| geneid | 8615 |
|---|---|
| ensemblid | ENSG00000138768.15 |
| hgncid | 30904 |
| symbol | USO1 |
| name | USO1 vesicle transport factor |
| refseq_nuc | NM_003715.4 |
| refseq_prot | NP_003706.2 |
| ensembl_nuc | ENST00000514213.7 |
| ensembl_prot | ENSP00000444850.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 75724577 |
| end | 75814286 |
| strand | + |
| ver | v1.2 |
| region | chr4:75724577-75814286 |
| region5000 | chr4:75719577-75819286 |
| regionname0 | USO1_chr4_75724577_75814286 |
| regionname5000 | USO1_chr4_75719577_75819286 |
| 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 | 962 | 277 | 80 | 65 | 78 | 14 | 38 | 66 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0002 | 0/0 | 962 | 4 | 0 | 0 | 0 | 0 | 4 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0003 | 0/0 | 962 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0004 | 0/0 | 962 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0005 | 0/0 | 962 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0006 | 0/0 | 962 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0007 | 0/0 | 962 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0008 | 0/0 | 962 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2889 | 107 | 19 | 30 | 37 | 4 | 17 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0002 | 0/0 | 2889 | 86 | 41 | 9 | 25 | 0 | 11 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0003 | 1/0 | 2889 | 42 | 17 | 14 | 1 | 4 | 5 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0004 | 0/1 | 2889 | 31 | 0 | 9 | 12 | 5 | 4 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0005 | 0/0 | 2889 | 4 | 0 | 0 | 0 | 0 | 4 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0006 | 0/0 | 2889 | 3 | 1 | 0 | 1 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0007 | 0/0 | 2889 | 2 | 0 | 1 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0008 | 0/0 | 2889 | 2 | 0 | 0 | 2 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0009 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0010 | 0/0 | 2889 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0011 | 0/0 | 2889 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0012 | 0/0 | 2889 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0013 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0014 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0015 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0016 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0017 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0018 | 0/0 | 2889 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| c0019 | 0/0 | 2889 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| 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 | 1235 | 245 | 76 | 55 | 69 | 9 | 36 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| t0002 | 0/1 | 1235 | 35 | 3 | 11 | 11 | 5 | 4 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| t0003 | 0/0 | 1235 | 2 | 2 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| t0004 | 0/0 | 1235 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| t0005 | 1/0 | 1235 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| t0006 | 0/0 | 1235 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| t0007 | 0/0 | 1235 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| t0008 | 0/0 | 1235 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| t0009 | 0/0 | 1235 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| 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 | 2 | 0 | 0 | 0 | 2 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0012 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0030 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2889 | 107 | 19 | 30 | 37 | 4 | 17 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0002 | 0/0 | 2889 | 86 | 41 | 9 | 25 | 0 | 11 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0003 | 1/0 | 2889 | 42 | 17 | 14 | 1 | 4 | 5 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0004 | 0/1 | 2889 | 31 | 0 | 9 | 12 | 5 | 4 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0006 | 0/0 | 2889 | 3 | 1 | 0 | 1 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0007 | 0/0 | 2889 | 2 | 0 | 1 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0009 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0010 | 0/0 | 2889 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0011 | 0/0 | 2889 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0012 | 0/0 | 2889 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0014 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0018 | 0/0 | 2889 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0002c0005 | 0/0 | 2889 | 4 | 0 | 0 | 0 | 0 | 4 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0003c0008 | 0/0 | 2889 | 2 | 0 | 0 | 2 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0004c0016 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0005c0015 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0006c0013 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0007c0017 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0008c0019 | 0/0 | 2889 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4123 | 105 | 17 | 30 | 37 | 4 | 17 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0001t0003 | 0/0 | 4123 | 2 | 2 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0002t0001 | 0/0 | 4123 | 83 | 39 | 9 | 25 | 0 | 10 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0002t0002 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0002t0006 | 0/0 | 4123 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0002t0009 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0003t0001 | 0/0 | 4123 | 38 | 16 | 13 | 1 | 4 | 4 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0003t0002 | 0/0 | 4123 | 2 | 1 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0003t0005 | 1/0 | 4123 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0003t0008 | 0/0 | 4123 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0004t0001 | 0/0 | 4123 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0004t0002 | 0/1 | 4123 | 30 | 0 | 9 | 11 | 5 | 4 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0006t0001 | 0/0 | 4123 | 3 | 1 | 0 | 1 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0007t0001 | 0/0 | 4123 | 2 | 0 | 1 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0009t0007 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0010t0002 | 0/0 | 4123 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0011t0001 | 0/0 | 4123 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0012t0001 | 0/0 | 4123 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0014t0002 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0001c0018t0001 | 0/0 | 4123 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0002c0005t0001 | 0/0 | 4123 | 4 | 0 | 0 | 0 | 0 | 4 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0003c0008t0001 | 0/0 | 4123 | 2 | 0 | 0 | 2 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0004c0016t0001 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0005c0015t0001 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0006c0013t0004 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0007c0017t0001 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| a0008c0019t0001 | 0/0 | 4123 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | copy fasta | chr4 | 75719577 | 75819286 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0006g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0002t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0005g0012 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0003t0008g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0030 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0004t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0006t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0006t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0006t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0007t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0007t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0009t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0010t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0011t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0012t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0014t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0001c0018t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0002c0005t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0002c0005t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0002c0005t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0002c0005t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0003c0008t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0003c0008t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0004c0016t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0005c0015t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0006c0013t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0007c0017t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| a0008c0019t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0002 | g0034 | EUR | GBR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0206 | EUR | GBR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00140 | hp2 | a0001 | c0004 | t0002 | g0009 | EUR | GBR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | FIN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0191 | EUR | FIN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0193 | EUR | FIN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00323 | hp2 | a0001 | c0004 | t0002 | g0015 | EUR | FIN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | CHS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00639 | hp1 | a0001 | c0012 | t0001 | g0054 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0259 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00741 | hp1 | a0001 | c0004 | t0002 | g0027 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0195 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0190 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0201 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0205 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01109 | hp2 | a0001 | c0004 | t0002 | g0031 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0280 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01168 | hp2 | a0001 | c0004 | t0002 | g0013 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0207 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0266 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0202 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01243 | hp1 | a0001 | c0010 | t0002 | g0006 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01243 | hp2 | a0001 | c0003 | t0002 | g0004 | AMR | PUR | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0200 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01257 | hp2 | a0008 | c0019 | t0001 | g0059 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0154 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0261 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01346 | hp2 | a0001 | c0004 | t0002 | g0035 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0278 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01433 | hp1 | a0001 | c0004 | t0002 | g0022 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01516 | hp1 | a0001 | c0004 | t0002 | g0001 | EUR | IBS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01516 | hp2 | a0001 | c0006 | t0001 | g0215 | EUR | IBS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01517 | hp2 | a0001 | c0004 | t0002 | g0001 | EUR | IBS | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01891 | hp2 | a0007 | c0017 | t0001 | g0162 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0265 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0208 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01943 | hp2 | a0001 | c0004 | t0002 | g0010 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0260 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01952 | hp2 | a0001 | c0004 | t0002 | g0033 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0188 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01981 | hp2 | a0001 | c0004 | t0002 | g0029 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0204 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0192 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02040 | hp1 | a0001 | c0006 | t0001 | g0216 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0198 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02074 | hp2 | a0001 | c0004 | t0002 | g0017 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02129 | hp2 | a0001 | c0004 | t0002 | g0008 | EAS | KHV | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02145 | hp1 | a0001 | c0003 | t0001 | g0203 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0209 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0281 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02273 | hp1 | a0001 | c0004 | t0002 | g0028 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0247 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0284 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0185 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0235 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0178 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0166 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0168 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0212 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0267 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0186 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0246 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0219 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0133 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02886 | hp2 | a0004 | c0016 | t0001 | g0180 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0176 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0276 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0174 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0275 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0153 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0158 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02976 | hp1 | a0001 | c0006 | t0001 | g0199 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0210 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03017 | hp1 | a0001 | c0004 | t0002 | g0014 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0194 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0240 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0189 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03098 | hp1 | a0001 | c0009 | t0007 | g0169 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0270 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0160 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03195 | hp2 | a0001 | c0002 | t0009 | g0159 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0241 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03225 | hp1 | a0005 | c0015 | t0001 | g0238 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03225 | hp2 | a0006 | c0013 | t0004 | g0038 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03239 | hp2 | a0001 | c0004 | t0002 | g0021 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0164 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03453 | hp2 | a0001 | c0014 | t0002 | g0036 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0214 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0273 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0248 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0220 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03491 | hp2 | a0002 | c0005 | t0001 | g0224 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0213 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0175 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0182 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03654 | hp2 | a0002 | c0005 | t0001 | g0222 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0244 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03688 | hp1 | a0002 | c0005 | t0001 | g0218 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03704 | hp1 | a0001 | c0004 | t0002 | g0026 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03710 | hp2 | a0001 | c0007 | t0001 | g0101 | SAS | PJL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03831 | hp2 | a0001 | c0002 | t0006 | g0228 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03927 | hp1 | a0001 | c0004 | t0002 | g0032 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0184 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04115 | hp2 | a0001 | c0003 | t0008 | g0170 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0254 | SAS | BEB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0243 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0183 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG04228 | hp2 | a0002 | c0005 | t0001 | g0221 | SAS | STU | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0277 | AFR | YRI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0171 | AFR | YRI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0197 | AFR | YRI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18966 | hp1 | a0003 | c0008 | t0001 | g0090 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18966 | hp2 | a0003 | c0008 | t0001 | g0129 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18970 | hp1 | a0001 | c0004 | t0002 | g0024 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18973 | hp1 | a0001 | c0004 | t0002 | g0016 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18979 | hp1 | a0001 | c0004 | t0001 | g0049 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18980 | hp1 | a0001 | c0004 | t0002 | g0020 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18999 | hp1 | a0001 | c0004 | t0002 | g0025 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19010 | hp1 | a0001 | c0004 | t0002 | g0023 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19010 | hp2 | a0001 | c0011 | t0001 | g0103 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0269 | AFR | LWK | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | LWK | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19054 | hp1 | a0001 | c0018 | t0001 | g0141 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19057 | hp2 | a0001 | c0004 | t0002 | g0011 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19062 | hp1 | a0001 | c0004 | t0002 | g0007 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19081 | hp2 | a0001 | c0004 | t0002 | g0019 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19087 | hp1 | a0001 | c0004 | t0002 | g0018 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0282 | AFR | YRI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0187 | EUR | TSI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | TSI | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | GIH | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0279 | SAS | GIH | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0181 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG01123 | hp2 | a0001 | c0007 | t0001 | g0151 | AMR | CLM | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0196 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0211 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0152 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | ACB | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0155 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | MSL | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG06807 | hp1 | a0001 | c0003 | t0002 | g0003 | AFR | USA | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0230 | AFR | USA | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | LWK | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0002 | g0030 | REF | REF | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0005 | g0012 | REF | REF | USO1_chr4_75719577_75819286 | USO1 | chr4 | 75719577 | 75819286 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75771105
|
C | G | 1 | a0008 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.523C>G | p.Leu175Val | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/24 | 766/4123 | 523/2889 | 175/962 | chr4 | 75771105 | ||
| chr4:75787081
|
C | G | 1 | a0003 | 2 | NA18966.hp1 NA18966.hp2 |
missense_variant | MODERATE | c.875C>G | p.Ser292Cys | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/24 | 1118/4123 | 875/2889 | 292/962 | chr4 | 75787081 | ||
| chr4:75787185
|
G | T | 1 | a0007 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.979G>T | p.Ala327Ser | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/24 | 1222/4123 | 979/2889 | 327/962 | chr4 | 75787185 | ||
| chr4:75804156
|
G | A | 1 | a0002 | 4 | HG03491.hp2 HG03654.hp2 HG03688.hp1 others(1): Show |
missense_variant | MODERATE | c.2009G>A | p.Arg670Lys | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/24 | 2252/4123 | 2009/2889 | 670/962 | chr4 | 75804156 | ||
| chr4:75809026
|
A | C | 1 | a0004 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.2450A>C | p.Glu817Ala | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/24 | 2693/4123 | 2450/2889 | 817/962 | chr4 | 75809026 | ||
| chr4:75810432
|
G | A | 1 | a0006 | 1 | HG03225.hp2 | missense_variant&splice_region_variant | MODERATE | c.2476G>A | p.Ala826Thr | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/24 | 2719/4123 | 2476/2889 | 826/962 | chr4 | 75810432 | ||
| chr4:75812236
|
T | C | 1 | a0005 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2660T>C | p.Ile887Thr | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/24 | 2903/4123 | 2660/2889 | 887/962 | chr4 | 75812236 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75774678
|
C | T | 1 | a0001c0018 | 1 | NA19054.hp1 | splice_region_variant&synonymous_variant | LOW | c.558C>T | p.Gly186Gly | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/24 | 801/4123 | 558/2889 | 186/962 | chr4 | 75774678 | ||
| chr4:75774774
|
A | G | 1 | a0001c0006 | 3 | HG01516.hp2 HG02040.hp1 HG02976.hp1 |
synonymous_variant | LOW | c.654A>G | p.Ser218Ser | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/24 | 897/4123 | 654/2889 | 218/962 | chr4 | 75774774 | ||
| chr4:75787172
|
T | A | 1 | a0001c0009 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.966T>A | p.Ala322Ala | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/24 | 1209/4123 | 966/2889 | 322/962 | chr4 | 75787172 | ||
| chr4:75790766
|
C | T | 1 | a0001c0009 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.1209C>T | p.Ile403Ile | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/24 | 1452/4123 | 1209/2889 | 403/962 | chr4 | 75790766 | ||
| chr4:75799732
|
T | C | 15 | a0001c0001a0001c0002a0001c0007others(12): Show | 211 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(208): Show |
splice_region_variant&synonymous_variant | LOW | c.1563T>C | p.Phe521Phe | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/24 | 1806/4123 | 1563/2889 | 521/962 | chr4 | 75799732 | ||
| chr4:75800431
|
G | A | 1 | a0001c0007 | 2 | HG01123.hp2 HG03710.hp2 |
synonymous_variant | LOW | c.1644G>A | p.Ser548Ser | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 15/24 | 1887/4123 | 1644/2889 | 548/962 | chr4 | 75800431 | ||
| chr4:75801200
|
G | A | 11 | a0001c0001a0001c0004a0001c0007others(8): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
splice_region_variant&synonymous_variant | LOW | c.1986G>A | p.Gln662Gln | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/24 | 2229/4123 | 1986/2889 | 662/962 | chr4 | 75801200 | ||
| chr4:75805294
|
T | C | 1 | a0001c0010 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.2280T>C | p.Ile760Ile | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/24 | 2523/4123 | 2280/2889 | 760/962 | chr4 | 75805294 | ||
| chr4:75806548
|
T | A | 1 | a0001c0011 | 1 | NA19010.hp2 | synonymous_variant | LOW | c.2352T>A | p.Ser784Ser | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/24 | 2595/4123 | 2352/2889 | 784/962 | chr4 | 75806548 | ||
| chr4:75809042
|
A | G | 2 | a0001c0004a0001c0014 | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
synonymous_variant | LOW | c.2466A>G | p.Thr822Thr | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/24 | 2709/4123 | 2466/2889 | 822/962 | chr4 | 75809042 | ||
| chr4:75809048
|
G | A | 1 | a0001c0012 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.2472G>A | p.Ala824Ala | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/24 | 2715/4123 | 2472/2889 | 824/962 | chr4 | 75809048 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75724680
|
G | A | 1 | a0006c0013t0004 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-140G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/24 | 140 | chr4 | 75724680 | |||||
| chr4:75724709
|
C | A | 1 | a0001c0001t0003 | 2 | HG02109.hp1 HG02818.hp1 |
5_prime_UTR_variant | MODIFIER | c.-111C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/24 | 111 | chr4 | 75724709 | |||||
| chr4:75724740
|
C | G | 21 | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(18): Show | 252 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(249): Show |
5_prime_UTR_variant | MODIFIER | c.-80C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/24 | 80 | chr4 | 75724740 | |||||
| chr4:75813396
|
T | G | 1 | a0001c0002t0006 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 24/24 | 101 | chr4 | 75813396 | |||||
| chr4:75813741
|
T | G | 1 | a0001c0009t0007 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*446T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 24/24 | 446 | chr4 | 75813741 | |||||
| chr4:75814034
|
G | T | 26 | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(23): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*739G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 24/24 | 739 | chr4 | 75814034 | |||||
| chr4:75814185
|
T | A | 1 | a0001c0003t0008 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*890T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 24/24 | 890 | chr4 | 75814185 | |||||
| chr4:75814224
|
T | C | 1 | a0001c0002t0009 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*929T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 24/24 | 929 | chr4 | 75814224 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75724992
|
C | G | 251 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(248): Show | 252 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.66+107C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75724992 | ||||||
| chr4:75725099
|
C | A | 1 | a0001c0002t0001g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.66+214C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75725099 | ||||||
| chr4:75725222
|
C | T | 2 | a0001c0001t0001g0285a0001c0001t0001g0286 | 2 | NA18998.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.66+337C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75725222 | ||||||
| chr4:75725259
|
C | T | 250 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(247): Show | 251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.66+374C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75725259 | ||||||
| chr4:75725588
|
C | T | 135 | a0001c0001t0001g0179a0001c0001t0001g0217a0001c0002t0001g0037others(132): Show | 136 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.66+703C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75725588 | ||||||
| chr4:75725617
|
T | TA | 114 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(111): Show | 114 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.66+747dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75725617 | |||||
| chr4:75725806
|
T | C | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.66+921T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75725806 | ||||||
| chr4:75726169
|
C | T | 250 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(247): Show | 251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.66+1284C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75726169 | ||||||
| chr4:75726195
|
C | T | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.66+1310C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75726195 | ||||||
| chr4:75726220
|
A | ACGGTGAG others(7): Show |
6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+1338_66+1351dup others(14): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75726220 | |||||
| chr4:75726281
|
C | CA | 114 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(111): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.66+1416dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75726281 | |||||
| chr4:75726281
|
C | CAA | 24 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(21): Show | 24 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.66+1415_66+1416dup others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75726281 | |||||
| chr4:75726281
|
CA | C | 6 | a0001c0001t0001g0140a0001c0002t0002g0005a0001c0003t0002g0003others(3): Show | 6 | HG01069.hp1 HG01243.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+1416delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75726281 | |||||
| chr4:75726293
|
AAAAAAAA others(57): Show |
A | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG01175.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.66+1411_66+1474del others(64): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75726293 | |||||
| chr4:75726301
|
A | G | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(1): Show | 4 | HG01943.hp1 HG02293.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+1416A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75726301 | ||||||
| chr4:75726567
|
C | CA | 111 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(108): Show | 111 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.66+1696dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75726567 | |||||
| chr4:75726797
|
C | G | 72 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(69): Show | 72 | HG00609.hp2 HG00733.hp2 HG01168.hp1 others(69): Show |
intron_variant | MODIFIER | c.66+1912C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75726797 | ||||||
| chr4:75726849
|
T | C | 1 | a0001c0003t0001g0178 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.66+1964T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75726849 | ||||||
| chr4:75727126
|
T | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+2241T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75727126 | ||||||
| chr4:75727205
|
T | G | 250 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(247): Show | 251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.66+2320T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75727205 | ||||||
| chr4:75727842
|
C | T | 1 | a0001c0007t0001g0151 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.66+2957C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75727842 | ||||||
| chr4:75727953
|
T | TA | 114 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(111): Show | 114 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.66+3071dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75727953 | |||||
| chr4:75728106
|
C | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+3221C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728106 | ||||||
| chr4:75728199
|
A | G | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.66+3314A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728199 | ||||||
| chr4:75728257
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.66+3372G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728257 | ||||||
| chr4:75728388
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.66+3503C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728388 | ||||||
| chr4:75728553
|
G | A | 2 | a0001c0003t0002g0003a0001c0003t0002g0004 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.66+3668G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728553 | ||||||
| chr4:75728859
|
C | T | 7 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(4): Show | 7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+3974C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728859 | ||||||
| chr4:75728895
|
T | A | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+4010T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728895 | ||||||
| chr4:75728958
|
C | T | 2 | a0001c0003t0002g0003a0001c0003t0002g0004 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.66+4073C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75728958 | ||||||
| chr4:75729088
|
A | G | 253 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(250): Show | 254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.66+4203A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729088 | ||||||
| chr4:75729139
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.66+4254A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729139 | ||||||
| chr4:75729286
|
A | T | 41 | a0001c0003t0001g0002a0001c0003t0001g0133a0001c0003t0001g0154others(38): Show | 42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.66+4401A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729286 | ||||||
| chr4:75729365
|
A | T | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.66+4480A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729365 | ||||||
| chr4:75729465
|
G | A | 1 | a0001c0004t0002g0007 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.66+4580G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729465 | ||||||
| chr4:75729484
|
T | C | 253 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(250): Show | 254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.66+4599T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729484 | ||||||
| chr4:75729737
|
A | C | 2 | a0001c0006t0001g0215a0001c0006t0001g0216 | 2 | HG01516.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.66+4852A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729737 | ||||||
| chr4:75729803
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.66+4918T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75729803 | ||||||
| chr4:75730097
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0130 | 2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.66+5212A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75730097 | ||||||
| chr4:75730361
|
A | C | 1 | a0001c0003t0001g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.66+5476A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75730361 | ||||||
| chr4:75730577
|
C | T | 2 | a0001c0003t0002g0003a0001c0003t0002g0004 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.66+5692C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75730577 | ||||||
| chr4:75730640
|
A | G | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.66+5755A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75730640 | ||||||
| chr4:75730822
|
T | G | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.66+5937T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75730822 | ||||||
| chr4:75731002
|
C | T | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+6117C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75731002 | ||||||
| chr4:75731362
|
G | A | 137 | a0001c0002t0001g0037a0001c0002t0001g0152a0001c0002t0001g0153others(134): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.66+6477G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75731362 | ||||||
| chr4:75731444
|
C | A | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.66+6559C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75731444 | ||||||
| chr4:75731488
|
C | G | 253 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(250): Show | 254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.66+6603C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75731488 | ||||||
| chr4:75731561
|
CA | C | 241 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(238): Show | 242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.66+6691delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75731561 | |||||
| chr4:75731709
|
C | G | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.66+6824C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75731709 | ||||||
| chr4:75731975
|
G | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+7090G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75731975 | ||||||
| chr4:75731983
|
G | A | 1 | a0001c0004t0002g0008 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.66+7098G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75731983 | ||||||
| chr4:75732052
|
A | G | 255 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.66+7167A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732052 | ||||||
| chr4:75732207
|
G | A | 1 | a0001c0004t0002g0009 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.66+7322G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732207 | ||||||
| chr4:75732260
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.66+7375T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732260 | ||||||
| chr4:75732271
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.66+7386G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732271 | ||||||
| chr4:75732315
|
T | A | 1 | a0001c0001t0001g0053 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.66+7430T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732315 | ||||||
| chr4:75732320
|
T | C | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+7435T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732320 | ||||||
| chr4:75732374
|
A | G | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.66+7489A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732374 | ||||||
| chr4:75732443
|
A | C | 1 | a0001c0004t0002g0035 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.66+7558A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732443 | ||||||
| chr4:75732666
|
G | C | 255 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.66+7781G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732666 | ||||||
| chr4:75732675
|
A | G | 254 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(251): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.66+7790A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732675 | ||||||
| chr4:75732771
|
T | A | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.66+7886T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732771 | ||||||
| chr4:75732835
|
C | T | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.66+7950C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732835 | ||||||
| chr4:75732876
|
T | TAAAA | 8 | a0001c0002t0001g0153a0001c0002t0001g0176a0001c0002t0001g0280others(5): Show | 8 | HG01168.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+8010_66+8013dup others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | |||||
| chr4:75732876
|
T | TAAAAA | 106 | a0001c0001t0001g0040a0001c0001t0001g0145a0001c0001t0001g0146others(103): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.66+8009_66+8013dup others(5): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | |||||
| chr4:75732876
|
T | TAAAAAA | 29 | a0001c0001t0001g0039a0001c0001t0001g0144a0001c0001t0001g0179others(26): Show | 29 | HG00609.hp2 HG01261.hp2 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.66+8008_66+8013dup others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | |||||
| chr4:75732876
|
T | TAAAAAAA | 61 | a0001c0001t0001g0041a0001c0001t0001g0045a0001c0001t0001g0047others(58): Show | 61 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.66+8007_66+8013dup others(7): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | |||||
| chr4:75732876
|
T | TAAAAAAA others(1): Show |
40 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(37): Show | 40 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.66+8006_66+8013dup others(8): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | |||||
| chr4:75732876
|
T | TAAAAAAA others(2): Show |
6 | a0001c0001t0001g0042a0001c0001t0001g0048a0001c0001t0001g0055others(3): Show | 6 | HG00438.hp2 HG01361.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+8005_66+8013dup others(9): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | |||||
| chr4:75732876
|
T | TAAAAAAA others(3): Show |
1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.66+8004_66+8013dup others(10): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | |||||
| chr4:75732876
|
T | TAAAAAAA others(6): Show |
2 | a0001c0012t0001g0054a0006c0013t0004g0038 | 2 | HG00639.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.66+8001_66+8013dup others(13): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75732876 | |||||
| chr4:75732918
|
T | A | 7 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(4): Show | 7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+8033T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75732918 | ||||||
| chr4:75733031
|
C | T | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.66+8146C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733031 | ||||||
| chr4:75733088
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.66+8203G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733088 | ||||||
| chr4:75733133
|
C | T | 41 | a0001c0003t0001g0002a0001c0003t0001g0133a0001c0003t0001g0154others(38): Show | 42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.66+8248C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733133 | ||||||
| chr4:75733208
|
G | A | 6 | a0001c0003t0001g0185a0001c0003t0001g0209a0001c0003t0001g0210others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+8323G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733208 | ||||||
| chr4:75733246
|
G | A | 12 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0056others(9): Show | 12 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.66+8361G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733246 | ||||||
| chr4:75733271
|
A | T | 3 | a0001c0002t0001g0235a0001c0002t0001g0278a0001c0002t0001g0279 | 3 | HG01358.hp2 HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.66+8386A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733271 | ||||||
| chr4:75733327
|
C | G | 3 | a0001c0002t0001g0219a0001c0002t0001g0223a0002c0005t0001g0224 | 3 | HG02738.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.66+8442C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733327 | ||||||
| chr4:75733522
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.66+8637G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733522 | ||||||
| chr4:75733556
|
C | G | 1 | a0001c0004t0002g0034 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.66+8671C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733556 | ||||||
| chr4:75733792
|
C | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.66+8907C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733792 | ||||||
| chr4:75733924
|
T | G | 2 | a0001c0003t0002g0003a0001c0003t0002g0004 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.66+9039T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75733924 | ||||||
| chr4:75733935
|
A | AT | 16 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0179others(13): Show | 16 | HG00741.hp1 HG01109.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.66+9076dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75733935 | |||||
| chr4:75733935
|
AT | A | 62 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0044others(59): Show | 63 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.66+9076delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75733935 | |||||
| chr4:75733935
|
ATT | A | 83 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0047others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.66+9075_66+9076del others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75733935 | |||||
| chr4:75733935
|
ATTTTTTT others(1): Show |
A | 70 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(67): Show | 70 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.66+9069_66+9076del others(8): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75733935 | |||||
| chr4:75734234
|
A | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+9349A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75734234 | ||||||
| chr4:75734298
|
G | C | 1 | a0001c0003t0001g0186 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.66+9413G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75734298 | ||||||
| chr4:75734312
|
A | T | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.66+9427A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75734312 | ||||||
| chr4:75734703
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG01175.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.66+9818C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75734703 | ||||||
| chr4:75734718
|
C | CT | 17 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(14): Show | 17 | HG00140.hp2 HG01109.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.66+9861dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75734718 | |||||
| chr4:75734718
|
C | CTT | 67 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0069others(64): Show | 68 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.66+9860_66+9861dup others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75734718 | |||||
| chr4:75734718
|
C | CTTT | 92 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0051others(89): Show | 92 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.66+9859_66+9861dup others(3): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75734718 | |||||
| chr4:75734718
|
C | CTTTT | 57 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(54): Show | 57 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.66+9858_66+9861dup others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75734718 | |||||
| chr4:75734718
|
C | CTTTTT | 22 | a0001c0001t0001g0045a0001c0001t0001g0065a0001c0001t0001g0067others(19): Show | 22 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.66+9857_66+9861dup others(5): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75734718 | |||||
| chr4:75734718
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0285 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.66+9852_66+9861del others(10): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75734718 | |||||
| chr4:75734718
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0286 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.66+9851_66+9861del others(11): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75734718 | |||||
| chr4:75734865
|
A | T | 4 | a0001c0004t0002g0018a0001c0004t0002g0023a0001c0004t0002g0024others(1): Show | 4 | NA18970.hp1 NA18999.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+9980A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75734865 | ||||||
| chr4:75735125
|
C | A | 137 | a0001c0002t0001g0037a0001c0002t0001g0152a0001c0002t0001g0153others(134): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.66+10240C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75735125 | ||||||
| chr4:75735316
|
A | G | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.66+10431A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75735316 | ||||||
| chr4:75735715
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.66+10830C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75735715 | ||||||
| chr4:75735721
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.66+10836A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75735721 | ||||||
| chr4:75735924
|
A | G | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+11039A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75735924 | ||||||
| chr4:75736250
|
G | A | 1 | a0001c0004t0002g0008 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.66+11365G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75736250 | ||||||
| chr4:75736307
|
C | CT | 29 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(26): Show | 29 | HG00323.hp2 HG00642.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.66+11450dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75736307 | |||||
| chr4:75736307
|
C | CTT | 11 | a0001c0001t0001g0042a0001c0001t0001g0058a0001c0001t0001g0063others(8): Show | 11 | HG00438.hp2 HG01517.hp1 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.66+11449_66+11450d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75736307 | |||||
| chr4:75736307
|
CTT | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0146others(3): Show | 6 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+11449_66+11450d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75736307 | |||||
| chr4:75736307
|
CTTT | C | 12 | a0001c0002t0001g0152a0001c0002t0001g0153a0001c0002t0001g0156others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+11448_66+11450d others(5): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75736307 | |||||
| chr4:75736307
|
CTTTT | C | 120 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0157others(117): Show | 121 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.66+11447_66+11450d others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75736307 | |||||
| chr4:75736362
|
G | C | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+11477G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75736362 | ||||||
| chr4:75736431
|
C | T | 6 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(3): Show | 6 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+11546C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75736431 | ||||||
| chr4:75736659
|
G | A | 3 | a0001c0003t0002g0003a0001c0003t0002g0004a0001c0009t0007g0169 | 3 | HG01243.hp2 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.66+11774G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75736659 | ||||||
| chr4:75736758
|
T | C | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+11873T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75736758 | ||||||
| chr4:75736889
|
T | C | 3 | a0001c0001t0001g0041a0001c0001t0001g0110a0001c0001t0001g0118 | 3 | NA18949.hp1 NA18973.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.66+12004T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75736889 | ||||||
| chr4:75737018
|
T | A | 254 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(251): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.66+12133T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737018 | ||||||
| chr4:75737057
|
G | C | 4 | a0001c0001t0001g0050a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | NA18962.hp2 NA18966.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+12172G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737057 | ||||||
| chr4:75737111
|
T | A | 1 | a0001c0004t0002g0033 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.66+12226T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737111 | ||||||
| chr4:75737153
|
A | G | 137 | a0001c0002t0001g0037a0001c0002t0001g0152a0001c0002t0001g0153others(134): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.66+12268A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737153 | ||||||
| chr4:75737281
|
AT | A | 3 | a0001c0006t0001g0199a0001c0006t0001g0215a0001c0006t0001g0216 | 3 | HG01516.hp2 HG02040.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.66+12397delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737281 | ||||||
| chr4:75737485
|
A | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+12600A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737485 | ||||||
| chr4:75737547
|
G | GA | 254 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(251): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.66+12663dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75737547 | |||||
| chr4:75737761
|
T | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.66+12876T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737761 | ||||||
| chr4:75737816
|
C | CATT | 8 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(5): Show | 8 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+12950_66+12952d others(5): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75737816 | |||||
| chr4:75737884
|
G | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.66+12999G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737884 | ||||||
| chr4:75737951
|
C | T | 7 | a0001c0002t0001g0231a0001c0002t0001g0259a0001c0002t0001g0260others(4): Show | 7 | HG00733.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+13066C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75737951 | ||||||
| chr4:75738139
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.66+13254C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738139 | ||||||
| chr4:75738188
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | HG01943.hp1 HG02293.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.66+13303A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738188 | ||||||
| chr4:75738241
|
A | G | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+13356A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738241 | ||||||
| chr4:75738389
|
G | A | 13 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.66+13504G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738389 | ||||||
| chr4:75738456
|
CA | C | 72 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(69): Show | 72 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(69): Show |
intron_variant | MODIFIER | c.66+13583delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75738456 | |||||
| chr4:75738539
|
G | A | 2 | a0001c0002t0001g0281a0001c0002t0002g0005 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.66+13654G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738539 | ||||||
| chr4:75738731
|
T | C | 253 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(250): Show | 254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.67-13642T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738731 | ||||||
| chr4:75738795
|
A | T | 1 | a0001c0002t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.67-13578A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738795 | ||||||
| chr4:75738865
|
T | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-13508T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738865 | ||||||
| chr4:75738955
|
C | T | 2 | a0001c0003t0002g0003a0001c0003t0002g0004 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.67-13418C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738955 | ||||||
| chr4:75738977
|
C | G | 1 | a0001c0003t0001g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.67-13396C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738977 | ||||||
| chr4:75738998
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.67-13375G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75738998 | ||||||
| chr4:75739001
|
C | T | 76 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(73): Show | 76 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.67-13372C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739001 | ||||||
| chr4:75739002
|
G | GC | 3 | a0001c0003t0002g0003a0001c0003t0002g0004a0001c0009t0007g0169 | 3 | HG01243.hp2 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.67-13369dupC | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75739002 | |||||
| chr4:75739095
|
G | A | 2 | a0001c0003t0002g0003a0001c0003t0002g0004 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.67-13278G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739095 | ||||||
| chr4:75739098
|
C | T | 10 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0267others(7): Show | 10 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.67-13275C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739098 | ||||||
| chr4:75739099
|
G | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-13274G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739099 | ||||||
| chr4:75739104
|
G | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-13269G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739104 | ||||||
| chr4:75739105
|
T | G | 255 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.67-13268T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739105 | ||||||
| chr4:75739144
|
G | T | 1 | a0001c0006t0001g0216 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.67-13229G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739144 | ||||||
| chr4:75739376
|
T | C | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.67-12997T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739376 | ||||||
| chr4:75739403
|
C | T | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-12970C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739403 | ||||||
| chr4:75739538
|
C | CT | 100 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(97): Show | 100 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.67-12815dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75739538 | |||||
| chr4:75739538
|
C | CTT | 10 | a0001c0001t0001g0041a0001c0001t0001g0056a0001c0001t0001g0071others(7): Show | 10 | HG00642.hp1 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-12816_67-12815d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75739538 | |||||
| chr4:75739538
|
CT | C | 16 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(13): Show | 16 | HG01099.hp1 HG01257.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.67-12815delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75739538 | |||||
| chr4:75739544
|
T | C | 4 | a0001c0002t0001g0220a0002c0005t0001g0218a0002c0005t0001g0221others(1): Show | 4 | HG03491.hp1 HG03654.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-12829T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739544 | ||||||
| chr4:75739708
|
A | G | 254 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(251): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.67-12665A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739708 | ||||||
| chr4:75739807
|
T | C | 137 | a0001c0002t0001g0037a0001c0002t0001g0152a0001c0002t0001g0153others(134): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.67-12566T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739807 | ||||||
| chr4:75739813
|
G | C | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-12560G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739813 | ||||||
| chr4:75739910
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.67-12463T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739910 | ||||||
| chr4:75739922
|
A | G | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.67-12451A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739922 | ||||||
| chr4:75739963
|
T | C | 254 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(251): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.67-12410T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739963 | ||||||
| chr4:75739989
|
T | C | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67-12384T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75739989 | ||||||
| chr4:75740074
|
A | G | 255 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.67-12299A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75740074 | ||||||
| chr4:75740450
|
G | T | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.67-11923G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75740450 | ||||||
| chr4:75740733
|
A | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67-11640A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75740733 | ||||||
| chr4:75740819
|
G | T | 5 | a0001c0001t0001g0077a0001c0001t0001g0080a0001c0001t0001g0089others(2): Show | 5 | HG01928.hp2 HG01993.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-11554G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75740819 | ||||||
| chr4:75740897
|
G | A | 1 | a0001c0002t0001g0243 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.67-11476G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75740897 | ||||||
| chr4:75740928
|
A | G | 2 | a0001c0003t0002g0003a0001c0003t0002g0004 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.67-11445A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75740928 | ||||||
| chr4:75740941
|
T | C | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.67-11432T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75740941 | ||||||
| chr4:75741094
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-11279G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75741094 | ||||||
| chr4:75741285
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.67-11088A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75741285 | ||||||
| chr4:75741536
|
G | A | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.67-10837G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75741536 | ||||||
| chr4:75741596
|
T | C | 3 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0087 | 3 | HG00140.hp1 HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.67-10777T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75741596 | ||||||
| chr4:75741601
|
CT | C | 213 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0045others(210): Show | 214 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.67-10749delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75741601 | |||||
| chr4:75741601
|
CTT | C | 14 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0002t0001g0239others(11): Show | 14 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-10750_67-10749d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75741601 | |||||
| chr4:75741661
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.67-10712A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75741661 | ||||||
| chr4:75741891
|
G | A | 3 | a0001c0002t0001g0243a0001c0002t0001g0244a0001c0002t0006g0228 | 3 | HG03669.hp2 HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.67-10482G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75741891 | ||||||
| chr4:75741984
|
C | T | 1 | a0001c0004t0002g0035 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.67-10389C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75741984 | ||||||
| chr4:75742004
|
C | A | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-10369C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742004 | ||||||
| chr4:75742060
|
T | G | 1 | a0001c0004t0002g0033 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.67-10313T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742060 | ||||||
| chr4:75742078
|
A | G | 3 | a0001c0006t0001g0199a0001c0006t0001g0215a0001c0006t0001g0216 | 3 | HG01516.hp2 HG02040.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.67-10295A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742078 | ||||||
| chr4:75742110
|
T | C | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.67-10263T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742110 | ||||||
| chr4:75742181
|
G | A | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.67-10192G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742181 | ||||||
| chr4:75742280
|
C | A | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.67-10093C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742280 | ||||||
| chr4:75742414
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.67-9959C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742414 | ||||||
| chr4:75742443
|
A | G | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67-9930A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742443 | ||||||
| chr4:75742478
|
G | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0119 | 2 | NA19057.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.67-9895G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742478 | ||||||
| chr4:75742525
|
C | T | 137 | a0001c0002t0001g0037a0001c0002t0001g0152a0001c0002t0001g0153others(134): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.67-9848C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742525 | ||||||
| chr4:75742893
|
C | T | 1 | a0005c0015t0001g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.67-9480C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742893 | ||||||
| chr4:75742913
|
G | A | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67-9460G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742913 | ||||||
| chr4:75742969
|
A | G | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.67-9404A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742969 | ||||||
| chr4:75742985
|
C | CT | 44 | a0001c0001t0001g0076a0001c0001t0001g0112a0001c0001t0001g0118others(41): Show | 45 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.67-9371dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75742985 | |||||
| chr4:75742999
|
T | A | 1 | a0001c0006t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.67-9374T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75742999 | ||||||
| chr4:75743083
|
C | T | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67-9290C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743083 | ||||||
| chr4:75743390
|
A | G | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.67-8983A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743390 | ||||||
| chr4:75743507
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-8866T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743507 | ||||||
| chr4:75743553
|
A | G | 4 | a0001c0003t0001g0182a0001c0003t0001g0183a0001c0003t0001g0184others(1): Show | 4 | HG03654.hp1 HG03942.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-8820A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743553 | ||||||
| chr4:75743593
|
G | T | 91 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(88): Show | 91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.67-8780G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743593 | ||||||
| chr4:75743643
|
C | T | 1 | a0001c0002t0001g0168 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.67-8730C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743643 | ||||||
| chr4:75743790
|
T | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-8583T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743790 | ||||||
| chr4:75743822
|
G | C | 137 | a0001c0002t0001g0037a0001c0002t0001g0152a0001c0002t0001g0153others(134): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.67-8551G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743822 | ||||||
| chr4:75743862
|
C | T | 7 | a0001c0004t0002g0009a0001c0004t0002g0014a0001c0004t0002g0028others(4): Show | 7 | HG00140.hp2 HG01346.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-8511C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75743862 | ||||||
| chr4:75744061
|
C | T | 6 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(3): Show | 6 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-8312C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744061 | ||||||
| chr4:75744307
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0179 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.67-8066C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744307 | ||||||
| chr4:75744354
|
G | A | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-8019G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744354 | ||||||
| chr4:75744443
|
G | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-7930G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744443 | ||||||
| chr4:75744669
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.67-7704C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744669 | ||||||
| chr4:75744676
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0001g0085 | 2 | NA18994.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.67-7697T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744676 | ||||||
| chr4:75744829
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.67-7544A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744829 | ||||||
| chr4:75744996
|
T | C | 254 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(251): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.67-7377T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75744996 | ||||||
| chr4:75745119
|
C | T | 1 | a0001c0003t0001g0198 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.67-7254C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745119 | ||||||
| chr4:75745212
|
T | A | 1 | a0001c0001t0001g0149 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.67-7161T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745212 | ||||||
| chr4:75745212
|
T | TTA | 4 | a0001c0002t0001g0239a0001c0002t0001g0240a0001c0002t0001g0241others(1): Show | 4 | HG01884.hp1 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-7148_67-7147dup others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75745212 | |||||
| chr4:75745312
|
G | T | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67-7061G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745312 | ||||||
| chr4:75745505
|
T | C | 1 | a0001c0003t0008g0170 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.67-6868T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745505 | ||||||
| chr4:75745514
|
C | T | 8 | a0001c0002t0001g0226a0001c0002t0001g0227a0001c0002t0001g0229others(5): Show | 8 | NA18941.hp2 NA18950.hp1 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.67-6859C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745514 | ||||||
| chr4:75745729
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.67-6644G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745729 | ||||||
| chr4:75745775
|
TTG | T | 90 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(87): Show | 90 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(87): Show |
intron_variant | MODIFIER | c.67-6596_67-6595del others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75745775 | |||||
| chr4:75745798
|
G | A | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67-6575G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745798 | ||||||
| chr4:75745922
|
G | A | 254 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(251): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.67-6451G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745922 | ||||||
| chr4:75745985
|
A | C | 8 | a0001c0002t0001g0225a0001c0002t0001g0232a0001c0002t0001g0237others(5): Show | 8 | HG00609.hp2 NA18940.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-6388A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75745985 | ||||||
| chr4:75746221
|
A | G | 7 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(4): Show | 7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-6152A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75746221 | ||||||
| chr4:75746886
|
G | T | 1 | a0001c0002t0001g0270 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67-5487G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75746886 | ||||||
| chr4:75747005
|
T | C | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.67-5368T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75747005 | ||||||
| chr4:75747065
|
A | T | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-5308A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75747065 | ||||||
| chr4:75747270
|
C | A | 41 | a0001c0003t0001g0002a0001c0003t0001g0133a0001c0003t0001g0154others(38): Show | 42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.67-5103C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75747270 | ||||||
| chr4:75747602
|
C | CT | 16 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0046others(13): Show | 16 | HG01168.hp2 HG01891.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.67-4746dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75747602 | |||||
| chr4:75747602
|
CT | C | 86 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(83): Show | 86 | HG00323.hp2 HG00609.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.67-4746delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75747602 | |||||
| chr4:75747602
|
CTT | C | 24 | a0001c0001t0001g0093a0001c0001t0001g0144a0001c0001t0001g0146others(21): Show | 24 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.67-4747_67-4746del others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75747602 | |||||
| chr4:75747620
|
T | C | 25 | a0001c0004t0001g0049a0001c0004t0002g0007a0001c0004t0002g0008others(22): Show | 25 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.67-4753T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75747620 | ||||||
| chr4:75747696
|
G | A | 158 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(155): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.67-4677G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75747696 | ||||||
| chr4:75747787
|
T | A | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-4586T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75747787 | ||||||
| chr4:75747900
|
C | CT | 20 | a0001c0002t0001g0156a0001c0002t0001g0163a0001c0002t0001g0226others(17): Show | 20 | HG01168.hp1 HG01346.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.67-4449dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75747900 | |||||
| chr4:75747900
|
CT | C | 117 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.67-4449delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75747900 | |||||
| chr4:75748019
|
T | A | 1 | a0001c0002t0001g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.67-4354T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748019 | ||||||
| chr4:75748065
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.67-4308G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748065 | ||||||
| chr4:75748095
|
C | T | 137 | a0001c0002t0001g0037a0001c0002t0001g0152a0001c0002t0001g0153others(134): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.67-4278C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748095 | ||||||
| chr4:75748123
|
C | G | 42 | a0001c0003t0001g0002a0001c0003t0001g0133a0001c0003t0001g0154others(39): Show | 43 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.67-4250C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748123 | ||||||
| chr4:75748181
|
G | A | 44 | a0001c0003t0001g0002a0001c0003t0001g0133a0001c0003t0001g0154others(41): Show | 45 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.67-4192G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748181 | ||||||
| chr4:75748201
|
G | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-4172G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748201 | ||||||
| chr4:75748211
|
C | CT | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.67-4144dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75748211 | |||||
| chr4:75748211
|
C | CTT | 106 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(103): Show | 106 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.67-4145_67-4144dup others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75748211 | |||||
| chr4:75748353
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.67-4020T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748353 | ||||||
| chr4:75748366
|
T | C | 73 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(70): Show | 73 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(70): Show |
intron_variant | MODIFIER | c.67-4007T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748366 | ||||||
| chr4:75748441
|
A | G | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-3932A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748441 | ||||||
| chr4:75748445
|
T | C | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.67-3928T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748445 | ||||||
| chr4:75748497
|
G | C | 6 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(3): Show | 6 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-3876G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748497 | ||||||
| chr4:75748524
|
A | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-3849A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748524 | ||||||
| chr4:75748554
|
T | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67-3819T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748554 | ||||||
| chr4:75748752
|
C | T | 1 | a0001c0003t0001g0002 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.67-3621C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748752 | ||||||
| chr4:75748854
|
T | A | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-3519T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748854 | ||||||
| chr4:75748944
|
T | TA | 28 | a0001c0004t0001g0049a0001c0004t0002g0001a0001c0004t0002g0007others(25): Show | 29 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.67-3421dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75748944 | |||||
| chr4:75748951
|
A | AT | 5 | a0001c0004t0002g0011a0001c0004t0002g0017a0001c0014t0002g0036others(2): Show | 5 | HG02074.hp2 HG02886.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-3422_67-3421ins others(1): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75748951 | ||||||
| chr4:75749115
|
T | G | 1 | a0001c0004t0002g0007 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.67-3258T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75749115 | ||||||
| chr4:75749404
|
G | T | 243 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(240): Show | 244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.67-2969G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75749404 | ||||||
| chr4:75749459
|
G | C | 1 | a0001c0003t0001g0002 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.67-2914G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75749459 | ||||||
| chr4:75749485
|
CT | C | 285 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(282): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.67-2886delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75749485 | |||||
| chr4:75749700
|
A | G | 2 | a0001c0004t0002g0011a0001c0004t0002g0017 | 2 | HG02074.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.67-2673A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75749700 | ||||||
| chr4:75749713
|
C | T | 1 | a0001c0003t0001g0002 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.67-2660C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75749713 | ||||||
| chr4:75749822
|
G | A | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-2551G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75749822 | ||||||
| chr4:75750247
|
A | G | 1 | a0001c0003t0001g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-2126A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750247 | ||||||
| chr4:75750278
|
A | G | 1 | a0001c0002t0001g0247 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.67-2095A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750278 | ||||||
| chr4:75750367
|
G | A | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-2006G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750367 | ||||||
| chr4:75750433
|
A | G | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.67-1940A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750433 | ||||||
| chr4:75750436
|
T | TA | 285 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(282): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.67-1928dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75750436 | |||||
| chr4:75750517
|
C | G | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-1856C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750517 | ||||||
| chr4:75750562
|
C | A | 1 | a0001c0001t0001g0107 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.67-1811C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750562 | ||||||
| chr4:75750576
|
C | T | 1 | a0001c0004t0002g0030 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.67-1797C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750576 | ||||||
| chr4:75750603
|
C | A | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.67-1770C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750603 | ||||||
| chr4:75750707
|
TCTCTTGA others(23): Show |
T | 82 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(79): Show | 82 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.67-1662_67-1633del others(30): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75750707 | |||||
| chr4:75750761
|
G | A | 2 | a0001c0003t0001g0189a0001c0003t0001g0203 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.67-1612G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750761 | ||||||
| chr4:75750772
|
C | T | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.67-1601C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750772 | ||||||
| chr4:75750784
|
A | G | 1 | a0001c0003t0001g0185 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.67-1589A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750784 | ||||||
| chr4:75750896
|
C | A | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-1477C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750896 | ||||||
| chr4:75750930
|
A | G | 83 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(80): Show | 83 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(80): Show |
intron_variant | MODIFIER | c.67-1443A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750930 | ||||||
| chr4:75750948
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0058 | 2 | HG00438.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.67-1425C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75750948 | ||||||
| chr4:75751129
|
A | G | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.67-1244A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751129 | ||||||
| chr4:75751185
|
ATTATT | A | 31 | a0001c0004t0001g0049a0001c0004t0002g0001a0001c0004t0002g0007others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.67-1165_67-1161del others(5): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75751185 | |||||
| chr4:75751235
|
G | A | 6 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(3): Show | 6 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-1138G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751235 | ||||||
| chr4:75751372
|
C | T | 1 | a0001c0004t0002g0007 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.67-1001C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751372 | ||||||
| chr4:75751557
|
G | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-816G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751557 | ||||||
| chr4:75751578
|
C | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-795C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751578 | ||||||
| chr4:75751688
|
A | G | 1 | a0001c0003t0001g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.67-685A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751688 | ||||||
| chr4:75751729
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.67-644G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751729 | ||||||
| chr4:75751763
|
C | T | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-610C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751763 | ||||||
| chr4:75751773
|
A | T | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-600A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751773 | ||||||
| chr4:75751798
|
C | T | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-575C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751798 | ||||||
| chr4:75751828
|
G | A | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.67-545G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75751828 | ||||||
| chr4:75752030
|
T | TA | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-342dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr4 | 75752030 | |||||
| chr4:75752040
|
A | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG01891.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.67-333A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75752040 | ||||||
| chr4:75752338
|
T | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0087 | 2 | HG00140.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.67-35T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 1/23 | chr4 | 75752338 | ||||||
| chr4:75752480
|
T | C | 1 | a0001c0002t0001g0239 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.153+21T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 2/23 | chr4 | 75752480 | ||||||
| chr4:75752488
|
T | C | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.153+29T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 2/23 | chr4 | 75752488 | ||||||
| chr4:75753040
|
TA | T | 73 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(70): Show | 73 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(70): Show |
intron_variant | MODIFIER | c.218+437delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753040 | ||||||
| chr4:75753124
|
G | A | 108 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(105): Show | 108 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.218+520G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753124 | ||||||
| chr4:75753217
|
G | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.218+613G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753217 | ||||||
| chr4:75753285
|
G | A | 1 | a0001c0002t0001g0259 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.218+681G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753285 | ||||||
| chr4:75753347
|
A | T | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+743A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753347 | ||||||
| chr4:75753360
|
C | T | 32 | a0001c0004t0001g0049a0001c0004t0002g0001a0001c0004t0002g0007others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.218+756C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753360 | ||||||
| chr4:75753371
|
AAAAATAA others(1): Show |
A | 91 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(88): Show | 91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.218+772_218+779del others(8): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75753371 | |||||
| chr4:75753439
|
T | C | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.218+835T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753439 | ||||||
| chr4:75753495
|
A | G | 1 | a0001c0002t0001g0236 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.218+891A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753495 | ||||||
| chr4:75753668
|
T | C | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+1064T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753668 | ||||||
| chr4:75753669
|
G | A | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+1065G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753669 | ||||||
| chr4:75753780
|
A | AT | 71 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0047others(68): Show | 73 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.218+1197dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75753780 | |||||
| chr4:75753780
|
AT | A | 9 | a0001c0001t0001g0093a0001c0001t0001g0100a0001c0001t0001g0121others(6): Show | 9 | HG01884.hp2 HG02004.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.218+1197delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75753780 | |||||
| chr4:75753814
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.218+1210C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75753814 | ||||||
| chr4:75754047
|
A | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.218+1443A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754047 | ||||||
| chr4:75754086
|
C | CT | 38 | a0001c0001t0001g0055a0001c0002t0001g0229a0001c0002t0001g0257others(35): Show | 39 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.218+1495dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75754086 | |||||
| chr4:75754086
|
CT | C | 6 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0102others(3): Show | 6 | HG01975.hp1 HG02004.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.218+1495delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75754086 | |||||
| chr4:75754139
|
A | G | 1 | a0001c0004t0002g0020 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.218+1535A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754139 | ||||||
| chr4:75754147
|
G | A | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+1543G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754147 | ||||||
| chr4:75754168
|
T | C | 264 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(261): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.218+1564T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754168 | ||||||
| chr4:75754232
|
C | T | 1 | a0001c0003t0001g0183 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.218+1628C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754232 | ||||||
| chr4:75754605
|
C | T | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.218+2001C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754605 | ||||||
| chr4:75754606
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.218+2002G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754606 | ||||||
| chr4:75754739
|
A | G | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.218+2135A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754739 | ||||||
| chr4:75754832
|
G | T | 14 | a0001c0003t0001g0002a0001c0003t0001g0133a0001c0003t0001g0178others(11): Show | 15 | HG02145.hp1 HG02258.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.218+2228G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75754832 | ||||||
| chr4:75755098
|
T | C | 1 | a0001c0004t0002g0009 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.219-2399T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75755098 | ||||||
| chr4:75755123
|
T | C | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.219-2374T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75755123 | ||||||
| chr4:75755124
|
A | G | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.219-2373A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75755124 | ||||||
| chr4:75755311
|
T | G | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.219-2186T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75755311 | ||||||
| chr4:75755322
|
G | A | 145 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(142): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.219-2175G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75755322 | ||||||
| chr4:75755529
|
C | T | 1 | a0001c0003t0008g0170 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.219-1968C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75755529 | ||||||
| chr4:75755810
|
C | A | 1 | a0001c0002t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.219-1687C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75755810 | ||||||
| chr4:75756077
|
G | A | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.219-1420G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756077 | ||||||
| chr4:75756126
|
C | T | 1 | a0001c0003t0001g0185 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.219-1371C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756126 | ||||||
| chr4:75756143
|
C | T | 1 | a0001c0003t0001g0002 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.219-1354C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756143 | ||||||
| chr4:75756169
|
C | CA | 124 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(121): Show | 124 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.219-1312dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75756169 | |||||
| chr4:75756292
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0087 | 2 | HG00140.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.219-1205A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756292 | ||||||
| chr4:75756347
|
G | A | 1 | a0001c0002t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.219-1150G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756347 | ||||||
| chr4:75756362
|
T | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.219-1135T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756362 | ||||||
| chr4:75756417
|
TATAAA | T | 41 | a0001c0003t0001g0002a0001c0003t0001g0133a0001c0003t0001g0154others(38): Show | 42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.219-1079_219-1075d others(7): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756417 | ||||||
| chr4:75756507
|
A | AT | 136 | a0001c0001t0001g0102a0001c0002t0001g0037a0001c0002t0001g0152others(133): Show | 137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.219-974dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75756507 | |||||
| chr4:75756507
|
A | ATT | 114 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(111): Show | 114 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.219-975_219-974dup others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75756507 | |||||
| chr4:75756585
|
C | G | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-912C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756585 | ||||||
| chr4:75756586
|
A | G | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-911A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756586 | ||||||
| chr4:75756589
|
C | G | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-908C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756589 | ||||||
| chr4:75756590
|
T | G | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-907T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756590 | ||||||
| chr4:75756592
|
T | A | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-905T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756592 | ||||||
| chr4:75756595
|
C | A | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-902C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756595 | ||||||
| chr4:75756632
|
G | A | 137 | a0001c0002t0001g0037a0001c0002t0001g0152a0001c0002t0001g0153others(134): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.219-865G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756632 | ||||||
| chr4:75756636
|
A | C | 1 | a0001c0001t0001g0120 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.219-861A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756636 | ||||||
| chr4:75756706
|
G | A | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219-791G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756706 | ||||||
| chr4:75756746
|
C | T | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.219-751C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756746 | ||||||
| chr4:75756764
|
C | T | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.219-733C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756764 | ||||||
| chr4:75756769
|
T | C | 1 | a0001c0002t0001g0231 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.219-728T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756769 | ||||||
| chr4:75756863
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.219-634A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756863 | ||||||
| chr4:75756958
|
C | CAT | 91 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(88): Show | 91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.219-531_219-530dup others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75756958 | |||||
| chr4:75756984
|
C | T | 253 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(250): Show | 254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.219-513C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75756984 | ||||||
| chr4:75757112
|
A | G | 253 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(250): Show | 254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.219-385A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75757112 | ||||||
| chr4:75757116
|
A | ACT | 253 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(250): Show | 254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.219-380_219-379dup others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr4 | 75757116 | |||||
| chr4:75757175
|
T | C | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.219-322T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75757175 | ||||||
| chr4:75757423
|
A | G | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.219-74A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 3/23 | chr4 | 75757423 | ||||||
| chr4:75757622
|
G | A | 1 | a0001c0003t0008g0170 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.295+49G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75757622 | ||||||
| chr4:75757790
|
A | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.295+217A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75757790 | ||||||
| chr4:75758066
|
C | T | 1 | a0001c0003t0001g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.295+493C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75758066 | ||||||
| chr4:75758306
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.295+733C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75758306 | ||||||
| chr4:75758543
|
A | T | 5 | a0001c0004t0002g0010a0001c0004t0002g0015a0001c0004t0002g0022others(2): Show | 5 | HG00323.hp2 HG00741.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.295+970A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75758543 | ||||||
| chr4:75758579
|
C | T | 73 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(70): Show | 73 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(70): Show |
intron_variant | MODIFIER | c.295+1006C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75758579 | ||||||
| chr4:75758729
|
A | T | 1 | a0001c0001t0001g0071 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.295+1156A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75758729 | ||||||
| chr4:75758903
|
C | T | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+1330C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75758903 | ||||||
| chr4:75759107
|
G | A | 1 | a0001c0006t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.295+1534G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75759107 | ||||||
| chr4:75759245
|
C | T | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+1672C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75759245 | ||||||
| chr4:75759246
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0001g0052a0001c0001t0001g0071a0001c0001t0001g0093others(5): Show | 8 | HG01069.hp1 HG01099.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.295+1684_295+1691d others(10): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759246
|
C | CTTTTTTT others(2): Show |
80 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(77): Show | 80 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.295+1683_295+1691d others(11): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759246
|
C | CTTTTTTT others(3): Show |
16 | a0001c0001t0001g0041a0001c0001t0001g0076a0001c0001t0001g0086others(13): Show | 16 | HG00280.hp1 HG01943.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.295+1682_295+1691d others(12): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759246
|
C | CTTTTTTT others(4): Show |
6 | a0001c0001t0001g0074a0001c0001t0001g0089a0001c0001t0001g0106others(3): Show | 6 | HG02300.hp1 HG02886.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+1681_295+1691d others(13): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759246
|
C | CTTTTTTT others(6): Show |
2 | a0001c0002t0001g0172a0001c0002t0001g0177 | 2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.295+1679_295+1691d others(15): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759246
|
C | CTTTTTTT others(7): Show |
2 | a0001c0002t0001g0173a0001c0002t0001g0174 | 2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.295+1678_295+1691d others(16): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759246
|
C | CTTTTTTT others(8): Show |
10 | a0001c0002t0001g0171a0001c0002t0001g0176a0001c0003t0001g0002others(7): Show | 11 | HG00099.hp2 HG02074.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.295+1677_295+1691d others(17): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759246
|
C | CTTTTTTT others(9): Show |
31 | a0001c0002t0001g0157a0001c0002t0001g0165a0001c0002t0001g0167others(28): Show | 31 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.295+1676_295+1691d others(18): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759246
|
C | CTTTTTTT others(10): Show |
33 | a0001c0002t0001g0153a0001c0002t0001g0158a0001c0002t0001g0166others(30): Show | 33 | HG00733.hp2 HG01261.hp2 HG01358.hp2 others(30): Show |
intron_variant | MODIFIER | c.295+1675_295+1691d others(19): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759246
|
C | CTTTTTTT others(11): Show |
23 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0160others(20): Show | 23 | HG00741.hp2 HG01168.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.295+1674_295+1691d others(20): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759246
|
C | CTTTTTTT others(12): Show |
14 | a0001c0001t0001g0040a0001c0001t0001g0179a0001c0002t0001g0156others(11): Show | 14 | HG02129.hp1 HG02145.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.295+1691_295+1692i others(21): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759246
|
C | CTTTTTTT others(13): Show |
8 | a0001c0001t0001g0039a0001c0002t0001g0152a0001c0002t0001g0225others(5): Show | 8 | HG00609.hp2 HG01243.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.295+1691_295+1692i others(22): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759246
|
C | CTTTTTTT others(14): Show |
1 | a0002c0005t0001g0222 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.295+1691_295+1692i others(23): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759246
|
C | CTTTTTTT others(15): Show |
7 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+1691_295+1692i others(24): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759246
|
C | CTTTTTTT others(16): Show |
1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.295+1691_295+1692i others(25): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759246
|
CT | C | 13 | a0001c0002t0001g0175a0001c0002t0001g0233a0001c0002t0001g0234others(10): Show | 13 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.295+1691delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759246 | |||||
| chr4:75759321
|
C | T | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+1748C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75759321 | ||||||
| chr4:75759736
|
C | T | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.295+2163C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75759736 | ||||||
| chr4:75759883
|
C | G | 1 | a0001c0001t0001g0115 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.295+2310C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75759883 | ||||||
| chr4:75759888
|
G | A | 1 | a0001c0002t0001g0263 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.295+2315G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75759888 | ||||||
| chr4:75759910
|
T | TA | 7 | a0001c0001t0001g0089a0001c0001t0001g0119a0001c0002t0001g0283others(4): Show | 7 | HG01981.hp2 HG02273.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.295+2354dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759910 | |||||
| chr4:75759910
|
TA | T | 7 | a0001c0001t0001g0068a0001c0001t0001g0095a0001c0001t0001g0102others(4): Show | 7 | HG00639.hp2 HG01109.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.295+2354delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75759910 | |||||
| chr4:75760073
|
G | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.295+2500G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760073 | ||||||
| chr4:75760126
|
T | C | 255 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.295+2553T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760126 | ||||||
| chr4:75760219
|
A | C | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.295+2646A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760219 | ||||||
| chr4:75760253
|
G | A | 12 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(9): Show | 12 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.295+2680G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760253 | ||||||
| chr4:75760376
|
A | G | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.295+2803A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760376 | ||||||
| chr4:75760388
|
C | T | 1 | a0001c0003t0001g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.295+2815C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760388 | ||||||
| chr4:75760418
|
T | A | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.295+2845T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760418 | ||||||
| chr4:75760429
|
A | G | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.295+2856A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760429 | ||||||
| chr4:75760872
|
C | T | 1 | a0001c0003t0001g0208 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.295+3299C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760872 | ||||||
| chr4:75760992
|
T | C | 255 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.295+3419T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75760992 | ||||||
| chr4:75761200
|
T | G | 1 | a0001c0001t0001g0082 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.295+3627T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75761200 | ||||||
| chr4:75761202
|
A | C | 1 | a0001c0002t0001g0172 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.295+3629A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75761202 | ||||||
| chr4:75761326
|
T | C | 254 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(251): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.295+3753T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75761326 | ||||||
| chr4:75761707
|
A | C | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.295+4134A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75761707 | ||||||
| chr4:75761734
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.295+4161A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75761734 | ||||||
| chr4:75761796
|
T | A | 1 | a0001c0003t0001g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.295+4223T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75761796 | ||||||
| chr4:75762164
|
C | CT | 21 | a0001c0001t0001g0040a0001c0001t0001g0179a0001c0003t0001g0002others(18): Show | 22 | HG02258.hp1 HG02486.hp1 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.295+4616dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75762164 | |||||
| chr4:75762164
|
CT | C | 128 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0047others(125): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.295+4616delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75762164 | |||||
| chr4:75762164
|
CTT | C | 103 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0045others(100): Show | 103 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.295+4615_295+4616d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75762164 | |||||
| chr4:75762383
|
C | T | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.295+4810C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75762383 | ||||||
| chr4:75762438
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.295+4865A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75762438 | ||||||
| chr4:75762495
|
T | C | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.295+4922T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75762495 | ||||||
| chr4:75762569
|
G | T | 1 | a0001c0002t0001g0241 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.295+4996G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75762569 | ||||||
| chr4:75762743
|
AT | A | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+5171delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75762743 | ||||||
| chr4:75762954
|
C | G | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+5381C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75762954 | ||||||
| chr4:75762955
|
A | G | 255 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.295+5382A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75762955 | ||||||
| chr4:75763057
|
C | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0134 | 2 | NA18971.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.295+5484C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75763057 | ||||||
| chr4:75763117
|
A | G | 1 | a0001c0002t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.295+5544A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75763117 | ||||||
| chr4:75763230
|
T | C | 3 | a0001c0003t0002g0003a0001c0003t0002g0004a0001c0009t0007g0169 | 3 | HG01243.hp2 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.295+5657T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75763230 | ||||||
| chr4:75763419
|
T | G | 1 | a0001c0001t0001g0119 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.295+5846T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75763419 | ||||||
| chr4:75763458
|
G | A | 137 | a0001c0002t0001g0037a0001c0002t0001g0152a0001c0002t0001g0153others(134): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.295+5885G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75763458 | ||||||
| chr4:75763480
|
G | A | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+5907G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75763480 | ||||||
| chr4:75763784
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.295+6211G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75763784 | ||||||
| chr4:75764142
|
A | G | 5 | a0001c0002t0001g0220a0002c0005t0001g0218a0002c0005t0001g0221others(2): Show | 5 | HG03491.hp1 HG03491.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-6297A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75764142 | ||||||
| chr4:75764191
|
T | C | 137 | a0001c0002t0001g0037a0001c0002t0001g0152a0001c0002t0001g0153others(134): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.296-6248T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75764191 | ||||||
| chr4:75764442
|
A | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0179 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.296-5997A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75764442 | ||||||
| chr4:75764523
|
C | G | 1 | a0001c0001t0001g0075 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.296-5916C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75764523 | ||||||
| chr4:75764678
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.296-5761C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75764678 | ||||||
| chr4:75764769
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.296-5670T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75764769 | ||||||
| chr4:75765040
|
A | T | 1 | a0001c0002t0001g0278 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.296-5399A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765040 | ||||||
| chr4:75765143
|
A | T | 1 | a0001c0001t0001g0105 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.296-5296A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765143 | ||||||
| chr4:75765148
|
G | A | 1 | a0001c0006t0001g0215 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.296-5291G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765148 | ||||||
| chr4:75765280
|
A | G | 1 | a0001c0002t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.296-5159A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765280 | ||||||
| chr4:75765316
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.296-5123T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765316 | ||||||
| chr4:75765322
|
A | G | 5 | a0001c0001t0001g0050a0001c0001t0001g0111a0001c0001t0001g0112others(2): Show | 5 | NA18962.hp2 NA18966.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-5117A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765322 | ||||||
| chr4:75765384
|
A | T | 7 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(4): Show | 7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.296-5055A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765384 | ||||||
| chr4:75765418
|
T | G | 1 | a0001c0002t0001g0268 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.296-5021T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765418 | ||||||
| chr4:75765437
|
T | C | 255 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.296-5002T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765437 | ||||||
| chr4:75765447
|
A | G | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.296-4992A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765447 | ||||||
| chr4:75765637
|
C | CT | 251 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(248): Show | 252 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.296-4788dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75765637 | |||||
| chr4:75765653
|
C | T | 41 | a0001c0003t0001g0002a0001c0003t0001g0133a0001c0003t0001g0154others(38): Show | 42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.296-4786C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765653 | ||||||
| chr4:75765787
|
G | C | 144 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(141): Show | 145 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.296-4652G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75765787 | ||||||
| chr4:75766038
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.296-4401C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75766038 | ||||||
| chr4:75766139
|
A | G | 255 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.296-4300A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75766139 | ||||||
| chr4:75766153
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.296-4286T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75766153 | ||||||
| chr4:75766391
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.296-4048A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75766391 | ||||||
| chr4:75766431
|
C | T | 2 | a0001c0002t0001g0165a0001c0002t0001g0282 | 2 | HG01109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.296-4008C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75766431 | ||||||
| chr4:75766559
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.296-3880C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75766559 | ||||||
| chr4:75766957
|
A | G | 2 | a0001c0003t0001g0189a0001c0003t0001g0203 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.296-3482A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75766957 | ||||||
| chr4:75767061
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG01891.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.296-3378G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75767061 | ||||||
| chr4:75767089
|
T | C | 2 | a0001c0003t0002g0003a0001c0003t0002g0004 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.296-3350T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75767089 | ||||||
| chr4:75767277
|
C | A | 253 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(250): Show | 254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.296-3162C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75767277 | ||||||
| chr4:75767735
|
T | C | 254 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(251): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.296-2704T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75767735 | ||||||
| chr4:75767756
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.296-2683G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75767756 | ||||||
| chr4:75768390
|
A | G | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.296-2049A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75768390 | ||||||
| chr4:75768450
|
T | TA | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.296-1988dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75768450 | |||||
| chr4:75768517
|
A | G | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.296-1922A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75768517 | ||||||
| chr4:75768994
|
T | C | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.296-1445T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75768994 | ||||||
| chr4:75769189
|
C | A | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.296-1250C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75769189 | ||||||
| chr4:75769340
|
C | T | 1 | a0001c0002t0001g0246 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.296-1099C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75769340 | ||||||
| chr4:75769392
|
G | A | 4 | a0001c0002t0001g0171a0001c0002t0001g0174a0001c0002t0001g0175others(1): Show | 4 | HG02895.hp2 HG02896.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-1047G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75769392 | ||||||
| chr4:75769599
|
G | T | 1 | a0001c0002t0001g0263 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.296-840G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75769599 | ||||||
| chr4:75769740
|
C | CT | 110 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(107): Show | 110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.296-683dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr4 | 75769740 | |||||
| chr4:75769795
|
A | C | 1 | a0001c0002t0001g0274 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.296-644A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75769795 | ||||||
| chr4:75770095
|
C | T | 82 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(79): Show | 82 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.296-344C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75770095 | ||||||
| chr4:75770130
|
C | A | 1 | a0001c0001t0001g0127 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.296-309C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 4/23 | chr4 | 75770130 | ||||||
| chr4:75770553
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.396+14C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 5/23 | chr4 | 75770553 | ||||||
| chr4:75770659
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.396+120G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 5/23 | chr4 | 75770659 | ||||||
| chr4:75770675
|
G | C | 253 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(250): Show | 254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.396+136G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 5/23 | chr4 | 75770675 | ||||||
| chr4:75770697
|
CACTT | C | 137 | a0001c0002t0001g0037a0001c0002t0001g0152a0001c0002t0001g0153others(134): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.397-123_397-120del others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr4 | 75770697 | |||||
| chr4:75771258
|
T | A | 1 | a0001c0002t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.555+121T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771258 | ||||||
| chr4:75771259
|
A | T | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+122A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771259 | ||||||
| chr4:75771290
|
G | C | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.555+153G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771290 | ||||||
| chr4:75771302
|
G | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.555+165G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771302 | ||||||
| chr4:75771375
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.555+238C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771375 | ||||||
| chr4:75771745
|
C | T | 255 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.555+608C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771745 | ||||||
| chr4:75771795
|
G | A | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+658G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771795 | ||||||
| chr4:75771813
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0058a0001c0001t0001g0082others(1): Show | 4 | HG00438.hp2 HG04184.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.555+676G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771813 | ||||||
| chr4:75771825
|
A | G | 137 | a0001c0002t0001g0037a0001c0002t0001g0152a0001c0002t0001g0153others(134): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.555+688A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771825 | ||||||
| chr4:75771838
|
A | G | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+701A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771838 | ||||||
| chr4:75771860
|
T | C | 137 | a0001c0002t0001g0037a0001c0002t0001g0152a0001c0002t0001g0153others(134): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.555+723T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771860 | ||||||
| chr4:75771875
|
A | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0179 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.555+738A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75771875 | ||||||
| chr4:75772197
|
G | A | 13 | a0001c0002t0001g0231a0001c0002t0001g0236a0001c0002t0001g0253others(10): Show | 13 | HG00733.hp2 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.555+1060G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772197 | ||||||
| chr4:75772399
|
G | A | 137 | a0001c0002t0001g0037a0001c0002t0001g0152a0001c0002t0001g0153others(134): Show | 138 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.555+1262G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772399 | ||||||
| chr4:75772505
|
G | A | 91 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(88): Show | 91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.555+1368G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772505 | ||||||
| chr4:75772533
|
G | A | 2 | a0001c0003t0002g0003a0001c0003t0002g0004 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.555+1396G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772533 | ||||||
| chr4:75772674
|
T | A | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.555+1537T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772674 | ||||||
| chr4:75772696
|
A | G | 254 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(251): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.555+1559A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772696 | ||||||
| chr4:75772751
|
AT | A | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.555+1617delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr4 | 75772751 | |||||
| chr4:75772815
|
G | A | 2 | a0001c0002t0001g0255a0001c0002t0001g0262 | 2 | NA18967.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.555+1678G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772815 | ||||||
| chr4:75772942
|
C | T | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.556-1734C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772942 | ||||||
| chr4:75772949
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.556-1727T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75772949 | ||||||
| chr4:75773194
|
TTTTA | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | NA18962.hp2 NA19007.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.556-1478_556-1475d others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr4 | 75773194 | |||||
| chr4:75773292
|
T | C | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.556-1384T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773292 | ||||||
| chr4:75773312
|
A | G | 1 | a0001c0004t0002g0010 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.556-1364A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773312 | ||||||
| chr4:75773365
|
TAA | T | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.556-1308_556-1307d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr4 | 75773365 | |||||
| chr4:75773389
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.556-1287C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773389 | ||||||
| chr4:75773451
|
A | T | 1 | a0001c0001t0001g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.556-1225A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773451 | ||||||
| chr4:75773469
|
A | G | 72 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(69): Show | 72 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(69): Show |
intron_variant | MODIFIER | c.556-1207A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773469 | ||||||
| chr4:75773502
|
A | G | 41 | a0001c0003t0001g0002a0001c0003t0001g0133a0001c0003t0001g0154others(38): Show | 42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.556-1174A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773502 | ||||||
| chr4:75773638
|
G | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.556-1038G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773638 | ||||||
| chr4:75773808
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.556-868T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773808 | ||||||
| chr4:75773913
|
CT | C | 255 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.556-755delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr4 | 75773913 | |||||
| chr4:75773986
|
G | A | 82 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(79): Show | 82 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.556-690G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75773986 | ||||||
| chr4:75774149
|
C | T | 150 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0058others(147): Show | 151 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.556-527C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | chr4 | 75774149 | ||||||
| chr4:75774657
|
TTCTC | T | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.556-17_556-14delCT others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr4 | 75774657 | |||||
| chr4:75774876
|
G | A | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.676+80G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75774876 | ||||||
| chr4:75775079
|
T | C | 32 | a0001c0004t0001g0049a0001c0004t0002g0001a0001c0004t0002g0007others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.676+283T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75775079 | ||||||
| chr4:75775329
|
A | G | 2 | a0001c0004t0002g0010a0001c0004t0002g0031 | 2 | HG01109.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.676+533A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75775329 | ||||||
| chr4:75775498
|
C | T | 7 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(4): Show | 7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.676+702C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75775498 | ||||||
| chr4:75775735
|
A | C | 1 | a0001c0002t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.676+939A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75775735 | ||||||
| chr4:75775809
|
A | G | 32 | a0001c0004t0001g0049a0001c0004t0002g0001a0001c0004t0002g0007others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.676+1013A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75775809 | ||||||
| chr4:75775844
|
A | G | 5 | a0001c0002t0001g0164a0001c0002t0001g0167a0001c0002t0001g0168others(2): Show | 5 | HG02258.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.676+1048A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75775844 | ||||||
| chr4:75776058
|
A | G | 83 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(80): Show | 83 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(80): Show |
intron_variant | MODIFIER | c.676+1262A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776058 | ||||||
| chr4:75776101
|
A | G | 1 | a0001c0006t0001g0199 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.676+1305A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776101 | ||||||
| chr4:75776199
|
C | T | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.676+1403C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776199 | ||||||
| chr4:75776230
|
T | A | 1 | a0001c0001t0001g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.676+1434T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776230 | ||||||
| chr4:75776240
|
T | G | 2 | a0001c0003t0001g0189a0001c0003t0001g0203 | 2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.676+1444T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776240 | ||||||
| chr4:75776730
|
T | C | 1 | a0001c0004t0002g0033 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.676+1934T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776730 | ||||||
| chr4:75776770
|
A | G | 1 | a0001c0003t0001g0194 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.676+1974A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776770 | ||||||
| chr4:75776811
|
G | A | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.676+2015G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776811 | ||||||
| chr4:75776898
|
A | G | 3 | a0001c0001t0001g0069a0001c0001t0003g0057a0001c0001t0003g0072 | 3 | HG02109.hp1 HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.676+2102A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776898 | ||||||
| chr4:75776918
|
A | G | 1 | a0001c0002t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.676+2122A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776918 | ||||||
| chr4:75776923
|
T | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.676+2127T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776923 | ||||||
| chr4:75776924
|
A | T | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.676+2128A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75776924 | ||||||
| chr4:75777171
|
A | G | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.676+2375A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75777171 | ||||||
| chr4:75777271
|
A | G | 247 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(244): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.676+2475A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75777271 | ||||||
| chr4:75777288
|
T | A | 1 | a0001c0002t0001g0231 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.676+2492T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75777288 | ||||||
| chr4:75777458
|
G | C | 1 | a0001c0001t0001g0086 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.676+2662G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75777458 | ||||||
| chr4:75777513
|
A | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.676+2717A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75777513 | ||||||
| chr4:75777715
|
C | G | 110 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(107): Show | 110 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.676+2919C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75777715 | ||||||
| chr4:75777869
|
A | G | 8 | a0001c0002t0001g0226a0001c0002t0001g0227a0001c0002t0001g0229others(5): Show | 8 | NA18941.hp2 NA18950.hp1 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.676+3073A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75777869 | ||||||
| chr4:75778053
|
G | C | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.676+3257G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778053 | ||||||
| chr4:75778270
|
G | T | 1 | a0001c0002t0001g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.676+3474G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778270 | ||||||
| chr4:75778374
|
G | C | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.676+3578G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778374 | ||||||
| chr4:75778463
|
A | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.676+3667A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778463 | ||||||
| chr4:75778469
|
G | A | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.676+3673G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778469 | ||||||
| chr4:75778502
|
C | T | 244 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(241): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.676+3706C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778502 | ||||||
| chr4:75778605
|
A | G | 2 | a0001c0006t0001g0215a0001c0006t0001g0216 | 2 | HG01516.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.676+3809A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778605 | ||||||
| chr4:75778737
|
A | G | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.676+3941A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778737 | ||||||
| chr4:75778786
|
G | A | 73 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(70): Show | 73 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(70): Show |
intron_variant | MODIFIER | c.677-3894G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778786 | ||||||
| chr4:75778841
|
A | G | 1 | a0001c0003t0001g0002 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.677-3839A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778841 | ||||||
| chr4:75778981
|
C | T | 1 | a0001c0002t0001g0245 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.677-3699C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75778981 | ||||||
| chr4:75779382
|
G | C | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.677-3298G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779382 | ||||||
| chr4:75779562
|
A | G | 1 | a0001c0002t0001g0234 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.677-3118A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779562 | ||||||
| chr4:75779630
|
A | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.677-3050A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779630 | ||||||
| chr4:75779714
|
A | G | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.677-2966A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779714 | ||||||
| chr4:75779750
|
A | G | 244 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(241): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.677-2930A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779750 | ||||||
| chr4:75779942
|
G | A | 2 | a0001c0003t0002g0003a0001c0003t0002g0004 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.677-2738G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779942 | ||||||
| chr4:75779948
|
A | G | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.677-2732A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779948 | ||||||
| chr4:75779994
|
A | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG01891.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.677-2686A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75779994 | ||||||
| chr4:75780335
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.677-2345C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75780335 | ||||||
| chr4:75780567
|
A | AGCCAATA others(2282): Show |
1 | a0001c0004t0002g0015 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.677-2095_677-2094i others(2291): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75780567 | |||||
| chr4:75780640
|
C | CT | 69 | a0001c0001t0001g0039a0001c0002t0001g0037a0001c0002t0001g0153others(66): Show | 69 | HG00733.hp2 HG01109.hp1 HG01168.hp1 others(66): Show |
intron_variant | MODIFIER | c.677-2015dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75780640 | |||||
| chr4:75780640
|
C | CTT | 25 | a0001c0002t0001g0156a0001c0002t0001g0160a0001c0002t0001g0164others(22): Show | 25 | HG00609.hp2 HG01346.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.677-2016_677-2015d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75780640 | |||||
| chr4:75780640
|
C | CTTTT | 23 | a0001c0004t0001g0049a0001c0004t0002g0001a0001c0004t0002g0007others(20): Show | 24 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.677-2018_677-2015d others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75780640 | |||||
| chr4:75780640
|
C | CTTTTT | 7 | a0001c0004t0002g0017a0001c0004t0002g0025a0001c0004t0002g0029others(4): Show | 7 | HG01109.hp2 HG01346.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.677-2019_677-2015d others(7): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75780640 | |||||
| chr4:75780640
|
C | CTTTTTTT others(4): Show |
1 | a0001c0004t0002g0015 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.677-2025_677-2015d others(13): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75780640 | |||||
| chr4:75780640
|
CT | C | 93 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.677-2015delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75780640 | |||||
| chr4:75780792
|
T | C | 244 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(241): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.677-1888T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75780792 | ||||||
| chr4:75781156
|
A | C | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.677-1524A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75781156 | ||||||
| chr4:75781340
|
G | A | 1 | a0001c0002t0001g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.677-1340G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75781340 | ||||||
| chr4:75781529
|
T | A | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.677-1151T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75781529 | ||||||
| chr4:75781760
|
TA | T | 111 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(108): Show | 111 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.677-910delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr4 | 75781760 | |||||
| chr4:75781761
|
A | T | 1 | a0001c0003t0001g0202 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.677-919A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75781761 | ||||||
| chr4:75781904
|
T | G | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.677-776T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75781904 | ||||||
| chr4:75782353
|
A | T | 1 | a0001c0001t0001g0111 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.677-327A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 8/23 | chr4 | 75782353 | ||||||
| chr4:75783325
|
C | T | 1 | a0001c0004t0002g0008 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.855+467C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783325 | ||||||
| chr4:75783526
|
A | G | 1 | a0001c0002t0001g0255 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.855+668A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783526 | ||||||
| chr4:75783613
|
C | T | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.855+755C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783613 | ||||||
| chr4:75783626
|
C | A | 91 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(88): Show | 91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.855+768C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783626 | ||||||
| chr4:75783674
|
C | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.855+816C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783674 | ||||||
| chr4:75783707
|
A | G | 108 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(105): Show | 108 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.855+849A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783707 | ||||||
| chr4:75783714
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.855+856G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783714 | ||||||
| chr4:75783861
|
A | T | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.855+1003A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75783861 | ||||||
| chr4:75784132
|
C | G | 1 | a0001c0001t0001g0079 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.855+1274C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75784132 | ||||||
| chr4:75784626
|
A | G | 41 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(38): Show | 42 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.855+1768A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75784626 | ||||||
| chr4:75784791
|
G | GA | 8 | a0001c0001t0001g0135a0001c0004t0001g0049a0001c0004t0002g0018others(5): Show | 8 | HG01993.hp2 NA18970.hp1 NA18979.hp1 others(5): Show |
intron_variant | MODIFIER | c.855+1947dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr4 | 75784791 | |||||
| chr4:75784940
|
T | A | 1 | a0001c0003t0001g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.855+2082T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75784940 | ||||||
| chr4:75785174
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.856-1888A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785174 | ||||||
| chr4:75785204
|
G | A | 2 | a0001c0002t0001g0230a0001c0002t0001g0284 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.856-1858G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785204 | ||||||
| chr4:75785323
|
T | C | 1 | a0001c0002t0001g0152 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.856-1739T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785323 | ||||||
| chr4:75785362
|
T | A | 8 | a0001c0001t0001g0041a0001c0001t0001g0097a0001c0001t0001g0107others(5): Show | 8 | HG01891.hp1 HG02922.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.856-1700T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785362 | ||||||
| chr4:75785413
|
C | G | 1 | a0001c0003t0001g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.856-1649C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785413 | ||||||
| chr4:75785543
|
C | T | 244 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(241): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.856-1519C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785543 | ||||||
| chr4:75785548
|
A | G | 6 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(3): Show | 6 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.856-1514A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785548 | ||||||
| chr4:75785704
|
A | G | 1 | a0001c0004t0002g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.856-1358A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785704 | ||||||
| chr4:75785741
|
A | G | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.856-1321A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785741 | ||||||
| chr4:75785755
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.856-1307A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785755 | ||||||
| chr4:75785927
|
A | T | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-1135A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75785927 | ||||||
| chr4:75786456
|
CTG | C | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.856-602_856-601del others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr4 | 75786456 | |||||
| chr4:75786775
|
G | A | 1 | a0001c0002t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.856-287G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75786775 | ||||||
| chr4:75786793
|
T | C | 10 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0267others(7): Show | 10 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.856-269T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75786793 | ||||||
| chr4:75786897
|
A | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.856-165A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75786897 | ||||||
| chr4:75786924
|
C | T | 4 | a0001c0001t0001g0056a0001c0001t0001g0063a0001c0001t0001g0099others(1): Show | 4 | HG00639.hp1 HG00738.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-138C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 9/23 | chr4 | 75786924 | ||||||
| chr4:75787349
|
A | G | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.996+147A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75787349 | ||||||
| chr4:75787403
|
T | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.996+201T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75787403 | ||||||
| chr4:75787479
|
G | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.996+277G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75787479 | ||||||
| chr4:75787539
|
C | T | 2 | a0001c0003t0002g0003a0001c0003t0002g0004 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.996+337C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75787539 | ||||||
| chr4:75787702
|
T | C | 1 | a0001c0004t0002g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.996+500T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75787702 | ||||||
| chr4:75787737
|
C | G | 1 | a0001c0001t0001g0123 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.996+535C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75787737 | ||||||
| chr4:75788145
|
C | T | 5 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0102others(2): Show | 5 | HG01975.hp1 HG02004.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.996+943C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788145 | ||||||
| chr4:75788165
|
TTA | T | 6 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(3): Show | 6 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.996+965_996+966del others(2): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75788165 | |||||
| chr4:75788166
|
TA | T | 4 | a0001c0001t0001g0116a0001c0003t0002g0003a0001c0003t0002g0004others(1): Show | 4 | HG01243.hp1 HG01243.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.996+965delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788166 | ||||||
| chr4:75788167
|
A | T | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.996+965A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788167 | ||||||
| chr4:75788170
|
T | A | 2 | a0001c0003t0002g0003a0001c0003t0002g0004 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.996+968T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788170 | ||||||
| chr4:75788170
|
TA | T | 47 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0115others(44): Show | 47 | HG00609.hp2 HG00733.hp2 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.996+969delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788170 | ||||||
| chr4:75788171
|
A | T | 18 | a0001c0001t0001g0116a0001c0001t0001g0130a0001c0002t0001g0167others(15): Show | 18 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.996+969A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788171 | ||||||
| chr4:75788171
|
AT | A | 113 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(110): Show | 113 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.996+984delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75788171 | |||||
| chr4:75788172
|
T | A | 1 | a0001c0003t0001g0209 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.996+970T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788172 | ||||||
| chr4:75788172
|
T | TTTA | 31 | a0001c0001t0001g0110a0001c0004t0001g0049a0001c0004t0002g0001others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.996+972_996+973ins others(3): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75788172 | |||||
| chr4:75788175
|
T | A | 23 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0267others(20): Show | 23 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.996+973T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788175 | ||||||
| chr4:75788176
|
T | A | 44 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0045others(41): Show | 45 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.996+974T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788176 | ||||||
| chr4:75788180
|
T | A | 39 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(36): Show | 40 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.996+978T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788180 | ||||||
| chr4:75788266
|
C | T | 1 | a0001c0002t0001g0282 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.996+1064C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788266 | ||||||
| chr4:75788329
|
G | A | 2 | a0001c0004t0002g0001a0001c0004t0002g0034 | 3 | HG00099.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.996+1127G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788329 | ||||||
| chr4:75788382
|
G | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0124a0001c0001t0001g0125 | 3 | HG01891.hp1 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.996+1180G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788382 | ||||||
| chr4:75788478
|
A | C | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.996+1276A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788478 | ||||||
| chr4:75788547
|
C | CTT | 36 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(33): Show | 37 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.996+1356_996+1357d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75788547 | |||||
| chr4:75788659
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0117 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.996+1457C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788659 | ||||||
| chr4:75788764
|
C | T | 1 | a0001c0002t0001g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.997-1386C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788764 | ||||||
| chr4:75788826
|
C | A | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.997-1324C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75788826 | ||||||
| chr4:75789096
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.997-1054G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789096 | ||||||
| chr4:75789230
|
T | G | 1 | a0001c0001t0001g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.997-920T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789230 | ||||||
| chr4:75789282
|
C | CTGT | 244 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(241): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.997-857_997-855dup others(3): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75789282 | |||||
| chr4:75789317
|
T | C | 6 | a0001c0003t0001g0185a0001c0003t0001g0209a0001c0003t0001g0210others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.997-833T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789317 | ||||||
| chr4:75789334
|
G | A | 2 | a0001c0003t0001g0194a0001c0003t0001g0195 | 2 | HG00741.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.997-816G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789334 | ||||||
| chr4:75789474
|
C | T | 2 | a0001c0007t0001g0101a0001c0007t0001g0151 | 2 | HG01123.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.997-676C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789474 | ||||||
| chr4:75789498
|
C | T | 10 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0267others(7): Show | 10 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.997-652C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789498 | ||||||
| chr4:75789731
|
A | G | 91 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(88): Show | 91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.997-419A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789731 | ||||||
| chr4:75789925
|
T | C | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.997-225T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789925 | ||||||
| chr4:75789937
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.997-213T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789937 | ||||||
| chr4:75789938
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.997-212T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789938 | ||||||
| chr4:75789944
|
T | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.997-206T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789944 | ||||||
| chr4:75789964
|
G | A | 5 | a0001c0003t0001g0181a0001c0003t0001g0188a0001c0003t0001g0192others(2): Show | 5 | HG01123.hp1 HG01934.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.997-186G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75789964 | ||||||
| chr4:75790047
|
T | TA | 84 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(81): Show | 84 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(81): Show |
intron_variant | MODIFIER | c.997-92dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75790047 | |||||
| chr4:75790047
|
TA | T | 133 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(130): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.997-92delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75790047 | |||||
| chr4:75790049
|
A | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0128 | 2 | HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.997-101A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75790049 | ||||||
| chr4:75790058
|
A | AAC | 7 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(4): Show | 7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.997-92_997-91insAC | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75790058 | ||||||
| chr4:75790059
|
C | A | 7 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(4): Show | 7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.997-91C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75790059 | ||||||
| chr4:75790069
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.997-81A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75790069 | ||||||
| chr4:75790070
|
G | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0098a0001c0001t0001g0104others(2): Show | 5 | HG00280.hp1 HG03490.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.997-80G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75790070 | ||||||
| chr4:75790071
|
AT | A | 31 | a0001c0004t0001g0049a0001c0004t0002g0001a0001c0004t0002g0007others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.997-71delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr4 | 75790071 | |||||
| chr4:75790073
|
T | C | 1 | a0001c0001t0001g0286 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.997-77T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 10/23 | chr4 | 75790073 | ||||||
| chr4:75790911
|
G | GA | 42 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(39): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.1240+126dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr4 | 75790911 | |||||
| chr4:75791020
|
A | G | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1240+223A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791020 | ||||||
| chr4:75791265
|
C | T | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1240+468C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791265 | ||||||
| chr4:75791309
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1240+512A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791309 | ||||||
| chr4:75791422
|
G | T | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1240+625G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791422 | ||||||
| chr4:75791517
|
G | C | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1240+720G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791517 | ||||||
| chr4:75791617
|
C | G | 1 | a0001c0006t0001g0216 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1240+820C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791617 | ||||||
| chr4:75791800
|
CA | C | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1240+1012delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr4 | 75791800 | |||||
| chr4:75791810
|
T | A | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1240+1013T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791810 | ||||||
| chr4:75791970
|
G | A | 91 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(88): Show | 91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.1240+1173G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791970 | ||||||
| chr4:75791985
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1240+1188C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75791985 | ||||||
| chr4:75792022
|
C | CT | 32 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(29): Show | 32 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1240+1241dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr4 | 75792022 | |||||
| chr4:75792022
|
CT | C | 7 | a0001c0001t0001g0119a0001c0001t0001g0136a0001c0002t0001g0153others(4): Show | 7 | HG01169.hp2 HG01943.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1240+1241delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr4 | 75792022 | |||||
| chr4:75792426
|
A | G | 1 | a0001c0002t0001g0279 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1241-1264A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75792426 | ||||||
| chr4:75792618
|
G | A | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1241-1072G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75792618 | ||||||
| chr4:75793205
|
CT | C | 80 | a0001c0001t0001g0048a0001c0001t0001g0115a0001c0002t0001g0037others(77): Show | 80 | HG00609.hp2 HG01109.hp1 HG01169.hp2 others(77): Show |
intron_variant | MODIFIER | c.1241-462delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr4 | 75793205 | |||||
| chr4:75793205
|
CTT | C | 114 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(111): Show | 115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1241-463_1241-462d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr4 | 75793205 | |||||
| chr4:75793205
|
CTTT | C | 30 | a0001c0001t0001g0040a0001c0001t0001g0119a0001c0001t0001g0135others(27): Show | 30 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1241-464_1241-462d others(5): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr4 | 75793205 | |||||
| chr4:75793368
|
C | T | 2 | a0001c0003t0002g0003a0001c0003t0002g0004 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1241-322C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75793368 | ||||||
| chr4:75793623
|
A | G | 1 | a0001c0003t0001g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1241-67A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 12/23 | chr4 | 75793623 | ||||||
| chr4:75794056
|
G | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1452+155G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794056 | ||||||
| chr4:75794152
|
T | G | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1452+251T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794152 | ||||||
| chr4:75794200
|
C | A | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1452+299C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794200 | ||||||
| chr4:75794355
|
C | T | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1452+454C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794355 | ||||||
| chr4:75794479
|
T | A | 1 | a0001c0003t0001g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1452+578T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794479 | ||||||
| chr4:75794525
|
T | C | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1452+624T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794525 | ||||||
| chr4:75794608
|
G | A | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1452+707G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794608 | ||||||
| chr4:75794678
|
T | C | 1 | a0001c0003t0001g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1452+777T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794678 | ||||||
| chr4:75794894
|
T | C | 2 | a0001c0004t0002g0024a0001c0014t0002g0036 | 2 | HG03453.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1452+993T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75794894 | ||||||
| chr4:75795209
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1452+1308A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75795209 | ||||||
| chr4:75795354
|
C | T | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1452+1453C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75795354 | ||||||
| chr4:75795562
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1452+1661G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75795562 | ||||||
| chr4:75795646
|
G | A | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1452+1745G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75795646 | ||||||
| chr4:75795708
|
G | A | 1 | a0001c0002t0001g0173 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1452+1807G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75795708 | ||||||
| chr4:75795769
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1452+1868C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75795769 | ||||||
| chr4:75795914
|
TTTTTG | T | 239 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(236): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1452+2045_1452+204 others(9): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75795914 | |||||
| chr4:75796140
|
A | G | 1 | a0001c0002t0001g0265 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1452+2239A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75796140 | ||||||
| chr4:75796318
|
ATCCCAGA others(4): Show |
A | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1452+2421_1452+243 others(15): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796318 | |||||
| chr4:75796341
|
C | CTTTTTTT others(7): Show |
3 | a0001c0004t0002g0019a0001c0004t0002g0026a0001c0014t0002g0036 | 3 | HG03453.hp2 HG03704.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1452+2452_1452+245 others(18): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796341 | |||||
| chr4:75796341
|
C | CTTTTTTT others(8): Show |
25 | a0001c0001t0001g0041a0001c0004t0001g0049a0001c0004t0002g0001others(22): Show | 26 | HG00099.hp1 HG00323.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1452+2452_1452+245 others(19): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796341 | |||||
| chr4:75796341
|
C | CTTTTTTT others(9): Show |
10 | a0001c0001t0001g0052a0001c0001t0001g0144a0001c0001t0001g0145others(7): Show | 10 | HG00140.hp2 HG01884.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1452+2452_1452+245 others(20): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796341 | |||||
| chr4:75796341
|
C | CTTTTTTT others(10): Show |
91 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(88): Show | 91 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1452+2452_1452+245 others(21): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796341 | |||||
| chr4:75796341
|
C | CTTTTTTT others(11): Show |
15 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0061others(12): Show | 15 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1452+2452_1452+245 others(22): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796341 | |||||
| chr4:75796341
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0001g0048a0001c0001t0001g0116 | 2 | HG04115.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1452+2452_1452+245 others(23): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796341 | |||||
| chr4:75796341
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0074 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1452+2452_1452+245 others(25): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796341 | |||||
| chr4:75796351
|
T | TTTTTTTT others(10): Show |
1 | a0001c0001t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1452+2452_1452+245 others(21): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796351 | |||||
| chr4:75796493
|
A | G | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1452+2592A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75796493 | ||||||
| chr4:75796500
|
G | A | 1 | a0001c0003t0001g0198 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1452+2599G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75796500 | ||||||
| chr4:75796571
|
G | T | 244 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(241): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1452+2670G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75796571 | ||||||
| chr4:75796829
|
A | G | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1453-2793A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75796829 | ||||||
| chr4:75796842
|
A | G | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1453-2780A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75796842 | ||||||
| chr4:75796875
|
AT | A | 112 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(109): Show | 112 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1453-2732delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796875 | |||||
| chr4:75796875
|
ATT | A | 31 | a0001c0004t0001g0049a0001c0004t0002g0001a0001c0004t0002g0007others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.1453-2733_1453-273 others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796875 | |||||
| chr4:75796890
|
T | TC | 16 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(13): Show | 16 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1453-2731dupC | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75796890 | |||||
| chr4:75796953
|
T | C | 91 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(88): Show | 91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.1453-2669T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75796953 | ||||||
| chr4:75797171
|
A | C | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1453-2451A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797171 | ||||||
| chr4:75797178
|
C | A | 1 | a0001c0002t0001g0278 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1453-2444C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797178 | ||||||
| chr4:75797221
|
T | C | 1 | a0001c0002t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1453-2401T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797221 | ||||||
| chr4:75797474
|
C | CTT | 121 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(118): Show | 122 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1453-2147_1453-214 others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75797474 | |||||
| chr4:75797474
|
CTCTTT | C | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1453-2146_1453-214 others(9): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75797474 | |||||
| chr4:75797560
|
C | CA | 106 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(103): Show | 106 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1453-2046dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75797560 | |||||
| chr4:75797560
|
CA | C | 87 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(84): Show | 87 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(84): Show |
intron_variant | MODIFIER | c.1453-2046delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75797560 | |||||
| chr4:75797686
|
G | T | 1 | a0001c0001t0001g0086 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1453-1936G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797686 | ||||||
| chr4:75797726
|
C | G | 7 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(4): Show | 7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1453-1896C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797726 | ||||||
| chr4:75797790
|
C | T | 30 | a0001c0004t0001g0049a0001c0004t0002g0001a0001c0004t0002g0007others(27): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1453-1832C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797790 | ||||||
| chr4:75797947
|
G | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0143 | 2 | HG01175.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.1453-1675G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797947 | ||||||
| chr4:75797966
|
G | A | 1 | a0001c0004t0002g0007 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1453-1656G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75797966 | ||||||
| chr4:75798231
|
C | T | 241 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(238): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1453-1391C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798231 | ||||||
| chr4:75798248
|
C | G | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1453-1374C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798248 | ||||||
| chr4:75798259
|
C | T | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1453-1363C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798259 | ||||||
| chr4:75798297
|
G | A | 10 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0001g0267others(7): Show | 10 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1453-1325G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798297 | ||||||
| chr4:75798387
|
G | A | 1 | a0001c0002t0001g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1453-1235G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798387 | ||||||
| chr4:75798395
|
G | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1453-1227G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798395 | ||||||
| chr4:75798574
|
A | G | 1 | a0001c0002t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1453-1048A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798574 | ||||||
| chr4:75798600
|
T | C | 1 | a0001c0001t0001g0119 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1453-1022T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798600 | ||||||
| chr4:75798703
|
G | C | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1453-919G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75798703 | ||||||
| chr4:75798821
|
A | AGTTTT | 39 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(36): Show | 40 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1453-790_1453-786d others(7): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | INFO_REALIGN_3_PRIME | chr4 | 75798821 | |||||
| chr4:75799148
|
G | A | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1453-474G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799148 | ||||||
| chr4:75799189
|
G | GT | 38 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(35): Show | 39 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1453-433_1453-432i others(3): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799189 | ||||||
| chr4:75799190
|
G | T | 285 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(282): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1453-432G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799190 | ||||||
| chr4:75799206
|
G | A | 5 | a0001c0002t0001g0164a0001c0002t0001g0167a0001c0002t0001g0168others(2): Show | 5 | HG02258.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1453-416G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799206 | ||||||
| chr4:75799259
|
A | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1453-363A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799259 | ||||||
| chr4:75799319
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0098 | 2 | HG03710.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1453-303C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799319 | ||||||
| chr4:75799374
|
A | G | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1453-248A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799374 | ||||||
| chr4:75799610
|
T | C | 1 | a0001c0001t0001g0080 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1453-12T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799610 | ||||||
| chr4:75799614
|
T | C | 3 | a0001c0003t0001g0209a0001c0003t0001g0210a0001c0003t0001g0212 | 3 | HG02258.hp1 HG02630.hp2 HG02976.hp2 |
splice_region_variant&intron_variant | LOW | c.1453-8T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 13/23 | chr4 | 75799614 | ||||||
| chr4:75799822
|
A | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1563+90A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75799822 | ||||||
| chr4:75799897
|
G | C | 83 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(80): Show | 83 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(80): Show |
intron_variant | MODIFIER | c.1563+165G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75799897 | ||||||
| chr4:75799920
|
C | G | 2 | a0001c0004t0002g0019a0001c0004t0002g0020 | 2 | NA18980.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1563+188C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75799920 | ||||||
| chr4:75799922
|
G | A | 7 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(4): Show | 7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1563+190G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75799922 | ||||||
| chr4:75800012
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1563+280C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75800012 | ||||||
| chr4:75800167
|
C | T | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1564-184C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75800167 | ||||||
| chr4:75800261
|
C | G | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1564-90C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75800261 | ||||||
| chr4:75800306
|
G | A | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1564-45G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 14/23 | chr4 | 75800306 | ||||||
| chr4:75800518
|
C | CTTT | 103 | a0001c0001t0001g0041a0001c0001t0001g0043a0001c0001t0001g0044others(100): Show | 103 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.1682+62_1682+64dup others(3): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr4 | 75800518 | |||||
| chr4:75800518
|
C | CTTTT | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0042others(8): Show | 11 | HG01123.hp2 HG02559.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1682+61_1682+64dup others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr4 | 75800518 | |||||
| chr4:75800518
|
CT | C | 8 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(5): Show | 8 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1682+64delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 15/23 | INFO_REALIGN_3_PRIME | chr4 | 75800518 | |||||
| chr4:75800552
|
C | G | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1683-66C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 15/23 | chr4 | 75800552 | ||||||
| chr4:75800602
|
A | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0179 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1683-16A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 15/23 | chr4 | 75800602 | ||||||
| chr4:75800888
|
G | A | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1864+89G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 16/23 | chr4 | 75800888 | ||||||
| chr4:75801269
|
T | C | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1986+69T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801269 | ||||||
| chr4:75801397
|
A | G | 1 | a0001c0004t0002g0031 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1986+197A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801397 | ||||||
| chr4:75801426
|
C | A | 39 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(36): Show | 40 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1986+226C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801426 | ||||||
| chr4:75801502
|
C | G | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1986+302C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801502 | ||||||
| chr4:75801683
|
C | T | 1 | a0001c0002t0001g0272 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1986+483C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801683 | ||||||
| chr4:75801747
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1986+547A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801747 | ||||||
| chr4:75801943
|
G | A | 3 | a0001c0003t0001g0154a0001c0003t0001g0196a0001c0003t0001g0202 | 3 | HG01192.hp1 HG01261.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1986+743G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801943 | ||||||
| chr4:75801977
|
G | A | 39 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(36): Show | 40 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1986+777G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75801977 | ||||||
| chr4:75802184
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1986+984G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802184 | ||||||
| chr4:75802584
|
C | A | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1986+1384C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802584 | ||||||
| chr4:75802585
|
A | C | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1986+1385A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802585 | ||||||
| chr4:75802736
|
C | CT | 44 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0092others(41): Show | 44 | HG00609.hp2 HG01243.hp2 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.1987-1373dupT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 75802736 | |||||
| chr4:75802736
|
C | CTT | 9 | a0001c0001t0001g0039a0001c0002t0001g0156a0001c0002t0001g0165others(6): Show | 9 | HG01109.hp1 HG02145.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1987-1374_1987-137 others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 75802736 | |||||
| chr4:75802736
|
CT | C | 78 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1987-1373delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 75802736 | |||||
| chr4:75802736
|
CTT | C | 31 | a0001c0001t0001g0096a0001c0001t0001g0113a0001c0004t0002g0001others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.1987-1374_1987-137 others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 75802736 | |||||
| chr4:75802742
|
T | C | 2 | a0001c0001t0001g0135a0004c0016t0001g0180 | 2 | HG01993.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1987-1392T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802742 | ||||||
| chr4:75802764
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0140 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1987-1370G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802764 | ||||||
| chr4:75802777
|
T | C | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1987-1357T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802777 | ||||||
| chr4:75802791
|
G | A | 30 | a0001c0004t0001g0049a0001c0004t0002g0001a0001c0004t0002g0007others(27): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1987-1343G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802791 | ||||||
| chr4:75802872
|
C | T | 1 | a0001c0004t0002g0035 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1987-1262C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802872 | ||||||
| chr4:75802880
|
C | T | 1 | a0001c0010t0002g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1987-1254C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802880 | ||||||
| chr4:75802887
|
A | C | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1987-1247A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75802887 | ||||||
| chr4:75803087
|
C | CA | 110 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1987-1034dupA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 75803087 | |||||
| chr4:75803087
|
C | CAA | 11 | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0001g0056others(8): Show | 11 | HG00738.hp1 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1987-1035_1987-103 others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr4 | 75803087 | |||||
| chr4:75803100
|
A | C | 1 | a0001c0009t0007g0169 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1987-1034A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803100 | ||||||
| chr4:75803238
|
G | C | 5 | a0001c0001t0001g0065a0001c0001t0001g0068a0001c0001t0001g0070others(2): Show | 5 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.1987-896G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803238 | ||||||
| chr4:75803284
|
A | T | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1987-850A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803284 | ||||||
| chr4:75803365
|
T | C | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.1987-769T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803365 | ||||||
| chr4:75803522
|
C | T | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1987-612C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803522 | ||||||
| chr4:75803527
|
G | A | 1 | a0001c0003t0001g0198 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1987-607G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803527 | ||||||
| chr4:75803762
|
T | A | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1987-372T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803762 | ||||||
| chr4:75803795
|
C | T | 2 | a0001c0002t0001g0230a0001c0002t0001g0284 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1987-339C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803795 | ||||||
| chr4:75803834
|
T | A | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1987-300T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803834 | ||||||
| chr4:75803856
|
A | T | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1987-278A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803856 | ||||||
| chr4:75803924
|
C | A | 1 | a0001c0001t0001g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1987-210C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803924 | ||||||
| chr4:75803940
|
G | A | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1987-194G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75803940 | ||||||
| chr4:75804075
|
A | G | 1 | a0001c0003t0001g0198 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1987-59A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75804075 | ||||||
| chr4:75804092
|
G | T | 274 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1987-42G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 17/23 | chr4 | 75804092 | ||||||
| chr4:75804393
|
A | C | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2125+121A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75804393 | ||||||
| chr4:75804454
|
T | C | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2125+182T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75804454 | ||||||
| chr4:75804471
|
A | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2125+199A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75804471 | ||||||
| chr4:75804817
|
G | A | 91 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(88): Show | 91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.2126-323G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75804817 | ||||||
| chr4:75804911
|
C | G | 31 | a0001c0004t0001g0049a0001c0004t0002g0001a0001c0004t0002g0007others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.2126-229C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75804911 | ||||||
| chr4:75804921
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2126-219C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75804921 | ||||||
| chr4:75804967
|
A | T | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2126-173A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75804967 | ||||||
| chr4:75805026
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2126-114A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75805026 | ||||||
| chr4:75805065
|
A | G | 1 | a0001c0004t0002g0008 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2126-75A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75805065 | ||||||
| chr4:75805106
|
C | T | 7 | a0001c0002t0001g0171a0001c0002t0001g0172a0001c0002t0001g0173others(4): Show | 7 | HG02895.hp2 HG02896.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.2126-34C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75805106 | ||||||
| chr4:75805127
|
G | C | 1 | a0001c0001t0001g0149 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2126-13G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 18/23 | chr4 | 75805127 | ||||||
| chr4:75805363
|
C | T | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2289+60C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805363 | ||||||
| chr4:75805375
|
T | C | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.2289+72T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805375 | ||||||
| chr4:75805386
|
C | T | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.2289+83C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805386 | ||||||
| chr4:75805468
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2289+165A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805468 | ||||||
| chr4:75805685
|
T | C | 2 | a0001c0003t0002g0003a0001c0003t0002g0004 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2289+382T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805685 | ||||||
| chr4:75805709
|
TA | T | 6 | a0001c0001t0001g0063a0001c0001t0001g0102a0001c0001t0001g0119others(3): Show | 6 | HG01517.hp1 HG01975.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.2289+423delA | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr4 | 75805709 | |||||
| chr4:75805770
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2289+467A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805770 | ||||||
| chr4:75805797
|
A | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0179 | 3 | HG02647.hp2 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2289+494A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805797 | ||||||
| chr4:75805916
|
T | C | 285 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(282): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.2290-570T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805916 | ||||||
| chr4:75805932
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2290-554T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805932 | ||||||
| chr4:75805944
|
C | G | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2290-542C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805944 | ||||||
| chr4:75805945
|
G | C | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2290-541G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75805945 | ||||||
| chr4:75806128
|
A | G | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2290-358A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75806128 | ||||||
| chr4:75806129
|
T | A | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2290-357T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75806129 | ||||||
| chr4:75806192
|
G | A | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.2290-294G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75806192 | ||||||
| chr4:75806304
|
A | T | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2290-182A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | chr4 | 75806304 | ||||||
| chr4:75806423
|
GT | G | 115 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(112): Show | 115 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.2290-54delT | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr4 | 75806423 | |||||
| chr4:75806779
|
C | T | 116 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.2376+207C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75806779 | ||||||
| chr4:75806974
|
A | G | 51 | a0001c0002t0001g0219a0001c0002t0001g0220a0001c0002t0001g0223others(48): Show | 51 | HG00609.hp2 HG00733.hp2 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.2376+402A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75806974 | ||||||
| chr4:75807306
|
T | C | 30 | a0001c0004t0001g0049a0001c0004t0002g0001a0001c0004t0002g0007others(27): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.2376+734T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75807306 | ||||||
| chr4:75807502
|
C | T | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2376+930C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75807502 | ||||||
| chr4:75807559
|
T | G | 1 | a0001c0001t0001g0064 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2376+987T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75807559 | ||||||
| chr4:75807668
|
CTT | C | 32 | a0001c0004t0001g0049a0001c0004t0002g0001a0001c0004t0002g0007others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.2376+1099_2376+110 others(6): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr4 | 75807668 | |||||
| chr4:75807774
|
A | C | 1 | a0001c0001t0001g0042 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2377-1179A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75807774 | ||||||
| chr4:75808038
|
A | G | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2377-915A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808038 | ||||||
| chr4:75808039
|
G | A | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2377-914G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808039 | ||||||
| chr4:75808103
|
T | C | 51 | a0001c0002t0001g0219a0001c0002t0001g0220a0001c0002t0001g0223others(48): Show | 51 | HG00609.hp2 HG00733.hp2 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.2377-850T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808103 | ||||||
| chr4:75808107
|
C | T | 2 | a0001c0003t0002g0003a0001c0003t0002g0004 | 2 | HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2377-846C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808107 | ||||||
| chr4:75808473
|
T | A | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2377-480T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808473 | ||||||
| chr4:75808621
|
A | C | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2377-332A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808621 | ||||||
| chr4:75808631
|
A | G | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2377-322A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808631 | ||||||
| chr4:75808739
|
A | ATT | 40 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0116others(37): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.2377-203_2377-202d others(4): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr4 | 75808739 | |||||
| chr4:75808739
|
A | ATTT | 107 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(104): Show | 107 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.2377-204_2377-202d others(5): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr4 | 75808739 | |||||
| chr4:75808768
|
G | A | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2377-185G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808768 | ||||||
| chr4:75808771
|
A | G | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2377-182A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808771 | ||||||
| chr4:75808779
|
T | G | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2377-174T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808779 | ||||||
| chr4:75808780
|
A | T | 1 | a0001c0011t0001g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2377-173A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808780 | ||||||
| chr4:75808784
|
G | C | 16 | a0001c0001t0001g0051a0001c0001t0001g0065a0001c0001t0001g0068others(13): Show | 16 | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.2377-169G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808784 | ||||||
| chr4:75808851
|
G | C | 244 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(241): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.2377-102G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808851 | ||||||
| chr4:75808908
|
T | A | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2377-45T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 20/23 | chr4 | 75808908 | ||||||
| chr4:75809105
|
T | C | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2475+54T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809105 | ||||||
| chr4:75809156
|
CTTTAGAT others(14): Show |
C | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2475+107_2475+127d others(23): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr4 | 75809156 | |||||
| chr4:75809220
|
T | C | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2475+169T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809220 | ||||||
| chr4:75809233
|
C | A | 39 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(36): Show | 40 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.2475+182C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809233 | ||||||
| chr4:75809282
|
C | T | 1 | a0001c0004t0002g0016 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2475+231C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809282 | ||||||
| chr4:75809291
|
T | A | 91 | a0001c0002t0001g0037a0001c0002t0001g0155a0001c0002t0001g0156others(88): Show | 91 | HG00609.hp2 HG00733.hp2 HG01109.hp1 others(88): Show |
intron_variant | MODIFIER | c.2475+240T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809291 | ||||||
| chr4:75809309
|
G | GA | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2475+258_2475+259i others(3): Show |
USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809309 | ||||||
| chr4:75809310
|
C | T | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2475+259C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809310 | ||||||
| chr4:75809348
|
G | A | 1 | a0001c0003t0001g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2475+297G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809348 | ||||||
| chr4:75809404
|
G | T | 1 | a0001c0002t0001g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2475+353G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809404 | ||||||
| chr4:75809532
|
G | A | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2475+481G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809532 | ||||||
| chr4:75809599
|
A | G | 1 | a0001c0003t0001g0187 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2475+548A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809599 | ||||||
| chr4:75809647
|
G | A | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2475+596G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809647 | ||||||
| chr4:75809755
|
T | C | 239 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(236): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.2476-677T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75809755 | ||||||
| chr4:75810094
|
A | T | 2 | a0001c0002t0001g0275a0001c0002t0001g0276 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2476-338A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75810094 | ||||||
| chr4:75810177
|
C | G | 1 | a0001c0001t0001g0126 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2476-255C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75810177 | ||||||
| chr4:75810179
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2476-253T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75810179 | ||||||
| chr4:75810275
|
G | C | 1 | a0001c0004t0002g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2476-157G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 21/23 | chr4 | 75810275 | ||||||
| chr4:75810587
|
A | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2583+48A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75810587 | ||||||
| chr4:75810604
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0128 | 2 | HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2583+65A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75810604 | ||||||
| chr4:75810668
|
T | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2583+129T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75810668 | ||||||
| chr4:75810965
|
G | A | 1 | a0001c0003t0001g0209 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2583+426G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75810965 | ||||||
| chr4:75810990
|
A | G | 1 | a0006c0013t0004g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2583+451A>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75810990 | ||||||
| chr4:75811143
|
C | T | 4 | a0001c0002t0001g0171a0001c0002t0001g0174a0001c0002t0001g0175others(1): Show | 4 | HG02895.hp2 HG02896.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2583+604C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811143 | ||||||
| chr4:75811157
|
C | T | 4 | a0001c0002t0001g0171a0001c0002t0001g0174a0001c0002t0001g0175others(1): Show | 4 | HG02895.hp2 HG02896.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2583+618C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811157 | ||||||
| chr4:75811217
|
A | T | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2583+678A>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811217 | ||||||
| chr4:75811243
|
C | T | 109 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.2583+704C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811243 | ||||||
| chr4:75811312
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2583+773T>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811312 | ||||||
| chr4:75811323
|
T | A | 1 | a0001c0001t0001g0052 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2583+784T>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811323 | ||||||
| chr4:75811409
|
G | C | 1 | a0001c0014t0002g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2584-751G>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811409 | ||||||
| chr4:75811416
|
C | A | 7 | a0001c0002t0001g0225a0001c0002t0001g0237a0001c0002t0001g0242others(4): Show | 7 | HG00609.hp2 NA18940.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.2584-744C>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811416 | ||||||
| chr4:75811416
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2584-744C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811416 | ||||||
| chr4:75811417
|
C | G | 1 | a0005c0015t0001g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2584-743C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811417 | ||||||
| chr4:75811460
|
T | G | 1 | a0001c0001t0001g0052 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2584-700T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811460 | ||||||
| chr4:75811555
|
G | A | 5 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2584-605G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811555 | ||||||
| chr4:75811577
|
C | G | 39 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(36): Show | 40 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.2584-583C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811577 | ||||||
| chr4:75811828
|
C | G | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2584-332C>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811828 | ||||||
| chr4:75811916
|
G | A | 1 | a0004c0016t0001g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2584-244G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 22/23 | chr4 | 75811916 | ||||||
| chr4:75812426
|
G | T | 1 | a0001c0002t0001g0248 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2799+51G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75812426 | ||||||
| chr4:75812579
|
C | T | 148 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.2799+204C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75812579 | ||||||
| chr4:75812701
|
G | T | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2799+326G>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75812701 | ||||||
| chr4:75812967
|
A | C | 1 | a0001c0001t0001g0149 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2800-239A>C | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75812967 | ||||||
| chr4:75813010
|
G | A | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0144others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2800-196G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75813010 | ||||||
| chr4:75813023
|
T | G | 149 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(146): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.2800-183T>G | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75813023 | ||||||
| chr4:75813067
|
C | T | 1 | a0001c0002t0001g0172 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2800-139C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75813067 | ||||||
| chr4:75813090
|
G | A | 1 | a0001c0002t0001g0267 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2800-116G>A | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75813090 | ||||||
| chr4:75813190
|
C | T | 83 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.2800-16C>T | USO1 | ENSG00000138768.15 | transcript | ENST00000514213.7 | protein_coding | 23/23 | chr4 | 75813190 |