| geneid | 25862 |
|---|---|
| ensemblid | ENSG00000164663.15 |
| hgncid | 20078 |
| symbol | USP49 |
| name | ubiquitin specific peptidase 49 |
| refseq_nuc | NM_001286554.2 |
| refseq_prot | NP_001273483.1 |
| ensembl_nuc | ENST00000682992.1 |
| ensembl_prot | ENSP00000507239.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 41789896 |
| end | 41895375 |
| strand | - |
| ver | v1.2 |
| region | chr6:41789896-41895375 |
| region5000 | chr6:41784896-41900375 |
| regionname0 | USP49_chr6_41789896_41895375 |
| regionname5000 | USP49_chr6_41784896_41900375 |
| 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 | 688 | 373 | 84 | 72 | 158 | 14 | 43 | 115 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0002 | 0/0 | 688 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0003 | 0/0 | 688 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0004 | 0/0 | 688 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0005 | 0/0 | 688 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0006 | 0/0 | 688 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2067 | 242 | 52 | 51 | 101 | 6 | 31 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| c0002 | 0/0 | 2067 | 67 | 20 | 8 | 27 | 4 | 8 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| c0003 | 1/0 | 2067 | 62 | 11 | 13 | 29 | 4 | 4 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| c0004 | 0/0 | 2067 | 5 | 0 | 0 | 5 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| c0005 | 0/0 | 2067 | 3 | 1 | 2 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| c0006 | 0/0 | 2067 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| c0007 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| c0008 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| c0009 | 0/0 | 2067 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| c0010 | 0/0 | 2067 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| 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 | 0/1 | 6875 | 135 | 23 | 28 | 55 | 5 | 23 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0002 | 0/0 | 6875 | 51 | 1 | 11 | 32 | 3 | 4 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0003 | 0/0 | 6874 | 40 | 3 | 2 | 26 | 2 | 7 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0004 | 0/0 | 6876 | 24 | 4 | 19 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0005 | 0/0 | 6875 | 23 | 6 | 1 | 15 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0006 | 0/0 | 6874 | 15 | 6 | 6 | 0 | 2 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0007 | 0/0 | 6875 | 10 | 0 | 0 | 10 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0008 | 0/0 | 6874 | 7 | 7 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0009 | 0/0 | 6875 | 7 | 6 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0010 | 1/0 | 6874 | 6 | 4 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0011 | 0/0 | 6876 | 6 | 0 | 0 | 6 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0012 | 0/0 | 6874 | 4 | 4 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0013 | 0/0 | 6875 | 4 | 4 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0014 | 0/0 | 6876 | 3 | 3 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0015 | 0/0 | 6875 | 3 | 3 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0016 | 0/0 | 6876 | 2 | 0 | 0 | 2 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0017 | 0/0 | 6875 | 2 | 0 | 0 | 0 | 0 | 2 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0018 | 0/0 | 6875 | 2 | 2 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0019 | 0/0 | 6875 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0020 | 0/0 | 6875 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0021 | 0/0 | 6874 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0022 | 0/0 | 6874 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0023 | 0/0 | 6908 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0024 | 0/0 | 6875 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0025 | 0/0 | 6875 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0026 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0027 | 0/0 | 6875 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0028 | 0/0 | 6875 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0029 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0030 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0031 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0032 | 0/0 | 6875 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0033 | 0/0 | 6875 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0034 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0035 | 0/0 | 6875 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0036 | 0/0 | 6875 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0037 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0038 | 0/0 | 6875 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0039 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0040 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0041 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0042 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0043 | 0/0 | 6875 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0044 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0045 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0046 | 0/0 | 6875 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0047 | 0/0 | 6875 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0048 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0049 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0050 | 0/0 | 6875 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0051 | 0/0 | 6875 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0052 | 0/0 | 6875 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0053 | 0/0 | 6871 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0054 | 0/0 | 6871 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0055 | 0/0 | 6871 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0056 | 0/0 | 6875 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0057 | 0/0 | 6875 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| t0058 | 0/0 | 6875 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| 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 | 2 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2067 | 242 | 52 | 51 | 101 | 6 | 31 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0002 | 0/0 | 2067 | 67 | 20 | 8 | 27 | 4 | 8 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0003 | 1/0 | 2067 | 62 | 11 | 13 | 29 | 4 | 4 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0007 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0010 | 0/0 | 2067 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0002c0004 | 0/0 | 2067 | 5 | 0 | 0 | 5 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0003c0005 | 0/0 | 2067 | 3 | 1 | 2 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0004c0008 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0005c0009 | 0/0 | 2067 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0006c0006 | 0/0 | 2067 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 8941 | 135 | 23 | 28 | 55 | 5 | 23 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0004 | 0/0 | 8942 | 24 | 4 | 19 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0005 | 0/0 | 8941 | 21 | 5 | 1 | 14 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0007 | 0/0 | 8941 | 10 | 0 | 0 | 10 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0009 | 0/0 | 8941 | 7 | 6 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0011 | 0/0 | 8942 | 6 | 0 | 0 | 6 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0014 | 0/0 | 8942 | 3 | 3 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0015 | 0/0 | 8941 | 3 | 3 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0016 | 0/0 | 8942 | 2 | 0 | 0 | 2 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0017 | 0/0 | 8941 | 2 | 0 | 0 | 0 | 0 | 2 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0018 | 0/0 | 8941 | 2 | 2 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0019 | 0/0 | 8941 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0029 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0030 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0031 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0032 | 0/0 | 8941 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0033 | 0/0 | 8941 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0034 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0035 | 0/0 | 8941 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0036 | 0/0 | 8941 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0037 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0039 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0040 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0041 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0042 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0043 | 0/0 | 8941 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0044 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0045 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0046 | 0/0 | 8941 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0047 | 0/0 | 8941 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0048 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0049 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0050 | 0/0 | 8941 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0051 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0052 | 0/0 | 8941 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0056 | 0/0 | 8941 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0057 | 0/0 | 8941 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0001t0058 | 0/0 | 8941 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0002t0003 | 0/0 | 8940 | 39 | 3 | 2 | 25 | 2 | 7 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0002t0006 | 0/0 | 8940 | 15 | 6 | 6 | 0 | 2 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0002t0008 | 0/0 | 8940 | 7 | 7 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0002t0012 | 0/0 | 8940 | 4 | 4 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0002t0021 | 0/0 | 8940 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0002t0022 | 0/0 | 8940 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0003t0002 | 0/0 | 8941 | 45 | 1 | 11 | 27 | 3 | 3 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0003t0010 | 1/0 | 8940 | 6 | 4 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0003t0013 | 0/0 | 8941 | 4 | 4 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0003t0020 | 0/0 | 8941 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0003t0023 | 0/0 | 8974 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0003t0024 | 0/0 | 8941 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0003t0025 | 0/0 | 8941 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0003t0026 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0003t0027 | 0/0 | 8941 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0003t0028 | 0/0 | 8941 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0007t0005 | 0/0 | 8941 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0001c0010t0003 | 0/0 | 8940 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0002c0004t0002 | 0/0 | 8941 | 5 | 0 | 0 | 5 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0003c0005t0053 | 0/0 | 8937 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0003c0005t0054 | 0/0 | 8937 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0003c0005t0055 | 0/0 | 8937 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0004c0008t0038 | 0/0 | 8941 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0005c0009t0002 | 0/0 | 8941 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| a0006c0006t0005 | 0/0 | 8941 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | copy fasta | chr6 | 41784896 | 41900375 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0007g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0007g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0007g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0007g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0007g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0007g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0007g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0007g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0007g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0009g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0009g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0009g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0011g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0011g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0011g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0011g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0011g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0011g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0014g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0014g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0014g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0015g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0015g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0015g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0016g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0016g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0017g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0017g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0018g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0018g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0019g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0029g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0030g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0031g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0032g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0033g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0034g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0035g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0036g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0037g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0039g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0040g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0041g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0042g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0043g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0044g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0045g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0046g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0047g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0048g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0049g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0050g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0051g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0052g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0056g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0057g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0001t0058g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0003g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0006g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0006g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0006g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0006g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0006g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0006g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0006g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0006g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0008g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0008g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0012g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0012g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0012g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0012g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0021g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0002t0022g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0010g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0010g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0010g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0010g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0013g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0013g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0013g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0013g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0020g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0023g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0024g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0025g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0026g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0027g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0003t0028g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0007t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0001c0010t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0002c0004t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0002c0004t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0002c0004t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0002c0004t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0002c0004t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0003c0005t0053g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0003c0005t0054g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0003c0005t0055g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0004c0008t0038g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0005c0009t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| a0006c0006t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0006 | g0339 | EUR | GBR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00099 | hp2 | a0001 | c0002 | t0003 | g0045 | EUR | GBR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00140 | hp1 | a0001 | c0002 | t0006 | g0256 | EUR | GBR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00280 | hp1 | a0001 | c0001 | t0019 | g0100 | EUR | FIN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00280 | hp2 | a0001 | c0003 | t0002 | g0176 | EUR | FIN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00323 | hp1 | a0001 | c0003 | t0002 | g0185 | EUR | FIN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | FIN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00408 | hp2 | a0001 | c0003 | t0002 | g0191 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0024 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00423 | hp2 | a0001 | c0003 | t0002 | g0200 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0354 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00544 | hp2 | a0001 | c0002 | t0021 | g0237 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00558 | hp1 | a0001 | c0001 | t0007 | g0351 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00558 | hp2 | a0001 | c0003 | t0002 | g0166 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00597 | hp2 | a0001 | c0001 | t0042 | g0128 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00609 | hp1 | a0001 | c0001 | t0040 | g0137 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00609 | hp2 | a0001 | c0003 | t0002 | g0173 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00621 | hp1 | a0001 | c0003 | t0002 | g0182 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | CHS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00639 | hp1 | a0001 | c0002 | t0006 | g0250 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00642 | hp1 | a0001 | c0002 | t0006 | g0254 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0224 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00733 | hp2 | a0001 | c0003 | t0002 | g0202 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00741 | hp1 | a0001 | c0003 | t0010 | g0056 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0080 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0195 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01070 | hp2 | a0001 | c0002 | t0006 | g0252 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01071 | hp2 | a0001 | c0002 | t0006 | g0251 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0029 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0084 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0319 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0072 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0087 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01168 | hp1 | a0003 | c0005 | t0054 | g0275 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01168 | hp2 | a0001 | c0003 | t0002 | g0201 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01192 | hp1 | a0001 | c0003 | t0002 | g0188 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01255 | hp2 | a0001 | c0001 | t0009 | g0160 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01256 | hp2 | a0001 | c0002 | t0006 | g0249 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0085 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01258 | hp1 | a0001 | c0002 | t0006 | g0253 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01261 | hp2 | a0001 | c0003 | t0002 | g0053 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0089 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0308 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01358 | hp1 | a0001 | c0003 | t0024 | g0377 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0184 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01361 | hp2 | a0003 | c0005 | t0053 | g0274 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0206 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01515 | hp1 | a0001 | c0003 | t0028 | g0193 | EUR | IBS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0328 | EUR | IBS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01516 | hp2 | a0001 | c0003 | t0002 | g0192 | EUR | IBS | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01884 | hp1 | a0001 | c0003 | t0002 | g0181 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01891 | hp1 | a0001 | c0001 | t0035 | g0380 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01891 | hp2 | a0001 | c0003 | t0013 | g0043 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0071 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01934 | hp2 | a0001 | c0003 | t0002 | g0179 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0074 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0073 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01975 | hp1 | a0001 | c0001 | t0032 | g0028 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0086 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0211 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01993 | hp1 | a0001 | c0001 | t0056 | g0304 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0083 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02015 | hp1 | a0001 | c0001 | t0037 | g0038 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02015 | hp2 | a0001 | c0002 | t0003 | g0341 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02040 | hp1 | a0001 | c0003 | t0002 | g0187 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02055 | hp1 | a0001 | c0002 | t0003 | g0240 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02055 | hp2 | a0001 | c0003 | t0010 | g0209 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0242 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02056 | hp2 | a0002 | c0004 | t0002 | g0197 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02071 | hp2 | a0001 | c0001 | t0039 | g0288 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02080 | hp1 | a0001 | c0001 | t0007 | g0356 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02080 | hp2 | a0001 | c0003 | t0002 | g0196 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0227 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02083 | hp2 | a0001 | c0001 | t0045 | g0358 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02129 | hp1 | a0001 | c0001 | t0007 | g0359 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0225 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02132 | hp1 | a0001 | c0001 | t0007 | g0360 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02132 | hp2 | a0001 | c0003 | t0002 | g0167 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02135 | hp2 | a0001 | c0002 | t0003 | g0232 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02145 | hp1 | a0001 | c0002 | t0006 | g0259 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02155 | hp1 | a0001 | c0001 | t0007 | g0362 | EAS | CDX | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0244 | EAS | CDX | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CDX | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02165 | hp2 | a0001 | c0001 | t0029 | g0292 | EAS | CDX | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0088 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02273 | hp2 | a0001 | c0003 | t0002 | g0307 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02280 | hp1 | a0001 | c0001 | t0018 | g0097 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02280 | hp2 | a0001 | c0001 | t0050 | g0113 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02293 | hp1 | a0001 | c0003 | t0002 | g0174 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0082 | AMR | PEL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02451 | hp2 | a0001 | c0002 | t0012 | g0161 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02523 | hp1 | a0001 | c0001 | t0041 | g0118 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02523 | hp2 | a0001 | c0003 | t0002 | g0190 | EAS | KHV | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02572 | hp1 | a0001 | c0002 | t0008 | g0270 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02602 | hp1 | a0001 | c0002 | t0003 | g0230 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02615 | hp2 | a0001 | c0002 | t0003 | g0040 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02622 | hp1 | a0001 | c0002 | t0008 | g0042 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02622 | hp2 | a0001 | c0001 | t0057 | g0059 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0096 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02630 | hp2 | a0001 | c0003 | t0013 | g0343 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02647 | hp1 | a0001 | c0002 | t0006 | g0257 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02698 | hp2 | a0001 | c0001 | t0036 | g0026 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0004 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02717 | hp2 | a0001 | c0002 | t0012 | g0162 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02723 | hp2 | a0001 | c0002 | t0008 | g0271 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02809 | hp1 | a0001 | c0003 | t0020 | g0061 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02818 | hp2 | a0001 | c0002 | t0012 | g0164 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02886 | hp1 | a0001 | c0002 | t0008 | g0041 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02886 | hp2 | a0001 | c0001 | t0043 | g0267 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02895 | hp1 | a0001 | c0002 | t0006 | g0067 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02897 | hp1 | a0001 | c0001 | t0015 | g0219 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02897 | hp2 | a0001 | c0002 | t0006 | g0255 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02922 | hp1 | a0001 | c0001 | t0058 | g0277 | AFR | ESN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02922 | hp2 | a0003 | c0005 | t0055 | g0273 | AFR | ESN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02976 | hp1 | a0001 | c0003 | t0010 | g0222 | AFR | ESN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02976 | hp2 | a0001 | c0007 | t0005 | g0036 | AFR | ESN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03017 | hp1 | a0001 | c0002 | t0006 | g0340 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03017 | hp2 | a0001 | c0003 | t0002 | g0177 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03041 | hp2 | a0001 | c0002 | t0008 | g0269 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03098 | hp1 | a0001 | c0001 | t0015 | g0063 | AFR | MSL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | MSL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03130 | hp2 | a0001 | c0002 | t0006 | g0258 | AFR | ESN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03139 | hp1 | a0001 | c0003 | t0013 | g0044 | AFR | ESN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03139 | hp2 | a0001 | c0001 | t0046 | g0151 | AFR | ESN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03195 | hp1 | a0001 | c0001 | t0015 | g0220 | AFR | ESN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0078 | AFR | ESN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03209 | hp1 | a0001 | c0001 | t0014 | g0069 | AFR | MSL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03209 | hp2 | a0004 | c0008 | t0038 | g0054 | AFR | MSL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03225 | hp1 | a0001 | c0003 | t0010 | g0064 | AFR | MSL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0030 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03453 | hp1 | a0001 | c0003 | t0013 | g0344 | AFR | MSL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03486 | hp1 | a0001 | c0002 | t0006 | g0218 | AFR | MSL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | MSL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03490 | hp1 | a0001 | c0002 | t0003 | g0246 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03491 | hp2 | a0001 | c0002 | t0003 | g0226 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03492 | hp2 | a0001 | c0002 | t0003 | g0233 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0210 | AFR | ESN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03540 | hp2 | a0001 | c0003 | t0025 | g0062 | AFR | GWD | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0159 | AFR | MSL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | MSL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03669 | hp1 | a0001 | c0002 | t0003 | g0234 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03688 | hp1 | a0001 | c0001 | t0033 | g0009 | SAS | STU | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0076 | SAS | STU | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0243 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03710 | hp2 | a0001 | c0001 | t0052 | g0014 | SAS | PJL | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03834 | hp1 | a0001 | c0003 | t0027 | g0378 | SAS | BEB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03834 | hp2 | a0001 | c0003 | t0002 | g0183 | SAS | BEB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0373 | SAS | BEB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03942 | hp1 | a0001 | c0001 | t0017 | g0120 | SAS | BEB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG03942 | hp2 | a0005 | c0009 | t0002 | g0170 | SAS | BEB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0278 | SAS | BEB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG04184 | hp2 | a0001 | c0001 | t0017 | g0132 | SAS | BEB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG04199 | hp1 | a0001 | c0001 | t0047 | g0300 | SAS | STU | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | STU | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0057 | SAS | STU | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | STU | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | YRI | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18522 | hp2 | a0001 | c0001 | t0014 | g0068 | AFR | YRI | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18747 | hp2 | a0001 | c0002 | t0003 | g0228 | EAS | CHB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18906 | hp1 | a0001 | c0003 | t0010 | g0055 | AFR | YRI | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | YRI | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18940 | hp1 | a0002 | c0004 | t0002 | g0169 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18941 | hp1 | a0001 | c0001 | t0034 | g0022 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0374 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18943 | hp1 | a0001 | c0001 | t0007 | g0345 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0379 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18945 | hp2 | a0001 | c0003 | t0002 | g0172 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18948 | hp1 | a0001 | c0003 | t0002 | g0047 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18948 | hp2 | a0001 | c0001 | t0011 | g0369 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18952 | hp1 | a0001 | c0010 | t0003 | g0248 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18952 | hp2 | a0001 | c0003 | t0026 | g0171 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18954 | hp1 | a0001 | c0002 | t0003 | g0065 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18954 | hp2 | a0001 | c0003 | t0002 | g0046 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18956 | hp1 | a0001 | c0001 | t0016 | g0034 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18956 | hp2 | a0001 | c0001 | t0007 | g0108 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18957 | hp1 | a0001 | c0003 | t0002 | g0186 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18957 | hp2 | a0001 | c0002 | t0003 | g0231 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18962 | hp2 | a0001 | c0002 | t0003 | g0235 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18963 | hp1 | a0001 | c0003 | t0002 | g0180 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0375 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18966 | hp1 | a0001 | c0002 | t0003 | g0223 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18966 | hp2 | a0001 | c0001 | t0031 | g0025 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18968 | hp2 | a0001 | c0002 | t0003 | g0236 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18969 | hp2 | a0001 | c0001 | t0007 | g0372 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18973 | hp2 | a0002 | c0004 | t0002 | g0203 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18974 | hp1 | a0001 | c0003 | t0023 | g0165 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18978 | hp1 | a0001 | c0001 | t0011 | g0349 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18978 | hp2 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18979 | hp1 | a0001 | c0001 | t0051 | g0023 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18982 | hp1 | a0002 | c0004 | t0002 | g0189 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18985 | hp1 | a0001 | c0003 | t0002 | g0178 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18985 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18989 | hp1 | a0006 | c0006 | t0005 | g0018 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18993 | hp2 | a0001 | c0002 | t0003 | g0212 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18994 | hp1 | a0001 | c0002 | t0003 | g0215 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18994 | hp2 | a0001 | c0003 | t0002 | g0051 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18995 | hp1 | a0001 | c0001 | t0011 | g0361 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18995 | hp2 | a0001 | c0002 | t0003 | g0245 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19000 | hp2 | a0001 | c0002 | t0003 | g0217 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19001 | hp2 | a0001 | c0003 | t0002 | g0198 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0214 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19002 | hp2 | a0001 | c0001 | t0007 | g0376 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19004 | hp1 | a0001 | c0003 | t0002 | g0050 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19006 | hp1 | a0001 | c0001 | t0044 | g0334 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19009 | hp2 | a0002 | c0004 | t0002 | g0276 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19010 | hp2 | a0001 | c0001 | t0048 | g0342 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19012 | hp1 | a0001 | c0003 | t0002 | g0049 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | LWK | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19030 | hp2 | a0001 | c0002 | t0008 | g0163 | AFR | LWK | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0070 | AFR | LWK | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19043 | hp2 | a0001 | c0001 | t0009 | g0004 | AFR | LWK | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19054 | hp1 | a0001 | c0003 | t0002 | g0205 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19054 | hp2 | a0001 | c0002 | t0003 | g0238 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19055 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19056 | hp2 | a0001 | c0003 | t0002 | g0204 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19058 | hp2 | a0001 | c0001 | t0049 | g0039 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19060 | hp2 | a0001 | c0001 | t0011 | g0370 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19063 | hp2 | a0001 | c0002 | t0003 | g0066 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19065 | hp1 | a0001 | c0002 | t0022 | g0247 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19067 | hp1 | a0001 | c0001 | t0011 | g0346 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19067 | hp2 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19070 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19078 | hp1 | a0001 | c0001 | t0016 | g0010 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0239 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19082 | hp1 | a0001 | c0001 | t0011 | g0348 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19082 | hp2 | a0001 | c0003 | t0002 | g0199 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19084 | hp1 | a0001 | c0002 | t0003 | g0216 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19084 | hp2 | a0001 | c0003 | t0002 | g0268 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0241 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19088 | hp1 | a0001 | c0002 | t0003 | g0229 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19088 | hp2 | a0001 | c0003 | t0002 | g0048 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19090 | hp2 | a0001 | c0003 | t0002 | g0052 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19091 | hp1 | a0001 | c0003 | t0002 | g0175 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | YRI | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA20129 | hp1 | a0001 | c0002 | t0008 | g0272 | AFR | ASW | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ASW | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA20752 | hp1 | a0001 | c0002 | t0003 | g0213 | EUR | TSI | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0262 | EUR | TSI | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | GIH | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | GIH | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG01123 | hp2 | a0001 | c0003 | t0002 | g0168 | AMR | CLM | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02109 | hp2 | a0001 | c0001 | t0018 | g0090 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0032 | AFR | ACB | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18955 | hp1 | a0001 | c0003 | t0002 | g0194 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA18955 | hp2 | a0001 | c0001 | t0030 | g0015 | EAS | JPT | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA20300 | hp1 | a0001 | c0001 | t0009 | g0060 | AFR | USA | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | USA | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA21309 | hp1 | a0001 | c0002 | t0012 | g0208 | AFR | LWK | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| NA21309 | hp2 | a0001 | c0001 | t0009 | g0098 | AFR | LWK | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0123 | REF | REF | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0010 | g0099 | REF | REF | USP49_chr6_41784896_41900375 | USP49 | chr6 | 41784896 | 41900375 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41805988
|
C | G | 1 | a0002 | 5 | HG02056.hp2 NA18940.hp1 NA18973.hp2 others(2): Show |
missense_variant | MODERATE | c.996G>C | p.Trp332Cys | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/8 | 1232/8940 | 996/2067 | 332/688 | chr6 | 41805988 | ||
| chr6:41806043
|
T | C | 1 | a0004 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.941A>G | p.Glu314Gly | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/8 | 1177/8940 | 941/2067 | 314/688 | chr6 | 41806043 | ||
| chr6:41806238
|
G | C | 1 | a0005 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.746C>G | p.Ala249Gly | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/8 | 982/8940 | 746/2067 | 249/688 | chr6 | 41806238 | ||
| chr6:41806602
|
G | T | 1 | a0003 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.382C>A | p.Leu128Met | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/8 | 618/8940 | 382/2067 | 128/688 | chr6 | 41806602 | ||
| chr6:41806830
|
C | T | 1 | a0006 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.154G>A | p.Asp52Asn | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/8 | 390/8940 | 154/2067 | 52/688 | chr6 | 41806830 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41798908
|
T | G | 1 | a0001c0007 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.1692A>C | p.Arg564Arg | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/8 | 1928/8940 | 1692/2067 | 564/688 | chr6 | 41798908 | ||
| chr6:41805838
|
G | C | 3 | a0001c0001a0001c0007a0006c0006 | 244 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(241): Show |
synonymous_variant | LOW | c.1146C>G | p.Leu382Leu | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/8 | 1382/8940 | 1146/2067 | 382/688 | chr6 | 41805838 | ||
| chr6:41805997
|
G | A | 2 | a0001c0002a0001c0010 | 68 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(65): Show |
synonymous_variant | LOW | c.987C>T | p.Gly329Gly | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/8 | 1223/8940 | 987/2067 | 329/688 | chr6 | 41805997 | ||
| chr6:41806321
|
C | A | 1 | a0001c0010 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.663G>T | p.Pro221Pro | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/8 | 899/8940 | 663/2067 | 221/688 | chr6 | 41806321 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41789925
|
T | C | 2 | a0001c0003t0020a0001c0003t0025 | 2 | HG02809.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6608A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 6608 | chr6 | 41789925 | |||||
| chr6:41789989
|
C | T | 1 | a0004c0008t0038 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6544G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 6544 | chr6 | 41789989 | |||||
| chr6:41790018
|
T | C | 1 | a0001c0001t0042 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6515A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 6515 | chr6 | 41790018 | |||||
| chr6:41790057
|
A | G | 3 | a0001c0001t0041a0003c0005t0054a0004c0008t0038 | 3 | HG01168.hp1 HG02523.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6476T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 6476 | chr6 | 41790057 | |||||
| chr6:41790098
|
C | A | 49 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(46): Show | 256 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*6435G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 6435 | chr6 | 41790098 | |||||
| chr6:41790255
|
G | T | 14 | a0001c0001t0005a0001c0001t0016a0001c0001t0030others(11): Show | 35 | HG00423.hp1 HG01074.hp1 HG01975.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*6278C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 6278 | chr6 | 41790255 | |||||
| chr6:41790383
|
G | A | 3 | a0003c0005t0053a0003c0005t0054a0003c0005t0055 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6150C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 6150 | chr6 | 41790383 | |||||
| chr6:41790405
|
G | T | 1 | a0001c0002t0021 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6128C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 6128 | chr6 | 41790405 | |||||
| chr6:41790421
|
C | T | 1 | a0001c0001t0014 | 3 | HG03195.hp2 HG03209.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6112G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 6112 | chr6 | 41790421 | |||||
| chr6:41790422
|
G | A | 1 | a0001c0002t0022 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6111C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 6111 | chr6 | 41790422 | |||||
| chr6:41790425
|
A | T | 2 | a0001c0003t0013a0004c0008t0038 | 5 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6108T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 6108 | chr6 | 41790425 | |||||
| chr6:41790445
|
A | T | 1 | a0001c0003t0013 | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6088T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 6088 | chr6 | 41790445 | |||||
| chr6:41790488
|
A | G | 2 | a0001c0003t0024a0001c0003t0027 | 2 | HG01358.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6045T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 6045 | chr6 | 41790488 | |||||
| chr6:41790592
|
G | T | 1 | a0001c0001t0040 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5941C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 5941 | chr6 | 41790592 | |||||
| chr6:41790642
|
T | C | 1 | a0001c0001t0018 | 2 | HG02109.hp2 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5891A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 5891 | chr6 | 41790642 | |||||
| chr6:41790845
|
G | A | 4 | a0001c0002t0003a0001c0002t0021a0001c0002t0022others(1): Show | 42 | HG00099.hp2 HG00544.hp2 HG00642.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*5688C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 5688 | chr6 | 41790845 | |||||
| chr6:41790954
|
C | G | 1 | a0001c0003t0026 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5579G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 5579 | chr6 | 41790954 | |||||
| chr6:41791031
|
C | A | 1 | a0001c0001t0035 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5502G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 5502 | chr6 | 41791031 | |||||
| chr6:41791191
|
G | C | 2 | a0003c0005t0054a0003c0005t0055 | 2 | HG01168.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5342C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 5342 | chr6 | 41791191 | |||||
| chr6:41791244
|
T | C | 1 | a0001c0001t0043 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5289A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 5289 | chr6 | 41791244 | |||||
| chr6:41791356
|
C | T | 1 | a0001c0001t0034 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5177G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 5177 | chr6 | 41791356 | |||||
| chr6:41791472
|
A | G | 1 | a0001c0001t0033 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5061T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 5061 | chr6 | 41791472 | |||||
| chr6:41791572
|
G | C | 1 | a0001c0001t0044 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4961C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 4961 | chr6 | 41791572 | |||||
| chr6:41792108
|
A | C | 6 | a0001c0003t0002a0001c0003t0023a0001c0003t0026others(3): Show | 54 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*4425T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 4425 | chr6 | 41792108 | |||||
| chr6:41792150
|
G | A | 1 | a0001c0001t0045 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4383C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 4383 | chr6 | 41792150 | |||||
| chr6:41792203
|
C | T | 1 | a0001c0001t0032 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4330G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 4330 | chr6 | 41792203 | |||||
| chr6:41792355
|
T | A | 1 | a0001c0001t0036 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4178A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 4178 | chr6 | 41792355 | |||||
| chr6:41792359
|
TTTTG | T | 3 | a0003c0005t0053a0003c0005t0054a0003c0005t0055 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4170_*4173delCAAA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 4170 | chr6 | 41792359 | |||||
| chr6:41792526
|
G | GC | 55 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(52): Show | 310 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*4006dupG | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 4006 | chr6 | 41792526 | |||||
| chr6:41792559
|
A | G | 1 | a0001c0001t0039 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3974T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 3974 | chr6 | 41792559 | |||||
| chr6:41792621
|
G | A | 1 | a0001c0001t0015 | 3 | HG02897.hp1 HG03098.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3912C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 3912 | chr6 | 41792621 | |||||
| chr6:41792634
|
C | G | 6 | a0001c0003t0002a0001c0003t0023a0001c0003t0026others(3): Show | 54 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*3899G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 3899 | chr6 | 41792634 | |||||
| chr6:41792827
|
T | A | 1 | a0001c0001t0037 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3706A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 3706 | chr6 | 41792827 | |||||
| chr6:41792840
|
G | A | 1 | a0001c0001t0046 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3693C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 3693 | chr6 | 41792840 | |||||
| chr6:41793002
|
G | A | 2 | a0001c0001t0009a0001c0001t0018 | 9 | HG01255.hp2 HG02109.hp2 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3531C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 3531 | chr6 | 41793002 | |||||
| chr6:41793122
|
T | G | 1 | a0001c0001t0047 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3411A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 3411 | chr6 | 41793122 | |||||
| chr6:41793252
|
T | G | 45 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(42): Show | 292 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*3281A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 3281 | chr6 | 41793252 | |||||
| chr6:41793252
|
T | TG | 1 | a0001c0001t0011 | 6 | NA18948.hp2 NA18978.hp1 NA18995.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3280_*3281insC | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 3280 | chr6 | 41793252 | |||||
| chr6:41793269
|
G | GT | 3 | a0001c0001t0004a0001c0001t0014a0001c0001t0016 | 29 | HG01069.hp2 HG01099.hp1 HG01099.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3263dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 3263 | chr6 | 41793269 | |||||
| chr6:41793281
|
A | G | 1 | a0001c0001t0057 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3252T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 3252 | chr6 | 41793281 | |||||
| chr6:41793292
|
C | T | 1 | a0001c0003t0013 | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3241G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 3241 | chr6 | 41793292 | |||||
| chr6:41793377
|
C | T | 1 | a0001c0001t0017 | 2 | HG03942.hp1 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3156G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 3156 | chr6 | 41793377 | |||||
| chr6:41793719
|
G | A | 1 | a0001c0001t0048 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2814C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 2814 | chr6 | 41793719 | |||||
| chr6:41793723
|
C | T | 15 | a0001c0001t0005a0001c0001t0016a0001c0001t0030others(12): Show | 36 | HG00423.hp1 HG01074.hp1 HG01891.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2810G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 2810 | chr6 | 41793723 | |||||
| chr6:41793757
|
T | C | 1 | a0001c0002t0006 | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2776A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 2776 | chr6 | 41793757 | |||||
| chr6:41793867
|
C | CCGGACGA others(26): Show |
1 | a0001c0003t0023 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2665_*2666insCTTC others(29): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 2665 | chr6 | 41793867 | |||||
| chr6:41793868
|
T | G | 1 | a0001c0003t0023 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2665A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 2665 | chr6 | 41793868 | |||||
| chr6:41793873
|
A | T | 1 | a0001c0003t0023 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2660T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 2660 | chr6 | 41793873 | |||||
| chr6:41793877
|
C | G | 1 | a0001c0002t0012 | 4 | HG02451.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2656G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 2656 | chr6 | 41793877 | |||||
| chr6:41793922
|
C | A | 1 | a0001c0001t0049 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2611G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 2611 | chr6 | 41793922 | |||||
| chr6:41794382
|
G | A | 1 | a0001c0001t0050 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2151C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 2151 | chr6 | 41794382 | |||||
| chr6:41794508
|
C | T | 1 | a0001c0001t0007 | 10 | HG00544.hp1 HG00558.hp1 HG02080.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2025G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 2025 | chr6 | 41794508 | |||||
| chr6:41794550
|
T | C | 1 | a0001c0001t0051 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1983A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 1983 | chr6 | 41794550 | |||||
| chr6:41794908
|
G | A | 1 | a0001c0001t0052 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1625C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 1625 | chr6 | 41794908 | |||||
| chr6:41794955
|
A | C | 1 | a0001c0001t0031 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1578T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 1578 | chr6 | 41794955 | |||||
| chr6:41795070
|
C | G | 7 | a0001c0002t0003a0001c0002t0006a0001c0002t0008others(4): Show | 68 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1463G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 1463 | chr6 | 41795070 | |||||
| chr6:41795095
|
C | A | 3 | a0003c0005t0053a0003c0005t0054a0003c0005t0055 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1438G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 1438 | chr6 | 41795095 | |||||
| chr6:41795304
|
A | G | 1 | a0001c0003t0020 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1229T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 1229 | chr6 | 41795304 | |||||
| chr6:41795719
|
C | A | 1 | a0001c0003t0027 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*814G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 814 | chr6 | 41795719 | |||||
| chr6:41795883
|
T | A | 62 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(59): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
3_prime_UTR_variant | MODIFIER | c.*650A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 650 | chr6 | 41795883 | |||||
| chr6:41796026
|
C | T | 1 | a0001c0001t0030 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*507G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 507 | chr6 | 41796026 | |||||
| chr6:41796112
|
C | A | 1 | a0001c0003t0028 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*421G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 421 | chr6 | 41796112 | |||||
| chr6:41796125
|
G | A | 1 | a0001c0001t0056 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*408C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 408 | chr6 | 41796125 | |||||
| chr6:41796136
|
A | G | 1 | a0001c0001t0029 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*397T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 397 | chr6 | 41796136 | |||||
| chr6:41796342
|
G | A | 45 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(42): Show | 252 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*191C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 191 | chr6 | 41796342 | |||||
| chr6:41796414
|
A | G | 1 | a0001c0001t0019 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*119T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 119 | chr6 | 41796414 | |||||
| chr6:41796513
|
C | A | 1 | a0001c0001t0057 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*20G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 8/8 | 20 | chr6 | 41796513 | |||||
| chr6:41891828
|
G | C | 1 | a0001c0001t0058 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-137C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/8 | 84845 | chr6 | 41891828 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41796874
|
T | C | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1877-151A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41796874 | ||||||
| chr6:41796920
|
C | T | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1877-197G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41796920 | ||||||
| chr6:41796945
|
A | AT | 6 | a0001c0001t0001g0109a0001c0001t0001g0147a0001c0001t0001g0156others(3): Show | 6 | HG01358.hp2 HG03139.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.1877-223dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41796945 | ||||||
| chr6:41796945
|
AT | A | 197 | a0001c0001t0001g0058a0001c0001t0001g0091a0001c0001t0001g0112others(194): Show | 200 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1877-223delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41796945 | ||||||
| chr6:41796945
|
ATT | A | 17 | a0001c0001t0001g0221a0001c0001t0001g0282a0001c0001t0004g0074others(14): Show | 17 | HG01168.hp1 HG01358.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1877-224_1877-223d others(4): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41796945 | ||||||
| chr6:41796958
|
T | G | 10 | a0001c0001t0001g0294a0001c0001t0001g0297a0001c0001t0001g0298others(7): Show | 10 | HG01943.hp2 HG01993.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1877-235A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41796958 | ||||||
| chr6:41797151
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1877-428C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41797151 | ||||||
| chr6:41797207
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1877-484C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41797207 | ||||||
| chr6:41797211
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1877-488G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41797211 | ||||||
| chr6:41797242
|
G | A | 36 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(33): Show | 36 | HG00423.hp1 HG01074.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1877-519C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41797242 | ||||||
| chr6:41797259
|
C | T | 4 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0001t0001g0333others(1): Show | 4 | HG02071.hp2 NA18968.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1877-536G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41797259 | ||||||
| chr6:41797320
|
C | G | 1 | a0001c0001t0001g0338 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1877-597G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41797320 | ||||||
| chr6:41797321
|
T | C | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1877-598A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41797321 | ||||||
| chr6:41797527
|
T | C | 54 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(51): Show | 54 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.1877-804A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41797527 | ||||||
| chr6:41797681
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(1): Show | 4 | HG02897.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1877-958C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41797681 | ||||||
| chr6:41797830
|
A | T | 2 | a0001c0002t0008g0041a0001c0002t0008g0042 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1876+894T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41797830 | ||||||
| chr6:41797972
|
A | G | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1876+752T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41797972 | ||||||
| chr6:41798059
|
A | G | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1876+665T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41798059 | ||||||
| chr6:41798280
|
T | G | 1 | a0001c0001t0009g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1876+444A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41798280 | ||||||
| chr6:41798282
|
A | ATTTTTTT others(33): Show |
1 | a0001c0001t0004g0073 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1876+441_1876+442i others(42): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41798282 | ||||||
| chr6:41798465
|
G | A | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1876+259C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41798465 | ||||||
| chr6:41798528
|
G | A | 2 | a0001c0001t0001g0260a0001c0001t0057g0059 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1876+196C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41798528 | ||||||
| chr6:41798567
|
C | T | 1 | a0001c0001t0007g0354 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1876+157G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41798567 | ||||||
| chr6:41798687
|
T | G | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1876+37A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41798687 | ||||||
| chr6:41798695
|
C | T | 1 | a0001c0003t0002g0179 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1876+29G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 7/7 | chr6 | 41798695 | ||||||
| chr6:41799079
|
C | CTTAT | 110 | a0001c0001t0001g0116a0001c0001t0001g0221a0001c0001t0001g0311others(107): Show | 110 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1671-154_1671-151d others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 6/7 | chr6 | 41799079 | ||||||
| chr6:41799079
|
C | CTTATTTA others(1): Show |
24 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0260others(21): Show | 27 | HG00323.hp1 HG01123.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.1671-158_1671-151d others(10): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 6/7 | chr6 | 41799079 | ||||||
| chr6:41799079
|
CTTAT | C | 157 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(154): Show | 158 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1671-154_1671-151d others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 6/7 | chr6 | 41799079 | ||||||
| chr6:41799156
|
A | T | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1671-227T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 6/7 | chr6 | 41799156 | ||||||
| chr6:41799241
|
G | A | 1 | a0001c0001t0007g0108 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1671-312C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 6/7 | chr6 | 41799241 | ||||||
| chr6:41799321
|
G | C | 2 | a0001c0002t0006g0257a0001c0002t0006g0258 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1671-392C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 6/7 | chr6 | 41799321 | ||||||
| chr6:41799347
|
T | G | 2 | a0001c0001t0001g0260a0001c0001t0057g0059 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1671-418A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 6/7 | chr6 | 41799347 | ||||||
| chr6:41799451
|
G | A | 1 | a0001c0001t0001g0365 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1670+379C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 6/7 | chr6 | 41799451 | ||||||
| chr6:41799631
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1670+199C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 6/7 | chr6 | 41799631 | ||||||
| chr6:41800285
|
C | G | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1562-347G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41800285 | ||||||
| chr6:41800429
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1562-491C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41800429 | ||||||
| chr6:41800505
|
G | A | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1562-567C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41800505 | ||||||
| chr6:41800772
|
T | C | 241 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(238): Show | 245 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.1562-834A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41800772 | ||||||
| chr6:41800842
|
A | G | 1 | a0001c0003t0002g0052 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1562-904T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41800842 | ||||||
| chr6:41801002
|
G | A | 1 | a0001c0001t0033g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1562-1064C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41801002 | ||||||
| chr6:41801016
|
G | C | 1 | a0001c0001t0001g0289 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1562-1078C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41801016 | ||||||
| chr6:41801294
|
G | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1562-1356C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41801294 | ||||||
| chr6:41801315
|
A | C | 5 | a0001c0001t0004g0071a0001c0001t0004g0073a0001c0001t0004g0074others(2): Show | 5 | HG01346.hp1 HG01928.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1562-1377T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41801315 | ||||||
| chr6:41801485
|
C | T | 1 | a0001c0003t0002g0048 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1562-1547G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41801485 | ||||||
| chr6:41801491
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1562-1553C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41801491 | ||||||
| chr6:41801765
|
G | A | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1562-1827C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41801765 | ||||||
| chr6:41801982
|
A | C | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1561+1824T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41801982 | ||||||
| chr6:41802025
|
G | GT | 41 | a0001c0001t0001g0146a0001c0001t0001g0326a0001c0001t0005g0005others(38): Show | 41 | HG00423.hp1 HG01074.hp1 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.1561+1780dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802025 | ||||||
| chr6:41802025
|
GT | G | 8 | a0001c0001t0001g0293a0001c0001t0001g0316a0001c0001t0001g0323others(5): Show | 8 | HG00558.hp1 HG00741.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1561+1780delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802025 | ||||||
| chr6:41802028
|
T | G | 1 | a0001c0003t0013g0344 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1561+1778A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802028 | ||||||
| chr6:41802182
|
T | C | 54 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(51): Show | 54 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.1561+1624A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802182 | ||||||
| chr6:41802206
|
C | G | 5 | a0001c0001t0001g0111a0001c0001t0001g0116a0001c0001t0001g0122others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1561+1600G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802206 | ||||||
| chr6:41802371
|
G | T | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1561+1435C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802371 | ||||||
| chr6:41802381
|
A | ATTTAT | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1561+1420_1561+142 others(9): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802381 | ||||||
| chr6:41802381
|
ATTTAT | A | 67 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(64): Show | 67 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.1561+1420_1561+142 others(9): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802381 | ||||||
| chr6:41802390
|
ATTTTATT others(10): Show |
A | 1 | a0001c0001t0001g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1561+1399_1561+141 others(21): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802390 | ||||||
| chr6:41802400
|
ATTTTATT | A | 7 | a0001c0001t0009g0004a0001c0001t0009g0060a0001c0001t0009g0096others(4): Show | 8 | HG01255.hp2 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1561+1399_1561+140 others(11): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802400 | ||||||
| chr6:41802405
|
A | T | 10 | a0001c0001t0001g0280a0001c0001t0001g0282a0001c0001t0001g0297others(7): Show | 10 | HG01943.hp2 HG01993.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1561+1401T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802405 | ||||||
| chr6:41802407
|
T | A | 10 | a0001c0001t0001g0280a0001c0001t0001g0282a0001c0001t0001g0297others(7): Show | 10 | HG01943.hp2 HG01993.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1561+1399A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802407 | ||||||
| chr6:41802407
|
T | TTTTTA | 24 | a0001c0002t0003g0040a0001c0002t0003g0045a0001c0002t0003g0057others(21): Show | 24 | HG00099.hp2 HG00642.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.1561+1394_1561+139 others(9): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802407 | ||||||
| chr6:41802407
|
T | TTTTTATT others(3): Show |
2 | a0001c0002t0003g0341a0001c0003t0002g0181 | 2 | HG01884.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.1561+1389_1561+139 others(14): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802407 | ||||||
| chr6:41802407
|
T | TTTTTATT others(8): Show |
9 | a0001c0003t0002g0047a0001c0003t0002g0172a0001c0003t0002g0174others(6): Show | 9 | HG01070.hp1 HG01168.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1561+1384_1561+139 others(19): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802407 | ||||||
| chr6:41802407
|
T | TTTTTATT others(13): Show |
4 | a0001c0003t0002g0053a0001c0003t0002g0177a0001c0003t0002g0200others(1): Show | 4 | HG00423.hp2 HG01261.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1561+1379_1561+139 others(24): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802407 | ||||||
| chr6:41802407
|
T | TTTTTATT others(18): Show |
1 | a0001c0003t0002g0185 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1561+1374_1561+139 others(29): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802407 | ||||||
| chr6:41802407
|
T | TTTTTATT others(23): Show |
1 | a0001c0003t0023g0165 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1561+1398_1561+139 others(34): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802407 | ||||||
| chr6:41802410
|
T | A | 154 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1561+1396A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802410 | ||||||
| chr6:41802412
|
A | T | 154 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1561+1394T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802412 | ||||||
| chr6:41802415
|
T | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(81): Show | 85 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1561+1391A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802415 | ||||||
| chr6:41802417
|
A | T | 84 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(81): Show | 85 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1561+1389T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802417 | ||||||
| chr6:41802419
|
TTTA | T | 7 | a0001c0001t0009g0004a0001c0001t0009g0060a0001c0001t0009g0096others(4): Show | 8 | HG01255.hp2 HG02109.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1561+1384_1561+138 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802419 | ||||||
| chr6:41802427
|
A | ATTTTATT others(17): Show |
1 | a0001c0003t0002g0180 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1561+1378_1561+137 others(28): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802427 | ||||||
| chr6:41802428
|
T | TTTTATTT others(1): Show |
4 | a0001c0002t0006g0257a0001c0002t0006g0259a0001c0002t0006g0339others(1): Show | 4 | HG00099.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1561+1370_1561+137 others(12): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802428 | ||||||
| chr6:41802428
|
T | TTTTATTT others(2): Show |
10 | a0001c0002t0003g0241a0001c0002t0003g0242a0001c0002t0003g0243others(7): Show | 10 | HG00621.hp1 HG00642.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1561+1377_1561+137 others(13): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802428 | ||||||
| chr6:41802428
|
T | TTTTATTT others(6): Show |
1 | a0001c0003t0002g0186 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1561+1377_1561+137 others(17): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802428 | ||||||
| chr6:41802428
|
T | TTTTATTT others(10): Show |
1 | a0001c0003t0002g0198 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1561+1377_1561+137 others(21): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802428 | ||||||
| chr6:41802428
|
T | TTTTATTT others(7): Show |
6 | a0001c0002t0003g0229a0001c0002t0003g0235a0001c0002t0003g0236others(3): Show | 6 | HG02886.hp1 HG03540.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.1561+1377_1561+137 others(18): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802428 | ||||||
| chr6:41802428
|
T | TTTTATTT others(11): Show |
1 | a0001c0002t0003g0228 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1561+1377_1561+137 others(22): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802428 | ||||||
| chr6:41802428
|
T | TTTTATTT others(12): Show |
19 | a0001c0003t0002g0048a0001c0003t0002g0049a0001c0003t0002g0050others(16): Show | 19 | HG00408.hp2 HG00733.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1561+1377_1561+137 others(23): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802428 | ||||||
| chr6:41802428
|
T | TTTTATTT others(16): Show |
2 | a0001c0003t0002g0052a0001c0003t0002g0176 | 2 | HG00280.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1561+1377_1561+137 others(27): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802428 | ||||||
| chr6:41802428
|
T | TTTTATTT others(17): Show |
4 | a0001c0003t0002g0166a0001c0003t0002g0167a0001c0003t0002g0168others(1): Show | 4 | HG00558.hp2 HG01123.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1561+1377_1561+137 others(28): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802428 | ||||||
| chr6:41802428
|
T | TTTTATTT others(22): Show |
1 | a0001c0003t0002g0196 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1561+1377_1561+137 others(33): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802428 | ||||||
| chr6:41802428
|
T | TTTTATTT others(16): Show |
1 | a0001c0003t0002g0046 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1561+1377_1561+137 others(27): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802428 | ||||||
| chr6:41802428
|
TTTTA | T | 7 | a0001c0001t0001g0291a0001c0001t0001g0316a0001c0001t0001g0321others(4): Show | 7 | HG00741.hp2 HG01123.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1561+1374_1561+137 others(8): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802428 | ||||||
| chr6:41802432
|
A | AT | 46 | a0001c0001t0001g0260a0001c0001t0001g0326a0001c0001t0004g0073others(43): Show | 46 | HG00423.hp1 HG00544.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.1561+1373dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802432 | ||||||
| chr6:41802432
|
A | ATTTTATT others(4): Show |
3 | a0001c0003t0002g0173a0001c0003t0026g0171a0005c0009t0002g0170 | 3 | HG00609.hp2 HG03942.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1561+1373_1561+137 others(15): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802432 | ||||||
| chr6:41802433
|
TTTA | T | 30 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0070others(27): Show | 32 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1561+1370_1561+137 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802433 | ||||||
| chr6:41802433
|
TTTATTTA | T | 4 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(1): Show | 4 | HG02897.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1561+1366_1561+137 others(11): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802433 | ||||||
| chr6:41802433
|
TTTATTTA others(8): Show |
T | 1 | a0001c0003t0027g0378 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1561+1358_1561+137 others(19): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802433 | ||||||
| chr6:41802434
|
TTA | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0092others(62): Show | 66 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1561+1370_1561+137 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802434 | ||||||
| chr6:41802435
|
T | TTA | 17 | a0001c0001t0001g0058a0001c0001t0001g0091a0001c0001t0001g0094others(14): Show | 17 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1561+1370_1561+137 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802435 | ||||||
| chr6:41802436
|
A | T | 17 | a0001c0001t0001g0058a0001c0001t0001g0091a0001c0001t0001g0094others(14): Show | 17 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1561+1370T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802436 | ||||||
| chr6:41802439
|
T | A | 65 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0092others(62): Show | 66 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1561+1367A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802439 | ||||||
| chr6:41802440
|
A | T | 65 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0092others(62): Show | 66 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1561+1366T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802440 | ||||||
| chr6:41802450
|
TTATTTAT others(7): Show |
T | 1 | a0001c0001t0001g0310 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1561+1342_1561+135 others(18): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802450 | ||||||
| chr6:41802451
|
T | TATTC | 3 | a0001c0002t0006g0067a0001c0002t0006g0218a0001c0002t0006g0255 | 3 | HG02895.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1561+1354_1561+135 others(8): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802451 | ||||||
| chr6:41802457
|
TTTA | T | 9 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(6): Show | 9 | HG00738.hp2 HG02280.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1561+1346_1561+134 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802457 | ||||||
| chr6:41802457
|
TTTATTTA | T | 3 | a0001c0001t0001g0315a0001c0001t0001g0330a0001c0001t0011g0369 | 3 | NA18522.hp1 NA18906.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1561+1342_1561+134 others(11): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802457 | ||||||
| chr6:41802458
|
TTATTTA | T | 13 | a0001c0001t0001g0290a0001c0001t0001g0294a0001c0001t0001g0295others(10): Show | 13 | HG00544.hp1 HG01099.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1561+1342_1561+134 others(10): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802458 | ||||||
| chr6:41802458
|
TTATTTAT others(3): Show |
T | 3 | a0001c0001t0001g0357a0001c0001t0001g0368a0001c0001t0009g0098 | 3 | NA18979.hp2 NA19091.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1561+1338_1561+134 others(14): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802458 | ||||||
| chr6:41802459
|
TATTTA | T | 6 | a0001c0001t0001g0323a0001c0001t0001g0327a0001c0001t0001g0338others(3): Show | 6 | HG00558.hp1 HG02559.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1561+1342_1561+134 others(9): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802459 | ||||||
| chr6:41802460
|
A | T | 6 | a0001c0001t0001g0281a0001c0001t0001g0291a0001c0001t0001g0306others(3): Show | 6 | HG01074.hp2 HG01123.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1561+1346T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802460 | ||||||
| chr6:41802462
|
TTA | T | 3 | a0001c0001t0001g0331a0001c0001t0004g0075a0001c0001t0043g0267 | 3 | HG01884.hp2 HG02886.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1561+1342_1561+134 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802462 | ||||||
| chr6:41802462
|
TTATTTA | T | 9 | a0001c0001t0001g0289a0001c0001t0001g0302a0001c0001t0001g0309others(6): Show | 9 | HG01943.hp2 HG02083.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1561+1338_1561+134 others(10): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802462 | ||||||
| chr6:41802463
|
T | A | 1 | a0001c0001t0001g0104 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1561+1343A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802463 | ||||||
| chr6:41802463
|
TA | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0114a0001c0001t0001g0121others(4): Show | 7 | HG00735.hp2 HG00738.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1561+1342delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802463 | ||||||
| chr6:41802464
|
A | T | 31 | a0001c0001t0001g0104a0001c0001t0001g0260a0001c0001t0001g0279others(28): Show | 31 | HG00323.hp2 HG00408.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1561+1342T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802464 | ||||||
| chr6:41802467
|
TA | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0103others(27): Show | 31 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.1561+1338delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802467 | ||||||
| chr6:41802468
|
A | T | 63 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0114others(60): Show | 63 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1561+1338T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802468 | ||||||
| chr6:41802468
|
AT | A | 25 | a0001c0001t0001g0109a0001c0001t0001g0139a0001c0001t0001g0153others(22): Show | 27 | HG00738.hp2 HG01069.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.1561+1337delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802468 | ||||||
| chr6:41802468
|
ATT | A | 4 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(1): Show | 4 | HG02897.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1561+1336_1561+133 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802468 | ||||||
| chr6:41802468
|
ATTT | A | 26 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(23): Show | 26 | HG00423.hp1 HG01891.hp1 HG01975.hp1 others(23): Show |
intron_variant | MODIFIER | c.1561+1335_1561+133 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802468 | ||||||
| chr6:41802468
|
ATTTTTTA others(7): Show |
A | 1 | a0001c0001t0018g0097 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1561+1324_1561+133 others(18): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802468 | ||||||
| chr6:41802469
|
T | A | 1 | a0003c0005t0053g0274 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1561+1337A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802469 | ||||||
| chr6:41802469
|
TTTTTTAT others(3): Show |
T | 6 | a0001c0001t0005g0031a0001c0001t0009g0004a0001c0001t0009g0060others(3): Show | 7 | HG01255.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1561+1327_1561+133 others(14): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802469 | ||||||
| chr6:41802471
|
T | TA | 6 | a0001c0001t0005g0017a0001c0001t0005g0032a0001c0001t0033g0009others(3): Show | 6 | HG02559.hp2 HG02809.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.1561+1334_1561+133 others(5): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802471 | ||||||
| chr6:41802472
|
T | A | 19 | a0001c0001t0001g0091a0001c0001t0001g0116a0001c0001t0001g0122others(16): Show | 19 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.1561+1334A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802472 | ||||||
| chr6:41802473
|
TTA | T | 5 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0001g0138others(2): Show | 5 | HG01981.hp2 HG02004.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1561+1331_1561+133 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802473 | ||||||
| chr6:41802473
|
TTATTTA | T | 20 | a0001c0001t0001g0298a0001c0001t0001g0326a0001c0001t0001g0353others(17): Show | 20 | HG01074.hp1 HG01993.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.1561+1327_1561+133 others(10): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802473 | ||||||
| chr6:41802474
|
T | A | 2 | a0001c0001t0001g0003a0003c0005t0053g0274 | 3 | HG01361.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1561+1332A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802474 | ||||||
| chr6:41802474
|
TA | T | 23 | a0001c0001t0001g0092a0001c0001t0001g0101a0001c0001t0001g0110others(20): Show | 23 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1561+1331delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802474 | ||||||
| chr6:41802474
|
TATTTA | T | 14 | a0001c0001t0001g0058a0001c0001t0001g0091a0001c0001t0001g0094others(11): Show | 14 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1561+1327_1561+133 others(9): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802474 | ||||||
| chr6:41802475
|
A | AT | 3 | a0001c0001t0001g0260a0001c0003t0024g0377a0003c0005t0054g0275 | 3 | HG01168.hp1 HG01358.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1561+1330dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802475 | ||||||
| chr6:41802475
|
A | T | 120 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0104others(117): Show | 121 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1561+1331T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802475 | ||||||
| chr6:41802477
|
T | A | 6 | a0001c0001t0001g0115a0001c0001t0001g0146a0001c0003t0013g0043others(3): Show | 6 | HG01515.hp2 HG01891.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1561+1329A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802477 | ||||||
| chr6:41802477
|
TTA | T | 8 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(5): Show | 8 | HG00738.hp2 HG02683.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1561+1327_1561+132 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802477 | ||||||
| chr6:41802478
|
TA | T | 20 | a0001c0001t0001g0221a0001c0001t0004g0001a0001c0001t0004g0002others(17): Show | 22 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1561+1327delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802478 | ||||||
| chr6:41802479
|
A | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0092others(144): Show | 148 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1561+1327T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802479 | ||||||
| chr6:41802479
|
AT | A | 62 | a0001c0001t0009g0096a0001c0002t0003g0040a0001c0002t0003g0045others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1561+1326delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802479 | ||||||
| chr6:41802479
|
ATTT | A | 31 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(28): Show | 31 | HG00423.hp1 HG01891.hp1 HG01975.hp1 others(28): Show |
intron_variant | MODIFIER | c.1561+1324_1561+132 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802479 | ||||||
| chr6:41802480
|
T | TTTA | 7 | a0001c0002t0006g0249a0001c0002t0006g0250a0001c0002t0006g0251others(4): Show | 7 | HG00140.hp1 HG00639.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.1561+1325_1561+132 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802480 | ||||||
| chr6:41802482
|
T | A | 2 | a0001c0001t0005g0031a0001c0001t0037g0038 | 2 | HG02015.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1561+1324A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802482 | ||||||
| chr6:41802483
|
T | A | 10 | a0001c0003t0002g0166a0001c0003t0002g0167a0001c0003t0002g0172others(7): Show | 10 | HG00558.hp2 HG00621.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1561+1323A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802483 | ||||||
| chr6:41802486
|
T | A | 1 | a0001c0007t0005g0036 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1561+1320A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802486 | ||||||
| chr6:41802505
|
G | A | 54 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(51): Show | 54 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.1561+1301C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802505 | ||||||
| chr6:41802535
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1561+1271C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802535 | ||||||
| chr6:41802544
|
G | A | 1 | a0001c0002t0003g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1561+1262C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802544 | ||||||
| chr6:41802574
|
G | A | 306 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(303): Show | 310 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.1561+1232C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802574 | ||||||
| chr6:41802598
|
ATTT | A | 54 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(51): Show | 54 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.1561+1205_1561+120 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802598 | ||||||
| chr6:41802733
|
T | A | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1561+1073A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802733 | ||||||
| chr6:41802866
|
G | A | 54 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(51): Show | 54 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.1561+940C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802866 | ||||||
| chr6:41802915
|
C | T | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1561+891G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802915 | ||||||
| chr6:41802989
|
T | G | 1 | a0003c0005t0053g0274 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1561+817A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41802989 | ||||||
| chr6:41803081
|
T | C | 8 | a0001c0001t0001g0152a0001c0001t0001g0221a0001c0001t0001g0260others(5): Show | 8 | HG02258.hp1 HG02622.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1561+725A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41803081 | ||||||
| chr6:41803161
|
G | A | 1 | a0001c0003t0002g0185 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1561+645C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41803161 | ||||||
| chr6:41803228
|
T | G | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1561+578A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41803228 | ||||||
| chr6:41803261
|
A | G | 1 | a0001c0001t0001g0337 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1561+545T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41803261 | ||||||
| chr6:41803297
|
TTTG | T | 159 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(156): Show | 160 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1561+506_1561+508d others(5): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41803297 | ||||||
| chr6:41803367
|
A | G | 376 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(373): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.1561+439T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41803367 | ||||||
| chr6:41803406
|
C | T | 2 | a0001c0001t0005g0035a0001c0001t0007g0360 | 2 | HG02132.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1561+400G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41803406 | ||||||
| chr6:41803671
|
A | G | 1 | a0001c0002t0003g0211 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1561+135T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41803671 | ||||||
| chr6:41803780
|
C | T | 1 | a0001c0001t0009g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1561+26G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 5/7 | chr6 | 41803780 | ||||||
| chr6:41804110
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1357-100A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/7 | chr6 | 41804110 | ||||||
| chr6:41804126
|
T | C | 20 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0070others(17): Show | 22 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1357-116A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/7 | chr6 | 41804126 | ||||||
| chr6:41804696
|
T | C | 2 | a0001c0001t0001g0260a0001c0001t0057g0059 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1357-686A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/7 | chr6 | 41804696 | ||||||
| chr6:41804730
|
C | G | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1357-720G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/7 | chr6 | 41804730 | ||||||
| chr6:41804733
|
C | G | 11 | a0001c0002t0008g0041a0001c0002t0008g0042a0001c0002t0008g0163others(8): Show | 11 | HG02451.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1357-723G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/7 | chr6 | 41804733 | ||||||
| chr6:41805504
|
T | C | 8 | a0001c0001t0009g0004a0001c0001t0009g0060a0001c0001t0009g0096others(5): Show | 9 | HG01255.hp2 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1356+124A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/7 | chr6 | 41805504 | ||||||
| chr6:41805532
|
G | A | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1356+96C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/7 | chr6 | 41805532 | ||||||
| chr6:41805584
|
G | A | 79 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(76): Show | 79 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1356+44C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 4/7 | chr6 | 41805584 | ||||||
| chr6:41807077
|
T | TA | 225 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(222): Show | 229 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-28-67dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41807077 | ||||||
| chr6:41807077
|
TA | T | 8 | a0001c0002t0003g0341a0001c0002t0006g0255a0001c0003t0002g0177others(5): Show | 8 | HG01168.hp1 HG01361.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28-67delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41807077 | ||||||
| chr6:41807270
|
T | C | 5 | a0001c0002t0008g0163a0001c0002t0012g0161a0001c0002t0012g0162others(2): Show | 5 | HG02451.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-259A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41807270 | ||||||
| chr6:41807388
|
A | G | 1 | a0001c0001t0001g0298 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-28-377T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41807388 | ||||||
| chr6:41807441
|
T | G | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-28-430A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41807441 | ||||||
| chr6:41807515
|
A | T | 1 | a0001c0001t0001g0298 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-28-504T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41807515 | ||||||
| chr6:41807588
|
C | T | 69 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0070others(66): Show | 72 | HG00423.hp1 HG01069.hp2 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.-28-577G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41807588 | ||||||
| chr6:41807602
|
C | T | 1 | a0005c0009t0002g0170 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-28-591G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41807602 | ||||||
| chr6:41807724
|
G | A | 1 | a0001c0001t0046g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-28-713C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41807724 | ||||||
| chr6:41807763
|
T | C | 17 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0071others(14): Show | 19 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.-28-752A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41807763 | ||||||
| chr6:41807922
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0007g0108 | 2 | HG01928.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.-28-911G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41807922 | ||||||
| chr6:41807932
|
C | T | 1 | a0001c0001t0001g0355 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-28-921G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41807932 | ||||||
| chr6:41808010
|
T | C | 79 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(76): Show | 79 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.-28-999A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808010 | ||||||
| chr6:41808042
|
G | T | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-1031C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808042 | ||||||
| chr6:41808183
|
C | T | 1 | a0001c0001t0018g0097 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-28-1172G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808183 | ||||||
| chr6:41808407
|
C | CT | 12 | a0001c0001t0001g0152a0001c0002t0003g0057a0001c0002t0003g0211others(9): Show | 12 | HG01256.hp2 HG01258.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.-28-1397dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808407 | ||||||
| chr6:41808407
|
CT | C | 134 | a0001c0001t0001g0138a0001c0001t0001g0150a0001c0001t0001g0221others(131): Show | 134 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-28-1397delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808407 | ||||||
| chr6:41808407
|
CTT | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(101): Show | 108 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-28-1398_-28-1397d others(4): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808407 | ||||||
| chr6:41808416
|
T | C | 1 | a0001c0001t0001g0367 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-28-1405A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808416 | ||||||
| chr6:41808440
|
T | C | 1 | a0001c0003t0002g0188 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-28-1429A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808440 | ||||||
| chr6:41808471
|
G | T | 2 | a0001c0001t0017g0120a0001c0001t0017g0132 | 2 | HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-28-1460C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808471 | ||||||
| chr6:41808647
|
T | A | 4 | a0001c0001t0001g0109a0001c0001t0001g0139a0001c0001t0001g0153others(1): Show | 4 | NA18956.hp2 NA19011.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-1636A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808647 | ||||||
| chr6:41808693
|
A | G | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-28-1682T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808693 | ||||||
| chr6:41808701
|
C | T | 7 | a0001c0003t0002g0166a0001c0003t0002g0167a0001c0003t0002g0172others(4): Show | 7 | HG00558.hp2 HG00609.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28-1690G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808701 | ||||||
| chr6:41808824
|
C | T | 1 | a0001c0002t0003g0224 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-28-1813G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808824 | ||||||
| chr6:41808885
|
C | T | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-28-1874G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808885 | ||||||
| chr6:41808943
|
T | C | 54 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(51): Show | 54 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.-28-1932A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808943 | ||||||
| chr6:41808999
|
C | T | 1 | a0001c0001t0005g0033 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-28-1988G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41808999 | ||||||
| chr6:41809024
|
C | T | 1 | a0001c0001t0005g0006 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-28-2013G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41809024 | ||||||
| chr6:41809226
|
T | TA | 238 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0091others(235): Show | 242 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.-28-2216dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41809226 | ||||||
| chr6:41809310
|
G | A | 1 | a0001c0001t0041g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-28-2299C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41809310 | ||||||
| chr6:41809369
|
A | T | 2 | a0001c0003t0013g0343a0001c0003t0013g0344 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-28-2358T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41809369 | ||||||
| chr6:41809475
|
A | G | 1 | a0001c0001t0043g0267 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-28-2464T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41809475 | ||||||
| chr6:41809482
|
G | A | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-28-2471C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41809482 | ||||||
| chr6:41809519
|
C | T | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-28-2508G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41809519 | ||||||
| chr6:41809549
|
G | A | 1 | a0001c0001t0005g0006 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-28-2538C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41809549 | ||||||
| chr6:41809620
|
A | G | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-28-2609T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41809620 | ||||||
| chr6:41809814
|
G | A | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-28-2803C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41809814 | ||||||
| chr6:41809816
|
G | A | 1 | a0001c0001t0044g0334 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-28-2805C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41809816 | ||||||
| chr6:41809853
|
A | T | 54 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(51): Show | 54 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.-28-2842T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41809853 | ||||||
| chr6:41809868
|
T | C | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-2857A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41809868 | ||||||
| chr6:41809880
|
G | C | 1 | a0001c0002t0003g0231 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-28-2869C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41809880 | ||||||
| chr6:41809942
|
A | G | 9 | a0001c0002t0006g0249a0001c0002t0006g0250a0001c0002t0006g0251others(6): Show | 9 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.-28-2931T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41809942 | ||||||
| chr6:41810012
|
C | G | 44 | a0001c0001t0001g0058a0001c0001t0001g0091a0001c0001t0001g0093others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.-28-3001G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810012 | ||||||
| chr6:41810031
|
A | G | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-3020T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810031 | ||||||
| chr6:41810061
|
G | A | 374 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(371): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.-28-3050C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810061 | ||||||
| chr6:41810096
|
G | A | 1 | a0001c0001t0007g0345 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-28-3085C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810096 | ||||||
| chr6:41810107
|
G | A | 1 | a0001c0001t0001g0363 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-28-3096C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810107 | ||||||
| chr6:41810143
|
C | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0117 | 2 | HG00733.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-28-3132G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810143 | ||||||
| chr6:41810200
|
G | C | 80 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(77): Show | 80 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-28-3189C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810200 | ||||||
| chr6:41810202
|
C | T | 1 | a0001c0003t0024g0377 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-28-3191G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810202 | ||||||
| chr6:41810255
|
C | T | 1 | a0001c0003t0002g0184 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-28-3244G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810255 | ||||||
| chr6:41810328
|
A | C | 4 | a0001c0001t0001g0311a0001c0001t0001g0315a0001c0001t0001g0329others(1): Show | 4 | HG03130.hp1 HG03225.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-3317T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810328 | ||||||
| chr6:41810387
|
A | G | 374 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(371): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.-28-3376T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810387 | ||||||
| chr6:41810455
|
C | T | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-3444G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810455 | ||||||
| chr6:41810550
|
CT | C | 372 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(369): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.-28-3540delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810550 | ||||||
| chr6:41810713
|
A | C | 1 | a0001c0001t0007g0354 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-28-3702T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810713 | ||||||
| chr6:41810806
|
G | A | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-28-3795C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810806 | ||||||
| chr6:41810848
|
C | T | 1 | a0001c0001t0005g0016 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-28-3837G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810848 | ||||||
| chr6:41810998
|
A | C | 1 | a0001c0001t0046g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-28-3987T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41810998 | ||||||
| chr6:41811037
|
G | A | 3 | a0001c0002t0006g0250a0001c0002t0006g0251a0001c0002t0006g0252 | 3 | HG00639.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-28-4026C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41811037 | ||||||
| chr6:41811610
|
T | G | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-4599A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41811610 | ||||||
| chr6:41811728
|
T | A | 1 | a0001c0001t0005g0006 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-28-4717A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41811728 | ||||||
| chr6:41811769
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-28-4758A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41811769 | ||||||
| chr6:41812013
|
ACAGATTT others(1): Show |
A | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-5010_-28-5003d others(10): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41812013 | ||||||
| chr6:41812236
|
C | T | 1 | a0001c0003t0013g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-28-5225G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41812236 | ||||||
| chr6:41812258
|
T | C | 242 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(239): Show | 246 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.-28-5247A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41812258 | ||||||
| chr6:41812322
|
G | A | 1 | a0001c0002t0003g0240 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-28-5311C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41812322 | ||||||
| chr6:41812348
|
G | C | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-28-5337C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41812348 | ||||||
| chr6:41812425
|
T | TG | 379 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(376): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.-28-5415dupC | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41812425 | ||||||
| chr6:41812469
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-28-5458C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41812469 | ||||||
| chr6:41812521
|
G | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0139 | 2 | NA19058.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.-28-5510C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41812521 | ||||||
| chr6:41812625
|
G | A | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-28-5614C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41812625 | ||||||
| chr6:41812795
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-28-5784C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41812795 | ||||||
| chr6:41812872
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-28-5861A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41812872 | ||||||
| chr6:41813217
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-28-6206C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41813217 | ||||||
| chr6:41813874
|
G | T | 1 | a0001c0001t0058g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-28-6863C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41813874 | ||||||
| chr6:41814210
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-28-7199C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41814210 | ||||||
| chr6:41814245
|
T | C | 6 | a0001c0001t0001g0152a0001c0001t0001g0260a0001c0001t0046g0151others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-7234A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41814245 | ||||||
| chr6:41814255
|
C | T | 2 | a0001c0001t0009g0096a0001c0001t0009g0098 | 2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-28-7244G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41814255 | ||||||
| chr6:41814269
|
A | G | 162 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(159): Show | 163 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.-28-7258T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41814269 | ||||||
| chr6:41814314
|
C | T | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-28-7303G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41814314 | ||||||
| chr6:41814334
|
A | C | 20 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0070others(17): Show | 22 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-28-7323T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41814334 | ||||||
| chr6:41814369
|
T | C | 54 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(51): Show | 54 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.-28-7358A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41814369 | ||||||
| chr6:41814438
|
A | T | 2 | a0001c0001t0014g0068a0001c0001t0014g0078 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-28-7427T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41814438 | ||||||
| chr6:41814661
|
CTACTT | C | 240 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(237): Show | 244 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.-28-7655_-28-7651d others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41814661 | ||||||
| chr6:41814690
|
G | A | 1 | a0001c0001t0001g0353 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-28-7679C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41814690 | ||||||
| chr6:41814727
|
T | C | 1 | a0001c0001t0005g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-28-7716A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41814727 | ||||||
| chr6:41815211
|
C | A | 1 | a0001c0001t0001g0134 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-28-8200G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41815211 | ||||||
| chr6:41815284
|
A | G | 1 | a0001c0003t0002g0200 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-28-8273T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41815284 | ||||||
| chr6:41815345
|
T | C | 2 | a0001c0001t0001g0353a0001c0001t0001g0367 | 2 | NA18940.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-28-8334A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41815345 | ||||||
| chr6:41815352
|
C | T | 1 | a0001c0001t0001g0352 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-28-8341G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41815352 | ||||||
| chr6:41815365
|
GAGCCAAG others(18): Show |
G | 1 | a0001c0001t0001g0155 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-28-8379_-28-8355d others(27): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41815365 | ||||||
| chr6:41815377
|
C | T | 1 | a0001c0003t0002g0178 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-28-8366G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41815377 | ||||||
| chr6:41815508
|
G | C | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-28-8497C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41815508 | ||||||
| chr6:41815511
|
A | G | 306 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(303): Show | 310 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.-28-8500T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41815511 | ||||||
| chr6:41815640
|
C | A | 10 | a0001c0003t0002g0178a0001c0003t0002g0180a0001c0003t0002g0182others(7): Show | 10 | HG00408.hp2 HG00621.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.-28-8629G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41815640 | ||||||
| chr6:41815717
|
C | T | 1 | a0001c0003t0025g0062 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-28-8706G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41815717 | ||||||
| chr6:41816079
|
G | A | 1 | a0001c0003t0013g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-28-9068C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41816079 | ||||||
| chr6:41816342
|
G | A | 1 | a0001c0003t0013g0344 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-28-9331C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41816342 | ||||||
| chr6:41816356
|
C | T | 241 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(238): Show | 245 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.-28-9345G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41816356 | ||||||
| chr6:41816443
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-28-9432A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41816443 | ||||||
| chr6:41816702
|
C | CTATTAT | 242 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(239): Show | 246 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.-28-9697_-28-9692d others(8): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41816702 | ||||||
| chr6:41816702
|
C | CTATTATT others(2): Show |
4 | a0001c0001t0001g0337a0003c0005t0053g0274a0003c0005t0054g0275others(1): Show | 4 | HG01168.hp1 HG01361.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-9700_-28-9692d others(11): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41816702 | ||||||
| chr6:41816702
|
C | CTATTATT others(8): Show |
1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-28-9706_-28-9692d others(17): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41816702 | ||||||
| chr6:41816702
|
C | CTATTATT others(11): Show |
4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-9709_-28-9692d others(20): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41816702 | ||||||
| chr6:41816832
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-28-9821C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41816832 | ||||||
| chr6:41816988
|
G | A | 1 | a0001c0001t0057g0059 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28-9977C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41816988 | ||||||
| chr6:41817144
|
C | G | 1 | a0001c0001t0001g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-28-10133G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817144 | ||||||
| chr6:41817150
|
C | CT | 11 | a0001c0002t0003g0215a0001c0002t0008g0163a0001c0003t0002g0179others(8): Show | 11 | HG00741.hp1 HG01891.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.-28-10140dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817150 | ||||||
| chr6:41817150
|
C | CTTT | 74 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(71): Show | 75 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-28-10142_-28-1014 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817150 | ||||||
| chr6:41817150
|
C | CTTTT | 83 | a0001c0001t0001g0091a0001c0001t0001g0106a0001c0001t0001g0117others(80): Show | 83 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-28-10143_-28-1014 others(8): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817150 | ||||||
| chr6:41817150
|
C | CTTTTT | 6 | a0001c0001t0001g0309a0001c0001t0001g0335a0001c0001t0001g0338others(3): Show | 6 | HG00621.hp2 HG03491.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-10144_-28-1014 others(9): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817150 | ||||||
| chr6:41817150
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0157a0001c0001t0001g0221a0001c0001t0015g0219others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-10150_-28-1014 others(15): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817150 | ||||||
| chr6:41817150
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0009g0098a0001c0001t0018g0090a0001c0001t0018g0097others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-10151_-28-1014 others(16): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817150 | ||||||
| chr6:41817150
|
C | CTTTTTTT others(6): Show |
5 | a0001c0001t0001g0158a0001c0001t0001g0260a0001c0001t0009g0096others(2): Show | 5 | HG01168.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-10152_-28-1014 others(17): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817150 | ||||||
| chr6:41817150
|
C | CTTTTTTT others(7): Show |
1 | a0003c0005t0055g0273 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-28-10153_-28-1014 others(18): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817150 | ||||||
| chr6:41817150
|
C | CTTTTTTT others(8): Show |
3 | a0001c0001t0057g0059a0001c0003t0025g0062a0003c0005t0053g0274 | 3 | HG01361.hp2 HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-28-10154_-28-1014 others(19): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817150 | ||||||
| chr6:41817150
|
C | CTTTTTTT others(11): Show |
10 | a0001c0001t0004g0001a0001c0001t0004g0074a0001c0001t0004g0080others(7): Show | 11 | HG01069.hp2 HG01099.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-28-10140_-28-1013 others(22): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817150 | ||||||
| chr6:41817150
|
C | CTTTTTTT others(12): Show |
10 | a0001c0001t0004g0002a0001c0001t0004g0071a0001c0001t0004g0072others(7): Show | 11 | HG01106.hp2 HG01261.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.-28-10140_-28-1013 others(23): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817150 | ||||||
| chr6:41817150
|
C | CTTTTTTT others(13): Show |
2 | a0001c0001t0004g0077a0001c0001t0004g0083 | 2 | HG02004.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-28-10140_-28-1013 others(24): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817150 | ||||||
| chr6:41817150
|
C | CTTTTTTT others(14): Show |
3 | a0001c0001t0004g0070a0001c0001t0004g0075a0001c0001t0004g0089 | 3 | HG01346.hp1 HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-28-10140_-28-1013 others(25): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817150 | ||||||
| chr6:41817166
|
TTG | T | 29 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0008others(26): Show | 29 | HG00423.hp1 HG01074.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.-28-10157_-28-1015 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817166 | ||||||
| chr6:41817167
|
TG | T | 6 | a0001c0001t0005g0007a0001c0001t0005g0012a0001c0001t0005g0021others(3): Show | 6 | HG03098.hp2 NA18978.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-10157delC | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817167 | ||||||
| chr6:41817168
|
G | T | 205 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(202): Show | 209 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.-28-10157C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817168 | ||||||
| chr6:41817234
|
G | A | 4 | a0001c0001t0005g0033a0001c0002t0003g0045a0001c0002t0003g0213others(1): Show | 4 | HG00099.hp2 HG03098.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-10223C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817234 | ||||||
| chr6:41817251
|
G | A | 1 | a0001c0003t0025g0062 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-28-10240C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817251 | ||||||
| chr6:41817282
|
G | A | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-28-10271C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817282 | ||||||
| chr6:41817304
|
T | C | 1 | a0001c0007t0005g0036 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-28-10293A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817304 | ||||||
| chr6:41817389
|
A | G | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-28-10378T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817389 | ||||||
| chr6:41817437
|
C | T | 3 | a0001c0003t0002g0190a0001c0003t0002g0196a0001c0003t0002g0204 | 3 | HG02080.hp2 HG02523.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-28-10426G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817437 | ||||||
| chr6:41817457
|
CT | C | 139 | a0001c0001t0001g0139a0001c0001t0001g0260a0001c0001t0001g0279others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.-28-10447delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817457 | ||||||
| chr6:41817457
|
CTT | C | 228 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(225): Show | 232 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.-28-10448_-28-1044 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817457 | ||||||
| chr6:41817462
|
T | C | 1 | a0001c0003t0024g0377 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-28-10451A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41817462 | ||||||
| chr6:41818051
|
T | C | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-28-11040A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41818051 | ||||||
| chr6:41818398
|
G | A | 232 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(229): Show | 236 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.-28-11387C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41818398 | ||||||
| chr6:41818405
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-28-11394A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41818405 | ||||||
| chr6:41818596
|
A | G | 1 | a0001c0003t0002g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-28-11585T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41818596 | ||||||
| chr6:41818715
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-28-11704A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41818715 | ||||||
| chr6:41818823
|
T | C | 1 | a0001c0003t0002g0048 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-28-11812A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41818823 | ||||||
| chr6:41818949
|
T | C | 1 | a0001c0003t0024g0377 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-28-11938A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41818949 | ||||||
| chr6:41819114
|
T | C | 1 | a0001c0003t0010g0064 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-28-12103A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41819114 | ||||||
| chr6:41819122
|
C | T | 1 | a0001c0001t0004g0076 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-28-12111G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41819122 | ||||||
| chr6:41819238
|
T | G | 59 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(56): Show | 59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.-28-12227A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41819238 | ||||||
| chr6:41819306
|
C | A | 1 | a0001c0003t0002g0278 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-28-12295G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41819306 | ||||||
| chr6:41819717
|
C | G | 3 | a0001c0001t0001g0316a0001c0001t0001g0323a0001c0001t0001g0327 | 3 | HG02258.hp2 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-28-12706G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41819717 | ||||||
| chr6:41819742
|
G | C | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-12731C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41819742 | ||||||
| chr6:41820002
|
C | A | 302 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(299): Show | 306 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.-28-12991G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41820002 | ||||||
| chr6:41820142
|
A | T | 8 | a0001c0001t0009g0004a0001c0001t0009g0060a0001c0001t0009g0096others(5): Show | 9 | HG01255.hp2 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-28-13131T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41820142 | ||||||
| chr6:41820181
|
GT | G | 300 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(297): Show | 304 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.-28-13171delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41820181 | ||||||
| chr6:41820257
|
G | T | 2 | a0001c0001t0001g0295a0001c0001t0044g0334 | 2 | NA19006.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-28-13246C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41820257 | ||||||
| chr6:41820324
|
C | G | 3 | a0001c0002t0006g0250a0001c0002t0006g0251a0001c0002t0006g0252 | 3 | HG00639.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-28-13313G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41820324 | ||||||
| chr6:41820413
|
T | C | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-28-13402A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41820413 | ||||||
| chr6:41820574
|
G | GA | 47 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0005g0005others(44): Show | 48 | HG00423.hp1 HG01074.hp1 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.-28-13564dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41820574 | ||||||
| chr6:41820642
|
T | G | 79 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(76): Show | 79 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.-28-13631A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41820642 | ||||||
| chr6:41820771
|
G | A | 1 | a0001c0001t0001g0355 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-28-13760C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41820771 | ||||||
| chr6:41820864
|
A | G | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-13853T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41820864 | ||||||
| chr6:41821095
|
A | C | 1 | a0001c0001t0001g0287 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-28-14084T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41821095 | ||||||
| chr6:41821190
|
C | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-28-14179G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41821190 | ||||||
| chr6:41821510
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-28-14499G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41821510 | ||||||
| chr6:41821771
|
T | C | 1 | a0001c0003t0002g0268 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-28-14760A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41821771 | ||||||
| chr6:41821878
|
A | G | 1 | a0001c0001t0046g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-28-14867T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41821878 | ||||||
| chr6:41821971
|
G | A | 36 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(33): Show | 36 | HG00423.hp1 HG01074.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-28-14960C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41821971 | ||||||
| chr6:41822033
|
T | G | 9 | a0001c0001t0001g0152a0001c0001t0001g0221a0001c0001t0001g0260others(6): Show | 9 | HG02258.hp1 HG02622.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-28-15022A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41822033 | ||||||
| chr6:41822159
|
C | A | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-28-15148G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41822159 | ||||||
| chr6:41822317
|
G | A | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-15306C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41822317 | ||||||
| chr6:41822318
|
A | G | 1 | a0001c0002t0003g0246 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-28-15307T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41822318 | ||||||
| chr6:41822535
|
T | C | 1 | a0001c0002t0003g0246 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-28-15524A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41822535 | ||||||
| chr6:41822652
|
C | G | 4 | a0001c0001t0001g0119a0001c0001t0001g0126a0001c0001t0001g0133others(1): Show | 4 | HG00597.hp2 HG02165.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-15641G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41822652 | ||||||
| chr6:41822717
|
C | T | 240 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(237): Show | 244 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.-28-15706G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41822717 | ||||||
| chr6:41822725
|
G | C | 71 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0004g0001others(68): Show | 74 | HG00423.hp1 HG01069.hp2 HG01074.hp1 others(71): Show |
intron_variant | MODIFIER | c.-28-15714C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41822725 | ||||||
| chr6:41822818
|
CA | C | 249 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(246): Show | 253 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.-28-15808delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41822818 | ||||||
| chr6:41822981
|
G | C | 1 | a0001c0001t0001g0107 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-28-15970C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41822981 | ||||||
| chr6:41823083
|
T | A | 5 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(2): Show | 5 | HG02109.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28-16072A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41823083 | ||||||
| chr6:41823832
|
G | C | 2 | a0001c0003t0010g0055a0001c0003t0010g0056 | 2 | HG00741.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-28-16821C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41823832 | ||||||
| chr6:41824008
|
T | C | 1 | a0001c0002t0003g0241 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-28-16997A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41824008 | ||||||
| chr6:41824291
|
A | C | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-28-17280T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41824291 | ||||||
| chr6:41824333
|
T | C | 1 | a0001c0001t0007g0356 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-28-17322A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41824333 | ||||||
| chr6:41824387
|
T | A | 4 | a0001c0002t0006g0067a0001c0002t0006g0218a0001c0002t0006g0255others(1): Show | 4 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-17376A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41824387 | ||||||
| chr6:41824481
|
C | T | 2 | a0001c0003t0013g0343a0001c0003t0013g0344 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-28-17470G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41824481 | ||||||
| chr6:41824549
|
A | G | 1 | a0001c0001t0004g0070 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-28-17538T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41824549 | ||||||
| chr6:41824673
|
T | G | 5 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28-17662A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41824673 | ||||||
| chr6:41824715
|
AAAACAAG others(9): Show |
A | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-28-17720_-28-1770 others(20): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41824715 | ||||||
| chr6:41824807
|
C | T | 55 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(52): Show | 55 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.-28-17796G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41824807 | ||||||
| chr6:41824845
|
G | C | 4 | a0001c0001t0001g0152a0001c0001t0001g0260a0001c0001t0046g0151others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-17834C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41824845 | ||||||
| chr6:41824915
|
G | A | 1 | a0001c0001t0057g0059 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28-17904C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41824915 | ||||||
| chr6:41824921
|
T | C | 52 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(49): Show | 52 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.-28-17910A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41824921 | ||||||
| chr6:41824946
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-28-17935G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41824946 | ||||||
| chr6:41825040
|
A | G | 1 | a0003c0005t0053g0274 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-28-18029T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41825040 | ||||||
| chr6:41825323
|
T | G | 1 | a0001c0001t0004g0308 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-28-18312A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41825323 | ||||||
| chr6:41825440
|
G | GA | 82 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(79): Show | 83 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.-28-18430dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41825440 | ||||||
| chr6:41825458
|
T | G | 1 | a0001c0003t0024g0377 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-28-18447A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41825458 | ||||||
| chr6:41825485
|
A | C | 5 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28-18474T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41825485 | ||||||
| chr6:41825516
|
G | A | 1 | a0001c0001t0004g0088 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-28-18505C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41825516 | ||||||
| chr6:41825565
|
A | G | 1 | a0001c0003t0024g0377 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-28-18554T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41825565 | ||||||
| chr6:41825731
|
T | C | 1 | a0001c0001t0014g0068 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-28-18720A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41825731 | ||||||
| chr6:41826331
|
CCTAT | C | 79 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(76): Show | 79 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-28-19324_-28-1932 others(8): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41826331 | ||||||
| chr6:41826497
|
T | C | 1 | a0001c0003t0024g0377 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-28-19486A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41826497 | ||||||
| chr6:41826600
|
T | C | 1 | a0001c0001t0005g0033 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-28-19589A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41826600 | ||||||
| chr6:41826743
|
C | T | 1 | a0001c0003t0002g0202 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-28-19732G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41826743 | ||||||
| chr6:41826798
|
ACTG | A | 4 | a0001c0001t0001g0152a0001c0001t0001g0260a0001c0001t0046g0151others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-19790_-28-1978 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41826798 | ||||||
| chr6:41827004
|
G | C | 1 | a0003c0005t0054g0275 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-28-19993C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41827004 | ||||||
| chr6:41827109
|
T | C | 1 | a0001c0003t0002g0177 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-28-20098A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41827109 | ||||||
| chr6:41827159
|
T | A | 1 | a0001c0003t0027g0378 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-28-20148A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41827159 | ||||||
| chr6:41827186
|
A | G | 1 | a0001c0001t0047g0300 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-28-20175T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41827186 | ||||||
| chr6:41827334
|
T | G | 1 | a0001c0001t0001g0125 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-28-20323A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41827334 | ||||||
| chr6:41827593
|
G | A | 67 | a0001c0002t0003g0040a0001c0002t0003g0045a0001c0002t0003g0057others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.-28-20582C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41827593 | ||||||
| chr6:41827632
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-28-20621G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41827632 | ||||||
| chr6:41827657
|
A | G | 3 | a0001c0001t0001g0110a0001c0001t0001g0145a0001c0001t0001g0156 | 3 | HG00438.hp2 NA18974.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-28-20646T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41827657 | ||||||
| chr6:41827671
|
T | C | 1 | a0001c0001t0057g0059 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28-20660A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41827671 | ||||||
| chr6:41827675
|
C | CA | 33 | a0001c0001t0001g0095a0001c0001t0001g0329a0001c0001t0001g0330others(30): Show | 35 | HG00558.hp1 HG01069.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.-28-20665dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41827675 | ||||||
| chr6:41827675
|
C | CAA | 184 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(181): Show | 186 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.-28-20666_-28-2066 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41827675 | ||||||
| chr6:41827675
|
C | CAAA | 20 | a0001c0001t0001g0091a0001c0001t0001g0104a0001c0001t0001g0105others(17): Show | 20 | HG00438.hp1 HG00735.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.-28-20667_-28-2066 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41827675 | ||||||
| chr6:41827675
|
CA | C | 7 | a0001c0001t0001g0221a0001c0001t0015g0219a0001c0002t0003g0066others(4): Show | 7 | HG01516.hp2 HG02451.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28-20665delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41827675 | ||||||
| chr6:41827906
|
T | A | 2 | a0001c0001t0011g0346a0001c0001t0011g0349 | 2 | NA18978.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-28-20895A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41827906 | ||||||
| chr6:41827939
|
G | A | 1 | a0001c0002t0003g0232 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-28-20928C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41827939 | ||||||
| chr6:41828108
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-28-21097G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41828108 | ||||||
| chr6:41828163
|
G | A | 4 | a0001c0002t0008g0163a0001c0002t0012g0161a0001c0002t0012g0162others(1): Show | 4 | HG02451.hp2 HG02717.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-21152C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41828163 | ||||||
| chr6:41828326
|
G | A | 25 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0070others(22): Show | 27 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.-28-21315C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41828326 | ||||||
| chr6:41828504
|
G | A | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-21493C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41828504 | ||||||
| chr6:41828551
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0139 | 2 | NA19058.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.-28-21540C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41828551 | ||||||
| chr6:41828727
|
T | C | 1 | a0001c0001t0004g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-28-21716A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41828727 | ||||||
| chr6:41828825
|
T | TTTTTTTT others(29): Show |
2 | a0001c0003t0013g0043a0001c0003t0013g0044 | 2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-28-21815_-28-2181 others(40): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41828825 | ||||||
| chr6:41828825
|
T | TTTTTTTT others(31): Show |
1 | a0001c0003t0013g0343 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-28-21815_-28-2181 others(42): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41828825 | ||||||
| chr6:41828825
|
T | TTTTTTTT others(32): Show |
1 | a0001c0003t0013g0344 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-28-21815_-28-2181 others(43): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41828825 | ||||||
| chr6:41828961
|
C | T | 3 | a0001c0001t0001g0303a0001c0001t0001g0317a0001c0001t0001g0371 | 3 | NA18975.hp1 NA19012.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-28-21950G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41828961 | ||||||
| chr6:41828967
|
T | C | 1 | a0001c0001t0019g0100 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-28-21956A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41828967 | ||||||
| chr6:41829079
|
A | G | 307 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(304): Show | 311 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.-28-22068T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41829079 | ||||||
| chr6:41829105
|
CA | C | 3 | a0001c0002t0006g0250a0001c0002t0006g0251a0001c0002t0006g0252 | 3 | HG00639.hp1 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-28-22095delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41829105 | ||||||
| chr6:41829152
|
T | C | 1 | a0001c0003t0002g0200 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-28-22141A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41829152 | ||||||
| chr6:41829211
|
A | G | 1 | a0001c0001t0007g0359 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-28-22200T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41829211 | ||||||
| chr6:41829232
|
T | C | 61 | a0001c0001t0001g0221a0001c0001t0001g0261a0001c0001t0015g0063others(58): Show | 61 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.-28-22221A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41829232 | ||||||
| chr6:41829316
|
A | AT | 6 | a0001c0001t0001g0131a0001c0001t0001g0139a0001c0001t0001g0147others(3): Show | 6 | HG01074.hp2 HG01358.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-22306dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41829316 | ||||||
| chr6:41829416
|
C | T | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-28-22405G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41829416 | ||||||
| chr6:41829425
|
T | C | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-28-22414A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41829425 | ||||||
| chr6:41829503
|
G | A | 1 | a0001c0001t0005g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-28-22492C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41829503 | ||||||
| chr6:41829603
|
G | A | 7 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0124others(4): Show | 7 | HG00735.hp1 HG01952.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28-22592C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41829603 | ||||||
| chr6:41829821
|
G | T | 1 | a0001c0002t0003g0242 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-28-22810C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41829821 | ||||||
| chr6:41829920
|
A | G | 1 | a0001c0001t0051g0023 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-28-22909T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41829920 | ||||||
| chr6:41830121
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-28-23110G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41830121 | ||||||
| chr6:41830273
|
A | G | 2 | a0001c0002t0006g0339a0001c0002t0006g0340 | 2 | HG00099.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-28-23262T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41830273 | ||||||
| chr6:41830362
|
T | C | 1 | a0001c0002t0003g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-28-23351A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41830362 | ||||||
| chr6:41830536
|
A | G | 1 | a0001c0003t0027g0378 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-28-23525T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41830536 | ||||||
| chr6:41830817
|
C | T | 30 | a0001c0001t0001g0326a0001c0001t0001g0347a0001c0001t0001g0350others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.-28-23806G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41830817 | ||||||
| chr6:41830840
|
T | A | 162 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(159): Show | 163 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.-28-23829A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41830840 | ||||||
| chr6:41830855
|
C | T | 1 | a0001c0003t0024g0377 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-28-23844G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41830855 | ||||||
| chr6:41831043
|
G | A | 1 | a0001c0003t0002g0181 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-28-24032C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41831043 | ||||||
| chr6:41831154
|
G | A | 1 | a0001c0003t0020g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-28-24143C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41831154 | ||||||
| chr6:41831234
|
A | G | 162 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(159): Show | 163 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.-28-24223T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41831234 | ||||||
| chr6:41831246
|
C | T | 1 | a0001c0001t0001g0003 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-28-24235G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41831246 | ||||||
| chr6:41831339
|
G | A | 1 | a0001c0003t0002g0196 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-28-24328C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41831339 | ||||||
| chr6:41831345
|
G | C | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-28-24334C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41831345 | ||||||
| chr6:41831375
|
G | C | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-28-24364C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41831375 | ||||||
| chr6:41831580
|
CA | C | 15 | a0001c0002t0003g0040a0001c0002t0006g0340a0001c0003t0002g0175others(12): Show | 15 | HG01168.hp1 HG01358.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.-28-24570delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41831580 | ||||||
| chr6:41831580
|
CAA | C | 75 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(72): Show | 78 | HG00423.hp1 HG01069.hp2 HG01074.hp1 others(75): Show |
intron_variant | MODIFIER | c.-28-24571_-28-2457 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41831580 | ||||||
| chr6:41831580
|
CAAA | C | 161 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(158): Show | 162 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.-28-24572_-28-2457 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41831580 | ||||||
| chr6:41831731
|
C | T | 5 | a0001c0001t0001g0302a0001c0001t0001g0311a0001c0001t0001g0315others(2): Show | 5 | HG02809.hp2 HG03130.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-24720G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41831731 | ||||||
| chr6:41831735
|
C | T | 5 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28-24724G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41831735 | ||||||
| chr6:41831880
|
C | T | 2 | a0001c0001t0009g0096a0001c0001t0009g0098 | 2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-28-24869G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41831880 | ||||||
| chr6:41832010
|
C | T | 1 | a0001c0003t0002g0181 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-28-24999G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41832010 | ||||||
| chr6:41832035
|
C | T | 1 | a0002c0004t0002g0197 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-28-25024G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41832035 | ||||||
| chr6:41832038
|
C | T | 1 | a0001c0003t0023g0165 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-28-25027G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41832038 | ||||||
| chr6:41832115
|
G | GT | 8 | a0001c0001t0001g0143a0001c0001t0001g0328a0001c0001t0015g0063others(5): Show | 8 | HG01361.hp2 HG01516.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28-25105dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41832115 | ||||||
| chr6:41832143
|
C | T | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-25132G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41832143 | ||||||
| chr6:41832172
|
T | G | 5 | a0001c0001t0009g0004a0001c0001t0009g0060a0001c0001t0009g0159others(2): Show | 6 | HG01255.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-25161A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41832172 | ||||||
| chr6:41832308
|
C | T | 1 | a0001c0003t0002g0202 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-28-25297G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41832308 | ||||||
| chr6:41832409
|
A | C | 1 | a0001c0001t0001g0289 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-28-25398T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41832409 | ||||||
| chr6:41832426
|
A | G | 1 | a0001c0002t0006g0257 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-28-25415T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41832426 | ||||||
| chr6:41832531
|
G | A | 1 | a0001c0003t0024g0377 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-28-25520C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41832531 | ||||||
| chr6:41832580
|
G | A | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-28-25569C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41832580 | ||||||
| chr6:41832891
|
T | C | 58 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.-28-25880A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41832891 | ||||||
| chr6:41832990
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-28-25979T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41832990 | ||||||
| chr6:41833020
|
CT | C | 78 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(75): Show | 78 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-28-26010delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41833020 | ||||||
| chr6:41833080
|
G | A | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-28-26069C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41833080 | ||||||
| chr6:41833085
|
C | T | 2 | a0001c0002t0003g0210a0001c0002t0003g0224 | 2 | HG00642.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-28-26074G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41833085 | ||||||
| chr6:41833277
|
A | G | 1 | a0001c0001t0001g0374 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-28-26266T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41833277 | ||||||
| chr6:41833284
|
G | A | 53 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-28-26273C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41833284 | ||||||
| chr6:41833305
|
CA | C | 7 | a0001c0003t0002g0200a0001c0003t0002g0268a0002c0004t0002g0169others(4): Show | 7 | HG00423.hp2 HG02056.hp2 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28-26295delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41833305 | ||||||
| chr6:41833306
|
A | G | 1 | a0001c0001t0035g0380 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-28-26295T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41833306 | ||||||
| chr6:41833335
|
G | T | 2 | a0001c0001t0001g0124a0001c0001t0041g0118 | 2 | HG02523.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-28-26324C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41833335 | ||||||
| chr6:41833463
|
A | C | 3 | a0001c0001t0001g0127a0001c0001t0001g0263a0001c0001t0001g0264 | 3 | NA18983.hp1 NA19009.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-28-26452T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41833463 | ||||||
| chr6:41833547
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-28-26536A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41833547 | ||||||
| chr6:41833891
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-28-26880G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41833891 | ||||||
| chr6:41833897
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-28-26886G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41833897 | ||||||
| chr6:41833907
|
C | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0126a0001c0001t0001g0133others(1): Show | 4 | HG00597.hp2 HG02165.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-26896G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41833907 | ||||||
| chr6:41833932
|
T | C | 1 | a0001c0002t0003g0341 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-28-26921A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41833932 | ||||||
| chr6:41833995
|
A | G | 1 | a0003c0005t0053g0274 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-28-26984T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41833995 | ||||||
| chr6:41834003
|
A | C | 1 | a0001c0001t0001g0306 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-28-26992T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41834003 | ||||||
| chr6:41834029
|
T | C | 5 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28-27018A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41834029 | ||||||
| chr6:41834062
|
C | T | 2 | a0001c0002t0006g0254a0001c0002t0006g0256 | 2 | HG00140.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.-28-27051G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41834062 | ||||||
| chr6:41834329
|
G | A | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-28-27318C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41834329 | ||||||
| chr6:41834498
|
G | A | 53 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-28-27487C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41834498 | ||||||
| chr6:41834520
|
G | A | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-28-27509C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41834520 | ||||||
| chr6:41834531
|
G | C | 1 | a0001c0001t0046g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-28-27520C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41834531 | ||||||
| chr6:41834587
|
A | C | 2 | a0001c0001t0001g0260a0001c0001t0057g0059 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-28-27576T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41834587 | ||||||
| chr6:41834616
|
G | A | 58 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.-28-27605C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41834616 | ||||||
| chr6:41834730
|
T | C | 1 | a0001c0001t0015g0220 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-28-27719A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41834730 | ||||||
| chr6:41835037
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-28-28026C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41835037 | ||||||
| chr6:41835305
|
C | T | 4 | a0001c0001t0001g0152a0001c0001t0001g0260a0001c0001t0046g0151others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-28294G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41835305 | ||||||
| chr6:41835373
|
T | C | 1 | a0001c0001t0009g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-28-28362A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41835373 | ||||||
| chr6:41835480
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(1): Show | 4 | HG02897.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-28469C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41835480 | ||||||
| chr6:41835495
|
C | T | 1 | a0001c0001t0057g0059 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28-28484G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41835495 | ||||||
| chr6:41835518
|
C | A | 1 | a0001c0002t0003g0207 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-28-28507G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41835518 | ||||||
| chr6:41835655
|
A | G | 1 | a0001c0002t0003g0245 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-28-28644T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41835655 | ||||||
| chr6:41835670
|
C | T | 1 | a0002c0004t0002g0197 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-28-28659G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41835670 | ||||||
| chr6:41835719
|
C | A | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-28-28708G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41835719 | ||||||
| chr6:41835719
|
C | CA | 13 | a0001c0001t0001g0126a0001c0001t0001g0131a0001c0001t0001g0147others(10): Show | 13 | HG00323.hp1 HG01070.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.-28-28709dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41835719 | ||||||
| chr6:41835721
|
G | A | 374 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(371): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.-28-28710C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41835721 | ||||||
| chr6:41835898
|
A | G | 4 | a0001c0001t0001g0119a0001c0001t0001g0126a0001c0001t0001g0133others(1): Show | 4 | HG00597.hp2 HG02165.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-28887T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41835898 | ||||||
| chr6:41835903
|
C | T | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-28-28892G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41835903 | ||||||
| chr6:41835924
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-28-28913T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41835924 | ||||||
| chr6:41836098
|
C | T | 77 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(74): Show | 78 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-28-29087G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41836098 | ||||||
| chr6:41836287
|
T | A | 1 | a0001c0003t0024g0377 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-28-29276A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41836287 | ||||||
| chr6:41836302
|
C | A | 2 | a0001c0001t0004g0001a0001c0001t0004g0085 | 3 | HG01257.hp2 HG01258.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-28-29291G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41836302 | ||||||
| chr6:41836507
|
G | A | 80 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(77): Show | 80 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-28-29496C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41836507 | ||||||
| chr6:41836737
|
C | T | 25 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0070others(22): Show | 27 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.-28-29726G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41836737 | ||||||
| chr6:41836857
|
G | GCA | 9 | a0001c0001t0015g0063a0001c0001t0015g0219a0001c0001t0015g0220others(6): Show | 9 | HG01361.hp2 HG01891.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28-29848_-28-2984 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41836857 | ||||||
| chr6:41836857
|
GCA | G | 4 | a0001c0001t0001g0152a0001c0001t0001g0260a0001c0001t0046g0151others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-29848_-28-2984 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41836857 | ||||||
| chr6:41836878
|
A | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-28-29867T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41836878 | ||||||
| chr6:41837138
|
G | T | 1 | a0001c0001t0009g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-28-30127C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41837138 | ||||||
| chr6:41837338
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-28-30327G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41837338 | ||||||
| chr6:41837384
|
G | A | 1 | a0001c0003t0002g0206 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-28-30373C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41837384 | ||||||
| chr6:41837473
|
T | G | 2 | a0003c0005t0054g0275a0003c0005t0055g0273 | 2 | HG01168.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-28-30462A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41837473 | ||||||
| chr6:41837519
|
A | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG00735.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-28-30508T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41837519 | ||||||
| chr6:41837583
|
A | G | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-28-30572T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41837583 | ||||||
| chr6:41837799
|
T | G | 1 | a0001c0001t0001g0373 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-28-30788A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41837799 | ||||||
| chr6:41837843
|
A | C | 52 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(49): Show | 52 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.-28-30832T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41837843 | ||||||
| chr6:41838132
|
A | G | 1 | a0001c0002t0003g0236 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-28-31121T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41838132 | ||||||
| chr6:41838560
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0117 | 2 | HG00733.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-28-31549T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41838560 | ||||||
| chr6:41838639
|
T | C | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-28-31628A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41838639 | ||||||
| chr6:41838734
|
C | A | 1 | a0001c0002t0003g0242 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-28-31723G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41838734 | ||||||
| chr6:41838862
|
A | G | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-28-31851T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41838862 | ||||||
| chr6:41838968
|
T | C | 2 | a0001c0001t0001g0109a0001c0001t0001g0139 | 2 | NA19058.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.-28-31957A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41838968 | ||||||
| chr6:41838970
|
T | A | 58 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.-28-31959A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41838970 | ||||||
| chr6:41839055
|
G | A | 58 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.-28-32044C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839055 | ||||||
| chr6:41839256
|
A | C | 2 | a0001c0002t0006g0257a0001c0002t0006g0258 | 2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-28-32245T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839256 | ||||||
| chr6:41839317
|
G | T | 1 | a0001c0003t0002g0201 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-29+32247C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839317 | ||||||
| chr6:41839338
|
G | A | 1 | a0001c0001t0009g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-29+32226C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839338 | ||||||
| chr6:41839401
|
T | C | 80 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(77): Show | 80 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-29+32163A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839401 | ||||||
| chr6:41839404
|
C | CA | 67 | a0001c0001t0001g0104a0001c0001t0001g0114a0001c0001t0001g0156others(64): Show | 67 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.-29+32159dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839404 | ||||||
| chr6:41839404
|
C | CAA | 33 | a0001c0002t0003g0057a0001c0002t0003g0207a0001c0002t0003g0211others(30): Show | 33 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.-29+32158_-29+3215 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839404 | ||||||
| chr6:41839404
|
C | CAAA | 15 | a0001c0002t0003g0240a0001c0002t0003g0243a0001c0002t0006g0249others(12): Show | 15 | HG00099.hp1 HG00558.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.-29+32157_-29+3215 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839404 | ||||||
| chr6:41839404
|
CA | C | 78 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(75): Show | 79 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.-29+32159delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839404 | ||||||
| chr6:41839404
|
CAA | C | 88 | a0001c0001t0001g0115a0001c0001t0001g0138a0001c0001t0001g0287others(85): Show | 91 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.-29+32158_-29+3215 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839404 | ||||||
| chr6:41839404
|
CAAA | C | 40 | a0001c0001t0001g0260a0001c0001t0001g0279a0001c0001t0001g0280others(37): Show | 40 | HG00423.hp1 HG01074.hp1 HG01358.hp1 others(37): Show |
intron_variant | MODIFIER | c.-29+32157_-29+3215 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839404 | ||||||
| chr6:41839404
|
CAAAA | C | 7 | a0001c0001t0001g0152a0001c0001t0001g0221a0001c0001t0005g0005others(4): Show | 7 | HG02258.hp1 HG02615.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+32156_-29+3215 others(8): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839404 | ||||||
| chr6:41839404
|
CAAAAAAA others(7): Show |
C | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+32146_-29+3215 others(18): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839404 | ||||||
| chr6:41839404
|
CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-29+32143_-29+3215 others(21): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839404 | ||||||
| chr6:41839532
|
G | A | 1 | a0001c0001t0005g0035 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-29+32032C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839532 | ||||||
| chr6:41839564
|
CA | C | 72 | a0001c0002t0003g0040a0001c0002t0003g0045a0001c0002t0003g0057others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.-29+31999delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41839564 | ||||||
| chr6:41840216
|
T | C | 39 | a0001c0002t0003g0045a0001c0002t0003g0057a0001c0002t0003g0065others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG01981.hp1 others(36): Show |
intron_variant | MODIFIER | c.-29+31348A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41840216 | ||||||
| chr6:41840292
|
T | C | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+31272A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41840292 | ||||||
| chr6:41840322
|
C | T | 1 | a0001c0002t0008g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-29+31242G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41840322 | ||||||
| chr6:41840328
|
T | C | 3 | a0001c0002t0008g0163a0001c0003t0020g0061a0001c0003t0025g0062 | 3 | HG02809.hp1 HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-29+31236A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41840328 | ||||||
| chr6:41840329
|
A | G | 1 | a0001c0002t0008g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-29+31235T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41840329 | ||||||
| chr6:41840373
|
C | CA | 6 | a0001c0001t0001g0101a0001c0001t0001g0263a0001c0001t0001g0367others(3): Show | 6 | HG00280.hp1 HG01257.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29+31190dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41840373 | ||||||
| chr6:41840373
|
CA | C | 10 | a0001c0001t0001g0103a0001c0001t0001g0111a0001c0001t0004g0082others(7): Show | 10 | HG01256.hp1 HG01261.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29+31190delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41840373 | ||||||
| chr6:41840385
|
A | G | 72 | a0001c0002t0003g0040a0001c0002t0003g0045a0001c0002t0003g0057others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.-29+31179T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41840385 | ||||||
| chr6:41840613
|
A | G | 130 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-29+30951T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41840613 | ||||||
| chr6:41840704
|
T | C | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+30860A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41840704 | ||||||
| chr6:41840738
|
T | A | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+30826A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41840738 | ||||||
| chr6:41840985
|
A | C | 1 | a0001c0002t0008g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-29+30579T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41840985 | ||||||
| chr6:41841019
|
A | C | 1 | a0001c0001t0001g0374 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-29+30545T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41841019 | ||||||
| chr6:41841031
|
A | C | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-29+30533T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41841031 | ||||||
| chr6:41841340
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-29+30224G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41841340 | ||||||
| chr6:41841342
|
T | A | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+30222A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41841342 | ||||||
| chr6:41841413
|
G | A | 5 | a0001c0003t0010g0055a0001c0003t0010g0056a0001c0003t0010g0064others(2): Show | 5 | HG00741.hp1 HG02055.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+30151C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41841413 | ||||||
| chr6:41841554
|
T | C | 3 | a0001c0001t0004g0070a0001c0001t0004g0075a0001c0001t0004g0077 | 3 | HG01884.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-29+30010A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41841554 | ||||||
| chr6:41841632
|
G | A | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+29932C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41841632 | ||||||
| chr6:41841634
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-29+29930T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41841634 | ||||||
| chr6:41841773
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-29+29791A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41841773 | ||||||
| chr6:41841810
|
A | G | 72 | a0001c0002t0003g0040a0001c0002t0003g0045a0001c0002t0003g0057others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.-29+29754T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41841810 | ||||||
| chr6:41842063
|
T | G | 302 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(299): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.-29+29501A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41842063 | ||||||
| chr6:41842363
|
ACT | A | 7 | a0001c0001t0001g0286a0001c0001t0001g0299a0001c0001t0001g0303others(4): Show | 7 | HG00735.hp2 HG01192.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+29199_-29+2920 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41842363 | ||||||
| chr6:41842436
|
T | C | 1 | a0001c0002t0008g0270 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-29+29128A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41842436 | ||||||
| chr6:41842456
|
G | C | 1 | a0001c0003t0025g0062 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-29+29108C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41842456 | ||||||
| chr6:41842603
|
G | A | 1 | a0001c0001t0005g0035 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-29+28961C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41842603 | ||||||
| chr6:41842898
|
C | T | 1 | a0001c0007t0005g0036 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-29+28666G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41842898 | ||||||
| chr6:41843059
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-29+28505G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843059 | ||||||
| chr6:41843163
|
C | T | 4 | a0001c0001t0001g0152a0001c0001t0001g0260a0001c0001t0046g0151others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29+28401G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843163 | ||||||
| chr6:41843167
|
G | A | 1 | a0001c0001t0005g0032 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-29+28397C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843167 | ||||||
| chr6:41843224
|
G | C | 1 | a0001c0001t0007g0351 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-29+28340C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843224 | ||||||
| chr6:41843256
|
T | C | 1 | a0001c0002t0003g0211 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-29+28308A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843256 | ||||||
| chr6:41843319
|
A | C | 5 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(2): Show | 5 | HG02109.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+28245T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843319 | ||||||
| chr6:41843329
|
G | A | 2 | a0001c0001t0001g0321a0001c0001t0004g0308 | 2 | HG01123.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.-29+28235C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843329 | ||||||
| chr6:41843399
|
G | T | 2 | a0001c0001t0001g0321a0001c0001t0004g0308 | 2 | HG01123.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.-29+28165C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843399 | ||||||
| chr6:41843407
|
A | G | 2 | a0001c0001t0001g0295a0001c0001t0044g0334 | 2 | NA19006.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-29+28157T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843407 | ||||||
| chr6:41843412
|
G | A | 6 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(3): Show | 6 | HG02897.hp1 HG03098.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29+28152C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843412 | ||||||
| chr6:41843588
|
C | T | 1 | a0001c0001t0001g0337 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-29+27976G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843588 | ||||||
| chr6:41843624
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-29+27940A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843624 | ||||||
| chr6:41843683
|
G | A | 5 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0095others(2): Show | 5 | NA18960.hp1 NA18964.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+27881C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843683 | ||||||
| chr6:41843872
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-29+27692C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843872 | ||||||
| chr6:41843929
|
A | C | 3 | a0001c0001t0001g0131a0001c0001t0001g0147a0001c0001t0001g0154 | 3 | HG01358.hp2 HG02300.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-29+27635T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843929 | ||||||
| chr6:41843961
|
T | C | 53 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-29+27603A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41843961 | ||||||
| chr6:41844025
|
C | T | 1 | a0001c0001t0005g0030 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-29+27539G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41844025 | ||||||
| chr6:41844098
|
G | A | 1 | a0003c0005t0053g0274 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-29+27466C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41844098 | ||||||
| chr6:41844251
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-29+27313A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41844251 | ||||||
| chr6:41844353
|
C | T | 1 | a0001c0001t0005g0006 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-29+27211G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41844353 | ||||||
| chr6:41844413
|
G | A | 130 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-29+27151C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41844413 | ||||||
| chr6:41844420
|
C | A | 78 | a0001c0001t0001g0155a0001c0001t0001g0283a0001c0001t0001g0284others(75): Show | 78 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-29+27144G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41844420 | ||||||
| chr6:41844462
|
C | T | 25 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0070others(22): Show | 27 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.-29+27102G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41844462 | ||||||
| chr6:41844475
|
G | A | 1 | a0001c0001t0007g0372 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-29+27089C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41844475 | ||||||
| chr6:41844556
|
G | A | 1 | a0001c0003t0013g0043 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-29+27008C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41844556 | ||||||
| chr6:41844761
|
AT | A | 140 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-29+26802delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41844761 | ||||||
| chr6:41844785
|
G | A | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+26779C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41844785 | ||||||
| chr6:41844910
|
T | C | 1 | a0001c0002t0003g0245 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-29+26654A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41844910 | ||||||
| chr6:41845045
|
C | T | 2 | a0001c0001t0004g0001a0001c0001t0004g0085 | 3 | HG01257.hp2 HG01258.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-29+26519G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41845045 | ||||||
| chr6:41845049
|
C | T | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+26515G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41845049 | ||||||
| chr6:41845452
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-29+26112C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41845452 | ||||||
| chr6:41845487
|
T | G | 1 | a0001c0003t0028g0193 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-29+26077A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41845487 | ||||||
| chr6:41845590
|
G | C | 2 | a0001c0002t0003g0210a0001c0002t0003g0224 | 2 | HG00642.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-29+25974C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41845590 | ||||||
| chr6:41845745
|
T | C | 1 | a0001c0001t0001g0365 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-29+25819A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41845745 | ||||||
| chr6:41845752
|
AT | A | 66 | a0001c0001t0001g0152a0001c0001t0001g0221a0001c0001t0015g0063others(63): Show | 66 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.-29+25811delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41845752 | ||||||
| chr6:41845847
|
T | C | 6 | a0001c0002t0008g0041a0001c0002t0008g0042a0001c0002t0008g0269others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+25717A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41845847 | ||||||
| chr6:41846271
|
C | T | 130 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-29+25293G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41846271 | ||||||
| chr6:41846274
|
G | A | 1 | a0001c0001t0015g0219 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-29+25290C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41846274 | ||||||
| chr6:41846457
|
A | G | 2 | a0001c0001t0007g0351a0001c0001t0007g0372 | 2 | HG00558.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-29+25107T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41846457 | ||||||
| chr6:41846518
|
G | C | 1 | a0001c0001t0001g0123 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-29+25046C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41846518 | ||||||
| chr6:41846594
|
T | A | 1 | a0002c0004t0002g0169 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-29+24970A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41846594 | ||||||
| chr6:41846706
|
T | C | 4 | a0001c0001t0001g0311a0001c0001t0001g0315a0001c0001t0001g0329others(1): Show | 4 | HG03130.hp1 HG03225.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+24858A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41846706 | ||||||
| chr6:41846769
|
A | AC | 67 | a0001c0002t0003g0040a0001c0002t0003g0045a0001c0002t0003g0057others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.-29+24794dupG | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41846769 | ||||||
| chr6:41846775
|
C | CG | 5 | a0001c0003t0010g0055a0001c0003t0010g0056a0001c0003t0010g0064others(2): Show | 5 | HG00741.hp1 HG02055.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+24788_-29+2478 others(5): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41846775 | ||||||
| chr6:41846777
|
C | A | 1 | a0001c0001t0001g0338 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-29+24787G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41846777 | ||||||
| chr6:41846952
|
T | A | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+24612A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41846952 | ||||||
| chr6:41847022
|
A | G | 146 | a0001c0001t0001g0152a0001c0001t0001g0221a0001c0001t0001g0260others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-29+24542T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41847022 | ||||||
| chr6:41847204
|
G | C | 5 | a0001c0003t0010g0055a0001c0003t0010g0056a0001c0003t0010g0064others(2): Show | 5 | HG00741.hp1 HG02055.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+24360C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41847204 | ||||||
| chr6:41847302
|
C | T | 1 | a0001c0003t0028g0193 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-29+24262G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41847302 | ||||||
| chr6:41847353
|
C | G | 3 | a0001c0001t0014g0068a0001c0001t0014g0069a0001c0001t0014g0078 | 3 | HG03195.hp2 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-29+24211G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41847353 | ||||||
| chr6:41847454
|
C | T | 53 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-29+24110G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41847454 | ||||||
| chr6:41847645
|
C | T | 58 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.-29+23919G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41847645 | ||||||
| chr6:41847653
|
G | T | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+23911C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41847653 | ||||||
| chr6:41847700
|
G | A | 2 | a0001c0003t0002g0173a0004c0008t0038g0054 | 2 | HG00609.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-29+23864C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41847700 | ||||||
| chr6:41847759
|
C | G | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+23805G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41847759 | ||||||
| chr6:41847784
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-29+23780C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41847784 | ||||||
| chr6:41848014
|
C | G | 1 | a0001c0001t0005g0020 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-29+23550G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41848014 | ||||||
| chr6:41848396
|
G | A | 85 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(82): Show | 85 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-29+23168C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41848396 | ||||||
| chr6:41848424
|
T | TGGCACTA others(17): Show |
2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+23116_-29+2313 others(28): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41848424 | ||||||
| chr6:41848442
|
G | A | 1 | a0001c0002t0003g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-29+23122C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41848442 | ||||||
| chr6:41848518
|
C | T | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+23046G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41848518 | ||||||
| chr6:41848541
|
T | A | 61 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(58): Show | 61 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.-29+23023A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41848541 | ||||||
| chr6:41848551
|
T | G | 1 | a0001c0003t0002g0192 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-29+23013A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41848551 | ||||||
| chr6:41848757
|
A | G | 1 | a0001c0001t0043g0267 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-29+22807T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41848757 | ||||||
| chr6:41848812
|
G | A | 1 | a0001c0001t0018g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-29+22752C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41848812 | ||||||
| chr6:41849040
|
T | C | 1 | a0001c0007t0005g0036 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-29+22524A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849040 | ||||||
| chr6:41849042
|
A | C | 1 | a0003c0005t0053g0274 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-29+22522T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849042 | ||||||
| chr6:41849058
|
T | A | 2 | a0001c0001t0001g0321a0001c0001t0004g0308 | 2 | HG01123.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.-29+22506A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849058 | ||||||
| chr6:41849064
|
G | A | 2 | a0001c0003t0002g0168a0001c0003t0002g0185 | 2 | HG00323.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.-29+22500C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849064 | ||||||
| chr6:41849434
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-29+22130A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849434 | ||||||
| chr6:41849536
|
C | A | 1 | a0001c0001t0005g0021 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-29+22028G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849536 | ||||||
| chr6:41849539
|
T | G | 3 | a0001c0001t0004g0070a0001c0001t0004g0075a0001c0001t0004g0077 | 3 | HG01884.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-29+22025A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849539 | ||||||
| chr6:41849611
|
C | CT | 11 | a0001c0001t0001g0091a0001c0001t0001g0148a0001c0001t0001g0260others(8): Show | 11 | HG00642.hp2 HG02293.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-29+21952dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849611 | ||||||
| chr6:41849757
|
G | A | 130 | a0001c0001t0001g0102a0001c0001t0001g0221a0001c0001t0015g0063others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-29+21807C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849757 | ||||||
| chr6:41849759
|
C | T | 1 | a0001c0003t0010g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-29+21805G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849759 | ||||||
| chr6:41849764
|
C | T | 1 | a0001c0001t0018g0097 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-29+21800G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849764 | ||||||
| chr6:41849794
|
G | C | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-29+21770C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849794 | ||||||
| chr6:41849818
|
A | G | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+21746T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849818 | ||||||
| chr6:41849839
|
C | G | 30 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0011others(27): Show | 30 | HG00423.hp1 HG01074.hp1 HG01975.hp1 others(27): Show |
intron_variant | MODIFIER | c.-29+21725G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849839 | ||||||
| chr6:41849975
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-29+21589G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849975 | ||||||
| chr6:41849996
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-29+21568T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41849996 | ||||||
| chr6:41850189
|
T | C | 5 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0095others(2): Show | 5 | NA18960.hp1 NA18964.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+21375A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41850189 | ||||||
| chr6:41850358
|
G | A | 3 | a0001c0002t0008g0269a0001c0002t0008g0270a0001c0002t0008g0272 | 3 | HG02572.hp1 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-29+21206C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41850358 | ||||||
| chr6:41850376
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-29+21188C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41850376 | ||||||
| chr6:41850387
|
G | A | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+21177C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41850387 | ||||||
| chr6:41850458
|
A | T | 11 | a0001c0001t0001g0152a0001c0001t0001g0260a0001c0001t0001g0279others(8): Show | 11 | HG02109.hp1 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-29+21106T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41850458 | ||||||
| chr6:41850462
|
A | T | 280 | a0001c0001t0001g0093a0001c0001t0001g0115a0001c0001t0001g0136others(277): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.-29+21102T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41850462 | ||||||
| chr6:41850464
|
A | C | 141 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.-29+21100T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41850464 | ||||||
| chr6:41850466
|
T | A | 1 | a0001c0001t0004g0077 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-29+21098A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41850466 | ||||||
| chr6:41850589
|
C | G | 1 | a0001c0003t0002g0052 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-29+20975G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41850589 | ||||||
| chr6:41850624
|
G | A | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-29+20940C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41850624 | ||||||
| chr6:41850739
|
G | A | 1 | a0001c0001t0001g0289 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-29+20825C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41850739 | ||||||
| chr6:41850853
|
G | A | 3 | a0001c0001t0001g0260a0001c0001t0001g0290a0001c0001t0057g0059 | 3 | HG02040.hp2 HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-29+20711C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41850853 | ||||||
| chr6:41850861
|
A | C | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+20703T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41850861 | ||||||
| chr6:41850891
|
G | A | 1 | a0001c0002t0012g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-29+20673C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41850891 | ||||||
| chr6:41850897
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-29+20667C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41850897 | ||||||
| chr6:41851298
|
G | A | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+20266C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851298 | ||||||
| chr6:41851330
|
A | G | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+20234T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851330 | ||||||
| chr6:41851379
|
A | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-29+20185T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851379 | ||||||
| chr6:41851559
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-29+20005G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851559 | ||||||
| chr6:41851649
|
T | C | 5 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(2): Show | 5 | HG02897.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+19915A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851649 | ||||||
| chr6:41851656
|
A | G | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-29+19908T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851656 | ||||||
| chr6:41851669
|
C | G | 302 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(299): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.-29+19895G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851669 | ||||||
| chr6:41851847
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-29+19717G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851847 | ||||||
| chr6:41851850
|
G | T | 13 | a0001c0001t0001g0221a0001c0001t0009g0004a0001c0001t0009g0060others(10): Show | 14 | HG01255.hp2 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-29+19714C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851850 | ||||||
| chr6:41851952
|
C | CA | 47 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0110others(44): Show | 49 | HG00597.hp2 HG00609.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.-29+19611dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851952 | ||||||
| chr6:41851952
|
C | CAA | 9 | a0001c0001t0001g0141a0001c0001t0001g0157a0001c0001t0001g0158others(6): Show | 9 | HG00639.hp2 HG01109.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+19610_-29+1961 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851952 | ||||||
| chr6:41851952
|
CA | C | 133 | a0001c0001t0001g0091a0001c0001t0001g0138a0001c0001t0001g0221others(130): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-29+19611delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851952 | ||||||
| chr6:41851952
|
CAA | C | 6 | a0001c0002t0003g0214a0001c0002t0003g0215a0001c0002t0003g0217others(3): Show | 6 | HG00323.hp1 NA18747.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+19610_-29+1961 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851952 | ||||||
| chr6:41851952
|
CAAA | C | 25 | a0001c0001t0005g0008a0001c0001t0005g0011a0001c0001t0005g0012others(22): Show | 25 | HG00423.hp1 HG01975.hp1 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.-29+19609_-29+1961 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851952 | ||||||
| chr6:41851952
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0305 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-29+19600_-29+1961 others(16): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851952 | ||||||
| chr6:41851970
|
A | G | 2 | a0001c0001t0009g0096a0001c0001t0009g0098 | 2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-29+19594T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851970 | ||||||
| chr6:41851973
|
A | G | 3 | a0001c0001t0019g0100a0001c0003t0020g0061a0001c0003t0025g0062 | 3 | HG00280.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+19591T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851973 | ||||||
| chr6:41851977
|
G | A | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-29+19587C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41851977 | ||||||
| chr6:41852256
|
C | T | 4 | a0001c0001t0001g0263a0003c0005t0053g0274a0003c0005t0054g0275others(1): Show | 4 | HG01168.hp1 HG01361.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29+19308G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41852256 | ||||||
| chr6:41852353
|
C | T | 3 | a0001c0002t0006g0067a0001c0002t0006g0218a0001c0002t0006g0255 | 3 | HG02895.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-29+19211G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41852353 | ||||||
| chr6:41852475
|
T | A | 1 | a0001c0001t0001g0134 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-29+19089A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41852475 | ||||||
| chr6:41852476
|
A | T | 1 | a0001c0003t0002g0168 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-29+19088T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41852476 | ||||||
| chr6:41852711
|
T | C | 1 | a0001c0001t0004g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-29+18853A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41852711 | ||||||
| chr6:41852916
|
A | G | 310 | a0001c0001t0001g0103a0001c0001t0001g0152a0001c0001t0001g0157others(307): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.-29+18648T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41852916 | ||||||
| chr6:41853011
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0046g0151 | 2 | HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-29+18553G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853011 | ||||||
| chr6:41853058
|
C | T | 2 | a0001c0001t0004g0070a0001c0001t0004g0075 | 2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-29+18506G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853058 | ||||||
| chr6:41853140
|
GGCGCCAT others(806): Show |
G | 1 | a0001c0001t0001g0363 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-29+17611_-29+1842 others(4): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853140 | ||||||
| chr6:41853225
|
T | G | 1 | a0001c0003t0024g0377 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-29+18339A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853225 | ||||||
| chr6:41853293
|
G | T | 3 | a0001c0002t0003g0241a0001c0002t0003g0242a0001c0002t0003g0379 | 3 | HG02056.hp1 NA18943.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-29+18271C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853293 | ||||||
| chr6:41853358
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-29+18206A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853358 | ||||||
| chr6:41853399
|
G | A | 45 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(42): Show | 45 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-29+18165C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853399 | ||||||
| chr6:41853767
|
C | G | 8 | a0001c0001t0009g0004a0001c0001t0009g0060a0001c0001t0009g0096others(5): Show | 9 | HG01255.hp2 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+17797G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853767 | ||||||
| chr6:41853800
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0057g0059 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-29+17764G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853800 | ||||||
| chr6:41853834
|
T | TA | 72 | a0001c0002t0003g0040a0001c0002t0003g0045a0001c0002t0003g0057others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.-29+17729dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853834 | ||||||
| chr6:41853907
|
G | C | 2 | a0001c0001t0001g0152a0001c0001t0046g0151 | 2 | HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-29+17657C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853907 | ||||||
| chr6:41853931
|
G | A | 2 | a0001c0001t0005g0029a0001c0001t0005g0030 | 2 | HG01074.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-29+17633C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853931 | ||||||
| chr6:41853955
|
C | T | 1 | a0001c0002t0003g0379 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-29+17609G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853955 | ||||||
| chr6:41853982
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+17582T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853982 | ||||||
| chr6:41853987
|
G | A | 2 | a0001c0001t0001g0353a0001c0001t0001g0367 | 2 | NA18940.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-29+17577C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853987 | ||||||
| chr6:41853999
|
C | CA | 111 | a0001c0001t0001g0221a0001c0001t0001g0260a0001c0001t0001g0293others(108): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.-29+17564_-29+1756 others(5): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853999 | ||||||
| chr6:41853999
|
C | CAA | 69 | a0001c0001t0005g0008a0001c0001t0005g0011a0001c0001t0005g0012others(66): Show | 69 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.-29+17564_-29+1756 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853999 | ||||||
| chr6:41853999
|
C | CAAA | 15 | a0001c0001t0016g0010a0001c0001t0051g0023a0001c0003t0002g0048others(12): Show | 15 | HG00408.hp2 HG00423.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.-29+17564_-29+1756 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41853999 | ||||||
| chr6:41854000
|
G | A | 305 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(302): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.-29+17564C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41854000 | ||||||
| chr6:41854000
|
G | GA | 6 | a0001c0001t0001g0105a0001c0001t0001g0111a0001c0001t0001g0117others(3): Show | 6 | HG00609.hp1 HG01256.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+17563dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41854000 | ||||||
| chr6:41854028
|
C | G | 1 | a0001c0002t0003g0212 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-29+17536G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41854028 | ||||||
| chr6:41854085
|
G | A | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-29+17479C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41854085 | ||||||
| chr6:41854249
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-29+17315C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41854249 | ||||||
| chr6:41854287
|
G | A | 1 | a0001c0002t0012g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-29+17277C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41854287 | ||||||
| chr6:41854316
|
C | CA | 15 | a0001c0001t0001g0158a0001c0001t0001g0261a0001c0001t0001g0262others(12): Show | 15 | HG00423.hp1 HG00597.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.-29+17247dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41854316 | ||||||
| chr6:41854316
|
CA | C | 131 | a0001c0001t0001g0138a0001c0001t0001g0221a0001c0001t0004g0085others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.-29+17247delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41854316 | ||||||
| chr6:41854316
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0046g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-29+17238_-29+1724 others(14): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41854316 | ||||||
| chr6:41854772
|
G | A | 1 | a0001c0003t0010g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-29+16792C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41854772 | ||||||
| chr6:41854945
|
A | G | 5 | a0001c0003t0010g0055a0001c0003t0010g0056a0001c0003t0010g0064others(2): Show | 5 | HG00741.hp1 HG02055.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+16619T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41854945 | ||||||
| chr6:41855050
|
G | A | 1 | a0001c0001t0004g0074 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-29+16514C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41855050 | ||||||
| chr6:41855324
|
G | A | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+16240C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41855324 | ||||||
| chr6:41855463
|
C | G | 2 | a0001c0002t0003g0225a0001c0002t0003g0227 | 2 | HG02083.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-29+16101G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41855463 | ||||||
| chr6:41855736
|
C | T | 1 | a0003c0005t0053g0274 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-29+15828G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41855736 | ||||||
| chr6:41855893
|
C | T | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+15671G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41855893 | ||||||
| chr6:41855997
|
G | C | 2 | a0001c0001t0001g0152a0001c0001t0046g0151 | 2 | HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-29+15567C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41855997 | ||||||
| chr6:41856047
|
CA | C | 54 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(51): Show | 54 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.-29+15516delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41856047 | ||||||
| chr6:41856145
|
G | C | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+15419C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41856145 | ||||||
| chr6:41856300
|
G | A | 55 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(52): Show | 55 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.-29+15264C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41856300 | ||||||
| chr6:41856338
|
G | A | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+15226C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41856338 | ||||||
| chr6:41856349
|
T | C | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+15215A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41856349 | ||||||
| chr6:41856374
|
C | CA | 39 | a0001c0001t0001g0003a0001c0001t0001g0135a0001c0001t0004g0001others(36): Show | 42 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.-29+15189dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41856374 | ||||||
| chr6:41856400
|
T | G | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+15164A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41856400 | ||||||
| chr6:41856480
|
T | C | 1 | a0001c0003t0024g0377 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-29+15084A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41856480 | ||||||
| chr6:41856482
|
T | G | 1 | a0001c0001t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-29+15082A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41856482 | ||||||
| chr6:41856506
|
C | A | 2 | a0001c0002t0008g0041a0001c0002t0008g0042 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-29+15058G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41856506 | ||||||
| chr6:41856596
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-29+14968G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41856596 | ||||||
| chr6:41856615
|
T | C | 1 | a0001c0001t0001g0328 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-29+14949A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41856615 | ||||||
| chr6:41856681
|
T | C | 1 | a0001c0003t0002g0168 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-29+14883A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41856681 | ||||||
| chr6:41856901
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-29+14663A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41856901 | ||||||
| chr6:41856960
|
A | G | 1 | a0001c0001t0031g0025 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-29+14604T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41856960 | ||||||
| chr6:41857078
|
G | A | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+14486C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41857078 | ||||||
| chr6:41857315
|
G | A | 26 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0070others(23): Show | 28 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-29+14249C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41857315 | ||||||
| chr6:41857346
|
T | G | 2 | a0001c0001t0001g0366a0001c0001t0001g0374 | 2 | NA18941.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-29+14218A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41857346 | ||||||
| chr6:41857371
|
G | A | 2 | a0001c0002t0008g0041a0001c0002t0008g0042 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-29+14193C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41857371 | ||||||
| chr6:41857373
|
G | T | 72 | a0001c0002t0003g0040a0001c0002t0003g0045a0001c0002t0003g0057others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.-29+14191C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41857373 | ||||||
| chr6:41857852
|
T | C | 15 | a0001c0002t0006g0067a0001c0002t0006g0218a0001c0002t0006g0249others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.-29+13712A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41857852 | ||||||
| chr6:41857902
|
A | G | 1 | a0001c0003t0002g0177 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-29+13662T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41857902 | ||||||
| chr6:41857950
|
A | C | 1 | a0001c0002t0006g0250 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-29+13614T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41857950 | ||||||
| chr6:41858119
|
C | T | 1 | a0001c0001t0046g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-29+13445G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41858119 | ||||||
| chr6:41858148
|
A | T | 1 | a0001c0001t0007g0376 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-29+13416T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41858148 | ||||||
| chr6:41858424
|
C | T | 1 | a0001c0001t0009g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-29+13140G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41858424 | ||||||
| chr6:41858628
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-29+12936G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41858628 | ||||||
| chr6:41858653
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-29+12911A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41858653 | ||||||
| chr6:41858894
|
C | T | 4 | a0001c0001t0001g0092a0001c0001t0001g0129a0001c0001t0001g0138others(1): Show | 4 | HG01496.hp2 NA19004.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+12670G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41858894 | ||||||
| chr6:41859203
|
C | G | 1 | a0001c0001t0007g0356 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-29+12361G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41859203 | ||||||
| chr6:41859273
|
A | G | 130 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-29+12291T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41859273 | ||||||
| chr6:41859455
|
A | G | 141 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.-29+12109T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41859455 | ||||||
| chr6:41859512
|
T | C | 1 | a0001c0001t0005g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-29+12052A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41859512 | ||||||
| chr6:41859598
|
C | T | 92 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(89): Show | 92 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-29+11966G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41859598 | ||||||
| chr6:41859606
|
A | T | 1 | a0001c0001t0005g0021 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-29+11958T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41859606 | ||||||
| chr6:41859665
|
T | G | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+11899A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41859665 | ||||||
| chr6:41859685
|
A | G | 5 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(2): Show | 5 | HG02897.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+11879T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41859685 | ||||||
| chr6:41859776
|
A | C | 1 | a0001c0001t0018g0097 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-29+11788T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41859776 | ||||||
| chr6:41860142
|
C | G | 1 | a0001c0001t0005g0012 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-29+11422G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41860142 | ||||||
| chr6:41860283
|
GAA | G | 3 | a0001c0002t0008g0269a0001c0002t0008g0270a0001c0002t0008g0272 | 3 | HG02572.hp1 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-29+11279_-29+1128 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41860283 | ||||||
| chr6:41860327
|
A | G | 2 | a0001c0003t0013g0343a0001c0003t0013g0344 | 2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-29+11237T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41860327 | ||||||
| chr6:41860332
|
T | A | 309 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(306): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.-29+11232A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41860332 | ||||||
| chr6:41860355
|
A | C | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+11209T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41860355 | ||||||
| chr6:41860396
|
T | C | 1 | a0001c0001t0005g0021 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-29+11168A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41860396 | ||||||
| chr6:41860506
|
A | G | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+11058T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41860506 | ||||||
| chr6:41860550
|
C | T | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-29+11014G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41860550 | ||||||
| chr6:41860674
|
AT | A | 146 | a0001c0001t0001g0152a0001c0001t0001g0221a0001c0001t0001g0260others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-29+10889delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41860674 | ||||||
| chr6:41860727
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-29+10837C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41860727 | ||||||
| chr6:41860770
|
A | G | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+10794T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41860770 | ||||||
| chr6:41860843
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-29+10721C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41860843 | ||||||
| chr6:41861028
|
C | G | 1 | a0001c0001t0001g0337 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-29+10536G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41861028 | ||||||
| chr6:41861042
|
T | C | 5 | a0001c0001t0001g0337a0001c0003t0013g0043a0001c0003t0013g0044others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+10522A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41861042 | ||||||
| chr6:41861166
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-29+10398C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41861166 | ||||||
| chr6:41861248
|
C | T | 1 | a0001c0001t0005g0037 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-29+10316G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41861248 | ||||||
| chr6:41861256
|
A | G | 1 | a0001c0002t0003g0212 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-29+10308T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41861256 | ||||||
| chr6:41861358
|
G | A | 1 | a0001c0002t0003g0211 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-29+10206C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41861358 | ||||||
| chr6:41861506
|
C | T | 1 | a0001c0001t0047g0300 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-29+10058G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41861506 | ||||||
| chr6:41861529
|
T | C | 309 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(306): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.-29+10035A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41861529 | ||||||
| chr6:41861593
|
G | A | 1 | a0003c0005t0054g0275 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-29+9971C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41861593 | ||||||
| chr6:41861708
|
C | CT | 6 | a0001c0001t0005g0021a0001c0001t0007g0108a0001c0003t0013g0043others(3): Show | 6 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29+9855dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41861708 | ||||||
| chr6:41861774
|
C | G | 2 | a0001c0001t0001g0260a0001c0001t0057g0059 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-29+9790G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41861774 | ||||||
| chr6:41861793
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-29+9771C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41861793 | ||||||
| chr6:41862073
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-29+9491C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41862073 | ||||||
| chr6:41862232
|
A | G | 53 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-29+9332T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41862232 | ||||||
| chr6:41862472
|
T | C | 8 | a0001c0001t0009g0004a0001c0001t0009g0060a0001c0001t0009g0096others(5): Show | 9 | HG01255.hp2 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+9092A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41862472 | ||||||
| chr6:41862531
|
G | A | 3 | a0001c0001t0015g0063a0001c0001t0015g0219a0001c0001t0015g0220 | 3 | HG02897.hp1 HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-29+9033C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41862531 | ||||||
| chr6:41862678
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-29+8886G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41862678 | ||||||
| chr6:41862872
|
C | A | 1 | a0001c0001t0001g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-29+8692G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41862872 | ||||||
| chr6:41862899
|
G | C | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+8665C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41862899 | ||||||
| chr6:41862907
|
A | G | 142 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.-29+8657T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41862907 | ||||||
| chr6:41862919
|
G | A | 1 | a0001c0002t0003g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-29+8645C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41862919 | ||||||
| chr6:41863019
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-29+8545G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41863019 | ||||||
| chr6:41863059
|
G | A | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+8505C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41863059 | ||||||
| chr6:41863162
|
T | C | 25 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0070others(22): Show | 27 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.-29+8402A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41863162 | ||||||
| chr6:41863189
|
T | C | 2 | a0001c0001t0001g0260a0001c0001t0057g0059 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-29+8375A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41863189 | ||||||
| chr6:41863282
|
C | G | 1 | a0001c0001t0001g0318 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-29+8282G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41863282 | ||||||
| chr6:41863405
|
G | A | 217 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0158others(214): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.-29+8159C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41863405 | ||||||
| chr6:41863448
|
T | C | 2 | a0001c0001t0015g0219a0001c0001t0015g0220 | 2 | HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-29+8116A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41863448 | ||||||
| chr6:41863514
|
A | C | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+8050T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41863514 | ||||||
| chr6:41863680
|
G | A | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+7884C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41863680 | ||||||
| chr6:41863690
|
C | T | 2 | a0001c0002t0003g0210a0001c0002t0003g0224 | 2 | HG00642.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-29+7874G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41863690 | ||||||
| chr6:41863933
|
A | AT | 67 | a0001c0001t0001g0114a0001c0001t0001g0142a0001c0001t0001g0338others(64): Show | 67 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.-29+7630dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41863933 | ||||||
| chr6:41863933
|
AT | A | 6 | a0001c0001t0001g0110a0001c0001t0001g0328a0001c0001t0005g0021others(3): Show | 7 | HG01255.hp2 HG01516.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29+7630delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41863933 | ||||||
| chr6:41864337
|
C | T | 1 | a0003c0005t0054g0275 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-29+7227G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41864337 | ||||||
| chr6:41864361
|
G | A | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+7203C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41864361 | ||||||
| chr6:41864392
|
G | GTCTC | 3 | a0001c0003t0010g0064a0001c0003t0010g0209a0001c0003t0010g0222 | 3 | HG02055.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-29+7168_-29+7171d others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41864392 | ||||||
| chr6:41864542
|
G | A | 1 | a0001c0003t0027g0378 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-29+7022C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41864542 | ||||||
| chr6:41864957
|
G | A | 1 | a0001c0001t0001g0335 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-29+6607C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41864957 | ||||||
| chr6:41865030
|
T | G | 1 | a0001c0001t0031g0025 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-29+6534A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865030 | ||||||
| chr6:41865034
|
T | A | 130 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-29+6530A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865034 | ||||||
| chr6:41865101
|
A | G | 311 | a0001c0001t0001g0103a0001c0001t0001g0152a0001c0001t0001g0157others(308): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-29+6463T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865101 | ||||||
| chr6:41865114
|
G | T | 1 | a0001c0001t0001g0335 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-29+6450C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865114 | ||||||
| chr6:41865205
|
C | T | 1 | a0001c0001t0005g0033 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-29+6359G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865205 | ||||||
| chr6:41865235
|
G | A | 36 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(33): Show | 36 | HG00423.hp1 HG01074.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-29+6329C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865235 | ||||||
| chr6:41865616
|
T | C | 1 | a0001c0001t0033g0009 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-29+5948A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865616 | ||||||
| chr6:41865636
|
C | T | 1 | a0001c0002t0003g0238 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-29+5928G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865636 | ||||||
| chr6:41865803
|
C | CT | 140 | a0001c0001t0001g0139a0001c0001t0001g0145a0001c0001t0001g0221others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-29+5760dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865803 | ||||||
| chr6:41865803
|
C | CTT | 7 | a0001c0001t0015g0063a0001c0002t0003g0341a0001c0003t0002g0184others(4): Show | 7 | HG01361.hp1 HG02015.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29+5759_-29+5760d others(4): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865803 | ||||||
| chr6:41865803
|
CT | C | 70 | a0001c0001t0001g0117a0001c0001t0001g0157a0001c0001t0001g0158others(67): Show | 73 | HG00423.hp1 HG01069.hp2 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.-29+5760delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865803 | ||||||
| chr6:41865805
|
TTTTTTTT others(104): Show |
T | 5 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(2): Show | 5 | HG02109.hp1 HG02818.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+5648_-29+5758d others(2): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865805 | ||||||
| chr6:41865818
|
T | C | 1 | a0001c0001t0005g0021 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-29+5746A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865818 | ||||||
| chr6:41865821
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-29+5743A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865821 | ||||||
| chr6:41865821
|
T | G | 1 | a0001c0001t0058g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-29+5743A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865821 | ||||||
| chr6:41865850
|
C | T | 2 | a0001c0002t0003g0226a0001c0002t0003g0233 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-29+5714G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865850 | ||||||
| chr6:41865916
|
C | CT | 74 | a0001c0001t0001g0081a0001c0001t0001g0092a0001c0001t0001g0104others(71): Show | 75 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.-29+5647dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865916 | ||||||
| chr6:41865916
|
C | CTT | 104 | a0001c0001t0001g0103a0001c0001t0001g0147a0001c0001t0001g0157others(101): Show | 106 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-29+5646_-29+5647d others(4): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865916 | ||||||
| chr6:41865916
|
C | CTTT | 23 | a0001c0001t0001g0003a0001c0001t0001g0149a0001c0001t0001g0309others(20): Show | 24 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.-29+5645_-29+5647d others(5): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865916 | ||||||
| chr6:41865916
|
C | T | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-29+5648G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865916 | ||||||
| chr6:41865916
|
CT | C | 56 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(53): Show | 56 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-29+5647delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865916 | ||||||
| chr6:41865916
|
CTT | C | 58 | a0001c0002t0003g0040a0001c0002t0003g0057a0001c0002t0003g0065others(55): Show | 58 | HG00140.hp1 HG00544.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-29+5646_-29+5647d others(4): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865916 | ||||||
| chr6:41865916
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0058g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-29+5638_-29+5647d others(12): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865916 | ||||||
| chr6:41865953
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-29+5611G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865953 | ||||||
| chr6:41865975
|
G | A | 25 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0070others(22): Show | 27 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.-29+5589C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41865975 | ||||||
| chr6:41866067
|
G | A | 1 | a0001c0001t0005g0011 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-29+5497C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41866067 | ||||||
| chr6:41866085
|
C | A | 67 | a0001c0002t0003g0040a0001c0002t0003g0045a0001c0002t0003g0057others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.-29+5479G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41866085 | ||||||
| chr6:41866119
|
A | G | 1 | a0001c0003t0002g0181 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-29+5445T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41866119 | ||||||
| chr6:41866299
|
C | A | 132 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.-29+5265G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41866299 | ||||||
| chr6:41866446
|
G | A | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+5118C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41866446 | ||||||
| chr6:41866566
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-29+4998T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41866566 | ||||||
| chr6:41866631
|
C | T | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+4933G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41866631 | ||||||
| chr6:41866764
|
TG | T | 24 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0070others(21): Show | 26 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.-29+4799delC | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41866764 | ||||||
| chr6:41866819
|
T | C | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+4745A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41866819 | ||||||
| chr6:41866833
|
T | C | 1 | a0001c0001t0005g0008 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-29+4731A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41866833 | ||||||
| chr6:41866964
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG00735.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-29+4600C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41866964 | ||||||
| chr6:41866965
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0147 | 2 | HG01358.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-29+4599C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41866965 | ||||||
| chr6:41867081
|
G | A | 4 | a0001c0001t0005g0011a0001c0001t0005g0016a0001c0001t0005g0021others(1): Show | 4 | HG01975.hp1 NA18985.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+4483C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41867081 | ||||||
| chr6:41867455
|
T | A | 25 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0070others(22): Show | 27 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.-29+4109A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41867455 | ||||||
| chr6:41867470
|
G | A | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+4094C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41867470 | ||||||
| chr6:41867570
|
C | T | 1 | a0001c0003t0002g0268 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-29+3994G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41867570 | ||||||
| chr6:41867587
|
C | CA | 10 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0327others(7): Show | 10 | HG00621.hp2 HG02622.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.-29+3976dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41867587 | ||||||
| chr6:41867587
|
C | CAA | 50 | a0001c0001t0005g0021a0001c0001t0047g0300a0001c0003t0002g0046others(47): Show | 50 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.-29+3975_-29+3976d others(4): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41867587 | ||||||
| chr6:41867612
|
A | G | 1 | a0001c0001t0005g0013 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-29+3952T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41867612 | ||||||
| chr6:41867683
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-29+3881G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41867683 | ||||||
| chr6:41867745
|
C | T | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-29+3819G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41867745 | ||||||
| chr6:41867757
|
ACAAACAA others(8): Show |
A | 2 | a0001c0001t0001g0081a0001c0001t0001g0106 | 2 | HG01981.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-29+3792_-29+3806d others(17): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41867757 | ||||||
| chr6:41867761
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-29+3803T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41867761 | ||||||
| chr6:41867836
|
A | G | 5 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(2): Show | 5 | HG02897.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+3728T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41867836 | ||||||
| chr6:41868074
|
G | A | 17 | a0001c0001t0004g0001a0001c0001t0004g0002a0001c0001t0004g0071others(14): Show | 19 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29+3490C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41868074 | ||||||
| chr6:41868084
|
C | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0117 | 2 | HG00733.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-29+3480G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41868084 | ||||||
| chr6:41868333
|
T | A | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+3231A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41868333 | ||||||
| chr6:41868420
|
C | T | 2 | a0001c0003t0020g0061a0001c0003t0025g0062 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+3144G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41868420 | ||||||
| chr6:41868444
|
C | T | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-29+3120G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41868444 | ||||||
| chr6:41868487
|
C | T | 2 | a0003c0005t0054g0275a0003c0005t0055g0273 | 2 | HG01168.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-29+3077G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41868487 | ||||||
| chr6:41868606
|
C | T | 2 | a0001c0003t0013g0043a0001c0003t0013g0044 | 2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-29+2958G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41868606 | ||||||
| chr6:41868677
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-29+2887C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41868677 | ||||||
| chr6:41868866
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-29+2698G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41868866 | ||||||
| chr6:41869039
|
C | T | 3 | a0001c0002t0003g0241a0001c0002t0003g0242a0001c0002t0003g0379 | 3 | HG02056.hp1 NA18943.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-29+2525G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41869039 | ||||||
| chr6:41869077
|
A | G | 89 | a0001c0001t0001g0103a0001c0001t0001g0283a0001c0001t0001g0284others(86): Show | 89 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.-29+2487T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41869077 | ||||||
| chr6:41869080
|
C | CT | 166 | a0001c0001t0001g0081a0001c0001t0001g0103a0001c0001t0001g0111others(163): Show | 169 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.-29+2483dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41869080 | ||||||
| chr6:41869080
|
CT | C | 9 | a0001c0001t0001g0058a0001c0001t0001g0116a0001c0001t0001g0126others(6): Show | 9 | HG01069.hp1 HG01070.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+2483delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41869080 | ||||||
| chr6:41869142
|
G | A | 1 | a0001c0003t0025g0062 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-29+2422C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41869142 | ||||||
| chr6:41869153
|
C | T | 1 | a0001c0002t0003g0213 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-29+2411G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41869153 | ||||||
| chr6:41869412
|
G | GA | 35 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(32): Show | 35 | HG00423.hp1 HG01074.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.-29+2151dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41869412 | ||||||
| chr6:41869499
|
C | A | 1 | a0001c0001t0001g0104 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-29+2065G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41869499 | ||||||
| chr6:41869623
|
T | C | 1 | a0001c0003t0027g0378 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-29+1941A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41869623 | ||||||
| chr6:41869707
|
CA | C | 8 | a0001c0001t0001g0095a0001c0001t0001g0101a0001c0001t0001g0260others(5): Show | 8 | HG00323.hp2 HG01257.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29+1856delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41869707 | ||||||
| chr6:41870136
|
C | T | 1 | a0001c0002t0006g0256 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-29+1428G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41870136 | ||||||
| chr6:41870140
|
T | C | 1 | a0001c0002t0003g0246 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-29+1424A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41870140 | ||||||
| chr6:41870173
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-29+1391G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41870173 | ||||||
| chr6:41870381
|
T | C | 130 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-29+1183A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41870381 | ||||||
| chr6:41870480
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-29+1084T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41870480 | ||||||
| chr6:41870556
|
TAAG | T | 26 | a0001c0001t0001g0081a0001c0001t0004g0001a0001c0001t0004g0002others(23): Show | 28 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-29+1005_-29+1007d others(5): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41870556 | ||||||
| chr6:41870646
|
G | C | 1 | a0001c0001t0015g0063 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-29+918C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41870646 | ||||||
| chr6:41870688
|
A | ATTTTTT | 197 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0091others(194): Show | 199 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.-29+870_-29+875dup others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41870688 | ||||||
| chr6:41870688
|
A | ATTTTTTT | 94 | a0001c0001t0001g0081a0001c0001t0001g0149a0001c0001t0001g0221others(91): Show | 96 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.-29+869_-29+875dup others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41870688 | ||||||
| chr6:41870688
|
A | ATTTTTTT others(1): Show |
8 | a0001c0001t0004g0072a0001c0001t0004g0077a0001c0001t0005g0033others(5): Show | 8 | HG01106.hp2 HG01168.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29+868_-29+875dup others(8): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41870688 | ||||||
| chr6:41870709
|
A | G | 1 | a0001c0001t0018g0097 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-29+855T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41870709 | ||||||
| chr6:41870896
|
CA | C | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+667delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41870896 | ||||||
| chr6:41870902
|
T | G | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+662A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41870902 | ||||||
| chr6:41870903
|
T | C | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+661A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41870903 | ||||||
| chr6:41870975
|
C | T | 1 | a0003c0005t0053g0274 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-29+589G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41870975 | ||||||
| chr6:41871059
|
A | C | 3 | a0001c0002t0006g0067a0001c0002t0006g0218a0001c0002t0006g0255 | 3 | HG02895.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-29+505T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41871059 | ||||||
| chr6:41871079
|
C | T | 72 | a0001c0002t0003g0040a0001c0002t0003g0045a0001c0002t0003g0057others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.-29+485G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41871079 | ||||||
| chr6:41871141
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG00735.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-29+423C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41871141 | ||||||
| chr6:41871143
|
C | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG00735.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-29+421G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41871143 | ||||||
| chr6:41871354
|
T | C | 142 | a0001c0001t0001g0221a0001c0001t0009g0060a0001c0001t0015g0063others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.-29+210A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41871354 | ||||||
| chr6:41871530
|
T | A | 72 | a0001c0002t0003g0040a0001c0002t0003g0045a0001c0002t0003g0057others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.-29+34A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 3/7 | chr6 | 41871530 | ||||||
| chr6:41871664
|
T | C | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-102-27A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41871664 | ||||||
| chr6:41871700
|
T | G | 142 | a0001c0001t0001g0221a0001c0001t0009g0060a0001c0001t0015g0063others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.-102-63A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41871700 | ||||||
| chr6:41871782
|
TA | T | 141 | a0001c0001t0001g0221a0001c0001t0009g0060a0001c0001t0015g0063others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.-102-146delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41871782 | ||||||
| chr6:41871826
|
A | C | 1 | a0001c0001t0035g0380 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-102-189T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41871826 | ||||||
| chr6:41871829
|
G | C | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-102-192C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41871829 | ||||||
| chr6:41872101
|
G | A | 4 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0018g0090others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-102-464C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872101 | ||||||
| chr6:41872167
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-102-530C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872167 | ||||||
| chr6:41872192
|
T | C | 1 | a0001c0002t0008g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-102-555A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872192 | ||||||
| chr6:41872258
|
C | T | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-102-621G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872258 | ||||||
| chr6:41872360
|
T | C | 1 | a0001c0003t0013g0344 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-102-723A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872360 | ||||||
| chr6:41872365
|
G | A | 1 | a0001c0001t0001g0352 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-102-728C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872365 | ||||||
| chr6:41872376
|
C | T | 1 | a0001c0001t0005g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-102-739G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872376 | ||||||
| chr6:41872452
|
C | T | 3 | a0001c0001t0009g0060a0001c0003t0020g0061a0001c0003t0025g0062 | 3 | HG02809.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-102-815G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872452 | ||||||
| chr6:41872742
|
C | A | 1 | a0001c0001t0001g0155 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-102-1105G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872742 | ||||||
| chr6:41872742
|
C | CA | 159 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0105others(156): Show | 159 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.-102-1106dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872742 | ||||||
| chr6:41872779
|
G | A | 53 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-102-1142C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872779 | ||||||
| chr6:41872855
|
A | G | 308 | a0001c0001t0001g0081a0001c0001t0001g0103a0001c0001t0001g0152others(305): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.-102-1218T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872855 | ||||||
| chr6:41872860
|
C | T | 1 | a0001c0001t0004g0076 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-102-1223G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872860 | ||||||
| chr6:41872902
|
C | A | 5 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0127others(2): Show | 5 | HG00735.hp1 HG01952.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.-102-1265G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872902 | ||||||
| chr6:41872905
|
C | CA | 9 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0001g0329others(6): Show | 9 | HG00423.hp2 HG01109.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-102-1269dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872905 | ||||||
| chr6:41872905
|
CA | C | 7 | a0001c0001t0001g0303a0001c0001t0001g0317a0001c0001t0001g0326others(4): Show | 7 | HG01168.hp1 HG02129.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.-102-1269delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872905 | ||||||
| chr6:41872917
|
A | G | 1 | a0001c0001t0042g0128 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-102-1280T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41872917 | ||||||
| chr6:41873217
|
A | G | 1 | a0001c0001t0005g0020 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-102-1580T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41873217 | ||||||
| chr6:41873257
|
TC | T | 35 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(32): Show | 35 | HG00423.hp1 HG01074.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.-102-1621delG | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41873257 | ||||||
| chr6:41873394
|
C | T | 92 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(89): Show | 92 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-102-1757G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41873394 | ||||||
| chr6:41873519
|
G | A | 1 | a0001c0001t0042g0128 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-102-1882C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41873519 | ||||||
| chr6:41873699
|
C | A | 4 | a0001c0001t0001g0303a0001c0001t0001g0317a0001c0001t0001g0326others(1): Show | 4 | NA18975.hp1 NA18975.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-102-2062G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41873699 | ||||||
| chr6:41873701
|
G | C | 1 | a0001c0002t0008g0272 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-102-2064C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41873701 | ||||||
| chr6:41873797
|
A | T | 58 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.-102-2160T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41873797 | ||||||
| chr6:41874306
|
T | C | 2 | a0001c0003t0010g0064a0001c0003t0010g0222 | 2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-102-2669A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874306 | ||||||
| chr6:41874378
|
A | T | 2 | a0003c0005t0054g0275a0003c0005t0055g0273 | 2 | HG01168.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-102-2741T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874378 | ||||||
| chr6:41874495
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-2858C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874495 | ||||||
| chr6:41874504
|
A | C | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-2867T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874504 | ||||||
| chr6:41874519
|
G | T | 1 | a0001c0001t0001g0279 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-102-2882C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874519 | ||||||
| chr6:41874525
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-102-2888A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874525 | ||||||
| chr6:41874533
|
C | A | 1 | a0001c0001t0018g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-102-2896G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874533 | ||||||
| chr6:41874539
|
C | T | 1 | a0001c0003t0027g0378 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-102-2902G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874539 | ||||||
| chr6:41874591
|
G | A | 1 | a0001c0001t0004g0071 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-102-2954C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874591 | ||||||
| chr6:41874640
|
A | C | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-3003T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874640 | ||||||
| chr6:41874651
|
C | G | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-3014G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874651 | ||||||
| chr6:41874652
|
C | G | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-3015G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874652 | ||||||
| chr6:41874654
|
A | T | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-3017T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874654 | ||||||
| chr6:41874655
|
G | T | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-3018C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874655 | ||||||
| chr6:41874656
|
G | C | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-3019C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874656 | ||||||
| chr6:41874657
|
T | A | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-3020A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874657 | ||||||
| chr6:41874659
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-3022A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874659 | ||||||
| chr6:41874667
|
T | G | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-3030A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874667 | ||||||
| chr6:41874669
|
G | T | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-3032C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874669 | ||||||
| chr6:41874670
|
G | C | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-3033C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874670 | ||||||
| chr6:41874671
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-3034T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874671 | ||||||
| chr6:41874738
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-3101C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874738 | ||||||
| chr6:41874754
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-3117C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874754 | ||||||
| chr6:41874807
|
A | T | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-3170T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41874807 | ||||||
| chr6:41875070
|
G | A | 4 | a0001c0001t0001g0152a0001c0001t0001g0260a0001c0001t0046g0151others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-102-3433C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41875070 | ||||||
| chr6:41875306
|
T | G | 130 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-102-3669A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41875306 | ||||||
| chr6:41875572
|
G | C | 7 | a0001c0001t0001g0318a0001c0001t0001g0331a0001c0001t0001g0332others(4): Show | 7 | HG01943.hp2 HG01993.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-102-3935C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41875572 | ||||||
| chr6:41875611
|
A | G | 2 | a0001c0001t0005g0012a0001c0001t0005g0019 | 2 | NA19010.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-102-3974T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41875611 | ||||||
| chr6:41875666
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-102-4029G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41875666 | ||||||
| chr6:41875673
|
G | A | 1 | a0001c0001t0048g0342 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-102-4036C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41875673 | ||||||
| chr6:41875879
|
G | A | 1 | a0001c0001t0004g0088 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-102-4242C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41875879 | ||||||
| chr6:41876074
|
C | T | 7 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(4): Show | 7 | HG01168.hp1 HG01361.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-102-4437G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41876074 | ||||||
| chr6:41876303
|
C | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0117 | 2 | HG00733.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-102-4666G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41876303 | ||||||
| chr6:41876343
|
A | AT | 72 | a0001c0002t0003g0040a0001c0002t0003g0045a0001c0002t0003g0057others(69): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.-102-4707dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41876343 | ||||||
| chr6:41876555
|
A | G | 2 | a0001c0003t0013g0043a0001c0003t0013g0044 | 2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-102-4918T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41876555 | ||||||
| chr6:41876648
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-102-5011C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41876648 | ||||||
| chr6:41877074
|
C | T | 1 | a0001c0002t0003g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-102-5437G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41877074 | ||||||
| chr6:41877127
|
A | G | 1 | a0001c0001t0009g0096 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-102-5490T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41877127 | ||||||
| chr6:41877479
|
G | T | 2 | a0001c0001t0001g0320a0001c0001t0004g0319 | 2 | HG01099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-102-5842C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41877479 | ||||||
| chr6:41877517
|
C | A | 1 | a0001c0001t0004g0086 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-102-5880G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41877517 | ||||||
| chr6:41877565
|
AT | A | 182 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0092others(179): Show | 183 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.-102-5929delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41877565 | ||||||
| chr6:41877565
|
ATT | A | 58 | a0001c0001t0001g0081a0001c0001t0001g0347a0001c0001t0004g0001others(55): Show | 60 | HG00423.hp1 HG01069.hp2 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.-102-5930_-102-592 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41877565 | ||||||
| chr6:41877593
|
C | T | 1 | a0001c0003t0002g0177 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-102-5956G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41877593 | ||||||
| chr6:41877690
|
AACTGGGA others(2): Show |
A | 87 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(84): Show | 87 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-102-6062_-102-605 others(13): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41877690 | ||||||
| chr6:41877841
|
G | A | 4 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0018g0090others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-102-6204C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41877841 | ||||||
| chr6:41877855
|
C | T | 2 | a0001c0001t0001g0291a0001c0001t0001g0338 | 2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-102-6218G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41877855 | ||||||
| chr6:41877875
|
T | A | 7 | a0001c0001t0009g0004a0001c0001t0009g0096a0001c0001t0009g0098others(4): Show | 8 | HG01255.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-102-6238A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41877875 | ||||||
| chr6:41877947
|
G | C | 26 | a0001c0001t0001g0081a0001c0001t0004g0001a0001c0001t0004g0002others(23): Show | 28 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-102-6310C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41877947 | ||||||
| chr6:41878001
|
C | T | 1 | a0001c0002t0012g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-102-6364G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41878001 | ||||||
| chr6:41878003
|
A | T | 1 | a0001c0001t0005g0030 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-102-6366T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41878003 | ||||||
| chr6:41878005
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0057g0059 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-102-6368G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41878005 | ||||||
| chr6:41878111
|
T | C | 1 | a0001c0007t0005g0036 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-102-6474A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41878111 | ||||||
| chr6:41878119
|
A | T | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-102-6482T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41878119 | ||||||
| chr6:41878222
|
T | C | 1 | a0001c0001t0007g0345 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-102-6585A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41878222 | ||||||
| chr6:41878307
|
T | C | 1 | a0001c0001t0004g0072 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-102-6670A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41878307 | ||||||
| chr6:41878372
|
T | G | 130 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-102-6735A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41878372 | ||||||
| chr6:41878533
|
T | C | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-102-6896A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41878533 | ||||||
| chr6:41878547
|
G | A | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-102-6910C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41878547 | ||||||
| chr6:41878684
|
T | A | 8 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0320others(5): Show | 8 | HG00323.hp2 HG01074.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-102-7047A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41878684 | ||||||
| chr6:41878695
|
T | C | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-102-7058A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41878695 | ||||||
| chr6:41878831
|
A | G | 142 | a0001c0001t0001g0221a0001c0001t0009g0060a0001c0001t0015g0063others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.-102-7194T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41878831 | ||||||
| chr6:41879057
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-102-7420G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879057 | ||||||
| chr6:41879110
|
G | A | 1 | a0001c0001t0035g0380 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-102-7473C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879110 | ||||||
| chr6:41879138
|
T | C | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-102-7501A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879138 | ||||||
| chr6:41879209
|
A | G | 1 | a0001c0002t0003g0246 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-102-7572T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879209 | ||||||
| chr6:41879216
|
G | A | 3 | a0001c0001t0009g0060a0001c0003t0020g0061a0001c0003t0025g0062 | 3 | HG02809.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-102-7579C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879216 | ||||||
| chr6:41879327
|
C | T | 53 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-102-7690G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879327 | ||||||
| chr6:41879395
|
A | T | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-102-7758T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879395 | ||||||
| chr6:41879505
|
T | A | 1 | a0001c0002t0012g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-102-7868A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879505 | ||||||
| chr6:41879506
|
G | A | 1 | a0001c0002t0012g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-102-7869C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879506 | ||||||
| chr6:41879613
|
T | C | 1 | a0002c0004t0002g0203 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-102-7976A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879613 | ||||||
| chr6:41879777
|
G | A | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-102-8140C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879777 | ||||||
| chr6:41879796
|
T | C | 7 | a0001c0002t0006g0249a0001c0002t0006g0250a0001c0002t0006g0251others(4): Show | 7 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.-102-8159A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879796 | ||||||
| chr6:41879803
|
A | T | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-102-8166T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879803 | ||||||
| chr6:41879910
|
G | C | 1 | a0001c0002t0003g0246 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-102-8273C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879910 | ||||||
| chr6:41879935
|
G | A | 2 | a0001c0001t0001g0260a0001c0001t0057g0059 | 2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-102-8298C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879935 | ||||||
| chr6:41879948
|
G | A | 1 | a0001c0001t0005g0035 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-102-8311C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879948 | ||||||
| chr6:41879972
|
T | C | 1 | a0001c0001t0007g0376 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-102-8335A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41879972 | ||||||
| chr6:41880002
|
G | T | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-102-8365C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41880002 | ||||||
| chr6:41880062
|
G | A | 58 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.-102-8425C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41880062 | ||||||
| chr6:41880141
|
GA | G | 130 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-102-8505delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41880141 | ||||||
| chr6:41880323
|
C | T | 1 | a0001c0003t0002g0176 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-102-8686G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41880323 | ||||||
| chr6:41880350
|
G | A | 58 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.-102-8713C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41880350 | ||||||
| chr6:41880377
|
A | G | 1 | a0003c0005t0055g0273 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-102-8740T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41880377 | ||||||
| chr6:41880378
|
G | A | 1 | a0003c0005t0055g0273 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-102-8741C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41880378 | ||||||
| chr6:41880506
|
C | T | 42 | a0001c0002t0003g0040a0001c0002t0003g0045a0001c0002t0003g0057others(39): Show | 42 | HG00099.hp2 HG00544.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-102-8869G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41880506 | ||||||
| chr6:41880572
|
G | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0145a0001c0001t0001g0156 | 3 | HG00438.hp2 NA18974.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-102-8935C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41880572 | ||||||
| chr6:41880586
|
A | G | 1 | a0001c0002t0003g0379 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-102-8949T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41880586 | ||||||
| chr6:41880817
|
G | A | 1 | a0001c0002t0006g0254 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-102-9180C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41880817 | ||||||
| chr6:41880876
|
T | C | 1 | a0001c0001t0005g0033 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-102-9239A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41880876 | ||||||
| chr6:41881026
|
G | A | 1 | a0001c0001t0014g0068 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-102-9389C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881026 | ||||||
| chr6:41881082
|
G | C | 7 | a0001c0001t0009g0004a0001c0001t0009g0096a0001c0001t0009g0098others(4): Show | 8 | HG01255.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-102-9445C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881082 | ||||||
| chr6:41881211
|
C | T | 1 | a0001c0001t0009g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-102-9574G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881211 | ||||||
| chr6:41881236
|
C | T | 1 | a0001c0001t0046g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-102-9599G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881236 | ||||||
| chr6:41881238
|
C | A | 6 | a0001c0001t0001g0092a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG01496.hp2 HG01993.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.-102-9601G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881238 | ||||||
| chr6:41881288
|
C | CA | 72 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0103others(69): Show | 73 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.-102-9652dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
C | CAA | 38 | a0001c0001t0001g0003a0001c0001t0001g0093a0001c0001t0001g0095others(35): Show | 39 | HG01109.hp2 HG01358.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.-102-9653_-102-965 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
C | CAAA | 14 | a0001c0001t0005g0019a0001c0001t0005g0020a0001c0001t0005g0021others(11): Show | 14 | HG00423.hp1 HG00609.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-102-9654_-102-965 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
C | CAAAA | 7 | a0001c0001t0001g0138a0001c0001t0004g0080a0001c0001t0014g0069others(4): Show | 7 | HG01069.hp2 HG03139.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-102-9655_-102-965 others(8): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
C | CAAAAA | 16 | a0001c0001t0001g0081a0001c0001t0004g0001a0001c0001t0004g0070others(13): Show | 17 | HG01099.hp1 HG01106.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-102-9656_-102-965 others(9): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
C | CAAAAAA | 6 | a0001c0001t0004g0002a0001c0001t0004g0073a0001c0001t0004g0074others(3): Show | 7 | HG01109.hp1 HG01261.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.-102-9657_-102-965 others(10): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
C | CAAAAAAA others(2): Show |
23 | a0001c0002t0003g0045a0001c0002t0003g0065a0001c0002t0003g0210others(20): Show | 23 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.-102-9660_-102-965 others(13): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
C | CAAAAAAA others(3): Show |
23 | a0001c0002t0003g0066a0001c0002t0003g0207a0001c0002t0003g0213others(20): Show | 23 | HG00140.hp1 HG00544.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.-102-9661_-102-965 others(14): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
C | CAAAAAAA others(4): Show |
9 | a0001c0001t0001g0260a0001c0002t0003g0040a0001c0002t0003g0217others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-102-9662_-102-965 others(15): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
C | CAAAAAAA others(5): Show |
2 | a0001c0002t0006g0218a0001c0010t0003g0248 | 2 | HG03486.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-102-9663_-102-965 others(16): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
C | CAAAAAAA others(6): Show |
3 | a0001c0002t0003g0241a0001c0002t0006g0339a0001c0002t0006g0340 | 3 | HG00099.hp1 HG03017.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-102-9664_-102-965 others(17): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
C | CAAAAAAA others(7): Show |
1 | a0001c0002t0003g0379 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-102-9665_-102-965 others(18): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
C | CAAAAAAA others(11): Show |
1 | a0001c0002t0003g0242 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-102-9669_-102-965 others(22): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
CAAAAAA | C | 9 | a0001c0003t0002g0050a0001c0003t0002g0053a0001c0003t0002g0175others(6): Show | 9 | HG00423.hp2 HG01261.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.-102-9657_-102-965 others(10): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
CAAAAAAA | C | 48 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(45): Show | 48 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-102-9658_-102-965 others(11): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0005g0030a0001c0002t0008g0042a0001c0002t0008g0269others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-102-9660_-102-965 others(13): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0005g0029a0004c0008t0038g0054 | 2 | HG01074.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-102-9661_-102-965 others(14): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0140 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-102-9662_-102-965 others(15): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
CAAAAAAA others(5): Show |
C | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-102-9663_-102-965 others(16): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0002t0003g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-102-9665_-102-965 others(18): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881288
|
CAAAAAAA others(13): Show |
C | 4 | a0001c0001t0001g0353a0001c0001t0001g0366a0001c0001t0001g0367others(1): Show | 4 | NA18940.hp2 NA18941.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.-102-9671_-102-965 others(24): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881288 | ||||||
| chr6:41881342
|
C | T | 2 | a0001c0002t0003g0210a0001c0002t0003g0224 | 2 | HG00642.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-102-9705G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881342 | ||||||
| chr6:41881451
|
G | A | 3 | a0001c0001t0009g0060a0001c0003t0020g0061a0001c0003t0025g0062 | 3 | HG02809.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-102-9814C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881451 | ||||||
| chr6:41881768
|
T | C | 1 | a0001c0003t0002g0174 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-103+10026A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881768 | ||||||
| chr6:41881963
|
A | G | 3 | a0001c0001t0009g0060a0001c0003t0020g0061a0001c0003t0025g0062 | 3 | HG02809.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-103+9831T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41881963 | ||||||
| chr6:41882031
|
T | A | 1 | a0001c0002t0003g0243 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-103+9763A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41882031 | ||||||
| chr6:41882137
|
A | G | 36 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(33): Show | 36 | HG00423.hp1 HG01074.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103+9657T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41882137 | ||||||
| chr6:41882320
|
A | T | 1 | a0001c0002t0003g0223 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-103+9474T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41882320 | ||||||
| chr6:41882390
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-103+9404T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41882390 | ||||||
| chr6:41882447
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-103+9347G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41882447 | ||||||
| chr6:41882504
|
A | G | 36 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(33): Show | 36 | HG00423.hp1 HG01074.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103+9290T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41882504 | ||||||
| chr6:41882560
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0001g0139a0001c0001t0001g0153others(1): Show | 4 | NA18956.hp2 NA19011.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+9234G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41882560 | ||||||
| chr6:41882626
|
G | GAAC | 142 | a0001c0001t0001g0221a0001c0001t0009g0060a0001c0001t0015g0063others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.-103+9165_-103+916 others(7): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41882626 | ||||||
| chr6:41883100
|
A | G | 1 | a0001c0002t0008g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-103+8694T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41883100 | ||||||
| chr6:41883180
|
T | A | 1 | a0001c0001t0057g0059 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-103+8614A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41883180 | ||||||
| chr6:41883227
|
A | G | 143 | a0001c0001t0001g0221a0001c0001t0009g0060a0001c0001t0015g0063others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-103+8567T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41883227 | ||||||
| chr6:41883353
|
C | CA | 50 | a0001c0001t0001g0095a0001c0001t0001g0139a0001c0001t0001g0140others(47): Show | 50 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.-103+8440dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41883353 | ||||||
| chr6:41883353
|
CA | C | 30 | a0001c0001t0005g0007a0001c0001t0005g0008a0001c0001t0005g0011others(27): Show | 30 | HG00423.hp1 HG01975.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.-103+8440delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41883353 | ||||||
| chr6:41883623
|
A | AAAAT | 120 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0283others(117): Show | 120 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-103+8167_-103+817 others(8): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41883623 | ||||||
| chr6:41883623
|
AAAATAAA others(1): Show |
A | 5 | a0001c0001t0058g0277a0001c0003t0013g0043a0001c0003t0013g0044others(2): Show | 5 | HG01891.hp2 HG02630.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103+8163_-103+817 others(12): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41883623 | ||||||
| chr6:41883647
|
T | A | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-103+8147A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41883647 | ||||||
| chr6:41883698
|
G | A | 1 | a0001c0002t0006g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-103+8096C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41883698 | ||||||
| chr6:41883711
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-103+8083A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41883711 | ||||||
| chr6:41883728
|
A | C | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+8066T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41883728 | ||||||
| chr6:41883794
|
G | A | 1 | a0001c0007t0005g0036 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-103+8000C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41883794 | ||||||
| chr6:41883847
|
T | TG | 4 | a0001c0001t0001g0152a0001c0001t0001g0260a0001c0001t0046g0151others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103+7946dupC | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41883847 | ||||||
| chr6:41883855
|
T | C | 3 | a0001c0001t0009g0060a0001c0003t0020g0061a0001c0003t0025g0062 | 3 | HG02809.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-103+7939A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41883855 | ||||||
| chr6:41884017
|
A | G | 1 | a0001c0001t0001g0352 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-103+7777T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884017 | ||||||
| chr6:41884033
|
T | G | 1 | a0001c0003t0002g0204 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-103+7761A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884033 | ||||||
| chr6:41884034
|
T | A | 3 | a0001c0001t0009g0004a0001c0001t0009g0159a0001c0001t0009g0160 | 4 | HG01255.hp2 HG02717.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+7760A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884034 | ||||||
| chr6:41884098
|
A | C | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG00735.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-103+7696T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884098 | ||||||
| chr6:41884149
|
G | A | 6 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0018g0090others(3): Show | 6 | HG01358.hp1 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103+7645C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884149 | ||||||
| chr6:41884185
|
A | G | 1 | a0001c0001t0001g0289 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-103+7609T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884185 | ||||||
| chr6:41884237
|
A | C | 142 | a0001c0001t0001g0221a0001c0001t0009g0060a0001c0001t0015g0063others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.-103+7557T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884237 | ||||||
| chr6:41884303
|
G | A | 15 | a0001c0002t0006g0067a0001c0002t0006g0218a0001c0002t0006g0249others(12): Show | 15 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.-103+7491C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884303 | ||||||
| chr6:41884325
|
T | C | 1 | a0001c0002t0003g0341 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-103+7469A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884325 | ||||||
| chr6:41884449
|
T | G | 377 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(374): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.-103+7345A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884449 | ||||||
| chr6:41884460
|
T | C | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-103+7334A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884460 | ||||||
| chr6:41884562
|
T | C | 1 | a0001c0002t0008g0163 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-103+7232A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884562 | ||||||
| chr6:41884585
|
C | T | 1 | a0001c0001t0001g0374 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-103+7209G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884585 | ||||||
| chr6:41884591
|
G | A | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+7203C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884591 | ||||||
| chr6:41884803
|
A | G | 1 | a0003c0005t0053g0274 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-103+6991T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884803 | ||||||
| chr6:41884878
|
T | A | 375 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0081others(372): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.-103+6916A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884878 | ||||||
| chr6:41884886
|
T | C | 4 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0150others(1): Show | 4 | NA18960.hp1 NA18964.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+6908A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884886 | ||||||
| chr6:41884934
|
A | G | 8 | a0001c0003t0002g0166a0001c0003t0002g0167a0001c0003t0002g0172others(5): Show | 8 | HG00558.hp2 HG00609.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.-103+6860T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884934 | ||||||
| chr6:41884943
|
C | A | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-103+6851G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884943 | ||||||
| chr6:41884982
|
G | C | 3 | a0001c0001t0009g0004a0001c0001t0009g0159a0001c0001t0009g0160 | 4 | HG01255.hp2 HG02717.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+6812C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41884982 | ||||||
| chr6:41885017
|
G | A | 215 | a0001c0001t0001g0081a0001c0001t0001g0152a0001c0001t0001g0157others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.-103+6777C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41885017 | ||||||
| chr6:41885056
|
G | A | 1 | a0001c0002t0012g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-103+6738C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41885056 | ||||||
| chr6:41885196
|
G | A | 3 | a0001c0001t0009g0060a0001c0003t0020g0061a0001c0003t0025g0062 | 3 | HG02809.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-103+6598C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41885196 | ||||||
| chr6:41885226
|
C | A | 2 | a0003c0005t0054g0275a0003c0005t0055g0273 | 2 | HG01168.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-103+6568G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41885226 | ||||||
| chr6:41885565
|
C | T | 5 | a0001c0003t0010g0055a0001c0003t0010g0056a0001c0003t0010g0064others(2): Show | 5 | HG00741.hp1 HG02055.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103+6229G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41885565 | ||||||
| chr6:41885929
|
G | A | 1 | a0001c0003t0002g0205 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-103+5865C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41885929 | ||||||
| chr6:41886038
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-103+5756C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41886038 | ||||||
| chr6:41886131
|
C | A | 1 | a0001c0003t0002g0206 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-103+5663G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41886131 | ||||||
| chr6:41886151
|
C | T | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-103+5643G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41886151 | ||||||
| chr6:41886419
|
G | A | 5 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0009g0060others(2): Show | 5 | HG02809.hp1 HG03225.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103+5375C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41886419 | ||||||
| chr6:41886648
|
A | T | 5 | a0001c0001t0001g0221a0001c0001t0015g0063a0001c0001t0015g0219others(2): Show | 5 | HG02897.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103+5146T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41886648 | ||||||
| chr6:41886663
|
G | A | 4 | a0001c0001t0001g0152a0001c0001t0001g0260a0001c0001t0046g0151others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103+5131C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41886663 | ||||||
| chr6:41886684
|
G | A | 1 | a0001c0001t0007g0376 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-103+5110C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41886684 | ||||||
| chr6:41886755
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-103+5039G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41886755 | ||||||
| chr6:41886993
|
T | G | 3 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0001t0001g0333 | 3 | NA18968.hp1 NA19057.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-103+4801A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41886993 | ||||||
| chr6:41887122
|
G | C | 1 | a0001c0001t0014g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-103+4672C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41887122 | ||||||
| chr6:41887294
|
C | A | 11 | a0001c0001t0001g0081a0001c0001t0004g0001a0001c0001t0004g0002others(8): Show | 13 | HG01069.hp2 HG01099.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-103+4500G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41887294 | ||||||
| chr6:41887325
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-103+4469C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41887325 | ||||||
| chr6:41887518
|
A | G | 1 | a0001c0001t0007g0351 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-103+4276T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41887518 | ||||||
| chr6:41887693
|
C | T | 1 | a0001c0001t0039g0288 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-103+4101G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41887693 | ||||||
| chr6:41887865
|
C | G | 1 | a0001c0002t0003g0207 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-103+3929G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41887865 | ||||||
| chr6:41887959
|
A | G | 4 | a0001c0001t0009g0096a0001c0001t0009g0098a0001c0001t0018g0090others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+3835T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41887959 | ||||||
| chr6:41888048
|
C | CT | 26 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(23): Show | 26 | HG00438.hp1 HG01109.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.-103+3745dupA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41888048 | ||||||
| chr6:41888048
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285 | 3 | HG02683.hp1 HG03704.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-103+3736_-103+374 others(14): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41888048 | ||||||
| chr6:41888048
|
CT | C | 72 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0265others(69): Show | 72 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.-103+3745delA | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41888048 | ||||||
| chr6:41888048
|
CTT | C | 63 | a0001c0001t0001g0221a0001c0001t0015g0219a0001c0001t0015g0220others(60): Show | 63 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(60): Show |
intron_variant | MODIFIER | c.-103+3744_-103+374 others(6): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41888048 | ||||||
| chr6:41888227
|
G | A | 1 | a0001c0001t0004g0089 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-103+3567C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41888227 | ||||||
| chr6:41888242
|
A | T | 1 | a0001c0003t0023g0165 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-103+3552T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41888242 | ||||||
| chr6:41888264
|
A | G | 53 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-103+3530T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41888264 | ||||||
| chr6:41888274
|
C | T | 1 | a0001c0001t0005g0006 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-103+3520G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41888274 | ||||||
| chr6:41888418
|
A | G | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-103+3376T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41888418 | ||||||
| chr6:41889051
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-103+2743C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41889051 | ||||||
| chr6:41889180
|
G | A | 1 | a0001c0002t0006g0259 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-103+2614C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41889180 | ||||||
| chr6:41889326
|
C | T | 1 | a0001c0001t0007g0345 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-103+2468G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41889326 | ||||||
| chr6:41889413
|
G | A | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-103+2381C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41889413 | ||||||
| chr6:41889466
|
G | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-103+2328C>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41889466 | ||||||
| chr6:41889527
|
T | C | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-103+2267A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41889527 | ||||||
| chr6:41889744
|
C | A | 2 | a0001c0001t0001g0335a0001c0001t0001g0336 | 2 | HG00741.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.-103+2050G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41889744 | ||||||
| chr6:41889749
|
T | G | 2 | a0001c0001t0001g0335a0001c0001t0001g0336 | 2 | HG00741.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.-103+2045A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41889749 | ||||||
| chr6:41889837
|
C | G | 26 | a0001c0001t0001g0081a0001c0001t0004g0001a0001c0001t0004g0002others(23): Show | 28 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-103+1957G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41889837 | ||||||
| chr6:41889868
|
C | T | 26 | a0001c0001t0001g0081a0001c0001t0004g0001a0001c0001t0004g0002others(23): Show | 28 | HG01069.hp2 HG01099.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-103+1926G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41889868 | ||||||
| chr6:41889882
|
T | C | 2 | a0001c0001t0009g0159a0001c0001t0009g0160 | 2 | HG01255.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-103+1912A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41889882 | ||||||
| chr6:41889953
|
C | T | 142 | a0001c0001t0001g0221a0001c0001t0009g0060a0001c0001t0015g0063others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.-103+1841G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41889953 | ||||||
| chr6:41890098
|
A | T | 10 | a0001c0002t0008g0041a0001c0002t0008g0042a0001c0002t0008g0163others(7): Show | 10 | HG02451.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-103+1696T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41890098 | ||||||
| chr6:41890130
|
C | T | 87 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(84): Show | 87 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-103+1664G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41890130 | ||||||
| chr6:41890220
|
A | T | 3 | a0001c0001t0009g0060a0001c0003t0020g0061a0001c0003t0025g0062 | 3 | HG02809.hp1 HG03540.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-103+1574T>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41890220 | ||||||
| chr6:41890301
|
C | G | 1 | a0001c0001t0057g0059 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-103+1493G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41890301 | ||||||
| chr6:41890378
|
C | CA | 132 | a0001c0001t0001g0221a0001c0001t0001g0260a0001c0001t0001g0261others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.-103+1415dupT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41890378 | ||||||
| chr6:41890433
|
C | G | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-103+1361G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41890433 | ||||||
| chr6:41890440
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-103+1354G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41890440 | ||||||
| chr6:41890456
|
T | C | 1 | a0001c0001t0043g0267 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-103+1338A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41890456 | ||||||
| chr6:41890470
|
C | T | 1 | a0001c0002t0003g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-103+1324G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41890470 | ||||||
| chr6:41890558
|
CA | C | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+1235delT | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41890558 | ||||||
| chr6:41890639
|
A | C | 2 | a0001c0003t0010g0055a0001c0003t0010g0056 | 2 | HG00741.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-103+1155T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41890639 | ||||||
| chr6:41890701
|
T | C | 1 | a0001c0003t0002g0268 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-103+1093A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41890701 | ||||||
| chr6:41891165
|
T | C | 3 | a0003c0005t0053g0274a0003c0005t0054g0275a0003c0005t0055g0273 | 3 | HG01168.hp1 HG01361.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-103+629A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41891165 | ||||||
| chr6:41891165
|
T | G | 4 | a0001c0002t0008g0269a0001c0002t0008g0270a0001c0002t0008g0271others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103+629A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41891165 | ||||||
| chr6:41891188
|
G | A | 1 | a0001c0001t0058g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-103+606C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41891188 | ||||||
| chr6:41891424
|
T | C | 1 | a0002c0004t0002g0276 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-103+370A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41891424 | ||||||
| chr6:41891481
|
T | C | 1 | a0001c0001t0001g0338 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-103+313A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41891481 | ||||||
| chr6:41891643
|
AAC | A | 35 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(32): Show | 35 | HG00423.hp1 HG01074.hp1 HG01975.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103+149_-103+150d others(4): Show |
USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 2/7 | chr6 | 41891643 | ||||||
| chr6:41891952
|
A | G | 1 | a0001c0001t0005g0005 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-184-77T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41891952 | ||||||
| chr6:41892005
|
T | C | 1 | a0001c0001t0037g0038 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-184-130A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41892005 | ||||||
| chr6:41892053
|
T | A | 1 | a0001c0001t0049g0039 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-184-178A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41892053 | ||||||
| chr6:41892056
|
A | G | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(1): Show | 4 | HG02109.hp1 HG02818.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-184-181T>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41892056 | ||||||
| chr6:41892237
|
T | C | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-184-362A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41892237 | ||||||
| chr6:41892325
|
C | T | 1 | a0004c0008t0038g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-184-450G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41892325 | ||||||
| chr6:41892340
|
G | A | 1 | a0001c0003t0002g0278 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-184-465C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41892340 | ||||||
| chr6:41892512
|
C | T | 1 | a0001c0003t0002g0053 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-184-637G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41892512 | ||||||
| chr6:41892514
|
T | C | 93 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(90): Show | 93 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-184-639A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41892514 | ||||||
| chr6:41892575
|
T | C | 2 | a0001c0002t0006g0339a0001c0002t0006g0340 | 2 | HG00099.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-184-700A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41892575 | ||||||
| chr6:41892977
|
T | C | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-184-1102A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41892977 | ||||||
| chr6:41892997
|
T | G | 1 | a0001c0002t0003g0341 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-184-1122A>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41892997 | ||||||
| chr6:41893007
|
G | T | 7 | a0001c0003t0002g0046a0001c0003t0002g0047a0001c0003t0002g0048others(4): Show | 7 | NA18948.hp1 NA18954.hp2 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.-184-1132C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41893007 | ||||||
| chr6:41893061
|
C | A | 1 | a0001c0001t0048g0342 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-184-1186G>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41893061 | ||||||
| chr6:41893150
|
T | C | 4 | a0001c0003t0013g0043a0001c0003t0013g0044a0001c0003t0013g0343others(1): Show | 4 | HG01891.hp2 HG02630.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-184-1275A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41893150 | ||||||
| chr6:41893225
|
C | T | 1 | a0001c0002t0003g0045 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-184-1350G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41893225 | ||||||
| chr6:41893314
|
C | G | 2 | a0001c0003t0013g0043a0001c0003t0013g0044 | 2 | HG01891.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-184-1439G>C | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41893314 | ||||||
| chr6:41893502
|
T | C | 32 | a0001c0001t0001g0347a0001c0001t0001g0350a0001c0001t0001g0352others(29): Show | 32 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.-184-1627A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41893502 | ||||||
| chr6:41893714
|
A | C | 2 | a0001c0002t0008g0041a0001c0002t0008g0042 | 2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-185+1610T>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41893714 | ||||||
| chr6:41893743
|
T | A | 2 | a0001c0003t0024g0377a0001c0003t0027g0378 | 2 | HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-185+1581A>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41893743 | ||||||
| chr6:41894198
|
T | C | 1 | a0001c0002t0003g0379 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-185+1126A>G | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41894198 | ||||||
| chr6:41894665
|
C | T | 1 | a0001c0002t0003g0040 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-185+659G>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41894665 | ||||||
| chr6:41895066
|
G | T | 36 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0005g0007others(33): Show | 36 | HG00423.hp1 HG01074.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-185+258C>A | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41895066 | ||||||
| chr6:41895177
|
G | A | 1 | a0001c0001t0035g0380 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-185+147C>T | USP49 | ENSG00000164663.15 | transcript | ENST00000682992.1 | protein_coding | 1/7 | chr6 | 41895177 |