Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4591 |
|---|---|
| ensemblid | ENSG00000108395.14 |
| hgncid | 7523 |
| symbol | TRIM37 |
| name | tripartite motif containing 37 |
| refseq_nuc | NM_015294.6 |
| refseq_prot | NP_056109.1 |
| ensembl_nuc | ENST00000262294.12 |
| ensembl_prot | ENSP00000262294.7 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 58998202 |
| end | 59106880 |
| strand | - |
| ver | v1.2 |
| region | chr17:58998202-59106880 |
| region5000 | chr17:58993202-59111880 |
| regionname0 | TRIM37_chr17_58998202_59106880 |
| regionname5000 | TRIM37_chr17_58993202_59111880 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 964 | 333 | 85 | 64 | 139 | 12 | 31 | 110 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0002 | 0/0 | 964 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0003 | 0/0 | 964 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0004 | 0/0 | 964 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0005 | 0/0 | 964 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0006 | 0/0 | 964 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2895 | 327 | 84 | 63 | 138 | 10 | 30 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| c0002 | 0/0 | 2895 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| c0003 | 0/0 | 2895 | 4 | 0 | 1 | 0 | 2 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| c0004 | 0/0 | 2895 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| c0005 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| c0006 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| c0007 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| c0008 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| c0009 | 0/0 | 2895 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1595 | 118 | 16 | 31 | 58 | 2 | 9 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0002 | 0/0 | 1595 | 100 | 23 | 18 | 41 | 5 | 13 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0003 | 0/0 | 1595 | 92 | 39 | 14 | 31 | 2 | 6 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0004 | 0/0 | 1594 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0005 | 0/0 | 1595 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0006 | 0/0 | 1595 | 4 | 0 | 1 | 0 | 2 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0007 | 0/0 | 1595 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0008 | 0/0 | 1595 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0009 | 0/0 | 1595 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0010 | 0/0 | 1595 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0011 | 0/0 | 1595 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0012 | 0/0 | 1595 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0013 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0014 | 0/0 | 1595 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0015 | 0/0 | 1595 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0016 | 0/0 | 1595 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0017 | 0/0 | 1595 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| t0018 | 0/0 | 1595 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0268 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0307 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2895 | 327 | 84 | 63 | 138 | 10 | 30 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0003 | 0/0 | 2895 | 4 | 0 | 1 | 0 | 2 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0006 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0008 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0002c0002 | 0/0 | 2895 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0003c0009 | 0/0 | 2895 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0004c0005 | 0/0 | 2895 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0005c0007 | 0/0 | 2895 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0006c0004 | 0/0 | 2895 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4489 | 117 | 16 | 30 | 58 | 2 | 9 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0002 | 0/0 | 4489 | 93 | 19 | 17 | 40 | 5 | 12 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0003 | 0/0 | 4489 | 89 | 37 | 14 | 30 | 2 | 6 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0004 | 0/0 | 4488 | 4 | 4 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0005 | 0/0 | 4489 | 4 | 0 | 0 | 4 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0007 | 0/0 | 4489 | 4 | 3 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0008 | 0/0 | 4489 | 3 | 0 | 0 | 3 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0009 | 0/0 | 4489 | 3 | 2 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0010 | 0/0 | 4489 | 2 | 2 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0011 | 0/0 | 4489 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0012 | 0/0 | 4489 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0013 | 0/0 | 4514 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0014 | 0/0 | 4489 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0015 | 0/0 | 4489 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0016 | 0/0 | 4489 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0017 | 0/0 | 4489 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0001t0018 | 0/0 | 4489 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0003t0006 | 0/0 | 4489 | 4 | 0 | 1 | 0 | 2 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0006t0003 | 0/0 | 4489 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0001c0008t0003 | 0/0 | 4489 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0002c0002t0002 | 0/0 | 4489 | 5 | 4 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0003c0009t0001 | 0/0 | 4489 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0004c0005t0003 | 0/0 | 4489 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0005c0007t0002 | 0/0 | 4489 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| a0006c0004t0002 | 0/0 | 4489 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | copy fasta | chr17 | 58993202 | 59111880 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0268 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0307 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0008g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0009g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0009g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0010g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0012g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0013g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0014g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0015g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0016g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0017g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0001t0018g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0003t0006g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0003t0006g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0003t0006g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0003t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0006t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0001c0008t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0002c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0002c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0002c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0003c0009t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0004c0005t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0005c0007t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| a0006c0004t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0211 | EUR | GBR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | GBR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | FIN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0015 | EUR | FIN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0165 | EUR | FIN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0300 | EUR | FIN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00597 | hp1 | a0005 | c0007 | t0002 | g0179 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00642 | hp1 | a0003 | c0009 | t0001 | g0294 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00642 | hp2 | a0001 | c0003 | t0006 | g0219 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0216 | AMR | PUR | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0161 | EUR | IBS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01515 | hp2 | a0001 | c0001 | t0012 | g0002 | EUR | IBS | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0207 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CDX | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | CDX | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0105 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02293 | hp1 | a0001 | c0001 | t0009 | g0169 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0167 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02615 | hp2 | a0002 | c0002 | t0002 | g0208 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02723 | hp1 | a0001 | c0001 | t0018 | g0342 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0182 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02735 | hp1 | a0001 | c0001 | t0017 | g0341 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0206 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02965 | hp2 | a0001 | c0006 | t0003 | g0106 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03017 | hp1 | a0001 | c0001 | t0013 | g0029 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0067 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0125 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03209 | hp2 | a0004 | c0005 | t0003 | g0084 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03516 | hp1 | a0001 | c0001 | t0010 | g0089 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | ESN | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0215 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03654 | hp1 | a0001 | c0001 | t0011 | g0001 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03704 | hp2 | a0001 | c0003 | t0006 | g0212 | SAS | PJL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03927 | hp2 | a0006 | c0004 | t0002 | g0144 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | BEB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0048 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | YRI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18522 | hp2 | a0001 | c0001 | t0007 | g0214 | AFR | YRI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | CHB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | CHB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | YRI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | YRI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0043 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18949 | hp2 | a0001 | c0001 | t0015 | g0332 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19006 | hp2 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0205 | AFR | LWK | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | LWK | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19055 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19056 | hp2 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19062 | hp2 | a0001 | c0001 | t0016 | g0236 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19064 | hp1 | a0001 | c0008 | t0003 | g0039 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19068 | hp2 | a0001 | c0001 | t0008 | g0032 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19084 | hp1 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | YRI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | YRI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ASW | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | ASW | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20752 | hp1 | a0001 | c0003 | t0006 | g0218 | EUR | TSI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0158 | EUR | TSI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20805 | hp1 | a0001 | c0003 | t0006 | g0217 | EUR | TSI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0168 | EUR | TSI | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | GIH | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | GIH | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02109 | hp1 | a0001 | c0001 | t0010 | g0078 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0213 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | MSL | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | USA | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0090 | AFR | USA | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18955 | hp1 | a0001 | c0001 | t0014 | g0271 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0071 | AFR | USA | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | USA | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | LWK | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | LWK | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0268 | REF | REF | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0307 | REF | REF | TRIM37_chr17_58993202_59111880 | TRIM37 | chr17 | 58993202 | 59111880 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59015674
|
C | T | 1 | a0002 | 5 | HG01952.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
missense_variant | MODERATE | c.2512G>A | p.Val838Ile | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/24 | 2931/4489 | 2512/2895 | 838/964 | chr17 | 59015674 | ||
| chr17:59041818
|
G | T | 1 | a0004 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1748C>A | p.Pro583His | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/24 | 2167/4489 | 1748/2895 | 583/964 | chr17 | 59041818 | ||
| chr17:59041827
|
G | A | 1 | a0005 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.1739C>T | p.Ala580Val | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/24 | 2158/4489 | 1739/2895 | 580/964 | chr17 | 59041827 | ||
| chr17:59041842
|
A | G | 1 | a0006 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.1724T>C | p.Met575Thr | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/24 | 2143/4489 | 1724/2895 | 575/964 | chr17 | 59041842 | ||
| chr17:59079795
|
C | A | 1 | a0003 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.575G>T | p.Arg192Leu | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/24 | 994/4489 | 575/2895 | 192/964 | chr17 | 59079795 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59028623
|
G | A | 1 | a0001c0006 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.2049C>T | p.Ala683Ala | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/24 | 2468/4489 | 2049/2895 | 683/964 | chr17 | 59028623 | ||
| chr17:59049378
|
G | A | 1 | a0001c0008 | 1 | NA19064.hp1 | synonymous_variant | LOW | c.1330C>T | p.Leu444Leu | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/24 | 1749/4489 | 1330/2895 | 444/964 | chr17 | 59049378 | ||
| chr17:59051264
|
A | G | 1 | a0001c0003 | 4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
synonymous_variant | LOW | c.1264T>C | p.Leu422Leu | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/24 | 1683/4489 | 1264/2895 | 422/964 | chr17 | 59051264 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:58998347
|
A | G | 1 | a0001c0001t0014 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1030T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 1030 | chr17 | 58998347 | |||||
| chr17:58998399
|
TG | T | 1 | a0001c0001t0004 | 4 | HG03516.hp2 HG06807.hp2 NA18906.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*977delC | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 977 | chr17 | 58998399 | |||||
| chr17:58998416
|
T | C | 1 | a0001c0001t0008 | 3 | NA19056.hp2 NA19068.hp2 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*961A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 961 | chr17 | 58998416 | |||||
| chr17:58998541
|
T | C | 1 | a0001c0001t0005 | 4 | NA18945.hp1 NA19006.hp2 NA19007.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*836A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 836 | chr17 | 58998541 | |||||
| chr17:58998618
|
A | G | 1 | a0001c0001t0009 | 3 | HG02293.hp1 HG02572.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*759T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 759 | chr17 | 58998618 | |||||
| chr17:58998628
|
C | CACTACAG others(18): Show |
1 | a0001c0001t0013 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*724_*748dupCTGCCT others(19): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 748 | chr17 | 58998628 | |||||
| chr17:58998743
|
T | A | 7 | a0001c0001t0002a0001c0001t0009a0001c0001t0011others(4): Show | 105 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*634A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 634 | chr17 | 58998743 | |||||
| chr17:58998954
|
C | A | 1 | a0001c0001t0016 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*423G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 423 | chr17 | 58998954 | |||||
| chr17:58999004
|
T | C | 1 | a0001c0001t0007 | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*373A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 373 | chr17 | 58999004 | |||||
| chr17:58999100
|
C | T | 1 | a0001c0001t0010 | 2 | HG02109.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*277G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 24/24 | 277 | chr17 | 58999100 | |||||
| chr17:59106596
|
C | G | 1 | a0001c0001t0012 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-135G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/24 | 135 | chr17 | 59106596 | |||||
| chr17:59106685
|
T | C | 2 | a0001c0001t0007a0001c0003t0006 | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-224A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/24 | chr17 | 59106685 | ||||||
| chr17:59106697
|
T | C | 1 | a0001c0001t0017 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-236A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/24 | 236 | chr17 | 59106697 | |||||
| chr17:59106706
|
C | T | 1 | a0001c0001t0011 | 1 | HG03654.hp1 | 5_prime_UTR_variant | MODIFIER | c.-245G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/24 | 245 | chr17 | 59106706 | |||||
| chr17:59106801
|
A | C | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(15): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(216): Show |
5_prime_UTR_variant | MODIFIER | c.-340T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/24 | 340 | chr17 | 59106801 | |||||
| chr17:59106871
|
G | A | 1 | a0001c0001t0018 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-410C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/24 | 410 | chr17 | 59106871 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:58999491
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2813-32T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 58999491 | ||||||
| chr17:58999532
|
T | A | 112 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(109): Show | 112 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.2813-73A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 58999532 | ||||||
| chr17:58999640
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2813-181G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 58999640 | ||||||
| chr17:59000389
|
C | A | 1 | a0001c0001t0001g0308 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2813-930G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59000389 | ||||||
| chr17:59000391
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2813-932C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59000391 | ||||||
| chr17:59000453
|
TAGCTGGA others(9): Show |
T | 1 | a0001c0001t0003g0060 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2813-1010_2813-995 others(19): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59000453 | ||||||
| chr17:59000547
|
G | A | 4 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2812+1051C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59000547 | ||||||
| chr17:59000799
|
G | GA | 21 | a0001c0001t0001g0223a0001c0001t0001g0242a0001c0001t0001g0274others(18): Show | 21 | HG00438.hp1 HG00438.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.2812+798dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59000799 | ||||||
| chr17:59001092
|
G | C | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2812+506C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001092 | ||||||
| chr17:59001156
|
C | T | 2 | a0001c0001t0003g0087a0001c0001t0003g0088 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2812+442G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001156 | ||||||
| chr17:59001199
|
C | CAA | 9 | a0001c0001t0003g0105a0001c0001t0007g0213a0001c0001t0007g0214others(6): Show | 9 | HG00642.hp2 HG01243.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2812+397_2812+398d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001199 | ||||||
| chr17:59001207
|
A | G | 1 | a0001c0001t0003g0070 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2812+391T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001207 | ||||||
| chr17:59001366
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2812+232C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001366 | ||||||
| chr17:59001454
|
TA | T | 9 | a0001c0001t0001g0222a0001c0001t0001g0230a0001c0001t0001g0244others(6): Show | 9 | HG01168.hp1 HG01256.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.2812+143delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001454 | ||||||
| chr17:59001502
|
G | A | 2 | a0001c0001t0001g0284a0001c0001t0001g0287 | 2 | HG00558.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.2812+96C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001502 | ||||||
| chr17:59001530
|
A | C | 2 | a0001c0001t0001g0295a0001c0006t0003g0106 | 2 | HG01071.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2812+68T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 23/23 | chr17 | 59001530 | ||||||
| chr17:59002221
|
C | T | 4 | a0001c0001t0003g0054a0001c0001t0003g0056a0001c0001t0003g0057others(1): Show | 4 | NA18612.hp2 NA18939.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2696-507G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59002221 | ||||||
| chr17:59002381
|
C | T | 88 | a0001c0001t0002g0108a0001c0001t0002g0124a0001c0001t0002g0126others(85): Show | 88 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.2696-667G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59002381 | ||||||
| chr17:59002489
|
C | A | 1 | a0001c0001t0003g0060 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2696-775G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59002489 | ||||||
| chr17:59002913
|
G | T | 1 | a0001c0001t0001g0226 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2696-1199C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59002913 | ||||||
| chr17:59002952
|
T | C | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2696-1238A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59002952 | ||||||
| chr17:59003052
|
T | C | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2696-1338A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003052 | ||||||
| chr17:59003110
|
G | A | 96 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.2696-1396C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003110 | ||||||
| chr17:59003436
|
G | A | 4 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0007others(1): Show | 4 | HG01978.hp2 HG03831.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2696-1722C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003436 | ||||||
| chr17:59003645
|
T | TA | 92 | a0001c0001t0001g0255a0001c0001t0001g0334a0001c0001t0001g0339others(89): Show | 92 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.2696-1932dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003645 | ||||||
| chr17:59003645
|
T | TAA | 12 | a0001c0001t0003g0011a0001c0001t0003g0049a0001c0001t0003g0052others(9): Show | 12 | HG02055.hp1 HG02559.hp1 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.2696-1933_2696-193 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003645 | ||||||
| chr17:59003663
|
C | A | 10 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(7): Show | 10 | NA18939.hp2 NA18954.hp2 NA18964.hp1 others(7): Show |
intron_variant | MODIFIER | c.2696-1949G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003663 | ||||||
| chr17:59003727
|
C | T | 1 | a0001c0001t0011g0001 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2696-2013G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003727 | ||||||
| chr17:59003919
|
C | A | 4 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(1): Show | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2696-2205G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003919 | ||||||
| chr17:59003922
|
T | TA | 124 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0227others(121): Show | 124 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2696-2209dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003922 | ||||||
| chr17:59003922
|
T | TAA | 11 | a0001c0001t0002g0155a0001c0001t0002g0156a0001c0001t0002g0164others(8): Show | 11 | HG02155.hp2 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.2696-2210_2696-220 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003922 | ||||||
| chr17:59003922
|
TA | T | 23 | a0001c0001t0001g0221a0001c0001t0001g0238a0001c0001t0001g0244others(20): Show | 23 | HG00639.hp2 HG01070.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.2696-2209delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59003922 | ||||||
| chr17:59004057
|
T | C | 1 | a0001c0001t0004g0090 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2696-2343A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004057 | ||||||
| chr17:59004090
|
C | A | 1 | a0001c0001t0001g0323 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2696-2376G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004090 | ||||||
| chr17:59004340
|
A | G | 1 | a0001c0001t0002g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2696-2626T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004340 | ||||||
| chr17:59004343
|
T | TTAAG | 338 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(335): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.2696-2630_2696-262 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004343 | ||||||
| chr17:59004524
|
G | A | 2 | a0001c0001t0002g0154a0001c0001t0002g0155 | 2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2696-2810C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004524 | ||||||
| chr17:59004552
|
T | A | 1 | a0001c0001t0003g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2696-2838A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004552 | ||||||
| chr17:59004652
|
C | A | 214 | a0001c0001t0001g0339a0001c0001t0002g0080a0001c0001t0002g0094others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.2696-2938G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004652 | ||||||
| chr17:59004741
|
T | A | 6 | a0001c0001t0003g0009a0001c0001t0003g0044a0001c0001t0005g0041others(3): Show | 6 | HG00438.hp1 NA18945.hp1 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.2696-3027A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004741 | ||||||
| chr17:59004761
|
T | G | 1 | a0001c0001t0001g0297 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2696-3047A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004761 | ||||||
| chr17:59004811
|
G | A | 2 | a0001c0001t0003g0012a0001c0001t0013g0029 | 2 | HG03017.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2696-3097C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004811 | ||||||
| chr17:59004864
|
G | A | 2 | a0001c0001t0002g0154a0001c0001t0002g0155 | 2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2696-3150C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004864 | ||||||
| chr17:59004885
|
C | T | 1 | a0001c0001t0002g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2696-3171G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004885 | ||||||
| chr17:59004936
|
A | T | 23 | a0001c0001t0002g0094a0001c0001t0002g0100a0001c0001t0003g0079others(20): Show | 23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.2696-3222T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59004936 | ||||||
| chr17:59005241
|
T | TA | 7 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(4): Show | 7 | HG02071.hp2 HG02293.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.2696-3528dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59005241 | ||||||
| chr17:59005261
|
T | C | 1 | a0001c0001t0003g0086 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2696-3547A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59005261 | ||||||
| chr17:59005282
|
C | T | 4 | a0001c0001t0001g0244a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG01168.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2696-3568G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59005282 | ||||||
| chr17:59005309
|
C | T | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2696-3595G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59005309 | ||||||
| chr17:59005529
|
C | T | 3 | a0001c0003t0006g0217a0001c0003t0006g0218a0001c0003t0006g0219 | 3 | HG00642.hp2 NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2696-3815G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59005529 | ||||||
| chr17:59005567
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2696-3853C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59005567 | ||||||
| chr17:59006093
|
C | G | 1 | a0001c0001t0001g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2696-4379G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006093 | ||||||
| chr17:59006244
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2696-4530C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006244 | ||||||
| chr17:59006295
|
T | C | 1 | a0001c0001t0001g0328 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2696-4581A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006295 | ||||||
| chr17:59006395
|
A | T | 2 | a0001c0001t0002g0152a0001c0001t0002g0174 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2696-4681T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006395 | ||||||
| chr17:59006396
|
T | A | 1 | a0001c0001t0002g0190 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2696-4682A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006396 | ||||||
| chr17:59006745
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2696-5031G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006745 | ||||||
| chr17:59006804
|
G | A | 2 | a0001c0001t0001g0311a0001c0001t0001g0312 | 2 | HG01433.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2696-5090C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006804 | ||||||
| chr17:59006842
|
T | C | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2696-5128A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59006842 | ||||||
| chr17:59007086
|
G | A | 1 | a0001c0001t0002g0177 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2695+5242C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007086 | ||||||
| chr17:59007158
|
A | AAC | 54 | a0001c0001t0001g0224a0001c0001t0001g0226a0001c0001t0001g0243others(51): Show | 54 | HG00544.hp2 HG00735.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.2695+5168_2695+516 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | ||||||
| chr17:59007158
|
A | AACAC | 62 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(59): Show | 62 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.2695+5166_2695+516 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | ||||||
| chr17:59007158
|
A | AACACAC | 20 | a0001c0001t0001g0227a0001c0001t0001g0230a0001c0001t0001g0232others(17): Show | 20 | HG01070.hp2 HG01175.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.2695+5164_2695+516 others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | ||||||
| chr17:59007158
|
A | AACACACA others(1): Show |
14 | a0001c0001t0001g0229a0001c0001t0001g0235a0001c0001t0001g0283others(11): Show | 14 | HG00621.hp2 HG01243.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.2695+5162_2695+516 others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | ||||||
| chr17:59007158
|
A | AACACACA others(5): Show |
4 | a0001c0001t0001g0239a0001c0001t0001g0303a0001c0001t0001g0313others(1): Show | 4 | NA18952.hp2 NA18979.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.2695+5158_2695+516 others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | ||||||
| chr17:59007158
|
A | AACACACA others(7): Show |
3 | a0001c0001t0001g0234a0001c0001t0001g0238a0001c0001t0003g0077 | 3 | HG03486.hp1 NA18964.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.2695+5156_2695+516 others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | ||||||
| chr17:59007158
|
A | AACACACA others(9): Show |
1 | a0001c0001t0001g0330 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2695+5154_2695+516 others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | ||||||
| chr17:59007158
|
AAC | A | 44 | a0001c0001t0001g0257a0001c0001t0001g0304a0001c0001t0001g0311others(41): Show | 44 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.2695+5168_2695+516 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | ||||||
| chr17:59007158
|
AACAC | A | 11 | a0001c0001t0002g0107a0001c0001t0002g0109a0001c0001t0002g0135others(8): Show | 11 | HG00673.hp1 HG00741.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.2695+5166_2695+516 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | ||||||
| chr17:59007158
|
AACACAC | A | 9 | a0001c0001t0001g0298a0001c0001t0002g0117a0001c0001t0003g0059others(6): Show | 9 | HG00642.hp2 HG02622.hp2 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.2695+5164_2695+516 others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | ||||||
| chr17:59007158
|
AACACACA others(3): Show |
A | 4 | a0001c0001t0002g0113a0001c0001t0002g0120a0001c0001t0002g0121others(1): Show | 4 | HG01257.hp2 HG01258.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.2695+5160_2695+516 others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | ||||||
| chr17:59007158
|
AACACACA others(5): Show |
A | 7 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0114others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2695+5158_2695+516 others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | ||||||
| chr17:59007158
|
AACACACA others(7): Show |
A | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2695+5156_2695+516 others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | ||||||
| chr17:59007158
|
AACACACA others(9): Show |
A | 6 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0006others(3): Show | 6 | HG01106.hp2 HG01978.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.2695+5154_2695+516 others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | ||||||
| chr17:59007158
|
AACACACA others(11): Show |
A | 1 | a0001c0001t0001g0242 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2695+5152_2695+516 others(22): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007158 | ||||||
| chr17:59007185
|
A | T | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5143T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007185 | ||||||
| chr17:59007186
|
C | A | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5142G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007186 | ||||||
| chr17:59007189
|
A | C | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5139T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007189 | ||||||
| chr17:59007195
|
A | C | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5133T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007195 | ||||||
| chr17:59007199
|
A | C | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5129T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007199 | ||||||
| chr17:59007201
|
A | ACACTAAA others(17): Show |
3 | a0001c0001t0008g0022a0001c0001t0008g0030a0001c0001t0008g0032 | 3 | NA19056.hp2 NA19068.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2695+5126_2695+512 others(28): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007201 | ||||||
| chr17:59007203
|
A | C | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5125T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007203 | ||||||
| chr17:59007207
|
T | C | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5121A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007207 | ||||||
| chr17:59007208
|
A | C | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5120T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007208 | ||||||
| chr17:59007210
|
A | C | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5118T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007210 | ||||||
| chr17:59007215
|
C | A | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5113G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007215 | ||||||
| chr17:59007217
|
C | A | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5111G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007217 | ||||||
| chr17:59007221
|
C | A | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2695+5107G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007221 | ||||||
| chr17:59007221
|
C | CCCCA | 96 | a0001c0001t0002g0080a0001c0001t0002g0107a0001c0001t0002g0108others(93): Show | 96 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.2695+5103_2695+510 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007221 | ||||||
| chr17:59007223
|
C | A | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5105G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007223 | ||||||
| chr17:59007227
|
C | A | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2695+5101G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007227 | ||||||
| chr17:59007231
|
C | A | 2 | a0001c0001t0001g0308a0001c0003t0006g0212 | 2 | HG00597.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2695+5097G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | ||||||
| chr17:59007231
|
C | CCACACAC others(13): Show |
4 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(1): Show | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2695+5096_2695+509 others(24): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | ||||||
| chr17:59007231
|
C | CCACACAC others(15): Show |
2 | a0001c0003t0006g0217a0001c0003t0006g0218 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2695+5096_2695+509 others(26): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | ||||||
| chr17:59007231
|
C | CCACACAC others(17): Show |
1 | a0001c0003t0006g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2695+5096_2695+509 others(28): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | ||||||
| chr17:59007231
|
C | CCACCCA | 6 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0006others(3): Show | 6 | HG01106.hp2 HG01978.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695+5096_2695+509 others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | ||||||
| chr17:59007231
|
C | CCACCCAC others(1): Show |
195 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(192): Show | 195 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.2695+5096_2695+509 others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | ||||||
| chr17:59007231
|
C | CCACCCAC others(3): Show |
18 | a0001c0001t0001g0248a0001c0001t0001g0302a0001c0001t0001g0303others(15): Show | 18 | HG02055.hp1 HG02523.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.2695+5096_2695+509 others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | ||||||
| chr17:59007231
|
C | CCACCCAC others(5): Show |
1 | a0001c0001t0001g0313 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2695+5096_2695+509 others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | ||||||
| chr17:59007231
|
C | CCACCCAC others(7): Show |
2 | a0001c0001t0001g0311a0001c0001t0001g0312 | 2 | HG01433.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2695+5096_2695+509 others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007231 | ||||||
| chr17:59007372
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2695+4956T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007372 | ||||||
| chr17:59007432
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2695+4896T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007432 | ||||||
| chr17:59007652
|
AAAT | A | 84 | a0001c0001t0001g0304a0001c0001t0001g0339a0001c0001t0002g0094others(81): Show | 84 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.2695+4673_2695+467 others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007652 | ||||||
| chr17:59007813
|
T | C | 1 | a0001c0001t0001g0268 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2695+4515A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007813 | ||||||
| chr17:59007916
|
G | A | 4 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2695+4412C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59007916 | ||||||
| chr17:59008190
|
T | G | 6 | a0001c0001t0001g0225a0001c0001t0001g0253a0001c0001t0001g0254others(3): Show | 6 | HG01070.hp2 HG01081.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.2695+4138A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59008190 | ||||||
| chr17:59008374
|
C | T | 2 | a0001c0001t0002g0120a0001c0001t0002g0121 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2695+3954G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59008374 | ||||||
| chr17:59008416
|
A | C | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2695+3912T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59008416 | ||||||
| chr17:59008664
|
T | C | 1 | a0001c0001t0001g0235 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2695+3664A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59008664 | ||||||
| chr17:59009106
|
G | A | 1 | a0001c0001t0003g0036 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2695+3222C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009106 | ||||||
| chr17:59009112
|
C | T | 119 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(116): Show | 119 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.2695+3216G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009112 | ||||||
| chr17:59009298
|
T | C | 11 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2695+3030A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009298 | ||||||
| chr17:59009443
|
C | CT | 12 | a0001c0001t0002g0100a0001c0001t0002g0107a0001c0001t0002g0128others(9): Show | 12 | HG00642.hp2 HG03453.hp1 HG03516.hp2 others(9): Show |
intron_variant | MODIFIER | c.2695+2884dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009443 | ||||||
| chr17:59009443
|
CT | C | 6 | a0001c0001t0002g0094a0001c0001t0002g0118a0001c0001t0002g0152others(3): Show | 6 | HG01070.hp1 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695+2884delA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009443 | ||||||
| chr17:59009448
|
T | TC | 118 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(115): Show | 118 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.2695+2879_2695+288 others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009448 | ||||||
| chr17:59009449
|
T | C | 2 | a0001c0001t0001g0229a0001c0001t0001g0317 | 2 | HG02897.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2695+2879A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009449 | ||||||
| chr17:59009531
|
C | T | 1 | a0001c0001t0002g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2695+2797G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009531 | ||||||
| chr17:59009607
|
A | G | 227 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(224): Show | 227 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.2695+2721T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009607 | ||||||
| chr17:59009761
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2695+2567G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009761 | ||||||
| chr17:59009885
|
A | T | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2695+2443T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009885 | ||||||
| chr17:59009931
|
G | T | 1 | a0001c0001t0003g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2695+2397C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009931 | ||||||
| chr17:59009976
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2695+2352G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009976 | ||||||
| chr17:59009977
|
G | A | 1 | a0001c0001t0002g0191 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2695+2351C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59009977 | ||||||
| chr17:59010016
|
T | G | 1 | a0001c0001t0002g0197 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2695+2312A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59010016 | ||||||
| chr17:59010069
|
A | G | 7 | a0001c0001t0003g0086a0001c0001t0003g0091a0001c0001t0003g0092others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2695+2259T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59010069 | ||||||
| chr17:59010448
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2695+1880G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59010448 | ||||||
| chr17:59010463
|
A | G | 5 | a0001c0001t0001g0232a0001c0001t0001g0244a0001c0001t0001g0246others(2): Show | 5 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2695+1865T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59010463 | ||||||
| chr17:59010784
|
C | T | 4 | a0001c0003t0006g0212a0001c0003t0006g0217a0001c0003t0006g0218others(1): Show | 4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.2695+1544G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59010784 | ||||||
| chr17:59010953
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | NA18963.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.2695+1375C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59010953 | ||||||
| chr17:59011164
|
G | A | 23 | a0001c0001t0002g0094a0001c0001t0002g0100a0001c0001t0003g0079others(20): Show | 23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.2695+1164C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011164 | ||||||
| chr17:59011172
|
G | GA | 7 | a0001c0001t0001g0238a0001c0001t0001g0246a0001c0001t0001g0311others(4): Show | 7 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2695+1155dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011172 | ||||||
| chr17:59011185
|
C | A | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2695+1143G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011185 | ||||||
| chr17:59011429
|
G | A | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2695+899C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011429 | ||||||
| chr17:59011516
|
G | A | 1 | a0001c0001t0003g0005 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2695+812C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011516 | ||||||
| chr17:59011651
|
G | A | 2 | a0001c0001t0003g0079a0001c0001t0003g0101 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2695+677C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011651 | ||||||
| chr17:59011674
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2695+654C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011674 | ||||||
| chr17:59011727
|
G | A | 1 | a0001c0001t0001g0340 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2695+601C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59011727 | ||||||
| chr17:59012132
|
T | C | 4 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2695+196A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012132 | ||||||
| chr17:59012153
|
C | T | 1 | a0001c0001t0001g0339 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2695+175G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012153 | ||||||
| chr17:59012215
|
C | CCAGCAGC others(8): Show |
2 | a0001c0001t0002g0126a0001c0001t0002g0143 | 2 | NA18995.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2695+112_2695+113i others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012215 | ||||||
| chr17:59012215
|
C | CCAGCAGC others(11): Show |
2 | a0001c0001t0001g0308a0001c0001t0003g0092 | 2 | HG00597.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2695+112_2695+113i others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012215 | ||||||
| chr17:59012215
|
C | CCAGCAGC others(14): Show |
3 | a0001c0001t0001g0262a0001c0001t0002g0107a0001c0001t0002g0109 | 3 | HG01978.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2695+112_2695+113i others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012215 | ||||||
| chr17:59012227
|
G | GCAGCAGC others(11): Show |
4 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0003g0048others(1): Show | 4 | HG00642.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2695+100_2695+101i others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | ||||||
| chr17:59012227
|
G | GCAGCAGC others(11): Show |
189 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(186): Show | 189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.2695+100_2695+101i others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | ||||||
| chr17:59012227
|
G | GCAGCAGC others(14): Show |
6 | a0001c0001t0002g0117a0001c0001t0003g0086a0001c0001t0004g0090others(3): Show | 6 | HG02615.hp1 HG02622.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695+100_2695+101i others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | ||||||
| chr17:59012227
|
G | GCAGCAGC others(14): Show |
24 | a0001c0001t0001g0258a0001c0001t0002g0112a0001c0001t0002g0113others(21): Show | 24 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.2695+100_2695+101i others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | ||||||
| chr17:59012227
|
G | GCAGCAGC others(17): Show |
3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2695+100_2695+101i others(26): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | ||||||
| chr17:59012227
|
G | GCAGCAGC others(17): Show |
6 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0077others(3): Show | 6 | HG03486.hp1 NA18952.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695+100_2695+101i others(26): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | ||||||
| chr17:59012227
|
G | GCAGCAGC others(20): Show |
6 | a0001c0001t0001g0281a0001c0001t0002g0080a0001c0001t0002g0114others(3): Show | 6 | HG01257.hp2 HG01258.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695+100_2695+101i others(29): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | ||||||
| chr17:59012227
|
G | GCAGCAGC others(23): Show |
3 | a0001c0001t0003g0073a0001c0001t0003g0075a0001c0001t0003g0076 | 3 | HG02630.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2695+100_2695+101i others(32): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | ||||||
| chr17:59012227
|
G | GCAGCAGC others(26): Show |
1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2695+100_2695+101i others(35): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012227 | ||||||
| chr17:59012250
|
ACCACCAC | A | 6 | a0001c0001t0001g0258a0001c0001t0003g0073a0001c0001t0003g0074others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695+71_2695+77del others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 22/23 | chr17 | 59012250 | ||||||
| chr17:59012767
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2577-321G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59012767 | ||||||
| chr17:59012854
|
C | T | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2577-408G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59012854 | ||||||
| chr17:59012875
|
C | CA | 102 | a0001c0001t0001g0304a0001c0001t0001g0322a0001c0001t0001g0339others(99): Show | 102 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.2577-430dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59012875 | ||||||
| chr17:59012889
|
A | T | 5 | a0001c0001t0001g0237a0001c0003t0006g0212a0001c0003t0006g0217others(2): Show | 5 | HG00642.hp2 HG03704.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.2577-443T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59012889 | ||||||
| chr17:59012890
|
T | A | 2 | a0001c0001t0003g0026a0001c0001t0003g0122 | 2 | NA18992.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2577-444A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59012890 | ||||||
| chr17:59012894
|
T | A | 3 | a0001c0001t0003g0019a0001c0001t0003g0026a0001c0001t0003g0122 | 3 | NA18992.hp2 NA19001.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2577-448A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59012894 | ||||||
| chr17:59012962
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2577-516C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59012962 | ||||||
| chr17:59013058
|
T | C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2577-612A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59013058 | ||||||
| chr17:59013330
|
T | C | 2 | a0001c0001t0001g0269a0001c0001t0001g0289 | 2 | HG01257.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.2577-884A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59013330 | ||||||
| chr17:59013367
|
G | A | 5 | a0001c0001t0003g0079a0001c0001t0003g0096a0001c0001t0003g0097others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.2577-921C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59013367 | ||||||
| chr17:59013506
|
G | C | 2 | a0001c0001t0001g0282a0001c0001t0001g0319 | 2 | HG00639.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2577-1060C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59013506 | ||||||
| chr17:59013636
|
A | G | 7 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0175others(4): Show | 7 | HG00558.hp2 HG02155.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.2577-1190T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59013636 | ||||||
| chr17:59013731
|
T | C | 4 | a0001c0003t0006g0212a0001c0003t0006g0217a0001c0003t0006g0218others(1): Show | 4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.2577-1285A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59013731 | ||||||
| chr17:59013734
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2577-1288G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59013734 | ||||||
| chr17:59014260
|
T | C | 6 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(3): Show | 6 | HG02559.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2576+1350A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014260 | ||||||
| chr17:59014307
|
G | A | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2576+1303C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014307 | ||||||
| chr17:59014371
|
T | A | 1 | a0001c0001t0001g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2576+1239A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014371 | ||||||
| chr17:59014473
|
G | A | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2576+1137C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014473 | ||||||
| chr17:59014515
|
C | T | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2576+1095G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014515 | ||||||
| chr17:59014546
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2576+1064T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014546 | ||||||
| chr17:59014631
|
T | C | 2 | a0001c0001t0002g0107a0001c0001t0002g0109 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2576+979A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014631 | ||||||
| chr17:59014714
|
G | GA | 11 | a0001c0001t0001g0224a0001c0001t0001g0258a0001c0001t0002g0132others(8): Show | 11 | HG01106.hp1 HG01978.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2576+895dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014714 | ||||||
| chr17:59014742
|
C | G | 1 | a0001c0001t0003g0173 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2576+868G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014742 | ||||||
| chr17:59014742
|
C | T | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2576+868G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014742 | ||||||
| chr17:59014881
|
A | C | 1 | a0001c0001t0002g0177 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2576+729T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014881 | ||||||
| chr17:59014911
|
C | CA | 10 | a0001c0001t0001g0304a0001c0001t0001g0321a0001c0001t0002g0180others(7): Show | 10 | HG02135.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2576+698dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59014911 | ||||||
| chr17:59015107
|
TA | T | 248 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(245): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.2576+502delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015107 | ||||||
| chr17:59015269
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2576+341C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015269 | ||||||
| chr17:59015364
|
G | C | 248 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(245): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.2576+246C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015364 | ||||||
| chr17:59015365
|
G | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2576+245C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015365 | ||||||
| chr17:59015426
|
C | A | 1 | a0001c0001t0002g0183 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2576+184G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015426 | ||||||
| chr17:59015427
|
G | A | 96 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.2576+183C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015427 | ||||||
| chr17:59015457
|
A | T | 1 | a0001c0001t0002g0170 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2576+153T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015457 | ||||||
| chr17:59015464
|
T | C | 1 | a0001c0001t0003g0173 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2576+146A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015464 | ||||||
| chr17:59015533
|
A | G | 2 | a0001c0001t0002g0154a0001c0001t0002g0155 | 2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2576+77T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 21/23 | chr17 | 59015533 | ||||||
| chr17:59015848
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2387-49C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59015848 | ||||||
| chr17:59015851
|
C | T | 1 | a0001c0001t0004g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2387-52G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59015851 | ||||||
| chr17:59016076
|
A | G | 1 | a0001c0001t0003g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2387-277T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016076 | ||||||
| chr17:59016254
|
C | G | 4 | a0001c0001t0002g0124a0001c0001t0002g0131a0001c0001t0002g0200others(1): Show | 4 | HG02132.hp1 NA18947.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2387-455G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016254 | ||||||
| chr17:59016275
|
T | C | 2 | a0001c0001t0003g0019a0001c0001t0003g0026 | 2 | NA19001.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2387-476A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016275 | ||||||
| chr17:59016329
|
G | A | 1 | a0001c0001t0003g0028 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2387-530C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016329 | ||||||
| chr17:59016396
|
C | CA | 29 | a0001c0001t0001g0224a0001c0001t0001g0244a0001c0001t0001g0274others(26): Show | 29 | HG00544.hp2 HG00642.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.2387-598dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016396 | ||||||
| chr17:59016396
|
CA | C | 19 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(16): Show | 19 | HG01346.hp1 HG02155.hp1 HG02300.hp1 others(16): Show |
intron_variant | MODIFIER | c.2387-598delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016396 | ||||||
| chr17:59016464
|
C | T | 248 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(245): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.2387-665G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016464 | ||||||
| chr17:59016557
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2386+739C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016557 | ||||||
| chr17:59016568
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2386+728C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016568 | ||||||
| chr17:59016599
|
C | CA | 37 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0124others(34): Show | 37 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.2386+696dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016599 | ||||||
| chr17:59016599
|
C | CAA | 11 | a0001c0001t0002g0172a0001c0001t0002g0184a0001c0001t0002g0187others(8): Show | 11 | HG01175.hp2 HG01256.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.2386+695_2386+696d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016599 | ||||||
| chr17:59016599
|
CA | C | 72 | a0001c0001t0001g0223a0001c0001t0001g0226a0001c0001t0001g0227others(69): Show | 72 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.2386+696delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016599 | ||||||
| chr17:59016599
|
CAA | C | 119 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(116): Show | 119 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.2386+695_2386+696d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016599 | ||||||
| chr17:59016599
|
CAAA | C | 42 | a0001c0001t0001g0232a0001c0001t0001g0244a0001c0001t0001g0249others(39): Show | 42 | HG00099.hp2 HG01099.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.2386+694_2386+696d others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016599 | ||||||
| chr17:59016599
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0002g0120a0001c0001t0002g0121 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2386+681_2386+696d others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016599 | ||||||
| chr17:59016720
|
C | T | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2386+576G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016720 | ||||||
| chr17:59016835
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2386+461A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016835 | ||||||
| chr17:59016999
|
T | C | 2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG00323.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.2386+297A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59016999 | ||||||
| chr17:59017088
|
C | T | 2 | a0001c0001t0002g0133a0001c0001t0002g0134 | 2 | HG00621.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2386+208G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59017088 | ||||||
| chr17:59017256
|
T | C | 252 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(249): Show | 252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.2386+40A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 20/23 | chr17 | 59017256 | ||||||
| chr17:59017486
|
T | C | 11 | a0001c0001t0001g0225a0001c0001t0001g0231a0001c0001t0001g0245others(8): Show | 11 | HG01070.hp2 HG01081.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.2258-62A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59017486 | ||||||
| chr17:59017583
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2258-159A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59017583 | ||||||
| chr17:59017630
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2258-206A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59017630 | ||||||
| chr17:59017851
|
C | T | 121 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(118): Show | 121 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.2258-427G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59017851 | ||||||
| chr17:59017889
|
A | G | 227 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(224): Show | 227 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.2258-465T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59017889 | ||||||
| chr17:59018722
|
G | GT | 10 | a0001c0001t0001g0220a0001c0001t0001g0226a0001c0001t0001g0259others(7): Show | 10 | HG01361.hp1 HG03688.hp1 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.2258-1299dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59018722 | ||||||
| chr17:59019014
|
G | A | 2 | a0001c0001t0003g0110a0001c0001t0003g0111 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2258-1590C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019014 | ||||||
| chr17:59019129
|
G | T | 1 | a0001c0001t0002g0135 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2258-1705C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019129 | ||||||
| chr17:59019444
|
T | C | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2258-2020A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019444 | ||||||
| chr17:59019445
|
C | T | 2 | a0001c0001t0003g0110a0001c0001t0003g0111 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2258-2021G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019445 | ||||||
| chr17:59019481
|
G | A | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2258-2057C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019481 | ||||||
| chr17:59019537
|
G | A | 2 | a0001c0001t0002g0107a0001c0001t0002g0109 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2258-2113C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019537 | ||||||
| chr17:59019615
|
G | A | 7 | a0001c0001t0002g0209a0001c0001t0002g0210a0002c0002t0002g0125others(4): Show | 7 | HG01952.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258-2191C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019615 | ||||||
| chr17:59019620
|
A | G | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2258-2196T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019620 | ||||||
| chr17:59019686
|
T | C | 246 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(243): Show | 246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.2258-2262A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019686 | ||||||
| chr17:59019703
|
G | A | 73 | a0001c0001t0001g0339a0001c0001t0003g0003a0001c0001t0003g0004others(70): Show | 73 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.2258-2279C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019703 | ||||||
| chr17:59019750
|
A | T | 2 | a0001c0001t0003g0087a0001c0001t0003g0088 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2258-2326T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59019750 | ||||||
| chr17:59020029
|
G | A | 122 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(119): Show | 122 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.2258-2605C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020029 | ||||||
| chr17:59020065
|
T | C | 1 | a0001c0001t0002g0116 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2258-2641A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020065 | ||||||
| chr17:59020094
|
G | C | 1 | a0001c0001t0003g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2258-2670C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020094 | ||||||
| chr17:59020230
|
C | CA | 9 | a0001c0001t0002g0121a0001c0001t0002g0130a0001c0001t0002g0132others(6): Show | 9 | HG00735.hp2 HG00741.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2258-2807dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020230 | ||||||
| chr17:59020230
|
CA | C | 58 | a0001c0001t0001g0251a0001c0001t0001g0280a0001c0001t0001g0305others(55): Show | 58 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.2258-2807delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020230 | ||||||
| chr17:59020230
|
CAA | C | 33 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0253others(30): Show | 33 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.2258-2808_2258-280 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020230 | ||||||
| chr17:59020230
|
CAAA | C | 77 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0231others(74): Show | 77 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.2258-2809_2258-280 others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020230 | ||||||
| chr17:59020230
|
CAAAA | C | 56 | a0001c0001t0001g0223a0001c0001t0001g0228a0001c0001t0001g0229others(53): Show | 56 | HG00280.hp1 HG00639.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.2258-2810_2258-280 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020230 | ||||||
| chr17:59020230
|
CAAAAA | C | 66 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0237others(63): Show | 66 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.2258-2811_2258-280 others(9): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020230 | ||||||
| chr17:59020230
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0003g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2258-2818_2258-280 others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020230 | ||||||
| chr17:59020391
|
A | G | 7 | a0001c0001t0002g0100a0001c0001t0003g0079a0001c0001t0003g0096others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.2258-2967T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020391 | ||||||
| chr17:59020417
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2258-2993T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020417 | ||||||
| chr17:59020691
|
G | A | 1 | a0001c0001t0001g0334 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2258-3267C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020691 | ||||||
| chr17:59020950
|
T | C | 22 | a0001c0001t0001g0339a0001c0001t0003g0005a0001c0001t0003g0010others(19): Show | 22 | HG01261.hp2 HG01943.hp1 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.2258-3526A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020950 | ||||||
| chr17:59020955
|
T | C | 7 | a0001c0001t0003g0086a0001c0001t0003g0091a0001c0001t0003g0092others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2258-3531A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59020955 | ||||||
| chr17:59021014
|
G | C | 1 | a0001c0001t0002g0161 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2258-3590C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59021014 | ||||||
| chr17:59021803
|
G | C | 1 | a0001c0001t0002g0129 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2258-4379C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59021803 | ||||||
| chr17:59021854
|
G | A | 3 | a0001c0001t0002g0126a0001c0001t0002g0143a0001c0001t0002g0146 | 3 | HG02071.hp1 NA18995.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2258-4430C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59021854 | ||||||
| chr17:59022051
|
T | G | 5 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0006others(2): Show | 5 | HG01106.hp2 HG01978.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.2258-4627A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59022051 | ||||||
| chr17:59022087
|
G | C | 10 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0064others(7): Show | 10 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2258-4663C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59022087 | ||||||
| chr17:59022475
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2258-5051C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59022475 | ||||||
| chr17:59022828
|
GAAATGGT others(10): Show |
G | 3 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0001g0252 | 3 | HG02004.hp2 NA18951.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2258-5421_2258-540 others(21): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59022828 | ||||||
| chr17:59022910
|
A | G | 1 | a0001c0001t0001g0286 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2258-5486T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59022910 | ||||||
| chr17:59022916
|
T | C | 1 | a0001c0001t0003g0035 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2258-5492A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59022916 | ||||||
| chr17:59022922
|
T | C | 2 | a0001c0001t0003g0014a0001c0001t0003g0015 | 2 | HG00099.hp2 HG00280.hp2 |
intron_variant | MODIFIER | c.2257+5493A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59022922 | ||||||
| chr17:59023185
|
A | C | 248 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(245): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.2257+5230T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59023185 | ||||||
| chr17:59023238
|
G | A | 4 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2257+5177C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59023238 | ||||||
| chr17:59023828
|
T | C | 1 | a0001c0001t0002g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2257+4587A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59023828 | ||||||
| chr17:59023872
|
A | G | 4 | a0001c0001t0001g0280a0001c0001t0001g0282a0001c0001t0001g0295others(1): Show | 4 | HG00639.hp2 HG01071.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2257+4543T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59023872 | ||||||
| chr17:59024009
|
T | C | 2 | a0001c0001t0002g0178a0001c0001t0002g0202 | 2 | HG00438.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.2257+4406A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024009 | ||||||
| chr17:59024082
|
C | A | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2257+4333G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024082 | ||||||
| chr17:59024144
|
G | A | 1 | a0001c0001t0008g0032 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2257+4271C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024144 | ||||||
| chr17:59024145
|
G | C | 1 | a0006c0004t0002g0144 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2257+4270C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024145 | ||||||
| chr17:59024177
|
G | A | 96 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.2257+4238C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024177 | ||||||
| chr17:59024210
|
G | A | 1 | a0001c0003t0006g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2257+4205C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024210 | ||||||
| chr17:59024214
|
C | CA | 12 | a0001c0001t0002g0080a0001c0001t0002g0108a0001c0001t0002g0115others(9): Show | 12 | HG00673.hp1 HG00741.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2257+4200dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024214 | ||||||
| chr17:59024214
|
CA | C | 106 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0229others(103): Show | 106 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.2257+4200delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024214 | ||||||
| chr17:59024214
|
CAA | C | 107 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0223others(104): Show | 107 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.2257+4199_2257+420 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024214 | ||||||
| chr17:59024214
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0009g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2257+4191_2257+420 others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024214 | ||||||
| chr17:59024239
|
AT | A | 3 | a0001c0001t0003g0077a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03486.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2257+4175delA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024239 | ||||||
| chr17:59024240
|
T | A | 1 | a0001c0001t0004g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2257+4175A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024240 | ||||||
| chr17:59024279
|
A | G | 4 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(1): Show | 4 | HG00639.hp1 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2257+4136T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024279 | ||||||
| chr17:59024369
|
T | C | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2257+4046A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024369 | ||||||
| chr17:59024474
|
G | C | 1 | a0001c0001t0001g0226 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2257+3941C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024474 | ||||||
| chr17:59024725
|
T | A | 1 | a0001c0001t0015g0332 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2257+3690A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024725 | ||||||
| chr17:59024772
|
T | C | 226 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(223): Show | 226 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.2257+3643A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59024772 | ||||||
| chr17:59025159
|
C | A | 1 | a0001c0001t0001g0256 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2257+3256G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025159 | ||||||
| chr17:59025160
|
A | C | 1 | a0001c0001t0003g0027 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2257+3255T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025160 | ||||||
| chr17:59025198
|
C | T | 1 | a0001c0001t0001g0336 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2257+3217G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025198 | ||||||
| chr17:59025381
|
T | G | 97 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.2257+3034A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025381 | ||||||
| chr17:59025659
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2257+2756A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025659 | ||||||
| chr17:59025712
|
G | A | 7 | a0001c0001t0001g0302a0001c0001t0001g0303a0001c0001t0001g0304others(4): Show | 7 | HG02523.hp2 NA18952.hp2 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.2257+2703C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025712 | ||||||
| chr17:59025747
|
G | A | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2257+2668C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025747 | ||||||
| chr17:59025779
|
T | C | 62 | a0001c0001t0001g0339a0001c0001t0003g0003a0001c0001t0003g0004others(59): Show | 62 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.2257+2636A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59025779 | ||||||
| chr17:59026051
|
C | G | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2257+2364G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59026051 | ||||||
| chr17:59026439
|
A | C | 1 | a0001c0001t0001g0336 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2257+1976T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59026439 | ||||||
| chr17:59026487
|
G | T | 4 | a0001c0001t0001g0324a0001c0001t0001g0329a0001c0001t0001g0331others(1): Show | 4 | HG00621.hp1 NA18612.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.2257+1928C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59026487 | ||||||
| chr17:59026509
|
T | C | 1 | a0001c0001t0003g0009 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2257+1906A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59026509 | ||||||
| chr17:59026581
|
C | A | 1 | a0001c0003t0006g0218 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2257+1834G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59026581 | ||||||
| chr17:59026743
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2257+1672G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59026743 | ||||||
| chr17:59027005
|
T | C | 1 | a0001c0001t0001g0268 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2257+1410A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027005 | ||||||
| chr17:59027025
|
T | A | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2257+1390A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027025 | ||||||
| chr17:59027153
|
G | T | 8 | a0001c0001t0003g0052a0001c0001t0003g0053a0001c0001t0003g0054others(5): Show | 8 | NA18612.hp2 NA18939.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.2257+1262C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027153 | ||||||
| chr17:59027274
|
T | A | 2 | a0001c0001t0002g0107a0001c0001t0002g0109 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2257+1141A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027274 | ||||||
| chr17:59027362
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2257+1053A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027362 | ||||||
| chr17:59027635
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2257+780A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027635 | ||||||
| chr17:59027862
|
C | T | 248 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(245): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.2257+553G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027862 | ||||||
| chr17:59027884
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2257+531C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027884 | ||||||
| chr17:59027954
|
T | A | 1 | a0001c0001t0002g0183 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2257+461A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027954 | ||||||
| chr17:59027996
|
C | G | 1 | a0001c0001t0002g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2257+419G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59027996 | ||||||
| chr17:59028193
|
T | C | 1 | a0001c0001t0002g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2257+222A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59028193 | ||||||
| chr17:59028257
|
T | C | 2 | a0001c0001t0003g0087a0001c0001t0003g0088 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2257+158A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59028257 | ||||||
| chr17:59028345
|
T | C | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2257+70A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 19/23 | chr17 | 59028345 | ||||||
| chr17:59028824
|
G | A | 5 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0001t0001g0265others(2): Show | 5 | HG01192.hp1 HG01943.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1949-101C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59028824 | ||||||
| chr17:59028932
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1949-209A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59028932 | ||||||
| chr17:59028945
|
C | T | 4 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(1): Show | 4 | HG00639.hp1 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1949-222G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59028945 | ||||||
| chr17:59029105
|
A | C | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1949-382T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029105 | ||||||
| chr17:59029208
|
G | A | 3 | a0001c0001t0001g0225a0001c0001t0001g0253a0001c0001t0001g0254 | 3 | NA18966.hp2 NA19005.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1949-485C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029208 | ||||||
| chr17:59029269
|
A | G | 130 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(127): Show | 130 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1949-546T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029269 | ||||||
| chr17:59029274
|
T | A | 7 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1949-551A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029274 | ||||||
| chr17:59029300
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1949-577T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029300 | ||||||
| chr17:59029544
|
A | C | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1949-821T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029544 | ||||||
| chr17:59029615
|
G | C | 2 | a0001c0001t0001g0284a0001c0001t0001g0287 | 2 | HG00558.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1949-892C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029615 | ||||||
| chr17:59029668
|
G | A | 2 | a0001c0001t0002g0107a0001c0001t0002g0109 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1949-945C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029668 | ||||||
| chr17:59029798
|
A | T | 1 | a0001c0001t0003g0123 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1949-1075T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029798 | ||||||
| chr17:59029987
|
TATTCATC others(3): Show |
T | 96 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1949-1274_1949-126 others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59029987 | ||||||
| chr17:59030056
|
C | T | 7 | a0001c0001t0002g0100a0001c0001t0003g0079a0001c0001t0003g0096others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1949-1333G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030056 | ||||||
| chr17:59030058
|
C | T | 1 | a0001c0001t0003g0055 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1949-1335G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030058 | ||||||
| chr17:59030202
|
T | G | 1 | a0001c0001t0002g0199 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1949-1479A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030202 | ||||||
| chr17:59030256
|
C | A | 4 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(1): Show | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1949-1533G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030256 | ||||||
| chr17:59030275
|
T | G | 1 | a0001c0001t0001g0242 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1949-1552A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030275 | ||||||
| chr17:59030367
|
C | T | 96 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1948+1529G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030367 | ||||||
| chr17:59030580
|
A | T | 1 | a0001c0001t0001g0277 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1948+1316T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030580 | ||||||
| chr17:59030610
|
C | T | 10 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0064others(7): Show | 10 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1948+1286G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030610 | ||||||
| chr17:59030697
|
T | C | 1 | a0001c0001t0003g0066 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1948+1199A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59030697 | ||||||
| chr17:59031076
|
G | C | 74 | a0001c0001t0001g0339a0001c0001t0003g0003a0001c0001t0003g0004others(71): Show | 74 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1948+820C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59031076 | ||||||
| chr17:59031182
|
A | G | 248 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(245): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1948+714T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59031182 | ||||||
| chr17:59031315
|
T | C | 1 | a0001c0001t0001g0335 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1948+581A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59031315 | ||||||
| chr17:59031539
|
G | A | 1 | a0001c0001t0014g0271 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1948+357C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59031539 | ||||||
| chr17:59031618
|
T | C | 1 | a0001c0001t0003g0052 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1948+278A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 18/23 | chr17 | 59031618 | ||||||
| chr17:59032251
|
C | T | 2 | a0001c0001t0002g0130a0001c0001t0002g0163 | 2 | HG00741.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1754-161G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032251 | ||||||
| chr17:59032254
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1754-164C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032254 | ||||||
| chr17:59032292
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1754-202C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032292 | ||||||
| chr17:59032322
|
GAGACCAT others(8514): Show |
G | 5 | a0001c0001t0001g0277a0001c0001t0001g0317a0001c0001t0001g0318others(2): Show | 5 | NA18943.hp2 NA18955.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.1753+970_1754-233d others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032322 | ||||||
| chr17:59032387
|
C | A | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1754-297G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032387 | ||||||
| chr17:59032398
|
G | T | 1 | a0001c0001t0002g0135 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1754-308C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032398 | ||||||
| chr17:59032531
|
C | CA | 123 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0223others(120): Show | 123 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.1754-442dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032531 | ||||||
| chr17:59032531
|
C | CAA | 11 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0244others(8): Show | 11 | HG01168.hp1 HG01952.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1754-443_1754-442d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032531 | ||||||
| chr17:59032531
|
CA | C | 89 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1754-442delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032531 | ||||||
| chr17:59032550
|
A | G | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1754-460T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032550 | ||||||
| chr17:59032554
|
G | C | 4 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(1): Show | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1754-464C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032554 | ||||||
| chr17:59032694
|
G | A | 8 | a0001c0001t0002g0135a0001c0001t0002g0141a0001c0001t0002g0142others(5): Show | 8 | HG00558.hp2 HG00673.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1754-604C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032694 | ||||||
| chr17:59032966
|
T | C | 116 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(113): Show | 116 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1754-876A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59032966 | ||||||
| chr17:59033558
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1754-1468C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033558 | ||||||
| chr17:59033712
|
C | A | 1 | a0001c0001t0002g0127 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1754-1622G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033712 | ||||||
| chr17:59033740
|
T | C | 116 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(113): Show | 116 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1754-1650A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033740 | ||||||
| chr17:59033827
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1754-1737C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033827 | ||||||
| chr17:59033889
|
G | A | 116 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(113): Show | 116 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1754-1799C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033889 | ||||||
| chr17:59033908
|
A | C | 72 | a0001c0001t0001g0224a0001c0001t0001g0226a0001c0001t0001g0227others(69): Show | 72 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1754-1818T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033908 | ||||||
| chr17:59033917
|
A | C | 1 | a0001c0001t0001g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1754-1827T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033917 | ||||||
| chr17:59033953
|
A | G | 1 | a0001c0001t0001g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1754-1863T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033953 | ||||||
| chr17:59033972
|
T | A | 1 | a0001c0001t0002g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1754-1882A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59033972 | ||||||
| chr17:59034050
|
T | G | 1 | a0001c0001t0001g0258 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1754-1960A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034050 | ||||||
| chr17:59034178
|
T | G | 1 | a0001c0001t0001g0227 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1754-2088A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034178 | ||||||
| chr17:59034245
|
G | C | 2 | a0001c0001t0002g0152a0001c0001t0002g0174 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1754-2155C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034245 | ||||||
| chr17:59034293
|
G | A | 336 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(333): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1754-2203C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034293 | ||||||
| chr17:59034509
|
A | G | 248 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(245): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1754-2419T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034509 | ||||||
| chr17:59034658
|
C | G | 1 | a0001c0001t0003g0046 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1754-2568G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034658 | ||||||
| chr17:59034824
|
T | C | 2 | a0001c0001t0003g0087a0001c0001t0003g0088 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1754-2734A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034824 | ||||||
| chr17:59034939
|
G | T | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1754-2849C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59034939 | ||||||
| chr17:59035007
|
G | A | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1754-2917C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035007 | ||||||
| chr17:59035093
|
T | C | 1 | a0001c0001t0001g0339 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1754-3003A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035093 | ||||||
| chr17:59035132
|
TCACCGCA others(12): Show |
T | 1 | a0001c0001t0001g0254 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1754-3061_1754-304 others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035132 | ||||||
| chr17:59035251
|
AG | A | 4 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(1): Show | 4 | HG00639.hp1 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1754-3162delC | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035251 | ||||||
| chr17:59035413
|
T | G | 2 | a0001c0001t0002g0107a0001c0001t0002g0109 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1754-3323A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035413 | ||||||
| chr17:59035755
|
ACAAAAAA others(1): Show |
A | 7 | a0001c0001t0001g0232a0001c0001t0001g0244a0001c0001t0001g0246others(4): Show | 7 | HG01099.hp2 HG01168.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1754-3673_1754-366 others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035755 | ||||||
| chr17:59035763
|
C | A | 109 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(106): Show | 109 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1754-3673G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035763 | ||||||
| chr17:59035958
|
GC | G | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1754-3869delG | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59035958 | ||||||
| chr17:59036191
|
T | C | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1754-4101A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036191 | ||||||
| chr17:59036330
|
A | C | 1 | a0001c0001t0002g0134 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1754-4240T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036330 | ||||||
| chr17:59036347
|
A | C | 4 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(1): Show | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1754-4257T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036347 | ||||||
| chr17:59036443
|
TGG | T | 4 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0076others(1): Show | 4 | HG02486.hp2 HG03486.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1754-4355_1754-435 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036443 | ||||||
| chr17:59036447
|
G | GGGGTGT | 7 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1754-4358_1754-435 others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | ||||||
| chr17:59036447
|
G | GGT | 121 | a0001c0001t0001g0225a0001c0001t0001g0231a0001c0001t0001g0232others(118): Show | 121 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.1754-4359_1754-435 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | ||||||
| chr17:59036447
|
G | GGTGT | 24 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(21): Show | 24 | HG00280.hp1 HG00733.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1754-4361_1754-435 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | ||||||
| chr17:59036447
|
G | GGTGTGT | 12 | a0001c0001t0001g0242a0001c0001t0001g0244a0001c0001t0001g0246others(9): Show | 12 | HG01168.hp1 HG01261.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1754-4363_1754-435 others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | ||||||
| chr17:59036447
|
G | GTGT | 3 | a0001c0001t0001g0270a0001c0001t0001g0283a0001c0001t0001g0325 | 3 | HG00544.hp1 HG03927.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1754-4358_1754-435 others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | ||||||
| chr17:59036447
|
G | T | 7 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(4): Show | 7 | HG00639.hp1 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1754-4357C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | ||||||
| chr17:59036447
|
GGT | G | 11 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0002g0175others(8): Show | 11 | HG01175.hp1 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1754-4359_1754-435 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | ||||||
| chr17:59036447
|
GGTGT | G | 6 | a0001c0001t0002g0186a0001c0001t0007g0213a0001c0001t0007g0214others(3): Show | 6 | HG00597.hp1 HG01243.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1754-4361_1754-435 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | ||||||
| chr17:59036447
|
GGTGTGTG others(1): Show |
G | 18 | a0001c0001t0001g0257a0001c0001t0001g0339a0001c0001t0003g0005others(15): Show | 18 | HG00642.hp2 HG01099.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1754-4365_1754-435 others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | ||||||
| chr17:59036447
|
GGTGTGTG others(5): Show |
G | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1754-4369_1754-435 others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036447 | ||||||
| chr17:59036449
|
T | G | 15 | a0001c0001t0002g0094a0001c0001t0002g0100a0001c0001t0002g0107others(12): Show | 15 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1754-4359A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036449 | ||||||
| chr17:59036451
|
T | G | 1 | a0001c0001t0002g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1754-4361A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036451 | ||||||
| chr17:59036483
|
T | C | 9 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(6): Show | 9 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1754-4393A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036483 | ||||||
| chr17:59036593
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1754-4503G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036593 | ||||||
| chr17:59036755
|
A | C | 2 | a0001c0001t0001g0324a0001c0001t0001g0329 | 2 | NA18612.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1754-4665T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036755 | ||||||
| chr17:59036787
|
C | G | 243 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(240): Show | 243 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1754-4697G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59036787 | ||||||
| chr17:59037136
|
C | G | 97 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1753+4677G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037136 | ||||||
| chr17:59037234
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1753+4579G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037234 | ||||||
| chr17:59037292
|
A | T | 1 | a0001c0001t0003g0005 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1753+4521T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037292 | ||||||
| chr17:59037354
|
C | T | 1 | a0001c0003t0006g0217 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1753+4459G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037354 | ||||||
| chr17:59037402
|
C | G | 4 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1753+4411G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037402 | ||||||
| chr17:59037427
|
G | A | 61 | a0001c0001t0001g0339a0001c0001t0003g0003a0001c0001t0003g0004others(58): Show | 61 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1753+4386C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037427 | ||||||
| chr17:59037442
|
C | T | 1 | a0001c0001t0002g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1753+4371G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037442 | ||||||
| chr17:59037490
|
G | A | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1753+4323C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037490 | ||||||
| chr17:59037535
|
G | T | 2 | a0001c0001t0003g0110a0001c0001t0003g0111 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1753+4278C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037535 | ||||||
| chr17:59037557
|
C | CA | 31 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0114others(28): Show | 31 | HG00673.hp1 HG00735.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1753+4255dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | ||||||
| chr17:59037557
|
C | CAA | 14 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0121others(11): Show | 14 | HG00558.hp2 HG01257.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1753+4254_1753+425 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | ||||||
| chr17:59037557
|
C | CAAAAAAA others(10): Show |
1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1753+4239_1753+425 others(21): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | ||||||
| chr17:59037557
|
C | CAAAAAAA others(13): Show |
2 | a0001c0001t0007g0215a0001c0001t0007g0216 | 2 | HG01243.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1753+4236_1753+425 others(24): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | ||||||
| chr17:59037557
|
C | CAAAAAAA others(15): Show |
2 | a0001c0001t0007g0213a0001c0001t0007g0214 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1753+4234_1753+425 others(26): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | ||||||
| chr17:59037557
|
CA | C | 6 | a0001c0001t0001g0235a0001c0001t0001g0254a0001c0001t0001g0258others(3): Show | 6 | HG00099.hp1 HG01358.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1753+4255delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | ||||||
| chr17:59037557
|
CAA | C | 42 | a0001c0001t0001g0220a0001c0001t0001g0223a0001c0001t0001g0224others(39): Show | 42 | HG00558.hp1 HG00597.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1753+4254_1753+425 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | ||||||
| chr17:59037557
|
CAAA | C | 69 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0225others(66): Show | 69 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1753+4253_1753+425 others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | ||||||
| chr17:59037557
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0003g0098a0001c0001t0003g0101a0001c0006t0003g0106 | 3 | HG01169.hp1 HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1753+4245_1753+425 others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | ||||||
| chr17:59037557
|
CAAAAAAA others(5): Show |
C | 22 | a0001c0001t0002g0094a0001c0001t0002g0100a0001c0001t0002g0119others(19): Show | 22 | HG01168.hp2 HG02109.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.1753+4244_1753+425 others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | ||||||
| chr17:59037557
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0002g0177 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1753+4240_1753+425 others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | ||||||
| chr17:59037557
|
CAAAAAAA others(13): Show |
C | 74 | a0001c0001t0001g0339a0001c0001t0003g0003a0001c0001t0003g0004others(71): Show | 74 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1753+4236_1753+425 others(24): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037557 | ||||||
| chr17:59037584
|
A | T | 1 | a0001c0001t0001g0260 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1753+4229T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037584 | ||||||
| chr17:59037591
|
G | C | 116 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(113): Show | 116 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1753+4222C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037591 | ||||||
| chr17:59037653
|
A | T | 1 | a0001c0001t0001g0270 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1753+4160T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59037653 | ||||||
| chr17:59038078
|
C | G | 1 | a0001c0001t0001g0257 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1753+3735G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038078 | ||||||
| chr17:59038090
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1753+3723G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038090 | ||||||
| chr17:59038155
|
T | C | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1753+3658A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038155 | ||||||
| chr17:59038305
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1753+3508A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038305 | ||||||
| chr17:59038338
|
T | A | 1 | a0001c0001t0001g0227 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1753+3475A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038338 | ||||||
| chr17:59038486
|
T | C | 1 | a0001c0001t0002g0194 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1753+3327A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038486 | ||||||
| chr17:59038753
|
T | C | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1753+3060A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038753 | ||||||
| chr17:59038761
|
C | G | 1 | a0001c0001t0001g0328 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1753+3052G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038761 | ||||||
| chr17:59038810
|
T | G | 1 | a0001c0001t0001g0254 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1753+3003A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59038810 | ||||||
| chr17:59039071
|
C | T | 3 | a0001c0001t0003g0086a0001c0001t0003g0092a0001c0001t0004g0090 | 3 | HG02615.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1753+2742G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039071 | ||||||
| chr17:59039151
|
A | T | 1 | a0001c0001t0001g0254 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1753+2662T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039151 | ||||||
| chr17:59039323
|
A | C | 1 | a0001c0003t0006g0217 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1753+2490T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039323 | ||||||
| chr17:59039350
|
CT | C | 62 | a0001c0001t0001g0254a0001c0001t0001g0339a0001c0001t0003g0003others(59): Show | 62 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1753+2462delA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039350 | ||||||
| chr17:59039448
|
G | A | 96 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1753+2365C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039448 | ||||||
| chr17:59039491
|
C | G | 4 | a0001c0001t0002g0149a0001c0001t0002g0156a0001c0001t0002g0211others(1): Show | 4 | HG00099.hp1 HG02602.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753+2322G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039491 | ||||||
| chr17:59039510
|
C | T | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1753+2303G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039510 | ||||||
| chr17:59039883
|
A | G | 11 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1753+1930T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039883 | ||||||
| chr17:59039974
|
T | C | 10 | a0001c0001t0003g0062a0001c0001t0003g0063a0001c0001t0003g0064others(7): Show | 10 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1753+1839A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59039974 | ||||||
| chr17:59040144
|
G | A | 1 | a0001c0001t0001g0328 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1753+1669C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040144 | ||||||
| chr17:59040356
|
G | A | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1753+1457C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040356 | ||||||
| chr17:59040461
|
C | T | 4 | a0001c0003t0006g0212a0001c0003t0006g0217a0001c0003t0006g0218others(1): Show | 4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1753+1352G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040461 | ||||||
| chr17:59040640
|
G | T | 1 | a0001c0001t0001g0254 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1753+1173C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040640 | ||||||
| chr17:59040760
|
T | C | 98 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1753+1053A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040760 | ||||||
| chr17:59040784
|
C | T | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1753+1029G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040784 | ||||||
| chr17:59040785
|
G | A | 11 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1753+1028C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040785 | ||||||
| chr17:59040843
|
A | C | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1753+970T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040843 | ||||||
| chr17:59040843
|
A | G | 222 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(219): Show | 222 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1753+970T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040843 | ||||||
| chr17:59040873
|
C | T | 2 | a0001c0001t0002g0120a0001c0001t0002g0121 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1753+940G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040873 | ||||||
| chr17:59040903
|
G | A | 1 | a0002c0002t0002g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1753+910C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040903 | ||||||
| chr17:59040907
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1753+906C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040907 | ||||||
| chr17:59040918
|
C | T | 3 | a0001c0001t0002g0132a0001c0001t0002g0158a0001c0001t0002g0159 | 3 | HG01106.hp1 HG01358.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1753+895G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59040918 | ||||||
| chr17:59041022
|
C | G | 3 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0121 | 3 | HG01257.hp2 HG01258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1753+791G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59041022 | ||||||
| chr17:59041036
|
G | A | 1 | a0001c0001t0003g0052 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1753+777C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59041036 | ||||||
| chr17:59041126
|
CTTTTAAT others(6): Show |
C | 1 | a0001c0001t0001g0238 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1753+674_1753+686d others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59041126 | ||||||
| chr17:59041285
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1753+528C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59041285 | ||||||
| chr17:59041310
|
T | C | 1 | a0001c0001t0003g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1753+503A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59041310 | ||||||
| chr17:59041331
|
T | A | 1 | a0001c0001t0001g0270 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1753+482A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59041331 | ||||||
| chr17:59041752
|
C | T | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1753+61G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 17/23 | chr17 | 59041752 | ||||||
| chr17:59042057
|
C | T | 1 | a0001c0001t0009g0167 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1668-159G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042057 | ||||||
| chr17:59042098
|
C | T | 2 | a0001c0001t0002g0107a0001c0001t0002g0109 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1668-200G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042098 | ||||||
| chr17:59042105
|
G | A | 6 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(3): Show | 6 | HG02559.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1668-207C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042105 | ||||||
| chr17:59042142
|
T | A | 1 | a0001c0001t0001g0296 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1668-244A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042142 | ||||||
| chr17:59042153
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1668-255C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042153 | ||||||
| chr17:59042251
|
C | T | 6 | a0001c0001t0001g0232a0001c0001t0001g0244a0001c0001t0001g0246others(3): Show | 6 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1668-353G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042251 | ||||||
| chr17:59042270
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1668-372C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042270 | ||||||
| chr17:59042293
|
G | A | 7 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1668-395C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042293 | ||||||
| chr17:59042304
|
A | G | 2 | a0001c0001t0002g0141a0001c0001t0002g0142 | 2 | HG00558.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1668-406T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042304 | ||||||
| chr17:59042374
|
C | CA | 11 | a0001c0001t0001g0235a0001c0001t0001g0314a0001c0001t0001g0315others(8): Show | 11 | HG02257.hp2 HG02486.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1668-477dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042374 | ||||||
| chr17:59042430
|
TTAA | T | 3 | a0001c0001t0003g0034a0001c0001t0008g0022a0001c0001t0008g0030 | 3 | NA18998.hp1 NA19056.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1668-535_1668-533d others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042430 | ||||||
| chr17:59042430
|
TTAAAAAA | T | 5 | a0001c0001t0003g0005a0001c0001t0003g0037a0001c0001t0003g0047others(2): Show | 5 | HG01099.hp1 HG01192.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1668-539_1668-533d others(9): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042430 | ||||||
| chr17:59042430
|
TTAAAAAA others(1): Show |
T | 7 | a0001c0001t0003g0009a0001c0001t0003g0040a0001c0001t0003g0044others(4): Show | 7 | HG00438.hp1 HG00733.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.1668-540_1668-533d others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042430 | ||||||
| chr17:59042430
|
TTAAAAAA others(4): Show |
T | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1668-543_1668-533d others(13): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042430 | ||||||
| chr17:59042430
|
TTAAAAAA others(7): Show |
T | 9 | a0001c0001t0001g0286a0001c0001t0007g0213a0001c0001t0007g0214others(6): Show | 9 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.1668-546_1668-533d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042430 | ||||||
| chr17:59042431
|
T | A | 199 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(196): Show | 199 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1668-533A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042431 | ||||||
| chr17:59042431
|
TA | T | 29 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(26): Show | 29 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.1668-534delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042431 | ||||||
| chr17:59042437
|
A | AATATATA others(3): Show |
1 | a0001c0001t0003g0101 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1668-540_1668-539i others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042437 | ||||||
| chr17:59042437
|
A | AATATATA others(11): Show |
2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1668-540_1668-539i others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042437 | ||||||
| chr17:59042437
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0003g0028 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1668-540_1668-539i others(37): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042437 | ||||||
| chr17:59042437
|
AAAAAAAA others(9): Show |
A | 5 | a0001c0001t0001g0232a0001c0001t0001g0244a0001c0001t0001g0246others(2): Show | 5 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1668-555_1668-540d others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042437 | ||||||
| chr17:59042438
|
AAAAAAAA others(8): Show |
A | 17 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0229others(14): Show | 17 | HG00639.hp1 HG00639.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.1668-555_1668-541d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042438 | ||||||
| chr17:59042439
|
A | AATATATA others(11): Show |
2 | a0001c0001t0010g0078a0001c0001t0010g0089 | 2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1668-542_1668-541i others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042439 | ||||||
| chr17:59042439
|
A | AATATATA others(13): Show |
1 | a0001c0001t0003g0079 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1668-542_1668-541i others(22): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042439 | ||||||
| chr17:59042439
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0008g0032 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1668-542_1668-541i others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042439 | ||||||
| chr17:59042439
|
A | T | 4 | a0001c0001t0003g0028a0001c0001t0003g0097a0001c0001t0003g0098others(1): Show | 4 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1668-541T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042439 | ||||||
| chr17:59042439
|
AAAAAAAA others(7): Show |
A | 3 | a0001c0001t0003g0086a0001c0001t0003g0092a0001c0001t0004g0090 | 3 | HG02615.hp1 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1668-555_1668-542d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042439 | ||||||
| chr17:59042439
|
AAAAAAAA others(9): Show |
A | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0247 | 3 | HG03098.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1668-557_1668-542d others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042439 | ||||||
| chr17:59042440
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0306 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1668-555_1668-543d others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042440 | ||||||
| chr17:59042440
|
AAAAAAAA others(8): Show |
A | 71 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(68): Show | 71 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1668-557_1668-543d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042440 | ||||||
| chr17:59042441
|
A | AATATATA others(3): Show |
1 | a0001c0001t0003g0013 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1668-544_1668-543i others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | ||||||
| chr17:59042441
|
A | AATATATA others(11): Show |
1 | a0001c0001t0003g0093 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1668-544_1668-543i others(20): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | ||||||
| chr17:59042441
|
A | AATATATA others(13): Show |
2 | a0001c0001t0003g0087a0001c0001t0003g0088 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1668-544_1668-543i others(22): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | ||||||
| chr17:59042441
|
A | AATATATA others(15): Show |
1 | a0001c0001t0003g0027 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1668-544_1668-543i others(24): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | ||||||
| chr17:59042441
|
A | AATATATA others(17): Show |
1 | a0001c0001t0003g0033 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1668-544_1668-543i others(26): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | ||||||
| chr17:59042441
|
A | ATATATAT others(2): Show |
3 | a0001c0001t0003g0085a0001c0001t0003g0095a0001c0001t0013g0029 | 3 | HG02647.hp1 HG03017.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1668-544_1668-543i others(11): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | ||||||
| chr17:59042441
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0003g0054 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1668-544_1668-543i others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | ||||||
| chr17:59042441
|
A | ATATATAT others(34): Show |
1 | a0001c0001t0003g0048 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1668-544_1668-543i others(43): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | ||||||
| chr17:59042441
|
A | T | 14 | a0001c0001t0002g0094a0001c0001t0002g0100a0001c0001t0003g0012others(11): Show | 14 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1668-543T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | ||||||
| chr17:59042441
|
AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0001g0317a0001c0001t0001g0318 | 2 | NA18943.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1668-555_1668-544d others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | ||||||
| chr17:59042441
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0252 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1668-557_1668-544d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | ||||||
| chr17:59042441
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1668-559_1668-544d others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042441 | ||||||
| chr17:59042442
|
AAAAAAAA others(8): Show |
A | 14 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0231others(11): Show | 14 | HG01169.hp2 HG02004.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1668-559_1668-545d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042442 | ||||||
| chr17:59042443
|
A | AATATATA others(3): Show |
1 | a0001c0001t0003g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1668-546_1668-545i others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | ||||||
| chr17:59042443
|
A | AATATATA others(5): Show |
1 | a0001c0001t0003g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1668-546_1668-545i others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | ||||||
| chr17:59042443
|
A | AATATATA others(13): Show |
2 | a0001c0001t0003g0018a0001c0001t0003g0019 | 2 | NA19001.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1668-546_1668-545i others(22): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | ||||||
| chr17:59042443
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0003g0081 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1668-546_1668-545i others(13): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | ||||||
| chr17:59042443
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0003g0058 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1668-546_1668-545i others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | ||||||
| chr17:59042443
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0003g0057 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1668-546_1668-545i others(21): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | ||||||
| chr17:59042443
|
A | ATATATAT others(14): Show |
3 | a0001c0001t0001g0339a0001c0001t0003g0011a0001c0001t0003g0122 | 3 | NA18944.hp1 NA18949.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1668-546_1668-545i others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | ||||||
| chr17:59042443
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0003g0016 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1668-546_1668-545i others(25): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | ||||||
| chr17:59042443
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0003g0038 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1668-546_1668-545i others(37): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | ||||||
| chr17:59042443
|
A | T | 27 | a0001c0001t0002g0094a0001c0001t0002g0100a0001c0001t0003g0012others(24): Show | 27 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.1668-545T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | ||||||
| chr17:59042443
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0320 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1668-559_1668-546d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042443 | ||||||
| chr17:59042444
|
AAAAAAAT others(8): Show |
A | 3 | a0001c0001t0001g0245a0001c0001t0001g0266a0001c0001t0001g0325 | 3 | HG01496.hp1 HG03927.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1668-561_1668-547d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042444 | ||||||
| chr17:59042445
|
A | AATATATA others(5): Show |
1 | a0001c0001t0003g0055 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
A | AATATATA others(13): Show |
1 | a0001c0001t0003g0026 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1668-548_1668-547i others(22): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
A | AATATATA others(17): Show |
1 | a0001c0001t0003g0015 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(26): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
A | AATATATA others(19): Show |
1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(28): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
A | AATATATA others(23): Show |
1 | a0001c0001t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(32): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
A | AATATATA others(31): Show |
1 | a0001c0001t0003g0056 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1668-548_1668-547i others(40): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
A | ATATATAT others(4): Show |
4 | a0001c0001t0003g0008a0001c0001t0003g0017a0001c0001t0003g0062others(1): Show | 4 | HG02027.hp1 HG02809.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1668-548_1668-547i others(13): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0003g0083 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1668-548_1668-547i others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0003g0059 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1668-548_1668-547i others(19): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0003g0046 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0003g0010 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(27): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
A | ATATATAT others(20): Show |
2 | a0001c0001t0003g0014a0001c0001t0003g0020 | 2 | HG00099.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1668-548_1668-547i others(29): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0003g0049 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(33): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
A | ATATATAT others(26): Show |
2 | a0001c0001t0003g0007a0001c0001t0003g0023 | 2 | HG01261.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1668-548_1668-547i others(35): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
A | ATATATAT others(34): Show |
1 | a0001c0001t0003g0035 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1668-548_1668-547i others(43): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
A | T | 47 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(44): Show | 47 | HG00741.hp1 HG01106.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.1668-547T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042445
|
AAAAAATA others(7): Show |
A | 1 | a0001c0001t0001g0254 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1668-561_1668-548d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042445 | ||||||
| chr17:59042447
|
A | AT | 4 | a0001c0001t0002g0109a0001c0001t0002g0129a0001c0001t0002g0138others(1): Show | 4 | HG02486.hp1 HG04204.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1668-550_1668-549i others(3): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042447 | ||||||
| chr17:59042447
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0003g0024a0001c0001t0003g0025 | 2 | NA18952.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1668-550_1668-549i others(23): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042447 | ||||||
| chr17:59042447
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0003g0021 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1668-550_1668-549i others(27): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042447 | ||||||
| chr17:59042447
|
A | ATATATAT others(22): Show |
4 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0053others(1): Show | 4 | HG01978.hp2 HG03831.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1668-550_1668-549i others(31): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042447 | ||||||
| chr17:59042447
|
A | T | 92 | a0001c0001t0001g0339a0001c0001t0002g0080a0001c0001t0002g0094others(89): Show | 92 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1668-549T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042447 | ||||||
| chr17:59042449
|
A | AAT | 9 | a0001c0001t0002g0128a0001c0001t0002g0165a0001c0001t0002g0187others(6): Show | 9 | HG00323.hp1 NA18944.hp2 NA18994.hp1 others(6): Show |
intron_variant | MODIFIER | c.1668-553_1668-552d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042449 | ||||||
| chr17:59042449
|
A | AATATATA others(5): Show |
1 | a0001c0001t0003g0063 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1668-563_1668-552d others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042449 | ||||||
| chr17:59042449
|
A | AT | 3 | a0001c0001t0002g0126a0001c0001t0002g0143a0001c0001t0002g0146 | 3 | HG02071.hp1 NA18995.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1668-552_1668-551i others(3): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042449 | ||||||
| chr17:59042449
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0003g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1668-552_1668-551i others(31): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042449 | ||||||
| chr17:59042449
|
A | ATATATAT others(38): Show |
1 | a0001c0001t0003g0052 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1668-552_1668-551i others(47): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042449 | ||||||
| chr17:59042449
|
A | T | 138 | a0001c0001t0001g0339a0001c0001t0002g0080a0001c0001t0002g0094others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1668-551T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042449 | ||||||
| chr17:59042450
|
AT | A | 4 | a0001c0001t0002g0210a0001c0001t0003g0110a0001c0001t0009g0167others(1): Show | 4 | HG02258.hp2 HG02293.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1668-553delA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042450 | ||||||
| chr17:59042450
|
ATAT | A | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1668-555_1668-553d others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042450 | ||||||
| chr17:59042451
|
T | A | 12 | a0001c0001t0001g0286a0001c0001t0003g0005a0001c0001t0003g0009others(9): Show | 12 | HG00438.hp1 HG01515.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1668-553A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042451 | ||||||
| chr17:59042453
|
T | A | 2 | a0001c0001t0003g0110a0001c0001t0003g0111 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1668-555A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042453 | ||||||
| chr17:59042472
|
A | C | 6 | a0001c0001t0003g0009a0001c0001t0003g0044a0001c0001t0005g0041others(3): Show | 6 | HG00438.hp1 NA18945.hp1 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.1668-574T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042472 | ||||||
| chr17:59042624
|
G | C | 1 | a0001c0001t0003g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1668-726C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042624 | ||||||
| chr17:59042730
|
T | A | 1 | a0001c0001t0001g0254 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1668-832A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042730 | ||||||
| chr17:59042742
|
G | A | 12 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0063others(9): Show | 12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1668-844C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042742 | ||||||
| chr17:59042894
|
C | G | 1 | a0001c0001t0001g0339 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1668-996G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59042894 | ||||||
| chr17:59043063
|
T | C | 12 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0063others(9): Show | 12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1668-1165A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043063 | ||||||
| chr17:59043165
|
T | G | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1668-1267A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043165 | ||||||
| chr17:59043419
|
A | G | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | NA18963.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1668-1521T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043419 | ||||||
| chr17:59043631
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0252 | 2 | NA18951.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1668-1733C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043631 | ||||||
| chr17:59043635
|
C | A | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1668-1737G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043635 | ||||||
| chr17:59043787
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1668-1889A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043787 | ||||||
| chr17:59043952
|
C | T | 129 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(126): Show | 129 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.1668-2054G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043952 | ||||||
| chr17:59043961
|
T | C | 3 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0310 | 3 | NA18993.hp2 NA19086.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1668-2063A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59043961 | ||||||
| chr17:59044393
|
T | G | 1 | a0001c0001t0001g0326 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1668-2495A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59044393 | ||||||
| chr17:59044398
|
T | A | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1668-2500A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59044398 | ||||||
| chr17:59044421
|
G | A | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1668-2523C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59044421 | ||||||
| chr17:59044875
|
A | G | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1667+2808T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59044875 | ||||||
| chr17:59044932
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1667+2751G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59044932 | ||||||
| chr17:59045453
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1667+2230G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59045453 | ||||||
| chr17:59045466
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1667+2217G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59045466 | ||||||
| chr17:59045470
|
T | C | 121 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(118): Show | 121 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1667+2213A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59045470 | ||||||
| chr17:59045545
|
A | C | 5 | a0001c0001t0003g0079a0001c0001t0003g0096a0001c0001t0003g0097others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.1667+2138T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59045545 | ||||||
| chr17:59045564
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1667+2119C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59045564 | ||||||
| chr17:59045915
|
C | T | 4 | a0001c0001t0001g0324a0001c0001t0001g0329a0001c0001t0001g0331others(1): Show | 4 | HG00621.hp1 NA18612.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.1667+1768G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59045915 | ||||||
| chr17:59045970
|
C | T | 11 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1667+1713G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59045970 | ||||||
| chr17:59046015
|
CA | C | 7 | a0001c0001t0002g0209a0001c0001t0002g0210a0002c0002t0002g0125others(4): Show | 7 | HG01952.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1667+1667delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046015 | ||||||
| chr17:59046164
|
T | C | 1 | a0001c0001t0003g0059 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1667+1519A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046164 | ||||||
| chr17:59046212
|
T | C | 5 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0006others(2): Show | 5 | HG01106.hp2 HG01978.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1667+1471A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046212 | ||||||
| chr17:59046314
|
C | T | 1 | a0001c0001t0002g0127 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1667+1369G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046314 | ||||||
| chr17:59046540
|
G | GT | 13 | a0001c0001t0001g0225a0001c0001t0001g0247a0001c0001t0001g0250others(10): Show | 13 | HG01978.hp1 HG02145.hp2 HG03098.hp1 others(10): Show |
intron_variant | MODIFIER | c.1667+1142dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046540 | ||||||
| chr17:59046550
|
T | C | 1 | a0001c0001t0003g0026 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1667+1133A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046550 | ||||||
| chr17:59046570
|
A | ACT | 248 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(245): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1667+1111_1667+111 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046570 | ||||||
| chr17:59046741
|
C | T | 1 | a0001c0001t0003g0065 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1667+942G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046741 | ||||||
| chr17:59046921
|
G | A | 7 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1667+762C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59046921 | ||||||
| chr17:59047011
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1667+672C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59047011 | ||||||
| chr17:59047075
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1667+608A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59047075 | ||||||
| chr17:59047077
|
C | T | 1 | a0001c0001t0001g0336 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1667+606G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59047077 | ||||||
| chr17:59047147
|
C | T | 2 | a0001c0001t0002g0190a0001c0001t0002g0191 | 2 | NA18970.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1667+536G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59047147 | ||||||
| chr17:59047662
|
G | A | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1667+21C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 16/23 | chr17 | 59047662 | ||||||
| chr17:59048007
|
A | G | 1 | a0001c0001t0002g0108 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1531-188T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048007 | ||||||
| chr17:59048019
|
G | A | 1 | a0001c0001t0001g0336 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1531-200C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048019 | ||||||
| chr17:59048068
|
C | G | 1 | a0001c0001t0003g0006 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1531-249G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048068 | ||||||
| chr17:59048300
|
A | C | 1 | a0001c0001t0002g0197 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1531-481T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048300 | ||||||
| chr17:59048343
|
C | G | 8 | a0001c0001t0001g0269a0001c0001t0001g0288a0001c0001t0001g0289others(5): Show | 8 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1531-524G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048343 | ||||||
| chr17:59048347
|
C | T | 2 | a0001c0001t0003g0031a0001c0001t0012g0002 | 2 | HG01515.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1531-528G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048347 | ||||||
| chr17:59048462
|
T | G | 1 | a0001c0001t0001g0261 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1531-643A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048462 | ||||||
| chr17:59048564
|
T | G | 1 | a0001c0001t0001g0323 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1530+614A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048564 | ||||||
| chr17:59048890
|
C | T | 11 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0063others(8): Show | 11 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1530+288G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 15/23 | chr17 | 59048890 | ||||||
| chr17:59049481
|
G | A | 73 | a0001c0001t0001g0339a0001c0001t0003g0003a0001c0001t0003g0004others(70): Show | 73 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1315-88C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59049481 | ||||||
| chr17:59049486
|
T | A | 4 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1315-93A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59049486 | ||||||
| chr17:59050008
|
A | G | 1 | a0001c0001t0002g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1315-615T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050008 | ||||||
| chr17:59050170
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1315-777C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050170 | ||||||
| chr17:59050318
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0252 | 2 | NA18951.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1314+896C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050318 | ||||||
| chr17:59050319
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0252 | 2 | NA18951.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1314+895G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050319 | ||||||
| chr17:59050363
|
C | G | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1314+851G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050363 | ||||||
| chr17:59050556
|
C | T | 2 | a0001c0001t0002g0154a0001c0001t0002g0155 | 2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1314+658G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050556 | ||||||
| chr17:59050838
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1314+376C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050838 | ||||||
| chr17:59050973
|
CCTT | C | 13 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(10): Show | 13 | HG00558.hp2 HG00673.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.1314+238_1314+240d others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59050973 | ||||||
| chr17:59051025
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1314+189T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 14/23 | chr17 | 59051025 | ||||||
| chr17:59051449
|
G | T | 1 | a0001c0001t0003g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1200-121C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59051449 | ||||||
| chr17:59051754
|
G | A | 4 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200-426C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59051754 | ||||||
| chr17:59051769
|
C | T | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1200-441G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59051769 | ||||||
| chr17:59051863
|
T | G | 131 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(128): Show | 131 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.1200-535A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59051863 | ||||||
| chr17:59052008
|
C | T | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1200-680G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052008 | ||||||
| chr17:59052213
|
TA | T | 247 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(244): Show | 247 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.1200-886delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052213 | ||||||
| chr17:59052280
|
C | T | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1200-952G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052280 | ||||||
| chr17:59052489
|
T | A | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1200-1161A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052489 | ||||||
| chr17:59052521
|
C | A | 93 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1200-1193G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052521 | ||||||
| chr17:59052531
|
C | T | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200-1203G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052531 | ||||||
| chr17:59052551
|
T | C | 1 | a0001c0001t0002g0170 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1200-1223A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052551 | ||||||
| chr17:59052661
|
AAGAG | A | 7 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200-1337_1200-133 others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052661 | ||||||
| chr17:59052753
|
G | C | 1 | a0001c0001t0002g0141 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1200-1425C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052753 | ||||||
| chr17:59052800
|
C | T | 11 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1200-1472G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052800 | ||||||
| chr17:59052824
|
G | A | 1 | a0001c0001t0002g0141 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1200-1496C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052824 | ||||||
| chr17:59052942
|
G | A | 4 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | NA18939.hp2 NA18954.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200-1614C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052942 | ||||||
| chr17:59052956
|
AAAAATC | A | 11 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1200-1634_1200-162 others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052956 | ||||||
| chr17:59052957
|
A | AAAATC | 50 | a0001c0001t0001g0224a0001c0001t0001g0232a0001c0001t0001g0244others(47): Show | 50 | HG00621.hp1 HG00642.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1200-1634_1200-163 others(9): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052957 | ||||||
| chr17:59052957
|
A | AAAATCAA others(3): Show |
73 | a0001c0001t0001g0249a0001c0001t0001g0284a0001c0001t0001g0287others(70): Show | 73 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1200-1639_1200-163 others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052957 | ||||||
| chr17:59052957
|
A | AAAATCAA others(8): Show |
8 | a0001c0001t0003g0011a0001c0001t0003g0018a0001c0001t0003g0031others(5): Show | 8 | HG00642.hp2 HG03139.hp2 HG03704.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200-1644_1200-163 others(19): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052957 | ||||||
| chr17:59052957
|
AAAATCAA others(8): Show |
A | 1 | a0001c0001t0001g0338 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1200-1644_1200-163 others(19): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59052957 | ||||||
| chr17:59053066
|
G | A | 23 | a0001c0001t0002g0094a0001c0001t0002g0100a0001c0001t0003g0079others(20): Show | 23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1200-1738C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053066 | ||||||
| chr17:59053186
|
C | T | 7 | a0001c0001t0002g0100a0001c0001t0003g0079a0001c0001t0003g0096others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200-1858G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053186 | ||||||
| chr17:59053227
|
T | G | 1 | a0001c0001t0002g0164 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1200-1899A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053227 | ||||||
| chr17:59053308
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1200-1980A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053308 | ||||||
| chr17:59053321
|
T | C | 1 | a0001c0001t0003g0048 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1200-1993A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053321 | ||||||
| chr17:59053351
|
G | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0025 | 2 | NA18952.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1200-2023C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053351 | ||||||
| chr17:59053424
|
C | T | 124 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(121): Show | 124 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1200-2096G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053424 | ||||||
| chr17:59053578
|
T | G | 1 | a0001c0001t0001g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1200-2250A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053578 | ||||||
| chr17:59053666
|
T | C | 1 | a0001c0001t0002g0131 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1200-2338A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053666 | ||||||
| chr17:59053726
|
A | G | 2 | a0001c0001t0002g0120a0001c0001t0002g0121 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1200-2398T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053726 | ||||||
| chr17:59053828
|
G | A | 1 | a0001c0001t0003g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1200-2500C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053828 | ||||||
| chr17:59053933
|
T | TAAACA | 227 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(224): Show | 227 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.1200-2610_1200-260 others(9): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053933 | ||||||
| chr17:59053990
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1200-2662G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59053990 | ||||||
| chr17:59054220
|
T | A | 121 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(118): Show | 121 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1199+2655A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054220 | ||||||
| chr17:59054311
|
G | A | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1199+2564C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054311 | ||||||
| chr17:59054360
|
G | C | 3 | a0001c0001t0003g0040a0001c0001t0003g0047a0001c0001t0003g0123 | 3 | HG00733.hp2 HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1199+2515C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054360 | ||||||
| chr17:59054389
|
C | G | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1199+2486G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054389 | ||||||
| chr17:59054404
|
C | T | 1 | a0001c0001t0003g0007 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1199+2471G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054404 | ||||||
| chr17:59054591
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1199+2284C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054591 | ||||||
| chr17:59054753
|
C | G | 1 | a0001c0001t0001g0323 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1199+2122G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054753 | ||||||
| chr17:59054809
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1199+2066G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054809 | ||||||
| chr17:59054991
|
A | G | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1199+1884T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59054991 | ||||||
| chr17:59055158
|
G | A | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1199+1717C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055158 | ||||||
| chr17:59055207
|
G | A | 229 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(226): Show | 229 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.1199+1668C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055207 | ||||||
| chr17:59055332
|
C | CA | 16 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(13): Show | 16 | HG00099.hp1 HG00438.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1199+1542dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055332 | ||||||
| chr17:59055332
|
C | CAA | 7 | a0001c0001t0002g0115a0001c0001t0002g0120a0001c0001t0002g0121others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1199+1541_1199+154 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055332 | ||||||
| chr17:59055332
|
C | CAAA | 6 | a0001c0001t0002g0117a0001c0001t0002g0119a0001c0001t0003g0073others(3): Show | 6 | HG02486.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1199+1540_1199+154 others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055332 | ||||||
| chr17:59055332
|
CA | C | 40 | a0001c0001t0001g0223a0001c0001t0001g0246a0001c0001t0001g0270others(37): Show | 40 | HG00544.hp1 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.1199+1542delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055332 | ||||||
| chr17:59055332
|
CAA | C | 178 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(175): Show | 178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1199+1541_1199+154 others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055332 | ||||||
| chr17:59055524
|
C | A | 6 | a0001c0001t0001g0232a0001c0001t0001g0244a0001c0001t0001g0246others(3): Show | 6 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1199+1351G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055524 | ||||||
| chr17:59055647
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1199+1228C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055647 | ||||||
| chr17:59055649
|
T | G | 249 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(246): Show | 249 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.1199+1226A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055649 | ||||||
| chr17:59055685
|
C | CA | 44 | a0001c0001t0001g0223a0001c0001t0001g0227a0001c0001t0001g0233others(41): Show | 44 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1199+1189dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055685 | ||||||
| chr17:59055685
|
CA | C | 19 | a0001c0001t0001g0243a0001c0001t0001g0252a0001c0001t0001g0338others(16): Show | 19 | HG00438.hp1 HG01099.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1199+1189delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055685 | ||||||
| chr17:59055768
|
T | C | 1 | a0001c0001t0002g0184 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1199+1107A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055768 | ||||||
| chr17:59055775
|
G | C | 1 | a0001c0001t0003g0037 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1199+1100C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055775 | ||||||
| chr17:59055816
|
T | C | 2 | a0001c0001t0003g0110a0001c0001t0003g0111 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1199+1059A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59055816 | ||||||
| chr17:59056068
|
T | G | 20 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(17): Show | 20 | HG01346.hp1 HG02071.hp1 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.1199+807A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056068 | ||||||
| chr17:59056179
|
T | A | 1 | a0001c0001t0001g0295 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1199+696A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056179 | ||||||
| chr17:59056267
|
C | T | 2 | a0001c0001t0002g0133a0001c0001t0002g0134 | 2 | HG00621.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1199+608G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056267 | ||||||
| chr17:59056298
|
C | T | 1 | a0001c0001t0003g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1199+577G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056298 | ||||||
| chr17:59056323
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1199+552G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056323 | ||||||
| chr17:59056446
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1199+429C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056446 | ||||||
| chr17:59056458
|
G | A | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1199+417C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056458 | ||||||
| chr17:59056495
|
C | A | 1 | a0001c0001t0003g0038 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1199+380G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056495 | ||||||
| chr17:59056586
|
C | T | 4 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(1): Show | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1199+289G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056586 | ||||||
| chr17:59056587
|
A | G | 251 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(248): Show | 251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1199+288T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056587 | ||||||
| chr17:59056593
|
G | A | 4 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(1): Show | 4 | NA18945.hp1 NA19006.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1199+282C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056593 | ||||||
| chr17:59056598
|
C | T | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1199+277G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056598 | ||||||
| chr17:59056649
|
G | C | 3 | a0001c0001t0003g0019a0001c0001t0003g0026a0001c0001t0003g0122 | 3 | NA18992.hp2 NA19001.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1199+226C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056649 | ||||||
| chr17:59056654
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1199+221G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056654 | ||||||
| chr17:59056661
|
C | T | 1 | a0001c0001t0003g0034 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1199+214G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056661 | ||||||
| chr17:59056667
|
T | C | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1199+208A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056667 | ||||||
| chr17:59056698
|
A | G | 254 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(251): Show | 254 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1199+177T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056698 | ||||||
| chr17:59056716
|
C | CA | 14 | a0001c0001t0001g0247a0001c0001t0001g0249a0001c0001t0002g0129others(11): Show | 14 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1199+158dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAA | 13 | a0001c0001t0001g0340a0001c0001t0002g0132a0001c0001t0002g0147others(10): Show | 13 | HG01106.hp1 HG01358.hp1 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.1199+157_1199+158d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAA | 13 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0107others(10): Show | 13 | HG00099.hp1 HG01261.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1199+156_1199+158d others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAA | 30 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0238others(27): Show | 30 | HG00597.hp1 HG00673.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1199+155_1199+158d others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAA | 41 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(38): Show | 41 | HG00438.hp2 HG00544.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1199+154_1199+158d others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAA | 39 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0226others(36): Show | 39 | HG00280.hp1 HG00558.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.1199+153_1199+158d others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA | 26 | a0001c0001t0001g0225a0001c0001t0001g0245a0001c0001t0001g0257others(23): Show | 26 | HG00544.hp2 HG00597.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1199+152_1199+158d others(9): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(1): Show |
24 | a0001c0001t0001g0233a0001c0001t0001g0242a0001c0001t0001g0248others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1199+151_1199+158d others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(2): Show |
23 | a0001c0001t0001g0231a0001c0001t0001g0250a0001c0001t0001g0252others(20): Show | 23 | HG01243.hp2 HG02135.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1199+150_1199+158d others(11): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(3): Show |
15 | a0001c0001t0001g0297a0001c0001t0001g0300a0001c0001t0001g0337others(12): Show | 15 | HG00323.hp2 HG00741.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1199+149_1199+158d others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(4): Show |
4 | a0001c0001t0003g0004a0001c0001t0003g0009a0001c0001t0008g0030others(1): Show | 4 | HG00438.hp1 HG03831.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1199+148_1199+158d others(13): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(5): Show |
7 | a0001c0001t0003g0011a0001c0001t0003g0014a0001c0001t0003g0060others(4): Show | 7 | HG00099.hp2 HG01515.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.1199+147_1199+158d others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0309a0001c0001t0003g0048a0001c0001t0005g0043 | 3 | HG02523.hp2 HG04228.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1199+146_1199+158d others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0243a0001c0001t0003g0070a0001c0001t0005g0041 | 3 | HG02155.hp1 HG03453.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1199+145_1199+158d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0339a0001c0001t0003g0007a0001c0001t0003g0034others(1): Show | 4 | HG01346.hp2 NA18944.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1199+144_1199+158d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0003g0008a0001c0001t0003g0037 | 2 | HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1199+143_1199+158d others(18): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0003g0012a0001c0001t0003g0035 | 2 | HG02040.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1199+140_1199+158d others(21): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(15): Show |
2 | a0001c0001t0003g0015a0001c0001t0003g0019 | 2 | HG00280.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1199+137_1199+158d others(24): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0298 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1199+136_1199+158d others(25): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0003g0026 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1199+134_1199+158d others(27): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(19): Show |
1 | a0001c0001t0003g0047 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1199+133_1199+158d others(28): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0003g0031 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1199+132_1199+158d others(29): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0003g0040 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1199+158_1199+159i others(34): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0003g0006 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1199+158_1199+159i others(35): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
CA | C | 6 | a0001c0001t0001g0228a0001c0001t0001g0230a0001c0001t0002g0119others(3): Show | 6 | HG00639.hp1 HG00642.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1199+158delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
CAA | C | 9 | a0001c0001t0001g0229a0001c0001t0002g0080a0001c0001t0002g0109others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1199+157_1199+158d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
CAAA | C | 6 | a0001c0001t0002g0112a0001c0001t0002g0114a0001c0001t0002g0118others(3): Show | 6 | HG01884.hp1 HG02451.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1199+156_1199+158d others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
CAAAAAA | C | 8 | a0001c0001t0002g0094a0001c0001t0003g0079a0001c0001t0003g0095others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1199+153_1199+158d others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
CAAAAAAA | C | 15 | a0001c0001t0002g0100a0001c0001t0003g0081a0001c0001t0003g0082others(12): Show | 15 | HG02109.hp1 HG02559.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1199+152_1199+158d others(9): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0008t0003g0039 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1199+149_1199+158d others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0046 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1199+148_1199+158d others(13): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1199+147_1199+158d others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056716
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0003g0003 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1199+144_1199+158d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056716 | ||||||
| chr17:59056763
|
G | T | 74 | a0001c0001t0001g0339a0001c0001t0003g0003a0001c0001t0003g0004others(71): Show | 74 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1199+112C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056763 | ||||||
| chr17:59056836
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1199+39G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 13/23 | chr17 | 59056836 | ||||||
| chr17:59057488
|
G | C | 23 | a0001c0001t0002g0094a0001c0001t0002g0100a0001c0001t0003g0079others(20): Show | 23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1020-434C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59057488 | ||||||
| chr17:59057522
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1020-468T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59057522 | ||||||
| chr17:59057588
|
G | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG00639.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1020-534C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59057588 | ||||||
| chr17:59057600
|
T | G | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1020-546A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59057600 | ||||||
| chr17:59057752
|
G | C | 4 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(1): Show | 4 | NA18945.hp1 NA19006.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1020-698C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59057752 | ||||||
| chr17:59057816
|
G | A | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020-762C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59057816 | ||||||
| chr17:59058342
|
G | C | 1 | a0001c0001t0011g0001 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1020-1288C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59058342 | ||||||
| chr17:59058516
|
G | A | 2 | a0001c0001t0002g0107a0001c0001t0002g0109 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1020-1462C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59058516 | ||||||
| chr17:59058690
|
T | A | 1 | a0001c0001t0001g0297 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1020-1636A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59058690 | ||||||
| chr17:59058700
|
C | T | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1020-1646G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59058700 | ||||||
| chr17:59058843
|
G | A | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1020-1789C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59058843 | ||||||
| chr17:59058850
|
C | T | 4 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020-1796G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59058850 | ||||||
| chr17:59059132
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1019+1900C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059132 | ||||||
| chr17:59059245
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1019+1787C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059245 | ||||||
| chr17:59059460
|
C | T | 23 | a0001c0001t0002g0094a0001c0001t0002g0100a0001c0001t0003g0079others(20): Show | 23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1019+1572G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059460 | ||||||
| chr17:59059513
|
C | T | 1 | a0002c0002t0002g0208 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1019+1519G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059513 | ||||||
| chr17:59059517
|
T | C | 2 | a0001c0001t0002g0107a0001c0001t0002g0109 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1019+1515A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059517 | ||||||
| chr17:59059577
|
T | C | 246 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(243): Show | 246 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1019+1455A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059577 | ||||||
| chr17:59059768
|
G | A | 133 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(130): Show | 133 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.1019+1264C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059768 | ||||||
| chr17:59059823
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1019+1209G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059823 | ||||||
| chr17:59059891
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1019+1141C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59059891 | ||||||
| chr17:59060052
|
G | A | 2 | a0001c0001t0002g0152a0001c0001t0002g0174 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1019+980C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59060052 | ||||||
| chr17:59060073
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1019+959A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59060073 | ||||||
| chr17:59060516
|
G | A | 4 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(1): Show | 4 | NA18945.hp1 NA19006.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1019+516C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59060516 | ||||||
| chr17:59060622
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1019+410C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59060622 | ||||||
| chr17:59060673
|
T | C | 1 | a0001c0001t0002g0127 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1019+359A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59060673 | ||||||
| chr17:59060760
|
A | T | 1 | a0001c0001t0001g0257 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1019+272T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 12/23 | chr17 | 59060760 | ||||||
| chr17:59061243
|
T | C | 5 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0114others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.943-135A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59061243 | ||||||
| chr17:59061501
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.943-393G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59061501 | ||||||
| chr17:59061561
|
G | T | 6 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(3): Show | 6 | HG02559.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.943-453C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59061561 | ||||||
| chr17:59061773
|
G | A | 97 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.943-665C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59061773 | ||||||
| chr17:59061932
|
G | A | 226 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(223): Show | 226 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.942+635C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59061932 | ||||||
| chr17:59061958
|
T | A | 4 | a0001c0003t0006g0212a0001c0003t0006g0217a0001c0003t0006g0218others(1): Show | 4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.942+609A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59061958 | ||||||
| chr17:59062098
|
G | A | 1 | a0001c0001t0002g0148 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.942+469C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59062098 | ||||||
| chr17:59062229
|
T | C | 1 | a0001c0001t0001g0339 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.942+338A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59062229 | ||||||
| chr17:59062453
|
A | G | 4 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(1): Show | 4 | HG02559.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.942+114T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59062453 | ||||||
| chr17:59062461
|
C | T | 2 | a0001c0001t0002g0149a0001c0001t0002g0211 | 2 | HG00099.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.942+106G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 11/23 | chr17 | 59062461 | ||||||
| chr17:59062654
|
G | A | 4 | a0001c0003t0006g0212a0001c0003t0006g0217a0001c0003t0006g0218others(1): Show | 4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.861-6C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59062654 | ||||||
| chr17:59062810
|
T | C | 1 | a0001c0001t0003g0023 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.861-162A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59062810 | ||||||
| chr17:59062940
|
A | G | 97 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.861-292T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59062940 | ||||||
| chr17:59062943
|
A | T | 248 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(245): Show | 248 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.861-295T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59062943 | ||||||
| chr17:59063233
|
G | A | 96 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(93): Show | 96 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.861-585C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063233 | ||||||
| chr17:59063242
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.861-594G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063242 | ||||||
| chr17:59063243
|
G | T | 1 | a0001c0001t0001g0243 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.861-595C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063243 | ||||||
| chr17:59063386
|
C | T | 3 | a0001c0003t0006g0217a0001c0003t0006g0218a0001c0003t0006g0219 | 3 | HG00642.hp2 NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.861-738G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063386 | ||||||
| chr17:59063412
|
C | T | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.861-764G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063412 | ||||||
| chr17:59063415
|
T | A | 12 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0063others(9): Show | 12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.861-767A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063415 | ||||||
| chr17:59063424
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.861-776G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063424 | ||||||
| chr17:59063427
|
C | G | 1 | a0001c0001t0002g0127 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.861-779G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063427 | ||||||
| chr17:59063684
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.860+671A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59063684 | ||||||
| chr17:59064162
|
G | C | 1 | a0001c0001t0001g0303 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.860+193C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 10/23 | chr17 | 59064162 | ||||||
| chr17:59064407
|
T | TA | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.810-3dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59064407 | ||||||
| chr17:59064552
|
T | G | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.810-147A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59064552 | ||||||
| chr17:59064785
|
C | A | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.810-380G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59064785 | ||||||
| chr17:59064930
|
A | C | 97 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.810-525T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59064930 | ||||||
| chr17:59064943
|
T | C | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.810-538A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59064943 | ||||||
| chr17:59065023
|
C | T | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.810-618G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59065023 | ||||||
| chr17:59065296
|
C | T | 325 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(322): Show | 325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.810-891G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59065296 | ||||||
| chr17:59065541
|
T | C | 1 | a0001c0001t0003g0173 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.810-1136A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59065541 | ||||||
| chr17:59065596
|
T | C | 1 | a0001c0001t0001g0257 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.810-1191A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59065596 | ||||||
| chr17:59065996
|
T | C | 4 | a0001c0003t0006g0212a0001c0003t0006g0217a0001c0003t0006g0218others(1): Show | 4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.810-1591A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59065996 | ||||||
| chr17:59066043
|
T | G | 90 | a0001c0001t0002g0108a0001c0001t0002g0124a0001c0001t0002g0126others(87): Show | 90 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.810-1638A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59066043 | ||||||
| chr17:59066431
|
G | A | 6 | a0001c0001t0001g0232a0001c0001t0001g0244a0001c0001t0001g0246others(3): Show | 6 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.810-2026C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59066431 | ||||||
| chr17:59066502
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0253a0001c0001t0001g0254 | 3 | NA18966.hp2 NA19005.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.810-2097T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59066502 | ||||||
| chr17:59066810
|
T | C | 1 | a0001c0001t0001g0305 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.810-2405A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59066810 | ||||||
| chr17:59066838
|
T | C | 1 | a0001c0001t0001g0313 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.810-2433A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59066838 | ||||||
| chr17:59066994
|
C | T | 114 | a0001c0001t0002g0080a0001c0001t0002g0107a0001c0001t0002g0108others(111): Show | 114 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.810-2589G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59066994 | ||||||
| chr17:59067006
|
C | T | 220 | a0001c0001t0001g0339a0001c0001t0002g0080a0001c0001t0002g0094others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.810-2601G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067006 | ||||||
| chr17:59067026
|
T | TTTTA | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.810-2625_810-2622d others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067026 | ||||||
| chr17:59067026
|
TTTTA | T | 8 | a0001c0001t0002g0147a0001c0001t0003g0009a0001c0001t0003g0013others(5): Show | 8 | HG00438.hp1 HG03831.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.810-2625_810-2622d others(6): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067026 | ||||||
| chr17:59067092
|
T | G | 2 | a0001c0001t0003g0110a0001c0001t0003g0111 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.810-2687A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067092 | ||||||
| chr17:59067175
|
C | G | 1 | a0001c0001t0002g0146 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.810-2770G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067175 | ||||||
| chr17:59067176
|
C | T | 1 | a0001c0001t0003g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.810-2771G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067176 | ||||||
| chr17:59067307
|
T | C | 2 | a0001c0001t0002g0190a0001c0001t0002g0191 | 2 | NA18970.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.810-2902A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067307 | ||||||
| chr17:59067737
|
TGTTGGTC others(107): Show |
T | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG01346.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.809+2972_809+3085d others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067737 | ||||||
| chr17:59067882
|
A | G | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.809+2941T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067882 | ||||||
| chr17:59067897
|
G | A | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.809+2926C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59067897 | ||||||
| chr17:59068135
|
C | G | 1 | a0001c0001t0002g0183 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.809+2688G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59068135 | ||||||
| chr17:59068269
|
G | C | 1 | a0001c0001t0003g0053 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.809+2554C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59068269 | ||||||
| chr17:59068352
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.809+2471A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59068352 | ||||||
| chr17:59068976
|
C | T | 2 | a0001c0001t0002g0107a0001c0001t0002g0109 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.809+1847G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59068976 | ||||||
| chr17:59069058
|
T | C | 1 | a0001c0001t0001g0300 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.809+1765A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59069058 | ||||||
| chr17:59069412
|
G | C | 2 | a0001c0001t0002g0107a0001c0001t0002g0109 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.809+1411C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59069412 | ||||||
| chr17:59070020
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.809+803A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59070020 | ||||||
| chr17:59070143
|
T | C | 4 | a0001c0003t0006g0212a0001c0003t0006g0217a0001c0003t0006g0218others(1): Show | 4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.809+680A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59070143 | ||||||
| chr17:59070259
|
A | G | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.809+564T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59070259 | ||||||
| chr17:59070339
|
T | G | 1 | a0001c0001t0002g0168 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.809+484A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59070339 | ||||||
| chr17:59070342
|
T | C | 6 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(3): Show | 6 | HG02559.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.809+481A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59070342 | ||||||
| chr17:59070666
|
C | T | 60 | a0001c0001t0001g0339a0001c0001t0003g0003a0001c0001t0003g0004others(57): Show | 60 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.809+157G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59070666 | ||||||
| chr17:59070738
|
T | TA | 11 | a0001c0001t0002g0128a0001c0001t0002g0148a0001c0001t0002g0187others(8): Show | 11 | HG02257.hp2 NA18747.hp2 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.809+84dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 9/23 | chr17 | 59070738 | ||||||
| chr17:59070999
|
C | T | 1 | a0001c0001t0003g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.685-52G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59070999 | ||||||
| chr17:59071283
|
C | CT | 15 | a0001c0001t0001g0224a0001c0001t0001g0245a0001c0001t0001g0247others(12): Show | 15 | HG01169.hp2 HG01978.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.685-337dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59071283 | ||||||
| chr17:59071397
|
T | C | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.685-450A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59071397 | ||||||
| chr17:59071478
|
G | C | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG00639.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.685-531C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59071478 | ||||||
| chr17:59071630
|
G | A | 219 | a0001c0001t0001g0339a0001c0001t0002g0080a0001c0001t0002g0094others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.685-683C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59071630 | ||||||
| chr17:59071659
|
C | T | 1 | a0001c0001t0003g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.685-712G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59071659 | ||||||
| chr17:59071784
|
T | C | 5 | a0002c0002t0002g0125a0002c0002t0002g0205a0002c0002t0002g0206others(2): Show | 5 | HG01952.hp2 HG02615.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-837A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59071784 | ||||||
| chr17:59072334
|
G | A | 219 | a0001c0001t0001g0339a0001c0001t0002g0080a0001c0001t0002g0094others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.685-1387C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59072334 | ||||||
| chr17:59072543
|
C | T | 95 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(92): Show | 95 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.685-1596G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59072543 | ||||||
| chr17:59072747
|
C | CA | 101 | a0001c0001t0001g0232a0001c0001t0001g0244a0001c0001t0001g0246others(98): Show | 101 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.685-1801dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59072747 | ||||||
| chr17:59073325
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.684+2322C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59073325 | ||||||
| chr17:59073371
|
G | A | 1 | a0001c0001t0002g0138 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.684+2276C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59073371 | ||||||
| chr17:59073491
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.684+2156T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59073491 | ||||||
| chr17:59073543
|
G | A | 2 | a0001c0001t0002g0107a0001c0001t0002g0109 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.684+2104C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59073543 | ||||||
| chr17:59073641
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.684+2006G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59073641 | ||||||
| chr17:59073998
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.684+1649G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59073998 | ||||||
| chr17:59074144
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.684+1503G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59074144 | ||||||
| chr17:59074145
|
T | G | 4 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(1): Show | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+1502A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59074145 | ||||||
| chr17:59074218
|
T | C | 95 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(92): Show | 95 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.684+1429A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59074218 | ||||||
| chr17:59074289
|
G | A | 4 | a0001c0001t0002g0149a0001c0001t0002g0156a0001c0001t0002g0211others(1): Show | 4 | HG00099.hp1 HG02602.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.684+1358C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59074289 | ||||||
| chr17:59074403
|
G | A | 7 | a0001c0001t0002g0100a0001c0001t0003g0079a0001c0001t0003g0096others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.684+1244C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59074403 | ||||||
| chr17:59074578
|
T | C | 1 | a0001c0001t0003g0059 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.684+1069A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59074578 | ||||||
| chr17:59074599
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.684+1048C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59074599 | ||||||
| chr17:59075021
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.684+626T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075021 | ||||||
| chr17:59075073
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.684+574A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075073 | ||||||
| chr17:59075103
|
T | C | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.684+544A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075103 | ||||||
| chr17:59075251
|
C | CA | 10 | a0001c0001t0001g0248a0001c0001t0001g0302a0001c0001t0001g0325others(7): Show | 10 | HG00597.hp1 HG01175.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.684+395dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075251 | ||||||
| chr17:59075399
|
T | C | 7 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(4): Show | 7 | HG02293.hp2 NA18946.hp2 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.684+248A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075399 | ||||||
| chr17:59075559
|
A | G | 220 | a0001c0001t0001g0339a0001c0001t0002g0080a0001c0001t0002g0094others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.684+88T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075559 | ||||||
| chr17:59075563
|
C | CA | 29 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0254others(26): Show | 29 | HG00438.hp2 HG01070.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.684+83dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075563 | ||||||
| chr17:59075563
|
CA | C | 90 | a0001c0001t0001g0243a0001c0001t0001g0339a0001c0001t0002g0080others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.684+83delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075563 | ||||||
| chr17:59075583
|
A | C | 1 | a0001c0001t0003g0019 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.684+64T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075583 | ||||||
| chr17:59075590
|
A | G | 1 | a0001c0001t0003g0018 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.684+57T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 8/23 | chr17 | 59075590 | ||||||
| chr17:59075827
|
T | C | 3 | a0001c0001t0001g0250a0001c0001t0001g0258a0001c0001t0001g0337 | 3 | HG02055.hp2 HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.617-113A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59075827 | ||||||
| chr17:59075914
|
A | T | 1 | a0001c0001t0001g0245 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.617-200T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59075914 | ||||||
| chr17:59076112
|
G | A | 1 | a0001c0003t0006g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.617-398C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076112 | ||||||
| chr17:59076135
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.617-421A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076135 | ||||||
| chr17:59076176
|
AG | A | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.617-463delC | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076176 | ||||||
| chr17:59076326
|
A | G | 1 | a0001c0001t0001g0277 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.617-612T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076326 | ||||||
| chr17:59076351
|
G | C | 7 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.617-637C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076351 | ||||||
| chr17:59076506
|
T | C | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.617-792A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076506 | ||||||
| chr17:59076827
|
T | A | 1 | a0001c0001t0003g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.617-1113A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076827 | ||||||
| chr17:59076865
|
C | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0314a0001c0001t0001g0315 | 3 | HG00544.hp1 NA18963.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.617-1151G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59076865 | ||||||
| chr17:59077267
|
C | CT | 6 | a0001c0001t0001g0302a0001c0001t0002g0115a0001c0001t0002g0158others(3): Show | 6 | HG01175.hp2 HG01358.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.617-1554dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077267 | ||||||
| chr17:59077308
|
T | C | 1 | a0001c0001t0001g0339 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.617-1594A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077308 | ||||||
| chr17:59077412
|
T | C | 1 | a0001c0001t0001g0322 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.617-1698A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077412 | ||||||
| chr17:59077617
|
C | T | 2 | a0001c0001t0003g0011a0001c0001t0003g0018 | 2 | NA18949.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.617-1903G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077617 | ||||||
| chr17:59077809
|
C | CA | 116 | a0001c0001t0001g0248a0001c0001t0001g0255a0001c0001t0001g0276others(113): Show | 116 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.616+1944dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077809 | ||||||
| chr17:59077809
|
C | CAA | 85 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(82): Show | 85 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.616+1943_616+1944d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077809 | ||||||
| chr17:59077809
|
C | CAAA | 10 | a0001c0001t0002g0134a0001c0001t0002g0138a0001c0001t0002g0145others(7): Show | 10 | HG00438.hp2 HG01361.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.616+1942_616+1944d others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077809 | ||||||
| chr17:59077881
|
C | T | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.616+1873G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077881 | ||||||
| chr17:59077888
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.616+1866G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59077888 | ||||||
| chr17:59078881
|
A | G | 4 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(1): Show | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.616+873T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59078881 | ||||||
| chr17:59079050
|
C | CA | 13 | a0001c0001t0001g0232a0001c0001t0001g0244a0001c0001t0001g0246others(10): Show | 13 | HG01168.hp1 HG01192.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.616+703dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59079050 | ||||||
| chr17:59079474
|
A | G | 1 | a0002c0002t0002g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.616+280T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59079474 | ||||||
| chr17:59079724
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.616+30C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 7/23 | chr17 | 59079724 | ||||||
| chr17:59080015
|
T | G | 2 | a0001c0001t0002g0120a0001c0001t0002g0121 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.493-138A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59080015 | ||||||
| chr17:59080085
|
C | T | 1 | a0001c0001t0003g0122 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.493-208G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59080085 | ||||||
| chr17:59080215
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.493-338A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59080215 | ||||||
| chr17:59080372
|
G | A | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.493-495C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59080372 | ||||||
| chr17:59080659
|
T | C | 1 | a0001c0001t0001g0338 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.492+438A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59080659 | ||||||
| chr17:59080984
|
T | C | 93 | a0001c0001t0002g0108a0001c0001t0002g0124a0001c0001t0002g0126others(90): Show | 93 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.492+113A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59080984 | ||||||
| chr17:59080993
|
T | C | 1 | a0001c0001t0001g0275 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.492+104A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59080993 | ||||||
| chr17:59081027
|
T | C | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.492+70A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59081027 | ||||||
| chr17:59081072
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.492+25T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 6/23 | chr17 | 59081072 | ||||||
| chr17:59081403
|
C | T | 8 | a0001c0001t0001g0269a0001c0001t0001g0288a0001c0001t0001g0289others(5): Show | 8 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.370-184G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081403 | ||||||
| chr17:59081479
|
G | A | 212 | a0001c0001t0001g0339a0001c0001t0002g0080a0001c0001t0002g0094others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.370-260C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081479 | ||||||
| chr17:59081558
|
C | A | 2 | a0001c0001t0002g0107a0001c0001t0002g0109 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.370-339G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081558 | ||||||
| chr17:59081579
|
A | G | 11 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.370-360T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081579 | ||||||
| chr17:59081645
|
T | C | 9 | a0001c0001t0001g0269a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 9 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.370-426A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081645 | ||||||
| chr17:59081737
|
G | A | 3 | a0001c0001t0002g0126a0001c0001t0002g0143a0001c0001t0002g0146 | 3 | HG02071.hp1 NA18995.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.370-518C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081737 | ||||||
| chr17:59081821
|
T | C | 2 | a0001c0001t0002g0120a0001c0001t0002g0121 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.370-602A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081821 | ||||||
| chr17:59081906
|
C | T | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.370-687G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081906 | ||||||
| chr17:59081907
|
A | C | 114 | a0001c0001t0002g0080a0001c0001t0002g0107a0001c0001t0002g0108others(111): Show | 114 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.370-688T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081907 | ||||||
| chr17:59081941
|
AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0010g0078a0001c0001t0010g0089 | 2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.370-734_370-723del others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081941 | ||||||
| chr17:59081944
|
A | T | 7 | a0001c0001t0001g0232a0001c0001t0001g0244a0001c0001t0001g0246others(4): Show | 7 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.370-725T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081944 | ||||||
| chr17:59081947
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.370-728T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081947 | ||||||
| chr17:59081949
|
AAAAT | A | 27 | a0001c0001t0002g0130a0001c0001t0002g0132a0001c0001t0002g0149others(24): Show | 27 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.370-734_370-731del others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081949 | ||||||
| chr17:59081950
|
A | T | 2 | a0001c0001t0007g0213a0001c0001t0007g0214 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.370-731T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081950 | ||||||
| chr17:59081950
|
AAAT | A | 55 | a0001c0001t0002g0108a0001c0001t0002g0124a0001c0001t0002g0126others(52): Show | 55 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.370-734_370-732del others(3): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081950 | ||||||
| chr17:59081951
|
AAT | A | 54 | a0001c0001t0001g0339a0001c0001t0002g0100a0001c0001t0002g0185others(51): Show | 54 | HG01261.hp2 HG01346.hp2 HG01943.hp1 others(51): Show |
intron_variant | MODIFIER | c.370-734_370-733del others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081951 | ||||||
| chr17:59081952
|
AT | A | 32 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0014others(29): Show | 32 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.370-734delA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081952 | ||||||
| chr17:59081953
|
T | A | 26 | a0001c0001t0002g0080a0001c0001t0002g0107a0001c0001t0002g0109others(23): Show | 26 | HG01106.hp2 HG01257.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.370-734A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081953 | ||||||
| chr17:59081953
|
TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0001g0305a0001c0001t0001g0313 | 2 | NA18979.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.370-745_370-735del others(11): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081953 | ||||||
| chr17:59081954
|
A | T | 1 | a0001c0001t0001g0243 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.370-735T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081954 | ||||||
| chr17:59081955
|
A | ATAATAAT | 3 | a0001c0001t0007g0214a0001c0001t0007g0215a0001c0001t0007g0216 | 3 | HG01243.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.370-737_370-736ins others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081955 | ||||||
| chr17:59081955
|
A | ATAATAAT others(3): Show |
1 | a0001c0001t0007g0213 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.370-737_370-736ins others(10): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081955 | ||||||
| chr17:59081955
|
A | T | 3 | a0001c0001t0002g0151a0001c0001t0003g0006a0001c0001t0003g0055 | 3 | HG01106.hp2 HG02965.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.370-736T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081955 | ||||||
| chr17:59081958
|
A | T | 24 | a0001c0001t0002g0094a0001c0001t0002g0117a0001c0001t0002g0138others(21): Show | 24 | HG01106.hp2 HG01243.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.370-739T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081958 | ||||||
| chr17:59081959
|
A | T | 1 | a0001c0001t0001g0338 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.370-740T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081959 | ||||||
| chr17:59081961
|
A | AAATAATA others(5): Show |
1 | a0001c0001t0002g0118 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.370-743_370-742ins others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081961 | ||||||
| chr17:59081961
|
A | AATAATAA others(4): Show |
1 | a0001c0001t0002g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.370-743_370-742ins others(11): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081961 | ||||||
| chr17:59081961
|
A | ATAATAAT others(6): Show |
1 | a0001c0001t0002g0116 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.370-743_370-742ins others(13): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081961 | ||||||
| chr17:59081961
|
A | T | 116 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0001g0252others(113): Show | 116 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.370-742T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081961 | ||||||
| chr17:59081964
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0002g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.370-746_370-745ins others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081964 | ||||||
| chr17:59081964
|
A | AAAAAAAT others(6): Show |
1 | a0001c0001t0002g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.370-746_370-745ins others(13): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081964 | ||||||
| chr17:59081964
|
A | AAAAATAA others(7): Show |
1 | a0001c0001t0002g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.370-746_370-745ins others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081964 | ||||||
| chr17:59081964
|
A | AAATAATA others(5): Show |
1 | a0001c0001t0002g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.370-757_370-746dup others(12): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081964 | ||||||
| chr17:59081964
|
A | T | 292 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0223others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.370-745T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081964 | ||||||
| chr17:59081967
|
T | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG01358.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.370-748A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081967 | ||||||
| chr17:59081970
|
T | A | 1 | a0001c0001t0001g0297 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.370-751A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59081970 | ||||||
| chr17:59082132
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.370-913C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082132 | ||||||
| chr17:59082137
|
G | A | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.370-918C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082137 | ||||||
| chr17:59082196
|
G | A | 4 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-977C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082196 | ||||||
| chr17:59082248
|
G | A | 1 | a0001c0001t0003g0036 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.370-1029C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082248 | ||||||
| chr17:59082274
|
A | G | 1 | a0001c0001t0003g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.370-1055T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082274 | ||||||
| chr17:59082513
|
A | C | 1 | a0001c0001t0002g0202 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.370-1294T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082513 | ||||||
| chr17:59082629
|
A | T | 95 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(92): Show | 95 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.369+1373T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082629 | ||||||
| chr17:59082753
|
T | C | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.369+1249A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082753 | ||||||
| chr17:59082856
|
T | C | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.369+1146A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59082856 | ||||||
| chr17:59083152
|
G | C | 97 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.369+850C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083152 | ||||||
| chr17:59083274
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.369+728T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083274 | ||||||
| chr17:59083302
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.369+700C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083302 | ||||||
| chr17:59083434
|
C | CA | 8 | a0001c0001t0002g0185a0001c0001t0002g0204a0001c0001t0003g0037others(5): Show | 8 | HG00733.hp2 HG01099.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.369+567dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083434 | ||||||
| chr17:59083497
|
C | G | 2 | a0001c0001t0002g0154a0001c0001t0002g0155 | 2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.369+505G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083497 | ||||||
| chr17:59083620
|
G | A | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.369+382C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083620 | ||||||
| chr17:59083752
|
T | C | 2 | a0001c0001t0002g0120a0001c0001t0002g0121 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.369+250A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083752 | ||||||
| chr17:59083773
|
T | C | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.369+229A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083773 | ||||||
| chr17:59083862
|
C | A | 1 | a0001c0008t0003g0039 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.369+140G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 5/23 | chr17 | 59083862 | ||||||
| chr17:59084300
|
T | C | 1 | a0001c0001t0001g0268 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.282-211A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59084300 | ||||||
| chr17:59084408
|
G | C | 12 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0063others(9): Show | 12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.282-319C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59084408 | ||||||
| chr17:59084517
|
T | G | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.282-428A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59084517 | ||||||
| chr17:59084774
|
A | G | 5 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0006others(2): Show | 5 | HG01106.hp2 HG01978.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-685T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59084774 | ||||||
| chr17:59084806
|
T | C | 2 | a0001c0001t0003g0040a0001c0001t0003g0047 | 2 | HG00733.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.282-717A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59084806 | ||||||
| chr17:59084835
|
G | A | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.282-746C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59084835 | ||||||
| chr17:59084848
|
A | G | 96 | a0001c0001t0001g0309a0001c0001t0002g0124a0001c0001t0002g0126others(93): Show | 96 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.282-759T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59084848 | ||||||
| chr17:59085103
|
A | T | 224 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.282-1014T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59085103 | ||||||
| chr17:59085292
|
A | C | 1 | a0001c0001t0001g0231 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.282-1203T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59085292 | ||||||
| chr17:59085515
|
G | C | 1 | a0001c0001t0003g0050 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.282-1426C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59085515 | ||||||
| chr17:59085667
|
C | T | 1 | a0001c0001t0001g0323 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.282-1578G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59085667 | ||||||
| chr17:59085787
|
G | A | 3 | a0001c0001t0002g0119a0001c0001t0002g0120a0001c0001t0002g0121 | 3 | HG01257.hp2 HG01258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.282-1698C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59085787 | ||||||
| chr17:59086012
|
T | C | 1 | a0001c0001t0003g0077 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.282-1923A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086012 | ||||||
| chr17:59086140
|
C | T | 97 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.282-2051G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086140 | ||||||
| chr17:59086161
|
G | C | 1 | a0001c0001t0003g0048 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.282-2072C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086161 | ||||||
| chr17:59086238
|
A | AT | 6 | a0001c0001t0002g0196a0001c0001t0002g0201a0001c0001t0003g0010others(3): Show | 6 | HG01981.hp2 HG03098.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.281+2052dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086238 | ||||||
| chr17:59086395
|
C | T | 11 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.281+1896G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086395 | ||||||
| chr17:59086430
|
G | A | 93 | a0001c0001t0002g0108a0001c0001t0002g0124a0001c0001t0002g0126others(90): Show | 93 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.281+1861C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086430 | ||||||
| chr17:59086511
|
T | A | 95 | a0001c0001t0002g0107a0001c0001t0002g0108a0001c0001t0002g0109others(92): Show | 95 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.281+1780A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086511 | ||||||
| chr17:59086632
|
A | G | 2 | a0001c0001t0003g0052a0001c0001t0003g0053 | 2 | NA18943.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.281+1659T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086632 | ||||||
| chr17:59086834
|
T | A | 74 | a0001c0001t0001g0339a0001c0001t0003g0003a0001c0001t0003g0004others(71): Show | 74 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.281+1457A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59086834 | ||||||
| chr17:59087028
|
C | A | 1 | a0001c0001t0002g0196 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.281+1263G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087028 | ||||||
| chr17:59087250
|
G | A | 6 | a0001c0001t0001g0232a0001c0001t0001g0244a0001c0001t0001g0246others(3): Show | 6 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.281+1041C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087250 | ||||||
| chr17:59087458
|
C | CT | 93 | a0001c0001t0001g0339a0001c0001t0002g0100a0001c0001t0003g0003others(90): Show | 93 | HG00099.hp2 HG00438.hp1 HG00733.hp2 others(90): Show |
intron_variant | MODIFIER | c.281+832dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087458 | ||||||
| chr17:59087458
|
CT | C | 15 | a0001c0001t0001g0229a0001c0001t0001g0257a0001c0001t0001g0300others(12): Show | 15 | HG00323.hp2 HG00642.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.281+832delA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087458 | ||||||
| chr17:59087662
|
G | A | 1 | a0001c0001t0009g0169 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.281+629C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087662 | ||||||
| chr17:59087735
|
AG | A | 7 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.281+555delC | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087735 | ||||||
| chr17:59087736
|
G | A | 213 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.281+555C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087736 | ||||||
| chr17:59087737
|
G | A | 7 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.281+554C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087737 | ||||||
| chr17:59087851
|
TCTTTC | T | 7 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.281+435_281+439del others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087851 | ||||||
| chr17:59087856
|
C | T | 23 | a0001c0001t0002g0094a0001c0001t0002g0100a0001c0001t0003g0079others(20): Show | 23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.281+435G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087856 | ||||||
| chr17:59087920
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281+371T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087920 | ||||||
| chr17:59087942
|
G | T | 1 | a0001c0001t0002g0094 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.281+349C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087942 | ||||||
| chr17:59087958
|
A | T | 1 | a0001c0001t0001g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.281+333T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 4/23 | chr17 | 59087958 | ||||||
| chr17:59088535
|
A | G | 1 | a0001c0001t0009g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.165-128T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59088535 | ||||||
| chr17:59088571
|
G | A | 2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG00323.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.165-164C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59088571 | ||||||
| chr17:59088847
|
A | G | 6 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(3): Show | 6 | HG02559.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.165-440T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59088847 | ||||||
| chr17:59088871
|
T | G | 4 | a0001c0003t0006g0212a0001c0003t0006g0217a0001c0003t0006g0218others(1): Show | 4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-464A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59088871 | ||||||
| chr17:59089132
|
C | T | 4 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(1): Show | 4 | HG01243.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.165-725G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089132 | ||||||
| chr17:59089228
|
T | C | 2 | a0001c0001t0001g0266a0001c0001t0001g0301 | 2 | HG01496.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.165-821A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089228 | ||||||
| chr17:59089414
|
G | A | 11 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.165-1007C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089414 | ||||||
| chr17:59089421
|
T | A | 1 | a0001c0001t0002g0146 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.165-1014A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089421 | ||||||
| chr17:59089458
|
T | C | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | HG02300.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.165-1051A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089458 | ||||||
| chr17:59089498
|
G | A | 1 | a0001c0001t0003g0061 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.165-1091C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089498 | ||||||
| chr17:59089616
|
G | T | 1 | a0001c0001t0002g0141 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.165-1209C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089616 | ||||||
| chr17:59089625
|
G | C | 1 | a0001c0001t0002g0150 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.165-1218C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089625 | ||||||
| chr17:59089822
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.165-1415C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59089822 | ||||||
| chr17:59090164
|
T | C | 4 | a0001c0001t0001g0244a0001c0001t0001g0246a0001c0001t0001g0247others(1): Show | 4 | HG01168.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.164+1136A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59090164 | ||||||
| chr17:59090242
|
T | A | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.164+1058A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59090242 | ||||||
| chr17:59090632
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.164+668C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59090632 | ||||||
| chr17:59090652
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.164+648C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59090652 | ||||||
| chr17:59090683
|
C | A | 2 | a0001c0001t0003g0110a0001c0001t0003g0111 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.164+617G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59090683 | ||||||
| chr17:59090688
|
C | T | 4 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.164+612G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59090688 | ||||||
| chr17:59090912
|
G | A | 1 | a0001c0001t0001g0268 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.164+388C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59090912 | ||||||
| chr17:59090933
|
C | T | 2 | a0001c0001t0003g0014a0001c0001t0003g0015 | 2 | HG00099.hp2 HG00280.hp2 |
intron_variant | MODIFIER | c.164+367G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59090933 | ||||||
| chr17:59091098
|
G | A | 1 | a0001c0001t0003g0008 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.164+202C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59091098 | ||||||
| chr17:59091134
|
T | G | 2 | a0001c0001t0003g0110a0001c0001t0003g0111 | 2 | HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.164+166A>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59091134 | ||||||
| chr17:59091217
|
G | A | 1 | a0005c0007t0002g0179 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.164+83C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 3/23 | chr17 | 59091217 | ||||||
| chr17:59091415
|
T | A | 1 | a0001c0001t0002g0137 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.124-75A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091415 | ||||||
| chr17:59091471
|
CATAATAT | C | 7 | a0001c0001t0001g0309a0001c0001t0003g0009a0001c0001t0003g0044others(4): Show | 7 | HG00438.hp1 HG02523.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-138_124-132del others(7): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091471 | ||||||
| chr17:59091483
|
TATATA | T | 8 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(5): Show | 8 | HG02293.hp2 HG02886.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-148_124-144del others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091483 | ||||||
| chr17:59091509
|
T | TTA | 4 | a0001c0003t0006g0212a0001c0003t0006g0217a0001c0003t0006g0218others(1): Show | 4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-170_124-169ins others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091509 | ||||||
| chr17:59091509
|
TCA | T | 127 | a0001c0001t0002g0080a0001c0001t0002g0107a0001c0001t0002g0108others(124): Show | 127 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.124-171_124-170del others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091509 | ||||||
| chr17:59091510
|
C | T | 103 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(100): Show | 103 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.124-170G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091510 | ||||||
| chr17:59091531
|
GTATAATA others(35): Show |
G | 16 | a0001c0001t0002g0126a0001c0001t0002g0135a0001c0001t0002g0136others(13): Show | 16 | HG00558.hp2 HG00673.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.124-233_124-192del others(42): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091531 | ||||||
| chr17:59091535
|
AATAATGT others(32): Show |
A | 202 | a0001c0001t0001g0339a0001c0001t0002g0080a0001c0001t0002g0094others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.124-234_124-196del others(39): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091535 | ||||||
| chr17:59091541
|
GTATAA | G | 5 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0001t0001g0265others(2): Show | 5 | HG01192.hp1 HG01943.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-206_124-202del others(5): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091541 | ||||||
| chr17:59091558
|
TTATATAT others(34): Show |
T | 2 | a0001c0001t0002g0117a0001c0001t0002g0128 | 2 | HG02622.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.124-259_124-219del others(41): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091558 | ||||||
| chr17:59091567
|
T | A | 4 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 4 | NA18946.hp2 NA18993.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-227A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091567 | ||||||
| chr17:59091568
|
A | AAT | 95 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(92): Show | 95 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.124-230_124-229dup others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091568 | ||||||
| chr17:59091568
|
A | AATATATA others(36): Show |
1 | a0001c0001t0001g0325 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.124-229_124-228ins others(43): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091568 | ||||||
| chr17:59091568
|
A | ATT | 12 | a0001c0001t0001g0225a0001c0001t0001g0245a0001c0001t0001g0251others(9): Show | 12 | HG01070.hp2 HG01081.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.124-229_124-228ins others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091568 | ||||||
| chr17:59091568
|
A | T | 4 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(1): Show | 4 | NA18946.hp2 NA18993.hp2 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-228T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091568 | ||||||
| chr17:59091595
|
C | T | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-255G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091595 | ||||||
| chr17:59091622
|
TATA | T | 3 | a0001c0003t0006g0217a0001c0003t0006g0218a0001c0003t0006g0219 | 3 | HG00642.hp2 NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.124-285_124-283del others(3): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091622 | ||||||
| chr17:59091640
|
A | G | 1 | a0001c0001t0003g0099 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.124-300T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091640 | ||||||
| chr17:59091828
|
A | C | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.124-488T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091828 | ||||||
| chr17:59091897
|
A | C | 1 | a0001c0001t0002g0131 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.124-557T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59091897 | ||||||
| chr17:59092055
|
G | GA | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-716dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092055 | ||||||
| chr17:59092120
|
C | T | 11 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.124-780G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092120 | ||||||
| chr17:59092232
|
A | G | 6 | a0001c0001t0001g0232a0001c0001t0001g0244a0001c0001t0001g0246others(3): Show | 6 | HG01168.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-892T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092232 | ||||||
| chr17:59092247
|
G | T | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.124-907C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092247 | ||||||
| chr17:59092348
|
G | A | 1 | a0002c0002t0002g0208 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.124-1008C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092348 | ||||||
| chr17:59092398
|
C | CA | 11 | a0001c0001t0001g0258a0001c0001t0001g0308a0001c0001t0001g0309others(8): Show | 11 | HG00597.hp2 HG01361.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.124-1059dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092398 | ||||||
| chr17:59092412
|
C | A | 2 | a0001c0001t0002g0116a0001c0001t0003g0060 | 2 | HG02886.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.124-1072G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092412 | ||||||
| chr17:59092412
|
C | CA | 8 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0322others(5): Show | 8 | HG01192.hp2 HG01433.hp2 NA18906.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-1073dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092412 | ||||||
| chr17:59092710
|
TATTTGTT others(90): Show |
T | 1 | a0001c0001t0015g0332 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.124-1467_124-1371d others(99): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092710 | ||||||
| chr17:59092808
|
G | C | 1 | a0001c0001t0015g0332 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.124-1468C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59092808 | ||||||
| chr17:59093026
|
T | C | 4 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-1686A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093026 | ||||||
| chr17:59093156
|
TAAAATA | T | 4 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0002g0139others(1): Show | 4 | NA18946.hp1 NA18964.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-1822_124-1817d others(8): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093156 | ||||||
| chr17:59093306
|
G | A | 6 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-1966C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093306 | ||||||
| chr17:59093504
|
G | C | 1 | a0001c0001t0003g0048 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.124-2164C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093504 | ||||||
| chr17:59093508
|
C | T | 1 | a0001c0001t0001g0324 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.124-2168G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093508 | ||||||
| chr17:59093737
|
T | C | 2 | a0001c0001t0001g0311a0001c0001t0001g0312 | 2 | HG01433.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.124-2397A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093737 | ||||||
| chr17:59093762
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.124-2422G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093762 | ||||||
| chr17:59093778
|
G | A | 1 | a0001c0001t0011g0001 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.124-2438C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093778 | ||||||
| chr17:59093778
|
G | T | 2 | a0001c0001t0002g0107a0001c0001t0002g0109 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.124-2438C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093778 | ||||||
| chr17:59093973
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124-2633G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59093973 | ||||||
| chr17:59094058
|
A | C | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.124-2718T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59094058 | ||||||
| chr17:59094556
|
C | T | 98 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.124-3216G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59094556 | ||||||
| chr17:59094692
|
G | A | 5 | a0001c0001t0002g0124a0001c0001t0002g0131a0001c0001t0002g0186others(2): Show | 5 | HG02132.hp1 HG02135.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-3352C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59094692 | ||||||
| chr17:59095088
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.124-3748C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59095088 | ||||||
| chr17:59095395
|
T | C | 2 | a0001c0001t0003g0097a0001c0001t0003g0098 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.124-4055A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59095395 | ||||||
| chr17:59095869
|
C | T | 3 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0014g0271 | 3 | NA18943.hp2 NA18955.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.124-4529G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59095869 | ||||||
| chr17:59096083
|
A | T | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.124-4743T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096083 | ||||||
| chr17:59096479
|
G | A | 62 | a0001c0001t0001g0339a0001c0001t0003g0003a0001c0001t0003g0004others(59): Show | 62 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.124-5139C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096479 | ||||||
| chr17:59096484
|
A | G | 220 | a0001c0001t0001g0339a0001c0001t0002g0080a0001c0001t0002g0094others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.124-5144T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096484 | ||||||
| chr17:59096548
|
TCAAAAAA others(7): Show |
T | 4 | a0001c0003t0006g0212a0001c0003t0006g0217a0001c0003t0006g0218others(1): Show | 4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-5222_124-5209d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096548 | ||||||
| chr17:59096549
|
C | CA | 109 | a0001c0001t0001g0223a0001c0001t0001g0227a0001c0001t0001g0267others(106): Show | 109 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.124-5210dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096549 | ||||||
| chr17:59096549
|
C | CAA | 6 | a0001c0001t0002g0155a0001c0001t0002g0174a0001c0001t0002g0197others(3): Show | 6 | HG01071.hp2 HG03516.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-5211_124-5210d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096549 | ||||||
| chr17:59096559
|
A | C | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | NA18963.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.124-5219T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096559 | ||||||
| chr17:59096563
|
C | A | 7 | a0001c0001t0002g0147a0001c0001t0002g0152a0001c0001t0002g0174others(4): Show | 7 | HG01070.hp1 HG01071.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-5223G>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096563 | ||||||
| chr17:59096563
|
CA | C | 72 | a0001c0001t0001g0245a0001c0001t0001g0339a0001c0001t0003g0003others(69): Show | 72 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.124-5224delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096563 | ||||||
| chr17:59096564
|
A | C | 1 | a0001c0001t0003g0010 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.124-5224T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096564 | ||||||
| chr17:59096626
|
A | C | 1 | a0001c0001t0001g0270 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.124-5286T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096626 | ||||||
| chr17:59096704
|
T | C | 23 | a0001c0001t0002g0094a0001c0001t0002g0100a0001c0001t0003g0079others(20): Show | 23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.124-5364A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096704 | ||||||
| chr17:59096896
|
C | T | 8 | a0001c0001t0007g0213a0001c0001t0007g0214a0001c0001t0007g0215others(5): Show | 8 | HG00642.hp2 HG01243.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.124-5556G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096896 | ||||||
| chr17:59096965
|
T | C | 2 | a0001c0001t0001g0314a0001c0001t0001g0315 | 2 | NA18963.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.124-5625A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59096965 | ||||||
| chr17:59097254
|
T | C | 2 | a0001c0001t0004g0103a0001c0001t0004g0104 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.124-5914A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59097254 | ||||||
| chr17:59097325
|
C | T | 23 | a0001c0001t0002g0094a0001c0001t0002g0100a0001c0001t0003g0079others(20): Show | 23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.124-5985G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59097325 | ||||||
| chr17:59097668
|
A | T | 2 | a0001c0001t0003g0087a0001c0001t0003g0088 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.124-6328T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59097668 | ||||||
| chr17:59097752
|
G | C | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.124-6412C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59097752 | ||||||
| chr17:59097837
|
G | C | 1 | a0001c0001t0002g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.123+6456C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59097837 | ||||||
| chr17:59097869
|
A | G | 1 | a0001c0001t0002g0181 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.123+6424T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59097869 | ||||||
| chr17:59098266
|
C | T | 23 | a0001c0001t0002g0094a0001c0001t0002g0100a0001c0001t0003g0079others(20): Show | 23 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.123+6027G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098266 | ||||||
| chr17:59098341
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.123+5952G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098341 | ||||||
| chr17:59098608
|
T | C | 43 | a0001c0001t0002g0124a0001c0001t0002g0126a0001c0001t0002g0127others(40): Show | 43 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.123+5685A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098608 | ||||||
| chr17:59098668
|
T | TA | 97 | a0001c0001t0001g0223a0001c0001t0002g0108a0001c0001t0002g0124others(94): Show | 97 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.123+5624dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098668 | ||||||
| chr17:59098668
|
TA | T | 11 | a0001c0001t0001g0230a0001c0001t0001g0269a0001c0001t0002g0080others(8): Show | 11 | HG01257.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.123+5624delT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098668 | ||||||
| chr17:59098700
|
A | G | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.123+5593T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098700 | ||||||
| chr17:59098745
|
A | T | 114 | a0001c0001t0002g0080a0001c0001t0002g0107a0001c0001t0002g0108others(111): Show | 114 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.123+5548T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098745 | ||||||
| chr17:59098922
|
C | T | 1 | a0001c0001t0001g0268 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.123+5371G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098922 | ||||||
| chr17:59098942
|
T | C | 1 | a0001c0001t0001g0316 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.123+5351A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098942 | ||||||
| chr17:59098977
|
G | C | 4 | a0001c0003t0006g0212a0001c0003t0006g0217a0001c0003t0006g0218others(1): Show | 4 | HG00642.hp2 HG03704.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+5316C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59098977 | ||||||
| chr17:59099058
|
C | G | 1 | a0001c0001t0002g0203 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.123+5235G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59099058 | ||||||
| chr17:59099163
|
C | T | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.123+5130G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59099163 | ||||||
| chr17:59099167
|
G | A | 2 | a0001c0001t0002g0120a0001c0001t0002g0121 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.123+5126C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59099167 | ||||||
| chr17:59099169
|
G | A | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+5124C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59099169 | ||||||
| chr17:59099741
|
T | C | 12 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0063others(9): Show | 12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+4552A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59099741 | ||||||
| chr17:59099873
|
G | C | 2 | a0001c0001t0002g0153a0001c0001t0002g0181 | 2 | HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.123+4420C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59099873 | ||||||
| chr17:59099996
|
T | A | 1 | a0001c0001t0001g0249 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.123+4297A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59099996 | ||||||
| chr17:59100188
|
G | A | 99 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0339others(96): Show | 99 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.123+4105C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100188 | ||||||
| chr17:59100246
|
C | T | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.123+4047G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100246 | ||||||
| chr17:59100317
|
C | T | 11 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.123+3976G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100317 | ||||||
| chr17:59100361
|
G | A | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.123+3932C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100361 | ||||||
| chr17:59100409
|
T | C | 93 | a0001c0001t0002g0108a0001c0001t0002g0124a0001c0001t0002g0126others(90): Show | 93 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.123+3884A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100409 | ||||||
| chr17:59100669
|
G | A | 2 | a0001c0001t0002g0120a0001c0001t0002g0121 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.123+3624C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100669 | ||||||
| chr17:59100792
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.123+3501C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100792 | ||||||
| chr17:59100908
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.123+3385C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100908 | ||||||
| chr17:59100917
|
G | C | 1 | a0001c0001t0003g0123 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.123+3376C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100917 | ||||||
| chr17:59100936
|
C | T | 1 | a0001c0001t0003g0086 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.123+3357G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100936 | ||||||
| chr17:59100970
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.123+3323C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59100970 | ||||||
| chr17:59101022
|
C | CA | 106 | a0001c0001t0002g0080a0001c0001t0002g0107a0001c0001t0002g0108others(103): Show | 106 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.123+3270dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101022 | ||||||
| chr17:59101209
|
A | C | 1 | a0001c0001t0002g0135 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.123+3084T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101209 | ||||||
| chr17:59101274
|
A | G | 6 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(3): Show | 6 | HG02559.hp1 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+3019T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101274 | ||||||
| chr17:59101477
|
A | G | 97 | a0001c0001t0001g0339a0001c0001t0002g0094a0001c0001t0002g0100others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.123+2816T>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101477 | ||||||
| chr17:59101531
|
G | T | 4 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(1): Show | 4 | HG02486.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+2762C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101531 | ||||||
| chr17:59101655
|
C | CA | 16 | a0001c0001t0001g0233a0001c0001t0001g0320a0001c0001t0001g0321others(13): Show | 16 | HG01256.hp1 HG02135.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.123+2637dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101655 | ||||||
| chr17:59101655
|
C | CAA | 23 | a0001c0001t0002g0109a0001c0001t0002g0124a0001c0001t0002g0131others(20): Show | 23 | HG00099.hp1 HG00544.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.123+2636_123+2637d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101655 | ||||||
| chr17:59101655
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003g0071 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.123+2625_123+2637d others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101655 | ||||||
| chr17:59101664
|
AAAAAAAA others(8): Show |
A | 11 | a0001c0001t0003g0012a0001c0001t0003g0061a0001c0001t0003g0062others(8): Show | 11 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.123+2614_123+2628d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101664 | ||||||
| chr17:59101665
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0012g0002 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.123+2614_123+2627d others(16): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101665 | ||||||
| chr17:59101666
|
AAAAAAAA others(6): Show |
A | 2 | a0001c0001t0003g0051a0001c0001t0003g0095 | 2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.123+2614_123+2626d others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101666 | ||||||
| chr17:59101666
|
AAAAAAAA others(8): Show |
A | 73 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(70): Show | 73 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.123+2612_123+2626d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101666 | ||||||
| chr17:59101667
|
AAAAAAAA others(5): Show |
A | 5 | a0001c0001t0003g0079a0001c0001t0003g0096a0001c0001t0003g0097others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+2614_123+2625d others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101667 | ||||||
| chr17:59101668
|
AAAAAAAA others(8): Show |
A | 2 | a0001c0001t0001g0339a0001c0001t0002g0094 | 2 | HG02809.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.123+2610_123+2624d others(17): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101668 | ||||||
| chr17:59101669
|
AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0002g0100a0001c0001t0003g0099 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.123+2612_123+2623d others(14): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101669 | ||||||
| chr17:59101670
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0006t0003g0106 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.123+2610_123+2622d others(15): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101670 | ||||||
| chr17:59101677
|
A | AAT | 6 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(3): Show | 6 | HG02647.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+2614_123+2615d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101677 | ||||||
| chr17:59101677
|
A | AT | 12 | a0001c0001t0001g0244a0001c0001t0001g0262a0001c0001t0001g0263others(9): Show | 12 | HG01070.hp2 HG01168.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+2615_123+2616i others(3): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101677 | ||||||
| chr17:59101677
|
A | T | 20 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(17): Show | 20 | HG01346.hp1 HG01361.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.123+2616T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101677 | ||||||
| chr17:59101678
|
AT | A | 11 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0323others(8): Show | 11 | HG00639.hp1 HG01070.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.123+2614delA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101678 | ||||||
| chr17:59101679
|
T | A | 92 | a0001c0001t0001g0230a0001c0001t0001g0233a0001c0001t0002g0080others(89): Show | 92 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.123+2614A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101679 | ||||||
| chr17:59101681
|
T | A | 58 | a0001c0001t0002g0117a0001c0001t0002g0128a0001c0001t0002g0129others(55): Show | 58 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.123+2612A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101681 | ||||||
| chr17:59101683
|
T | A | 1 | a0001c0001t0002g0132 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.123+2610A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101683 | ||||||
| chr17:59101685
|
T | A | 1 | a0001c0001t0002g0132 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.123+2608A>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101685 | ||||||
| chr17:59101693
|
T | C | 2 | a0001c0001t0002g0120a0001c0001t0002g0121 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.123+2600A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101693 | ||||||
| chr17:59101695
|
T | C | 11 | a0001c0001t0001g0324a0001c0001t0001g0333a0001c0001t0001g0334others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.123+2598A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101695 | ||||||
| chr17:59101695
|
T | TAC | 8 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0327others(5): Show | 8 | HG00621.hp1 HG02040.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.123+2596_123+2597d others(4): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101695 | ||||||
| chr17:59101697
|
C | T | 134 | a0001c0001t0001g0225a0001c0001t0001g0228a0001c0001t0001g0229others(131): Show | 134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.123+2596G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101697 | ||||||
| chr17:59101699
|
C | T | 2 | a0001c0001t0001g0233a0001c0001t0002g0132 | 2 | HG01106.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.123+2594G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101699 | ||||||
| chr17:59101723
|
T | C | 1 | a0001c0001t0002g0202 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.123+2570A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101723 | ||||||
| chr17:59101727
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.123+2566A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101727 | ||||||
| chr17:59101777
|
T | C | 1 | a0001c0001t0003g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.123+2516A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101777 | ||||||
| chr17:59101796
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.123+2497C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101796 | ||||||
| chr17:59101877
|
C | T | 220 | a0001c0001t0001g0339a0001c0001t0002g0080a0001c0001t0002g0094others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.123+2416G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101877 | ||||||
| chr17:59101938
|
C | CA | 12 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0063others(9): Show | 12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+2354dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59101938 | ||||||
| chr17:59102215
|
C | T | 3 | a0001c0001t0004g0102a0001c0001t0004g0103a0001c0001t0004g0104 | 3 | HG03516.hp2 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.123+2078G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59102215 | ||||||
| chr17:59102263
|
T | C | 2 | a0001c0001t0003g0007a0001c0001t0003g0008 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.123+2030A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59102263 | ||||||
| chr17:59102287
|
A | T | 1 | a0001c0001t0002g0131 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.123+2006T>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59102287 | ||||||
| chr17:59102811
|
G | C | 1 | a0001c0001t0002g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.123+1482C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59102811 | ||||||
| chr17:59102873
|
A | C | 98 | a0001c0001t0001g0232a0001c0001t0001g0339a0001c0001t0002g0094others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.123+1420T>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59102873 | ||||||
| chr17:59102896
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.123+1397G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59102896 | ||||||
| chr17:59102936
|
CATCTCTG others(47): Show |
C | 1 | a0001c0001t0001g0231 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.123+1303_123+1356d others(56): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59102936 | ||||||
| chr17:59103169
|
G | A | 1 | a0001c0001t0001g0335 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.123+1124C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59103169 | ||||||
| chr17:59103189
|
T | C | 11 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0113others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.123+1104A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59103189 | ||||||
| chr17:59103373
|
G | T | 1 | a0001c0003t0006g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.123+920C>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59103373 | ||||||
| chr17:59103631
|
C | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG00639.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.123+662G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59103631 | ||||||
| chr17:59103635
|
C | G | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+658G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59103635 | ||||||
| chr17:59103650
|
G | GT | 14 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(11): Show | 14 | HG00438.hp1 HG01175.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.123+642dupA | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59103650 | ||||||
| chr17:59103729
|
C | T | 5 | a0001c0001t0003g0073a0001c0001t0003g0074a0001c0001t0003g0075others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+564G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59103729 | ||||||
| chr17:59104141
|
T | C | 1 | a0001c0001t0001g0336 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.123+152A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59104141 | ||||||
| chr17:59104144
|
G | A | 7 | a0001c0001t0002g0209a0001c0001t0002g0210a0002c0002t0002g0125others(4): Show | 7 | HG01952.hp2 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.123+149C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59104144 | ||||||
| chr17:59104163
|
C | T | 74 | a0001c0001t0001g0339a0001c0001t0003g0003a0001c0001t0003g0004others(71): Show | 74 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.123+130G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 2/23 | chr17 | 59104163 | ||||||
| chr17:59104921
|
G | A | 1 | a0001c0001t0003g0122 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.22-527C>T | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59104921 | ||||||
| chr17:59104947
|
C | G | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22-553G>C | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59104947 | ||||||
| chr17:59105091
|
C | CA | 214 | a0001c0001t0001g0337a0001c0001t0001g0338a0001c0001t0001g0339others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.22-698dupT | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59105091 | ||||||
| chr17:59105278
|
AATCCAGA others(31): Show |
A | 1 | a0001c0001t0003g0123 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.22-922_22-885delCT others(36): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59105278 | ||||||
| chr17:59105432
|
G | C | 220 | a0001c0001t0001g0339a0001c0001t0002g0080a0001c0001t0002g0094others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.21+1009C>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59105432 | ||||||
| chr17:59105483
|
C | T | 4 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | NA18939.hp2 NA18954.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.21+958G>A | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59105483 | ||||||
| chr17:59105669
|
T | C | 1 | a0001c0001t0001g0340 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.21+772A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59105669 | ||||||
| chr17:59105905
|
CATAT | C | 89 | a0001c0001t0002g0124a0001c0001t0002g0126a0001c0001t0002g0127others(86): Show | 89 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.21+532_21+535delAT others(2): Show |
TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59105905 | ||||||
| chr17:59106082
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.21+359A>G | TRIM37 | ENSG00000108395.14 | transcript | ENST00000262294.12 | protein_coding | 1/23 | chr17 | 59106082 |