Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7375 |
|---|---|
| ensemblid | ENSG00000114316.13 |
| hgncid | 12627 |
| symbol | USP4 |
| name | ubiquitin specific peptidase 4 |
| refseq_nuc | NM_003363.4 |
| refseq_prot | NP_003354.2 |
| ensembl_nuc | ENST00000265560.9 |
| ensembl_prot | ENSP00000265560.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 49277144 |
| end | 49340053 |
| strand | - |
| ver | v1.2 |
| region | chr3:49277144-49340053 |
| region5000 | chr3:49272144-49345053 |
| regionname0 | USP4_chr3_49277144_49340053 |
| regionname5000 | USP4_chr3_49272144_49345053 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 963 | 217 | 75 | 58 | 48 | 12 | 22 | 40 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0002 | 0/0 | 963 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0003 | 0/0 | 963 | 3 | 1 | 0 | 0 | 2 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0004 | 0/0 | 963 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0005 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2892 | 155 | 60 | 35 | 29 | 10 | 19 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| c0002 | 0/0 | 2892 | 39 | 2 | 14 | 18 | 2 | 3 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| c0003 | 0/0 | 2892 | 15 | 13 | 2 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| c0004 | 0/0 | 2892 | 4 | 0 | 4 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| c0005 | 0/0 | 2892 | 3 | 0 | 3 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| c0006 | 0/0 | 2892 | 3 | 1 | 0 | 0 | 2 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| c0007 | 0/0 | 2892 | 2 | 2 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| c0008 | 0/0 | 2892 | 2 | 0 | 0 | 2 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| c0009 | 0/0 | 2892 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| c0010 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| c0011 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1178 | 169 | 63 | 42 | 42 | 6 | 16 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| t0002 | 1/1 | 1179 | 22 | 2 | 8 | 1 | 5 | 4 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| t0003 | 0/0 | 1178 | 18 | 0 | 7 | 6 | 3 | 2 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| t0004 | 0/0 | 1178 | 12 | 12 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| t0005 | 0/0 | 1178 | 2 | 2 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| t0006 | 0/0 | 1179 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| t0007 | 0/0 | 1178 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| t0008 | 0/0 | 1178 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0166 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0181 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2892 | 155 | 60 | 35 | 29 | 10 | 19 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0002 | 0/0 | 2892 | 39 | 2 | 14 | 18 | 2 | 3 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0003 | 0/0 | 2892 | 15 | 13 | 2 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0004 | 0/0 | 2892 | 4 | 0 | 4 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0005 | 0/0 | 2892 | 3 | 0 | 3 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0009 | 0/0 | 2892 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0002c0007 | 0/0 | 2892 | 2 | 2 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0002c0010 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0003c0006 | 0/0 | 2892 | 3 | 1 | 0 | 0 | 2 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0004c0008 | 0/0 | 2892 | 2 | 0 | 0 | 2 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0005c0011 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4069 | 119 | 45 | 26 | 27 | 6 | 15 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0001t0002 | 1/1 | 4070 | 19 | 1 | 8 | 1 | 3 | 4 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0001t0003 | 0/0 | 4069 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0001t0004 | 0/0 | 4069 | 12 | 12 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0001t0005 | 0/0 | 4069 | 2 | 2 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0001t0006 | 0/0 | 4070 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0001t0008 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0002t0001 | 0/0 | 4069 | 21 | 1 | 7 | 12 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0002t0003 | 0/0 | 4069 | 17 | 0 | 7 | 6 | 2 | 2 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0002t0007 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0003t0001 | 0/0 | 4069 | 15 | 13 | 2 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0004t0001 | 0/0 | 4069 | 4 | 0 | 4 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0005t0001 | 0/0 | 4069 | 3 | 0 | 3 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0001c0009t0001 | 0/0 | 4069 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0002c0007t0001 | 0/0 | 4069 | 2 | 2 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0002c0010t0001 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0003c0006t0002 | 0/0 | 4070 | 3 | 1 | 0 | 0 | 2 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0004c0008t0001 | 0/0 | 4069 | 2 | 0 | 0 | 2 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| a0005c0011t0001 | 0/0 | 4069 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | copy fasta | chr3 | 49272144 | 49345053 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0166 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0002g0181 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0001t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0002t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0004t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0004t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0004t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0004t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0005t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0005t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0001c0009t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0002c0007t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0002c0007t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0002c0010t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0003c0006t0002g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0003c0006t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0004c0008t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0004c0008t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| a0005c0011t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0163 | EUR | GBR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | CHS | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00639 | hp2 | a0001 | c0002 | t0003 | g0107 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00642 | hp1 | a0001 | c0005 | t0001 | g0005 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00733 | hp1 | a0001 | c0002 | t0003 | g0141 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00735 | hp2 | a0001 | c0002 | t0003 | g0145 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0148 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0153 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0207 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01081 | hp1 | a0001 | c0004 | t0001 | g0043 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0113 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0097 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0112 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0102 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01192 | hp1 | a0001 | c0004 | t0001 | g0125 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0209 | AMR | PUR | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01255 | hp2 | a0001 | c0004 | t0001 | g0038 | AMR | CLM | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01256 | hp1 | a0001 | c0005 | t0001 | g0001 | AMR | CLM | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0111 | AMR | CLM | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01258 | hp1 | a0001 | c0005 | t0001 | g0001 | AMR | CLM | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0115 | AMR | CLM | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0149 | AMR | CLM | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0101 | EUR | IBS | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01516 | hp2 | a0003 | c0006 | t0002 | g0004 | EUR | IBS | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01517 | hp1 | a0003 | c0006 | t0002 | g0004 | EUR | IBS | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01517 | hp2 | a0001 | c0002 | t0003 | g0002 | EUR | IBS | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0196 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0211 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02027 | hp1 | a0001 | c0001 | t0008 | g0137 | EAS | KHV | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0067 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02257 | hp2 | a0003 | c0006 | t0002 | g0157 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02280 | hp2 | a0001 | c0002 | t0007 | g0116 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PEL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02300 | hp2 | a0001 | c0004 | t0001 | g0129 | AMR | PEL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0206 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0188 | SAS | PJL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0216 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02886 | hp2 | a0002 | c0007 | t0001 | g0109 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0175 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0205 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0197 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0198 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0219 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0200 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0199 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0202 | AFR | MSL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0222 | AFR | MSL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0212 | AFR | MSL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0201 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0204 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0220 | AFR | GWD | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0215 | AFR | MSL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | STU | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0142 | SAS | BEB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | BEB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0002 | SAS | BEB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | BEB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0214 | AFR | YRI | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18747 | hp2 | a0001 | c0002 | t0003 | g0010 | EAS | CHB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18952 | hp1 | a0004 | c0008 | t0001 | g0143 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0106 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0099 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18979 | hp2 | a0001 | c0002 | t0003 | g0098 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19030 | hp2 | a0005 | c0011 | t0001 | g0208 | AFR | LWK | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19057 | hp1 | a0001 | c0002 | t0003 | g0103 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19080 | hp2 | a0001 | c0002 | t0003 | g0104 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19082 | hp1 | a0004 | c0008 | t0001 | g0100 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19090 | hp1 | a0001 | c0009 | t0001 | g0185 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ASW | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0210 | AFR | ASW | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0056 | EUR | TSI | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0162 | EUR | TSI | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | TSI | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0169 | EUR | TSI | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | GIH | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0217 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0195 | AFR | MSL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0068 | AFR | MSL | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | USA | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0213 | AFR | USA | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | USA | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA20300 | hp2 | a0002 | c0007 | t0001 | g0110 | AFR | USA | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| NA21309 | hp2 | a0002 | c0010 | t0001 | g0009 | AFR | LWK | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0181 | REF | REF | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0166 | REF | REF | USP4_chr3_49272144_49345053 | USP4 | chr3 | 49272144 | 49345053 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49283991
|
T | C | 1 | a0003 | 3 | HG01516.hp2 HG01517.hp1 HG02257.hp2 |
missense_variant | MODERATE | c.2536A>G | p.Ile846Val | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/22 | 2565/4070 | 2536/2892 | 846/963 | chr3 | 49283991 | ||
| chr3:49294431
|
T | C | 1 | a0002 | 3 | HG02886.hp2 NA20300.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.1859A>G | p.Tyr620Cys | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 14/22 | 1888/4070 | 1859/2892 | 620/963 | chr3 | 49294431 | ||
| chr3:49294526
|
C | A | 1 | a0004 | 2 | NA18952.hp1 NA19082.hp1 |
missense_variant | MODERATE | c.1764G>T | p.Lys588Asn | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 14/22 | 1793/4070 | 1764/2892 | 588/963 | chr3 | 49294526 | ||
| chr3:49335570
|
T | C | 1 | a0005 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.128A>G | p.Lys43Arg | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/22 | 157/4070 | 128/2892 | 43/963 | chr3 | 49335570 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49278889
|
C | T | 1 | a0001c0009 | 1 | NA19090.hp1 | synonymous_variant | LOW | c.2658G>A | p.Ala886Ala | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 21/22 | 2687/4070 | 2658/2892 | 886/963 | chr3 | 49278889 | ||
| chr3:49280775
|
G | A | 1 | a0001c0005 | 3 | HG00642.hp1 HG01256.hp1 HG01258.hp1 |
synonymous_variant | LOW | c.2613C>T | p.Ser871Ser | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 20/22 | 2642/4070 | 2613/2892 | 871/963 | chr3 | 49280775 | ||
| chr3:49284579
|
G | A | 1 | a0001c0003 | 15 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
synonymous_variant | LOW | c.2277C>T | p.Tyr759Tyr | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 18/22 | 2306/4070 | 2277/2892 | 759/963 | chr3 | 49284579 | ||
| chr3:49298624
|
A | G | 1 | a0001c0004 | 4 | HG01081.hp1 HG01192.hp1 HG01255.hp2 others(1): Show |
synonymous_variant | LOW | c.1524T>C | p.Thr508Thr | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 12/22 | 1553/4070 | 1524/2892 | 508/963 | chr3 | 49298624 | ||
| chr3:49305742
|
G | A | 4 | a0001c0002a0001c0009a0002c0007others(1): Show | 44 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(41): Show |
synonymous_variant | LOW | c.1101C>T | p.Asp367Asp | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/22 | 1130/4070 | 1101/2892 | 367/963 | chr3 | 49305742 | ||
| chr3:49324936
|
C | T | 4 | a0001c0002a0001c0009a0002c0007others(1): Show | 44 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(41): Show |
synonymous_variant | LOW | c.591G>A | p.Lys197Lys | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 5/22 | 620/4070 | 591/2892 | 197/963 | chr3 | 49324936 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49277156
|
G | C | 1 | a0001c0001t0006 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1137C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 22/22 | 1137 | chr3 | 49277156 | |||||
| chr3:49277401
|
A | T | 1 | a0001c0001t0005 | 2 | HG02055.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*892T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 22/22 | 892 | chr3 | 49277401 | |||||
| chr3:49277527
|
G | A | 2 | a0001c0001t0003a0001c0002t0003 | 18 | HG00639.hp2 HG00733.hp1 HG00735.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*766C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 22/22 | 766 | chr3 | 49277527 | |||||
| chr3:49277680
|
T | A | 1 | a0001c0002t0007 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*613A>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 22/22 | 613 | chr3 | 49277680 | |||||
| chr3:49278142
|
CT | C | 16 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(13): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*150delA | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 22/22 | 150 | chr3 | 49278142 | |||||
| chr3:49278152
|
T | G | 1 | a0001c0001t0008 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*141A>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 22/22 | 141 | chr3 | 49278152 | |||||
| chr3:49340035
|
G | C | 1 | a0001c0001t0004 | 12 | HG01884.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-11C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/22 | 11 | chr3 | 49340035 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:49278523
|
C | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0120 | 3 | HG02559.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2734-72G>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 21/21 | chr3 | 49278523 | ||||||
| chr3:49278664
|
A | G | 3 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0072 | 3 | HG01109.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2733+150T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 21/21 | chr3 | 49278664 | ||||||
| chr3:49278731
|
A | G | 2 | a0001c0005t0001g0001a0001c0005t0001g0005 | 3 | HG00642.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2733+83T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 21/21 | chr3 | 49278731 | ||||||
| chr3:49279278
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2645-376T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 20/21 | chr3 | 49279278 | ||||||
| chr3:49279890
|
G | C | 1 | a0001c0001t0001g0018 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2644+854C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 20/21 | chr3 | 49279890 | ||||||
| chr3:49279905
|
T | C | 178 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(175): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2644+839A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 20/21 | chr3 | 49279905 | ||||||
| chr3:49280294
|
C | G | 178 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(175): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2644+450G>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 20/21 | chr3 | 49280294 | ||||||
| chr3:49280332
|
C | T | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2644+412G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 20/21 | chr3 | 49280332 | ||||||
| chr3:49280516
|
C | T | 13 | a0001c0001t0001g0135a0001c0003t0001g0195a0001c0003t0001g0196others(10): Show | 13 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2644+228G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 20/21 | chr3 | 49280516 | ||||||
| chr3:49280555
|
G | T | 1 | a0001c0001t0001g0013 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2644+189C>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 20/21 | chr3 | 49280555 | ||||||
| chr3:49280559
|
C | CA | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0033others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2644+184dupT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 20/21 | chr3 | 49280559 | ||||||
| chr3:49280682
|
G | T | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2644+62C>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 20/21 | chr3 | 49280682 | ||||||
| chr3:49280683
|
G | T | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2644+61C>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 20/21 | chr3 | 49280683 | ||||||
| chr3:49281063
|
G | A | 2 | a0001c0001t0004g0212a0001c0001t0004g0213 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2541-216C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281063 | ||||||
| chr3:49281089
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2541-242C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281089 | ||||||
| chr3:49281199
|
G | A | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2541-352C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281199 | ||||||
| chr3:49281366
|
G | A | 3 | a0002c0007t0001g0109a0002c0007t0001g0110a0002c0010t0001g0009 | 3 | HG02886.hp2 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2541-519C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281366 | ||||||
| chr3:49281442
|
C | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0039others(10): Show | 13 | HG00544.hp2 HG00735.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.2541-595G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281442 | ||||||
| chr3:49281472
|
A | ATG | 37 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0023others(34): Show | 38 | HG00642.hp1 HG01109.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.2541-627_2541-626d others(4): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281472 | ||||||
| chr3:49281476
|
G | GTATA | 3 | a0001c0001t0001g0135a0001c0003t0001g0195a0005c0011t0001g0208 | 3 | HG03471.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2541-633_2541-630d others(6): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281476 | ||||||
| chr3:49281476
|
G | GTGTA | 6 | a0001c0001t0001g0123a0001c0001t0001g0173a0001c0003t0001g0175others(3): Show | 6 | HG02622.hp2 HG02683.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.2541-630_2541-629i others(6): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281476 | ||||||
| chr3:49281476
|
GTA | G | 6 | a0001c0002t0001g0111a0001c0002t0001g0115a0001c0002t0001g0140others(3): Show | 6 | HG00544.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2541-631_2541-630d others(4): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281476 | ||||||
| chr3:49281476
|
GTATA | G | 15 | a0001c0002t0001g0108a0001c0002t0001g0144a0001c0002t0001g0146others(12): Show | 15 | HG00733.hp1 HG02735.hp1 HG02886.hp2 others(12): Show |
intron_variant | MODIFIER | c.2541-633_2541-630d others(6): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281476 | ||||||
| chr3:49281476
|
GTATATA | G | 10 | a0001c0001t0003g0056a0001c0002t0003g0002a0001c0002t0003g0003others(7): Show | 12 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.2541-635_2541-630d others(8): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281476 | ||||||
| chr3:49281476
|
GTATATAT others(1): Show |
G | 2 | a0001c0002t0003g0145a0001c0002t0007g0116 | 2 | HG00735.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2541-637_2541-630d others(10): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281476 | ||||||
| chr3:49281478
|
A | G | 99 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0012others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.2541-631T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281478 | ||||||
| chr3:49281480
|
A | G | 2 | a0001c0002t0001g0111a0001c0002t0001g0115 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2541-633T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281480 | ||||||
| chr3:49281485
|
T | C | 2 | a0001c0002t0001g0147a0001c0002t0003g0098 | 2 | NA18979.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.2541-638A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281485 | ||||||
| chr3:49281487
|
T | C | 7 | a0001c0001t0001g0150a0001c0002t0001g0140a0001c0002t0001g0147others(4): Show | 7 | HG00544.hp1 HG02723.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.2541-640A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281487 | ||||||
| chr3:49281489
|
T | C | 24 | a0001c0001t0001g0023a0001c0001t0001g0081a0001c0001t0001g0150others(21): Show | 24 | HG00544.hp1 HG00733.hp1 HG02698.hp2 others(21): Show |
intron_variant | MODIFIER | c.2541-642A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281489 | ||||||
| chr3:49281489
|
T | TAC | 2 | a0001c0001t0002g0164a0001c0001t0002g0165 | 2 | HG00733.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.2541-643_2541-642i others(4): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281489 | ||||||
| chr3:49281489
|
TATACACA others(13): Show |
T | 1 | a0001c0001t0001g0020 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2541-662_2541-643d others(22): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281489 | ||||||
| chr3:49281491
|
T | C | 60 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0013others(57): Show | 62 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.2541-644A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281491 | ||||||
| chr3:49281491
|
T | TAC | 6 | a0001c0001t0001g0156a0001c0001t0002g0162a0001c0001t0002g0167others(3): Show | 7 | HG01516.hp2 HG01517.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2541-646_2541-645d others(4): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281491 | ||||||
| chr3:49281491
|
T | TACAC | 5 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0174others(2): Show | 5 | HG01884.hp2 HG02027.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2541-648_2541-645d others(6): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281491 | ||||||
| chr3:49281491
|
T | TACACAC | 11 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0171others(8): Show | 11 | HG01069.hp2 HG01070.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.2541-650_2541-645d others(8): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281491 | ||||||
| chr3:49281491
|
T | TACACACA others(3): Show |
1 | a0001c0001t0002g0170 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2541-654_2541-645d others(12): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281491 | ||||||
| chr3:49281491
|
T | TACACACA others(5): Show |
1 | a0001c0001t0002g0181 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2541-656_2541-645d others(14): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281491 | ||||||
| chr3:49281491
|
TAC | T | 35 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(32): Show | 35 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.2541-646_2541-645d others(4): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281491 | ||||||
| chr3:49281491
|
TACAC | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0030a0001c0001t0001g0035others(8): Show | 11 | HG00639.hp1 HG00735.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.2541-648_2541-645d others(6): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281491 | ||||||
| chr3:49281491
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0044 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2541-656_2541-645d others(14): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281491 | ||||||
| chr3:49281493
|
C | T | 41 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(38): Show | 41 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.2541-646G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281493 | ||||||
| chr3:49281495
|
C | T | 43 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0032others(40): Show | 43 | HG00544.hp2 HG00597.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.2541-648G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281495 | ||||||
| chr3:49281497
|
C | T | 17 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0030others(14): Show | 17 | HG00735.hp1 HG01975.hp1 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.2541-650G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281497 | ||||||
| chr3:49281505
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2541-658G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281505 | ||||||
| chr3:49281527
|
CACACAT | C | 8 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(5): Show | 8 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2541-686_2541-681d others(8): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281527 | ||||||
| chr3:49281533
|
T | C | 5 | a0001c0001t0001g0191a0001c0001t0004g0219a0001c0001t0004g0222others(2): Show | 6 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2541-686A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281533 | ||||||
| chr3:49281709
|
C | T | 1 | a0001c0001t0004g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2541-862G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281709 | ||||||
| chr3:49281714
|
C | CA | 53 | a0001c0001t0001g0026a0001c0001t0001g0078a0001c0001t0001g0082others(50): Show | 55 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.2541-868dupT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281714 | ||||||
| chr3:49281740
|
C | T | 4 | a0001c0002t0001g0011a0001c0002t0001g0105a0004c0008t0001g0100others(1): Show | 4 | NA18952.hp1 NA18983.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.2541-893G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281740 | ||||||
| chr3:49281903
|
C | T | 33 | a0001c0001t0003g0056a0001c0002t0001g0108a0001c0002t0001g0140others(30): Show | 35 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.2541-1056G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281903 | ||||||
| chr3:49281904
|
A | G | 33 | a0001c0001t0003g0056a0001c0002t0001g0108a0001c0002t0001g0140others(30): Show | 35 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.2541-1057T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49281904 | ||||||
| chr3:49282036
|
A | C | 13 | a0001c0003t0001g0195a0001c0003t0001g0196a0001c0003t0001g0197others(10): Show | 14 | HG00642.hp1 HG01074.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.2541-1189T>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49282036 | ||||||
| chr3:49282268
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2541-1421T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49282268 | ||||||
| chr3:49282568
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0117 | 2 | HG03688.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2540+1419G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49282568 | ||||||
| chr3:49282650
|
G | C | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2540+1337C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49282650 | ||||||
| chr3:49282750
|
G | C | 207 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(204): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2540+1237C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49282750 | ||||||
| chr3:49282857
|
ACCACCAC others(301): Show |
A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0004g0211 | 3 | HG01884.hp2 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2540+822_2540+1129 others(3): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49282857 | ||||||
| chr3:49283008
|
C | CT | 61 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0024others(58): Show | 63 | HG00597.hp1 HG00597.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.2540+978dupA | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283008 | ||||||
| chr3:49283008
|
C | CTT | 10 | a0001c0002t0001g0149a0001c0002t0003g0098a0001c0002t0003g0101others(7): Show | 10 | HG00639.hp2 HG00735.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.2540+977_2540+978d others(4): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283008 | ||||||
| chr3:49283008
|
C | T | 2 | a0001c0002t0001g0140a0001c0002t0001g0147 | 2 | NA19003.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2540+979G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283008 | ||||||
| chr3:49283008
|
CT | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0134a0001c0001t0001g0156others(2): Show | 5 | HG03041.hp1 HG03098.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.2540+978delA | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283008 | ||||||
| chr3:49283165
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2540+822C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283165 | ||||||
| chr3:49283189
|
C | T | 8 | a0001c0001t0001g0154a0001c0001t0001g0171a0001c0001t0001g0172others(5): Show | 8 | HG02451.hp1 HG02486.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2540+798G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283189 | ||||||
| chr3:49283204
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0059a0001c0001t0001g0192others(1): Show | 4 | HG00642.hp2 HG01074.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2540+783A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283204 | ||||||
| chr3:49283216
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2540+771T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283216 | ||||||
| chr3:49283221
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0020 | 3 | HG02280.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2540+766C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283221 | ||||||
| chr3:49283228
|
A | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0117 | 2 | HG03688.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2540+759T>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283228 | ||||||
| chr3:49283236
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0004g0211 | 3 | HG01884.hp2 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2540+751C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283236 | ||||||
| chr3:49283238
|
T | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0004g0211 | 3 | HG01884.hp2 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2540+749A>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283238 | ||||||
| chr3:49283243
|
A | T | 17 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0061others(14): Show | 17 | HG01074.hp1 HG01109.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.2540+744T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283243 | ||||||
| chr3:49283249
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0004g0211 | 3 | HG01884.hp2 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2540+738A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283249 | ||||||
| chr3:49283250
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0004g0211 | 3 | HG01884.hp2 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2540+737C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283250 | ||||||
| chr3:49283255
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2540+732G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283255 | ||||||
| chr3:49283256
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0004g0211 | 3 | HG01884.hp2 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2540+731A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283256 | ||||||
| chr3:49283257
|
G | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(1): Show | 4 | HG00099.hp1 HG01884.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.2540+730C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283257 | ||||||
| chr3:49283261
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2540+726T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283261 | ||||||
| chr3:49283291
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0123 | 2 | HG02683.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2540+696T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283291 | ||||||
| chr3:49283304
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2540+683C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283304 | ||||||
| chr3:49283305
|
T | C | 3 | a0001c0001t0001g0020a0001c0001t0004g0212a0001c0001t0004g0213 | 3 | HG03453.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2540+682A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283305 | ||||||
| chr3:49283394
|
T | C | 7 | a0001c0001t0004g0214a0001c0001t0004g0215a0001c0001t0004g0216others(4): Show | 7 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2540+593A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283394 | ||||||
| chr3:49283549
|
C | T | 12 | a0001c0001t0001g0155a0001c0003t0001g0195a0001c0003t0001g0196others(9): Show | 12 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2540+438G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283549 | ||||||
| chr3:49283763
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2540+224G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283763 | ||||||
| chr3:49283871
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2540+116G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 19/21 | chr3 | 49283871 | ||||||
| chr3:49284144
|
G | C | 1 | a0001c0001t0001g0150 | 1 | HG02723.hp2 | splice_region_variant&intron_variant | LOW | c.2391-8C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 18/21 | chr3 | 49284144 | ||||||
| chr3:49284292
|
T | TG | 5 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0065others(2): Show | 5 | HG01109.hp1 HG03831.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.2391-157dupC | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 18/21 | chr3 | 49284292 | ||||||
| chr3:49284594
|
T | A | 52 | a0001c0001t0001g0150a0001c0001t0004g0211a0001c0001t0004g0212others(49): Show | 54 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.2272-10A>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 17/21 | chr3 | 49284594 | ||||||
| chr3:49284674
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2272-90A>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 17/21 | chr3 | 49284674 | ||||||
| chr3:49284676
|
T | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0174 | 2 | HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2272-92A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 17/21 | chr3 | 49284676 | ||||||
| chr3:49285521
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0073others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2200+577G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 16/21 | chr3 | 49285521 | ||||||
| chr3:49285740
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2200+358C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 16/21 | chr3 | 49285740 | ||||||
| chr3:49286624
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1973-299G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49286624 | ||||||
| chr3:49286816
|
C | CTCTA | 70 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(67): Show | 71 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1973-495_1973-492d others(6): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49286816 | ||||||
| chr3:49286816
|
C | CTCTATCT others(1): Show |
40 | a0001c0001t0001g0021a0001c0001t0001g0030a0001c0001t0001g0031others(37): Show | 41 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1973-499_1973-492d others(10): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49286816 | ||||||
| chr3:49286816
|
C | CTCTATCT others(5): Show |
33 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0035others(30): Show | 34 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1973-503_1973-492d others(14): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49286816 | ||||||
| chr3:49286816
|
C | CTCTATCT others(9): Show |
2 | a0001c0001t0001g0026a0001c0002t0003g0104 | 2 | NA19003.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1973-507_1973-492d others(18): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49286816 | ||||||
| chr3:49286816
|
CTCTA | C | 23 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0060others(20): Show | 24 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.1973-495_1973-492d others(6): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49286816 | ||||||
| chr3:49286816
|
CTCTATCT others(1): Show |
C | 10 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.1973-499_1973-492d others(10): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49286816 | ||||||
| chr3:49286816
|
CTCTATCT others(5): Show |
C | 2 | a0001c0001t0001g0020a0001c0002t0001g0108 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1973-503_1973-492d others(14): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49286816 | ||||||
| chr3:49287022
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1973-697T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49287022 | ||||||
| chr3:49287022
|
A | T | 116 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.1973-697T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49287022 | ||||||
| chr3:49287098
|
G | A | 1 | a0002c0007t0001g0109 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1973-773C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49287098 | ||||||
| chr3:49287240
|
C | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0073others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1973-915G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49287240 | ||||||
| chr3:49287349
|
G | A | 115 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(112): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.1973-1024C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49287349 | ||||||
| chr3:49287375
|
C | T | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1973-1050G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49287375 | ||||||
| chr3:49287421
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1973-1096A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49287421 | ||||||
| chr3:49287620
|
G | A | 10 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1973-1295C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49287620 | ||||||
| chr3:49287625
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1973-1300T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49287625 | ||||||
| chr3:49287877
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1973-1552C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49287877 | ||||||
| chr3:49288122
|
G | C | 3 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0193 | 3 | HG01175.hp2 HG01257.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1973-1797C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49288122 | ||||||
| chr3:49288164
|
A | C | 15 | a0001c0003t0001g0175a0001c0003t0001g0195a0001c0003t0001g0196others(12): Show | 15 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1973-1839T>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49288164 | ||||||
| chr3:49288210
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1973-1885A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49288210 | ||||||
| chr3:49288379
|
A | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0073others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1973-2054T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49288379 | ||||||
| chr3:49288745
|
A | G | 52 | a0001c0001t0001g0150a0001c0001t0004g0211a0001c0001t0004g0212others(49): Show | 54 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1973-2420T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49288745 | ||||||
| chr3:49288832
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0002g0164 | 2 | HG02300.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1973-2507C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49288832 | ||||||
| chr3:49289268
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1973-2943A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49289268 | ||||||
| chr3:49289511
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1972+2999T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49289511 | ||||||
| chr3:49290078
|
C | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0052 | 2 | NA19012.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1972+2432G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49290078 | ||||||
| chr3:49290186
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1972+2324C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49290186 | ||||||
| chr3:49290436
|
C | T | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0073others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1972+2074G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49290436 | ||||||
| chr3:49290583
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1972+1927G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49290583 | ||||||
| chr3:49290666
|
T | G | 15 | a0001c0003t0001g0175a0001c0003t0001g0195a0001c0003t0001g0196others(12): Show | 15 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1972+1844A>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49290666 | ||||||
| chr3:49290674
|
C | T | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1972+1836G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49290674 | ||||||
| chr3:49290742
|
T | C | 1 | a0001c0002t0001g0140 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1972+1768A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49290742 | ||||||
| chr3:49291125
|
C | T | 1 | a0001c0002t0007g0116 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1972+1385G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49291125 | ||||||
| chr3:49291185
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1972+1325G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49291185 | ||||||
| chr3:49291209
|
C | G | 1 | a0001c0002t0003g0141 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1972+1301G>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49291209 | ||||||
| chr3:49291279
|
T | TA | 6 | a0001c0001t0001g0086a0001c0001t0001g0136a0001c0002t0001g0011others(3): Show | 6 | HG01496.hp2 NA18952.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1972+1230dupT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49291279 | ||||||
| chr3:49291343
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1972+1167C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49291343 | ||||||
| chr3:49291400
|
A | C | 175 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(172): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1972+1110T>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49291400 | ||||||
| chr3:49291573
|
CA | C | 5 | a0001c0001t0001g0039a0001c0001t0001g0057a0001c0001t0001g0096others(2): Show | 5 | HG01069.hp2 HG01070.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1972+936delT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49291573 | ||||||
| chr3:49291657
|
A | T | 39 | a0001c0002t0001g0108a0001c0002t0001g0111a0001c0002t0001g0112others(36): Show | 41 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.1972+853T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49291657 | ||||||
| chr3:49292090
|
A | G | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1972+420T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49292090 | ||||||
| chr3:49292098
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1972+412G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49292098 | ||||||
| chr3:49292288
|
G | GA | 7 | a0001c0001t0001g0118a0001c0001t0001g0121a0001c0001t0001g0133others(4): Show | 7 | HG01243.hp2 HG01934.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1972+221dupT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49292288 | ||||||
| chr3:49292356
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1972+154C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 15/21 | chr3 | 49292356 | ||||||
| chr3:49293465
|
AAAAC | A | 7 | a0001c0001t0004g0214a0001c0001t0004g0215a0001c0001t0004g0216others(4): Show | 7 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1884-871_1884-868d others(6): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 14/21 | chr3 | 49293465 | ||||||
| chr3:49293627
|
T | C | 52 | a0001c0001t0001g0150a0001c0001t0004g0211a0001c0001t0004g0212others(49): Show | 54 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1883+780A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 14/21 | chr3 | 49293627 | ||||||
| chr3:49293810
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1883+597G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 14/21 | chr3 | 49293810 | ||||||
| chr3:49293878
|
A | G | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1883+529T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 14/21 | chr3 | 49293878 | ||||||
| chr3:49293976
|
A | AT | 8 | a0001c0001t0001g0030a0001c0001t0001g0118a0001c0001t0001g0121others(5): Show | 8 | HG01192.hp2 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1883+430dupA | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 14/21 | chr3 | 49293976 | ||||||
| chr3:49294392
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1883+15T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 14/21 | chr3 | 49294392 | ||||||
| chr3:49294952
|
C | A | 1 | a0001c0002t0003g0104 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1692-354G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49294952 | ||||||
| chr3:49295085
|
T | G | 1 | a0001c0001t0002g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1692-487A>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295085 | ||||||
| chr3:49295105
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1692-507G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295105 | ||||||
| chr3:49295106
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1692-508C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295106 | ||||||
| chr3:49295169
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1692-571C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295169 | ||||||
| chr3:49295276
|
G | A | 19 | a0001c0002t0001g0108a0001c0002t0003g0002a0001c0002t0003g0003others(16): Show | 21 | HG00639.hp2 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1692-678C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295276 | ||||||
| chr3:49295288
|
C | CA | 25 | a0001c0001t0001g0007a0001c0001t0001g0059a0001c0001t0001g0073others(22): Show | 25 | HG00639.hp1 HG00642.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.1692-691dupT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295288 | ||||||
| chr3:49295288
|
C | CAA | 8 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0046others(5): Show | 8 | HG00597.hp1 HG00597.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1692-692_1692-691d others(4): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295288 | ||||||
| chr3:49295288
|
C | CAAAAAAA others(9): Show |
3 | a0001c0002t0001g0113a0001c0002t0001g0114a0001c0002t0001g0147 | 3 | HG01081.hp2 HG01169.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1692-706_1692-691d others(18): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295288 | ||||||
| chr3:49295288
|
C | CAAAAAAA others(10): Show |
7 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0115others(4): Show | 7 | HG00738.hp1 HG01099.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1692-707_1692-691d others(19): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295288 | ||||||
| chr3:49295288
|
C | CAAAAAAA others(23): Show |
1 | a0001c0002t0007g0116 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1692-691_1692-690i others(32): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295288 | ||||||
| chr3:49295288
|
CA | C | 63 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(60): Show | 64 | HG00099.hp1 HG00544.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1692-691delT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295288 | ||||||
| chr3:49295288
|
CAA | C | 5 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0001t0001g0074others(2): Show | 5 | HG01069.hp1 HG01884.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1692-692_1692-691d others(4): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295288 | ||||||
| chr3:49295382
|
G | C | 21 | a0001c0001t0001g0150a0001c0002t0001g0111a0001c0002t0001g0112others(18): Show | 21 | HG00544.hp1 HG00738.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1692-784C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295382 | ||||||
| chr3:49295466
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1692-868C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295466 | ||||||
| chr3:49295646
|
T | C | 1 | a0001c0001t0001g0020 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1692-1048A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295646 | ||||||
| chr3:49295697
|
C | CGT | 2 | a0001c0001t0001g0061a0001c0001t0001g0072 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1692-1101_1692-110 others(6): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295697 | ||||||
| chr3:49295701
|
T | TGC | 13 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0006g0153others(10): Show | 13 | HG00738.hp1 HG01069.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1692-1105_1692-110 others(6): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295701 | ||||||
| chr3:49295701
|
T | TGCGCGCG others(9): Show |
2 | a0001c0002t0001g0182a0001c0009t0001g0185 | 2 | NA19079.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1692-1104_1692-110 others(20): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295701 | ||||||
| chr3:49295701
|
T | TGCGCGCG others(11): Show |
3 | a0001c0002t0001g0183a0001c0002t0001g0184a0001c0002t0001g0186 | 3 | HG00544.hp1 NA18951.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1692-1104_1692-110 others(22): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295701 | ||||||
| chr3:49295706
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0073others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1692-1108C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295706 | ||||||
| chr3:49295709
|
C | CGCGCGCG others(12): Show |
1 | a0001c0002t0001g0187 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1692-1112_1692-111 others(23): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295709 | ||||||
| chr3:49295714
|
G | A | 1 | a0003c0006t0002g0157 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1692-1116C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295714 | ||||||
| chr3:49295714
|
G | GCA | 7 | a0001c0001t0001g0020a0001c0001t0001g0053a0001c0001t0001g0066others(4): Show | 7 | HG02109.hp2 HG02486.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.1692-1118_1692-111 others(6): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295714 | ||||||
| chr3:49295714
|
G | GCACACAC others(3): Show |
1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1692-1126_1692-111 others(14): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295714 | ||||||
| chr3:49295714
|
G | GCACACAC others(7): Show |
1 | a0001c0001t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1692-1130_1692-111 others(18): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295714 | ||||||
| chr3:49295714
|
G | GCGCGCA | 2 | a0001c0001t0004g0213a0001c0002t0001g0189 | 2 | HG06807.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1692-1117_1692-111 others(10): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295714 | ||||||
| chr3:49295714
|
G | GCGCGCAC others(13): Show |
3 | a0001c0001t0004g0214a0001c0001t0004g0218a0001c0001t0004g0220 | 3 | HG02572.hp2 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1692-1117_1692-111 others(24): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295714 | ||||||
| chr3:49295714
|
G | GCGCGCAC others(17): Show |
3 | a0001c0001t0004g0215a0001c0001t0004g0216a0001c0001t0004g0221 | 3 | HG02486.hp1 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1692-1117_1692-111 others(28): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295714 | ||||||
| chr3:49295714
|
G | GCGCGCGC others(13): Show |
1 | a0001c0001t0004g0217 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1692-1117_1692-111 others(24): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295714 | ||||||
| chr3:49295714
|
G | GCGCGCGC others(19): Show |
1 | a0001c0001t0004g0219 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1692-1117_1692-111 others(30): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295714 | ||||||
| chr3:49295714
|
G | GCGCGCGC others(17): Show |
2 | a0001c0001t0004g0212a0001c0001t0004g0222 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1692-1117_1692-111 others(28): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295714 | ||||||
| chr3:49295714
|
G | GCGCGCGC others(9): Show |
1 | a0001c0002t0001g0188 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1692-1117_1692-111 others(20): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295714 | ||||||
| chr3:49295714
|
G | GCTGCGCG others(10): Show |
1 | a0001c0002t0001g0146 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1692-1117_1692-111 others(21): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295714 | ||||||
| chr3:49295716
|
A | G | 10 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(7): Show | 10 | HG01099.hp2 HG01109.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1692-1118T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295716 | ||||||
| chr3:49295734
|
ACC | A | 22 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0037others(19): Show | 22 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1692-1138_1692-113 others(6): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295734 | ||||||
| chr3:49295735
|
C | CA | 4 | a0001c0001t0001g0133a0001c0001t0001g0136a0001c0001t0004g0212others(1): Show | 4 | HG01934.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1692-1138_1692-113 others(5): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295735 | ||||||
| chr3:49295736
|
C | A | 194 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1692-1138G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295736 | ||||||
| chr3:49295737
|
C | A | 3 | a0001c0001t0001g0136a0001c0001t0004g0212a0001c0001t0004g0222 | 3 | HG03453.hp1 HG03453.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1692-1139G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295737 | ||||||
| chr3:49295738
|
C | A | 32 | a0001c0001t0001g0087a0001c0001t0001g0150a0001c0001t0004g0211others(29): Show | 32 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1692-1140G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295738 | ||||||
| chr3:49295739
|
C | A | 2 | a0001c0001t0004g0212a0001c0001t0004g0222 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1692-1141G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49295739 | ||||||
| chr3:49296008
|
T | G | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1692-1410A>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49296008 | ||||||
| chr3:49296037
|
A | C | 1 | a0001c0001t0001g0127 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1692-1439T>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49296037 | ||||||
| chr3:49296038
|
G | A | 2 | a0001c0003t0001g0175a0001c0003t0001g0205 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1692-1440C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49296038 | ||||||
| chr3:49296064
|
G | C | 1 | a0001c0001t0001g0127 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1692-1466C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49296064 | ||||||
| chr3:49296078
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1692-1480A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49296078 | ||||||
| chr3:49296285
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1691+1585T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49296285 | ||||||
| chr3:49296518
|
G | A | 1 | a0001c0003t0001g0202 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1691+1352C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49296518 | ||||||
| chr3:49296636
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1691+1234C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49296636 | ||||||
| chr3:49296784
|
T | A | 1 | a0001c0001t0001g0049 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1691+1086A>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49296784 | ||||||
| chr3:49297175
|
G | C | 123 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(120): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.1691+695C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49297175 | ||||||
| chr3:49297194
|
G | A | 20 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(17): Show | 20 | HG00544.hp1 HG00738.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.1691+676C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49297194 | ||||||
| chr3:49297335
|
G | A | 152 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1691+535C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49297335 | ||||||
| chr3:49297364
|
A | G | 20 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(17): Show | 20 | HG00544.hp1 HG00738.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.1691+506T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49297364 | ||||||
| chr3:49297578
|
AG | A | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1691+291delC | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49297578 | ||||||
| chr3:49297614
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1691+256T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 13/21 | chr3 | 49297614 | ||||||
| chr3:49297982
|
C | T | 1 | a0005c0011t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1597-18G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 12/21 | chr3 | 49297982 | ||||||
| chr3:49298312
|
C | T | 21 | a0001c0001t0001g0150a0001c0002t0001g0111a0001c0002t0001g0112others(18): Show | 21 | HG00544.hp1 HG00738.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1596+240G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 12/21 | chr3 | 49298312 | ||||||
| chr3:49298482
|
G | A | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596+70C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 12/21 | chr3 | 49298482 | ||||||
| chr3:49298799
|
T | C | 95 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(92): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.1513-164A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 11/21 | chr3 | 49298799 | ||||||
| chr3:49298867
|
A | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0123 | 2 | HG02683.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1513-232T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 11/21 | chr3 | 49298867 | ||||||
| chr3:49299068
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1513-433G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 11/21 | chr3 | 49299068 | ||||||
| chr3:49299207
|
A | G | 4 | a0001c0003t0001g0175a0001c0003t0001g0204a0001c0003t0001g0205others(1): Show | 4 | HG02622.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1513-572T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 11/21 | chr3 | 49299207 | ||||||
| chr3:49299493
|
C | G | 55 | a0001c0001t0001g0150a0001c0001t0004g0211a0001c0001t0004g0212others(52): Show | 57 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1513-858G>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 11/21 | chr3 | 49299493 | ||||||
| chr3:49299497
|
A | G | 1 | a0001c0001t0001g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1513-862T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 11/21 | chr3 | 49299497 | ||||||
| chr3:49299538
|
G | A | 21 | a0001c0001t0001g0031a0001c0001t0001g0046a0001c0001t0001g0049others(18): Show | 21 | HG00597.hp1 HG00597.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1513-903C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 11/21 | chr3 | 49299538 | ||||||
| chr3:49299628
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | NA18954.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1512+839C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 11/21 | chr3 | 49299628 | ||||||
| chr3:49299653
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1512+814T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 11/21 | chr3 | 49299653 | ||||||
| chr3:49299687
|
C | T | 111 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.1512+780G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 11/21 | chr3 | 49299687 | ||||||
| chr3:49299688
|
G | A | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1512+779C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 11/21 | chr3 | 49299688 | ||||||
| chr3:49299708
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0117 | 2 | HG03688.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1512+759C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 11/21 | chr3 | 49299708 | ||||||
| chr3:49299838
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1512+629A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 11/21 | chr3 | 49299838 | ||||||
| chr3:49300108
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1512+359C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 11/21 | chr3 | 49300108 | ||||||
| chr3:49301032
|
G | A | 111 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.1288-341C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 10/21 | chr3 | 49301032 | ||||||
| chr3:49301450
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1288-759C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 10/21 | chr3 | 49301450 | ||||||
| chr3:49301550
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1287+834A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 10/21 | chr3 | 49301550 | ||||||
| chr3:49301559
|
G | A | 43 | a0001c0001t0001g0150a0001c0002t0001g0011a0001c0002t0001g0105others(40): Show | 45 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.1287+825C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 10/21 | chr3 | 49301559 | ||||||
| chr3:49301594
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1287+790T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 10/21 | chr3 | 49301594 | ||||||
| chr3:49301894
|
A | G | 2 | a0001c0003t0001g0197a0001c0003t0001g0200 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1287+490T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 10/21 | chr3 | 49301894 | ||||||
| chr3:49302014
|
T | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0002c0010t0001g0009 | 3 | HG02572.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1287+370A>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 10/21 | chr3 | 49302014 | ||||||
| chr3:49302088
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0002c0010t0001g0009 | 3 | HG02572.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1287+296G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 10/21 | chr3 | 49302088 | ||||||
| chr3:49302189
|
TA | T | 6 | a0001c0001t0001g0041a0001c0001t0001g0063a0001c0001t0001g0082others(3): Show | 6 | HG01256.hp2 HG01257.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287+194delT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 10/21 | chr3 | 49302189 | ||||||
| chr3:49302747
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1129-205C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49302747 | ||||||
| chr3:49302765
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1129-223C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49302765 | ||||||
| chr3:49303098
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1129-556C>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49303098 | ||||||
| chr3:49303168
|
C | T | 1 | a0001c0003t0001g0202 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1129-626G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49303168 | ||||||
| chr3:49303174
|
C | T | 2 | a0002c0007t0001g0109a0002c0007t0001g0110 | 2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1129-632G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49303174 | ||||||
| chr3:49303438
|
C | CA | 27 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0065others(24): Show | 27 | HG00544.hp2 HG00733.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1129-897dupT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49303438 | ||||||
| chr3:49303438
|
CA | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0073others(3): Show | 6 | HG01496.hp1 HG02451.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1129-897delT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49303438 | ||||||
| chr3:49303665
|
G | C | 1 | a0001c0001t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1129-1123C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49303665 | ||||||
| chr3:49303753
|
C | A | 1 | a0001c0001t0001g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1129-1211G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49303753 | ||||||
| chr3:49303839
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1129-1297C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49303839 | ||||||
| chr3:49304033
|
G | A | 4 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(1): Show | 4 | HG01081.hp2 HG01099.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1129-1491C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49304033 | ||||||
| chr3:49304722
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1128+993C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49304722 | ||||||
| chr3:49304755
|
T | TTTG | 3 | a0001c0001t0001g0048a0001c0001t0001g0126a0001c0002t0001g0183 | 3 | HG00544.hp1 NA18963.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1128+957_1128+959d others(5): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49304755 | ||||||
| chr3:49304911
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1128+804C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49304911 | ||||||
| chr3:49304984
|
G | A | 19 | a0001c0002t0001g0011a0001c0002t0001g0105a0001c0002t0003g0002others(16): Show | 21 | HG00639.hp2 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1128+731C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49304984 | ||||||
| chr3:49305005
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0193 | 3 | HG01175.hp2 HG01257.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1128+710C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305005 | ||||||
| chr3:49305065
|
T | TTTG | 3 | a0001c0001t0001g0024a0001c0001t0001g0078a0001c0001t0001g0121 | 3 | HG02055.hp2 HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1128+647_1128+649d others(5): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305065 | ||||||
| chr3:49305157
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1128+558G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305157 | ||||||
| chr3:49305249
|
T | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0073others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+466A>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305249 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1250): Show |
1 | a0001c0002t0001g0112 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1128+393_1128+394i others(1259): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1251): Show |
1 | a0001c0001t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1128+393_1128+394i others(1260): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1251): Show |
2 | a0001c0001t0004g0212a0001c0001t0004g0222 | 2 | HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1128+393_1128+394i others(1260): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1251): Show |
38 | a0001c0002t0001g0011a0001c0002t0001g0105a0001c0002t0001g0108others(35): Show | 40 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.1128+393_1128+394i others(1260): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1252): Show |
9 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0001t0004g0215others(6): Show | 9 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1128+393_1128+394i others(1261): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1252): Show |
3 | a0001c0002t0001g0140a0001c0002t0001g0146a0001c0002t0001g0184 | 3 | NA18951.hp2 NA18963.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1128+393_1128+394i others(1261): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1251): Show |
2 | a0001c0001t0001g0049a0001c0001t0001g0079 | 2 | HG00741.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1128+393_1128+394i others(1260): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1236): Show |
1 | a0001c0001t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1128+393_1128+394i others(1245): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1250): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0054a0001c0001t0001g0122 | 3 | HG02280.hp1 HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1128+393_1128+394i others(1259): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1251): Show |
1 | a0001c0001t0001g0030 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1128+393_1128+394i others(1260): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1251): Show |
4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0073others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+393_1128+394i others(1260): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1251): Show |
12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0023others(9): Show | 12 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.1128+393_1128+394i others(1260): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1251): Show |
76 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0016others(73): Show | 77 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1128+393_1128+394i others(1260): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1251): Show |
1 | a0001c0001t0001g0192 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1128+393_1128+394i others(1260): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1252): Show |
1 | a0001c0001t0001g0096 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1128+393_1128+394i others(1261): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1252): Show |
2 | a0001c0001t0001g0057a0001c0001t0001g0078 | 2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1128+393_1128+394i others(1261): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1252): Show |
15 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(12): Show | 15 | HG00735.hp1 HG01175.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.1128+393_1128+394i others(1261): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1256): Show |
1 | a0001c0001t0001g0087 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1128+393_1128+394i others(1265): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305321
|
G | GCCCGCCT others(1250): Show |
1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1128+393_1128+394i others(1259): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305321 | ||||||
| chr3:49305330
|
A | G | 28 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0154others(25): Show | 28 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.1128+385T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305330 | ||||||
| chr3:49305347
|
G | A | 174 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1128+368C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305347 | ||||||
| chr3:49305602
|
T | C | 1 | a0001c0001t0002g0119 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1128+113A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 9/21 | chr3 | 49305602 | ||||||
| chr3:49306007
|
A | G | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0073others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-119T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49306007 | ||||||
| chr3:49306024
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.955-136C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49306024 | ||||||
| chr3:49306045
|
G | A | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.955-157C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49306045 | ||||||
| chr3:49306123
|
TA | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0069others(3): Show | 6 | HG02055.hp1 HG02559.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.955-236delT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49306123 | ||||||
| chr3:49306168
|
T | G | 22 | a0001c0002t0001g0011a0001c0002t0001g0105a0001c0002t0001g0108others(19): Show | 24 | HG00639.hp2 HG00733.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.955-280A>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49306168 | ||||||
| chr3:49306201
|
T | G | 2 | a0001c0001t0001g0135a0001c0005t0001g0005 | 2 | HG00642.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.955-313A>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49306201 | ||||||
| chr3:49306210
|
G | GT | 13 | a0001c0001t0001g0171a0001c0001t0004g0211a0001c0001t0004g0212others(10): Show | 13 | HG01884.hp2 HG02027.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.955-323dupA | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49306210 | ||||||
| chr3:49306210
|
G | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0002t0001g0146 | 3 | HG02572.hp1 HG02922.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.955-322C>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49306210 | ||||||
| chr3:49306210
|
GT | G | 16 | a0001c0003t0001g0175a0001c0003t0001g0195a0001c0003t0001g0196others(13): Show | 16 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.955-323delA | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49306210 | ||||||
| chr3:49306818
|
C | G | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.955-930G>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49306818 | ||||||
| chr3:49306972
|
T | C | 10 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.955-1084A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49306972 | ||||||
| chr3:49307134
|
C | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0053 | 2 | NA18940.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.955-1246G>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49307134 | ||||||
| chr3:49307138
|
C | G | 1 | a0001c0001t0001g0021 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.955-1250G>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49307138 | ||||||
| chr3:49307455
|
T | A | 1 | a0005c0011t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.955-1567A>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49307455 | ||||||
| chr3:49307724
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.955-1836C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49307724 | ||||||
| chr3:49307779
|
C | CACAAA | 7 | a0001c0001t0004g0214a0001c0001t0004g0215a0001c0001t0004g0216others(4): Show | 7 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.955-1896_955-1892d others(7): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49307779 | ||||||
| chr3:49307779
|
CACAAAAC others(3): Show |
C | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.955-1901_955-1892d others(12): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49307779 | ||||||
| chr3:49308258
|
G | A | 1 | a0002c0010t0001g0009 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.954+2362C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49308258 | ||||||
| chr3:49308509
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0052 | 2 | NA19012.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.954+2111G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49308509 | ||||||
| chr3:49308520
|
T | C | 1 | a0001c0002t0001g0147 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.954+2100A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49308520 | ||||||
| chr3:49308697
|
T | C | 174 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.954+1923A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49308697 | ||||||
| chr3:49308717
|
A | G | 1 | a0001c0001t0008g0137 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.954+1903T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49308717 | ||||||
| chr3:49308729
|
G | A | 1 | a0005c0011t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.954+1891C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49308729 | ||||||
| chr3:49309033
|
C | CA | 46 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0073others(43): Show | 48 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.954+1586dupT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309033 | ||||||
| chr3:49309033
|
C | CAA | 7 | a0001c0002t0001g0108a0001c0002t0001g0111a0001c0002t0001g0113others(4): Show | 7 | HG00738.hp1 HG01081.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+1585_954+1586d others(4): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309033 | ||||||
| chr3:49309033
|
CA | C | 7 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0061others(4): Show | 7 | HG01167.hp1 HG01975.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+1586delT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309033 | ||||||
| chr3:49309370
|
T | C | 11 | a0001c0003t0001g0195a0001c0003t0001g0196a0001c0003t0001g0197others(8): Show | 11 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.954+1250A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309370 | ||||||
| chr3:49309464
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.954+1156G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309464 | ||||||
| chr3:49309528
|
T | A | 1 | a0001c0001t0001g0130 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.954+1092A>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309528 | ||||||
| chr3:49309547
|
C | T | 6 | a0001c0001t0002g0138a0001c0001t0002g0151a0001c0001t0002g0158others(3): Show | 6 | HG01069.hp2 HG01070.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.954+1073G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309547 | ||||||
| chr3:49309612
|
G | A | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.954+1008C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309612 | ||||||
| chr3:49309619
|
C | CT | 98 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(95): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.954+1000dupA | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309619 | ||||||
| chr3:49309619
|
C | CTT | 14 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0052others(11): Show | 14 | HG00544.hp2 HG00738.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.954+999_954+1000du others(3): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309619 | ||||||
| chr3:49309619
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.954+989_954+1000de others(13): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309619 | ||||||
| chr3:49309656
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.954+964G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309656 | ||||||
| chr3:49309714
|
T | C | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.954+906A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309714 | ||||||
| chr3:49309924
|
C | A | 174 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.954+696G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309924 | ||||||
| chr3:49309943
|
C | CTTTTTTT others(1): Show |
17 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0029others(14): Show | 17 | HG00099.hp1 HG01169.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.954+669_954+676dup others(8): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309943 | ||||||
| chr3:49309943
|
C | CTTTTTTT others(2): Show |
71 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(68): Show | 72 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.954+668_954+676dup others(9): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309943 | ||||||
| chr3:49309943
|
C | CTTTTTTT others(3): Show |
51 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0021others(48): Show | 53 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.954+667_954+676dup others(10): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309943 | ||||||
| chr3:49309943
|
C | CTTTTTTT others(4): Show |
23 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0087others(20): Show | 23 | HG00544.hp1 HG00733.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.954+666_954+676dup others(11): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309943 | ||||||
| chr3:49309943
|
C | CTTTTTTT others(5): Show |
9 | a0001c0002t0003g0098a0001c0003t0001g0195a0001c0003t0001g0197others(6): Show | 9 | HG01074.hp1 HG01243.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.954+665_954+676dup others(12): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309943 | ||||||
| chr3:49309943
|
C | CTTTTTTT others(6): Show |
15 | a0001c0001t0001g0135a0001c0001t0001g0155a0001c0001t0001g0156others(12): Show | 16 | HG01069.hp2 HG01516.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.954+664_954+676dup others(13): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309943 | ||||||
| chr3:49309943
|
C | CTTTTTTT others(7): Show |
8 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0203others(5): Show | 8 | HG01192.hp2 HG01981.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.954+663_954+676dup others(14): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309943 | ||||||
| chr3:49309943
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0154a0001c0001t0001g0173 | 2 | HG02451.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.954+662_954+676dup others(15): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309943 | ||||||
| chr3:49309943
|
C | CTTTTTTT others(9): Show |
3 | a0001c0001t0001g0134a0001c0001t0001g0171a0001c0001t0002g0138 | 3 | HG01070.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.954+661_954+676dup others(16): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309943 | ||||||
| chr3:49309943
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0002g0179 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.954+660_954+676dup others(17): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309943 | ||||||
| chr3:49309943
|
CTTTTT | C | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.954+672_954+676del others(5): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49309943 | ||||||
| chr3:49310308
|
A | C | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.954+312T>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 8/21 | chr3 | 49310308 | ||||||
| chr3:49310807
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.837-70C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 7/21 | chr3 | 49310807 | ||||||
| chr3:49311176
|
CG | C | 119 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.836+337delC | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 7/21 | chr3 | 49311176 | ||||||
| chr3:49311879
|
A | T | 1 | a0001c0001t0002g0119 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.696-225T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49311879 | ||||||
| chr3:49312011
|
G | C | 120 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.696-357C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49312011 | ||||||
| chr3:49312049
|
C | T | 8 | a0001c0001t0001g0054a0001c0002t0001g0111a0001c0002t0001g0112others(5): Show | 8 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.696-395G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49312049 | ||||||
| chr3:49312233
|
C | T | 2 | a0001c0001t0004g0212a0001c0001t0004g0213 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.696-579G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49312233 | ||||||
| chr3:49312248
|
C | T | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.696-594G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49312248 | ||||||
| chr3:49312414
|
G | A | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.696-760C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49312414 | ||||||
| chr3:49312458
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.696-804C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49312458 | ||||||
| chr3:49312460
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.696-806C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49312460 | ||||||
| chr3:49312600
|
A | C | 42 | a0001c0002t0001g0011a0001c0002t0001g0105a0001c0002t0001g0108others(39): Show | 44 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.696-946T>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49312600 | ||||||
| chr3:49312866
|
A | G | 10 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(7): Show | 10 | HG01109.hp1 HG01243.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.696-1212T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49312866 | ||||||
| chr3:49312867
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0002c0010t0001g0009 | 3 | HG02572.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.696-1213G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49312867 | ||||||
| chr3:49312976
|
C | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0073others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1322G>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49312976 | ||||||
| chr3:49313185
|
C | A | 1 | a0001c0001t0001g0027 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.696-1531G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49313185 | ||||||
| chr3:49314103
|
A | T | 1 | a0001c0001t0001g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.696-2449T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49314103 | ||||||
| chr3:49314159
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.696-2505C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49314159 | ||||||
| chr3:49314497
|
A | T | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.696-2843T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49314497 | ||||||
| chr3:49314549
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.696-2895T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49314549 | ||||||
| chr3:49314794
|
G | A | 2 | a0001c0005t0001g0001a0001c0005t0001g0005 | 3 | HG00642.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.696-3140C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49314794 | ||||||
| chr3:49314848
|
G | C | 1 | a0005c0011t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.696-3194C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49314848 | ||||||
| chr3:49315045
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.696-3391G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49315045 | ||||||
| chr3:49315089
|
A | T | 192 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(189): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.696-3435T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49315089 | ||||||
| chr3:49315104
|
A | T | 4 | a0001c0001t0001g0203a0001c0003t0001g0204a0001c0003t0001g0205others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-3450T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49315104 | ||||||
| chr3:49315186
|
T | C | 55 | a0001c0001t0001g0150a0001c0001t0004g0211a0001c0001t0004g0212others(52): Show | 57 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.696-3532A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49315186 | ||||||
| chr3:49315218
|
C | T | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.696-3564G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49315218 | ||||||
| chr3:49315571
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.696-3917A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49315571 | ||||||
| chr3:49315628
|
A | G | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.696-3974T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49315628 | ||||||
| chr3:49315681
|
T | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0073others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.696-4027A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49315681 | ||||||
| chr3:49315715
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.696-4061C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49315715 | ||||||
| chr3:49315768
|
A | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0190 | 2 | NA18995.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.696-4114T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49315768 | ||||||
| chr3:49316009
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.696-4355C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49316009 | ||||||
| chr3:49316077
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.696-4423G>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49316077 | ||||||
| chr3:49316184
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.696-4530C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49316184 | ||||||
| chr3:49316285
|
ATTTAAC | A | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.696-4637_696-4632d others(8): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49316285 | ||||||
| chr3:49316469
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0054 | 2 | HG02280.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.696-4815C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49316469 | ||||||
| chr3:49317018
|
T | C | 1 | a0001c0002t0001g0147 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.696-5364A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49317018 | ||||||
| chr3:49317289
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.696-5635C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49317289 | ||||||
| chr3:49317297
|
A | G | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.696-5643T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49317297 | ||||||
| chr3:49317327
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.696-5673G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49317327 | ||||||
| chr3:49317447
|
T | A | 2 | a0002c0007t0001g0109a0002c0007t0001g0110 | 2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.696-5793A>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49317447 | ||||||
| chr3:49317542
|
GT | G | 169 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(166): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.696-5889delA | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49317542 | ||||||
| chr3:49317546
|
T | G | 1 | a0001c0001t0001g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.696-5892A>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49317546 | ||||||
| chr3:49317547
|
T | G | 7 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0086others(4): Show | 8 | HG01256.hp1 HG01258.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.696-5893A>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49317547 | ||||||
| chr3:49317572
|
T | C | 61 | a0001c0001t0001g0150a0001c0001t0001g0154a0001c0001t0001g0171others(58): Show | 63 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.696-5918A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49317572 | ||||||
| chr3:49317708
|
G | GT | 6 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0035others(3): Show | 6 | HG02145.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-6055dupA | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49317708 | ||||||
| chr3:49317941
|
G | T | 200 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(197): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.696-6287C>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49317941 | ||||||
| chr3:49318605
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0002g0181 | 2 | HG01167.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.695+6097T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49318605 | ||||||
| chr3:49318825
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.695+5877C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49318825 | ||||||
| chr3:49318909
|
C | CA | 7 | a0001c0001t0001g0194a0001c0001t0002g0162a0001c0001t0002g0163others(4): Show | 7 | HG00140.hp2 HG02145.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.695+5792dupT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49318909 | ||||||
| chr3:49319141
|
CA | C | 24 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0023others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.695+5560delT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49319141 | ||||||
| chr3:49319144
|
A | G | 35 | a0001c0001t0001g0150a0001c0002t0001g0011a0001c0002t0001g0105others(32): Show | 37 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.695+5558T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49319144 | ||||||
| chr3:49319145
|
A | G | 8 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(5): Show | 8 | HG00738.hp1 HG01081.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.695+5557T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49319145 | ||||||
| chr3:49319238
|
C | T | 119 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.695+5464G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49319238 | ||||||
| chr3:49319268
|
A | G | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.695+5434T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49319268 | ||||||
| chr3:49319452
|
T | G | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.695+5250A>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49319452 | ||||||
| chr3:49319599
|
A | ATGTT | 210 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(207): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.695+5099_695+5102d others(6): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49319599 | ||||||
| chr3:49319599
|
A | ATGTTTGT others(1): Show |
3 | a0001c0001t0001g0156a0001c0001t0001g0174a0001c0001t0001g0190 | 3 | HG03098.hp1 NA18995.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.695+5095_695+5102d others(10): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49319599 | ||||||
| chr3:49319654
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.695+5048G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49319654 | ||||||
| chr3:49319881
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0002c0010t0001g0009 | 3 | HG02572.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.695+4821C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49319881 | ||||||
| chr3:49319994
|
A | G | 174 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.695+4708T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49319994 | ||||||
| chr3:49320066
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0002c0010t0001g0009 | 3 | HG02572.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.695+4636C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49320066 | ||||||
| chr3:49320423
|
C | T | 1 | a0001c0003t0001g0196 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.695+4279G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49320423 | ||||||
| chr3:49320447
|
A | AAAAAAG | 174 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.695+4249_695+4254d others(8): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49320447 | ||||||
| chr3:49320658
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0073others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.695+4044C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49320658 | ||||||
| chr3:49320703
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.695+3999A>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49320703 | ||||||
| chr3:49320814
|
A | G | 1 | a0005c0011t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.695+3888T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49320814 | ||||||
| chr3:49321116
|
G | GTCAGAAA others(6): Show |
2 | a0001c0001t0001g0079a0001c0001t0001g0087 | 2 | HG00741.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.695+3573_695+3585d others(15): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49321116 | ||||||
| chr3:49321213
|
G | A | 55 | a0001c0001t0001g0150a0001c0001t0004g0211a0001c0001t0004g0212others(52): Show | 57 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.695+3489C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49321213 | ||||||
| chr3:49321669
|
A | G | 49 | a0001c0001t0001g0150a0001c0001t0001g0154a0001c0001t0001g0171others(46): Show | 51 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.695+3033T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49321669 | ||||||
| chr3:49321719
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.695+2983G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49321719 | ||||||
| chr3:49321755
|
A | G | 1 | a0001c0003t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.695+2947T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49321755 | ||||||
| chr3:49321825
|
C | T | 6 | a0001c0001t0001g0154a0001c0001t0001g0171a0001c0001t0001g0172others(3): Show | 6 | HG02451.hp1 HG02486.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.695+2877G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49321825 | ||||||
| chr3:49322510
|
T | C | 42 | a0001c0002t0001g0011a0001c0002t0001g0105a0001c0002t0001g0108others(39): Show | 44 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.695+2192A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49322510 | ||||||
| chr3:49322706
|
C | T | 15 | a0001c0001t0001g0203a0001c0003t0001g0195a0001c0003t0001g0196others(12): Show | 15 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.695+1996G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49322706 | ||||||
| chr3:49322787
|
A | AG | 221 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(218): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.695+1914dupC | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49322787 | ||||||
| chr3:49323009
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.695+1693G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49323009 | ||||||
| chr3:49323270
|
T | A | 1 | a0001c0001t0001g0085 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.695+1432A>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49323270 | ||||||
| chr3:49323271
|
T | TA | 26 | a0001c0001t0001g0024a0001c0001t0001g0052a0001c0001t0001g0053others(23): Show | 26 | HG00642.hp2 HG00738.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.695+1430dupT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49323271 | ||||||
| chr3:49323271
|
TA | T | 45 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0072others(42): Show | 47 | HG00544.hp1 HG00597.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.695+1430delT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49323271 | ||||||
| chr3:49323271
|
TAA | T | 10 | a0001c0001t0004g0212a0001c0001t0004g0214a0001c0001t0004g0215others(7): Show | 10 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.695+1429_695+1430d others(4): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49323271 | ||||||
| chr3:49323271
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.695+1421_695+1430d others(12): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49323271 | ||||||
| chr3:49323271
|
TAAAAAAA others(5): Show |
T | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0002c0010t0001g0009 | 3 | HG02572.hp1 HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.695+1419_695+1430d others(14): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49323271 | ||||||
| chr3:49323272
|
A | T | 1 | a0001c0001t0001g0032 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.695+1430T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49323272 | ||||||
| chr3:49323297
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.695+1405T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49323297 | ||||||
| chr3:49323357
|
C | A | 1 | a0001c0001t0001g0173 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.695+1345G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49323357 | ||||||
| chr3:49323826
|
C | T | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.695+876G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49323826 | ||||||
| chr3:49323891
|
C | A | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.695+811G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49323891 | ||||||
| chr3:49324358
|
A | G | 77 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(74): Show | 78 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.695+344T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 6/21 | chr3 | 49324358 | ||||||
| chr3:49325085
|
G | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0174 | 2 | HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.488-46C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 4/21 | chr3 | 49325085 | ||||||
| chr3:49325251
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.488-212C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 4/21 | chr3 | 49325251 | ||||||
| chr3:49325354
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.488-315G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 4/21 | chr3 | 49325354 | ||||||
| chr3:49325459
|
A | G | 119 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.487+260T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 4/21 | chr3 | 49325459 | ||||||
| chr3:49325631
|
A | G | 7 | a0001c0001t0001g0150a0001c0001t0001g0154a0001c0001t0001g0171others(4): Show | 7 | HG02451.hp1 HG02486.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.487+88T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 4/21 | chr3 | 49325631 | ||||||
| chr3:49325898
|
T | C | 1 | a0001c0001t0006g0153 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.361-53A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49325898 | ||||||
| chr3:49326055
|
G | A | 2 | a0001c0001t0001g0176a0001c0003t0001g0175 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.361-210C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49326055 | ||||||
| chr3:49326159
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG00639.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.361-314T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49326159 | ||||||
| chr3:49326318
|
C | T | 2 | a0001c0001t0005g0067a0001c0001t0005g0068 | 2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.361-473G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49326318 | ||||||
| chr3:49326326
|
A | T | 119 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.361-481T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49326326 | ||||||
| chr3:49326328
|
T | A | 2 | a0001c0003t0001g0202a0005c0011t0001g0208 | 2 | HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.361-483A>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49326328 | ||||||
| chr3:49326337
|
A | T | 37 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0031others(34): Show | 37 | HG00597.hp1 HG00639.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.361-492T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49326337 | ||||||
| chr3:49326339
|
T | A | 44 | a0001c0001t0001g0150a0001c0002t0001g0011a0001c0002t0001g0105others(41): Show | 46 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.361-494A>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49326339 | ||||||
| chr3:49326616
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.361-771G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49326616 | ||||||
| chr3:49326707
|
C | CT | 109 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(106): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.361-863dupA | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49326707 | ||||||
| chr3:49326751
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.361-906G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49326751 | ||||||
| chr3:49326826
|
C | T | 18 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0203others(15): Show | 18 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.360+860G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49326826 | ||||||
| chr3:49327067
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.360+619T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49327067 | ||||||
| chr3:49327163
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.360+523A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49327163 | ||||||
| chr3:49327397
|
G | A | 111 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.360+289C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49327397 | ||||||
| chr3:49327435
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.360+251G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 3/21 | chr3 | 49327435 | ||||||
| chr3:49327836
|
C | T | 110 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(107): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.230-20G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49327836 | ||||||
| chr3:49328108
|
T | TCC | 12 | a0001c0001t0004g0211a0001c0001t0004g0212a0001c0001t0004g0213others(9): Show | 12 | HG01884.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.230-293_230-292ins others(2): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49328108 | ||||||
| chr3:49328155
|
T | G | 2 | a0001c0001t0004g0212a0001c0001t0004g0213 | 2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.230-339A>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49328155 | ||||||
| chr3:49328168
|
G | A | 1 | a0001c0001t0004g0219 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.230-352C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49328168 | ||||||
| chr3:49328215
|
G | A | 4 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0139others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.230-399C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49328215 | ||||||
| chr3:49328314
|
C | T | 1 | a0001c0001t0004g0213 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.230-498G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49328314 | ||||||
| chr3:49328408
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.230-592C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49328408 | ||||||
| chr3:49328577
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.230-761T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49328577 | ||||||
| chr3:49328644
|
G | T | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.230-828C>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49328644 | ||||||
| chr3:49329215
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.230-1399G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49329215 | ||||||
| chr3:49329299
|
C | T | 1 | a0001c0001t0004g0222 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.230-1483G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49329299 | ||||||
| chr3:49329308
|
G | C | 55 | a0001c0001t0001g0150a0001c0001t0004g0211a0001c0001t0004g0212others(52): Show | 57 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.230-1492C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49329308 | ||||||
| chr3:49329396
|
G | T | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0073others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.230-1580C>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49329396 | ||||||
| chr3:49329638
|
G | A | 2 | a0003c0006t0002g0004a0003c0006t0002g0157 | 3 | HG01516.hp2 HG01517.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.230-1822C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49329638 | ||||||
| chr3:49329673
|
T | A | 1 | a0001c0002t0001g0147 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.230-1857A>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49329673 | ||||||
| chr3:49330087
|
C | G | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.230-2271G>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49330087 | ||||||
| chr3:49330171
|
A | AAAAC | 182 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.230-2359_230-2356d others(6): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49330171 | ||||||
| chr3:49330171
|
AAAACAAA others(5): Show |
A | 2 | a0001c0001t0001g0091a0001c0001t0008g0137 | 2 | HG02027.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.230-2367_230-2356d others(14): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49330171 | ||||||
| chr3:49330335
|
C | CT | 11 | a0001c0003t0001g0195a0001c0003t0001g0196a0001c0003t0001g0197others(8): Show | 11 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.230-2520dupA | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49330335 | ||||||
| chr3:49330388
|
C | T | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.230-2572G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49330388 | ||||||
| chr3:49330573
|
C | T | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.230-2757G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49330573 | ||||||
| chr3:49330884
|
A | G | 174 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.230-3068T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49330884 | ||||||
| chr3:49330932
|
C | G | 1 | a0001c0002t0001g0147 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.230-3116G>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49330932 | ||||||
| chr3:49330933
|
G | C | 1 | a0001c0002t0001g0147 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.230-3117C>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49330933 | ||||||
| chr3:49331030
|
A | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027 | 3 | HG01975.hp2 NA19003.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.230-3214T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49331030 | ||||||
| chr3:49331048
|
G | A | 1 | a0001c0001t0004g0220 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.230-3232C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49331048 | ||||||
| chr3:49331088
|
G | A | 119 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.230-3272C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49331088 | ||||||
| chr3:49331146
|
C | A | 1 | a0001c0003t0001g0207 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.230-3330G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49331146 | ||||||
| chr3:49331319
|
CA | C | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.230-3504delT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49331319 | ||||||
| chr3:49331320
|
A | AAAAAAAA others(8097): Show |
1 | a0001c0003t0001g0209 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.230-3505_230-3504i others(8106): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49331320 | ||||||
| chr3:49331455
|
T | C | 3 | a0001c0002t0001g0108a0002c0007t0001g0109a0002c0007t0001g0110 | 3 | HG02886.hp2 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.230-3639A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49331455 | ||||||
| chr3:49331473
|
T | C | 2 | a0002c0007t0001g0109a0002c0007t0001g0110 | 2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.230-3657A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49331473 | ||||||
| chr3:49331777
|
A | G | 12 | a0001c0001t0004g0211a0001c0001t0004g0212a0001c0001t0004g0213others(9): Show | 12 | HG01884.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.229+3692T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49331777 | ||||||
| chr3:49331950
|
C | T | 192 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(189): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.229+3519G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49331950 | ||||||
| chr3:49331969
|
C | CA | 56 | a0001c0001t0001g0017a0001c0001t0001g0070a0001c0001t0001g0092others(53): Show | 58 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.229+3499dupT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49331969 | ||||||
| chr3:49331985
|
A | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0078others(1): Show | 4 | HG02055.hp2 HG02698.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+3484T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49331985 | ||||||
| chr3:49332070
|
C | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0120 | 3 | HG02559.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.229+3399G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49332070 | ||||||
| chr3:49332102
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.229+3367C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49332102 | ||||||
| chr3:49332110
|
T | C | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.229+3359A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49332110 | ||||||
| chr3:49332350
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.229+3119G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49332350 | ||||||
| chr3:49332451
|
C | CA | 12 | a0001c0001t0001g0176a0001c0001t0004g0212a0001c0001t0004g0213others(9): Show | 12 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.229+3017dupT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49332451 | ||||||
| chr3:49332477
|
G | A | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.229+2992C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49332477 | ||||||
| chr3:49332514
|
T | C | 7 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(4): Show | 7 | HG00738.hp1 HG01081.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.229+2955A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49332514 | ||||||
| chr3:49332525
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.229+2944G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49332525 | ||||||
| chr3:49332624
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.229+2845C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49332624 | ||||||
| chr3:49332703
|
T | A | 1 | a0001c0001t0002g0170 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.229+2766A>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49332703 | ||||||
| chr3:49332764
|
T | G | 1 | a0001c0001t0002g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.229+2705A>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49332764 | ||||||
| chr3:49333052
|
C | A | 1 | a0001c0001t0001g0096 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.229+2417G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49333052 | ||||||
| chr3:49333064
|
T | A | 1 | a0001c0001t0004g0221 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.229+2405A>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49333064 | ||||||
| chr3:49333111
|
C | G | 210 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(207): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.229+2358G>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49333111 | ||||||
| chr3:49333144
|
CTTTT | C | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.229+2321_229+2324d others(6): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49333144 | ||||||
| chr3:49334252
|
A | T | 11 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(8): Show | 11 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.229+1217T>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49334252 | ||||||
| chr3:49334740
|
C | G | 1 | a0001c0001t0001g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.229+729G>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49334740 | ||||||
| chr3:49334890
|
A | C | 1 | a0001c0003t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.229+579T>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49334890 | ||||||
| chr3:49334961
|
G | T | 1 | a0001c0001t0001g0072 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.229+508C>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49334961 | ||||||
| chr3:49335294
|
G | T | 1 | a0001c0001t0001g0019 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.229+175C>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49335294 | ||||||
| chr3:49335419
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.229+50T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 2/21 | chr3 | 49335419 | ||||||
| chr3:49335612
|
A | G | 42 | a0001c0002t0001g0011a0001c0002t0001g0105a0001c0002t0001g0108others(39): Show | 44 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.102-16T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49335612 | ||||||
| chr3:49335663
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.102-67A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49335663 | ||||||
| chr3:49335845
|
A | C | 1 | a0001c0001t0006g0153 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.102-249T>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49335845 | ||||||
| chr3:49335862
|
GTCTT | G | 2 | a0001c0001t0001g0071a0001c0002t0001g0115 | 2 | HG01258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.102-270_102-267del others(4): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49335862 | ||||||
| chr3:49335903
|
G | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0130a0001c0001t0001g0131others(3): Show | 6 | HG01934.hp2 HG02109.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.102-307C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49335903 | ||||||
| chr3:49336165
|
C | CT | 123 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(120): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.102-570dupA | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49336165 | ||||||
| chr3:49336165
|
C | CTT | 48 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 50 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.102-571_102-570dup others(2): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49336165 | ||||||
| chr3:49336531
|
CT | C | 20 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(17): Show | 20 | HG00639.hp1 HG00741.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.102-936delA | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49336531 | ||||||
| chr3:49336719
|
T | C | 2 | a0001c0001t0002g0138a0001c0001t0002g0179 | 2 | HG01070.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.102-1123A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49336719 | ||||||
| chr3:49336817
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG00099.hp2 HG00140.hp1 |
intron_variant | MODIFIER | c.102-1221G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49336817 | ||||||
| chr3:49337465
|
G | A | 5 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-1869C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49337465 | ||||||
| chr3:49337631
|
C | CTTGCTAT others(19): Show |
1 | a0001c0002t0001g0189 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.102-2036_102-2035i others(28): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49337631 | ||||||
| chr3:49337830
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.101+2094C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49337830 | ||||||
| chr3:49337898
|
T | C | 2 | a0001c0001t0002g0181a0001c0001t0004g0211 | 2 | HG01884.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.101+2026A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49337898 | ||||||
| chr3:49337916
|
C | G | 43 | a0001c0001t0001g0150a0001c0002t0001g0011a0001c0002t0001g0105others(40): Show | 45 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.101+2008G>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49337916 | ||||||
| chr3:49338032
|
G | A | 1 | a0001c0001t0002g0169 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.101+1892C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49338032 | ||||||
| chr3:49338044
|
C | CA | 13 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(10): Show | 13 | HG01175.hp1 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.101+1879dupT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49338044 | ||||||
| chr3:49338044
|
CA | C | 66 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(63): Show | 68 | HG00544.hp1 HG00639.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.101+1879delT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49338044 | ||||||
| chr3:49338044
|
CAA | C | 97 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(94): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.101+1878_101+1879d others(4): Show |
USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49338044 | ||||||
| chr3:49338113
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.101+1811C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49338113 | ||||||
| chr3:49338440
|
C | T | 1 | a0001c0001t0004g0211 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.101+1484G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49338440 | ||||||
| chr3:49338662
|
C | CA | 13 | a0001c0001t0001g0180a0001c0001t0001g0190a0001c0001t0001g0191others(10): Show | 13 | HG00544.hp1 HG02735.hp1 NA18940.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+1261dupT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49338662 | ||||||
| chr3:49338662
|
CA | C | 12 | a0001c0001t0004g0211a0001c0001t0004g0212a0001c0001t0004g0213others(9): Show | 12 | HG01884.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.101+1261delT | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49338662 | ||||||
| chr3:49338675
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG02280.hp1 HG02572.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.101+1249T>C | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49338675 | ||||||
| chr3:49338878
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.101+1046A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49338878 | ||||||
| chr3:49338973
|
C | T | 2 | a0001c0005t0001g0001a0001c0005t0001g0005 | 3 | HG00642.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.101+951G>A | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49338973 | ||||||
| chr3:49339115
|
C | A | 1 | a0001c0001t0004g0222 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.101+809G>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49339115 | ||||||
| chr3:49339624
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.101+300C>T | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49339624 | ||||||
| chr3:49339780
|
T | C | 16 | a0001c0001t0001g0203a0001c0003t0001g0195a0001c0003t0001g0196others(13): Show | 16 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.101+144A>G | USP4 | ENSG00000114316.13 | transcript | ENST00000265560.9 | protein_coding | 1/21 | chr3 | 49339780 |