geneid | 11154 |
---|---|
ensemblid | ENSG00000100478.16 |
hgncid | 575 |
symbol | AP4S1 |
name | adaptor related protein complex 4 subunit sigma 1 |
refseq_nuc | NM_001128126.3 |
refseq_prot | NP_001121598.1 |
ensembl_nuc | ENST00000542754.7 |
ensembl_prot | ENSP00000438170.2 |
mane_status | MANE Select |
chr | chr14 |
start | 31025649 |
end | 31096450 |
strand | + |
ver | v1.2 |
region | chr14:31025649-31096450 |
region5000 | chr14:31020649-31101450 |
regionname0 | AP4S1_chr14_31025649_31096450 |
regionname5000 | AP4S1_chr14_31020649_31101450 |
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 | 144 | 346 | 82 | 56 | 152 | 12 | 42 | 108 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
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 | 1/1 | 435 | 346 | 82 | 56 | 152 | 12 | 42 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
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 | 1/0 | 3626 | 179 | 30 | 24 | 95 | 7 | 22 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0002 | 0/0 | 3626 | 30 | 1 | 2 | 24 | 0 | 3 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0003 | 0/1 | 3628 | 23 | 4 | 12 | 0 | 3 | 3 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0004 | 0/0 | 3629 | 15 | 2 | 5 | 3 | 1 | 4 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0005 | 0/0 | 3627 | 13 | 4 | 3 | 3 | 0 | 3 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0006 | 0/0 | 3627 | 9 | 9 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0007 | 0/0 | 3628 | 8 | 2 | 1 | 0 | 0 | 5 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0008 | 0/0 | 3625 | 5 | 1 | 3 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0009 | 0/0 | 3628 | 5 | 1 | 4 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0010 | 0/0 | 3628 | 5 | 0 | 0 | 5 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0011 | 0/0 | 3628 | 4 | 0 | 0 | 4 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0012 | 0/0 | 3628 | 3 | 3 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0013 | 0/0 | 3626 | 3 | 0 | 0 | 3 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0014 | 0/0 | 3629 | 3 | 3 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0015 | 0/0 | 3627 | 3 | 1 | 1 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0016 | 0/0 | 3627 | 2 | 2 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0017 | 0/0 | 3626 | 2 | 0 | 0 | 2 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0018 | 0/0 | 3626 | 2 | 2 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0019 | 0/0 | 3627 | 2 | 2 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0020 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0021 | 0/0 | 3627 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0022 | 0/0 | 3626 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0023 | 0/0 | 3626 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0024 | 0/0 | 3626 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0025 | 0/0 | 3627 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0026 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0027 | 0/0 | 3627 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0028 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0029 | 0/0 | 3627 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0030 | 0/0 | 3626 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0031 | 0/0 | 3626 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0032 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0033 | 0/0 | 3626 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0034 | 0/0 | 3626 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0035 | 0/0 | 3625 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0036 | 0/0 | 3626 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0037 | 0/0 | 3625 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0038 | 0/0 | 3626 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0039 | 0/0 | 3628 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0040 | 0/0 | 3626 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0041 | 0/0 | 3627 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0042 | 0/0 | 3627 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0043 | 0/0 | 3627 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0044 | 0/0 | 3628 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0045 | 0/0 | 3628 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0046 | 0/0 | 3627 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0047 | 0/0 | 3627 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0048 | 0/0 | 3629 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
t0049 | 0/0 | 3628 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
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 | 3 | 0 | 0 | 3 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
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 | 1/1 | 435 | 346 | 82 | 56 | 152 | 12 | 42 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4060 | 179 | 30 | 24 | 95 | 7 | 22 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0002 | 0/0 | 4060 | 30 | 1 | 2 | 24 | 0 | 3 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0003 | 0/1 | 4062 | 23 | 4 | 12 | 0 | 3 | 3 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0004 | 0/0 | 4063 | 15 | 2 | 5 | 3 | 1 | 4 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0005 | 0/0 | 4061 | 13 | 4 | 3 | 3 | 0 | 3 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0006 | 0/0 | 4061 | 9 | 9 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0007 | 0/0 | 4062 | 8 | 2 | 1 | 0 | 0 | 5 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0008 | 0/0 | 4059 | 5 | 1 | 3 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0009 | 0/0 | 4062 | 5 | 1 | 4 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0010 | 0/0 | 4062 | 5 | 0 | 0 | 5 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0011 | 0/0 | 4062 | 4 | 0 | 0 | 4 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0012 | 0/0 | 4062 | 3 | 3 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0013 | 0/0 | 4060 | 3 | 0 | 0 | 3 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0014 | 0/0 | 4063 | 3 | 3 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0015 | 0/0 | 4061 | 3 | 1 | 1 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0016 | 0/0 | 4061 | 2 | 2 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0017 | 0/0 | 4060 | 2 | 0 | 0 | 2 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0018 | 0/0 | 4060 | 2 | 2 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0019 | 0/0 | 4061 | 2 | 2 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0020 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0021 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0022 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0023 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0024 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0025 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0026 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0027 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0028 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0029 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0030 | 0/0 | 4060 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0031 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0032 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0033 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0034 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0035 | 0/0 | 4059 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0036 | 0/0 | 4060 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0037 | 0/0 | 4059 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0038 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0039 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0040 | 0/0 | 4060 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0041 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0042 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0043 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0044 | 0/0 | 4062 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0045 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0046 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0047 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0048 | 0/0 | 4063 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
a0001c0001t0049 | 0/0 | 4062 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | copy fasta | chr14 | 31020649 | 31101450 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0005g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0006g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0006g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0007g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0007g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0007g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0007g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0007g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0008g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0008g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0008g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0008g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0009g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0009g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0009g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0009g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0009g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0010g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0010g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0010g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0010g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0010g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0011g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0011g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0011g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0011g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0012g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0012g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0013g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0013g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0013g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0014g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0014g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0014g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0015g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0015g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0015g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0016g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0016g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0017g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0017g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0018g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0018g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0019g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0019g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0020g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0022g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0023g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0024g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0025g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0026g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0027g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0028g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0029g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0030g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0031g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0032g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0033g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0034g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0035g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0036g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0037g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0038g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0039g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0040g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0041g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0042g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0043g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0044g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0045g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0046g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0047g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0048g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
a0001c0001t0049g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0152 | EUR | GBR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | GBR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00140 | hp1 | a0001 | c0001 | t0015 | g0211 | EUR | GBR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | GBR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0042 | EUR | FIN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | FIN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | FIN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0245 | EUR | FIN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00558 | hp1 | a0001 | c0001 | t0011 | g0088 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00609 | hp1 | a0001 | c0001 | t0011 | g0082 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0242 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | CHS | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0255 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0260 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0258 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01069 | hp2 | a0001 | c0001 | t0009 | g0262 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0150 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01081 | hp2 | a0001 | c0001 | t0008 | g0244 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01106 | hp2 | a0001 | c0001 | t0007 | g0157 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0083 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0209 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01169 | hp1 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0254 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01255 | hp2 | a0001 | c0001 | t0044 | g0131 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01256 | hp2 | a0001 | c0001 | t0008 | g0061 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01257 | hp2 | a0001 | c0001 | t0015 | g0143 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0259 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01361 | hp2 | a0001 | c0001 | t0009 | g0065 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0145 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01884 | hp1 | a0001 | c0001 | t0031 | g0326 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01891 | hp1 | a0001 | c0001 | t0012 | g0200 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01928 | hp1 | a0001 | c0001 | t0009 | g0038 | AMR | PEL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0095 | AMR | PEL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0305 | AMR | PEL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PEL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02056 | hp2 | a0001 | c0001 | t0040 | g0323 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02071 | hp2 | a0001 | c0001 | t0011 | g0090 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02074 | hp2 | a0001 | c0001 | t0010 | g0273 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02135 | hp1 | a0001 | c0001 | t0022 | g0167 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02145 | hp1 | a0001 | c0001 | t0032 | g0250 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02145 | hp2 | a0001 | c0001 | t0039 | g0133 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02155 | hp1 | a0001 | c0001 | t0048 | g0129 | EAS | CDX | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02155 | hp2 | a0001 | c0001 | t0045 | g0086 | EAS | CDX | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CDX | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CDX | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02257 | hp2 | a0001 | c0001 | t0018 | g0101 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02280 | hp2 | a0001 | c0001 | t0027 | g0164 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02572 | hp2 | a0001 | c0001 | t0014 | g0160 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0044 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02630 | hp1 | a0001 | c0001 | t0042 | g0014 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02630 | hp2 | a0001 | c0001 | t0041 | g0227 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0327 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02683 | hp1 | a0001 | c0001 | t0007 | g0268 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0148 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02723 | hp1 | a0001 | c0001 | t0036 | g0091 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0249 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02809 | hp1 | a0001 | c0001 | t0037 | g0041 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02886 | hp2 | a0001 | c0001 | t0020 | g0202 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02896 | hp1 | a0001 | c0001 | t0016 | g0198 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02897 | hp1 | a0001 | c0001 | t0016 | g0197 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02970 | hp1 | a0001 | c0001 | t0043 | g0204 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03017 | hp1 | a0001 | c0001 | t0030 | g0068 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03041 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0328 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03195 | hp2 | a0001 | c0001 | t0018 | g0205 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03209 | hp1 | a0001 | c0001 | t0014 | g0158 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03209 | hp2 | a0001 | c0001 | t0015 | g0263 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0265 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0248 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0064 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0016 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03516 | hp1 | a0001 | c0001 | t0019 | g0008 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03540 | hp2 | a0001 | c0001 | t0028 | g0193 | AFR | GWD | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03579 | hp2 | a0001 | c0001 | t0007 | g0161 | AFR | MSL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0156 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0253 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03704 | hp2 | a0001 | c0001 | t0007 | g0266 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0226 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0094 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0149 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03927 | hp2 | a0001 | c0001 | t0007 | g0269 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG03942 | hp2 | a0001 | c0001 | t0049 | g0229 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | STU | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | STU | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG04184 | hp1 | a0001 | c0001 | t0007 | g0208 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | BEB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG04199 | hp1 | a0001 | c0001 | t0005 | g0279 | SAS | STU | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0043 | SAS | STU | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0267 | SAS | STU | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18747 | hp2 | a0001 | c0001 | t0038 | g0089 | EAS | CHB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18906 | hp1 | a0001 | c0001 | t0026 | g0194 | AFR | YRI | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | YRI | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18944 | hp1 | a0001 | c0001 | t0013 | g0301 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18945 | hp1 | a0001 | c0001 | t0024 | g0190 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18950 | hp1 | a0001 | c0001 | t0033 | g0116 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18951 | hp1 | a0001 | c0001 | t0013 | g0317 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18957 | hp1 | a0001 | c0001 | t0017 | g0078 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18971 | hp2 | a0001 | c0001 | t0010 | g0272 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18972 | hp1 | a0001 | c0001 | t0023 | g0181 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18982 | hp2 | a0001 | c0001 | t0011 | g0085 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18983 | hp2 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18985 | hp1 | a0001 | c0001 | t0046 | g0087 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18987 | hp2 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18989 | hp2 | a0001 | c0001 | t0010 | g0275 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA18999 | hp2 | a0001 | c0001 | t0017 | g0077 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19011 | hp2 | a0001 | c0001 | t0025 | g0186 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | LWK | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19043 | hp2 | a0001 | c0001 | t0014 | g0159 | AFR | LWK | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19057 | hp2 | a0001 | c0001 | t0010 | g0271 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19067 | hp1 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19067 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19075 | hp2 | a0001 | c0001 | t0010 | g0274 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19078 | hp1 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19078 | hp2 | a0001 | c0001 | t0013 | g0276 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19082 | hp1 | a0001 | c0001 | t0035 | g0034 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | TSI | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0130 | EUR | TSI | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0252 | EUR | TSI | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01123 | hp1 | a0001 | c0001 | t0009 | g0070 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0278 | AMR | CLM | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02109 | hp1 | a0001 | c0001 | t0047 | g0264 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02109 | hp2 | a0001 | c0001 | t0012 | g0201 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0216 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02486 | hp2 | a0001 | c0001 | t0019 | g0007 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02559 | hp1 | a0001 | c0001 | t0012 | g0199 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ACB | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG06807 | hp1 | a0001 | c0001 | t0034 | g0010 | AFR | USA | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | USA | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA20300 | hp1 | a0001 | c0001 | t0009 | g0069 | AFR | USA | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | USA | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA21309 | hp1 | a0001 | c0001 | t0029 | g0243 | AFR | LWK | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0071 | REF | REF | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0111 | REF | REF | AP4S1_chr14_31020649_31101450 | AP4S1 | chr14 | 31020649 | 31101450 |
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 |
---|
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:31025703
|
G | A | 3 | a0001c0001t0012a0001c0001t0016a0001c0001t0020 | 6 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-156G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/6 | 40494 | chr14 | 31025703 | |||||
chr14:31025758
|
G | A | 1 | a0001c0001t0020 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-101G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/6 | 40439 | chr14 | 31025758 | |||||
chr14:31025782
|
G | A | 9 | a0001c0001t0002a0001c0001t0021a0001c0001t0022others(6): Show | 38 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-77G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/6 | 40415 | chr14 | 31025782 | |||||
chr14:31093218
|
T | C | 1 | a0001c0001t0029 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*183T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 183 | chr14 | 31093218 | |||||
chr14:31093352
|
A | G | 2 | a0001c0001t0010a0001c0001t0049 | 6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*317A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 317 | chr14 | 31093352 | |||||
chr14:31093465
|
A | AT | 14 | a0001c0001t0003a0001c0001t0004a0001c0001t0009others(11): Show | 59 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*443dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 444 | INFO_REALIGN_3_PRIME | chr14 | 31093465 | ||||
chr14:31093465
|
A | ATT | 4 | a0001c0001t0012a0001c0001t0020a0001c0001t0028others(1): Show | 6 | HG01891.hp1 HG02109.hp2 HG02155.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*442_*443dupTT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 444 | INFO_REALIGN_3_PRIME | chr14 | 31093465 | ||||
chr14:31093635
|
C | T | 5 | a0001c0001t0012a0001c0001t0016a0001c0001t0020others(2): Show | 8 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*600C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 600 | chr14 | 31093635 | |||||
chr14:31093787
|
C | T | 1 | a0001c0001t0040 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*752C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 752 | chr14 | 31093787 | |||||
chr14:31094332
|
C | T | 1 | a0001c0001t0047 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1297C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1297 | chr14 | 31094332 | |||||
chr14:31094380
|
G | A | 1 | a0001c0001t0006 | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1345G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1345 | chr14 | 31094380 | |||||
chr14:31094453
|
G | A | 1 | a0001c0001t0049 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1418G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1418 | chr14 | 31094453 | |||||
chr14:31094467
|
A | G | 4 | a0001c0001t0011a0001c0001t0045a0001c0001t0046others(1): Show | 7 | HG00558.hp1 HG00609.hp1 HG02071.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1432A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1432 | chr14 | 31094467 | |||||
chr14:31094611
|
G | A | 1 | a0001c0001t0030 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1576G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1576 | chr14 | 31094611 | |||||
chr14:31094627
|
G | A | 1 | a0001c0001t0029 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1592G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1592 | chr14 | 31094627 | |||||
chr14:31094641
|
C | T | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(15): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1606C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1606 | chr14 | 31094641 | |||||
chr14:31094742
|
T | C | 28 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(25): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1707T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 1707 | chr14 | 31094742 | |||||
chr14:31095061
|
G | A | 5 | a0001c0001t0012a0001c0001t0016a0001c0001t0020others(2): Show | 8 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2026G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2026 | chr14 | 31095061 | |||||
chr14:31095081
|
C | G | 1 | a0001c0001t0014 | 3 | HG02572.hp2 HG03209.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2046C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2046 | chr14 | 31095081 | |||||
chr14:31095086
|
C | G | 1 | a0001c0001t0038 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2051C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2051 | chr14 | 31095086 | |||||
chr14:31095119
|
A | G | 1 | a0001c0001t0017 | 2 | NA18957.hp1 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2084A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2084 | chr14 | 31095119 | |||||
chr14:31095410
|
C | T | 2 | a0001c0001t0019a0001c0001t0039 | 3 | HG02145.hp2 HG02486.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2375C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2375 | chr14 | 31095410 | |||||
chr14:31095638
|
C | T | 1 | a0001c0001t0006 | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2603C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2603 | chr14 | 31095638 | |||||
chr14:31095671
|
C | T | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG02723.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2636C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2636 | chr14 | 31095671 | |||||
chr14:31095753
|
A | G | 1 | a0001c0001t0024 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2718A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2718 | chr14 | 31095753 | |||||
chr14:31095768
|
A | T | 2 | a0001c0001t0010a0001c0001t0049 | 6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2733A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2733 | chr14 | 31095768 | |||||
chr14:31095817
|
C | T | 3 | a0001c0001t0013a0001c0001t0023a0001c0001t0035 | 5 | NA18944.hp1 NA18951.hp1 NA18972.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2782C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2782 | chr14 | 31095817 | |||||
chr14:31095821
|
C | T | 1 | a0001c0001t0034 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2786C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2786 | chr14 | 31095821 | |||||
chr14:31095822
|
G | A | 1 | a0001c0001t0009 | 5 | HG01069.hp2 HG01123.hp1 HG01361.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2787G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2787 | chr14 | 31095822 | |||||
chr14:31095846
|
C | T | 1 | a0001c0001t0044 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2811C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2811 | chr14 | 31095846 | |||||
chr14:31095929
|
C | T | 1 | a0001c0001t0022 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2894C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 2894 | chr14 | 31095929 | |||||
chr14:31096089
|
C | CA | 16 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(13): Show | 71 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*3076dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3077 | INFO_REALIGN_3_PRIME | chr14 | 31096089 | ||||
chr14:31096089
|
C | CAA | 5 | a0001c0001t0004a0001c0001t0007a0001c0001t0014others(2): Show | 28 | HG00280.hp1 HG00733.hp1 HG01106.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3075_*3076dupAA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3077 | INFO_REALIGN_3_PRIME | chr14 | 31096089 | ||||
chr14:31096089
|
CA | C | 3 | a0001c0001t0008a0001c0001t0035a0001c0001t0037 | 7 | HG01081.hp2 HG01169.hp1 HG01256.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3076delA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3076 | INFO_REALIGN_3_PRIME | chr14 | 31096089 | ||||
chr14:31096139
|
A | G | 1 | a0001c0001t0049 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3104A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3104 | chr14 | 31096139 | |||||
chr14:31096173
|
C | T | 8 | a0001c0001t0006a0001c0001t0010a0001c0001t0012others(5): Show | 23 | HG01891.hp1 HG02055.hp2 HG02074.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3138C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3138 | chr14 | 31096173 | |||||
chr14:31096215
|
A | AT | 2 | a0001c0001t0010a0001c0001t0049 | 6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3182dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3183 | INFO_REALIGN_3_PRIME | chr14 | 31096215 | ||||
chr14:31096254
|
C | CA | 1 | a0001c0001t0014 | 3 | HG02572.hp2 HG03209.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3223dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3224 | INFO_REALIGN_3_PRIME | chr14 | 31096254 | ||||
chr14:31096284
|
G | A | 1 | a0001c0001t0043 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3249G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3249 | chr14 | 31096284 | |||||
chr14:31096356
|
G | A | 5 | a0001c0001t0012a0001c0001t0016a0001c0001t0020others(2): Show | 8 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3321G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3321 | chr14 | 31096356 | |||||
chr14:31096386
|
A | G | 1 | a0001c0001t0033 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3351A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3351 | chr14 | 31096386 | |||||
chr14:31096408
|
C | T | 5 | a0001c0001t0012a0001c0001t0016a0001c0001t0020others(2): Show | 8 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3373C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 6/6 | 3373 | chr14 | 31096408 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:31025823
|
G | C | 1 | a0001c0001t0001g0004 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-72+36G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31025823 | ||||||
chr14:31025916
|
C | T | 1 | a0001c0001t0001g0342 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-72+129C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31025916 | ||||||
chr14:31026108
|
C | A | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-72+321C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026108 | ||||||
chr14:31026140
|
C | T | 63 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(60): Show | 63 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-72+353C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026140 | ||||||
chr14:31026299
|
G | A | 1 | a0001c0001t0002g0006 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-72+512G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026299 | ||||||
chr14:31026341
|
G | T | 1 | a0001c0001t0004g0278 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-72+554G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026341 | ||||||
chr14:31026386
|
C | G | 1 | a0001c0001t0002g0277 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-72+599C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026386 | ||||||
chr14:31026419
|
C | T | 187 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(184): Show | 188 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.-72+632C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026419 | ||||||
chr14:31026507
|
A | C | 7 | a0001c0001t0001g0270a0001c0001t0010g0271a0001c0001t0010g0272others(4): Show | 7 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72+720A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026507 | ||||||
chr14:31026568
|
G | T | 5 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0014g0158others(2): Show | 5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+781G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026568 | ||||||
chr14:31026633
|
C | A | 40 | a0001c0001t0001g0004a0001c0001t0001g0192a0001c0001t0001g0195others(37): Show | 41 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-72+846C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026633 | ||||||
chr14:31026665
|
G | A | 2 | a0001c0001t0019g0007a0001c0001t0019g0008 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-72+878G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026665 | ||||||
chr14:31026722
|
C | G | 7 | a0001c0001t0001g0270a0001c0001t0010g0271a0001c0001t0010g0272others(4): Show | 7 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72+935C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026722 | ||||||
chr14:31026722
|
C | T | 4 | a0001c0001t0007g0266a0001c0001t0007g0267a0001c0001t0007g0268others(1): Show | 4 | HG02683.hp1 HG03704.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72+935C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026722 | ||||||
chr14:31026773
|
C | G | 1 | a0001c0001t0007g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-72+986C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026773 | ||||||
chr14:31026813
|
C | T | 1 | a0001c0001t0047g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-72+1026C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026813 | ||||||
chr14:31026826
|
C | T | 5 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0014g0158others(2): Show | 5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+1039C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026826 | ||||||
chr14:31026869
|
AG | A | 28 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0135others(25): Show | 29 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-72+1083delG | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026869 | ||||||
chr14:31026905
|
C | T | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-72+1118C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31026905 | ||||||
chr14:31027006
|
T | C | 233 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-72+1219T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31027006 | ||||||
chr14:31027162
|
G | C | 1 | a0001c0001t0005g0279 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-72+1375G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31027162 | ||||||
chr14:31027459
|
C | T | 1 | a0001c0001t0048g0129 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-72+1672C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31027459 | ||||||
chr14:31027535
|
ACCTGTAG others(2): Show |
A | 7 | a0001c0001t0001g0270a0001c0001t0010g0271a0001c0001t0010g0272others(4): Show | 7 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72+1751_-72+1759d others(11): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31027535 | |||||
chr14:31027574
|
A | G | 1 | a0001c0001t0001g0341 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-72+1787A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31027574 | ||||||
chr14:31027928
|
T | A | 7 | a0001c0001t0001g0270a0001c0001t0010g0271a0001c0001t0010g0272others(4): Show | 7 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72+2141T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31027928 | ||||||
chr14:31028037
|
A | G | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 106 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-72+2250A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028037 | ||||||
chr14:31028183
|
AT | A | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(211): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.-72+2408delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31028183 | |||||
chr14:31028394
|
T | C | 1 | a0001c0001t0002g0162 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-72+2607T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028394 | ||||||
chr14:31028539
|
G | A | 1 | a0001c0001t0002g0163 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-72+2752G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028539 | ||||||
chr14:31028596
|
T | TAC | 72 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(69): Show | 73 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(70): Show |
intron_variant | MODIFIER | c.-72+2831_-72+2832d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31028596 | |||||
chr14:31028596
|
T | TACAC | 57 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(54): Show | 57 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.-72+2829_-72+2832d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31028596 | |||||
chr14:31028596
|
T | TACACAC | 17 | a0001c0001t0001g0003a0001c0001t0001g0280a0001c0001t0001g0281others(14): Show | 17 | HG00323.hp2 HG01081.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.-72+2827_-72+2832d others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31028596 | |||||
chr14:31028596
|
T | TACACACA others(1): Show |
3 | a0001c0001t0012g0199a0001c0001t0016g0197a0001c0001t0016g0198 | 3 | HG02559.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-72+2825_-72+2832d others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31028596 | |||||
chr14:31028596
|
TAC | T | 5 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(2): Show | 5 | HG00741.hp2 HG02015.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+2831_-72+2832d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31028596 | |||||
chr14:31028667
|
C | T | 1 | a0001c0001t0003g0002 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-72+2880C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028667 | ||||||
chr14:31028798
|
C | T | 3 | a0001c0001t0001g0206a0001c0001t0018g0205a0001c0001t0043g0204 | 3 | HG02451.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-72+3011C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028798 | ||||||
chr14:31028850
|
G | C | 317 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(314): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.-72+3063G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028850 | ||||||
chr14:31028851
|
T | C | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.-72+3064T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028851 | ||||||
chr14:31028879
|
C | A | 7 | a0001c0001t0001g0270a0001c0001t0010g0271a0001c0001t0010g0272others(4): Show | 7 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72+3092C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028879 | ||||||
chr14:31028921
|
A | G | 10 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0001t0001g0333others(7): Show | 10 | NA18939.hp1 NA18947.hp2 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.-72+3134A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31028921 | ||||||
chr14:31029025
|
A | G | 4 | a0001c0001t0001g0192a0001c0001t0026g0194a0001c0001t0027g0164others(1): Show | 4 | HG02280.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+3238A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029025 | ||||||
chr14:31029096
|
T | A | 1 | a0001c0001t0008g0022 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-72+3309T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029096 | ||||||
chr14:31029112
|
A | C | 2 | a0001c0001t0019g0007a0001c0001t0019g0008 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-72+3325A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029112 | ||||||
chr14:31029129
|
TC | T | 3 | a0001c0001t0001g0206a0001c0001t0018g0205a0001c0001t0043g0204 | 3 | HG02451.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-72+3343delC | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029129 | ||||||
chr14:31029204
|
T | A | 23 | a0001c0001t0001g0207a0001c0001t0001g0210a0001c0001t0001g0212others(20): Show | 23 | HG00140.hp1 HG00621.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.-72+3417T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029204 | ||||||
chr14:31029341
|
A | G | 5 | a0001c0001t0001g0240a0001c0001t0005g0241a0001c0001t0005g0242others(2): Show | 5 | HG00639.hp2 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+3554A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029341 | ||||||
chr14:31029357
|
A | G | 1 | a0001c0001t0018g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-72+3570A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029357 | ||||||
chr14:31029518
|
T | C | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG02074.hp1 NA18977.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+3731T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029518 | ||||||
chr14:31029558
|
C | A | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-72+3771C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029558 | ||||||
chr14:31029576
|
C | T | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | NA18995.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-72+3789C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029576 | ||||||
chr14:31029675
|
A | G | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0029g0243 | 3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-72+3888A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029675 | ||||||
chr14:31029849
|
C | CA | 7 | a0001c0001t0001g0270a0001c0001t0010g0271a0001c0001t0010g0272others(4): Show | 7 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72+4074dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31029849 | |||||
chr14:31029851
|
A | C | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-72+4064A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029851 | ||||||
chr14:31029876
|
C | T | 40 | a0001c0001t0001g0004a0001c0001t0001g0192a0001c0001t0001g0195others(37): Show | 41 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-72+4089C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31029876 | ||||||
chr14:31030007
|
A | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG00544.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.-72+4220A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030007 | ||||||
chr14:31030076
|
G | A | 2 | a0001c0001t0019g0007a0001c0001t0019g0008 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-72+4289G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030076 | ||||||
chr14:31030185
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-72+4398G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030185 | ||||||
chr14:31030223
|
T | C | 2 | a0001c0001t0012g0200a0001c0001t0012g0201 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-72+4436T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030223 | ||||||
chr14:31030307
|
G | C | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.-72+4520G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030307 | ||||||
chr14:31030342
|
T | C | 70 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0192others(67): Show | 71 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.-72+4555T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030342 | ||||||
chr14:31030553
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0035g0034 | 2 | NA18943.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-72+4766T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030553 | ||||||
chr14:31030571
|
A | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0246a0001c0001t0001g0251others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.-72+4784A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030571 | ||||||
chr14:31030578
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0007g0208 | 2 | HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-72+4791G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030578 | ||||||
chr14:31030628
|
C | T | 1 | a0001c0001t0007g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-72+4841C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030628 | ||||||
chr14:31030650
|
G | A | 1 | a0001c0001t0002g0165 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-72+4863G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030650 | ||||||
chr14:31030754
|
A | C | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-72+4967A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030754 | ||||||
chr14:31030779
|
A | G | 2 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | NA18968.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-72+4992A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030779 | ||||||
chr14:31030869
|
A | G | 10 | a0001c0001t0001g0206a0001c0001t0001g0270a0001c0001t0010g0271others(7): Show | 10 | HG02074.hp2 HG02451.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-72+5082A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31030869 | ||||||
chr14:31031102
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-72+5315C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031102 | ||||||
chr14:31031197
|
T | C | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-72+5410T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031197 | ||||||
chr14:31031224
|
T | C | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-72+5437T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031224 | ||||||
chr14:31031331
|
T | A | 64 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(61): Show | 64 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-72+5544T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031331 | ||||||
chr14:31031440
|
C | G | 3 | a0001c0001t0001g0206a0001c0001t0018g0205a0001c0001t0043g0204 | 3 | HG02451.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-72+5653C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031440 | ||||||
chr14:31031478
|
C | T | 1 | a0001c0001t0019g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-72+5691C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031478 | ||||||
chr14:31031553
|
A | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 106 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-72+5766A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031553 | ||||||
chr14:31031745
|
C | G | 1 | a0001c0001t0047g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-72+5958C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031745 | ||||||
chr14:31031828
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-72+6041A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031828 | ||||||
chr14:31031842
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-72+6055C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031842 | ||||||
chr14:31031906
|
A | G | 3 | a0001c0001t0006g0327a0001c0001t0006g0328a0001c0001t0031g0326 | 3 | HG01884.hp1 HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-72+6119A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031906 | ||||||
chr14:31031914
|
TG | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.-72+6131delG | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31031914 | |||||
chr14:31031947
|
A | G | 1 | a0001c0001t0002g0191 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-72+6160A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031947 | ||||||
chr14:31031958
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-72+6171G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31031958 | ||||||
chr14:31032071
|
C | CA | 11 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0037others(8): Show | 11 | HG00738.hp2 HG01928.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-72+6304dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032071 | |||||
chr14:31032071
|
CAAAAA | C | 24 | a0001c0001t0001g0207a0001c0001t0001g0210a0001c0001t0001g0212others(21): Show | 24 | HG00140.hp1 HG00621.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-72+6300_-72+6304d others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032071 | |||||
chr14:31032071
|
CAAAAAA | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 153 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.-72+6299_-72+6304d others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032071 | |||||
chr14:31032071
|
CAAAAAAA | C | 10 | a0001c0001t0001g0206a0001c0001t0001g0270a0001c0001t0010g0271others(7): Show | 10 | HG02074.hp2 HG02451.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-72+6298_-72+6304d others(9): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032071 | |||||
chr14:31032087
|
A | G | 2 | a0001c0001t0019g0007a0001c0001t0019g0008 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-72+6300A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032087 | ||||||
chr14:31032255
|
G | A | 3 | a0001c0001t0001g0206a0001c0001t0018g0205a0001c0001t0043g0204 | 3 | HG02451.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-72+6468G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032255 | ||||||
chr14:31032274
|
A | G | 2 | a0001c0001t0006g0327a0001c0001t0006g0328 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-72+6487A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032274 | ||||||
chr14:31032299
|
C | T | 234 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-72+6512C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032299 | ||||||
chr14:31032403
|
C | T | 3 | a0001c0001t0003g0025a0001c0001t0003g0026a0001c0001t0003g0027 | 3 | HG02559.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-72+6616C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032403 | ||||||
chr14:31032523
|
A | ATT | 65 | a0001c0001t0001g0270a0001c0001t0001g0280a0001c0001t0001g0281others(62): Show | 65 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-72+6750_-72+6751d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032523 | |||||
chr14:31032523
|
A | ATTT | 72 | a0001c0001t0001g0003a0001c0001t0001g0206a0001c0001t0001g0207others(69): Show | 72 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.-72+6749_-72+6751d others(5): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032523 | |||||
chr14:31032523
|
A | ATTTT | 47 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0192others(44): Show | 48 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-72+6748_-72+6751d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032523 | |||||
chr14:31032523
|
AT | A | 6 | a0001c0001t0001g0040a0001c0001t0007g0157a0001c0001t0007g0161others(3): Show | 6 | HG00621.hp2 HG01106.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-72+6751delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31032523 | |||||
chr14:31032587
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-72+6800G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032587 | ||||||
chr14:31032689
|
C | A | 5 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0014g0158others(2): Show | 5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+6902C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032689 | ||||||
chr14:31032697
|
G | A | 23 | a0001c0001t0001g0207a0001c0001t0001g0210a0001c0001t0001g0212others(20): Show | 23 | HG00140.hp1 HG00621.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.-72+6910G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032697 | ||||||
chr14:31032727
|
G | A | 9 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(6): Show | 9 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.-72+6940G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032727 | ||||||
chr14:31032760
|
T | C | 10 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(7): Show | 10 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-72+6973T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032760 | ||||||
chr14:31032762
|
C | T | 1 | a0001c0001t0047g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-72+6975C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032762 | ||||||
chr14:31032771
|
T | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-72+6984T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032771 | ||||||
chr14:31032776
|
C | T | 10 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(7): Show | 10 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-72+6989C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31032776 | ||||||
chr14:31033220
|
A | AT | 7 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(4): Show | 7 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-72+7444dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31033220 | |||||
chr14:31033253
|
A | G | 186 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.-72+7466A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31033253 | ||||||
chr14:31033275
|
G | A | 1 | a0001c0001t0015g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-72+7488G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31033275 | ||||||
chr14:31033430
|
C | T | 64 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(61): Show | 64 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-72+7643C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31033430 | ||||||
chr14:31033431
|
C | T | 1 | a0001c0001t0007g0161 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-72+7644C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31033431 | ||||||
chr14:31033440
|
C | T | 4 | a0001c0001t0006g0018a0001c0001t0006g0019a0001c0001t0006g0020others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72+7653C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31033440 | ||||||
chr14:31033606
|
G | A | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-72+7819G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31033606 | ||||||
chr14:31034068
|
A | G | 3 | a0001c0001t0001g0206a0001c0001t0018g0205a0001c0001t0043g0204 | 3 | HG02451.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-72+8281A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034068 | ||||||
chr14:31034108
|
G | C | 1 | a0001c0001t0001g0292 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-72+8321G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034108 | ||||||
chr14:31034255
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-72+8468C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034255 | ||||||
chr14:31034277
|
C | T | 41 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 42 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-72+8490C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034277 | ||||||
chr14:31034392
|
G | A | 2 | a0001c0001t0007g0157a0001c0001t0007g0161 | 2 | HG01106.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-72+8605G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034392 | ||||||
chr14:31034413
|
C | T | 5 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0014g0158others(2): Show | 5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+8626C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034413 | ||||||
chr14:31034468
|
T | G | 41 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(38): Show | 42 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-72+8681T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034468 | ||||||
chr14:31034570
|
C | T | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-72+8783C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034570 | ||||||
chr14:31034609
|
A | AT | 82 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0029others(79): Show | 83 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.-72+8847dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31034609 | |||||
chr14:31034609
|
A | ATT | 11 | a0001c0001t0001g0239a0001c0001t0002g0163a0001c0001t0002g0165others(8): Show | 11 | HG00438.hp1 HG02572.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.-72+8846_-72+8847d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31034609 | |||||
chr14:31034609
|
AT | A | 73 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0144others(70): Show | 73 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-72+8847delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31034609 | |||||
chr14:31034687
|
G | A | 67 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(64): Show | 67 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.-72+8900G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034687 | ||||||
chr14:31034703
|
C | T | 2 | a0001c0001t0003g0152a0001c0001t0003g0153 | 2 | HG00099.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-72+8916C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034703 | ||||||
chr14:31034766
|
C | T | 35 | a0001c0001t0001g0003a0001c0001t0001g0230a0001c0001t0001g0231others(32): Show | 35 | HG00140.hp2 HG00323.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.-72+8979C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034766 | ||||||
chr14:31034839
|
C | A | 2 | a0001c0001t0019g0007a0001c0001t0019g0008 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-72+9052C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034839 | ||||||
chr14:31034880
|
G | T | 1 | a0001c0001t0041g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-72+9093G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034880 | ||||||
chr14:31034910
|
A | T | 1 | a0001c0001t0018g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-72+9123A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034910 | ||||||
chr14:31034970
|
A | T | 1 | a0001c0001t0024g0190 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-72+9183A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31034970 | ||||||
chr14:31035036
|
T | G | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-72+9249T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035036 | ||||||
chr14:31035122
|
T | G | 11 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(8): Show | 11 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.-72+9335T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035122 | ||||||
chr14:31035138
|
T | C | 5 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0014g0158others(2): Show | 5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+9351T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035138 | ||||||
chr14:31035193
|
C | CT | 188 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(185): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.-72+9426dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31035193 | |||||
chr14:31035193
|
C | CTT | 47 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(44): Show | 47 | HG00438.hp2 HG00621.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.-72+9425_-72+9426d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31035193 | |||||
chr14:31035232
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-72+9445A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035232 | ||||||
chr14:31035332
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-72+9545T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035332 | ||||||
chr14:31035395
|
A | ATG | 224 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(221): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.-72+9609_-72+9610i others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31035395 | |||||
chr14:31035405
|
A | C | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-72+9618A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035405 | ||||||
chr14:31035562
|
T | TAAAAAAA others(317): Show |
2 | a0001c0001t0005g0242a0001c0001t0029g0243 | 2 | HG00639.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-72+9789_-72+9790i others(326): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31035562 | |||||
chr14:31035562
|
T | TAAAAAAA others(339): Show |
1 | a0001c0001t0005g0241 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-72+9789_-72+9790i others(348): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31035562 | |||||
chr14:31035563
|
A | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0093others(53): Show | 56 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.-72+9776A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035563 | ||||||
chr14:31035627
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-72+9840C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035627 | ||||||
chr14:31035638
|
C | CT | 74 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(71): Show | 75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.-72+9866dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31035638 | |||||
chr14:31035770
|
C | T | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-72+9983C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035770 | ||||||
chr14:31035790
|
T | C | 8 | a0001c0001t0001g0206a0001c0001t0012g0199a0001c0001t0012g0200others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-72+10003T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035790 | ||||||
chr14:31035831
|
T | G | 1 | a0001c0001t0006g0328 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-72+10044T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035831 | ||||||
chr14:31035842
|
G | A | 234 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-72+10055G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035842 | ||||||
chr14:31035843
|
C | T | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0029g0243 | 3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-72+10056C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035843 | ||||||
chr14:31035850
|
CT | C | 168 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(165): Show | 169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.-72+10065delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31035850 | |||||
chr14:31035883
|
A | G | 24 | a0001c0001t0001g0035a0001c0001t0001g0096a0001c0001t0001g0097others(21): Show | 24 | HG00140.hp1 HG00621.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-72+10096A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035883 | ||||||
chr14:31035912
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-72+10125G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035912 | ||||||
chr14:31035920
|
C | T | 2 | a0001c0001t0001g0338a0001c0001t0013g0317 | 2 | NA18951.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.-72+10133C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035920 | ||||||
chr14:31035931
|
C | T | 2 | a0001c0001t0003g0130a0001c0001t0044g0131 | 2 | HG01255.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-72+10144C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035931 | ||||||
chr14:31035932
|
A | G | 2 | a0001c0001t0003g0130a0001c0001t0044g0131 | 2 | HG01255.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-72+10145A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035932 | ||||||
chr14:31035955
|
A | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0098 | 2 | HG00733.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-72+10168A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035955 | ||||||
chr14:31035972
|
C | T | 7 | a0001c0001t0001g0270a0001c0001t0010g0271a0001c0001t0010g0272others(4): Show | 7 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72+10185C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035972 | ||||||
chr14:31035981
|
T | C | 1 | a0001c0001t0003g0152 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-72+10194T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035981 | ||||||
chr14:31035982
|
G | A | 1 | a0001c0001t0003g0152 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-72+10195G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31035982 | ||||||
chr14:31036021
|
T | C | 5 | a0001c0001t0001g0106a0001c0001t0001g0121a0001c0001t0002g0187others(2): Show | 5 | HG02135.hp1 HG02970.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+10234T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036021 | ||||||
chr14:31036025
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-72+10238T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036025 | ||||||
chr14:31036133
|
TTA | T | 22 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0100others(19): Show | 22 | HG00140.hp1 HG00621.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.-72+10347_-72+1034 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036133 | ||||||
chr14:31036134
|
T | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0206a0001c0001t0007g0157others(6): Show | 9 | HG01106.hp2 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-72+10347T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036134 | ||||||
chr14:31036142
|
T | A | 22 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0100others(19): Show | 22 | HG00140.hp1 HG00621.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.-72+10355T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036142 | ||||||
chr14:31036190
|
AT | A | 78 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0093others(75): Show | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.-72+10404delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036190 | ||||||
chr14:31036201
|
A | G | 6 | a0001c0001t0012g0199a0001c0001t0012g0200a0001c0001t0012g0201others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72+10414A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036201 | ||||||
chr14:31036572
|
C | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG00438.hp2 HG01099.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+10785C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036572 | ||||||
chr14:31036589
|
A | G | 29 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0337others(26): Show | 29 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-72+10802A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31036589 | ||||||
chr14:31036969
|
T | TGCCCGGC others(186): Show |
1 | a0001c0001t0005g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-72+11198_-72+1119 others(197): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31036969 | |||||
chr14:31036969
|
T | TGCCCGGC others(187): Show |
1 | a0001c0001t0005g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-72+11198_-72+1119 others(198): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31036969 | |||||
chr14:31036969
|
T | TGCCCGGC others(190): Show |
1 | a0001c0001t0032g0250 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-72+11198_-72+1119 others(201): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31036969 | |||||
chr14:31037003
|
A | G | 3 | a0001c0001t0005g0248a0001c0001t0005g0249a0001c0001t0032g0250 | 3 | HG02145.hp1 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-72+11216A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037003 | ||||||
chr14:31037070
|
C | T | 1 | a0001c0001t0044g0131 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-72+11283C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037070 | ||||||
chr14:31037143
|
A | G | 85 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-72+11356A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037143 | ||||||
chr14:31037181
|
C | G | 1 | a0001c0001t0001g0290 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-72+11394C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037181 | ||||||
chr14:31037203
|
A | G | 1 | a0001c0001t0002g0189 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-72+11416A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037203 | ||||||
chr14:31037205
|
C | G | 85 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-72+11418C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037205 | ||||||
chr14:31037299
|
T | C | 288 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(285): Show | 290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.-72+11512T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037299 | ||||||
chr14:31037339
|
A | C | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-72+11552A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037339 | ||||||
chr14:31037376
|
T | C | 85 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-72+11589T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037376 | ||||||
chr14:31037410
|
T | C | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG00438.hp2 HG01099.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+11623T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037410 | ||||||
chr14:31037427
|
C | CT | 85 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-72+11643dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31037427 | |||||
chr14:31037439
|
C | T | 1 | a0001c0001t0007g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-72+11652C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037439 | ||||||
chr14:31037926
|
T | C | 6 | a0001c0001t0001g0029a0001c0001t0001g0104a0001c0001t0001g0109others(3): Show | 6 | HG00544.hp1 HG00558.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72+12139T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037926 | ||||||
chr14:31037943
|
C | A | 2 | a0001c0001t0001g0206a0001c0001t0047g0264 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-72+12156C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037943 | ||||||
chr14:31037953
|
A | T | 50 | a0001c0001t0001g0118a0001c0001t0001g0251a0001c0001t0001g0252others(47): Show | 50 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-72+12166A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037953 | ||||||
chr14:31037973
|
C | A | 17 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0003g0002others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-72+12186C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31037973 | ||||||
chr14:31038014
|
T | C | 85 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-72+12227T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31038014 | ||||||
chr14:31038193
|
A | G | 1 | a0001c0001t0010g0275 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-72+12406A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31038193 | ||||||
chr14:31038653
|
TC | T | 22 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0100others(19): Show | 22 | HG00408.hp2 HG00609.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-72+12868delC | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31038653 | |||||
chr14:31038753
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-72+12966T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31038753 | ||||||
chr14:31038788
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-72+13001C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31038788 | ||||||
chr14:31038820
|
A | G | 1 | a0001c0001t0031g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-72+13033A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31038820 | ||||||
chr14:31038870
|
A | G | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-72+13083A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31038870 | ||||||
chr14:31038992
|
GT | G | 214 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0023others(211): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-72+13219delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31038992 | |||||
chr14:31039118
|
G | T | 286 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(283): Show | 288 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.-72+13331G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039118 | ||||||
chr14:31039216
|
C | T | 1 | a0001c0001t0004g0095 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-72+13429C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039216 | ||||||
chr14:31039220
|
C | G | 6 | a0001c0001t0012g0199a0001c0001t0012g0200a0001c0001t0012g0201others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72+13433C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039220 | ||||||
chr14:31039225
|
G | A | 35 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0100others(32): Show | 35 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-72+13438G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039225 | ||||||
chr14:31039567
|
G | GTT | 18 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0001g0332others(15): Show | 19 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.-72+13783_-72+1378 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31039567 | |||||
chr14:31039570
|
T | TTTTG | 5 | a0001c0001t0001g0315a0001c0001t0001g0319a0001c0001t0001g0322others(2): Show | 5 | HG00544.hp2 HG01192.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+13784_-72+1378 others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31039570 | |||||
chr14:31039571
|
T | TTTG | 62 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(59): Show | 62 | HG00140.hp2 HG00423.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.-72+13784_-72+1378 others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039571 | ||||||
chr14:31039572
|
G | GT | 10 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0142others(7): Show | 10 | HG01981.hp1 HG02109.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.-72+13803dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31039572 | |||||
chr14:31039572
|
G | T | 68 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(65): Show | 68 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.-72+13785G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039572 | ||||||
chr14:31039577
|
T | G | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG01243.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-72+13790T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039577 | ||||||
chr14:31039578
|
T | TG | 16 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0003g0002others(13): Show | 17 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.-72+13791_-72+1379 others(5): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039578 | ||||||
chr14:31039579
|
T | G | 122 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(119): Show | 123 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.-72+13792T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039579 | ||||||
chr14:31039588
|
T | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG00639.hp1 HG01106.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72+13801T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039588 | ||||||
chr14:31039663
|
CCCGGGTT others(11): Show |
C | 1 | a0001c0001t0001g0125 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-72+13897_-72+1391 others(22): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31039663 | |||||
chr14:31039840
|
C | T | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-72+14053C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039840 | ||||||
chr14:31039868
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-72+14081C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039868 | ||||||
chr14:31039878
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0019g0007a0001c0001t0019g0008 | 3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-72+14091C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039878 | ||||||
chr14:31039881
|
G | A | 85 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-72+14094G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039881 | ||||||
chr14:31039884
|
C | T | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+14097C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31039884 | ||||||
chr14:31040041
|
T | G | 1 | a0001c0001t0011g0082 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-72+14254T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040041 | ||||||
chr14:31040089
|
A | G | 1 | a0001c0001t0004g0216 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-72+14302A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040089 | ||||||
chr14:31040148
|
C | CT | 244 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(241): Show | 246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-72+14379dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31040148 | |||||
chr14:31040148
|
C | CTT | 9 | a0001c0001t0001g0039a0001c0001t0001g0079a0001c0001t0001g0080others(6): Show | 9 | HG00280.hp2 HG02071.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-72+14378_-72+1437 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31040148 | |||||
chr14:31040165
|
T | C | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-72+14378T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040165 | ||||||
chr14:31040244
|
C | G | 1 | a0001c0001t0041g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-72+14457C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040244 | ||||||
chr14:31040292
|
G | A | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | NA18988.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-72+14505G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040292 | ||||||
chr14:31040456
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-72+14669A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040456 | ||||||
chr14:31040822
|
G | T | 3 | a0001c0001t0001g0092a0001c0001t0019g0007a0001c0001t0019g0008 | 3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-72+15035G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040822 | ||||||
chr14:31040827
|
G | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0050 | 2 | HG00621.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-72+15040G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040827 | ||||||
chr14:31040902
|
G | A | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+15115G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31040902 | ||||||
chr14:31041075
|
C | CA | 132 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(129): Show | 133 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.-72+15303dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31041075 | |||||
chr14:31041075
|
CA | C | 36 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0100others(33): Show | 36 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.-72+15303delA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31041075 | |||||
chr14:31041131
|
T | G | 121 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(118): Show | 122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.-72+15344T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041131 | ||||||
chr14:31041211
|
G | C | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-72+15424G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041211 | ||||||
chr14:31041228
|
C | G | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-72+15441C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041228 | ||||||
chr14:31041338
|
G | C | 289 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(286): Show | 291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.-72+15551G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041338 | ||||||
chr14:31041613
|
C | T | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72+15826C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041613 | ||||||
chr14:31041673
|
A | C | 53 | a0001c0001t0001g0118a0001c0001t0001g0251a0001c0001t0001g0252others(50): Show | 53 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-72+15886A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041673 | ||||||
chr14:31041687
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-72+15900A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041687 | ||||||
chr14:31041747
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-72+15960G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041747 | ||||||
chr14:31041807
|
T | G | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-72+16020T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041807 | ||||||
chr14:31041853
|
A | AT | 13 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(10): Show | 13 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-72+16072dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31041853 | |||||
chr14:31041913
|
C | T | 1 | a0001c0001t0005g0081 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-72+16126C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041913 | ||||||
chr14:31041915
|
G | A | 1 | a0001c0001t0018g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-72+16128G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041915 | ||||||
chr14:31041953
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-72+16166G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31041953 | ||||||
chr14:31042145
|
T | C | 50 | a0001c0001t0001g0118a0001c0001t0001g0251a0001c0001t0001g0252others(47): Show | 50 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-72+16358T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042145 | ||||||
chr14:31042170
|
T | C | 53 | a0001c0001t0001g0118a0001c0001t0001g0251a0001c0001t0001g0252others(50): Show | 53 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-72+16383T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042170 | ||||||
chr14:31042182
|
A | G | 343 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.-72+16395A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042182 | ||||||
chr14:31042282
|
C | G | 35 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0100others(32): Show | 35 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-72+16495C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042282 | ||||||
chr14:31042376
|
A | G | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | NA18946.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.-72+16589A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042376 | ||||||
chr14:31042537
|
G | A | 50 | a0001c0001t0001g0118a0001c0001t0001g0251a0001c0001t0001g0252others(47): Show | 50 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-72+16750G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042537 | ||||||
chr14:31042557
|
G | A | 1 | a0001c0001t0005g0249 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-72+16770G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042557 | ||||||
chr14:31042707
|
A | G | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0029g0243 | 3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-72+16920A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042707 | ||||||
chr14:31042848
|
G | T | 1 | a0001c0001t0002g0168 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-72+17061G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042848 | ||||||
chr14:31042992
|
G | A | 2 | a0001c0001t0005g0083a0001c0001t0005g0084 | 2 | HG01109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-72+17205G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31042992 | ||||||
chr14:31043034
|
G | A | 1 | a0001c0001t0025g0186 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-72+17247G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043034 | ||||||
chr14:31043094
|
G | T | 1 | a0001c0001t0029g0243 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-72+17307G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043094 | ||||||
chr14:31043146
|
G | A | 118 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(115): Show | 119 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.-72+17359G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043146 | ||||||
chr14:31043182
|
C | T | 90 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(87): Show | 91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.-72+17395C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043182 | ||||||
chr14:31043225
|
G | A | 1 | a0001c0001t0001g0304 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-72+17438G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043225 | ||||||
chr14:31043225
|
G | GAA | 84 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(81): Show | 85 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.-72+17449_-72+1745 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31043225 | |||||
chr14:31043283
|
T | G | 1 | a0001c0001t0005g0305 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-72+17496T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043283 | ||||||
chr14:31043310
|
C | G | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-72+17523C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043310 | ||||||
chr14:31043405
|
G | T | 1 | a0001c0001t0002g0185 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-72+17618G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043405 | ||||||
chr14:31043525
|
C | T | 35 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0100others(32): Show | 35 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-72+17738C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043525 | ||||||
chr14:31043710
|
T | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0109 | 2 | HG02135.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-72+17923T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043710 | ||||||
chr14:31043893
|
A | T | 85 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(82): Show | 86 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-72+18106A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31043893 | ||||||
chr14:31044100
|
G | C | 130 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(127): Show | 131 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-72+18313G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044100 | ||||||
chr14:31044106
|
A | G | 29 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 30 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.-72+18319A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044106 | ||||||
chr14:31044219
|
C | T | 5 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG00438.hp2 HG01099.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+18432C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044219 | ||||||
chr14:31044260
|
G | A | 6 | a0001c0001t0001g0102a0001c0001t0001g0106a0001c0001t0001g0112others(3): Show | 6 | NA18971.hp1 NA19007.hp2 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72+18473G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044260 | ||||||
chr14:31044289
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-72+18502T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044289 | ||||||
chr14:31044408
|
C | T | 7 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(4): Show | 7 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-72+18621C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044408 | ||||||
chr14:31044413
|
A | T | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-72+18626A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044413 | ||||||
chr14:31044527
|
T | A | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-72+18740T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044527 | ||||||
chr14:31044637
|
C | T | 5 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0314others(2): Show | 5 | HG00140.hp2 HG01175.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72+18850C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044637 | ||||||
chr14:31044719
|
C | G | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0029g0243 | 3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-72+18932C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044719 | ||||||
chr14:31044811
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-72+19024C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044811 | ||||||
chr14:31044836
|
T | C | 1 | a0001c0001t0020g0202 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-72+19049T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044836 | ||||||
chr14:31044851
|
G | T | 121 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(118): Show | 122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.-72+19064G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044851 | ||||||
chr14:31044875
|
A | G | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-72+19088A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044875 | ||||||
chr14:31044906
|
A | AT | 6 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0213others(3): Show | 6 | HG02280.hp2 HG02622.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72+19133dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31044906 | |||||
chr14:31044994
|
C | T | 26 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0337others(23): Show | 26 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.-72+19207C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31044994 | ||||||
chr14:31045032
|
G | A | 2 | a0001c0001t0002g0169a0001c0001t0002g0185 | 2 | NA18954.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-72+19245G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045032 | ||||||
chr14:31045050
|
C | T | 1 | a0001c0001t0002g0185 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-72+19263C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045050 | ||||||
chr14:31045167
|
G | T | 3 | a0001c0001t0012g0199a0001c0001t0012g0200a0001c0001t0012g0201 | 3 | HG01891.hp1 HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-72+19380G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045167 | ||||||
chr14:31045283
|
G | T | 29 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(26): Show | 30 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.-72+19496G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045283 | ||||||
chr14:31045392
|
G | A | 82 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(79): Show | 83 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-72+19605G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045392 | ||||||
chr14:31045493
|
G | A | 12 | a0001c0001t0005g0083a0001c0001t0005g0084a0001c0001t0011g0082others(9): Show | 12 | HG00558.hp1 HG00609.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-72+19706G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045493 | ||||||
chr14:31045626
|
C | T | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-72+19839C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045626 | ||||||
chr14:31045627
|
G | A | 1 | a0001c0001t0004g0278 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-72+19840G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045627 | ||||||
chr14:31045663
|
A | C | 82 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(79): Show | 83 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-72+19876A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045663 | ||||||
chr14:31045753
|
G | A | 1 | a0001c0001t0012g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-72+19966G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045753 | ||||||
chr14:31045790
|
A | G | 56 | a0001c0001t0001g0092a0001c0001t0001g0118a0001c0001t0001g0251others(53): Show | 56 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.-72+20003A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045790 | ||||||
chr14:31045866
|
T | G | 1 | a0001c0001t0025g0186 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-72+20079T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045866 | ||||||
chr14:31045910
|
T | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0337others(27): Show | 30 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-72+20123T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045910 | ||||||
chr14:31045964
|
A | AT | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(12): Show | 15 | HG00099.hp2 HG00544.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.-71-20143dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31045964 | |||||
chr14:31045964
|
AT | A | 172 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(169): Show | 173 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.-71-20143delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31045964 | |||||
chr14:31045988
|
C | T | 1 | a0001c0001t0009g0038 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-71-20138C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31045988 | ||||||
chr14:31046057
|
C | T | 1 | a0001c0001t0003g0149 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-71-20069C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31046057 | ||||||
chr14:31046257
|
A | G | 17 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0003g0002others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-19869A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31046257 | ||||||
chr14:31046567
|
C | T | 90 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(87): Show | 91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.-71-19559C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31046567 | ||||||
chr14:31046573
|
C | T | 1 | a0001c0001t0004g0255 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-71-19553C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31046573 | ||||||
chr14:31046703
|
G | A | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0029g0243 | 3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-71-19423G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31046703 | ||||||
chr14:31046795
|
G | A | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-19331G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31046795 | ||||||
chr14:31046845
|
C | CA | 33 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(30): Show | 33 | HG01361.hp1 HG01891.hp1 HG02109.hp2 others(30): Show |
intron_variant | MODIFIER | c.-71-19262dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31046845 | |||||
chr14:31046845
|
C | CAA | 7 | a0001c0001t0006g0015a0001c0001t0006g0017a0001c0001t0010g0271others(4): Show | 7 | HG02055.hp2 HG02074.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-19263_-71-1926 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31046845 | |||||
chr14:31046862
|
AAAG | A | 7 | a0001c0001t0001g0003a0001c0001t0004g0094a0001c0001t0004g0095others(4): Show | 7 | HG01081.hp2 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-19257_-71-1925 others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31046862 | |||||
chr14:31046884
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-71-19242A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31046884 | ||||||
chr14:31047178
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-71-18948C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31047178 | ||||||
chr14:31047385
|
C | CT | 12 | a0001c0001t0001g0076a0001c0001t0001g0195a0001c0001t0001g0232others(9): Show | 12 | HG00741.hp2 HG01175.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-71-18721dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31047385 | |||||
chr14:31047385
|
CT | C | 7 | a0001c0001t0001g0206a0001c0001t0001g0240a0001c0001t0001g0337others(4): Show | 7 | HG01109.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71-18721delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31047385 | |||||
chr14:31047411
|
G | A | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-71-18715G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31047411 | ||||||
chr14:31047537
|
G | A | 1 | a0001c0001t0039g0133 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-71-18589G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31047537 | ||||||
chr14:31047564
|
T | G | 1 | a0001c0001t0007g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-71-18562T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31047564 | ||||||
chr14:31047630
|
T | G | 8 | a0001c0001t0011g0082a0001c0001t0011g0085a0001c0001t0011g0088others(5): Show | 8 | HG00558.hp1 HG00609.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-71-18496T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31047630 | ||||||
chr14:31047631
|
G | A | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-71-18495G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31047631 | ||||||
chr14:31047789
|
A | AT | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0029g0243 | 3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-71-18336dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31047789 | |||||
chr14:31047850
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-71-18276A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31047850 | ||||||
chr14:31048093
|
A | AT | 10 | a0001c0001t0001g0039a0001c0001t0002g0169a0001c0001t0002g0183others(7): Show | 10 | HG00673.hp1 HG02071.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-71-18016dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31048093 | |||||
chr14:31048093
|
AT | A | 9 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0228others(6): Show | 9 | HG01069.hp1 HG01074.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.-71-18016delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31048093 | |||||
chr14:31048239
|
G | A | 17 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0003g0002others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-17887G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31048239 | ||||||
chr14:31048266
|
T | A | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-17860T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31048266 | ||||||
chr14:31048600
|
G | T | 2 | a0001c0001t0019g0007a0001c0001t0019g0008 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-71-17526G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31048600 | ||||||
chr14:31048799
|
G | A | 297 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-71-17327G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31048799 | ||||||
chr14:31048870
|
C | T | 1 | a0001c0001t0015g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-71-17256C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31048870 | ||||||
chr14:31049025
|
G | T | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-71-17101G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049025 | ||||||
chr14:31049180
|
G | A | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-16946G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049180 | ||||||
chr14:31049184
|
C | T | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-16942C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049184 | ||||||
chr14:31049188
|
T | C | 285 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(282): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.-71-16938T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049188 | ||||||
chr14:31049199
|
G | T | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-16927G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049199 | ||||||
chr14:31049210
|
G | A | 17 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0003g0002others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-16916G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049210 | ||||||
chr14:31049413
|
C | CA | 8 | a0001c0001t0001g0012a0001c0001t0001g0060a0001c0001t0001g0110others(5): Show | 8 | HG01257.hp1 HG01258.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-71-16697dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049413 | |||||
chr14:31049426
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-71-16700A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049426 | ||||||
chr14:31049426
|
AAAATATA others(5): Show |
A | 1 | a0001c0001t0010g0275 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-71-16698_-71-1668 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049426 | |||||
chr14:31049426
|
AAAATATA others(9): Show |
A | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-71-16698_-71-1668 others(20): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049426 | |||||
chr14:31049427
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-71-16699A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049427 | ||||||
chr14:31049427
|
AAATATAT others(2): Show |
A | 6 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 6 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-16697_-71-1668 others(13): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049427 | |||||
chr14:31049428
|
A | AAAAAAAA others(18): Show |
1 | a0001c0001t0003g0145 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(29): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0003g0002 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-71-16697_-71-1669 others(22): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0003g0149 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(26): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0003g0146 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(28): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0098 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(17): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0003g0130 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(19): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0003g0151 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(23): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0003g0150 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(27): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0003g0148 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0003g0245 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(22): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0003g0153 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(24): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AAAAAAAA others(15): Show |
2 | a0001c0001t0003g0152a0001c0001t0044g0131 | 2 | HG00099.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.-71-16697_-71-1669 others(26): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AAAAAATA others(9): Show |
1 | a0001c0001t0001g0144 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(20): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AAATATAT others(8): Show |
1 | a0001c0001t0001g0141 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-71-16697_-71-1669 others(19): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AAT | 6 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0114others(3): Show | 6 | HG00544.hp1 HG00558.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-16665_-71-1666 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0028 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-71-16673_-71-1666 others(14): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AATATATA others(5): Show |
1 | a0001c0001t0018g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-71-16675_-71-1666 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
A | AT | 10 | a0001c0001t0001g0049a0001c0001t0001g0072a0001c0001t0001g0234others(7): Show | 10 | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-71-16698_-71-1669 others(5): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049428 | ||||||
chr14:31049428
|
A | ATAT | 8 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0113others(5): Show | 8 | HG01099.hp1 HG03516.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.-71-16698_-71-1669 others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049428 | ||||||
chr14:31049428
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0154 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-71-16698_-71-1669 others(17): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049428 | ||||||
chr14:31049428
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0025g0186 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-71-16698_-71-1669 others(19): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049428 | ||||||
chr14:31049428
|
A | T | 11 | a0001c0001t0001g0037a0001c0001t0001g0073a0001c0001t0001g0074others(8): Show | 11 | HG01192.hp2 HG02055.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.-71-16698A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049428 | ||||||
chr14:31049428
|
AAT | A | 12 | a0001c0001t0001g0093a0001c0001t0001g0303a0001c0001t0001g0306others(9): Show | 12 | HG00558.hp1 HG02056.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.-71-16665_-71-1666 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
AATAT | A | 40 | a0001c0001t0001g0029a0001c0001t0001g0118a0001c0001t0001g0119others(37): Show | 40 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.-71-16667_-71-1666 others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
AATATAT | A | 32 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0100others(29): Show | 32 | HG00408.hp2 HG00609.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.-71-16669_-71-1666 others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
AATATATA others(3): Show |
A | 5 | a0001c0001t0003g0147a0001c0001t0007g0208a0001c0001t0007g0266others(2): Show | 5 | HG01099.hp2 HG02886.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-16673_-71-1666 others(14): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
AATATATA others(5): Show |
A | 4 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(1): Show | 4 | HG02074.hp2 NA18971.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71-16675_-71-1666 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049428
|
AATATATA others(9): Show |
A | 2 | a0001c0001t0001g0206a0001c0001t0047g0264 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-71-16679_-71-1666 others(20): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049428 | |||||
chr14:31049429
|
AT | A | 7 | a0001c0001t0001g0092a0001c0001t0001g0246a0001c0001t0001g0302others(4): Show | 7 | HG01256.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71-16696delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049429 | ||||||
chr14:31049429
|
ATAT | A | 3 | a0001c0001t0001g0311a0001c0001t0001g0315a0001c0001t0001g0335 | 3 | HG01346.hp2 HG02602.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.-71-16696_-71-1669 others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049429 | ||||||
chr14:31049429
|
ATATATAT others(2): Show |
A | 19 | a0001c0001t0001g0011a0001c0001t0001g0132a0001c0001t0001g0337others(16): Show | 19 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.-71-16696_-71-1668 others(13): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049429 | ||||||
chr14:31049429
|
ATATATAT others(4): Show |
A | 7 | a0001c0001t0001g0003a0001c0001t0008g0003a0001c0001t0012g0199others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-16696_-71-1668 others(15): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049429 | ||||||
chr14:31049429
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-71-16696_-71-1668 others(17): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049429 | ||||||
chr14:31049430
|
T | A | 31 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0046others(28): Show | 31 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-71-16696T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049430 | ||||||
chr14:31049432
|
T | A | 20 | a0001c0001t0001g0055a0001c0001t0001g0093a0001c0001t0001g0246others(17): Show | 20 | HG01109.hp1 HG01257.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.-71-16694T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049432 | ||||||
chr14:31049434
|
T | A | 42 | a0001c0001t0001g0055a0001c0001t0001g0093a0001c0001t0001g0118others(39): Show | 42 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.-71-16692T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049434 | ||||||
chr14:31049436
|
T | A | 6 | a0001c0001t0001g0281a0001c0001t0001g0307a0001c0001t0001g0316others(3): Show | 6 | HG02080.hp1 HG02280.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-16690T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049436 | ||||||
chr14:31049438
|
T | A | 1 | a0001c0001t0004g0261 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-71-16688T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049438 | ||||||
chr14:31049440
|
T | A | 20 | a0001c0001t0001g0011a0001c0001t0001g0132a0001c0001t0003g0147others(17): Show | 20 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.-71-16686T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049440 | ||||||
chr14:31049442
|
T | A | 6 | a0001c0001t0001g0003a0001c0001t0003g0147a0001c0001t0004g0255others(3): Show | 6 | HG00733.hp1 HG01099.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-16684T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049442 | ||||||
chr14:31049442
|
T | C | 7 | a0001c0001t0011g0082a0001c0001t0011g0085a0001c0001t0011g0090others(4): Show | 7 | HG00609.hp1 HG02071.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-16684T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049442 | ||||||
chr14:31049444
|
T | A | 1 | a0001c0001t0003g0147 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-71-16682T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049444 | ||||||
chr14:31049444
|
T | C | 1 | a0001c0001t0011g0088 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-71-16682T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049444 | ||||||
chr14:31049446
|
T | A | 2 | a0001c0001t0001g0206a0001c0001t0003g0147 | 2 | HG01099.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-71-16680T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049446 | ||||||
chr14:31049447
|
A | G | 3 | a0001c0001t0001g0218a0001c0001t0014g0158a0001c0001t0015g0211 | 3 | HG00140.hp1 HG03209.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.-71-16679A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049447 | ||||||
chr14:31049453
|
A | ATG | 8 | a0001c0001t0001g0045a0001c0001t0001g0062a0001c0001t0002g0166others(5): Show | 8 | HG00438.hp1 HG02040.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.-71-16672_-71-1667 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049453 | |||||
chr14:31049453
|
A | G | 140 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(137): Show | 141 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.-71-16673A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049453 | ||||||
chr14:31049455
|
A | G | 13 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0099others(10): Show | 13 | HG02055.hp1 HG02083.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-71-16671A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049455 | ||||||
chr14:31049457
|
A | G | 3 | a0001c0001t0001g0218a0001c0001t0014g0158a0001c0001t0015g0211 | 3 | HG00140.hp1 HG03209.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.-71-16669A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049457 | ||||||
chr14:31049459
|
ATATG | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0218a0001c0001t0002g0189 | 3 | NA18612.hp2 NA18957.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-71-16663_-71-1666 others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049459 | |||||
chr14:31049459
|
ATATGTAT others(7): Show |
A | 1 | a0001c0001t0014g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-71-16664_-71-1665 others(18): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049459 | |||||
chr14:31049460
|
T | C | 1 | a0001c0001t0015g0211 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-71-16666T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049460 | ||||||
chr14:31049461
|
ATGTATAT others(5): Show |
A | 1 | a0001c0001t0015g0211 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-71-16663_-71-1665 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049461 | |||||
chr14:31049463
|
G | A | 24 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0032others(21): Show | 24 | HG02055.hp1 HG02055.hp2 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.-71-16663G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049463 | ||||||
chr14:31049464
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-71-16662T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049464 | ||||||
chr14:31049464
|
T | TAC | 12 | a0001c0001t0001g0040a0001c0001t0001g0054a0001c0001t0001g0060others(9): Show | 12 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.-71-16661_-71-1666 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049464 | |||||
chr14:31049464
|
T | TACAC | 3 | a0001c0001t0001g0063a0001c0001t0008g0022a0001c0001t0017g0077 | 3 | NA18987.hp2 NA18999.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-71-16661_-71-1666 others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049464 | |||||
chr14:31049464
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0005g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-71-16660_-71-1664 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049464 | |||||
chr14:31049465
|
A | G | 10 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0099others(7): Show | 10 | HG02055.hp1 HG02083.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-71-16661A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049465 | ||||||
chr14:31049465
|
ATATATAT others(1): Show |
A | 3 | a0001c0001t0001g0093a0001c0001t0007g0267a0001c0001t0007g0268 | 3 | HG02683.hp1 HG03540.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-71-16658_-71-1665 others(12): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049465 | |||||
chr14:31049466
|
T | C | 145 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(142): Show | 146 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.-71-16660T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049466 | ||||||
chr14:31049467
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-71-16659A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049467 | ||||||
chr14:31049467
|
ATATATG | A | 11 | a0001c0001t0001g0320a0001c0001t0002g0001a0001c0001t0002g0163others(8): Show | 12 | HG01257.hp1 HG01258.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.-71-16656_-71-1665 others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049467 | |||||
chr14:31049468
|
T | C | 144 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(141): Show | 144 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-71-16658T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049468 | ||||||
chr14:31049469
|
A | G | 2 | a0001c0001t0001g0134a0001c0001t0002g0189 | 2 | NA18612.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-71-16657A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049469 | ||||||
chr14:31049469
|
ATATG | A | 17 | a0001c0001t0001g0215a0001c0001t0001g0225a0001c0001t0001g0228others(14): Show | 17 | HG01074.hp2 HG01106.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.-71-16654_-71-1665 others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049469 | |||||
chr14:31049470
|
T | C | 128 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.-71-16656T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049470 | ||||||
chr14:31049471
|
ATG | A | 50 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(47): Show | 50 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.-71-16653_-71-1665 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049471 | |||||
chr14:31049472
|
T | C | 80 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(77): Show | 80 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.-71-16654T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049472 | ||||||
chr14:31049473
|
G | A | 81 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(78): Show | 81 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-71-16653G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049473 | ||||||
chr14:31049474
|
T | C | 163 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(160): Show | 164 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.-71-16652T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049474 | ||||||
chr14:31049474
|
T | TAC | 31 | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0120others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.-71-16618_-71-1661 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | |||||
chr14:31049474
|
T | TACAC | 5 | a0001c0001t0001g0098a0001c0001t0003g0002a0001c0001t0003g0245others(2): Show | 6 | HG00323.hp2 HG00733.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-16620_-71-1661 others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | |||||
chr14:31049474
|
T | TACACACA others(3): Show |
3 | a0001c0001t0001g0292a0001c0001t0006g0327a0001c0001t0006g0328 | 3 | HG02129.hp2 HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-71-16626_-71-1661 others(14): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | |||||
chr14:31049474
|
T | TACACACA others(5): Show |
2 | a0001c0001t0001g0252a0001c0001t0001g0281 | 2 | HG04115.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-71-16628_-71-1661 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | |||||
chr14:31049474
|
T | TACACACA others(7): Show |
10 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(7): Show | 10 | HG01081.hp1 HG01243.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.-71-16630_-71-1661 others(18): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | |||||
chr14:31049474
|
T | TACACACA others(9): Show |
9 | a0001c0001t0001g0118a0001c0001t0001g0302a0001c0001t0001g0303others(6): Show | 9 | HG01109.hp2 HG01175.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.-71-16632_-71-1661 others(20): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | |||||
chr14:31049474
|
T | TACACACA others(11): Show |
17 | a0001c0001t0001g0251a0001c0001t0001g0288a0001c0001t0001g0291others(14): Show | 17 | HG00140.hp2 HG00423.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.-71-16634_-71-1661 others(22): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | |||||
chr14:31049474
|
T | TACACACA others(13): Show |
7 | a0001c0001t0001g0280a0001c0001t0001g0282a0001c0001t0001g0286others(4): Show | 7 | HG00544.hp2 HG02602.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71-16636_-71-1661 others(24): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | |||||
chr14:31049474
|
T | TACACACA others(15): Show |
3 | a0001c0001t0001g0311a0001c0001t0001g0332a0001c0001t0001g0333 | 3 | HG01346.hp2 NA18947.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-71-16638_-71-1661 others(26): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | |||||
chr14:31049474
|
TAC | T | 6 | a0001c0001t0005g0241a0001c0001t0012g0199a0001c0001t0012g0200others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-16618_-71-1661 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | |||||
chr14:31049474
|
TACAC | T | 4 | a0001c0001t0001g0011a0001c0001t0006g0015a0001c0001t0016g0197others(1): Show | 4 | HG02280.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-71-16620_-71-1661 others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | |||||
chr14:31049474
|
TACACAC | T | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-16622_-71-1661 others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31049474 | |||||
chr14:31049476
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0092others(10): Show | 13 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-71-16650C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049476 | ||||||
chr14:31049477
|
A | ATATATG | 6 | a0001c0001t0001g0012a0001c0001t0006g0016a0001c0001t0006g0018others(3): Show | 6 | HG02257.hp1 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-16649_-71-1664 others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049477 | ||||||
chr14:31049477
|
A | G | 1 | a0001c0001t0008g0013 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-71-16649A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049477 | ||||||
chr14:31049478
|
C | T | 12 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0092others(9): Show | 12 | HG02257.hp1 HG02486.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.-71-16648C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049478 | ||||||
chr14:31049480
|
C | T | 5 | a0001c0001t0001g0009a0001c0001t0001g0092a0001c0001t0006g0020others(2): Show | 5 | HG02486.hp2 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71-16646C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049480 | ||||||
chr14:31049481
|
A | ATG | 3 | a0001c0001t0001g0092a0001c0001t0019g0007a0001c0001t0019g0008 | 3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-71-16645_-71-1664 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049481 | ||||||
chr14:31049482
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0019g0007a0001c0001t0019g0008 | 3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-71-16644C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049482 | ||||||
chr14:31049510
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-71-16616T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049510 | ||||||
chr14:31049547
|
G | C | 35 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0100others(32): Show | 35 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-71-16579G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049547 | ||||||
chr14:31049761
|
G | A | 66 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0096others(63): Show | 66 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-71-16365G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049761 | ||||||
chr14:31049821
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-71-16305C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049821 | ||||||
chr14:31049866
|
T | C | 285 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(282): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.-71-16260T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31049866 | ||||||
chr14:31050141
|
C | T | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-71-15985C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050141 | ||||||
chr14:31050152
|
C | T | 50 | a0001c0001t0001g0118a0001c0001t0001g0251a0001c0001t0001g0252others(47): Show | 50 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-71-15974C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050152 | ||||||
chr14:31050213
|
C | T | 15 | a0001c0001t0001g0003a0001c0001t0004g0042a0001c0001t0004g0043others(12): Show | 15 | HG00280.hp1 HG01081.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.-71-15913C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050213 | ||||||
chr14:31050222
|
T | C | 1 | a0001c0001t0001g0287 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-71-15904T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050222 | ||||||
chr14:31050350
|
G | A | 7 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(4): Show | 7 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-15776G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050350 | ||||||
chr14:31050382
|
G | A | 1 | a0001c0001t0047g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-71-15744G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050382 | ||||||
chr14:31050450
|
A | T | 1 | a0001c0001t0002g0180 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-71-15676A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050450 | ||||||
chr14:31050525
|
G | C | 1 | a0001c0001t0041g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-71-15601G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050525 | ||||||
chr14:31050562
|
A | G | 1 | a0001c0001t0017g0077 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-71-15564A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050562 | ||||||
chr14:31050573
|
T | C | 1 | a0001c0001t0005g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-71-15553T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050573 | ||||||
chr14:31050802
|
C | T | 6 | a0001c0001t0006g0021a0001c0001t0010g0271a0001c0001t0010g0272others(3): Show | 6 | HG02074.hp2 HG02965.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-15324C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050802 | ||||||
chr14:31050806
|
C | T | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-15320C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050806 | ||||||
chr14:31050813
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-15313C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050813 | ||||||
chr14:31050823
|
A | G | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-71-15303A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050823 | ||||||
chr14:31050932
|
T | A | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-71-15194T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31050932 | ||||||
chr14:31051255
|
C | CA | 12 | a0001c0001t0001g0054a0001c0001t0001g0060a0001c0001t0001g0073others(9): Show | 12 | HG01346.hp1 HG01981.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-71-14855dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31051255 | |||||
chr14:31051274
|
C | A | 1 | a0001c0001t0001g0220 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-71-14852C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051274 | ||||||
chr14:31051313
|
A | G | 2 | a0001c0001t0005g0242a0001c0001t0029g0243 | 2 | HG00639.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-71-14813A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051313 | ||||||
chr14:31051370
|
G | A | 17 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0003g0002others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-14756G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051370 | ||||||
chr14:31051476
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-14650G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051476 | ||||||
chr14:31051477
|
C | G | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-14649C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051477 | ||||||
chr14:31051516
|
C | CA | 5 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0014g0158others(2): Show | 5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71-14603dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31051516 | |||||
chr14:31051605
|
C | T | 234 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.-71-14521C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051605 | ||||||
chr14:31051747
|
C | T | 2 | a0001c0001t0001g0316a0001c0001t0001g0322 | 2 | HG00544.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-71-14379C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051747 | ||||||
chr14:31051754
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-71-14372G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051754 | ||||||
chr14:31051945
|
G | A | 4 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(1): Show | 4 | HG02572.hp1 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71-14181G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051945 | ||||||
chr14:31051962
|
A | T | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-14164A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051962 | ||||||
chr14:31051963
|
T | A | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-14163T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051963 | ||||||
chr14:31051964
|
A | T | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-14162A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051964 | ||||||
chr14:31051992
|
C | T | 2 | a0001c0001t0016g0197a0001c0001t0016g0198 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-71-14134C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051992 | ||||||
chr14:31051993
|
G | A | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0029g0243 | 3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-71-14133G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31051993 | ||||||
chr14:31052039
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG01243.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-71-14087C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052039 | ||||||
chr14:31052257
|
G | C | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-71-13869G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052257 | ||||||
chr14:31052426
|
T | A | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-13700T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052426 | ||||||
chr14:31052544
|
G | A | 31 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(28): Show | 32 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-71-13582G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052544 | ||||||
chr14:31052670
|
C | T | 1 | a0001c0001t0001g0302 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-71-13456C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052670 | ||||||
chr14:31052728
|
C | CA | 21 | a0001c0001t0001g0033a0001c0001t0001g0072a0001c0001t0001g0074others(18): Show | 21 | HG00741.hp2 HG01175.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.-71-13379dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31052728 | |||||
chr14:31052728
|
CA | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0280others(9): Show | 12 | HG01496.hp1 HG02056.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-71-13379delA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31052728 | |||||
chr14:31052730
|
A | G | 1 | a0001c0001t0005g0241 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-71-13396A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052730 | ||||||
chr14:31052760
|
C | A | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-13366C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052760 | ||||||
chr14:31052801
|
C | A | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-13325C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052801 | ||||||
chr14:31052862
|
C | T | 6 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(3): Show | 6 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-13264C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31052862 | ||||||
chr14:31052934
|
A | AT | 139 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(136): Show | 140 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.-71-13169dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31052934 | |||||
chr14:31052934
|
A | ATT | 13 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0039others(10): Show | 13 | HG00280.hp2 HG00741.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.-71-13170_-71-1316 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31052934 | |||||
chr14:31053024
|
T | C | 51 | a0001c0001t0001g0118a0001c0001t0001g0251a0001c0001t0001g0252others(48): Show | 51 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.-71-13102T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053024 | ||||||
chr14:31053067
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-71-13059A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053067 | ||||||
chr14:31053069
|
T | A | 6 | a0001c0001t0012g0199a0001c0001t0012g0200a0001c0001t0012g0201others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-13057T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053069 | ||||||
chr14:31053078
|
T | A | 5 | a0001c0001t0007g0208a0001c0001t0007g0266a0001c0001t0007g0267others(2): Show | 5 | HG02683.hp1 HG03704.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-13048T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053078 | ||||||
chr14:31053258
|
A | G | 1 | a0001c0001t0002g0277 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-71-12868A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053258 | ||||||
chr14:31053268
|
T | G | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG01243.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-71-12858T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053268 | ||||||
chr14:31053420
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-71-12706C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053420 | ||||||
chr14:31053473
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-71-12653G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053473 | ||||||
chr14:31053502
|
G | C | 3 | a0001c0001t0001g0092a0001c0001t0019g0007a0001c0001t0019g0008 | 3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-71-12624G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053502 | ||||||
chr14:31053543
|
T | C | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-12583T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053543 | ||||||
chr14:31053589
|
C | CT | 25 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0106others(22): Show | 25 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.-71-12508dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31053589 | |||||
chr14:31053589
|
CT | C | 168 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(165): Show | 170 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.-71-12508delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31053589 | |||||
chr14:31053589
|
CTT | C | 25 | a0001c0001t0001g0047a0001c0001t0001g0056a0001c0001t0001g0093others(22): Show | 25 | HG00609.hp2 HG01891.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-71-12509_-71-1250 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31053589 | |||||
chr14:31053589
|
CTTT | C | 22 | a0001c0001t0001g0096a0001c0001t0001g0100a0001c0001t0001g0207others(19): Show | 22 | HG00140.hp1 HG00408.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-71-12510_-71-1250 others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31053589 | |||||
chr14:31053589
|
CTTTTT | C | 7 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG00099.hp2 HG00642.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-12512_-71-1250 others(9): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31053589 | |||||
chr14:31053589
|
CTTTTTTT | C | 17 | a0001c0001t0001g0003a0001c0001t0001g0337a0001c0001t0001g0340others(14): Show | 17 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.-71-12514_-71-1250 others(11): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31053589 | |||||
chr14:31053589
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0035g0034 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-71-12518_-71-1250 others(15): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31053589 | |||||
chr14:31053950
|
A | G | 2 | a0001c0001t0045g0086a0001c0001t0046g0087 | 2 | HG02155.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-71-12176A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31053950 | ||||||
chr14:31054377
|
A | T | 17 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0003g0002others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-11749A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054377 | ||||||
chr14:31054378
|
T | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0050 | 2 | HG00621.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-71-11748T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054378 | ||||||
chr14:31054573
|
T | G | 1 | a0001c0001t0001g0246 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-71-11553T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054573 | ||||||
chr14:31054738
|
C | T | 234 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.-71-11388C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054738 | ||||||
chr14:31054859
|
C | T | 1 | a0001c0001t0048g0129 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-71-11267C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054859 | ||||||
chr14:31054867
|
C | CA | 33 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(30): Show | 33 | HG00642.hp2 HG01106.hp2 HG02080.hp2 others(30): Show |
intron_variant | MODIFIER | c.-71-11230dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | |||||
chr14:31054867
|
C | CAA | 37 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0280others(34): Show | 37 | HG00140.hp2 HG00423.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.-71-11231_-71-1123 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | |||||
chr14:31054867
|
C | CAAA | 16 | a0001c0001t0001g0118a0001c0001t0001g0281a0001c0001t0001g0284others(13): Show | 16 | HG00544.hp2 HG00673.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-71-11232_-71-1123 others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | |||||
chr14:31054867
|
CA | C | 51 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(48): Show | 52 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-71-11230delA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | |||||
chr14:31054867
|
CAA | C | 102 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0036others(99): Show | 103 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.-71-11231_-71-1123 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | |||||
chr14:31054867
|
CAAA | C | 24 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0132others(21): Show | 24 | HG00733.hp1 HG01069.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-71-11232_-71-1123 others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | |||||
chr14:31054867
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0011g0090 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-71-11241_-71-1123 others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | |||||
chr14:31054867
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0125 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-71-11243_-71-1123 others(18): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | |||||
chr14:31054867
|
CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0001g0023a0001c0001t0001g0055 | 2 | HG01496.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-71-11248_-71-1123 others(23): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31054867 | |||||
chr14:31054870
|
A | T | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-71-11256A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054870 | ||||||
chr14:31054904
|
A | G | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-71-11222A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054904 | ||||||
chr14:31054930
|
G | A | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-71-11196G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31054930 | ||||||
chr14:31055131
|
A | G | 2 | a0001c0001t0001g0311a0001c0001t0001g0315 | 2 | HG01346.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-71-10995A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31055131 | ||||||
chr14:31055229
|
T | G | 51 | a0001c0001t0001g0118a0001c0001t0001g0251a0001c0001t0001g0252others(48): Show | 51 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.-71-10897T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31055229 | ||||||
chr14:31055293
|
C | G | 31 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(28): Show | 32 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-71-10833C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31055293 | ||||||
chr14:31055554
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-71-10572A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31055554 | ||||||
chr14:31055728
|
T | TTG | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.-71-10390_-71-1038 others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31055728 | |||||
chr14:31055856
|
T | G | 1 | a0001c0001t0031g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-71-10270T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31055856 | ||||||
chr14:31055957
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-71-10169C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31055957 | ||||||
chr14:31055989
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-71-10137G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31055989 | ||||||
chr14:31056209
|
G | T | 285 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(282): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.-71-9917G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056209 | ||||||
chr14:31056446
|
C | T | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-9680C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056446 | ||||||
chr14:31056458
|
G | A | 288 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(285): Show | 290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.-71-9668G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056458 | ||||||
chr14:31056548
|
G | A | 2 | a0001c0001t0006g0327a0001c0001t0006g0328 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-71-9578G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056548 | ||||||
chr14:31056601
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0050 | 2 | HG00621.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-71-9525C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056601 | ||||||
chr14:31056660
|
A | G | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-71-9466A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056660 | ||||||
chr14:31056881
|
A | G | 1 | a0001c0001t0044g0131 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-71-9245A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056881 | ||||||
chr14:31056982
|
G | A | 2 | a0001c0001t0004g0094a0001c0001t0004g0095 | 2 | HG01928.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-71-9144G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31056982 | ||||||
chr14:31057044
|
A | G | 229 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(226): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.-71-9082A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057044 | ||||||
chr14:31057189
|
G | A | 234 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.-71-8937G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057189 | ||||||
chr14:31057234
|
A | C | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-71-8892A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057234 | ||||||
chr14:31057540
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-71-8586G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057540 | ||||||
chr14:31057556
|
A | G | 3 | a0001c0001t0001g0092a0001c0001t0019g0007a0001c0001t0019g0008 | 3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-71-8570A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057556 | ||||||
chr14:31057598
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-71-8528T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057598 | ||||||
chr14:31057637
|
T | C | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-71-8489T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057637 | ||||||
chr14:31057648
|
C | T | 118 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(115): Show | 119 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.-71-8478C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057648 | ||||||
chr14:31057740
|
C | T | 21 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0337others(18): Show | 21 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.-71-8386C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057740 | ||||||
chr14:31057782
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-71-8344C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057782 | ||||||
chr14:31057932
|
G | T | 2 | a0001c0001t0001g0059a0001c0001t0008g0061 | 2 | HG01256.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-71-8194G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057932 | ||||||
chr14:31057935
|
T | G | 1 | a0001c0001t0004g0095 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-71-8191T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057935 | ||||||
chr14:31057958
|
C | T | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-8168C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31057958 | ||||||
chr14:31058086
|
GT | G | 230 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(227): Show | 232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-71-8034delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058086 | |||||
chr14:31058173
|
G | A | 4 | a0001c0001t0003g0247a0001c0001t0003g0258a0001c0001t0003g0259others(1): Show | 4 | HG00738.hp1 HG01069.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-71-7953G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058173 | ||||||
chr14:31058285
|
A | C | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-71-7841A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058285 | ||||||
chr14:31058363
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-7763C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058363 | ||||||
chr14:31058517
|
C | CTG | 6 | a0001c0001t0001g0100a0001c0001t0001g0221a0001c0001t0001g0225others(3): Show | 6 | HG01243.hp1 NA18944.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-7601_-71-7600d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | |||||
chr14:31058517
|
C | CTGTG | 6 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0004g0042others(3): Show | 6 | HG00140.hp1 HG00280.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71-7603_-71-7600d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | |||||
chr14:31058517
|
C | CTGTGTGT others(3): Show |
2 | a0001c0001t0001g0340a0001c0001t0004g0043 | 2 | HG04204.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-71-7600_-71-7599i others(12): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | |||||
chr14:31058517
|
C | CTGTGTGT others(9): Show |
1 | a0001c0001t0004g0253 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-71-7600_-71-7599i others(18): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | |||||
chr14:31058517
|
CTGTGTGT others(3): Show |
C | 2 | a0001c0001t0007g0157a0001c0001t0007g0161 | 2 | HG01106.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-71-7599_-71-7590d others(12): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | |||||
chr14:31058517
|
CTGTGTGT others(5): Show |
C | 2 | a0001c0001t0006g0327a0001c0001t0006g0328 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-71-7599_-71-7588d others(14): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | |||||
chr14:31058517
|
CTGTGTGT others(7): Show |
C | 1 | a0001c0001t0001g0011 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-71-7599_-71-7586d others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | |||||
chr14:31058517
|
CTGTGTGT others(11): Show |
C | 14 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0003g0145others(11): Show | 14 | HG00741.hp1 HG01074.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.-71-7599_-71-7582d others(20): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | |||||
chr14:31058517
|
CTGTGTGT others(13): Show |
C | 14 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0003g0002others(11): Show | 15 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.-71-7599_-71-7580d others(22): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058517 | |||||
chr14:31058519
|
GTGTGTGT others(1): Show |
G | 6 | a0001c0001t0001g0005a0001c0001t0007g0268a0001c0001t0014g0158others(3): Show | 6 | HG02145.hp2 HG02572.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-7599_-71-7592d others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058519 | |||||
chr14:31058523
|
GTGTA | G | 8 | a0001c0001t0001g0003a0001c0001t0001g0215a0001c0001t0001g0219others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.-71-7599_-71-7596d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058523 | |||||
chr14:31058525
|
GTA | G | 10 | a0001c0001t0001g0210a0001c0001t0001g0214a0001c0001t0001g0217others(7): Show | 10 | HG00621.hp1 HG01081.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-71-7599_-71-7598d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058525 | |||||
chr14:31058527
|
A | ATG | 12 | a0001c0001t0001g0029a0001c0001t0001g0110a0001c0001t0001g0113others(9): Show | 12 | HG01891.hp2 HG02056.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-71-7551_-71-7550d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | |||||
chr14:31058527
|
A | ATGTG | 5 | a0001c0001t0001g0136a0001c0001t0001g0139a0001c0001t0001g0155others(2): Show | 5 | HG00642.hp2 HG01123.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71-7553_-71-7550d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | |||||
chr14:31058527
|
A | ATGTGTG | 4 | a0001c0001t0001g0140a0001c0001t0003g0024a0001c0001t0019g0007others(1): Show | 4 | HG00099.hp2 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-71-7555_-71-7550d others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | |||||
chr14:31058527
|
A | ATGTGTGT others(1): Show |
7 | a0001c0001t0001g0142a0001c0001t0001g0206a0001c0001t0003g0247others(4): Show | 7 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-7557_-71-7550d others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | |||||
chr14:31058527
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0001g0092 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-71-7561_-71-7550d others(14): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | |||||
chr14:31058527
|
A | G | 31 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0100others(28): Show | 31 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(28): Show |
intron_variant | MODIFIER | c.-71-7599A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058527 | ||||||
chr14:31058527
|
ATG | A | 11 | a0001c0001t0001g0103a0001c0001t0001g0124a0001c0001t0001g0125others(8): Show | 11 | HG00544.hp1 HG02083.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.-71-7551_-71-7550d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | |||||
chr14:31058527
|
ATGTGTG | A | 9 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0289others(6): Show | 9 | HG00544.hp2 HG01243.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.-71-7555_-71-7550d others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | |||||
chr14:31058527
|
ATGTGTGT others(1): Show |
A | 46 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0251others(43): Show | 46 | HG00140.hp2 HG00423.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.-71-7557_-71-7550d others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | |||||
chr14:31058527
|
ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0001g0119 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-71-7565_-71-7550d others(18): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | |||||
chr14:31058527
|
ATGTGTGT others(13): Show |
A | 1 | a0001c0001t0001g0320 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-71-7569_-71-7550d others(22): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | |||||
chr14:31058527
|
ATGTGTGT others(17): Show |
A | 127 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(124): Show | 128 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.-71-7573_-71-7550d others(26): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | |||||
chr14:31058527
|
ATGTGTGT others(21): Show |
A | 1 | a0001c0001t0009g0262 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-71-7577_-71-7550d others(30): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058527 | |||||
chr14:31058531
|
G | C | 2 | a0001c0001t0006g0327a0001c0001t0006g0328 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-71-7595G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058531 | ||||||
chr14:31058533
|
G | C | 1 | a0001c0001t0001g0011 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-71-7593G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058533 | ||||||
chr14:31058537
|
G | C | 14 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0003g0145others(11): Show | 14 | HG00741.hp1 HG01074.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.-71-7589G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058537 | ||||||
chr14:31058539
|
G | C | 17 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0003g0002others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-7587G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058539 | ||||||
chr14:31058541
|
G | C | 14 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0003g0002others(11): Show | 15 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.-71-7585G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058541 | ||||||
chr14:31058584
|
T | C | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-71-7542T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058584 | ||||||
chr14:31058718
|
C | G | 1 | a0001c0001t0043g0204 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-71-7408C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058718 | ||||||
chr14:31058720
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-71-7406G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058720 | ||||||
chr14:31058731
|
C | CT | 6 | a0001c0001t0001g0097a0001c0001t0001g0289a0001c0001t0002g0173others(3): Show | 6 | HG02080.hp2 HG02280.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-7382dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31058731 | |||||
chr14:31058752
|
TTTTAGTA others(3): Show |
T | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-7373_-71-7364d others(12): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058752 | ||||||
chr14:31058756
|
A | G | 4 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(1): Show | 4 | HG00639.hp1 HG01106.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71-7370A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058756 | ||||||
chr14:31058912
|
G | A | 22 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0100others(19): Show | 22 | HG00408.hp2 HG00609.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-71-7214G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31058912 | ||||||
chr14:31059121
|
T | C | 2 | a0001c0001t0036g0091a0001c0001t0037g0041 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-71-7005T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31059121 | ||||||
chr14:31059613
|
G | A | 6 | a0001c0001t0012g0199a0001c0001t0012g0200a0001c0001t0012g0201others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71-6513G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31059613 | ||||||
chr14:31059758
|
A | G | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-6368A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31059758 | ||||||
chr14:31059866
|
G | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0337others(26): Show | 29 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-71-6260G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31059866 | ||||||
chr14:31059930
|
A | AAT | 7 | a0001c0001t0001g0005a0001c0001t0002g0184a0001c0001t0010g0271others(4): Show | 7 | HG02074.hp2 HG03041.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71-6181_-71-6180d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31059930 | |||||
chr14:31059930
|
A | T | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0029g0243 | 3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-71-6196A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31059930 | ||||||
chr14:31059932
|
T | A | 23 | a0001c0001t0001g0057a0001c0001t0001g0093a0001c0001t0001g0098others(20): Show | 24 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.-71-6194T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31059932 | ||||||
chr14:31059943
|
A | T | 4 | a0001c0001t0001g0132a0001c0001t0001g0206a0001c0001t0015g0263others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71-6183A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31059943 | ||||||
chr14:31059963
|
ATATATGT others(25): Show |
A | 98 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(95): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.-71-6127_-71-6096d others(34): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31059963 | |||||
chr14:31059995
|
TTATATGT others(11): Show |
T | 2 | a0001c0001t0001g0206a0001c0001t0047g0264 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-71-6127_-71-6110d others(20): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31059995 | |||||
chr14:31060032
|
T | A | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG01243.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-71-6094T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060032 | ||||||
chr14:31060058
|
T | C | 3 | a0001c0001t0001g0280a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | NA18953.hp2 NA18987.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-71-6068T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060058 | ||||||
chr14:31060210
|
A | G | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-71-5916A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060210 | ||||||
chr14:31060275
|
T | C | 100 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(97): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.-71-5851T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060275 | ||||||
chr14:31060347
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-71-5779G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060347 | ||||||
chr14:31060354
|
A | C | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-5772A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060354 | ||||||
chr14:31060456
|
A | G | 2 | a0001c0001t0006g0327a0001c0001t0006g0328 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-71-5670A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060456 | ||||||
chr14:31060703
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-71-5423A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060703 | ||||||
chr14:31060724
|
T | G | 1 | a0001c0001t0001g0291 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-71-5402T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060724 | ||||||
chr14:31060829
|
A | G | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-71-5297A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060829 | ||||||
chr14:31060958
|
C | T | 7 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(4): Show | 7 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71-5168C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060958 | ||||||
chr14:31060961
|
T | C | 285 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(282): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.-71-5165T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060961 | ||||||
chr14:31060976
|
G | A | 1 | a0001c0001t0005g0083 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-71-5150G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31060976 | ||||||
chr14:31061065
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-71-5061T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061065 | ||||||
chr14:31061287
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-71-4839G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061287 | ||||||
chr14:31061446
|
G | C | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-4680G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061446 | ||||||
chr14:31061493
|
T | A | 117 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(114): Show | 118 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-71-4633T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061493 | ||||||
chr14:31061499
|
C | T | 94 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(91): Show | 95 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.-71-4627C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061499 | ||||||
chr14:31061647
|
A | AT | 30 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0337others(27): Show | 30 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-71-4465dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31061647 | |||||
chr14:31061852
|
G | A | 129 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(126): Show | 130 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-71-4274G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061852 | ||||||
chr14:31061881
|
C | G | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-4245C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061881 | ||||||
chr14:31061914
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0039g0133 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-71-4212G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061914 | ||||||
chr14:31061941
|
G | A | 229 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(226): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.-71-4185G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31061941 | ||||||
chr14:31061987
|
CCACATTT others(9): Show |
C | 1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-4136_-71-4121d others(18): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31061987 | |||||
chr14:31062127
|
T | C | 21 | a0001c0001t0001g0003a0001c0001t0001g0337a0001c0001t0001g0340others(18): Show | 21 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-71-3999T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062127 | ||||||
chr14:31062271
|
G | T | 69 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.-71-3855G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062271 | ||||||
chr14:31062274
|
T | C | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-3852T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062274 | ||||||
chr14:31062315
|
T | C | 17 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0003g0002others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-3811T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062315 | ||||||
chr14:31062355
|
T | G | 1 | a0001c0001t0019g0007 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-71-3771T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062355 | ||||||
chr14:31062649
|
T | C | 129 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(126): Show | 130 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-71-3477T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062649 | ||||||
chr14:31062727
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-71-3399G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062727 | ||||||
chr14:31062745
|
A | G | 1 | a0001c0001t0017g0077 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-71-3381A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062745 | ||||||
chr14:31062872
|
T | C | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-3254T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062872 | ||||||
chr14:31062926
|
C | T | 35 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0100others(32): Show | 35 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-71-3200C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062926 | ||||||
chr14:31062927
|
A | G | 70 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(67): Show | 71 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.-71-3199A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062927 | ||||||
chr14:31062963
|
C | T | 117 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(114): Show | 118 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-71-3163C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062963 | ||||||
chr14:31062969
|
C | CA | 9 | a0001c0001t0001g0004a0001c0001t0001g0039a0001c0001t0001g0103others(6): Show | 9 | HG01175.hp1 HG01433.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.-71-3143dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31062969 | |||||
chr14:31062977
|
A | C | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-3149A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062977 | ||||||
chr14:31062997
|
A | C | 17 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0003g0002others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-71-3129A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31062997 | ||||||
chr14:31063006
|
G | C | 1 | a0001c0001t0001g0035 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-71-3120G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063006 | ||||||
chr14:31063228
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-71-2898C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063228 | ||||||
chr14:31063246
|
C | G | 50 | a0001c0001t0001g0118a0001c0001t0001g0251a0001c0001t0001g0252others(47): Show | 50 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-71-2880C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063246 | ||||||
chr14:31063259
|
A | G | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-2867A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063259 | ||||||
chr14:31063458
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-71-2668A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063458 | ||||||
chr14:31063580
|
A | T | 3 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0142 | 3 | HG00099.hp2 HG00642.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-71-2546A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063580 | ||||||
chr14:31063901
|
T | C | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-2225T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063901 | ||||||
chr14:31063964
|
C | T | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-2162C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31063964 | ||||||
chr14:31064070
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-71-2056A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31064070 | ||||||
chr14:31064275
|
G | A | 4 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(1): Show | 4 | HG02559.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71-1851G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31064275 | ||||||
chr14:31064407
|
C | T | 1 | a0001c0001t0005g0279 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-71-1719C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31064407 | ||||||
chr14:31064477
|
A | G | 1 | a0001c0001t0035g0034 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-71-1649A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31064477 | ||||||
chr14:31064506
|
G | C | 1 | a0001c0001t0002g0189 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-71-1620G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31064506 | ||||||
chr14:31065265
|
T | C | 285 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(282): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.-71-861T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065265 | ||||||
chr14:31065418
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-71-708A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065418 | ||||||
chr14:31065434
|
G | A | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71-692G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065434 | ||||||
chr14:31065472
|
TCAGAAGA others(3): Show |
T | 69 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.-71-653_-71-644del others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065472 | ||||||
chr14:31065500
|
A | C | 229 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(226): Show | 231 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.-71-626A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065500 | ||||||
chr14:31065531
|
G | A | 3 | a0001c0001t0001g0092a0001c0001t0019g0007a0001c0001t0019g0008 | 3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-71-595G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065531 | ||||||
chr14:31065546
|
A | AATGAATG others(3): Show |
1 | a0001c0001t0001g0280 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-71-578_-71-569dup others(10): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 31065546 | |||||
chr14:31065574
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-71-552A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065574 | ||||||
chr14:31065716
|
A | G | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0029g0243 | 3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-71-410A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065716 | ||||||
chr14:31065776
|
T | G | 3 | a0001c0001t0004g0042a0001c0001t0004g0043a0001c0001t0004g0044 | 3 | HG00280.hp1 HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-71-350T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065776 | ||||||
chr14:31065851
|
A | G | 230 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(227): Show | 232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-71-275A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065851 | ||||||
chr14:31065911
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0008g0003a0001c0001t0008g0244 | 3 | HG01081.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-71-215C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065911 | ||||||
chr14:31065956
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-71-170G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 1/5 | chr14 | 31065956 | ||||||
chr14:31066397
|
G | C | 315 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(312): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.138+63G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31066397 | ||||||
chr14:31066550
|
C | G | 288 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(285): Show | 290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.138+216C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31066550 | ||||||
chr14:31066750
|
C | A | 1 | a0001c0001t0005g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.138+416C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31066750 | ||||||
chr14:31066790
|
G | A | 51 | a0001c0001t0001g0118a0001c0001t0001g0251a0001c0001t0001g0252others(48): Show | 51 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.138+456G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31066790 | ||||||
chr14:31066969
|
G | T | 315 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(312): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.138+635G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31066969 | ||||||
chr14:31067112
|
G | A | 1 | a0001c0001t0007g0267 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.138+778G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31067112 | ||||||
chr14:31067208
|
C | CA | 50 | a0001c0001t0001g0110a0001c0001t0001g0118a0001c0001t0001g0251others(47): Show | 50 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.138+888dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 31067208 | |||||
chr14:31067208
|
CA | C | 222 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(219): Show | 224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.138+888delA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 31067208 | |||||
chr14:31067209
|
A | T | 1 | a0001c0001t0002g0187 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.138+875A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31067209 | ||||||
chr14:31067251
|
C | T | 1 | a0001c0001t0005g0305 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.138+917C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31067251 | ||||||
chr14:31067256
|
T | A | 1 | a0001c0001t0008g0013 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.138+922T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31067256 | ||||||
chr14:31067424
|
C | T | 12 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+1090C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31067424 | ||||||
chr14:31067516
|
A | AT | 54 | a0001c0001t0001g0072a0001c0001t0001g0118a0001c0001t0001g0251others(51): Show | 54 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.138+1198dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 31067516 | |||||
chr14:31067516
|
AT | A | 6 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0002g0176others(3): Show | 6 | HG01891.hp2 HG02074.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+1198delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 31067516 | |||||
chr14:31067739
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0047g0264 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.138+1405G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31067739 | ||||||
chr14:31067814
|
A | G | 3 | a0001c0001t0005g0241a0001c0001t0005g0242a0001c0001t0029g0243 | 3 | HG00639.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.138+1480A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31067814 | ||||||
chr14:31067876
|
A | AT | 38 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0100others(35): Show | 38 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.138+1554dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 31067876 | |||||
chr14:31068029
|
C | T | 1 | a0001c0001t0002g0187 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.138+1695C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068029 | ||||||
chr14:31068078
|
G | A | 1 | a0001c0001t0004g0255 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.138+1744G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068078 | ||||||
chr14:31068132
|
T | A | 233 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(230): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.139-1711T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068132 | ||||||
chr14:31068163
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.139-1680C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068163 | ||||||
chr14:31068210
|
C | T | 1 | a0001c0001t0030g0068 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.139-1633C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068210 | ||||||
chr14:31068379
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.139-1464T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068379 | ||||||
chr14:31068693
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.139-1150C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068693 | ||||||
chr14:31068738
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0074a0001c0001t0001g0075others(1): Show | 4 | HG02055.hp1 HG02622.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-1105T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068738 | ||||||
chr14:31068777
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.139-1066G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31068777 | ||||||
chr14:31069161
|
C | T | 5 | a0001c0001t0007g0208a0001c0001t0007g0266a0001c0001t0007g0267others(2): Show | 5 | HG02683.hp1 HG03704.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-682C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069161 | ||||||
chr14:31069180
|
G | A | 15 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(12): Show | 15 | HG00544.hp2 HG00673.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.139-663G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069180 | ||||||
chr14:31069258
|
A | T | 1 | a0001c0001t0031g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.139-585A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069258 | ||||||
chr14:31069360
|
G | A | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.139-483G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069360 | ||||||
chr14:31069422
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.139-421T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069422 | ||||||
chr14:31069443
|
A | C | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.139-400A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069443 | ||||||
chr14:31069568
|
C | G | 6 | a0001c0001t0012g0199a0001c0001t0012g0200a0001c0001t0012g0201others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-275C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069568 | ||||||
chr14:31069694
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.139-149G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069694 | ||||||
chr14:31069733
|
A | G | 129 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(126): Show | 130 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.139-110A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069733 | ||||||
chr14:31069753
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0019g0007a0001c0001t0019g0008 | 3 | HG02486.hp2 HG02647.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.139-90C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069753 | ||||||
chr14:31069778
|
C | G | 231 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 233 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.139-65C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 2/5 | chr14 | 31069778 | ||||||
chr14:31070296
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.225+367A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31070296 | ||||||
chr14:31070569
|
G | C | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.225+640G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31070569 | ||||||
chr14:31070631
|
G | C | 6 | a0001c0001t0012g0199a0001c0001t0012g0200a0001c0001t0012g0201others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.225+702G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31070631 | ||||||
chr14:31070778
|
C | T | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+849C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31070778 | ||||||
chr14:31071404
|
C | A | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.225+1475C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071404 | ||||||
chr14:31071545
|
T | G | 129 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(126): Show | 130 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.226-1360T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071545 | ||||||
chr14:31071554
|
A | G | 287 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(284): Show | 289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.226-1351A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071554 | ||||||
chr14:31071578
|
G | A | 1 | a0001c0001t0015g0211 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.226-1327G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071578 | ||||||
chr14:31071626
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.226-1279G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071626 | ||||||
chr14:31071683
|
G | T | 1 | a0001c0001t0002g0191 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.226-1222G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071683 | ||||||
chr14:31071695
|
G | A | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-1210G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071695 | ||||||
chr14:31071887
|
AC | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG02040.hp1 HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.226-1017delC | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071887 | ||||||
chr14:31071922
|
A | AT | 252 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(249): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.226-975dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr14 | 31071922 | |||||
chr14:31071930
|
T | G | 17 | a0001c0001t0001g0098a0001c0001t0001g0144a0001c0001t0003g0002others(14): Show | 18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.226-975T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071930 | ||||||
chr14:31071931
|
G | T | 187 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0023others(184): Show | 187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.226-974G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31071931 | ||||||
chr14:31072061
|
C | T | 2 | a0001c0001t0027g0164a0001c0001t0028g0193 | 2 | HG02280.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.226-844C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072061 | ||||||
chr14:31072088
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0080a0001c0001t0005g0081 | 3 | NA18983.hp2 NA19000.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.226-817G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072088 | ||||||
chr14:31072146
|
G | T | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-759G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072146 | ||||||
chr14:31072274
|
T | C | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | HG01346.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.226-631T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072274 | ||||||
chr14:31072288
|
C | T | 236 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(233): Show | 238 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.226-617C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072288 | ||||||
chr14:31072344
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.226-561G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072344 | ||||||
chr14:31072417
|
C | T | 127 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0031others(124): Show | 128 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.226-488C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072417 | ||||||
chr14:31072473
|
C | T | 5 | a0001c0001t0007g0208a0001c0001t0007g0266a0001c0001t0007g0267others(2): Show | 5 | HG02683.hp1 HG03704.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.226-432C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072473 | ||||||
chr14:31072543
|
A | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG02622.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.226-362A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072543 | ||||||
chr14:31072560
|
A | C | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.226-345A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072560 | ||||||
chr14:31072670
|
C | CA | 12 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.226-227dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr14 | 31072670 | |||||
chr14:31072678
|
A | T | 1 | a0001c0001t0002g0187 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.226-227A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072678 | ||||||
chr14:31072707
|
C | A | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.226-198C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072707 | ||||||
chr14:31072732
|
CAAGT | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0132a0001c0001t0001g0337others(26): Show | 29 | HG00280.hp1 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.226-172_226-169del others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072732 | ||||||
chr14:31072811
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.226-94G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 3/5 | chr14 | 31072811 | ||||||
chr14:31073046
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.294+73T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073046 | ||||||
chr14:31073167
|
G | T | 5 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(2): Show | 5 | HG02074.hp2 NA18971.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.294+194G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073167 | ||||||
chr14:31073185
|
G | GA | 68 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0037others(65): Show | 68 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.294+227dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31073185 | |||||
chr14:31073185
|
G | GAA | 9 | a0001c0001t0001g0118a0001c0001t0001g0283a0001c0001t0001g0284others(6): Show | 9 | HG00423.hp2 HG01109.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.294+226_294+227dup others(2): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31073185 | |||||
chr14:31073195
|
A | AC | 8 | a0001c0001t0001g0056a0001c0001t0005g0226a0001c0001t0010g0271others(5): Show | 8 | HG02074.hp2 HG03490.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.294+222_294+223ins others(1): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073195 | ||||||
chr14:31073212
|
A | C | 15 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0057others(12): Show | 15 | HG00642.hp1 HG00738.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.294+239A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073212 | ||||||
chr14:31073218
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.294+245C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073218 | ||||||
chr14:31073220
|
A | G | 21 | a0001c0001t0001g0132a0001c0001t0005g0084a0001c0001t0005g0241others(18): Show | 21 | HG00639.hp2 HG01106.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.294+247A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073220 | ||||||
chr14:31073226
|
C | T | 2 | a0001c0001t0007g0208a0001c0001t0007g0266 | 2 | HG03704.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.294+253C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073226 | ||||||
chr14:31073256
|
T | C | 77 | a0001c0001t0001g0045a0001c0001t0001g0118a0001c0001t0001g0126others(74): Show | 78 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.294+283T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073256 | ||||||
chr14:31073257
|
A | G | 77 | a0001c0001t0001g0045a0001c0001t0001g0118a0001c0001t0001g0126others(74): Show | 78 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.294+284A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073257 | ||||||
chr14:31073261
|
T | C | 2 | a0001c0001t0002g0196a0001c0001t0030g0068 | 2 | HG02896.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.294+288T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073261 | ||||||
chr14:31073266
|
A | G | 3 | a0001c0001t0002g0182a0001c0001t0002g0196a0001c0001t0030g0068 | 3 | HG01192.hp2 HG02896.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.294+293A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073266 | ||||||
chr14:31073269
|
T | A | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.294+296T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073269 | ||||||
chr14:31073273
|
A | G | 87 | a0001c0001t0001g0045a0001c0001t0001g0118a0001c0001t0001g0126others(84): Show | 88 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.294+300A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073273 | ||||||
chr14:31073286
|
G | C | 267 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(264): Show | 269 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.294+313G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073286 | ||||||
chr14:31073286
|
G | T | 7 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 7 | HG02630.hp1 HG02647.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+313G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073286 | ||||||
chr14:31073290
|
A | G | 1 | a0001c0001t0015g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.294+317A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073290 | ||||||
chr14:31073293
|
A | G | 7 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(4): Show | 7 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.294+320A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073293 | ||||||
chr14:31073294
|
T | C | 3 | a0001c0001t0005g0083a0001c0001t0008g0013a0001c0001t0047g0264 | 3 | HG01109.hp1 HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.294+321T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073294 | ||||||
chr14:31073297
|
T | C | 58 | a0001c0001t0001g0005a0001c0001t0001g0074a0001c0001t0001g0098others(55): Show | 59 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.294+324T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073297 | ||||||
chr14:31073301
|
T | A | 1 | a0001c0001t0005g0226 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.294+328T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073301 | ||||||
chr14:31073301
|
T | C | 2 | a0001c0001t0002g0188a0001c0001t0027g0164 | 2 | HG00438.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.294+328T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073301 | ||||||
chr14:31073304
|
T | C | 133 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0029others(130): Show | 134 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.294+331T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073304 | ||||||
chr14:31073306
|
C | A | 1 | a0001c0001t0011g0085 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.294+333C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073306 | ||||||
chr14:31073306
|
C | T | 7 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0012g0200others(4): Show | 7 | HG01106.hp2 HG01891.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.294+333C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073306 | ||||||
chr14:31073306
|
CGGTGAAA others(829): Show |
C | 1 | a0001c0001t0019g0007 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.294+344_294+1179de others(1): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31073306 | |||||
chr14:31073314
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.294+341C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073314 | ||||||
chr14:31073317
|
C | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0032others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.294+344C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073317 | ||||||
chr14:31073317
|
C | T | 5 | a0001c0001t0001g0107a0001c0001t0001g0128a0001c0001t0002g0177others(2): Show | 5 | HG00323.hp1 HG00408.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.294+344C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073317 | ||||||
chr14:31073318
|
G | A | 1 | a0001c0001t0002g0182 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.294+345G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073318 | ||||||
chr14:31073320
|
C | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0049 | 2 | HG00639.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.294+347C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073320 | ||||||
chr14:31073346
|
T | C | 134 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0028others(131): Show | 135 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.294+373T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073346 | ||||||
chr14:31073351
|
G | A | 1 | a0001c0001t0003g0152 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.294+378G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073351 | ||||||
chr14:31073353
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0015g0211a0001c0001t0015g0263 | 3 | HG00140.hp1 HG03209.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.294+380G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073353 | ||||||
chr14:31073356
|
G | A | 64 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0060others(61): Show | 64 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.294+383G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073356 | ||||||
chr14:31073357
|
G | T | 1 | a0001c0001t0003g0152 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.294+384G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073357 | ||||||
chr14:31073358
|
T | C | 204 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.294+385T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073358 | ||||||
chr14:31073360
|
G | T | 4 | a0001c0001t0001g0056a0001c0001t0001g0132a0001c0001t0004g0203others(1): Show | 4 | HG01891.hp2 HG03098.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+387G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073360 | ||||||
chr14:31073361
|
G | A | 85 | a0001c0001t0001g0004a0001c0001t0001g0023a0001c0001t0001g0033others(82): Show | 86 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.294+388G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073361 | ||||||
chr14:31073362
|
C | T | 3 | a0001c0001t0005g0083a0001c0001t0005g0084a0001c0001t0047g0264 | 3 | HG01109.hp1 HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.294+389C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073362 | ||||||
chr14:31073363
|
G | C | 3 | a0001c0001t0005g0083a0001c0001t0005g0084a0001c0001t0047g0264 | 3 | HG01109.hp1 HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.294+390G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073363 | ||||||
chr14:31073364
|
C | T | 27 | a0001c0001t0002g0174a0001c0001t0003g0002a0001c0001t0003g0024others(24): Show | 28 | HG00099.hp1 HG00323.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.294+391C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073364 | ||||||
chr14:31073372
|
C | A | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.294+399C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073372 | ||||||
chr14:31073382
|
C | T | 3 | a0001c0001t0012g0200a0001c0001t0012g0201a0001c0001t0041g0227 | 3 | HG01891.hp1 HG02109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.294+409C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073382 | ||||||
chr14:31073383
|
C | A | 1 | a0001c0001t0001g0053 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.294+410C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073383 | ||||||
chr14:31073383
|
C | G | 6 | a0001c0001t0001g0313a0001c0001t0004g0256a0001c0001t0004g0261others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+410C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073383 | ||||||
chr14:31073419
|
G | A | 2 | a0001c0001t0004g0209a0001c0001t0015g0211 | 2 | HG00140.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.294+446G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073419 | ||||||
chr14:31073427
|
T | C | 31 | a0001c0001t0001g0005a0001c0001t0001g0037a0001c0001t0001g0074others(28): Show | 31 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(28): Show |
intron_variant | MODIFIER | c.294+454T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073427 | ||||||
chr14:31073433
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.294+460T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073433 | ||||||
chr14:31073439
|
G | A | 11 | a0001c0001t0001g0053a0001c0001t0001g0128a0001c0001t0002g0177others(8): Show | 11 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(8): Show |
intron_variant | MODIFIER | c.294+466G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073439 | ||||||
chr14:31073445
|
C | G | 238 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(235): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.294+472C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073445 | ||||||
chr14:31073446
|
C | T | 231 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(228): Show | 233 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.294+473C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073446 | ||||||
chr14:31073460
|
A | T | 5 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0014g0158others(2): Show | 5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+487A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073460 | ||||||
chr14:31073461
|
G | A | 1 | a0001c0001t0002g0162 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.294+488G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073461 | ||||||
chr14:31073468
|
C | T | 2 | a0001c0001t0004g0216a0001c0001t0044g0131 | 2 | HG01255.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.294+495C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073468 | ||||||
chr14:31073469
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 143 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.294+496A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073469 | ||||||
chr14:31073473
|
G | C | 5 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0014g0158others(2): Show | 5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.294+500G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073473 | ||||||
chr14:31073476
|
C | G | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.294+503C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073476 | ||||||
chr14:31073485
|
G | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.294+512G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073485 | ||||||
chr14:31073487
|
C | G | 1 | a0001c0001t0015g0211 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.294+514C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073487 | ||||||
chr14:31073491
|
G | GA | 15 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0056others(12): Show | 15 | HG02055.hp1 HG02074.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.294+530dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31073491 | |||||
chr14:31073536
|
T | C | 1 | a0001c0001t0001g0222 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.294+563T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073536 | ||||||
chr14:31073633
|
C | T | 4 | a0001c0001t0001g0098a0001c0001t0005g0248a0001c0001t0005g0249others(1): Show | 4 | HG00733.hp2 HG02145.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+660C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073633 | ||||||
chr14:31073640
|
G | A | 1 | a0001c0001t0031g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.294+667G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073640 | ||||||
chr14:31073834
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.294+861G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073834 | ||||||
chr14:31073854
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.294+881T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073854 | ||||||
chr14:31073964
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.294+991G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31073964 | ||||||
chr14:31074097
|
T | C | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(272): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.294+1124T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074097 | ||||||
chr14:31074153
|
T | A | 1 | a0001c0001t0019g0007 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.294+1180T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074153 | ||||||
chr14:31074178
|
T | G | 2 | a0001c0001t0004g0255a0001c0001t0004g0278 | 2 | HG00733.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.294+1205T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074178 | ||||||
chr14:31074270
|
A | C | 1 | a0001c0001t0044g0131 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.294+1297A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074270 | ||||||
chr14:31074312
|
G | A | 32 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(29): Show | 32 | HG00639.hp2 HG01109.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.294+1339G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074312 | ||||||
chr14:31074320
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0005g0226 | 2 | HG03490.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.294+1347G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074320 | ||||||
chr14:31074324
|
C | CAAAT | 14 | a0001c0001t0001g0045a0001c0001t0001g0115a0001c0001t0001g0270others(11): Show | 14 | HG01106.hp2 HG02040.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.294+1391_294+1394d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31074324 | |||||
chr14:31074324
|
CAAAT | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(125): Show | 129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.294+1391_294+1394d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31074324 | |||||
chr14:31074324
|
CAAATAAA others(5): Show |
C | 58 | a0001c0001t0001g0093a0001c0001t0001g0118a0001c0001t0001g0141others(55): Show | 58 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.294+1383_294+1394d others(14): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31074324 | |||||
chr14:31074364
|
T | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0057others(2): Show | 5 | HG00642.hp1 HG00738.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.294+1391T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074364 | ||||||
chr14:31074365
|
A | T | 5 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0057others(2): Show | 5 | HG00642.hp1 HG00738.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.294+1392A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074365 | ||||||
chr14:31074367
|
A | G | 1 | a0001c0001t0018g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.294+1394A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074367 | ||||||
chr14:31074377
|
G | A | 9 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.294+1404G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074377 | ||||||
chr14:31074419
|
G | A | 1 | a0001c0001t0015g0263 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.294+1446G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074419 | ||||||
chr14:31074483
|
T | G | 7 | a0001c0001t0012g0199a0001c0001t0012g0200a0001c0001t0012g0201others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+1510T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074483 | ||||||
chr14:31074551
|
G | A | 49 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0251others(46): Show | 49 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.294+1578G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074551 | ||||||
chr14:31074555
|
G | A | 1 | a0001c0001t0031g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.294+1582G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074555 | ||||||
chr14:31074589
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.294+1616C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074589 | ||||||
chr14:31074590
|
G | A | 3 | a0001c0001t0015g0263a0001c0001t0018g0205a0001c0001t0047g0264 | 3 | HG02109.hp1 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.294+1617G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074590 | ||||||
chr14:31074597
|
T | C | 39 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0096others(36): Show | 39 | HG00099.hp2 HG00621.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.294+1624T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074597 | ||||||
chr14:31074696
|
G | A | 3 | a0001c0001t0019g0007a0001c0001t0019g0008a0001c0001t0039g0133 | 3 | HG02145.hp2 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.294+1723G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31074696 | ||||||
chr14:31074826
|
T | TC | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(124): Show | 128 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.294+1857dupC | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31074826 | |||||
chr14:31075083
|
T | G | 6 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(3): Show | 6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+2110T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31075083 | ||||||
chr14:31075104
|
T | A | 1 | a0001c0001t0005g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.294+2131T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31075104 | ||||||
chr14:31075336
|
A | G | 2 | a0001c0001t0027g0164a0001c0001t0043g0204 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.294+2363A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31075336 | ||||||
chr14:31075348
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0005g0226 | 2 | HG03490.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.294+2375A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31075348 | ||||||
chr14:31075438
|
G | C | 1 | a0001c0001t0001g0319 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.294+2465G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31075438 | ||||||
chr14:31075547
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.294+2574C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31075547 | ||||||
chr14:31075741
|
A | AT | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.294+2783dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31075741 | |||||
chr14:31075741
|
A | ATT | 36 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0093others(33): Show | 36 | HG00621.hp1 HG02040.hp2 HG02074.hp1 others(33): Show |
intron_variant | MODIFIER | c.294+2782_294+2783d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31075741 | |||||
chr14:31075801
|
G | A | 7 | a0001c0001t0012g0199a0001c0001t0012g0200a0001c0001t0012g0201others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+2828G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31075801 | ||||||
chr14:31076002
|
C | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0342 | 2 | HG00438.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.294+3029C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076002 | ||||||
chr14:31076104
|
C | T | 215 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.294+3131C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076104 | ||||||
chr14:31076121
|
A | G | 6 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(3): Show | 6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+3148A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076121 | ||||||
chr14:31076154
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.294+3181C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076154 | ||||||
chr14:31076292
|
T | C | 7 | a0001c0001t0012g0199a0001c0001t0012g0200a0001c0001t0012g0201others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.294+3319T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076292 | ||||||
chr14:31076597
|
C | G | 4 | a0001c0001t0005g0083a0001c0001t0005g0084a0001c0001t0005g0241others(1): Show | 4 | HG00639.hp2 HG01109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+3624C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076597 | ||||||
chr14:31076665
|
A | G | 6 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(3): Show | 6 | HG01884.hp2 HG02818.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.294+3692A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076665 | ||||||
chr14:31076759
|
T | C | 51 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(48): Show | 52 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.294+3786T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076759 | ||||||
chr14:31076781
|
A | G | 1 | a0001c0001t0005g0279 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.295-3792A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076781 | ||||||
chr14:31076815
|
G | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 13 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.295-3758G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076815 | ||||||
chr14:31076872
|
G | A | 4 | a0001c0001t0005g0083a0001c0001t0005g0084a0001c0001t0005g0241others(1): Show | 4 | HG00639.hp2 HG01109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-3701G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076872 | ||||||
chr14:31076915
|
G | A | 5 | a0001c0001t0001g0093a0001c0001t0005g0083a0001c0001t0005g0084others(2): Show | 5 | HG00639.hp2 HG01109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-3658G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31076915 | ||||||
chr14:31077000
|
C | T | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.295-3573C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077000 | ||||||
chr14:31077018
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.295-3555G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077018 | ||||||
chr14:31077087
|
G | A | 6 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(3): Show | 6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-3486G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077087 | ||||||
chr14:31077151
|
C | G | 20 | a0001c0001t0001g0093a0001c0001t0001g0315a0001c0001t0005g0083others(17): Show | 20 | HG00639.hp2 HG01109.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.295-3422C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077151 | ||||||
chr14:31077186
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.295-3387C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077186 | ||||||
chr14:31077292
|
A | G | 1 | a0001c0001t0025g0186 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.295-3281A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077292 | ||||||
chr14:31077390
|
A | G | 3 | a0001c0001t0015g0263a0001c0001t0018g0205a0001c0001t0047g0264 | 3 | HG02109.hp1 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.295-3183A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077390 | ||||||
chr14:31077410
|
G | C | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.295-3163G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077410 | ||||||
chr14:31077435
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0195a0001c0001t0002g0182 | 3 | HG00741.hp2 HG01192.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.295-3138G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077435 | ||||||
chr14:31077578
|
C | A | 3 | a0001c0001t0003g0025a0001c0001t0003g0026a0001c0001t0003g0027 | 3 | HG02559.hp2 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.295-2995C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077578 | ||||||
chr14:31077585
|
A | G | 1 | a0001c0001t0005g0226 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.295-2988A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077585 | ||||||
chr14:31077587
|
C | T | 11 | a0001c0001t0012g0199a0001c0001t0012g0200a0001c0001t0012g0201others(8): Show | 11 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.295-2986C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077587 | ||||||
chr14:31077629
|
CTTCCAGG others(3): Show |
C | 1 | a0001c0001t0034g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.295-2930_295-2921d others(12): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31077629 | |||||
chr14:31077683
|
T | A | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.295-2890T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077683 | ||||||
chr14:31077739
|
C | CT | 51 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(48): Show | 52 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.295-2819dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31077739 | |||||
chr14:31077739
|
CT | C | 26 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0096others(23): Show | 26 | HG00621.hp1 HG02074.hp1 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.295-2819delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31077739 | |||||
chr14:31077805
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.295-2768G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077805 | ||||||
chr14:31077983
|
C | A | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.295-2590C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31077983 | ||||||
chr14:31078128
|
G | A | 1 | a0001c0001t0001g0321 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.295-2445G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31078128 | ||||||
chr14:31078406
|
C | T | 1 | a0001c0001t0025g0186 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.295-2167C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31078406 | ||||||
chr14:31078615
|
G | T | 7 | a0001c0001t0012g0199a0001c0001t0012g0200a0001c0001t0012g0201others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.295-1958G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31078615 | ||||||
chr14:31078767
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.295-1806G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31078767 | ||||||
chr14:31078906
|
C | T | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.295-1667C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31078906 | ||||||
chr14:31079136
|
G | C | 9 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.295-1437G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31079136 | ||||||
chr14:31079245
|
T | C | 5 | a0001c0001t0001g0093a0001c0001t0005g0083a0001c0001t0005g0084others(2): Show | 5 | HG00639.hp2 HG01109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.295-1328T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31079245 | ||||||
chr14:31079313
|
T | C | 4 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(1): Show | 4 | HG02572.hp1 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-1260T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31079313 | ||||||
chr14:31079332
|
G | A | 70 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(67): Show | 71 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.295-1241G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31079332 | ||||||
chr14:31079497
|
A | G | 6 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(3): Show | 6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.295-1076A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31079497 | ||||||
chr14:31079757
|
T | C | 19 | a0001c0001t0001g0093a0001c0001t0005g0083a0001c0001t0005g0084others(16): Show | 19 | HG00639.hp2 HG01109.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.295-816T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31079757 | ||||||
chr14:31079900
|
T | TTAC | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.295-671_295-669dup others(3): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 31079900 | |||||
chr14:31080155
|
C | G | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.295-418C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31080155 | ||||||
chr14:31080237
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.295-336G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31080237 | ||||||
chr14:31080413
|
T | C | 19 | a0001c0001t0001g0093a0001c0001t0005g0083a0001c0001t0005g0084others(16): Show | 19 | HG00639.hp2 HG01109.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.295-160T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31080413 | ||||||
chr14:31080460
|
A | T | 3 | a0001c0001t0016g0197a0001c0001t0016g0198a0001c0001t0041g0227 | 3 | HG02630.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.295-113A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31080460 | ||||||
chr14:31080539
|
T | G | 276 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(273): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.295-34T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31080539 | ||||||
chr14:31080557
|
T | C | 2 | a0001c0001t0010g0272a0001c0001t0010g0274 | 2 | NA18971.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.295-16T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 4/5 | chr14 | 31080557 | ||||||
chr14:31080626
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0067 | 2 | HG02165.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.306+42G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31080626 | ||||||
chr14:31080949
|
G | A | 6 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(3): Show | 6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+365G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31080949 | ||||||
chr14:31081072
|
G | A | 8 | a0001c0001t0001g0093a0001c0001t0005g0083a0001c0001t0005g0084others(5): Show | 8 | HG00639.hp2 HG01109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.306+488G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081072 | ||||||
chr14:31081089
|
G | A | 1 | a0001c0001t0004g0216 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.306+505G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081089 | ||||||
chr14:31081136
|
C | A | 1 | a0001c0001t0002g0174 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.306+552C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081136 | ||||||
chr14:31081388
|
T | C | 5 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0014g0158others(2): Show | 5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+804T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081388 | ||||||
chr14:31081463
|
G | C | 4 | a0001c0001t0005g0083a0001c0001t0005g0084a0001c0001t0005g0241others(1): Show | 4 | HG00639.hp2 HG01109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+879G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081463 | ||||||
chr14:31081517
|
G | C | 1 | a0001c0001t0001g0106 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.306+933G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081517 | ||||||
chr14:31081526
|
G | A | 1 | a0001c0001t0012g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.306+942G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081526 | ||||||
chr14:31081976
|
C | T | 4 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(1): Show | 4 | HG02074.hp2 NA18971.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+1392C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31081976 | ||||||
chr14:31082341
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.306+1757A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082341 | ||||||
chr14:31082357
|
A | G | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.306+1773A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082357 | ||||||
chr14:31082556
|
T | A | 8 | a0001c0001t0001g0093a0001c0001t0005g0083a0001c0001t0005g0084others(5): Show | 8 | HG00639.hp2 HG01109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.306+1972T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082556 | ||||||
chr14:31082569
|
T | C | 35 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 35 | HG00099.hp2 HG00642.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.306+1985T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082569 | ||||||
chr14:31082654
|
T | A | 1 | a0001c0001t0003g0151 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.306+2070T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082654 | ||||||
chr14:31082724
|
G | A | 73 | a0001c0001t0001g0033a0001c0001t0001g0096a0001c0001t0001g0097others(70): Show | 73 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.306+2140G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082724 | ||||||
chr14:31082753
|
G | A | 2 | a0001c0001t0005g0241a0001c0001t0005g0242 | 2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.306+2169G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082753 | ||||||
chr14:31082765
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.306+2181G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082765 | ||||||
chr14:31082778
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.306+2194C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082778 | ||||||
chr14:31082788
|
T | C | 8 | a0001c0001t0001g0093a0001c0001t0005g0083a0001c0001t0005g0084others(5): Show | 8 | HG00639.hp2 HG01109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.306+2204T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082788 | ||||||
chr14:31082812
|
C | T | 8 | a0001c0001t0001g0093a0001c0001t0005g0083a0001c0001t0005g0084others(5): Show | 8 | HG00639.hp2 HG01109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.306+2228C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082812 | ||||||
chr14:31082813
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+2229G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082813 | ||||||
chr14:31082813
|
G | T | 2 | a0001c0001t0015g0263a0001c0001t0047g0264 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.306+2229G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082813 | ||||||
chr14:31082820
|
C | T | 5 | a0001c0001t0007g0208a0001c0001t0007g0266a0001c0001t0007g0267others(2): Show | 5 | HG02683.hp1 HG03704.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.306+2236C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082820 | ||||||
chr14:31082825
|
G | A | 1 | a0001c0001t0001g0332 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.306+2241G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082825 | ||||||
chr14:31082846
|
A | C | 1 | a0001c0001t0001g0314 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.306+2262A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082846 | ||||||
chr14:31082850
|
T | G | 3 | a0001c0001t0001g0005a0001c0001t0015g0263a0001c0001t0047g0264 | 3 | HG02109.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.306+2266T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082850 | ||||||
chr14:31082862
|
C | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+2278C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082862 | ||||||
chr14:31082883
|
G | A | 3 | a0001c0001t0019g0007a0001c0001t0019g0008a0001c0001t0039g0133 | 3 | HG02145.hp2 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.306+2299G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31082883 | ||||||
chr14:31082895
|
C | CA | 6 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0073others(3): Show | 6 | HG02165.hp2 HG03540.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+2326dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31082895 | |||||
chr14:31082895
|
C | CAA | 24 | a0001c0001t0001g0144a0001c0001t0003g0002a0001c0001t0003g0024others(21): Show | 25 | HG00099.hp1 HG00323.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.306+2325_306+2326d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31082895 | |||||
chr14:31083070
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0012g0199a0001c0001t0012g0200others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.306+2486A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31083070 | ||||||
chr14:31083414
|
T | C | 22 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(19): Show | 22 | HG00099.hp2 HG00642.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.306+2830T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31083414 | ||||||
chr14:31083433
|
A | AGTG | 3 | a0001c0001t0015g0263a0001c0001t0018g0205a0001c0001t0047g0264 | 3 | HG02109.hp1 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.306+2852_306+2854d others(5): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083433 | |||||
chr14:31083467
|
G | A | 7 | a0001c0001t0001g0331a0001c0001t0001g0333a0001c0001t0001g0334others(4): Show | 7 | NA18939.hp1 NA18947.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.306+2883G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31083467 | ||||||
chr14:31083494
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0039g0133 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.306+2911_306+2912i others(21): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083494 | |||||
chr14:31083496
|
C | CT | 57 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(54): Show | 57 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.306+2938dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTT | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0023others(106): Show | 110 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.306+2937_306+2938d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTT | 68 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0039others(65): Show | 68 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.306+2936_306+2938d others(5): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTT | 34 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0100others(31): Show | 34 | HG01106.hp2 HG01175.hp1 HG02080.hp1 others(31): Show |
intron_variant | MODIFIER | c.306+2935_306+2938d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTTT | 10 | a0001c0001t0001g0210a0001c0001t0001g0219a0001c0001t0001g0223others(7): Show | 10 | HG00099.hp1 HG00621.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.306+2934_306+2938d others(7): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTTTT | 17 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(14): Show | 18 | HG00323.hp2 HG00741.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.306+2933_306+2938d others(8): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTTTTT | 7 | a0001c0001t0003g0026a0001c0001t0003g0130a0001c0001t0003g0145others(4): Show | 7 | HG01257.hp2 HG01361.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.306+2932_306+2938d others(9): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0006g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.306+2928_306+2938d others(13): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTTTTT others(5): Show |
7 | a0001c0001t0001g0005a0001c0001t0006g0015a0001c0001t0006g0018others(4): Show | 7 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.306+2927_306+2938d others(14): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0006g0016a0001c0001t0006g0017a0001c0001t0006g0327others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+2926_306+2938d others(15): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0047g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.306+2925_306+2938d others(16): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0012g0199a0001c0001t0018g0205 | 2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.306+2924_306+2938d others(17): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTTTTT others(9): Show |
7 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0140others(4): Show | 7 | HG00099.hp2 HG02886.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.306+2923_306+2938d others(18): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTTTTT others(10): Show |
5 | a0001c0001t0001g0139a0001c0001t0005g0241a0001c0001t0010g0272others(2): Show | 5 | HG00642.hp2 HG02074.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.306+2922_306+2938d others(19): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0142a0001c0001t0005g0242 | 2 | HG00639.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.306+2921_306+2938d others(20): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0136 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.306+2920_306+2938d others(21): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0019g0008 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.306+2917_306+2938d others(24): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTTTTT others(16): Show |
2 | a0001c0001t0001g0093a0001c0001t0019g0007 | 2 | HG02486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.306+2916_306+2938d others(25): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0049g0229 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.306+2914_306+2938d others(27): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31083496 | |||||
chr14:31083496
|
C | T | 1 | a0001c0001t0039g0133 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.306+2912C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31083496 | ||||||
chr14:31083930
|
T | C | 72 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(69): Show | 73 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.306+3346T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31083930 | ||||||
chr14:31083934
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.306+3350G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31083934 | ||||||
chr14:31083940
|
G | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.306+3356G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31083940 | ||||||
chr14:31084055
|
C | T | 5 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0014g0158others(2): Show | 5 | HG01106.hp2 HG02572.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+3471C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084055 | ||||||
chr14:31084104
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0099 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.306+3520A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084104 | ||||||
chr14:31084214
|
G | T | 6 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(3): Show | 6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+3630G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084214 | ||||||
chr14:31084373
|
G | A | 1 | a0001c0001t0009g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.306+3789G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084373 | ||||||
chr14:31084514
|
T | G | 70 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(67): Show | 71 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.306+3930T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084514 | ||||||
chr14:31084519
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.306+3935T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084519 | ||||||
chr14:31084587
|
C | T | 5 | a0001c0001t0001g0281a0001c0001t0001g0307a0001c0001t0001g0312others(2): Show | 5 | HG03654.hp2 HG03834.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.306+4003C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084587 | ||||||
chr14:31084903
|
A | G | 1 | a0001c0001t0015g0211 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.306+4319A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084903 | ||||||
chr14:31084929
|
C | G | 1 | a0001c0001t0004g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.306+4345C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31084929 | ||||||
chr14:31085076
|
G | A | 2 | a0001c0001t0001g0316a0001c0001t0001g0322 | 2 | HG00544.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.306+4492G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085076 | ||||||
chr14:31085137
|
C | T | 1 | a0001c0001t0005g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.306+4553C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085137 | ||||||
chr14:31085138
|
G | T | 1 | a0001c0001t0031g0326 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.306+4554G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085138 | ||||||
chr14:31085270
|
T | C | 1 | a0001c0001t0005g0279 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.306+4686T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085270 | ||||||
chr14:31085295
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.306+4711C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085295 | ||||||
chr14:31085312
|
G | T | 1 | a0001c0001t0001g0060 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.306+4728G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085312 | ||||||
chr14:31085523
|
C | T | 4 | a0001c0001t0011g0082a0001c0001t0011g0088a0001c0001t0011g0090others(1): Show | 4 | HG00558.hp1 HG00609.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+4939C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085523 | ||||||
chr14:31085600
|
C | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+5016C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085600 | ||||||
chr14:31085664
|
T | C | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.306+5080T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085664 | ||||||
chr14:31085957
|
A | G | 22 | a0001c0001t0001g0005a0001c0001t0006g0015a0001c0001t0006g0016others(19): Show | 22 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.306+5373A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085957 | ||||||
chr14:31085972
|
G | A | 6 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(3): Show | 6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.306+5388G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31085972 | ||||||
chr14:31086198
|
A | G | 1 | a0001c0001t0026g0194 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.306+5614A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31086198 | ||||||
chr14:31086314
|
C | A | 16 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(13): Show | 16 | HG01884.hp1 HG02055.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.306+5730C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31086314 | ||||||
chr14:31086377
|
G | C | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.306+5793G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31086377 | ||||||
chr14:31086383
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0012g0199a0001c0001t0012g0200others(6): Show | 9 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.306+5799G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31086383 | ||||||
chr14:31086410
|
A | ATTTG | 3 | a0001c0001t0001g0005a0001c0001t0001g0240a0001c0001t0005g0084 | 3 | HG02818.hp1 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.306+5850_306+5853d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31086410 | |||||
chr14:31086410
|
ATTTG | A | 3 | a0001c0001t0019g0007a0001c0001t0019g0008a0001c0001t0039g0133 | 3 | HG02145.hp2 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.306+5850_306+5853d others(6): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31086410 | |||||
chr14:31086583
|
T | C | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.306+5999T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31086583 | ||||||
chr14:31086707
|
C | T | 1 | a0001c0001t0005g0084 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.306+6123C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31086707 | ||||||
chr14:31086843
|
C | T | 2 | a0001c0001t0005g0083a0001c0001t0005g0084 | 2 | HG01109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.307-6064C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31086843 | ||||||
chr14:31087160
|
C | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0228 | 2 | HG02129.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.307-5747C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087160 | ||||||
chr14:31087380
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0029g0243 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.307-5527G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087380 | ||||||
chr14:31087399
|
C | T | 1 | a0001c0001t0024g0190 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.307-5508C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087399 | ||||||
chr14:31087601
|
C | T | 1 | a0001c0001t0005g0108 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.307-5306C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087601 | ||||||
chr14:31087673
|
T | A | 185 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(182): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.307-5234T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087673 | ||||||
chr14:31087717
|
A | G | 1 | a0001c0001t0047g0264 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.307-5190A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087717 | ||||||
chr14:31087754
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0029g0243 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.307-5153C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087754 | ||||||
chr14:31087761
|
T | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0008g0061 | 3 | HG01106.hp1 HG01256.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.307-5146T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31087761 | ||||||
chr14:31088123
|
G | C | 179 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0032others(176): Show | 180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.307-4784G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088123 | ||||||
chr14:31088129
|
A | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0240a0001c0001t0015g0263 | 3 | HG03041.hp1 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.307-4778A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088129 | ||||||
chr14:31088178
|
G | C | 2 | a0001c0001t0015g0263a0001c0001t0018g0205 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.307-4729G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088178 | ||||||
chr14:31088250
|
T | C | 1 | a0001c0001t0026g0194 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.307-4657T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088250 | ||||||
chr14:31088487
|
G | A | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-4420G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088487 | ||||||
chr14:31088714
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.307-4193G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088714 | ||||||
chr14:31088807
|
C | CA | 81 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(78): Show | 81 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.307-4077dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31088807 | |||||
chr14:31088807
|
C | CAA | 29 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0096others(26): Show | 29 | HG00621.hp1 HG02040.hp2 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.307-4078_307-4077d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31088807 | |||||
chr14:31088807
|
CA | C | 31 | a0001c0001t0001g0029a0001c0001t0001g0052a0001c0001t0001g0104others(28): Show | 31 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.307-4077delA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31088807 | |||||
chr14:31088807
|
CAA | C | 8 | a0001c0001t0012g0199a0001c0001t0012g0200a0001c0001t0012g0201others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-4078_307-4077d others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31088807 | |||||
chr14:31088807
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.307-4086_307-4077d others(12): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31088807 | |||||
chr14:31088886
|
G | A | 1 | a0001c0001t0029g0243 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.307-4021G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088886 | ||||||
chr14:31088966
|
A | T | 6 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(3): Show | 6 | HG02074.hp2 HG03942.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.307-3941A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31088966 | ||||||
chr14:31089027
|
C | T | 18 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.307-3880C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089027 | ||||||
chr14:31089163
|
C | A | 12 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0007g0208others(9): Show | 12 | HG01106.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.307-3744C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089163 | ||||||
chr14:31089163
|
C | CA | 25 | a0001c0001t0001g0079a0001c0001t0006g0015a0001c0001t0006g0016others(22): Show | 25 | HG00280.hp2 HG01891.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.307-3726dupA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31089163 | |||||
chr14:31089163
|
CA | C | 55 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0003g0002others(52): Show | 56 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.307-3726delA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31089163 | |||||
chr14:31089328
|
T | A | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.307-3579T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089328 | ||||||
chr14:31089463
|
A | G | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-3444A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089463 | ||||||
chr14:31089465
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.307-3442T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089465 | ||||||
chr14:31089584
|
C | T | 52 | a0001c0001t0003g0002a0001c0001t0003g0024a0001c0001t0003g0025others(49): Show | 53 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.307-3323C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089584 | ||||||
chr14:31089642
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(2): Show | 5 | HG02630.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-3265T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089642 | ||||||
chr14:31089746
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.307-3161G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089746 | ||||||
chr14:31089914
|
G | A | 3 | a0001c0001t0001g0047a0001c0001t0027g0164a0001c0001t0043g0204 | 3 | HG02280.hp2 HG02735.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.307-2993G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31089914 | ||||||
chr14:31090027
|
T | G | 8 | a0001c0001t0012g0199a0001c0001t0012g0200a0001c0001t0012g0201others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-2880T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31090027 | ||||||
chr14:31090053
|
G | C | 1 | a0001c0001t0018g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.307-2854G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31090053 | ||||||
chr14:31090081
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.307-2826G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31090081 | ||||||
chr14:31090282
|
G | C | 1 | a0001c0001t0029g0243 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.307-2625G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31090282 | ||||||
chr14:31090402
|
G | C | 200 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(197): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.307-2505G>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31090402 | ||||||
chr14:31090615
|
A | G | 2 | a0001c0001t0036g0091a0001c0001t0037g0041 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.307-2292A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31090615 | ||||||
chr14:31090632
|
A | T | 9 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.307-2275A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31090632 | ||||||
chr14:31091199
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.307-1708G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091199 | ||||||
chr14:31091219
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.307-1688T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091219 | ||||||
chr14:31091362
|
T | C | 6 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.307-1545T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091362 | ||||||
chr14:31091402
|
G | T | 8 | a0001c0001t0012g0199a0001c0001t0012g0200a0001c0001t0012g0201others(5): Show | 8 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-1505G>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091402 | ||||||
chr14:31091525
|
C | CT | 13 | a0001c0001t0001g0039a0001c0001t0001g0076a0001c0001t0002g0172others(10): Show | 13 | HG01106.hp2 HG01175.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.307-1368dupT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31091525 | |||||
chr14:31091648
|
C | G | 12 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0007g0208others(9): Show | 12 | HG01106.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.307-1259C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091648 | ||||||
chr14:31091788
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.307-1119G>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091788 | ||||||
chr14:31091890
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(2): Show | 5 | HG02630.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.307-1017A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091890 | ||||||
chr14:31091933
|
A | G | 1 | a0001c0001t0001g0313 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.307-974A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091933 | ||||||
chr14:31091962
|
C | G | 66 | a0001c0001t0001g0035a0001c0001t0001g0072a0001c0001t0001g0118others(63): Show | 67 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.307-945C>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091962 | ||||||
chr14:31091969
|
C | A | 24 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(21): Show | 24 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.307-938C>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31091969 | ||||||
chr14:31092467
|
AACAT | A | 3 | a0001c0001t0019g0007a0001c0001t0019g0008a0001c0001t0039g0133 | 3 | HG02145.hp2 HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.307-435_307-432del others(4): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31092467 | |||||
chr14:31092496
|
A | C | 1 | a0001c0001t0001g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.307-411A>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092496 | ||||||
chr14:31092547
|
TTAC | T | 5 | a0001c0001t0001g0037a0001c0001t0001g0074a0001c0001t0001g0075others(2): Show | 5 | HG02055.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-357_307-355del others(3): Show |
AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 31092547 | |||||
chr14:31092571
|
A | T | 1 | a0001c0001t0003g0245 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.307-336A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092571 | ||||||
chr14:31092626
|
A | G | 2 | a0001c0001t0005g0083a0001c0001t0005g0084 | 2 | HG01109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.307-281A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092626 | ||||||
chr14:31092684
|
C | T | 100 | a0001c0001t0001g0093a0001c0001t0003g0002a0001c0001t0003g0024others(97): Show | 101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.307-223C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092684 | ||||||
chr14:31092732
|
T | A | 3 | a0001c0001t0003g0145a0001c0001t0003g0146a0001c0001t0003g0150 | 3 | HG00741.hp1 HG01074.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.307-175T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092732 | ||||||
chr14:31092860
|
T | TA | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-47_307-46insA | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092860 | ||||||
chr14:31092864
|
A | T | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-43A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092864 | ||||||
chr14:31092866
|
T | A | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-41T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092866 | ||||||
chr14:31092866
|
T | C | 17 | a0001c0001t0010g0271a0001c0001t0010g0272a0001c0001t0010g0273others(14): Show | 17 | HG01891.hp1 HG02074.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.307-41T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092866 | ||||||
chr14:31092868
|
A | G | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-39A>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092868 | ||||||
chr14:31092871
|
T | A | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-36T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092871 | ||||||
chr14:31092872
|
T | A | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-35T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092872 | ||||||
chr14:31092873
|
T | A | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-34T>A | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092873 | ||||||
chr14:31092876
|
C | T | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-31C>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092876 | ||||||
chr14:31092878
|
T | G | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-29T>G | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092878 | ||||||
chr14:31092880
|
A | T | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-27A>T | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092880 | ||||||
chr14:31092883
|
CT | C | 10 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0017others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.307-23delT | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092883 | ||||||
chr14:31092896
|
T | C | 12 | a0001c0001t0007g0157a0001c0001t0007g0161a0001c0001t0007g0208others(9): Show | 12 | HG01106.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.307-11T>C | AP4S1 | ENSG00000100478.16 | transcript | ENST00000542754.7 | protein_coding | 5/5 | chr14 | 31092896 |