2043+82T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 14/21 | chr1 | 3829709 | ||||||
chr1:3830019
|
G | T | 115 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(112): Show | 143 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1837-22C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830019 | ||||||
chr1:3830021
|
T | G | 44 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(41): Show | 50 | HG00323.hp1 HG00423.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1837-24A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830021 | ||||||
chr1:3830025
|
C | G | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1837-28G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830025 | ||||||
chr1:3830071
|
A | G | 5 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0251others(2): Show | 7 | HG00642.hp2 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837-74T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830071 | ||||||
chr1:3830146
|
C | T | 23 | a0001c0001t0008g0013a0001c0001t0008g0024a0001c0001t0008g0248others(20): Show | 26 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.1837-149G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830146 | ||||||
chr1:3830248
|
T | C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1837-251A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830248 | ||||||
chr1:3830255
|
C | T | 3 | a0001c0001t0009g0242a0001c0001t0009g0243a0005c0008t0015g0140 | 3 | HG02109.hp2 HG02451.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1837-258G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830255 | ||||||
chr1:3830459
|
C | G | 44 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(41): Show | 50 | HG00323.hp1 HG00423.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1837-462G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830459 | ||||||
chr1:3830483
|
T | C | 1 | a0002c0002t0001g0078 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1837-486A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830483 | ||||||
chr1:3830496
|
G | A | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1837-499C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830496 | ||||||
chr1:3830604
|
T | A | 1 | a0003c0004t0002g0198 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1836+442A>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830604 | ||||||
chr1:3830735
|
C | T | 2 | a0001c0001t0003g0276a0001c0001t0003g0277 | 2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1836+311G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830735 | ||||||
chr1:3830736
|
A | G | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1836+310T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830736 | ||||||
chr1:3830755
|
C | T | 73 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(70): Show | 98 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1836+291G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830755 | ||||||
chr1:3830776
|
CA | C | 157 | a0001c0001t0003g0028a0001c0001t0003g0279a0001c0001t0003g0281others(154): Show | 192 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.1836+269delT | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830776 | ||||||
chr1:3830776
|
CAA | C | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 84 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1836+268_1836+269d others(4): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830776 | ||||||
chr1:3830833
|
A | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1836+213T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830833 | ||||||
chr1:3830978
|
C | G | 11 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(8): Show | 12 | HG01952.hp1 HG02129.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.1836+68G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3830978 | ||||||
chr1:3831009
|
T | C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1836+37A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3831009 | ||||||
chr1:3831016
|
C | T | 114 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(111): Show | 142 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1836+30G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3831016 | ||||||
chr1:3831032
|
C | T | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1836+14G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3831032 | ||||||
chr1:3831039
|
T | C | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
splice_region_variant&intron_variant | LOW | c.1836+7A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 13/21 | chr1 | 3831039 | ||||||
chr1:3831263
|
T | C | 11 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(8): Show | 17 | HG00642.hp2 HG00741.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1660-41A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3831263 | ||||||
chr1:3831455
|
C | T | 2 | a0001c0001t0007g0272a0002c0002t0001g0120 | 2 | HG01257.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1660-233G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3831455 | ||||||
chr1:3831456
|
G | A | 1 | a0003c0003t0002g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1660-234C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3831456 | ||||||
chr1:3831521
|
A | G | 159 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(156): Show | 193 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.1660-299T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3831521 | ||||||
chr1:3831532
|
C | T | 1 | a0002c0002t0001g0035 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1660-310G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3831532 | ||||||
chr1:3831543
|
T | C | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1660-321A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3831543 | ||||||
chr1:3831607
|
T | C | 114 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(111): Show | 142 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1660-385A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3831607 | ||||||
chr1:3831650
|
G | A | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1660-428C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3831650 | ||||||
chr1:3831711
|
A | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1660-489T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3831711 | ||||||
chr1:3831728
|
T | C | 1 | a0002c0002t0001g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1660-506A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3831728 | ||||||
chr1:3831757
|
G | A | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1660-535C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3831757 | ||||||
chr1:3831898
|
T | A | 2 | a0001c0001t0009g0242a0001c0001t0009g0243 | 2 | HG02109.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1660-676A>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3831898 | ||||||
chr1:3831949
|
G | T | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1660-727C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3831949 | ||||||
chr1:3832041
|
G | A | 44 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(41): Show | 50 | HG00323.hp1 HG00423.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1660-819C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832041 | ||||||
chr1:3832050
|
C | A | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1660-828G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832050 | ||||||
chr1:3832091
|
C | G | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.1660-869G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832091 | ||||||
chr1:3832124
|
A | C | 104 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(101): Show | 132 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1660-902T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832124 | ||||||
chr1:3832238
|
CGTAACCA others(10): Show |
C | 207 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(204): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1660-1033_1660-101 others(21): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832238 | ||||||
chr1:3832239
|
G | A | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1660-1017C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832239 | ||||||
chr1:3832336
|
T | G | 2 | a0001c0001t0003g0314a0001c0001t0037g0312 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1660-1114A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832336 | ||||||
chr1:3832370
|
G | A | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1660-1148C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832370 | ||||||
chr1:3832372
|
A | AACCAGGA others(41): Show |
2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1660-1151_1660-115 others(52): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832372 | ||||||
chr1:3832372
|
AACCAGGA others(41): Show |
A | 23 | a0001c0001t0004g0002a0001c0001t0004g0142a0001c0001t0004g0143others(20): Show | 28 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1660-1198_1660-115 others(52): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832372 | ||||||
chr1:3832394
|
GTGACCAG others(17): Show |
G | 131 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(128): Show | 160 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.1660-1196_1660-117 others(28): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832394 | ||||||
chr1:3832396
|
G | A | 1 | a0002c0002t0001g0100 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1660-1174C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832396 | ||||||
chr1:3832410
|
CGTAGGTC others(89): Show |
C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1660-1284_1660-118 others(100): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832410 | ||||||
chr1:3832418
|
C | G | 81 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(78): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1660-1196G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832418 | ||||||
chr1:3832420
|
G | GACCAGGA others(73): Show |
1 | a0001c0001t0007g0284 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1660-1199_1660-119 others(84): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832420 | ||||||
chr1:3832420
|
G | GACCAGGA others(73): Show |
66 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(63): Show | 79 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1660-1199_1660-119 others(84): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832420 | ||||||
chr1:3832434
|
C | T | 6 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0259others(3): Show | 6 | HG02895.hp2 HG03195.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1660-1212G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832434 | ||||||
chr1:3832442
|
G | A | 1 | a0003c0003t0002g0216 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1660-1220C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832442 | ||||||
chr1:3832444
|
G | GACCAGGA others(49): Show |
6 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0259others(3): Show | 6 | HG02895.hp2 HG03195.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1660-1223_1660-122 others(60): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832444 | ||||||
chr1:3832444
|
GACCAGGA others(89): Show |
G | 2 | a0002c0002t0001g0072a0002c0002t0001g0096 | 2 | HG01884.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1660-1318_1660-122 others(100): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832444 | ||||||
chr1:3832465
|
C | T | 1 | a0002c0002t0001g0052 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1660-1243G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832465 | ||||||
chr1:3832468
|
GACCAGGA others(65): Show |
G | 1 | a0002c0002t0001g0052 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1660-1318_1660-124 others(76): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832468 | ||||||
chr1:3832492
|
GACCAGGA others(41): Show |
G | 111 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(108): Show | 139 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1660-1318_1660-127 others(52): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832492 | ||||||
chr1:3832506
|
T | C | 25 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(22): Show | 26 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.1660-1284A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832506 | ||||||
chr1:3832513
|
C | T | 1 | a0003c0003t0002g0172 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1660-1291G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832513 | ||||||
chr1:3832538
|
A | G | 8 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0259others(5): Show | 8 | HG02451.hp2 HG02559.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1660-1316T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832538 | ||||||
chr1:3832540
|
A | G | 7 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0259others(4): Show | 7 | HG02895.hp2 HG02922.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1660-1318T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832540 | ||||||
chr1:3832551
|
T | C | 104 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(101): Show | 132 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1659+1311A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832551 | ||||||
chr1:3832710
|
T | C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1659+1152A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832710 | ||||||
chr1:3832753
|
C | T | 2 | a0001c0001t0020g0286a0001c0001t0020g0287 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1659+1109G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832753 | ||||||
chr1:3832793
|
G | A | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1659+1069C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832793 | ||||||
chr1:3832797
|
C | T | 1 | a0001c0001t0003g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1659+1065G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832797 | ||||||
chr1:3832842
|
G | A | 4 | a0003c0003t0002g0023a0003c0003t0002g0180a0003c0003t0002g0220others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1659+1020C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832842 | ||||||
chr1:3832938
|
C | T | 1 | a0012c0019t0032g0234 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1659+924G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832938 | ||||||
chr1:3832973
|
G | A | 1 | a0001c0001t0005g0293 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1659+889C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832973 | ||||||
chr1:3832987
|
C | CT | 118 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(115): Show | 146 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.1659+874dupA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832987 | ||||||
chr1:3832987
|
CT | C | 5 | a0001c0001t0003g0028a0001c0001t0003g0279a0001c0001t0003g0281others(2): Show | 6 | HG01168.hp2 HG01192.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1659+874delA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832987 | ||||||
chr1:3832987
|
CTT | C | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 84 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1659+873_1659+874d others(4): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3832987 | ||||||
chr1:3833024
|
T | C | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1659+838A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833024 | ||||||
chr1:3833046
|
G | A | 43 | a0001c0001t0004g0002a0001c0001t0004g0142a0001c0001t0004g0143others(40): Show | 49 | HG00323.hp1 HG00423.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1659+816C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833046 | ||||||
chr1:3833055
|
G | A | 2 | a0003c0003t0002g0170a0003c0003t0002g0172 | 2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1659+807C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833055 | ||||||
chr1:3833083
|
C | G | 114 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(111): Show | 142 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1659+779G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833083 | ||||||
chr1:3833084
|
G | A | 114 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(111): Show | 142 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1659+778C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833084 | ||||||
chr1:3833129
|
C | T | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1659+733G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833129 | ||||||
chr1:3833130
|
A | G | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1659+732T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833130 | ||||||
chr1:3833141
|
C | T | 1 | a0001c0001t0003g0310 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1659+721G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833141 | ||||||
chr1:3833187
|
G | C | 1 | a0001c0001t0004g0149 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1659+675C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833187 | ||||||
chr1:3833209
|
A | G | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1659+653T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833209 | ||||||
chr1:3833338
|
C | T | 1 | a0002c0002t0001g0054 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1659+524G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833338 | ||||||
chr1:3833506
|
A | T | 1 | a0003c0003t0002g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1659+356T>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833506 | ||||||
chr1:3833511
|
T | C | 75 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(72): Show | 88 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.1659+351A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833511 | ||||||
chr1:3833574
|
A | T | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1659+288T>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833574 | ||||||
chr1:3833594
|
A | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1659+268T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833594 | ||||||
chr1:3833603
|
G | A | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1659+259C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833603 | ||||||
chr1:3833621
|
A | C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1659+241T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833621 | ||||||
chr1:3833651
|
AC | A | 117 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(114): Show | 145 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1659+210delG | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833651 | ||||||
chr1:3833760
|
A | G | 1 | a0002c0002t0001g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1659+102T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 12/21 | chr1 | 3833760 | ||||||
chr1:3834071
|
C | T | 1 | a0002c0002t0001g0075 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1486-36G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834071 | ||||||
chr1:3834122
|
C | T | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1486-87G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834122 | ||||||
chr1:3834165
|
A | G | 115 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(112): Show | 143 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1486-130T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834165 | ||||||
chr1:3834167
|
T | G | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1486-132A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834167 | ||||||
chr1:3834252
|
CATCTTCC others(46): Show |
C | 115 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(112): Show | 143 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1486-270_1486-218d others(55): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834252 | ||||||
chr1:3834322
|
G | A | 1 | a0003c0003t0002g0216 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1486-287C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834322 | ||||||
chr1:3834361
|
C | T | 2 | a0003c0003t0002g0022a0003c0003t0002g0188 | 3 | HG02129.hp1 HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1486-326G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834361 | ||||||
chr1:3834421
|
T | C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1486-386A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834421 | ||||||
chr1:3834428
|
G | A | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1486-393C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834428 | ||||||
chr1:3834476
|
A | T | 1 | a0002c0002t0001g0071 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1486-441T>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834476 | ||||||
chr1:3834539
|
T | G | 73 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(70): Show | 86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1485+386A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834539 | ||||||
chr1:3834557
|
A | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1485+368T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834557 | ||||||
chr1:3834652
|
C | T | 3 | a0001c0006t0021g0117a0003c0003t0016g0230a0003c0003t0016g0231 | 3 | HG02723.hp2 HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1485+273G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834652 | ||||||
chr1:3834714
|
C | G | 114 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(111): Show | 142 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1485+211G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834714 | ||||||
chr1:3834820
|
C | T | 1 | a0003c0003t0002g0172 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1485+105G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834820 | ||||||
chr1:3834873
|
C | T | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1485+52G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834873 | ||||||
chr1:3834895
|
C | A | 7 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311others(4): Show | 7 | HG01496.hp2 HG02683.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1485+30G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834895 | ||||||
chr1:3834905
|
C | T | 1 | a0001c0001t0003g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1485+20G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 11/21 | chr1 | 3834905 | ||||||
chr1:3835164
|
G | GT | 73 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(70): Show | 86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1318-73dupA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3835164 | ||||||
chr1:3835247
|
T | A | 1 | a0002c0002t0001g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1318-155A>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3835247 | ||||||
chr1:3835365
|
G | T | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1318-273C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3835365 | ||||||
chr1:3835373
|
C | T | 10 | a0001c0001t0007g0014a0001c0001t0007g0272a0001c0001t0007g0273others(7): Show | 12 | HG02109.hp1 HG02559.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1318-281G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3835373 | ||||||
chr1:3835402
|
C | G | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.1318-310G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3835402 | ||||||
chr1:3835491
|
G | A | 4 | a0001c0001t0003g0030a0001c0001t0003g0306a0001c0001t0003g0307others(1): Show | 5 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1318-399C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3835491 | ||||||
chr1:3835557
|
G | A | 20 | a0001c0001t0003g0028a0001c0001t0003g0030a0001c0001t0003g0237others(17): Show | 22 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.1318-465C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3835557 | ||||||
chr1:3835770
|
C | T | 3 | a0001c0001t0010g0244a0001c0001t0010g0247a0001c0001t0010g0260 | 3 | HG01074.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1318-678G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3835770 | ||||||
chr1:3835904
|
T | C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1317+591A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3835904 | ||||||
chr1:3836005
|
TA | T | 214 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(211): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1317+489delT | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836005 | ||||||
chr1:3836079
|
A | C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1317+416T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836079 | ||||||
chr1:3836175
|
G | A | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1317+320C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836175 | ||||||
chr1:3836184
|
T | C | 7 | a0002c0002t0001g0007a0002c0002t0001g0015a0002c0002t0001g0016others(4): Show | 12 | NA18954.hp2 NA18970.hp2 NA18971.hp1 others(9): Show |
intron_variant | MODIFIER | c.1317+311A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836184 | ||||||
chr1:3836228
|
G | A | 22 | a0001c0001t0004g0002a0001c0001t0004g0142a0001c0001t0004g0143others(19): Show | 27 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1317+267C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836228 | ||||||
chr1:3836237
|
C | T | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1317+258G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836237 | ||||||
chr1:3836243
|
T | G | 4 | a0001c0001t0003g0027a0001c0001t0003g0251a0001c0001t0003g0253others(1): Show | 5 | HG00642.hp2 HG02280.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1317+252A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836243 | ||||||
chr1:3836293
|
A | G | 73 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(70): Show | 86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1317+202T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836293 | ||||||
chr1:3836298
|
C | A | 1 | a0001c0001t0003g0310 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1317+197G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836298 | ||||||
chr1:3836304
|
CA | C | 9 | a0001c0001t0005g0292a0001c0001t0005g0303a0001c0001t0007g0285others(6): Show | 9 | HG01168.hp1 HG02004.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1317+190delT | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836304 | ||||||
chr1:3836304
|
CAA | C | 198 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(195): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1317+189_1317+190d others(4): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836304 | ||||||
chr1:3836304
|
CAAA | C | 29 | a0001c0001t0003g0276a0001c0001t0003g0281a0001c0001t0004g0002others(26): Show | 34 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1317+188_1317+190d others(5): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836304 | ||||||
chr1:3836377
|
C | T | 5 | a0001c0001t0007g0272a0001c0001t0007g0283a0001c0001t0007g0284others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1317+118G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836377 | ||||||
chr1:3836449
|
G | C | 73 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(70): Show | 86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1317+46C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836449 | ||||||
chr1:3836467
|
C | T | 1 | a0002c0002t0001g0109 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1317+28G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836467 | ||||||
chr1:3836468
|
G | GT | 134 | a0001c0001t0004g0146a0001c0001t0004g0148a0001c0001t0004g0149others(131): Show | 170 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.1317+26dupA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836468 | ||||||
chr1:3836468
|
G | GTT | 59 | a0001c0001t0003g0237a0001c0001t0003g0257a0001c0001t0003g0258others(56): Show | 65 | HG00741.hp1 HG01109.hp1 HG01175.hp2 others(62): Show |
intron_variant | MODIFIER | c.1317+25_1317+26dup others(2): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836468 | ||||||
chr1:3836468
|
G | GTTT | 32 | a0001c0001t0003g0009a0001c0001t0003g0026a0001c0001t0003g0027others(29): Show | 41 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.1317+24_1317+26dup others(3): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836468 | ||||||
chr1:3836468
|
G | GTTTT | 5 | a0001c0001t0003g0025a0001c0001t0003g0254a0001c0001t0003g0308others(2): Show | 6 | HG00280.hp2 HG01243.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1317+23_1317+26dup others(4): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 10/21 | chr1 | 3836468 | ||||||
chr1:3836751
|
G | C | 20 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(17): Show | 21 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.1120-59C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 9/21 | chr1 | 3836751 | ||||||
chr1:3836870
|
A | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1120-178T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 9/21 | chr1 | 3836870 | ||||||
chr1:3836905
|
C | T | 1 | a0003c0003t0002g0172 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1120-213G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 9/21 | chr1 | 3836905 | ||||||
chr1:3837249
|
T | C | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1119+43A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 9/21 | chr1 | 3837249 | ||||||
chr1:3837260
|
A | G | 3 | a0003c0004t0002g0012a0003c0004t0002g0197a0003c0004t0002g0198 | 5 | NA18957.hp1 NA18975.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119+32T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 9/21 | chr1 | 3837260 | ||||||
chr1:3837917
|
G | A | 1 | a0002c0002t0001g0081 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.892-398C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 8/21 | chr1 | 3837917 | ||||||
chr1:3837925
|
G | C | 114 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(111): Show | 142 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.892-406C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 8/21 | chr1 | 3837925 | ||||||
chr1:3838032
|
G | T | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.892-513C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 8/21 | chr1 | 3838032 | ||||||
chr1:3838206
|
G | A | 1 | a0001c0006t0021g0117 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.892-687C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 8/21 | chr1 | 3838206 | ||||||
chr1:3838238
|
G | A | 3 | a0001c0006t0006g0127a0001c0006t0006g0133a0018c0010t0006g0125 | 3 | HG02145.hp2 HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.892-719C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 8/21 | chr1 | 3838238 | ||||||
chr1:3838348
|
T | TCTATGTT others(22): Show |
3 | a0001c0001t0005g0295a0001c0001t0005g0301a0001c0001t0005g0304 | 3 | HG00423.hp2 HG00609.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.891+587_891+615dup others(29): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 8/21 | chr1 | 3838348 | ||||||
chr1:3838431
|
G | A | 1 | a0002c0002t0001g0086 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.891+533C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 8/21 | chr1 | 3838431 | ||||||
chr1:3838480
|
C | T | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.891+484G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 8/21 | chr1 | 3838480 | ||||||
chr1:3838526
|
C | T | 1 | a0001c0001t0003g0310 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.891+438G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 8/21 | chr1 | 3838526 | ||||||
chr1:3838829
|
T | C | 1 | a0001c0001t0003g0278 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.891+135A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 8/21 | chr1 | 3838829 | ||||||
chr1:3839143
|
T | C | 1 | a0003c0004t0002g0214 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.736-24A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 7/21 | chr1 | 3839143 | ||||||
chr1:3839199
|
G | A | 1 | a0002c0002t0001g0039 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.736-80C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 7/21 | chr1 | 3839199 | ||||||
chr1:3839206
|
C | A | 2 | a0003c0003t0012g0289a0003c0003t0012g0290 | 2 | HG02738.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.736-87G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 7/21 | chr1 | 3839206 | ||||||
chr1:3839208
|
G | A | 1 | a0002c0002t0001g0082 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.736-89C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 7/21 | chr1 | 3839208 | ||||||
chr1:3839305
|
T | C | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.736-186A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 7/21 | chr1 | 3839305 | ||||||
chr1:3839311
|
T | G | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.736-192A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 7/21 | chr1 | 3839311 | ||||||
chr1:3839354
|
T | C | 4 | a0003c0003t0014g0137a0003c0003t0014g0138a0003c0003t0016g0230others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.736-235A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 7/21 | chr1 | 3839354 | ||||||
chr1:3839401
|
C | T | 2 | a0001c0001t0009g0242a0001c0001t0009g0243 | 2 | HG02109.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.735+207G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 7/21 | chr1 | 3839401 | ||||||
chr1:3839510
|
C | A | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.735+98G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 7/21 | chr1 | 3839510 | ||||||
chr1:3839556
|
A | G | 134 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(131): Show | 163 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.735+52T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 7/21 | chr1 | 3839556 | ||||||
chr1:3839583
|
G | A | 1 | a0003c0003t0018g0215 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.735+25C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 7/21 | chr1 | 3839583 | ||||||
chr1:3839591
|
T | C | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.735+17A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 7/21 | chr1 | 3839591 | ||||||
chr1:3839814
|
C | T | 1 | a0002c0002t0001g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.567-38G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3839814 | ||||||
chr1:3839898
|
C | T | 3 | a0001c0001t0008g0248a0001c0001t0008g0261a0001c0001t0008g0262 | 3 | HG02074.hp2 NA18965.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.567-122G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3839898 | ||||||
chr1:3839929
|
T | C | 239 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(236): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.567-153A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3839929 | ||||||
chr1:3839966
|
C | A | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.567-190G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3839966 | ||||||
chr1:3839968
|
T | C | 134 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(131): Show | 163 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.567-192A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3839968 | ||||||
chr1:3840072
|
C | T | 1 | a0015c0021t0012g0255 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.567-296G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3840072 | ||||||
chr1:3840113
|
T | C | 1 | a0001c0001t0007g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.567-337A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3840113 | ||||||
chr1:3840209
|
C | A | 1 | a0001c0001t0010g0249 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.567-433G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3840209 | ||||||
chr1:3840259
|
C | T | 4 | a0001c0001t0027g0145a0001c0001t0028g0161a0005c0008t0015g0139others(1): Show | 4 | HG02451.hp2 HG02559.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.567-483G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3840259 | ||||||
chr1:3840329
|
C | T | 1 | a0016c0022t0034g0269 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.567-553G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3840329 | ||||||
chr1:3840345
|
T | C | 25 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(22): Show | 30 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.567-569A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3840345 | ||||||
chr1:3840427
|
G | A | 23 | a0001c0001t0008g0013a0001c0001t0008g0024a0001c0001t0008g0248others(20): Show | 26 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.567-651C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3840427 | ||||||
chr1:3840530
|
G | A | 1 | a0001c0001t0004g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.567-754C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3840530 | ||||||
chr1:3840697
|
C | T | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.567-921G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3840697 | ||||||
chr1:3840736
|
C | T | 114 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(111): Show | 142 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.567-960G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3840736 | ||||||
chr1:3841017
|
A | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.567-1241T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841017 | ||||||
chr1:3841143
|
C | T | 1 | a0003c0003t0002g0196 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.567-1367G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841143 | ||||||
chr1:3841185
|
G | A | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.567-1409C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841185 | ||||||
chr1:3841286
|
C | A | 1 | a0002c0002t0001g0083 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.567-1510G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841286 | ||||||
chr1:3841318
|
C | T | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.567-1542G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841318 | ||||||
chr1:3841320
|
GTAC | G | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.567-1547_567-1545d others(5): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841320 | ||||||
chr1:3841325
|
T | G | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.567-1549A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841325 | ||||||
chr1:3841326
|
C | T | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.567-1550G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841326 | ||||||
chr1:3841468
|
C | A | 1 | a0001c0001t0004g0156 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.567-1692G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841468 | ||||||
chr1:3841629
|
C | A | 1 | a0003c0003t0002g0216 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.567-1853G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841629 | ||||||
chr1:3841636
|
C | T | 6 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311others(3): Show | 6 | HG01496.hp2 HG02683.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.567-1860G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841636 | ||||||
chr1:3841647
|
G | A | 1 | a0001c0001t0004g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.567-1871C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841647 | ||||||
chr1:3841929
|
T | C | 22 | a0001c0001t0004g0002a0001c0001t0004g0142a0001c0001t0004g0143others(19): Show | 27 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.567-2153A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841929 | ||||||
chr1:3841969
|
C | T | 2 | a0002c0002t0001g0065a0002c0002t0001g0067 | 2 | HG00597.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.567-2193G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841969 | ||||||
chr1:3841995
|
C | T | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.567-2219G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841995 | ||||||
chr1:3841996
|
A | G | 2 | a0001c0001t0020g0286a0001c0001t0020g0287 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.567-2220T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3841996 | ||||||
chr1:3842086
|
TTTTTTA | T | 25 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(22): Show | 30 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.567-2316_567-2311d others(8): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842086 | ||||||
chr1:3842093
|
T | A | 1 | a0016c0022t0034g0269 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.567-2317A>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842093 | ||||||
chr1:3842117
|
C | T | 16 | a0001c0001t0003g0028a0001c0001t0003g0030a0001c0001t0003g0264others(13): Show | 18 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.567-2341G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842117 | ||||||
chr1:3842151
|
G | A | 5 | a0002c0002t0001g0044a0002c0002t0001g0085a0002c0002t0001g0086others(2): Show | 5 | HG02071.hp1 HG02132.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.567-2375C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842151 | ||||||
chr1:3842154
|
T | C | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.567-2378A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842154 | ||||||
chr1:3842162
|
G | A | 4 | a0003c0003t0014g0137a0003c0003t0014g0138a0003c0003t0016g0230others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.567-2386C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842162 | ||||||
chr1:3842192
|
A | G | 237 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(234): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.567-2416T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842192 | ||||||
chr1:3842281
|
C | T | 1 | a0001c0001t0003g0264 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.567-2505G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842281 | ||||||
chr1:3842415
|
C | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.566+2492G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842415 | ||||||
chr1:3842547
|
C | T | 1 | a0001c0006t0006g0127 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.566+2360G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842547 | ||||||
chr1:3842701
|
A | G | 33 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(30): Show | 41 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.566+2206T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842701 | ||||||
chr1:3842765
|
T | C | 1 | a0002c0002t0001g0114 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.566+2142A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842765 | ||||||
chr1:3842769
|
A | G | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.566+2138T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842769 | ||||||
chr1:3842772
|
T | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.566+2135A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842772 | ||||||
chr1:3842788
|
T | A | 115 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(112): Show | 143 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.566+2119A>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842788 | ||||||
chr1:3842800
|
G | A | 2 | a0001c0001t0004g0142a0001c0001t0004g0157 | 2 | HG00323.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.566+2107C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842800 | ||||||
chr1:3842810
|
T | C | 1 | a0001c0006t0006g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.566+2097A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842810 | ||||||
chr1:3842936
|
C | T | 10 | a0001c0001t0010g0235a0001c0001t0010g0244a0001c0001t0010g0246others(7): Show | 10 | HG00140.hp2 HG01074.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.566+1971G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842936 | ||||||
chr1:3842989
|
T | C | 1 | a0002c0002t0001g0104 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.566+1918A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3842989 | ||||||
chr1:3843026
|
G | A | 4 | a0003c0003t0014g0137a0003c0003t0014g0138a0003c0003t0016g0230others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.566+1881C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843026 | ||||||
chr1:3843027
|
A | G | 5 | a0002c0002t0001g0037a0002c0002t0001g0050a0002c0002t0001g0064others(2): Show | 5 | HG00438.hp2 HG00609.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.566+1880T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843027 | ||||||
chr1:3843032
|
C | T | 1 | a0001c0001t0007g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.566+1875G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843032 | ||||||
chr1:3843068
|
G | A | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.566+1839C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843068 | ||||||
chr1:3843072
|
G | A | 1 | a0001c0001t0005g0304 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.566+1835C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843072 | ||||||
chr1:3843196
|
C | A | 6 | a0002c0002t0001g0036a0002c0002t0001g0058a0002c0002t0001g0087others(3): Show | 6 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.566+1711G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843196 | ||||||
chr1:3843216
|
G | A | 1 | a0002c0002t0001g0046 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.566+1691C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843216 | ||||||
chr1:3843220
|
A | G | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.566+1687T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843220 | ||||||
chr1:3843244
|
G | C | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.566+1663C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843244 | ||||||
chr1:3843310
|
C | T | 2 | a0001c0001t0003g0308a0003c0003t0002g0195 | 2 | HG03486.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.566+1597G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843310 | ||||||
chr1:3843322
|
T | A | 1 | a0002c0002t0001g0059 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.566+1585A>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843322 | ||||||
chr1:3843325
|
T | TA | 112 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(109): Show | 140 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.566+1581dupT | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843325 | ||||||
chr1:3843325
|
T | TAA | 20 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(17): Show | 21 | HG00438.hp1 HG00609.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.566+1580_566+1581d others(4): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843325 | ||||||
chr1:3843349
|
G | A | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.566+1558C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843349 | ||||||
chr1:3843373
|
A | G | 104 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(101): Show | 132 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.566+1534T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843373 | ||||||
chr1:3843375
|
A | AC | 18 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0293others(15): Show | 19 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.566+1531_566+1532i others(3): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843375 | ||||||
chr1:3843376
|
A | AT | 134 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(131): Show | 167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.566+1530dupA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843376 | ||||||
chr1:3843376
|
A | ATT | 6 | a0001c0001t0004g0151a0001c0001t0004g0152a0001c0006t0006g0127others(3): Show | 6 | HG01517.hp1 HG02135.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+1529_566+1530d others(4): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843376 | ||||||
chr1:3843376
|
A | C | 1 | a0001c0001t0005g0292 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.566+1531T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843376 | ||||||
chr1:3843376
|
A | T | 18 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0293others(15): Show | 19 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.566+1531T>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843376 | ||||||
chr1:3843497
|
G | A | 115 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(112): Show | 143 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.566+1410C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843497 | ||||||
chr1:3843544
|
GTTTTGA | G | 74 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(71): Show | 87 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.566+1357_566+1362d others(8): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843544 | ||||||
chr1:3843550
|
A | G | 159 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(156): Show | 193 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.566+1357T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843550 | ||||||
chr1:3843565
|
C | T | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.566+1342G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843565 | ||||||
chr1:3843637
|
C | G | 1 | a0001c0001t0003g0276 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.566+1270G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843637 | ||||||
chr1:3843637
|
C | T | 4 | a0001c0001t0007g0014a0001c0001t0007g0273a0001c0001t0007g0275others(1): Show | 6 | HG02109.hp1 HG03195.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.566+1270G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843637 | ||||||
chr1:3843666
|
C | T | 237 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(234): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.566+1241G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843666 | ||||||
chr1:3843670
|
G | A | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.566+1237C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843670 | ||||||
chr1:3843745
|
G | A | 70 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(67): Show | 83 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.566+1162C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843745 | ||||||
chr1:3843792
|
T | C | 237 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(234): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.566+1115A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843792 | ||||||
chr1:3843954
|
A | G | 237 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(234): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.566+953T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3843954 | ||||||
chr1:3844106
|
C | G | 74 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(71): Show | 87 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.566+801G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844106 | ||||||
chr1:3844108
|
A | G | 2 | a0002c0002t0001g0054a0002c0002t0001g0063 | 2 | HG00733.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.566+799T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844108 | ||||||
chr1:3844248
|
C | T | 1 | a0001c0001t0010g0235 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.566+659G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844248 | ||||||
chr1:3844420
|
C | T | 13 | a0001c0001t0003g0028a0001c0001t0003g0030a0001c0001t0003g0264others(10): Show | 15 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.566+487G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844420 | ||||||
chr1:3844494
|
C | T | 33 | a0001c0001t0007g0014a0001c0001t0007g0272a0001c0001t0007g0273others(30): Show | 38 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.566+413G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844494 | ||||||
chr1:3844542
|
C | T | 31 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(28): Show | 39 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.566+365G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844542 | ||||||
chr1:3844696
|
C | T | 1 | a0001c0006t0006g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.566+211G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844696 | ||||||
chr1:3844697
|
T | TTAAAAAA others(8): Show |
1 | a0001c0006t0006g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.566+209_566+210ins others(15): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844697 | ||||||
chr1:3844698
|
C | A | 1 | a0001c0006t0006g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.566+209G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844698 | ||||||
chr1:3844698
|
C | CAAAAAAA others(6): Show |
3 | a0001c0006t0006g0126a0005c0008t0015g0139a0005c0008t0015g0140 | 3 | HG02451.hp2 HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.566+208_566+209ins others(13): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844698 | ||||||
chr1:3844698
|
C | CAAAAAAA others(7): Show |
68 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(65): Show | 81 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.566+208_566+209ins others(14): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844698 | ||||||
chr1:3844698
|
C | CAAAAAAA others(8): Show |
30 | a0001c0001t0003g0280a0001c0001t0003g0309a0001c0001t0003g0310others(27): Show | 35 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.566+208_566+209ins others(15): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844698 | ||||||
chr1:3844698
|
C | CAAAAAAA others(9): Show |
4 | a0001c0001t0004g0143a0001c0001t0004g0159a0001c0001t0013g0031others(1): Show | 4 | HG02615.hp1 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.566+208_566+209ins others(16): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844698 | ||||||
chr1:3844707
|
A | AAAAAAAA others(10): Show |
2 | a0001c0001t0005g0302a0001c0001t0020g0286 | 2 | HG01175.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.566+199_566+200ins others(17): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844707 | ||||||
chr1:3844707
|
A | AAAAAAAA others(9): Show |
20 | a0001c0001t0003g0237a0001c0001t0003g0258a0001c0001t0005g0029others(17): Show | 21 | HG00423.hp2 HG00609.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.566+199_566+200ins others(16): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844707 | ||||||
chr1:3844707
|
A | AAAAAAAA others(8): Show |
12 | a0001c0001t0003g0257a0001c0001t0005g0294a0002c0002t0001g0037others(9): Show | 12 | HG00423.hp1 HG00438.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.566+199_566+200ins others(15): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844707 | ||||||
chr1:3844707
|
A | AAAAAAAA others(7): Show |
91 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(88): Show | 119 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.566+199_566+200ins others(14): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844707 | ||||||
chr1:3844707
|
A | AAAAAAAA others(6): Show |
1 | a0002c0002t0001g0062 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.566+199_566+200ins others(13): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844707 | ||||||
chr1:3844709
|
G | A | 126 | a0001c0001t0003g0237a0001c0001t0003g0257a0001c0001t0003g0258others(123): Show | 155 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.566+198C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844709 | ||||||
chr1:3844901
|
T | A | 31 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(28): Show | 39 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(36): Show |
splice_region_variant&intron_variant | LOW | c.566+6A>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 6/21 | chr1 | 3844901 | ||||||
chr1:3845086
|
A | G | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.490-103T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 5/21 | chr1 | 3845086 | ||||||
chr1:3845113
|
T | C | 4 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0259others(1): Show | 4 | HG02895.hp2 HG03195.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-130A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 5/21 | chr1 | 3845113 | ||||||
chr1:3845178
|
G | A | 1 | a0003c0003t0012g0290 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.489+111C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 5/21 | chr1 | 3845178 | ||||||
chr1:3845208
|
C | T | 22 | a0001c0001t0004g0002a0001c0001t0004g0142a0001c0001t0004g0143others(19): Show | 27 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.489+81G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 5/21 | chr1 | 3845208 | ||||||
chr1:3845499
|
C | G | 9 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(6): Show | 15 | HG00642.hp2 HG00741.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.427-148G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3845499 | ||||||
chr1:3845512
|
T | C | 114 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(111): Show | 142 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.427-161A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3845512 | ||||||
chr1:3845516
|
T | C | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.427-165A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3845516 | ||||||
chr1:3845689
|
TATTA | T | 6 | a0001c0001t0003g0314a0001c0001t0004g0148a0001c0001t0004g0149others(3): Show | 6 | HG02572.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.427-342_427-339del others(4): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3845689 | ||||||
chr1:3845852
|
C | A | 115 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(112): Show | 143 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.427-501G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3845852 | ||||||
chr1:3845878
|
G | A | 1 | a0003c0003t0002g0217 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.427-527C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3845878 | ||||||
chr1:3845897
|
G | A | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.427-546C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3845897 | ||||||
chr1:3845904
|
A | G | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.427-553T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3845904 | ||||||
chr1:3845977
|
G | A | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.427-626C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3845977 | ||||||
chr1:3845993
|
T | G | 1 | a0002c0002t0001g0017 | 2 | HG01943.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.427-642A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3845993 | ||||||
chr1:3846040
|
C | T | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.427-689G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846040 | ||||||
chr1:3846086
|
C | CA | 58 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(55): Show | 69 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.427-736dupT | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846086 | ||||||
chr1:3846086
|
C | CAA | 14 | a0001c0001t0003g0254a0001c0001t0007g0014a0001c0001t0007g0272others(11): Show | 16 | HG02109.hp1 HG02145.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.427-737_427-736dup others(2): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846086 | ||||||
chr1:3846086
|
C | CAAA | 7 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311others(4): Show | 7 | HG01496.hp2 HG02683.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.427-738_427-736dup others(3): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846086 | ||||||
chr1:3846086
|
CA | C | 11 | a0002c0002t0001g0017a0002c0002t0001g0061a0002c0002t0011g0136others(8): Show | 12 | HG00597.hp1 HG01069.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.427-736delT | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846086 | ||||||
chr1:3846086
|
CAAAAAAA others(3): Show |
C | 43 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(40): Show | 49 | HG00323.hp1 HG00423.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.427-745_427-736del others(10): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846086 | ||||||
chr1:3846086
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0005g0292 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.427-746_427-736del others(11): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846086 | ||||||
chr1:3846157
|
A | T | 233 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(230): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.427-806T>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846157 | ||||||
chr1:3846183
|
T | C | 72 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(69): Show | 85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.427-832A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846183 | ||||||
chr1:3846251
|
T | C | 25 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(22): Show | 30 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.427-900A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846251 | ||||||
chr1:3846304
|
C | A | 1 | a0003c0003t0002g0021 | 2 | NA18967.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.427-953G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846304 | ||||||
chr1:3846307
|
T | C | 6 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311others(3): Show | 6 | HG01496.hp2 HG02683.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.427-956A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846307 | ||||||
chr1:3846325
|
C | T | 75 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(72): Show | 88 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.427-974G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846325 | ||||||
chr1:3846414
|
G | A | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.426+1061C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846414 | ||||||
chr1:3846600
|
G | A | 4 | a0003c0003t0014g0137a0003c0003t0014g0138a0003c0003t0016g0230others(1): Show | 4 | HG01109.hp1 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.426+875C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846600 | ||||||
chr1:3846721
|
C | T | 1 | a0002c0002t0001g0016 | 2 | NA19000.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.426+754G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846721 | ||||||
chr1:3846830
|
T | A | 17 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(14): Show | 18 | HG00423.hp2 HG00609.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.426+645A>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3846830 | ||||||
chr1:3847003
|
T | C | 8 | a0001c0001t0004g0158a0001c0001t0004g0162a0003c0003t0014g0137others(5): Show | 8 | HG01109.hp1 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.426+472A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3847003 | ||||||
chr1:3847198
|
T | A | 5 | a0001c0001t0007g0272a0001c0001t0007g0283a0001c0001t0007g0284others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.426+277A>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3847198 | ||||||
chr1:3847203
|
C | T | 2 | a0001c0001t0003g0263a0001c0001t0003g0271 | 2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.426+272G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3847203 | ||||||
chr1:3847206
|
G | A | 1 | a0003c0003t0002g0188 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.426+269C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3847206 | ||||||
chr1:3847263
|
C | CTGGGCAC others(15): Show |
2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.426+190_426+211dup others(22): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3847263 | ||||||
chr1:3847300
|
G | A | 104 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(101): Show | 132 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.426+175C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3847300 | ||||||
chr1:3847387
|
GA | G | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.426+87delT | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3847387 | ||||||
chr1:3847408
|
T | G | 1 | a0002c0002t0001g0101 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.426+67A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 4/21 | chr1 | 3847408 | ||||||
chr1:3847652
|
C | T | 23 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(20): Show | 28 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.288-39G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3847652 | ||||||
chr1:3847695
|
C | A | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.288-82G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3847695 | ||||||
chr1:3847897
|
C | T | 106 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(103): Show | 134 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.288-284G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3847897 | ||||||
chr1:3847928
|
G | A | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.288-315C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3847928 | ||||||
chr1:3847952
|
A | C | 1 | a0001c0001t0004g0147 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.288-339T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3847952 | ||||||
chr1:3847959
|
C | T | 1 | a0001c0001t0004g0146 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.288-346G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3847959 | ||||||
chr1:3847966
|
C | T | 1 | a0001c0001t0003g0314 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.288-353G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3847966 | ||||||
chr1:3847968
|
G | A | 2 | a0003c0003t0016g0230a0003c0003t0016g0231 | 2 | HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.288-355C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3847968 | ||||||
chr1:3848047
|
T | C | 104 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(101): Show | 132 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.288-434A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848047 | ||||||
chr1:3848064
|
A | C | 2 | a0001c0001t0020g0286a0001c0001t0020g0287 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.288-451T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848064 | ||||||
chr1:3848081
|
C | G | 1 | a0003c0003t0014g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.288-468G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848081 | ||||||
chr1:3848116
|
T | C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.287+492A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848116 | ||||||
chr1:3848127
|
G | A | 13 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(10): Show | 13 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.287+481C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848127 | ||||||
chr1:3848150
|
A | G | 1 | a0002c0002t0011g0136 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.287+458T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848150 | ||||||
chr1:3848156
|
G | C | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.287+452C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848156 | ||||||
chr1:3848164
|
T | A | 1 | a0002c0002t0001g0102 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.287+444A>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848164 | ||||||
chr1:3848270
|
C | T | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.287+338G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848270 | ||||||
chr1:3848314
|
C | T | 102 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(99): Show | 116 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.287+294G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848314 | ||||||
chr1:3848404
|
C | G | 6 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311others(3): Show | 6 | HG01496.hp2 HG02683.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.287+204G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848404 | ||||||
chr1:3848406
|
C | G | 1 | a0002c0002t0001g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.287+202G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848406 | ||||||
chr1:3848415
|
C | A | 102 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(99): Show | 116 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.287+193G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848415 | ||||||
chr1:3848464
|
A | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.287+144T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848464 | ||||||
chr1:3848491
|
C | T | 91 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(88): Show | 105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.287+117G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848491 | ||||||
chr1:3848518
|
C | T | 1 | a0012c0019t0032g0234 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.287+90G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848518 | ||||||
chr1:3848531
|
C | CA | 35 | a0001c0001t0004g0159a0001c0001t0004g0160a0001c0001t0005g0029others(32): Show | 37 | HG00423.hp2 HG00609.hp2 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.287+76dupT | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848531 | ||||||
chr1:3848531
|
C | CAAAAA | 95 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(92): Show | 123 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.287+72_287+76dupTT others(3): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 3/21 | chr1 | 3848531 | ||||||
chr1:3848822
|
G | A | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.114-41C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3848822 | ||||||
chr1:3848860
|
G | T | 23 | a0001c0001t0008g0013a0001c0001t0008g0024a0001c0001t0008g0248others(20): Show | 26 | HG00140.hp2 HG01074.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.114-79C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3848860 | ||||||
chr1:3848895
|
A | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.114-114T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3848895 | ||||||
chr1:3848902
|
T | C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.114-121A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3848902 | ||||||
chr1:3848985
|
G | A | 231 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(228): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.114-204C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3848985 | ||||||
chr1:3848999
|
T | C | 103 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(100): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.114-218A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3848999 | ||||||
chr1:3849107
|
G | C | 25 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(22): Show | 30 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.114-326C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849107 | ||||||
chr1:3849114
|
C | T | 206 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(203): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.114-333G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849114 | ||||||
chr1:3849191
|
T | C | 130 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(127): Show | 163 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.114-410A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849191 | ||||||
chr1:3849194
|
C | T | 6 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311others(3): Show | 6 | HG01496.hp2 HG02683.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.114-413G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849194 | ||||||
chr1:3849266
|
C | CT | 7 | a0003c0003t0002g0170a0003c0003t0002g0172a0003c0003t0002g0176others(4): Show | 7 | HG02056.hp1 HG02738.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.114-486dupA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849266 | ||||||
chr1:3849266
|
CT | C | 223 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(220): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.114-486delA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849266 | ||||||
chr1:3849320
|
C | T | 3 | a0001c0001t0008g0024a0005c0008t0015g0139a0005c0008t0015g0140 | 4 | HG01123.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-539G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849320 | ||||||
chr1:3849343
|
T | C | 1 | a0002c0002t0001g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.114-562A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849343 | ||||||
chr1:3849347
|
T | C | 1 | a0005c0008t0015g0140 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.114-566A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849347 | ||||||
chr1:3849348
|
G | T | 1 | a0002c0002t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.114-567C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849348 | ||||||
chr1:3849407
|
T | C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.114-626A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849407 | ||||||
chr1:3849408
|
G | C | 1 | a0003c0003t0002g0189 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.114-627C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849408 | ||||||
chr1:3849451
|
G | A | 1 | a0001c0001t0013g0032 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.114-670C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849451 | ||||||
chr1:3849477
|
C | T | 1 | a0003c0003t0002g0174 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.114-696G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849477 | ||||||
chr1:3849495
|
G | T | 310 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(307): Show | 376 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.114-714C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849495 | ||||||
chr1:3849527
|
A | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.114-746T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849527 | ||||||
chr1:3849675
|
C | T | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.114-894G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849675 | ||||||
chr1:3849676
|
A | G | 35 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(32): Show | 40 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.114-895T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849676 | ||||||
chr1:3849722
|
G | T | 131 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(128): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.114-941C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849722 | ||||||
chr1:3849833
|
T | TA | 26 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(23): Show | 31 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.114-1053dupT | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849833 | ||||||
chr1:3849833
|
TA | T | 11 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(8): Show | 11 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.114-1053delT | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849833 | ||||||
chr1:3849877
|
C | T | 104 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(101): Show | 132 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.114-1096G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849877 | ||||||
chr1:3849891
|
A | C | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.114-1110T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849891 | ||||||
chr1:3849963
|
T | C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.114-1182A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849963 | ||||||
chr1:3849987
|
C | A | 2 | a0002c0002t0001g0104a0007c0011t0001g0049 | 2 | HG01433.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.114-1206G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3849987 | ||||||
chr1:3850023
|
G | A | 25 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(22): Show | 30 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.114-1242C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850023 | ||||||
chr1:3850105
|
T | A | 1 | a0002c0002t0001g0105 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.114-1324A>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850105 | ||||||
chr1:3850108
|
G | T | 1 | a0002c0002t0001g0105 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.114-1327C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850108 | ||||||
chr1:3850109
|
T | A | 1 | a0002c0002t0001g0105 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.114-1328A>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850109 | ||||||
chr1:3850110
|
T | C | 1 | a0002c0002t0001g0105 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.114-1329A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850110 | ||||||
chr1:3850111
|
T | A | 1 | a0002c0002t0001g0105 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.114-1330A>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850111 | ||||||
chr1:3850113
|
A | T | 1 | a0002c0002t0001g0105 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.114-1332T>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850113 | ||||||
chr1:3850114
|
G | A | 1 | a0002c0002t0001g0105 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.114-1333C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850114 | ||||||
chr1:3850116
|
G | GCTGTACC others(7): Show |
1 | a0002c0002t0001g0105 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.114-1336_114-1335i others(16): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850116 | ||||||
chr1:3850130
|
C | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.114-1349G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850130 | ||||||
chr1:3850151
|
C | T | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.114-1370G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850151 | ||||||
chr1:3850160
|
G | A | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.114-1379C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850160 | ||||||
chr1:3850283
|
T | G | 1 | a0003c0003t0002g0172 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.114-1502A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850283 | ||||||
chr1:3850420
|
C | A | 1 | a0002c0002t0001g0106 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.114-1639G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850420 | ||||||
chr1:3850426
|
G | C | 1 | a0002c0005t0001g0107 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.114-1645C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850426 | ||||||
chr1:3850523
|
T | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.114-1742A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850523 | ||||||
chr1:3850611
|
T | C | 3 | a0001c0001t0007g0283a0001c0001t0007g0284a0001c0001t0007g0285 | 3 | HG02559.hp2 HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.113+1684A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850611 | ||||||
chr1:3850654
|
C | T | 1 | a0001c0006t0006g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.113+1641G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850654 | ||||||
chr1:3850703
|
G | A | 20 | a0001c0001t0003g0028a0001c0001t0003g0030a0001c0001t0003g0237others(17): Show | 22 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.113+1592C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850703 | ||||||
chr1:3850718
|
C | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.113+1577G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850718 | ||||||
chr1:3850765
|
C | A | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.113+1530G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850765 | ||||||
chr1:3850912
|
G | A | 2 | a0002c0002t0001g0108a0002c0002t0001g0109 | 2 | NA18747.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.113+1383C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3850912 | ||||||
chr1:3851034
|
A | G | 232 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(229): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.113+1261T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3851034 | ||||||
chr1:3851096
|
G | C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.113+1199C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3851096 | ||||||
chr1:3851127
|
G | A | 1 | a0001c0001t0004g0160 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.113+1168C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3851127 | ||||||
chr1:3851132
|
C | T | 194 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(191): Show | 236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.113+1163G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3851132 | ||||||
chr1:3851193
|
C | T | 2 | a0002c0005t0001g0038a0002c0005t0001g0111 | 2 | NA18940.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.113+1102G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3851193 | ||||||
chr1:3851195
|
C | T | 5 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311others(2): Show | 5 | HG01496.hp2 HG02683.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+1100G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3851195 | ||||||
chr1:3851251
|
C | T | 1 | a0003c0003t0014g0137 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.113+1044G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3851251 | ||||||
chr1:3851255
|
C | T | 17 | a0001c0001t0003g0028a0001c0001t0003g0030a0001c0001t0003g0256others(14): Show | 19 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.113+1040G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3851255 | ||||||
chr1:3851326
|
A | C | 1 | a0007c0011t0001g0049 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.113+969T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3851326 | ||||||
chr1:3851424
|
C | T | 6 | a0003c0003t0002g0011a0003c0003t0002g0184a0003c0003t0002g0185others(3): Show | 8 | HG02523.hp2 HG03704.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.113+871G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3851424 | ||||||
chr1:3851488
|
G | C | 1 | a0003c0003t0002g0221 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.113+807C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3851488 | ||||||
chr1:3851530
|
A | G | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.113+765T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3851530 | ||||||
chr1:3851615
|
T | C | 1 | a0012c0019t0032g0234 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.113+680A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3851615 | ||||||
chr1:3851784
|
G | A | 1 | a0003c0003t0002g0222 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.113+511C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3851784 | ||||||
chr1:3851958
|
C | T | 3 | a0001c0001t0003g0276a0001c0001t0003g0277a0001c0001t0003g0278 | 3 | HG03486.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.113+337G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3851958 | ||||||
chr1:3852001
|
G | A | 105 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(102): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.113+294C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3852001 | ||||||
chr1:3852004
|
T | C | 25 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(22): Show | 30 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.113+291A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3852004 | ||||||
chr1:3852141
|
C | T | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.113+154G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3852141 | ||||||
chr1:3852155
|
T | C | 131 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(128): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.113+140A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3852155 | ||||||
chr1:3852165
|
T | C | 131 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(128): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.113+130A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3852165 | ||||||
chr1:3852179
|
G | A | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.113+116C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3852179 | ||||||
chr1:3852191
|
G | A | 4 | a0001c0001t0007g0014a0001c0001t0007g0273a0001c0001t0007g0275others(1): Show | 6 | HG02109.hp1 HG03195.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+104C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3852191 | ||||||
chr1:3852251
|
C | T | 2 | a0001c0001t0020g0286a0001c0001t0020g0287 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.113+44G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 2/21 | chr1 | 3852251 | ||||||
chr1:3852469
|
A | T | 94 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(91): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-14-48T>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3852469 | ||||||
chr1:3852470
|
A | T | 94 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(91): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-14-49T>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3852470 | ||||||
chr1:3852608
|
T | C | 20 | a0001c0001t0003g0028a0001c0001t0003g0030a0001c0001t0003g0237others(17): Show | 22 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.-14-187A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3852608 | ||||||
chr1:3852667
|
A | G | 131 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(128): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.-14-246T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3852667 | ||||||
chr1:3852678
|
T | C | 1 | a0001c0001t0004g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-14-257A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3852678 | ||||||
chr1:3852698
|
C | T | 94 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(91): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-14-277G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3852698 | ||||||
chr1:3852712
|
G | C | 131 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(128): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.-14-291C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3852712 | ||||||
chr1:3852722
|
C | T | 131 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(128): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.-14-301G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3852722 | ||||||
chr1:3852739
|
T | C | 1 | a0010c0020t0003g0313 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-14-318A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3852739 | ||||||
chr1:3852765
|
A | G | 131 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(128): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.-14-344T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3852765 | ||||||
chr1:3852801
|
G | C | 131 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(128): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.-14-380C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3852801 | ||||||
chr1:3852813
|
C | T | 131 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(128): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.-14-392G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3852813 | ||||||
chr1:3852901
|
C | CGGCCAAG others(2): Show |
104 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(101): Show | 132 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-14-489_-14-481dup others(9): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3852901 | ||||||
chr1:3852915
|
T | C | 131 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(128): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.-14-494A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3852915 | ||||||
chr1:3853000
|
T | C | 236 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(233): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.-14-579A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853000 | ||||||
chr1:3853026
|
G | C | 131 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(128): Show | 164 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.-14-605C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853026 | ||||||
chr1:3853036
|
T | C | 11 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(8): Show | 11 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-615A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853036 | ||||||
chr1:3853196
|
G | A | 2 | a0001c0001t0020g0286a0001c0001t0020g0287 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-14-775C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853196 | ||||||
chr1:3853273
|
A | C | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-14-852T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853273 | ||||||
chr1:3853307
|
G | C | 24 | a0001c0001t0004g0002a0001c0001t0004g0142a0001c0001t0004g0143others(21): Show | 29 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-14-886C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853307 | ||||||
chr1:3853352
|
C | T | 1 | a0016c0022t0034g0269 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-14-931G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853352 | ||||||
chr1:3853400
|
C | CG | 11 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(8): Show | 11 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-980dupC | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853400 | ||||||
chr1:3853400
|
C | T | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-14-979G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853400 | ||||||
chr1:3853405
|
G | GGA | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.-14-985_-14-984ins others(2): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853405 | ||||||
chr1:3853405
|
GA | G | 26 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(23): Show | 31 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-14-985delT | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853405 | ||||||
chr1:3853406
|
A | G | 177 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(174): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.-14-985T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853406 | ||||||
chr1:3853407
|
A | G | 26 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(23): Show | 31 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-14-986T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853407 | ||||||
chr1:3853408
|
A | G | 6 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311others(3): Show | 6 | HG01496.hp2 HG02683.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-987T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853408 | ||||||
chr1:3853444
|
G | T | 2 | a0005c0008t0015g0139a0005c0008t0015g0140 | 2 | HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-14-1023C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853444 | ||||||
chr1:3853516
|
C | T | 4 | a0002c0002t0001g0118a0002c0002t0001g0120a0002c0002t0001g0121others(1): Show | 4 | HG00741.hp1 HG01192.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-1095G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853516 | ||||||
chr1:3853640
|
G | C | 6 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311others(3): Show | 6 | HG01496.hp2 HG02683.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-1219C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853640 | ||||||
chr1:3853800
|
CA | C | 105 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(102): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-14-1380delT | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853800 | ||||||
chr1:3853831
|
C | A | 240 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(237): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.-14-1410G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853831 | ||||||
chr1:3853860
|
C | T | 1 | a0002c0002t0001g0047 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-14-1439G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853860 | ||||||
chr1:3853861
|
G | A | 104 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(101): Show | 132 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-14-1440C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853861 | ||||||
chr1:3853886
|
G | C | 24 | a0001c0001t0004g0002a0001c0001t0004g0142a0001c0001t0004g0143others(21): Show | 29 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-14-1465C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853886 | ||||||
chr1:3853922
|
C | T | 5 | a0001c0001t0009g0239a0001c0001t0009g0240a0001c0001t0009g0259others(2): Show | 5 | HG02895.hp2 HG03195.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-1501G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3853922 | ||||||
chr1:3854056
|
C | T | 6 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311others(3): Show | 6 | HG01496.hp2 HG02683.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-1635G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854056 | ||||||
chr1:3854078
|
G | A | 25 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(22): Show | 30 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-14-1657C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854078 | ||||||
chr1:3854169
|
G | T | 21 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(18): Show | 22 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-14-1748C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854169 | ||||||
chr1:3854172
|
T | C | 104 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(101): Show | 132 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-14-1751A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854172 | ||||||
chr1:3854236
|
G | A | 105 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(102): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-14-1815C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854236 | ||||||
chr1:3854350
|
A | G | 25 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(22): Show | 30 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-14-1929T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854350 | ||||||
chr1:3854365
|
C | T | 25 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(22): Show | 30 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-14-1944G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854365 | ||||||
chr1:3854396
|
C | G | 1 | a0001c0001t0004g0141 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-14-1975G>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854396 | ||||||
chr1:3854520
|
G | A | 25 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(22): Show | 30 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-14-2099C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854520 | ||||||
chr1:3854529
|
C | T | 1 | a0003c0003t0002g0181 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-14-2108G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854529 | ||||||
chr1:3854544
|
T | C | 106 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(103): Show | 134 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-14-2123A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854544 | ||||||
chr1:3854550
|
C | A | 1 | a0003c0003t0002g0223 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-14-2129G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854550 | ||||||
chr1:3854556
|
T | C | 104 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(101): Show | 132 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-14-2135A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854556 | ||||||
chr1:3854599
|
G | A | 104 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(101): Show | 132 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-14-2178C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854599 | ||||||
chr1:3854635
|
A | AT | 38 | a0001c0001t0013g0031a0001c0006t0006g0124a0001c0006t0006g0126others(35): Show | 40 | HG00438.hp1 HG00597.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.-14-2215dupA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854635 | ||||||
chr1:3854635
|
AT | A | 12 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311others(9): Show | 12 | HG01496.hp2 HG02683.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-14-2215delA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854635 | ||||||
chr1:3854635
|
ATT | A | 30 | a0001c0001t0003g0264a0001c0001t0003g0267a0001c0001t0004g0002others(27): Show | 35 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.-14-2216_-14-2215d others(4): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854635 | ||||||
chr1:3854635
|
ATTT | A | 68 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(65): Show | 81 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.-14-2217_-14-2215d others(5): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854635 | ||||||
chr1:3854635
|
ATTTT | A | 14 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0294others(11): Show | 15 | HG00423.hp2 HG00609.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.-14-2218_-14-2215d others(6): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854635 | ||||||
chr1:3854708
|
C | T | 1 | a0002c0002t0001g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-15+2181G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854708 | ||||||
chr1:3854784
|
C | T | 105 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(102): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-15+2105G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854784 | ||||||
chr1:3854805
|
T | C | 106 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(103): Show | 134 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-15+2084A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854805 | ||||||
chr1:3854870
|
A | AT | 134 | a0001c0001t0003g0263a0001c0001t0003g0281a0001c0001t0003g0282others(131): Show | 167 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.-15+2018dupA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854870 | ||||||
chr1:3854870
|
A | ATT | 83 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(80): Show | 97 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.-15+2017_-15+2018d others(4): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854870 | ||||||
chr1:3854940
|
C | T | 2 | a0001c0001t0020g0286a0001c0001t0020g0287 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-15+1949G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854940 | ||||||
chr1:3854983
|
C | T | 130 | a0001c0001t0004g0002a0001c0001t0004g0142a0001c0001t0004g0143others(127): Show | 163 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.-15+1906G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3854983 | ||||||
chr1:3855018
|
C | T | 11 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(8): Show | 11 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+1871G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855018 | ||||||
chr1:3855119
|
G | A | 1 | a0002c0002t0001g0114 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-15+1770C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855119 | ||||||
chr1:3855159
|
A | T | 240 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(237): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.-15+1730T>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855159 | ||||||
chr1:3855169
|
C | A | 2 | a0003c0003t0016g0230a0003c0003t0016g0231 | 2 | HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-15+1720G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855169 | ||||||
chr1:3855174
|
A | AT | 10 | a0001c0001t0003g0310a0001c0001t0003g0311a0001c0001t0037g0312others(7): Show | 10 | HG01496.hp2 HG02683.hp2 HG03540.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+1714dupA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855174 | ||||||
chr1:3855174
|
AT | A | 54 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(51): Show | 63 | HG00140.hp2 HG00642.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.-15+1714delA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855174 | ||||||
chr1:3855174
|
ATT | A | 55 | a0001c0001t0003g0028a0001c0001t0003g0030a0001c0001t0003g0264others(52): Show | 64 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.-15+1713_-15+1714d others(4): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855174 | ||||||
chr1:3855174
|
ATTT | A | 23 | a0001c0001t0005g0029a0001c0001t0005g0292a0001c0001t0005g0293others(20): Show | 24 | HG00423.hp2 HG00609.hp2 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.-15+1712_-15+1714d others(5): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855174 | ||||||
chr1:3855174
|
ATTTT | A | 101 | a0001c0001t0005g0304a0002c0002t0001g0001a0002c0002t0001g0006others(98): Show | 129 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.-15+1711_-15+1714d others(6): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855174 | ||||||
chr1:3855209
|
C | T | 1 | a0001c0001t0010g0235 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-15+1680G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855209 | ||||||
chr1:3855330
|
T | C | 21 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(18): Show | 22 | HG00423.hp2 HG00609.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-15+1559A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855330 | ||||||
chr1:3855348
|
CT | C | 132 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(129): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.-15+1540delA | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855348 | ||||||
chr1:3855348
|
CTT | C | 103 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(100): Show | 131 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.-15+1539_-15+1540d others(4): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855348 | ||||||
chr1:3855449
|
G | A | 1 | a0003c0003t0002g0232 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-15+1440C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855449 | ||||||
chr1:3855459
|
G | A | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-15+1430C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855459 | ||||||
chr1:3855491
|
T | C | 19 | a0001c0001t0005g0029a0001c0001t0005g0291a0001c0001t0005g0292others(16): Show | 20 | HG00423.hp2 HG00609.hp2 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15+1398A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855491 | ||||||
chr1:3855665
|
T | G | 2 | a0001c0001t0004g0163a0001c0001t0004g0164 | 2 | HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.-15+1224A>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855665 | ||||||
chr1:3855711
|
G | T | 106 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(103): Show | 134 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-15+1178C>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855711 | ||||||
chr1:3855795
|
C | T | 105 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(102): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-15+1094G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855795 | ||||||
chr1:3855896
|
T | C | 4 | a0001c0001t0003g0030a0001c0001t0003g0306a0001c0001t0003g0307others(1): Show | 5 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+993A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855896 | ||||||
chr1:3855946
|
C | A | 1 | a0001c0001t0003g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-15+943G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3855946 | ||||||
chr1:3856237
|
C | A | 1 | a0002c0002t0024g0115 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-15+652G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856237 | ||||||
chr1:3856302
|
A | G | 25 | a0001c0001t0004g0002a0001c0001t0004g0141a0001c0001t0004g0142others(22): Show | 30 | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-15+587T>C | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856302 | ||||||
chr1:3856365
|
G | C | 1 | a0001c0006t0021g0117 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-15+524C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856365 | ||||||
chr1:3856375
|
G | C | 105 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(102): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.-15+514C>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856375 | ||||||
chr1:3856392
|
G | A | 1 | a0002c0002t0001g0116 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-15+497C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856392 | ||||||
chr1:3856470
|
T | C | 94 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(91): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-15+419A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856470 | ||||||
chr1:3856515
|
G | A | 6 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311others(3): Show | 6 | HG01496.hp2 HG02683.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+374C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856515 | ||||||
chr1:3856525
|
T | C | 94 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(91): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-15+364A>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856525 | ||||||
chr1:3856542
|
C | T | 104 | a0002c0002t0001g0001a0002c0002t0001g0006a0002c0002t0001g0007others(101): Show | 132 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.-15+347G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856542 | ||||||
chr1:3856544
|
C | T | 1 | a0001c0001t0004g0142 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-15+345G>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856544 | ||||||
chr1:3856592
|
G | A | 7 | a0002c0002t0001g0020a0002c0002t0001g0118a0002c0002t0001g0119others(4): Show | 8 | HG00741.hp1 HG01175.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+297C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856592 | ||||||
chr1:3856628
|
A | T | 1 | a0003c0003t0002g0166 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-15+261T>A | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856628 | ||||||
chr1:3856687
|
A | C | 96 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(93): Show | 110 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-15+202T>G | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856687 | ||||||
chr1:3856688
|
C | A | 115 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(112): Show | 143 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-15+201G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856688 | ||||||
chr1:3856811
|
G | A | 6 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311others(3): Show | 6 | HG01496.hp2 HG02683.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+78C>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856811 | ||||||
chr1:3856816
|
G | GCCCGCGC | 10 | a0001c0006t0006g0124a0001c0006t0006g0126a0001c0006t0006g0127others(7): Show | 10 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+66_-15+72dupGC others(5): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856816 | ||||||
chr1:3856816
|
GCCCGCGC | G | 94 | a0001c0001t0003g0009a0001c0001t0003g0025a0001c0001t0003g0026others(91): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-15+66_-15+72delGC others(5): Show |
CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856816 | ||||||
chr1:3856830
|
C | A | 1 | a0003c0003t0002g0233 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-15+59G>T | CEP104 | ENSG00000116198.14 | transcript | ENST00000378230.8 | protein_coding | 1/21 | chr1 | 3856830 |