| geneid | 26228 |
|---|---|
| ensemblid | ENSG00000035720.8 |
| hgncid | 24133 |
| symbol | STAP1 |
| name | signal transducing adaptor family member 1 |
| refseq_nuc | NM_012108.4 |
| refseq_prot | NP_036240.1 |
| ensembl_nuc | ENST00000265404.7 |
| ensembl_prot | ENSP00000265404.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 67558727 |
| end | 67607337 |
| strand | + |
| ver | v1.2 |
| region | chr4:67558727-67607337 |
| region5000 | chr4:67553727-67612337 |
| regionname0 | STAP1_chr4_67558727_67607337 |
| regionname5000 | STAP1_chr4_67553727_67612337 |
| 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 | 295 | 378 | 86 | 78 | 163 | 14 | 35 | 119 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0002 | 0/0 | 295 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0003 | 0/0 | 295 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0004 | 0/0 | 295 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| 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 | 888 | 253 | 46 | 52 | 125 | 5 | 23 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| c0002 | 0/0 | 888 | 93 | 27 | 15 | 38 | 5 | 8 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| c0003 | 0/0 | 888 | 30 | 12 | 11 | 0 | 4 | 3 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| c0004 | 0/0 | 888 | 2 | 0 | 0 | 2 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| c0005 | 0/0 | 888 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| c0006 | 0/0 | 888 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| c0007 | 0/0 | 888 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| c0008 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1064 | 226 | 45 | 60 | 87 | 11 | 23 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| t0002 | 0/1 | 1064 | 109 | 12 | 12 | 70 | 3 | 11 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| t0003 | 1/0 | 1064 | 30 | 18 | 5 | 4 | 0 | 2 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| t0004 | 0/0 | 1064 | 5 | 4 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| t0005 | 0/0 | 1064 | 3 | 0 | 0 | 3 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| t0006 | 0/0 | 1064 | 3 | 3 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| t0007 | 0/0 | 1064 | 2 | 2 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| t0008 | 0/0 | 1064 | 2 | 0 | 0 | 2 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| t0009 | 0/0 | 1064 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| t0010 | 0/0 | 1064 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| 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 | 7 | 0 | 1 | 5 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0005 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0233 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| 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 | 888 | 253 | 46 | 52 | 125 | 5 | 23 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0002 | 0/0 | 888 | 93 | 27 | 15 | 38 | 5 | 8 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0003 | 0/0 | 888 | 30 | 12 | 11 | 0 | 4 | 3 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0005 | 0/0 | 888 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0008 | 0/0 | 888 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0002c0004 | 0/0 | 888 | 2 | 0 | 0 | 2 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0003c0006 | 0/0 | 888 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0004c0007 | 0/0 | 888 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1951 | 135 | 23 | 38 | 57 | 2 | 15 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0001t0002 | 0/1 | 1951 | 86 | 7 | 9 | 59 | 3 | 7 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0001t0003 | 1/0 | 1951 | 20 | 9 | 5 | 4 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0001t0004 | 0/0 | 1951 | 2 | 2 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0001t0005 | 0/0 | 1951 | 3 | 0 | 0 | 3 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0001t0006 | 0/0 | 1951 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0001t0007 | 0/0 | 1951 | 2 | 2 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0001t0008 | 0/0 | 1951 | 2 | 0 | 0 | 2 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0001t0009 | 0/0 | 1951 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0001t0010 | 0/0 | 1951 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0002t0001 | 0/0 | 1951 | 63 | 13 | 14 | 27 | 5 | 4 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0002t0002 | 0/0 | 1951 | 18 | 4 | 0 | 11 | 0 | 3 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0002t0003 | 0/0 | 1951 | 7 | 6 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0002t0004 | 0/0 | 1951 | 3 | 2 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0002t0006 | 0/0 | 1951 | 2 | 2 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0003t0001 | 0/0 | 1951 | 23 | 8 | 8 | 0 | 4 | 3 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0003t0002 | 0/0 | 1951 | 4 | 1 | 3 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0003t0003 | 0/0 | 1951 | 3 | 3 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0005t0001 | 0/0 | 1951 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0001c0008t0001 | 0/0 | 1951 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0002c0004t0001 | 0/0 | 1951 | 2 | 0 | 0 | 2 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0003c0006t0001 | 0/0 | 1951 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| a0004c0007t0002 | 0/0 | 1951 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | copy fasta | chr4 | 67553727 | 67612337 |
| 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 | 4 | 0 | 4 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 1 | 5 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0233 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0008g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0008g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0009g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0001t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0005 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0004g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0002t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0003t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0001c0008t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0002c0004t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0002c0004t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0003c0006t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| a0004c0007t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0013 | EUR | GBR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0342 | EUR | GBR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0352 | EUR | GBR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0237 | EUR | GBR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0207 | EUR | FIN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0335 | EUR | FIN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0313 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0324 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0289 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0152 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00735 | hp1 | a0001 | c0003 | t0002 | g0341 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0348 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0278 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0288 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0328 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0292 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0330 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0337 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0325 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0334 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0333 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0308 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0291 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0347 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0290 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0293 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0262 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0183 | EUR | IBS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0353 | EUR | IBS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0346 | EUR | IBS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0011 | EUR | IBS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0192 | EUR | IBS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0011 | EUR | IBS | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0160 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01891 | hp1 | a0001 | c0002 | t0003 | g0266 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0338 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02056 | hp1 | a0003 | c0006 | t0001 | g0027 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0309 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0318 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0161 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0351 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CDX | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0179 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0311 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02300 | hp2 | a0001 | c0003 | t0002 | g0287 | AMR | PEL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0340 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02523 | hp2 | a0002 | c0004 | t0001 | g0042 | EAS | KHV | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02572 | hp1 | a0001 | c0002 | t0003 | g0163 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0132 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02615 | hp2 | a0001 | c0002 | t0004 | g0336 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0176 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0286 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02647 | hp2 | a0001 | c0008 | t0001 | g0258 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02717 | hp1 | a0001 | c0003 | t0002 | g0283 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0239 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0151 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0247 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0356 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02818 | hp1 | a0001 | c0002 | t0003 | g0155 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0245 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0339 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0149 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0153 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0175 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0285 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02965 | hp2 | a0001 | c0003 | t0003 | g0295 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0284 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02976 | hp2 | a0001 | c0002 | t0006 | g0173 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0180 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0282 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0182 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0244 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0174 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0150 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03209 | hp2 | a0001 | c0003 | t0003 | g0349 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0158 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0186 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03239 | hp2 | a0001 | c0002 | t0003 | g0322 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0159 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0268 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03516 | hp1 | a0001 | c0001 | t0009 | g0249 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0350 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03540 | hp2 | a0001 | c0002 | t0006 | g0162 | AFR | GWD | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03579 | hp1 | a0001 | c0002 | t0004 | g0154 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | MSL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0280 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0323 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0281 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0093 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG03942 | hp2 | a0001 | c0005 | t0001 | g0041 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0177 | SAS | STU | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | BEB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | STU | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04199 | hp2 | a0004 | c0007 | t0002 | g0212 | SAS | STU | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0213 | SAS | STU | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0111 | AFR | YRI | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | CHB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0270 | AFR | YRI | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | YRI | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18942 | hp2 | a0001 | c0001 | t0008 | g0238 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18964 | hp2 | a0002 | c0004 | t0001 | g0073 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0354 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0317 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0355 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18987 | hp2 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | LWK | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | LWK | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0267 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19089 | hp2 | a0001 | c0001 | t0008 | g0205 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19240 | hp1 | a0001 | c0003 | t0003 | g0294 | AFR | YRI | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0148 | AFR | YRI | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ASW | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0279 | AFR | ASW | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0272 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | ACB | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | USA | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | USA | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | USA | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | USA | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0233 | REF | REF | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0047 | REF | REF | STAP1_chr4_67553727_67612337 | STAP1 | chr4 | 67553727 | 67612337 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:67558814
|
T | C | 1 | a0002 | 2 | HG02523.hp2 NA18964.hp2 |
missense_variant | MODERATE | c.5T>C | p.Met2Thr | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/9 | 88/1951 | 5/888 | 2/295 | chr4 | 67558814 | ||
| chr4:67581459
|
A | G | 1 | a0004 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.518A>G | p.Asn173Ser | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/9 | 601/1951 | 518/888 | 173/295 | chr4 | 67581459 | ||
| chr4:67581464
|
A | G | 1 | a0003 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.523A>G | p.Met175Val | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/9 | 606/1951 | 523/888 | 175/295 | chr4 | 67581464 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:67577250
|
A | G | 2 | a0001c0002a0001c0003 | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
synonymous_variant | LOW | c.354A>G | p.Thr118Thr | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/9 | 437/1951 | 354/888 | 118/295 | chr4 | 67577250 | ||
| chr4:67581322
|
C | T | 2 | a0001c0003a0001c0008 | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(28): Show |
synonymous_variant | LOW | c.381C>T | p.Asn127Asn | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/9 | 464/1951 | 381/888 | 127/295 | chr4 | 67581322 | ||
| chr4:67581355
|
G | C | 1 | a0001c0005 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.414G>C | p.Leu138Leu | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/9 | 497/1951 | 414/888 | 138/295 | chr4 | 67581355 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:67606562
|
C | T | 3 | a0001c0001t0006a0001c0001t0010a0001c0002t0006 | 4 | HG02572.hp2 HG02976.hp2 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*205C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 205 | chr4 | 67606562 | |||||
| chr4:67606710
|
T | C | 7 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(4): Show | 114 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*353T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 353 | chr4 | 67606710 | |||||
| chr4:67606732
|
A | G | 1 | a0001c0001t0009 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*375A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 375 | chr4 | 67606732 | |||||
| chr4:67606886
|
T | C | 18 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(15): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
3_prime_UTR_variant | MODIFIER | c.*529T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 529 | chr4 | 67606886 | |||||
| chr4:67606984
|
G | A | 1 | a0001c0001t0005 | 3 | NA18959.hp2 NA18987.hp2 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*627G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 627 | chr4 | 67606984 | |||||
| chr4:67606991
|
C | T | 1 | a0001c0001t0008 | 2 | NA18942.hp2 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*634C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 634 | chr4 | 67606991 | |||||
| chr4:67607018
|
G | A | 1 | a0001c0001t0007 | 2 | HG02922.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*661G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 661 | chr4 | 67607018 | |||||
| chr4:67607258
|
G | T | 1 | a0001c0001t0010 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*901G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 901 | chr4 | 67607258 | |||||
| chr4:67607265
|
A | G | 2 | a0001c0001t0004a0001c0002t0004 | 5 | HG01167.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*908A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 908 | chr4 | 67607265 | |||||
| chr4:67607296
|
C | A | 1 | a0001c0001t0009 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*939C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 9/9 | 939 | chr4 | 67607296 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:67559031
|
A | G | 1 | a0001c0001t0001g0357 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.120+102A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67559031 | ||||||
| chr4:67559384
|
A | G | 94 | a0001c0001t0001g0012a0001c0001t0001g0269a0001c0001t0001g0296others(91): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.120+455A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67559384 | ||||||
| chr4:67559536
|
T | G | 12 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(9): Show | 12 | HG00408.hp1 HG02083.hp1 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.120+607T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67559536 | ||||||
| chr4:67559688
|
A | C | 1 | a0001c0001t0005g0267 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.120+759A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67559688 | ||||||
| chr4:67559850
|
A | G | 91 | a0001c0001t0001g0012a0001c0001t0001g0296a0001c0001t0001g0297others(88): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.120+921A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67559850 | ||||||
| chr4:67560040
|
C | G | 2 | a0001c0001t0001g0269a0001c0001t0003g0270 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.120+1111C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560040 | ||||||
| chr4:67560106
|
A | G | 179 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(176): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.120+1177A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560106 | ||||||
| chr4:67560168
|
T | A | 2 | a0001c0001t0001g0198a0001c0001t0003g0197 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.120+1239T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560168 | ||||||
| chr4:67560219
|
A | G | 1 | a0001c0001t0002g0025 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.120+1290A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560219 | ||||||
| chr4:67560230
|
TC | T | 179 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(176): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.120+1303delC | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560230 | |||||
| chr4:67560294
|
A | T | 1 | a0001c0003t0001g0356 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.120+1365A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560294 | ||||||
| chr4:67560347
|
G | A | 1 | a0001c0002t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.120+1418G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560347 | ||||||
| chr4:67560454
|
A | C | 200 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(197): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.120+1525A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560454 | ||||||
| chr4:67560637
|
T | TGTGGGGG others(1): Show |
5 | a0001c0002t0001g0274a0001c0002t0001g0275a0001c0002t0001g0276others(2): Show | 5 | HG00621.hp1 HG01123.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+1711_120+1712i others(10): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560637 | |||||
| chr4:67560641
|
T | TGG | 79 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(76): Show | 81 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.120+1714_120+1715d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560641 | |||||
| chr4:67560643
|
G | GGGGT | 20 | a0001c0001t0001g0246a0001c0001t0001g0248a0001c0001t0001g0253others(17): Show | 21 | HG00558.hp2 HG00639.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.120+1715_120+1716i others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560643 | |||||
| chr4:67560643
|
G | GGGGTGT | 10 | a0001c0001t0003g0262a0001c0002t0001g0279a0001c0003t0001g0278others(7): Show | 10 | HG01081.hp1 HG01496.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.120+1715_120+1716i others(8): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560643 | |||||
| chr4:67560643
|
G | GGGGTGTG others(1): Show |
61 | a0001c0001t0001g0012a0001c0001t0001g0296a0001c0001t0001g0297others(58): Show | 69 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.120+1715_120+1716i others(10): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560643 | |||||
| chr4:67560643
|
G | GGGGTGTG others(3): Show |
10 | a0001c0001t0001g0343a0001c0001t0001g0344a0001c0001t0001g0345others(7): Show | 10 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.120+1715_120+1716i others(12): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560643 | |||||
| chr4:67560643
|
G | GGGGTGTG others(5): Show |
1 | a0001c0001t0001g0351 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.120+1715_120+1716i others(14): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560643 | |||||
| chr4:67560643
|
G | GGTGTGT | 4 | a0001c0001t0001g0198a0001c0001t0001g0269a0001c0001t0004g0268others(1): Show | 4 | HG01884.hp1 HG02965.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+1717_120+1722d others(8): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560643 | |||||
| chr4:67560643
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0003g0270 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.120+1722_120+1723i others(12): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560643 | |||||
| chr4:67560643
|
G | T | 6 | a0001c0002t0001g0274a0001c0002t0001g0275a0001c0002t0001g0276others(3): Show | 6 | HG00621.hp1 HG01123.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+1714G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560643 | ||||||
| chr4:67560645
|
T | G | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0002t0001g0176 | 3 | HG01256.hp1 HG01258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.120+1716T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560645 | ||||||
| chr4:67560650
|
GTC | G | 4 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0007g0174others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+1723_120+1724d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560650 | |||||
| chr4:67560652
|
C | CTG | 5 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 5 | HG02129.hp2 HG02132.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+1744_120+1745d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67560652 | |||||
| chr4:67560652
|
C | G | 198 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(195): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.120+1723C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560652 | ||||||
| chr4:67560741
|
T | A | 1 | a0001c0001t0003g0026 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.120+1812T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560741 | ||||||
| chr4:67560816
|
C | A | 1 | a0003c0006t0001g0027 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.120+1887C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560816 | ||||||
| chr4:67560827
|
T | A | 1 | a0001c0001t0001g0028 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.120+1898T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560827 | ||||||
| chr4:67560904
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.120+1975C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560904 | ||||||
| chr4:67560923
|
AC | A | 13 | a0001c0003t0001g0011a0001c0003t0001g0272a0001c0003t0001g0278others(10): Show | 14 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.120+1995delC | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560923 | ||||||
| chr4:67560930
|
T | C | 2 | a0001c0003t0003g0294a0001c0003t0003g0295 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.120+2001T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560930 | ||||||
| chr4:67560992
|
G | A | 8 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0035others(5): Show | 8 | HG00609.hp1 HG00621.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.120+2063G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67560992 | ||||||
| chr4:67561178
|
G | A | 1 | a0001c0003t0001g0352 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.120+2249G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561178 | ||||||
| chr4:67561543
|
A | G | 26 | a0001c0001t0001g0243a0001c0002t0001g0009a0001c0002t0001g0176others(23): Show | 27 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.120+2614A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561543 | ||||||
| chr4:67561722
|
G | T | 1 | a0001c0001t0002g0024 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.120+2793G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561722 | ||||||
| chr4:67561729
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0003g0197 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.120+2800T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561729 | ||||||
| chr4:67561773
|
A | G | 5 | a0001c0001t0001g0257a0001c0001t0001g0260a0001c0001t0002g0259others(2): Show | 5 | HG02615.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+2844A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561773 | ||||||
| chr4:67561814
|
A | C | 198 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(195): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.120+2885A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561814 | ||||||
| chr4:67561879
|
C | T | 1 | a0001c0001t0002g0261 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.120+2950C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561879 | ||||||
| chr4:67561893
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.120+2964G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561893 | ||||||
| chr4:67561898
|
C | T | 55 | a0001c0002t0001g0009a0001c0002t0001g0176a0001c0002t0001g0177others(52): Show | 57 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.120+2969C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67561898 | ||||||
| chr4:67562021
|
G | A | 17 | a0001c0001t0001g0012a0001c0001t0001g0297a0001c0001t0001g0298others(14): Show | 18 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.120+3092G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562021 | ||||||
| chr4:67562027
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.120+3098G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562027 | ||||||
| chr4:67562068
|
CA | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 135 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.120+3162delA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562068 | |||||
| chr4:67562068
|
CAA | C | 8 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0007g0174others(5): Show | 8 | HG01167.hp2 HG01255.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.120+3161_120+3162d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562068 | |||||
| chr4:67562068
|
CAAA | C | 73 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(70): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.120+3160_120+3162d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562068 | |||||
| chr4:67562068
|
CAAAA | C | 110 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(107): Show | 111 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.120+3159_120+3162d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562068 | |||||
| chr4:67562068
|
CAAAAA | C | 7 | a0001c0001t0001g0198a0001c0001t0001g0241a0001c0001t0001g0269others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+3158_120+3162d others(7): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562068 | |||||
| chr4:67562068
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0297 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.120+3153_120+3162d others(12): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562068 | |||||
| chr4:67562068
|
CAAAAAAA others(4): Show |
C | 16 | a0001c0001t0001g0012a0001c0001t0001g0298a0001c0001t0001g0299others(13): Show | 17 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.120+3152_120+3162d others(13): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562068 | |||||
| chr4:67562087
|
A | G | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.120+3158A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562087 | ||||||
| chr4:67562088
|
A | G | 62 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0002g0310others(59): Show | 68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.120+3159A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562088 | ||||||
| chr4:67562104
|
GAAAGAAA others(8): Show |
G | 2 | a0001c0001t0007g0174a0001c0001t0007g0175 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.120+3188_120+3202d others(17): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562104 | |||||
| chr4:67562328
|
C | T | 22 | a0001c0001t0001g0012a0001c0001t0001g0257a0001c0001t0001g0260others(19): Show | 23 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.120+3399C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562328 | ||||||
| chr4:67562365
|
GCTGT | G | 4 | a0001c0001t0001g0198a0001c0001t0002g0053a0001c0001t0002g0054others(1): Show | 4 | HG01884.hp1 NA18948.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+3439_120+3442d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562365 | |||||
| chr4:67562485
|
G | A | 1 | a0001c0002t0002g0309 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.120+3556G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562485 | ||||||
| chr4:67562493
|
T | C | 2 | a0001c0003t0001g0278a0001c0003t0001g0288 | 2 | HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.120+3564T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562493 | ||||||
| chr4:67562571
|
C | T | 3 | a0001c0001t0002g0242a0001c0001t0003g0240a0001c0001t0004g0239 | 3 | HG02280.hp1 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.120+3642C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562571 | ||||||
| chr4:67562574
|
G | C | 197 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(194): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.120+3645G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562574 | ||||||
| chr4:67562601
|
T | TA | 164 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(161): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.120+3693dupA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562601 | |||||
| chr4:67562601
|
T | TAA | 6 | a0001c0001t0001g0206a0001c0001t0002g0242a0001c0001t0003g0262others(3): Show | 6 | HG00735.hp1 HG01496.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.120+3692_120+3693d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562601 | |||||
| chr4:67562601
|
T | TAAAA | 13 | a0001c0001t0001g0012a0001c0001t0001g0297a0001c0001t0001g0298others(10): Show | 14 | HG00735.hp2 HG01071.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.120+3690_120+3693d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562601 | |||||
| chr4:67562601
|
TA | T | 7 | a0001c0001t0001g0143a0001c0001t0002g0051a0001c0001t0002g0052others(4): Show | 7 | HG01167.hp2 HG02015.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+3693delA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67562601 | |||||
| chr4:67562665
|
A | G | 1 | a0001c0001t0002g0023 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.120+3736A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562665 | ||||||
| chr4:67562708
|
C | T | 1 | a0001c0002t0001g0335 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.120+3779C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562708 | ||||||
| chr4:67562710
|
T | C | 1 | a0001c0002t0001g0335 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.120+3781T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562710 | ||||||
| chr4:67562720
|
G | C | 1 | a0001c0001t0001g0014 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.120+3791G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562720 | ||||||
| chr4:67562761
|
G | A | 15 | a0001c0002t0001g0149a0001c0002t0001g0153a0001c0002t0001g0156others(12): Show | 15 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+3832G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562761 | ||||||
| chr4:67562765
|
C | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0263 | 2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.120+3836C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562765 | ||||||
| chr4:67562918
|
C | G | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.120+3989C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67562918 | ||||||
| chr4:67563015
|
G | T | 199 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(196): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.120+4086G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563015 | ||||||
| chr4:67563108
|
C | A | 1 | a0001c0001t0002g0207 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.120+4179C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563108 | ||||||
| chr4:67563190
|
G | A | 1 | a0001c0002t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.120+4261G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563190 | ||||||
| chr4:67563262
|
G | T | 65 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 67 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.120+4333G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563262 | ||||||
| chr4:67563331
|
C | A | 218 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(215): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.120+4402C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563331 | ||||||
| chr4:67563527
|
G | A | 1 | a0001c0002t0002g0179 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.120+4598G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563527 | ||||||
| chr4:67563590
|
G | C | 218 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(215): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.120+4661G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563590 | ||||||
| chr4:67563596
|
G | A | 1 | a0001c0002t0001g0244 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.120+4667G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563596 | ||||||
| chr4:67563690
|
G | A | 4 | a0001c0001t0001g0269a0001c0001t0003g0240a0001c0001t0003g0270others(1): Show | 4 | HG02280.hp1 HG02965.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+4761G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563690 | ||||||
| chr4:67563818
|
G | A | 1 | a0001c0001t0003g0050 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.120+4889G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563818 | ||||||
| chr4:67563844
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.120+4915A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563844 | ||||||
| chr4:67563873
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.120+4944G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563873 | ||||||
| chr4:67563939
|
TA | T | 168 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(165): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.120+5025delA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67563939 | |||||
| chr4:67563939
|
TAA | T | 11 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0260others(8): Show | 11 | HG00733.hp2 HG01167.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.120+5024_120+5025d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67563939 | |||||
| chr4:67563962
|
G | A | 2 | a0001c0001t0007g0174a0001c0001t0007g0175 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.120+5033G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67563962 | ||||||
| chr4:67564130
|
C | T | 34 | a0001c0002t0001g0009a0001c0002t0001g0244a0001c0002t0001g0245others(31): Show | 36 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.120+5201C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564130 | ||||||
| chr4:67564147
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.120+5218A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564147 | ||||||
| chr4:67564405
|
C | T | 178 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(175): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.120+5476C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564405 | ||||||
| chr4:67564467
|
T | G | 1 | a0001c0001t0001g0343 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.120+5538T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564467 | ||||||
| chr4:67564518
|
G | A | 1 | a0001c0002t0001g0180 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.120+5589G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564518 | ||||||
| chr4:67564668
|
T | C | 2 | a0001c0001t0002g0060a0001c0001t0002g0061 | 2 | NA18959.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.120+5739T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564668 | ||||||
| chr4:67564683
|
C | T | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.120+5754C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564683 | ||||||
| chr4:67564733
|
T | C | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.120+5804T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564733 | ||||||
| chr4:67564774
|
A | G | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.120+5845A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564774 | ||||||
| chr4:67564892
|
C | T | 178 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(175): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.120+5963C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564892 | ||||||
| chr4:67564944
|
A | G | 3 | a0001c0002t0001g0009a0001c0002t0001g0244a0001c0002t0001g0245 | 4 | HG02559.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+6015A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564944 | ||||||
| chr4:67564979
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.120+6050C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67564979 | ||||||
| chr4:67565290
|
T | G | 2 | a0001c0001t0001g0198a0001c0001t0003g0197 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.121-5794T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67565290 | ||||||
| chr4:67565322
|
T | C | 1 | a0001c0001t0002g0056 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.121-5762T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67565322 | ||||||
| chr4:67565323
|
C | T | 1 | a0001c0001t0002g0056 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.121-5761C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67565323 | ||||||
| chr4:67565324
|
T | C | 1 | a0001c0001t0002g0056 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.121-5760T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67565324 | ||||||
| chr4:67565412
|
A | G | 22 | a0001c0001t0001g0012a0001c0001t0001g0257a0001c0001t0001g0260others(19): Show | 23 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.121-5672A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67565412 | ||||||
| chr4:67565725
|
T | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.121-5359T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67565725 | ||||||
| chr4:67565740
|
C | G | 2 | a0001c0001t0001g0297a0001c0001t0001g0307 | 2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.121-5344C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67565740 | ||||||
| chr4:67565934
|
C | CT | 57 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0048others(54): Show | 58 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.121-5120dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67565934 | |||||
| chr4:67565934
|
CT | C | 42 | a0001c0001t0001g0012a0001c0001t0001g0065a0001c0001t0001g0066others(39): Show | 46 | HG00544.hp2 HG00673.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.121-5120delT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67565934 | |||||
| chr4:67565934
|
CTT | C | 15 | a0001c0001t0001g0204a0001c0001t0001g0263a0001c0001t0003g0240others(12): Show | 15 | HG00621.hp1 HG01109.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.121-5121_121-5120d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67565934 | |||||
| chr4:67565934
|
CTTT | C | 70 | a0001c0001t0001g0064a0001c0001t0001g0198a0001c0001t0001g0248others(67): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(75): Show |
intron_variant | MODIFIER | c.121-5122_121-5120d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67565934 | |||||
| chr4:67566035
|
G | A | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.121-5049G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566035 | ||||||
| chr4:67566047
|
C | A | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.121-5037C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566047 | ||||||
| chr4:67566102
|
C | T | 10 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(7): Show | 10 | HG00423.hp1 HG02071.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.121-4982C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566102 | ||||||
| chr4:67566120
|
A | G | 2 | a0001c0001t0001g0198a0001c0001t0003g0197 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.121-4964A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566120 | ||||||
| chr4:67566217
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.121-4867C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566217 | ||||||
| chr4:67566490
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.121-4594C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566490 | ||||||
| chr4:67566498
|
G | A | 31 | a0001c0002t0001g0009a0001c0002t0001g0244a0001c0002t0001g0245others(28): Show | 33 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.121-4586G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566498 | ||||||
| chr4:67566776
|
C | A | 1 | a0001c0001t0003g0067 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.121-4308C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566776 | ||||||
| chr4:67566799
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.121-4285G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67566799 | ||||||
| chr4:67567088
|
A | G | 93 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(90): Show | 96 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.121-3996A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67567088 | ||||||
| chr4:67567167
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.121-3917G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67567167 | ||||||
| chr4:67567257
|
T | G | 1 | a0001c0001t0002g0116 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.121-3827T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67567257 | ||||||
| chr4:67567266
|
C | T | 5 | a0001c0001t0001g0204a0001c0001t0001g0248a0001c0001t0001g0263others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-3818C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67567266 | ||||||
| chr4:67567367
|
C | CT | 25 | a0001c0002t0001g0009a0001c0002t0001g0137a0001c0002t0001g0176others(22): Show | 26 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.121-3716dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67567367 | |||||
| chr4:67567368
|
T | TG | 85 | a0001c0001t0001g0198a0001c0001t0001g0204a0001c0001t0001g0248others(82): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.121-3710dupG | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67567368 | |||||
| chr4:67567765
|
G | C | 52 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0031others(49): Show | 56 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.121-3319G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67567765 | ||||||
| chr4:67567894
|
C | T | 109 | a0001c0001t0001g0198a0001c0001t0001g0204a0001c0001t0001g0248others(106): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.121-3190C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67567894 | ||||||
| chr4:67567895
|
G | A | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.121-3189G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67567895 | ||||||
| chr4:67568136
|
T | C | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.121-2948T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568136 | ||||||
| chr4:67568137
|
C | T | 111 | a0001c0001t0001g0198a0001c0001t0001g0204a0001c0001t0001g0248others(108): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.121-2947C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568137 | ||||||
| chr4:67568221
|
T | C | 41 | a0001c0001t0002g0329a0001c0002t0001g0004a0001c0002t0001g0005others(38): Show | 47 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.121-2863T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568221 | ||||||
| chr4:67568243
|
A | G | 1 | a0001c0001t0002g0019 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.121-2841A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568243 | ||||||
| chr4:67568301
|
T | C | 124 | a0001c0001t0001g0198a0001c0001t0001g0204a0001c0001t0001g0248others(121): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.121-2783T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568301 | ||||||
| chr4:67568310
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.121-2774C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568310 | ||||||
| chr4:67568376
|
A | C | 15 | a0001c0002t0001g0149a0001c0002t0001g0153a0001c0002t0001g0156others(12): Show | 15 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.121-2708A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568376 | ||||||
| chr4:67568450
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.121-2634C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568450 | ||||||
| chr4:67568508
|
T | A | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.121-2576T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568508 | ||||||
| chr4:67568517
|
A | G | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.121-2567A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568517 | ||||||
| chr4:67568532
|
A | C | 1 | a0001c0002t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.121-2552A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568532 | ||||||
| chr4:67568579
|
T | C | 3 | a0001c0001t0005g0069a0001c0001t0005g0070a0001c0001t0005g0267 | 3 | NA18959.hp2 NA18987.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.121-2505T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568579 | ||||||
| chr4:67568744
|
C | T | 126 | a0001c0001t0001g0198a0001c0001t0001g0204a0001c0001t0001g0248others(123): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.121-2340C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568744 | ||||||
| chr4:67568754
|
G | A | 126 | a0001c0001t0001g0198a0001c0001t0001g0204a0001c0001t0001g0248others(123): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.121-2330G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568754 | ||||||
| chr4:67568880
|
C | T | 4 | a0001c0003t0001g0011a0001c0003t0001g0272a0001c0003t0002g0287others(1): Show | 5 | HG01123.hp1 HG01361.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-2204C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568880 | ||||||
| chr4:67568952
|
A | G | 2 | a0001c0001t0007g0174a0001c0001t0007g0175 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.121-2132A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67568952 | ||||||
| chr4:67569011
|
A | T | 1 | a0001c0001t0001g0122 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.121-2073A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67569011 | ||||||
| chr4:67569045
|
C | T | 1 | a0001c0002t0001g0152 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.121-2039C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67569045 | ||||||
| chr4:67569058
|
T | C | 4 | a0001c0002t0001g0176a0001c0002t0001g0181a0001c0002t0001g0182others(1): Show | 4 | HG01243.hp1 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-2026T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67569058 | ||||||
| chr4:67569326
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.121-1758G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67569326 | ||||||
| chr4:67569480
|
CTTGT | C | 42 | a0001c0001t0002g0329a0001c0002t0001g0004a0001c0002t0001g0005others(39): Show | 48 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.121-1601_121-1598d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67569480 | |||||
| chr4:67569677
|
C | T | 1 | a0001c0001t0002g0233 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.121-1407C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67569677 | ||||||
| chr4:67569732
|
T | TTG | 35 | a0001c0002t0001g0137a0001c0002t0001g0149a0001c0002t0001g0153others(32): Show | 35 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.121-1337_121-1336d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67569732 | |||||
| chr4:67569761
|
G | C | 5 | a0001c0001t0001g0204a0001c0001t0001g0248a0001c0001t0001g0263others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-1323G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67569761 | ||||||
| chr4:67569974
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.121-1110G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67569974 | ||||||
| chr4:67570010
|
G | A | 124 | a0001c0001t0001g0198a0001c0001t0001g0204a0001c0001t0001g0248others(121): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.121-1074G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570010 | ||||||
| chr4:67570138
|
T | A | 218 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(215): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.121-946T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570138 | ||||||
| chr4:67570254
|
T | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.121-830T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570254 | ||||||
| chr4:67570262
|
G | A | 1 | a0001c0002t0001g0330 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.121-822G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570262 | ||||||
| chr4:67570295
|
C | T | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.121-789C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570295 | ||||||
| chr4:67570526
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.121-558G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570526 | ||||||
| chr4:67570576
|
T | G | 4 | a0001c0001t0007g0174a0001c0001t0007g0175a0001c0002t0001g0152others(1): Show | 4 | HG00733.hp2 HG02735.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-508T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570576 | ||||||
| chr4:67570608
|
G | A | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.121-476G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570608 | ||||||
| chr4:67570665
|
A | G | 37 | a0001c0002t0001g0137a0001c0002t0001g0149a0001c0002t0001g0153others(34): Show | 37 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.121-419A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570665 | ||||||
| chr4:67570691
|
GGAAA | G | 65 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 67 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.121-378_121-375del others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67570691 | |||||
| chr4:67570711
|
A | AAAGG | 5 | a0001c0001t0001g0257a0001c0001t0001g0260a0001c0001t0002g0259others(2): Show | 5 | HG02615.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-356_121-353dup others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 67570711 | |||||
| chr4:67570785
|
C | T | 31 | a0001c0002t0001g0009a0001c0002t0001g0244a0001c0002t0001g0245others(28): Show | 33 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.121-299C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570785 | ||||||
| chr4:67570836
|
A | G | 1 | a0001c0002t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.121-248A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570836 | ||||||
| chr4:67570858
|
T | C | 104 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(101): Show | 107 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.121-226T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570858 | ||||||
| chr4:67570921
|
A | G | 2 | a0001c0003t0003g0294a0001c0003t0003g0295 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.121-163A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570921 | ||||||
| chr4:67570978
|
C | T | 1 | a0001c0002t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.121-106C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 1/8 | chr4 | 67570978 | ||||||
| chr4:67571165
|
T | C | 219 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(216): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.192+10T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571165 | ||||||
| chr4:67571257
|
T | C | 1 | a0001c0002t0001g0190 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.192+102T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571257 | ||||||
| chr4:67571302
|
C | T | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.192+147C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571302 | ||||||
| chr4:67571415
|
T | G | 53 | a0001c0002t0001g0009a0001c0002t0001g0137a0001c0002t0001g0176others(50): Show | 55 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.192+260T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571415 | ||||||
| chr4:67571509
|
C | T | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.192+354C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571509 | ||||||
| chr4:67571533
|
C | T | 112 | a0001c0001t0002g0329a0001c0002t0001g0004a0001c0002t0001g0005others(109): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.192+378C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571533 | ||||||
| chr4:67571629
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.192+474G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571629 | ||||||
| chr4:67571918
|
T | G | 1 | a0001c0002t0004g0154 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.192+763T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571918 | ||||||
| chr4:67571979
|
G | A | 210 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(207): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.192+824G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67571979 | ||||||
| chr4:67572118
|
T | A | 1 | a0001c0002t0003g0155 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.192+963T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572118 | ||||||
| chr4:67572135
|
A | G | 26 | a0001c0003t0001g0011a0001c0003t0001g0272a0001c0003t0001g0278others(23): Show | 27 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.192+980A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572135 | ||||||
| chr4:67572414
|
G | A | 3 | a0001c0002t0001g0009a0001c0002t0001g0244a0001c0002t0001g0245 | 4 | HG02559.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+1259G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572414 | ||||||
| chr4:67572530
|
C | T | 22 | a0001c0001t0001g0012a0001c0001t0001g0257a0001c0001t0001g0260others(19): Show | 23 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.192+1375C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572530 | ||||||
| chr4:67572673
|
T | A | 1 | a0001c0002t0002g0160 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.192+1518T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572673 | ||||||
| chr4:67572756
|
C | A | 1 | a0001c0001t0001g0211 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.192+1601C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572756 | ||||||
| chr4:67572770
|
G | A | 1 | a0001c0001t0004g0239 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.192+1615G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572770 | ||||||
| chr4:67572786
|
G | T | 219 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(216): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.192+1631G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572786 | ||||||
| chr4:67572997
|
TAA | T | 4 | a0001c0001t0001g0049a0001c0001t0003g0026a0001c0001t0003g0043others(1): Show | 4 | NA18987.hp1 NA18995.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+1843_192+1844d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67572997 | ||||||
| chr4:67573116
|
C | A | 1 | a0001c0001t0001g0040 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.192+1961C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67573116 | ||||||
| chr4:67573200
|
G | C | 1 | a0001c0003t0001g0338 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.192+2045G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67573200 | ||||||
| chr4:67573640
|
A | G | 1 | a0001c0003t0001g0356 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.193-1745A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67573640 | ||||||
| chr4:67573652
|
G | A | 1 | a0004c0007t0002g0212 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.193-1733G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67573652 | ||||||
| chr4:67574038
|
G | A | 3 | a0001c0002t0001g0180a0001c0002t0001g0183a0001c0002t0001g0192 | 3 | HG01515.hp1 HG01517.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.193-1347G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574038 | ||||||
| chr4:67574056
|
T | G | 2 | a0001c0001t0007g0174a0001c0001t0007g0175 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.193-1329T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574056 | ||||||
| chr4:67574365
|
T | C | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.193-1020T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574365 | ||||||
| chr4:67574476
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.193-909G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574476 | ||||||
| chr4:67574533
|
C | G | 1 | a0001c0001t0001g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.193-852C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574533 | ||||||
| chr4:67574616
|
T | A | 1 | a0001c0001t0001g0169 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.193-769T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574616 | ||||||
| chr4:67574625
|
T | A | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.193-760T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574625 | ||||||
| chr4:67574653
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.193-732G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574653 | ||||||
| chr4:67574909
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.193-476T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67574909 | ||||||
| chr4:67575215
|
G | C | 55 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0044others(52): Show | 64 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.193-170G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67575215 | ||||||
| chr4:67575244
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0003g0197 | 2 | HG01884.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.193-141G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67575244 | ||||||
| chr4:67575373
|
T | C | 41 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0013others(38): Show | 47 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.193-12T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 2/8 | chr4 | 67575373 | ||||||
| chr4:67575582
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.306+84T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67575582 | ||||||
| chr4:67575713
|
T | C | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.306+215T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67575713 | ||||||
| chr4:67575799
|
C | T | 1 | a0001c0001t0009g0249 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.306+301C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67575799 | ||||||
| chr4:67575857
|
C | T | 96 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(93): Show | 99 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.306+359C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67575857 | ||||||
| chr4:67575865
|
T | C | 41 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0013others(38): Show | 47 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.306+367T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67575865 | ||||||
| chr4:67575974
|
A | G | 1 | a0001c0001t0002g0207 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.306+476A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67575974 | ||||||
| chr4:67576109
|
C | A | 1 | a0001c0001t0002g0237 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.306+611C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576109 | ||||||
| chr4:67576136
|
G | A | 1 | a0001c0001t0003g0067 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.306+638G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576136 | ||||||
| chr4:67576229
|
C | G | 118 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0002t0001g0004others(115): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.306+731C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576229 | ||||||
| chr4:67576424
|
T | C | 41 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0013others(38): Show | 47 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.307-779T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576424 | ||||||
| chr4:67576610
|
A | G | 4 | a0001c0001t0001g0099a0001c0001t0002g0097a0001c0001t0002g0098others(1): Show | 4 | NA18960.hp2 NA18992.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-593A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576610 | ||||||
| chr4:67576757
|
G | C | 1 | a0001c0001t0004g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.307-446G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576757 | ||||||
| chr4:67576770
|
A | G | 2 | a0001c0002t0002g0160a0001c0002t0002g0161 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.307-433A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576770 | ||||||
| chr4:67576878
|
G | A | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.307-325G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576878 | ||||||
| chr4:67576912
|
A | T | 114 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0009others(111): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.307-291A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67576912 | ||||||
| chr4:67577036
|
C | T | 40 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0013others(37): Show | 46 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.307-167C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 3/8 | chr4 | 67577036 | ||||||
| chr4:67577546
|
G | A | 1 | a0001c0001t0001g0031 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.363+287G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577546 | ||||||
| chr4:67577590
|
T | G | 96 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(93): Show | 99 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.363+331T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577590 | ||||||
| chr4:67577635
|
T | TTTTC | 71 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(68): Show | 73 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.363+392_363+395dup others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 67577635 | |||||
| chr4:67577650
|
TC | T | 67 | a0001c0002t0001g0009a0001c0002t0001g0137a0001c0002t0001g0149others(64): Show | 69 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.363+392delC | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577650 | ||||||
| chr4:67577651
|
C | CTTTCT | 23 | a0001c0001t0001g0012a0001c0001t0001g0198a0001c0001t0001g0206others(20): Show | 24 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.363+395_363+396ins others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 67577651 | |||||
| chr4:67577651
|
C | T | 48 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0013others(45): Show | 54 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.363+392C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577651 | ||||||
| chr4:67577653
|
T | C | 48 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0013others(45): Show | 54 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.363+394T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577653 | ||||||
| chr4:67577654
|
T | C | 67 | a0001c0002t0001g0009a0001c0002t0001g0137a0001c0002t0001g0149others(64): Show | 69 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.363+395T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577654 | ||||||
| chr4:67577779
|
G | C | 2 | a0001c0001t0001g0100a0001c0001t0003g0131 | 2 | HG02559.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.363+520G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577779 | ||||||
| chr4:67577853
|
T | G | 2 | a0001c0001t0002g0242a0001c0001t0004g0239 | 2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.363+594T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67577853 | ||||||
| chr4:67578023
|
C | T | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.363+764C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578023 | ||||||
| chr4:67578230
|
T | C | 1 | a0001c0001t0001g0353 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.363+971T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578230 | ||||||
| chr4:67578233
|
C | T | 5 | a0001c0002t0001g0274a0001c0002t0001g0275a0001c0002t0001g0276others(2): Show | 5 | HG00621.hp1 NA18942.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+974C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578233 | ||||||
| chr4:67578384
|
C | A | 28 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(25): Show | 28 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(25): Show |
intron_variant | MODIFIER | c.363+1125C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578384 | ||||||
| chr4:67578462
|
G | A | 97 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(94): Show | 100 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.363+1203G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578462 | ||||||
| chr4:67578474
|
G | A | 30 | a0001c0002t0004g0336a0001c0002t0004g0337a0001c0003t0001g0011others(27): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.363+1215G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578474 | ||||||
| chr4:67578513
|
T | C | 2 | a0001c0001t0001g0269a0001c0001t0003g0270 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.363+1254T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578513 | ||||||
| chr4:67578539
|
G | A | 211 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(208): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.363+1280G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578539 | ||||||
| chr4:67578584
|
T | C | 38 | a0001c0002t0001g0137a0001c0002t0001g0149a0001c0002t0001g0153others(35): Show | 38 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.363+1325T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578584 | ||||||
| chr4:67578702
|
G | C | 1 | a0001c0003t0001g0280 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.363+1443G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578702 | ||||||
| chr4:67578741
|
T | G | 2 | a0001c0001t0007g0174a0001c0001t0007g0175 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.363+1482T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578741 | ||||||
| chr4:67578830
|
A | AT | 96 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(93): Show | 99 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.363+1587dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 67578830 | |||||
| chr4:67578830
|
AT | A | 96 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0009others(93): Show | 103 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.363+1587delT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 67578830 | |||||
| chr4:67578880
|
G | A | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0303 | 3 | HG01167.hp1 HG01169.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.363+1621G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578880 | ||||||
| chr4:67578975
|
C | T | 8 | a0001c0001t0002g0008a0001c0001t0002g0210a0001c0001t0002g0222others(5): Show | 9 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.363+1716C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578975 | ||||||
| chr4:67578989
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 3 | HG01952.hp2 HG01981.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.363+1730C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67578989 | ||||||
| chr4:67579145
|
C | T | 4 | a0001c0002t0001g0188a0001c0002t0001g0189a0001c0002t0001g0194others(1): Show | 4 | NA18944.hp1 NA18971.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1886C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67579145 | ||||||
| chr4:67579422
|
T | A | 1 | a0001c0002t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.364-1883T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67579422 | ||||||
| chr4:67579559
|
T | G | 97 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(94): Show | 100 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.364-1746T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67579559 | ||||||
| chr4:67579584
|
A | G | 1 | a0001c0002t0003g0163 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.364-1721A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67579584 | ||||||
| chr4:67579989
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.364-1316C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67579989 | ||||||
| chr4:67580191
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.364-1114G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580191 | ||||||
| chr4:67580277
|
C | T | 100 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0009others(97): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.364-1028C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580277 | ||||||
| chr4:67580311
|
T | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0263a0001c0001t0003g0235 | 3 | HG01891.hp2 HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.364-994T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580311 | ||||||
| chr4:67580405
|
C | T | 5 | a0001c0003t0001g0284a0001c0003t0001g0285a0001c0003t0001g0286others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-900C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580405 | ||||||
| chr4:67580584
|
G | C | 39 | a0001c0002t0001g0137a0001c0002t0001g0149a0001c0002t0001g0153others(36): Show | 39 | HG00544.hp2 HG01106.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.364-721G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580584 | ||||||
| chr4:67580594
|
C | T | 30 | a0001c0003t0001g0011a0001c0003t0001g0159a0001c0003t0001g0272others(27): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.364-711C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580594 | ||||||
| chr4:67580619
|
C | A | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0009others(72): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.364-686C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580619 | ||||||
| chr4:67580703
|
T | C | 67 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 69 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.364-602T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580703 | ||||||
| chr4:67580827
|
T | G | 220 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(217): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.364-478T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580827 | ||||||
| chr4:67580831
|
C | A | 2 | a0001c0002t0002g0160a0001c0002t0002g0161 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.364-474C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580831 | ||||||
| chr4:67580908
|
T | A | 174 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(171): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.364-397T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580908 | ||||||
| chr4:67580970
|
G | A | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0303 | 3 | HG01167.hp1 HG01169.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.364-335G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67580970 | ||||||
| chr4:67581041
|
G | C | 3 | a0001c0003t0001g0280a0001c0003t0001g0281a0001c0003t0001g0282 | 3 | HG03017.hp2 HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.364-264G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67581041 | ||||||
| chr4:67581042
|
G | A | 5 | a0001c0003t0001g0284a0001c0003t0001g0285a0001c0003t0001g0286others(2): Show | 5 | HG02630.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-263G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 4/8 | chr4 | 67581042 | ||||||
| chr4:67581482
|
A | G | 83 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0009others(80): Show | 90 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.530+11A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581482 | ||||||
| chr4:67581512
|
A | G | 1 | a0001c0003t0002g0293 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.530+41A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581512 | ||||||
| chr4:67581531
|
A | G | 71 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(68): Show | 73 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.530+60A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581531 | ||||||
| chr4:67581539
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0009g0249 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.530+68G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581539 | ||||||
| chr4:67581634
|
A | G | 220 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(217): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.530+163A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581634 | ||||||
| chr4:67581667
|
C | G | 1 | a0001c0001t0004g0268 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.530+196C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581667 | ||||||
| chr4:67581691
|
C | T | 2 | a0001c0003t0003g0294a0001c0003t0003g0295 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.530+220C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581691 | ||||||
| chr4:67581716
|
T | G | 32 | a0001c0002t0004g0336a0001c0002t0004g0337a0001c0003t0001g0011others(29): Show | 33 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.530+245T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581716 | ||||||
| chr4:67581777
|
T | G | 2 | a0001c0002t0004g0336a0001c0002t0004g0337 | 2 | HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.530+306T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581777 | ||||||
| chr4:67581927
|
A | C | 1 | a0001c0001t0002g0096 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.530+456A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581927 | ||||||
| chr4:67581958
|
T | C | 2 | a0001c0001t0002g0030a0001c0001t0002g0036 | 2 | NA19009.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.530+487T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67581958 | ||||||
| chr4:67582229
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.530+758T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582229 | ||||||
| chr4:67582272
|
G | A | 217 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(214): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.530+801G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582272 | ||||||
| chr4:67582303
|
T | G | 1 | a0001c0001t0005g0069 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.530+832T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582303 | ||||||
| chr4:67582311
|
T | TTG | 94 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(91): Show | 97 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.530+840_530+841ins others(2): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582311 | ||||||
| chr4:67582312
|
G | T | 96 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(93): Show | 99 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.530+841G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582312 | ||||||
| chr4:67582321
|
G | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0263a0001c0001t0003g0235 | 3 | HG01891.hp2 HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.530+850G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582321 | ||||||
| chr4:67582459
|
C | G | 97 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(94): Show | 100 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.530+988C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582459 | ||||||
| chr4:67582555
|
G | A | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.531-1019G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582555 | ||||||
| chr4:67582630
|
G | GT | 161 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(158): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.531-933dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 67582630 | |||||
| chr4:67582656
|
A | G | 97 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(94): Show | 100 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.531-918A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582656 | ||||||
| chr4:67582785
|
C | A | 3 | a0001c0001t0001g0198a0001c0001t0003g0197a0001c0001t0003g0240 | 3 | HG01884.hp1 HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.531-789C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582785 | ||||||
| chr4:67582883
|
A | G | 66 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0009others(63): Show | 73 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.531-691A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582883 | ||||||
| chr4:67582908
|
A | G | 3 | a0001c0001t0001g0198a0001c0001t0003g0197a0001c0001t0003g0240 | 3 | HG01884.hp1 HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.531-666A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67582908 | ||||||
| chr4:67583108
|
A | G | 2 | a0001c0003t0001g0288a0001c0003t0001g0292 | 2 | HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.531-466A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67583108 | ||||||
| chr4:67583199
|
G | A | 1 | a0001c0001t0004g0239 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.531-375G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67583199 | ||||||
| chr4:67583389
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.531-185A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67583389 | ||||||
| chr4:67583546
|
A | G | 2 | a0001c0001t0007g0174a0001c0001t0007g0175 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.531-28A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | chr4 | 67583546 | ||||||
| chr4:67583551
|
G | GT | 26 | a0001c0002t0001g0009a0001c0002t0001g0137a0001c0002t0001g0176others(23): Show | 27 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.531-16dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 67583551 | |||||
| chr4:67583830
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.659+128G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67583830 | ||||||
| chr4:67583873
|
C | T | 1 | a0001c0003t0003g0349 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.659+171C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67583873 | ||||||
| chr4:67583923
|
C | T | 1 | a0001c0001t0002g0055 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.659+221C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67583923 | ||||||
| chr4:67583993
|
G | A | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.659+291G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67583993 | ||||||
| chr4:67584098
|
G | GA | 156 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(153): Show | 170 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.659+414dupA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67584098 | |||||
| chr4:67584098
|
GAA | G | 94 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(91): Show | 97 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.659+413_659+414del others(2): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67584098 | |||||
| chr4:67584116
|
A | AAAAT | 38 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0013others(35): Show | 44 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.659+414_659+415ins others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584116 | ||||||
| chr4:67584116
|
A | AAAT | 31 | a0001c0002t0001g0009a0001c0002t0001g0176a0001c0002t0001g0181others(28): Show | 32 | HG00642.hp2 HG00735.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.659+414_659+415ins others(3): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584116 | ||||||
| chr4:67584116
|
A | AAT | 29 | a0001c0002t0001g0137a0001c0002t0001g0177a0001c0002t0001g0178others(26): Show | 30 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.659+414_659+415ins others(2): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584116 | ||||||
| chr4:67584116
|
A | T | 97 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(94): Show | 100 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.659+414A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584116 | ||||||
| chr4:67584306
|
G | A | 1 | a0001c0001t0002g0097 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.659+604G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584306 | ||||||
| chr4:67584325
|
A | G | 1 | a0001c0003t0001g0292 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.659+623A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584325 | ||||||
| chr4:67584510
|
C | G | 1 | a0001c0002t0001g0189 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.659+808C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584510 | ||||||
| chr4:67584517
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.659+815A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584517 | ||||||
| chr4:67584584
|
C | T | 76 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0009others(73): Show | 84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.659+882C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584584 | ||||||
| chr4:67584654
|
A | T | 1 | a0001c0001t0002g0230 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.659+952A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584654 | ||||||
| chr4:67584688
|
TAGA | T | 71 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(68): Show | 73 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.659+991_659+993del others(3): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67584688 | |||||
| chr4:67584693
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.659+991G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584693 | ||||||
| chr4:67584780
|
A | G | 1 | a0001c0002t0001g0326 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.659+1078A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584780 | ||||||
| chr4:67584876
|
C | T | 10 | a0001c0002t0001g0153a0001c0002t0001g0156a0001c0002t0001g0157others(7): Show | 10 | HG02572.hp1 HG02818.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.659+1174C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584876 | ||||||
| chr4:67584967
|
A | G | 2 | a0001c0002t0001g0152a0001c0002t0002g0151 | 2 | HG00733.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.659+1265A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67584967 | ||||||
| chr4:67585137
|
C | A | 1 | a0001c0001t0001g0072 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.659+1435C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585137 | ||||||
| chr4:67585150
|
G | A | 173 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(170): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.659+1448G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585150 | ||||||
| chr4:67585270
|
A | G | 173 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(170): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.659+1568A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585270 | ||||||
| chr4:67585276
|
A | G | 74 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0009others(71): Show | 82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.659+1574A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585276 | ||||||
| chr4:67585437
|
G | C | 1 | a0004c0007t0002g0212 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.659+1735G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585437 | ||||||
| chr4:67585658
|
T | C | 97 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0009others(94): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.659+1956T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585658 | ||||||
| chr4:67585881
|
A | T | 97 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0009others(94): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.659+2179A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585881 | ||||||
| chr4:67585916
|
C | T | 99 | a0001c0001t0007g0174a0001c0001t0007g0175a0001c0002t0001g0004others(96): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.659+2214C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67585916 | ||||||
| chr4:67586060
|
T | C | 1 | a0001c0001t0002g0087 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.659+2358T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586060 | ||||||
| chr4:67586091
|
C | A | 30 | a0001c0003t0001g0011a0001c0003t0001g0159a0001c0003t0001g0272others(27): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.659+2389C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586091 | ||||||
| chr4:67586093
|
T | A | 30 | a0001c0003t0001g0011a0001c0003t0001g0159a0001c0003t0001g0272others(27): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.659+2391T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586093 | ||||||
| chr4:67586106
|
C | T | 99 | a0001c0001t0007g0174a0001c0001t0007g0175a0001c0002t0001g0004others(96): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.659+2404C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586106 | ||||||
| chr4:67586237
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.659+2535T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586237 | ||||||
| chr4:67586364
|
G | A | 18 | a0001c0002t0001g0004a0001c0002t0001g0312a0001c0002t0001g0315others(15): Show | 21 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.659+2662G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586364 | ||||||
| chr4:67586527
|
G | A | 3 | a0001c0003t0001g0280a0001c0003t0001g0281a0001c0003t0001g0282 | 3 | HG03017.hp2 HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.659+2825G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586527 | ||||||
| chr4:67586586
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0057a0001c0001t0001g0058 | 3 | HG00544.hp1 NA18973.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.659+2884T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586586 | ||||||
| chr4:67586587
|
G | A | 99 | a0001c0001t0007g0174a0001c0001t0007g0175a0001c0002t0001g0004others(96): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.659+2885G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586587 | ||||||
| chr4:67586745
|
T | G | 99 | a0001c0001t0007g0174a0001c0001t0007g0175a0001c0002t0001g0004others(96): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.659+3043T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586745 | ||||||
| chr4:67586819
|
T | C | 2 | a0001c0001t0001g0269a0001c0001t0003g0270 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.659+3117T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586819 | ||||||
| chr4:67586842
|
C | T | 99 | a0001c0001t0007g0174a0001c0001t0007g0175a0001c0002t0001g0004others(96): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.659+3140C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67586842 | ||||||
| chr4:67587155
|
G | C | 30 | a0001c0003t0001g0011a0001c0003t0001g0159a0001c0003t0001g0272others(27): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.659+3453G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587155 | ||||||
| chr4:67587159
|
G | A | 2 | a0001c0002t0001g0327a0001c0002t0001g0331 | 2 | NA19079.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.659+3457G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587159 | ||||||
| chr4:67587218
|
C | CA | 3 | a0001c0001t0001g0204a0001c0001t0001g0263a0001c0001t0003g0235 | 3 | HG01891.hp2 HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.659+3520dupA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67587218 | |||||
| chr4:67587264
|
A | C | 1 | a0001c0001t0001g0066 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.659+3562A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587264 | ||||||
| chr4:67587441
|
T | C | 1 | a0001c0002t0004g0154 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.660-3443T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587441 | ||||||
| chr4:67587446
|
A | G | 67 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0009others(64): Show | 74 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.660-3438A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587446 | ||||||
| chr4:67587471
|
T | C | 99 | a0001c0001t0007g0174a0001c0001t0007g0175a0001c0002t0001g0004others(96): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.660-3413T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587471 | ||||||
| chr4:67587478
|
A | G | 2 | a0001c0001t0001g0269a0001c0001t0003g0270 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.660-3406A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587478 | ||||||
| chr4:67587616
|
G | A | 1 | a0001c0001t0002g0055 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.660-3268G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587616 | ||||||
| chr4:67587636
|
C | A | 99 | a0001c0001t0007g0174a0001c0001t0007g0175a0001c0002t0001g0004others(96): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.660-3248C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587636 | ||||||
| chr4:67587685
|
T | A | 1 | a0001c0001t0001g0138 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-3199T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587685 | ||||||
| chr4:67587719
|
CT | C | 80 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0044others(77): Show | 89 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.660-3147delT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67587719 | |||||
| chr4:67587719
|
CTTT | C | 62 | a0001c0001t0001g0012a0001c0001t0001g0257a0001c0001t0001g0260others(59): Show | 67 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.660-3149_660-3147d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67587719 | |||||
| chr4:67587719
|
CTTTT | C | 134 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(131): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.660-3150_660-3147d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67587719 | |||||
| chr4:67587781
|
C | T | 196 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(193): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.660-3103C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587781 | ||||||
| chr4:67587798
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.660-3086A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587798 | ||||||
| chr4:67587803
|
T | C | 99 | a0001c0001t0007g0174a0001c0001t0007g0175a0001c0002t0001g0004others(96): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.660-3081T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587803 | ||||||
| chr4:67587966
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.660-2918C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67587966 | ||||||
| chr4:67588039
|
T | TA | 119 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0028others(116): Show | 132 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.660-2819dupA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | |||||
| chr4:67588039
|
T | TAA | 21 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0045others(18): Show | 22 | HG00323.hp1 HG00733.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.660-2820_660-2819d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | |||||
| chr4:67588039
|
T | TAAAAA | 19 | a0001c0003t0001g0011a0001c0003t0001g0278a0001c0003t0001g0281others(16): Show | 20 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.660-2823_660-2819d others(7): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | |||||
| chr4:67588039
|
T | TAAAAAA | 10 | a0001c0003t0001g0159a0001c0003t0001g0272a0001c0003t0001g0284others(7): Show | 10 | HG00642.hp2 HG01106.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.660-2824_660-2819d others(8): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | |||||
| chr4:67588039
|
TA | T | 7 | a0001c0001t0001g0204a0001c0001t0003g0235a0001c0001t0009g0249others(4): Show | 7 | HG00544.hp2 HG01891.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.660-2819delA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | |||||
| chr4:67588039
|
TAA | T | 27 | a0001c0001t0001g0012a0001c0001t0001g0201a0001c0001t0001g0209others(24): Show | 28 | HG00733.hp2 HG01071.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.660-2820_660-2819d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | |||||
| chr4:67588039
|
TAAA | T | 101 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(98): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.660-2821_660-2819d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | |||||
| chr4:67588039
|
TAAAA | T | 11 | a0001c0001t0001g0200a0001c0001t0001g0226a0001c0001t0001g0253others(8): Show | 11 | HG01168.hp2 HG01256.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.660-2822_660-2819d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | |||||
| chr4:67588039
|
TAAAAAAA others(3): Show |
T | 2 | a0001c0001t0001g0085a0001c0001t0001g0138 | 2 | NA18972.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.660-2828_660-2819d others(12): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588039 | |||||
| chr4:67588083
|
T | C | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.660-2801T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588083 | ||||||
| chr4:67588101
|
A | T | 1 | a0001c0001t0001g0167 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.660-2783A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588101 | ||||||
| chr4:67588277
|
G | A | 180 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.660-2607G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588277 | ||||||
| chr4:67588341
|
A | AGAC | 99 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(96): Show | 102 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.660-2531_660-2529d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588341 | |||||
| chr4:67588353
|
C | CGAT | 30 | a0001c0001t0001g0204a0001c0001t0001g0248a0001c0001t0001g0263others(27): Show | 31 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.660-2509_660-2507d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588353 | |||||
| chr4:67588353
|
CGAT | C | 44 | a0001c0001t0001g0269a0001c0001t0002g0068a0001c0001t0003g0270others(41): Show | 50 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.660-2509_660-2507d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67588353 | |||||
| chr4:67588356
|
T | C | 35 | a0001c0001t0001g0040a0001c0001t0001g0059a0001c0001t0001g0253others(32): Show | 36 | HG00544.hp2 HG01106.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.660-2528T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588356 | ||||||
| chr4:67588359
|
T | C | 40 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0013others(37): Show | 46 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.660-2525T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588359 | ||||||
| chr4:67588391
|
T | G | 167 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(164): Show | 177 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.660-2493T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588391 | ||||||
| chr4:67588496
|
G | A | 1 | a0001c0001t0002g0018 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.660-2388G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588496 | ||||||
| chr4:67588534
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.660-2350C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588534 | ||||||
| chr4:67588630
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.660-2254C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588630 | ||||||
| chr4:67588691
|
G | A | 3 | a0001c0001t0001g0269a0001c0001t0003g0270a0001c0001t0004g0268 | 3 | HG02965.hp1 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.660-2193G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588691 | ||||||
| chr4:67588801
|
T | C | 19 | a0001c0001t0001g0012a0001c0001t0001g0064a0001c0001t0001g0088others(16): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.660-2083T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588801 | ||||||
| chr4:67588807
|
G | A | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.660-2077G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588807 | ||||||
| chr4:67588932
|
A | G | 354 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(351): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.660-1952A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588932 | ||||||
| chr4:67588991
|
C | A | 14 | a0001c0002t0001g0149a0001c0002t0001g0153a0001c0002t0001g0156others(11): Show | 14 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.660-1893C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67588991 | ||||||
| chr4:67589007
|
C | T | 2 | a0001c0002t0002g0179a0001c0002t0002g0186 | 2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.660-1877C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589007 | ||||||
| chr4:67589028
|
A | G | 2 | a0001c0002t0004g0336a0001c0002t0004g0337 | 2 | HG01167.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.660-1856A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589028 | ||||||
| chr4:67589095
|
C | T | 1 | a0001c0001t0002g0254 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.660-1789C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589095 | ||||||
| chr4:67589229
|
A | G | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.660-1655A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589229 | ||||||
| chr4:67589486
|
A | T | 1 | a0001c0001t0001g0138 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-1398A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589486 | ||||||
| chr4:67589538
|
T | G | 1 | a0001c0001t0001g0198 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.660-1346T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589538 | ||||||
| chr4:67589575
|
T | C | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.660-1309T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589575 | ||||||
| chr4:67589584
|
C | G | 97 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(94): Show | 100 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.660-1300C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589584 | ||||||
| chr4:67589682
|
G | T | 99 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(96): Show | 102 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.660-1202G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589682 | ||||||
| chr4:67589715
|
C | T | 1 | a0001c0002t0002g0316 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.660-1169C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589715 | ||||||
| chr4:67589809
|
A | AT | 40 | a0001c0001t0001g0135a0001c0001t0001g0206a0001c0001t0001g0211others(37): Show | 41 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.660-1062dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67589809 | |||||
| chr4:67589813
|
T | C | 1 | a0001c0002t0001g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.660-1071T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589813 | ||||||
| chr4:67589863
|
G | A | 1 | a0001c0001t0002g0237 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.660-1021G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589863 | ||||||
| chr4:67589879
|
A | C | 2 | a0001c0001t0007g0174a0001c0001t0007g0175 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.660-1005A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67589879 | ||||||
| chr4:67590102
|
T | A | 1 | a0001c0001t0001g0138 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-782T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590102 | ||||||
| chr4:67590103
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-781C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590103 | ||||||
| chr4:67590109
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-775C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590109 | ||||||
| chr4:67590111
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-773T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590111 | ||||||
| chr4:67590125
|
C | T | 2 | a0001c0001t0001g0269a0001c0001t0003g0270 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.660-759C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590125 | ||||||
| chr4:67590286
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.660-598T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590286 | ||||||
| chr4:67590338
|
C | G | 1 | a0001c0001t0002g0116 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.660-546C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590338 | ||||||
| chr4:67590356
|
C | T | 165 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(162): Show | 175 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.660-528C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590356 | ||||||
| chr4:67590426
|
G | A | 5 | a0001c0001t0001g0204a0001c0001t0001g0248a0001c0001t0001g0263others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.660-458G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590426 | ||||||
| chr4:67590438
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-446A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590438 | ||||||
| chr4:67590462
|
G | T | 2 | a0001c0001t0007g0174a0001c0001t0007g0175 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.660-422G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590462 | ||||||
| chr4:67590650
|
A | C | 1 | a0001c0001t0001g0138 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.660-234A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590650 | ||||||
| chr4:67590679
|
A | G | 2 | a0001c0001t0001g0269a0001c0001t0003g0270 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.660-205A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590679 | ||||||
| chr4:67590741
|
A | G | 3 | a0001c0001t0001g0198a0001c0001t0003g0197a0001c0001t0003g0240 | 3 | HG01884.hp1 HG02280.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.660-143A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590741 | ||||||
| chr4:67590745
|
A | AT | 19 | a0001c0001t0001g0084a0001c0001t0001g0112a0001c0001t0001g0121others(16): Show | 19 | HG00621.hp1 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.660-119dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67590745 | |||||
| chr4:67590745
|
A | ATT | 63 | a0001c0001t0001g0088a0001c0001t0001g0248a0001c0001t0001g0269others(60): Show | 70 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.660-120_660-119dup others(2): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67590745 | |||||
| chr4:67590745
|
A | ATTT | 28 | a0001c0001t0001g0012a0001c0001t0001g0064a0001c0001t0001g0257others(25): Show | 29 | HG01070.hp1 HG01071.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.660-121_660-119dup others(3): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67590745 | |||||
| chr4:67590745
|
A | ATTTT | 60 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(57): Show | 62 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.660-122_660-119dup others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67590745 | |||||
| chr4:67590745
|
A | ATTTTT | 13 | a0001c0001t0001g0206a0001c0001t0001g0211a0001c0001t0001g0215others(10): Show | 13 | HG00733.hp2 HG01358.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.660-123_660-119dup others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67590745 | |||||
| chr4:67590745
|
AT | A | 9 | a0001c0001t0001g0044a0001c0001t0001g0099a0001c0001t0001g0133others(6): Show | 9 | HG00438.hp2 HG00597.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.660-119delT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 67590745 | |||||
| chr4:67590801
|
A | G | 1 | a0001c0005t0001g0041 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.660-83A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590801 | ||||||
| chr4:67590840
|
C | A | 1 | a0001c0001t0001g0117 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.660-44C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 6/8 | chr4 | 67590840 | ||||||
| chr4:67591062
|
A | G | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.729+109A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591062 | ||||||
| chr4:67591277
|
A | C | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.729+324A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591277 | ||||||
| chr4:67591331
|
T | A | 162 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(159): Show | 172 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.729+378T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591331 | ||||||
| chr4:67591432
|
A | G | 1 | a0001c0003t0001g0290 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.729+479A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591432 | ||||||
| chr4:67591685
|
C | G | 102 | a0001c0001t0001g0012a0001c0001t0001g0083a0001c0001t0001g0084others(99): Show | 110 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.729+732C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591685 | ||||||
| chr4:67591793
|
C | A | 1 | a0001c0001t0001g0269 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.729+840C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591793 | ||||||
| chr4:67591847
|
A | G | 1 | a0001c0002t0001g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.729+894A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591847 | ||||||
| chr4:67591936
|
C | CT | 8 | a0001c0001t0001g0141a0001c0001t0002g0110a0001c0001t0004g0239others(5): Show | 8 | HG01167.hp2 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.729+984dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 67591936 | |||||
| chr4:67591977
|
A | G | 183 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0082others(180): Show | 192 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.729+1024A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67591977 | ||||||
| chr4:67592036
|
G | A | 3 | a0001c0001t0001g0204a0001c0001t0001g0263a0001c0001t0003g0235 | 3 | HG01891.hp2 HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.729+1083G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592036 | ||||||
| chr4:67592058
|
A | T | 17 | a0001c0002t0001g0013a0001c0002t0001g0152a0001c0002t0001g0323others(14): Show | 18 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.729+1105A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592058 | ||||||
| chr4:67592088
|
C | T | 8 | a0001c0001t0001g0248a0001c0001t0001g0257a0001c0001t0001g0260others(5): Show | 9 | HG02559.hp1 HG02615.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.729+1135C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592088 | ||||||
| chr4:67592113
|
T | G | 17 | a0001c0001t0001g0100a0001c0001t0001g0257a0001c0001t0001g0260others(14): Show | 17 | HG02572.hp1 HG02615.hp1 HG02818.hp1 others(14): Show |
intron_variant | MODIFIER | c.730-1147T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592113 | ||||||
| chr4:67592126
|
A | AT | 307 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(304): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.730-1123dupT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 67592126 | |||||
| chr4:67592126
|
A | ATT | 8 | a0001c0001t0001g0248a0001c0001t0001g0260a0001c0001t0002g0259others(5): Show | 9 | HG02559.hp1 HG02615.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.730-1124_730-1123d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 67592126 | |||||
| chr4:67592126
|
AT | A | 6 | a0001c0001t0001g0102a0001c0001t0002g0101a0001c0002t0002g0160others(3): Show | 6 | HG01167.hp2 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.730-1123delT | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 67592126 | |||||
| chr4:67592156
|
G | A | 86 | a0001c0001t0001g0012a0001c0001t0001g0090a0001c0001t0001g0125others(83): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.730-1104G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592156 | ||||||
| chr4:67592253
|
C | T | 5 | a0001c0001t0001g0204a0001c0001t0001g0263a0001c0001t0003g0235others(2): Show | 5 | HG01891.hp2 HG02055.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.730-1007C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592253 | ||||||
| chr4:67592286
|
G | T | 1 | a0001c0001t0002g0020 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.730-974G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592286 | ||||||
| chr4:67592335
|
T | C | 1 | a0001c0001t0002g0023 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.730-925T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592335 | ||||||
| chr4:67592401
|
G | A | 3 | a0001c0002t0001g0176a0001c0002t0001g0181a0001c0002t0001g0182 | 3 | HG02622.hp2 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.730-859G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592401 | ||||||
| chr4:67592401
|
G | C | 1 | a0001c0001t0001g0126 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.730-859G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592401 | ||||||
| chr4:67592478
|
A | G | 1 | a0001c0003t0002g0283 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.730-782A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592478 | ||||||
| chr4:67592570
|
C | T | 1 | a0001c0001t0002g0223 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.730-690C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592570 | ||||||
| chr4:67592692
|
T | C | 184 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0049others(181): Show | 199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.730-568T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592692 | ||||||
| chr4:67592725
|
C | A | 2 | a0001c0003t0003g0294a0001c0003t0003g0295 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.730-535C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592725 | ||||||
| chr4:67592774
|
C | T | 1 | a0001c0002t0001g0335 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.730-486C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592774 | ||||||
| chr4:67592865
|
G | A | 35 | a0001c0001t0001g0077a0001c0001t0001g0106a0001c0001t0001g0246others(32): Show | 37 | HG00639.hp2 HG01261.hp2 HG01358.hp2 others(34): Show |
intron_variant | MODIFIER | c.730-395G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592865 | ||||||
| chr4:67592920
|
A | G | 59 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0077others(56): Show | 64 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.730-340A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67592920 | ||||||
| chr4:67593090
|
G | A | 40 | a0001c0001t0001g0077a0001c0001t0001g0106a0001c0001t0001g0246others(37): Show | 42 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.730-170G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67593090 | ||||||
| chr4:67593219
|
G | C | 181 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0040others(178): Show | 198 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.730-41G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 7/8 | chr4 | 67593219 | ||||||
| chr4:67593472
|
T | C | 1 | a0001c0002t0001g0177 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.826+116T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67593472 | ||||||
| chr4:67593504
|
T | G | 1 | a0001c0002t0002g0355 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.826+148T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67593504 | ||||||
| chr4:67593727
|
C | T | 43 | a0001c0001t0001g0077a0001c0001t0001g0106a0001c0001t0001g0246others(40): Show | 45 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.826+371C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67593727 | ||||||
| chr4:67593798
|
T | C | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.826+442T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67593798 | ||||||
| chr4:67594015
|
T | C | 62 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0077others(59): Show | 67 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.826+659T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594015 | ||||||
| chr4:67594036
|
A | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0077others(61): Show | 69 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.826+680A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594036 | ||||||
| chr4:67594437
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.826+1081C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594437 | ||||||
| chr4:67594537
|
T | C | 62 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0077others(59): Show | 67 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.826+1181T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594537 | ||||||
| chr4:67594799
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.826+1443G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594799 | ||||||
| chr4:67594822
|
T | C | 62 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0077others(59): Show | 67 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.826+1466T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594822 | ||||||
| chr4:67594926
|
G | A | 3 | a0001c0001t0002g0242a0001c0001t0007g0174a0001c0001t0007g0175 | 3 | HG02818.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.826+1570G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594926 | ||||||
| chr4:67594950
|
A | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0062a0001c0001t0001g0063 | 3 | HG02895.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.826+1594A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67594950 | ||||||
| chr4:67595000
|
T | C | 62 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0077others(59): Show | 67 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.826+1644T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595000 | ||||||
| chr4:67595024
|
C | A | 20 | a0001c0001t0001g0077a0001c0001t0001g0246a0001c0001t0003g0010others(17): Show | 21 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.826+1668C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595024 | ||||||
| chr4:67595031
|
T | G | 2 | a0001c0001t0003g0108a0001c0001t0003g0216 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.826+1675T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595031 | ||||||
| chr4:67595149
|
C | T | 1 | a0001c0002t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.826+1793C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595149 | ||||||
| chr4:67595365
|
G | A | 62 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0077others(59): Show | 67 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.826+2009G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595365 | ||||||
| chr4:67595372
|
C | CA | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0028others(39): Show | 42 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.826+2045dupA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | |||||
| chr4:67595372
|
C | CAA | 8 | a0001c0001t0001g0074a0001c0001t0001g0124a0001c0001t0002g0019others(5): Show | 8 | HG00738.hp2 HG01361.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.826+2044_826+2045d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | |||||
| chr4:67595372
|
CA | C | 49 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0045others(46): Show | 51 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.826+2045delA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | |||||
| chr4:67595372
|
CAA | C | 12 | a0001c0001t0001g0169a0001c0001t0001g0171a0001c0001t0001g0299others(9): Show | 12 | HG01169.hp1 HG02132.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.826+2044_826+2045d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | |||||
| chr4:67595372
|
CAAA | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0077others(31): Show | 38 | HG00408.hp1 HG00544.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.826+2043_826+2045d others(5): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | |||||
| chr4:67595372
|
CAAAA | C | 10 | a0001c0001t0001g0246a0001c0001t0003g0010a0001c0001t0003g0026others(7): Show | 11 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.826+2042_826+2045d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | |||||
| chr4:67595372
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0006a0001c0001t0001g0303 | 3 | HG02145.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.826+2035_826+2045d others(13): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | |||||
| chr4:67595372
|
CAAAAAAA others(5): Show |
C | 70 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0057others(67): Show | 76 | HG00323.hp2 HG00558.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.826+2034_826+2045d others(14): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | |||||
| chr4:67595372
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0002t0002g0314 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.826+2032_826+2045d others(16): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595372 | |||||
| chr4:67595401
|
A | T | 1 | a0001c0001t0002g0222 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.826+2045A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595401 | ||||||
| chr4:67595500
|
C | T | 1 | a0001c0002t0001g0333 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.826+2144C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595500 | ||||||
| chr4:67595525
|
C | T | 1 | a0001c0001t0007g0175 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.826+2169C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595525 | ||||||
| chr4:67595668
|
T | A | 3 | a0001c0001t0002g0242a0001c0001t0007g0174a0001c0001t0007g0175 | 3 | HG02818.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.826+2312T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595668 | ||||||
| chr4:67595784
|
C | A | 43 | a0001c0001t0001g0077a0001c0001t0001g0106a0001c0001t0001g0246others(40): Show | 45 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.826+2428C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595784 | ||||||
| chr4:67595818
|
G | T | 1 | a0003c0006t0001g0027 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.826+2462G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67595818 | ||||||
| chr4:67595976
|
T | TTTTG | 62 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0077others(59): Show | 67 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.826+2621_826+2624d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67595976 | |||||
| chr4:67596082
|
G | A | 1 | a0001c0001t0001g0353 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.826+2726G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596082 | ||||||
| chr4:67596148
|
TG | T | 43 | a0001c0001t0001g0077a0001c0001t0001g0106a0001c0001t0001g0246others(40): Show | 45 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.826+2796delG | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67596148 | |||||
| chr4:67596160
|
G | A | 3 | a0001c0001t0001g0057a0001c0001t0001g0099a0001c0001t0001g0133 | 3 | HG02071.hp2 NA18993.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.826+2804G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596160 | ||||||
| chr4:67596330
|
A | G | 43 | a0001c0001t0001g0077a0001c0001t0001g0106a0001c0001t0001g0246others(40): Show | 45 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.826+2974A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596330 | ||||||
| chr4:67596421
|
T | A | 2 | a0001c0001t0002g0023a0001c0001t0002g0025 | 2 | NA18990.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.826+3065T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596421 | ||||||
| chr4:67596448
|
A | G | 43 | a0001c0001t0001g0077a0001c0001t0001g0106a0001c0001t0001g0246others(40): Show | 45 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.826+3092A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596448 | ||||||
| chr4:67596474
|
G | A | 1 | a0001c0001t0002g0091 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.826+3118G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596474 | ||||||
| chr4:67596641
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.826+3285G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596641 | ||||||
| chr4:67596815
|
T | C | 2 | a0001c0001t0007g0174a0001c0001t0007g0175 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.826+3459T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596815 | ||||||
| chr4:67596912
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.826+3556A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67596912 | ||||||
| chr4:67597074
|
G | A | 2 | a0001c0001t0007g0174a0001c0001t0007g0175 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.826+3718G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597074 | ||||||
| chr4:67597166
|
T | C | 1 | a0002c0004t0001g0073 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.826+3810T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597166 | ||||||
| chr4:67597264
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0138 | 2 | NA18972.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.826+3908G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597264 | ||||||
| chr4:67597395
|
G | A | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.826+4039G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597395 | ||||||
| chr4:67597484
|
C | A | 1 | a0001c0002t0001g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.826+4128C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597484 | ||||||
| chr4:67597495
|
C | G | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.826+4139C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597495 | ||||||
| chr4:67597562
|
T | C | 62 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0077others(59): Show | 67 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.826+4206T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597562 | ||||||
| chr4:67597679
|
G | A | 1 | a0001c0002t0001g0279 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.826+4323G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597679 | ||||||
| chr4:67597691
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.826+4335T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597691 | ||||||
| chr4:67597961
|
A | G | 4 | a0001c0001t0001g0140a0001c0001t0001g0298a0001c0001t0001g0299others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+4605A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597961 | ||||||
| chr4:67597984
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.826+4628C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67597984 | ||||||
| chr4:67598092
|
T | C | 356 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(353): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.826+4736T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598092 | ||||||
| chr4:67598101
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0269 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.826+4745G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598101 | ||||||
| chr4:67598248
|
C | T | 1 | a0001c0001t0009g0249 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.826+4892C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598248 | ||||||
| chr4:67598353
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.826+4997C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598353 | ||||||
| chr4:67598387
|
A | G | 1 | a0001c0001t0002g0091 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.826+5031A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598387 | ||||||
| chr4:67598402
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0269 | 2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.826+5046G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598402 | ||||||
| chr4:67598403
|
T | C | 2 | a0001c0001t0005g0069a0001c0001t0005g0267 | 2 | NA18987.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.826+5047T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598403 | ||||||
| chr4:67598445
|
T | C | 1 | a0001c0002t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.826+5089T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598445 | ||||||
| chr4:67598476
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.826+5120A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598476 | ||||||
| chr4:67598635
|
G | A | 46 | a0001c0001t0001g0077a0001c0001t0001g0106a0001c0001t0001g0246others(43): Show | 48 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.826+5279G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598635 | ||||||
| chr4:67598665
|
C | T | 46 | a0001c0001t0001g0077a0001c0001t0001g0106a0001c0001t0001g0246others(43): Show | 48 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.826+5309C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598665 | ||||||
| chr4:67598858
|
T | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0077others(64): Show | 72 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.826+5502T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598858 | ||||||
| chr4:67598879
|
T | A | 13 | a0001c0001t0001g0077a0001c0001t0001g0246a0001c0001t0003g0010others(10): Show | 14 | HG00639.hp2 HG01261.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.826+5523T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598879 | ||||||
| chr4:67598926
|
C | T | 46 | a0001c0001t0001g0077a0001c0001t0001g0106a0001c0001t0001g0246others(43): Show | 48 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.826+5570C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598926 | ||||||
| chr4:67598941
|
T | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0064others(17): Show | 22 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.826+5585T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598941 | ||||||
| chr4:67598960
|
C | G | 1 | a0001c0001t0001g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.826+5604C>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67598960 | ||||||
| chr4:67599033
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.826+5677G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599033 | ||||||
| chr4:67599056
|
G | A | 46 | a0001c0001t0001g0077a0001c0001t0001g0106a0001c0001t0001g0246others(43): Show | 48 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.826+5700G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599056 | ||||||
| chr4:67599080
|
G | A | 1 | a0001c0003t0001g0356 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.826+5724G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599080 | ||||||
| chr4:67599096
|
T | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0077others(64): Show | 72 | HG00408.hp1 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.826+5740T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599096 | ||||||
| chr4:67599097
|
G | A | 46 | a0001c0001t0001g0077a0001c0001t0001g0106a0001c0001t0001g0246others(43): Show | 48 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.826+5741G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599097 | ||||||
| chr4:67599115
|
T | C | 46 | a0001c0001t0001g0077a0001c0001t0001g0106a0001c0001t0001g0246others(43): Show | 48 | HG00639.hp2 HG01167.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.826+5759T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599115 | ||||||
| chr4:67599353
|
T | C | 1 | a0001c0003t0001g0342 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.826+5997T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599353 | ||||||
| chr4:67599641
|
T | C | 2 | a0001c0002t0002g0160a0001c0002t0002g0161 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.826+6285T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599641 | ||||||
| chr4:67599683
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.826+6327C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599683 | ||||||
| chr4:67599687
|
A | T | 1 | a0001c0001t0001g0202 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.826+6331A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599687 | ||||||
| chr4:67599716
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.826+6360A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599716 | ||||||
| chr4:67599736
|
G | A | 23 | a0001c0001t0002g0008a0001c0001t0002g0051a0001c0001t0002g0054others(20): Show | 24 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.826+6380G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599736 | ||||||
| chr4:67599861
|
C | T | 2 | a0001c0001t0001g0202a0001c0003t0001g0356 | 2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.827-6435C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599861 | ||||||
| chr4:67599928
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.827-6368C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599928 | ||||||
| chr4:67599987
|
T | G | 1 | a0001c0002t0001g0321 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.827-6309T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67599987 | ||||||
| chr4:67600015
|
A | G | 310 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(307): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.827-6281A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600015 | ||||||
| chr4:67600071
|
G | A | 3 | a0001c0001t0002g0259a0001c0001t0002g0261a0001c0003t0002g0283 | 3 | HG02717.hp1 HG02896.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.827-6225G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600071 | ||||||
| chr4:67600195
|
T | C | 310 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(307): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.827-6101T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600195 | ||||||
| chr4:67600203
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.827-6093C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600203 | ||||||
| chr4:67600377
|
C | T | 1 | a0001c0003t0002g0283 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.827-5919C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600377 | ||||||
| chr4:67600391
|
T | A | 2 | a0001c0001t0002g0091a0001c0001t0002g0127 | 2 | NA18966.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.827-5905T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600391 | ||||||
| chr4:67600548
|
T | C | 2 | a0001c0003t0003g0294a0001c0003t0003g0295 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.827-5748T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600548 | ||||||
| chr4:67600725
|
C | T | 1 | a0001c0002t0003g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.827-5571C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600725 | ||||||
| chr4:67600744
|
A | G | 40 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0032others(37): Show | 49 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.827-5552A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600744 | ||||||
| chr4:67600855
|
A | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG02129.hp2 HG02132.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.827-5441A>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600855 | ||||||
| chr4:67600912
|
T | C | 1 | a0001c0003t0001g0342 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.827-5384T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67600912 | ||||||
| chr4:67601080
|
G | T | 1 | a0001c0002t0001g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.827-5216G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601080 | ||||||
| chr4:67601215
|
G | A | 291 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(288): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.827-5081G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601215 | ||||||
| chr4:67601252
|
G | T | 1 | a0001c0001t0001g0202 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.827-5044G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601252 | ||||||
| chr4:67601277
|
C | A | 72 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0040others(69): Show | 79 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.827-5019C>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601277 | ||||||
| chr4:67601317
|
T | A | 4 | a0001c0001t0006g0132a0001c0001t0010g0111a0001c0002t0006g0162others(1): Show | 4 | HG02572.hp2 HG02976.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-4979T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601317 | ||||||
| chr4:67601520
|
G | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0088 | 2 | HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.827-4776G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601520 | ||||||
| chr4:67601574
|
T | C | 310 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(307): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.827-4722T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601574 | ||||||
| chr4:67601579
|
A | G | 308 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(305): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.827-4717A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601579 | ||||||
| chr4:67601585
|
T | C | 1 | a0001c0001t0001g0353 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.827-4711T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601585 | ||||||
| chr4:67601650
|
G | A | 1 | a0001c0001t0002g0071 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.827-4646G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601650 | ||||||
| chr4:67601836
|
G | T | 291 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(288): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.827-4460G>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601836 | ||||||
| chr4:67601935
|
A | G | 291 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(288): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.827-4361A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601935 | ||||||
| chr4:67601967
|
T | C | 291 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(288): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.827-4329T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67601967 | ||||||
| chr4:67602302
|
C | T | 291 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(288): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.827-3994C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67602302 | ||||||
| chr4:67602318
|
C | CAT | 286 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(283): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.827-3978_827-3977i others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67602318 | ||||||
| chr4:67602510
|
G | A | 118 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0017others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.827-3786G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67602510 | ||||||
| chr4:67602534
|
G | A | 2 | a0001c0001t0007g0174a0001c0001t0007g0175 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.827-3762G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67602534 | ||||||
| chr4:67602625
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.827-3671C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67602625 | ||||||
| chr4:67602727
|
C | T | 1 | a0001c0001t0002g0022 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.827-3569C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67602727 | ||||||
| chr4:67602737
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.827-3559G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67602737 | ||||||
| chr4:67602812
|
GTGCT | G | 291 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(288): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.827-3479_827-3476d others(6): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67602812 | |||||
| chr4:67603040
|
G | A | 291 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(288): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.827-3256G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603040 | ||||||
| chr4:67603280
|
G | A | 289 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(286): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.827-3016G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603280 | ||||||
| chr4:67603600
|
T | C | 1 | a0001c0003t0001g0356 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.827-2696T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603600 | ||||||
| chr4:67603612
|
T | C | 310 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(307): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.827-2684T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603612 | ||||||
| chr4:67603657
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.827-2639G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603657 | ||||||
| chr4:67603677
|
G | A | 1 | a0001c0001t0002g0242 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.827-2619G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603677 | ||||||
| chr4:67603864
|
G | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0304 | 2 | HG02165.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.827-2432G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603864 | ||||||
| chr4:67603907
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.827-2389C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603907 | ||||||
| chr4:67603937
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0138 | 2 | NA18972.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.827-2359A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603937 | ||||||
| chr4:67603950
|
C | T | 3 | a0001c0001t0002g0242a0001c0001t0007g0174a0001c0001t0007g0175 | 3 | HG02818.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.827-2346C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603950 | ||||||
| chr4:67603991
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.827-2305G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67603991 | ||||||
| chr4:67604244
|
A | G | 1 | a0001c0002t0001g0319 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.827-2052A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604244 | ||||||
| chr4:67604268
|
A | G | 1 | a0001c0001t0001g0303 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.827-2028A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604268 | ||||||
| chr4:67604272
|
A | G | 2 | a0001c0002t0002g0179a0001c0002t0002g0186 | 2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.827-2024A>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604272 | ||||||
| chr4:67604330
|
G | C | 1 | a0001c0001t0003g0235 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.827-1966G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604330 | ||||||
| chr4:67604416
|
T | C | 310 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(307): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.827-1880T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604416 | ||||||
| chr4:67604506
|
T | A | 3 | a0001c0001t0002g0242a0001c0001t0007g0174a0001c0001t0007g0175 | 3 | HG02818.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.827-1790T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604506 | ||||||
| chr4:67604713
|
G | C | 1 | a0001c0001t0002g0022 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.827-1583G>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604713 | ||||||
| chr4:67604737
|
T | C | 99 | a0001c0001t0001g0257a0001c0001t0002g0001a0001c0001t0002g0002others(96): Show | 109 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.827-1559T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604737 | ||||||
| chr4:67604801
|
T | C | 1 | a0001c0002t0003g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.827-1495T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604801 | ||||||
| chr4:67604804
|
T | C | 116 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0017others(113): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.827-1492T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604804 | ||||||
| chr4:67604818
|
TTC | T | 116 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0017others(113): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.827-1472_827-1471d others(4): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67604818 | |||||
| chr4:67604887
|
T | G | 37 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0032others(34): Show | 46 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.827-1409T>G | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67604887 | ||||||
| chr4:67605034
|
G | A | 1 | a0001c0001t0002g0219 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.827-1262G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605034 | ||||||
| chr4:67605168
|
T | A | 1 | a0001c0003t0001g0356 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.827-1128T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605168 | ||||||
| chr4:67605170
|
A | T | 1 | a0001c0001t0001g0234 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.827-1126A>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605170 | ||||||
| chr4:67605295
|
T | C | 3 | a0001c0001t0002g0242a0001c0001t0007g0174a0001c0001t0007g0175 | 3 | HG02818.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.827-1001T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605295 | ||||||
| chr4:67605334
|
T | C | 318 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(315): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.827-962T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605334 | ||||||
| chr4:67605388
|
C | CA | 119 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0017others(116): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.827-893dupA | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67605388 | |||||
| chr4:67605388
|
C | CAA | 204 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(201): Show | 225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.827-894_827-893dup others(2): Show |
STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 67605388 | |||||
| chr4:67605481
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.827-815C>T | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605481 | ||||||
| chr4:67605482
|
G | A | 1 | a0001c0001t0002g0236 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.827-814G>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605482 | ||||||
| chr4:67605825
|
T | A | 1 | a0001c0001t0001g0246 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.827-471T>A | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605825 | ||||||
| chr4:67605871
|
T | C | 100 | a0001c0001t0001g0257a0001c0001t0002g0001a0001c0001t0002g0002others(97): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.827-425T>C | STAP1 | ENSG00000035720.8 | transcript | ENST00000265404.7 | protein_coding | 8/8 | chr4 | 67605871 |