| geneid | 283209 |
|---|---|
| ensemblid | ENSG00000165434.8 |
| hgncid | 20898 |
| symbol | PGM2L1 |
| name | phosphoglucomutase 2 like 1 |
| refseq_nuc | NM_173582.6 |
| refseq_prot | NP_775853.2 |
| ensembl_nuc | ENST00000298198.5 |
| ensembl_prot | ENSP00000298198.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 74330316 |
| end | 74398433 |
| strand | - |
| ver | v1.2 |
| region | chr11:74330316-74398433 |
| region5000 | chr11:74325316-74403433 |
| regionname0 | PGM2L1_chr11_74330316_74398433 |
| regionname5000 | PGM2L1_chr11_74325316_74403433 |
| 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 | 0/1 | 622 | 182 | 63 | 26 | 67 | 6 | 19 | 51 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0002 | 1/0 | 622 | 94 | 19 | 13 | 50 | 3 | 8 | 43 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003 | 0/0 | 622 | 89 | 8 | 7 | 63 | 3 | 8 | 46 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0004 | 0/0 | 622 | 7 | 1 | 2 | 0 | 0 | 4 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0005 | 0/0 | 622 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0006 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0007 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0008 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0009 | 0/0 | 622 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0010 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1869 | 123 | 16 | 21 | 62 | 6 | 17 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| c0002 | 1/0 | 1869 | 94 | 19 | 13 | 50 | 3 | 8 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| c0003 | 0/0 | 1869 | 86 | 5 | 7 | 63 | 3 | 8 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| c0004 | 0/0 | 1869 | 57 | 45 | 5 | 5 | 0 | 2 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| c0005 | 0/0 | 1869 | 7 | 1 | 2 | 0 | 0 | 4 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| c0006 | 0/0 | 1869 | 3 | 3 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| c0007 | 0/0 | 1869 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| c0008 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| c0009 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| c0010 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| c0011 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| c0012 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| c0013 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| c0014 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 6613 | 56 | 1 | 6 | 45 | 1 | 3 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0002 | 0/0 | 6611 | 49 | 7 | 4 | 30 | 3 | 5 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0003 | 0/1 | 6613 | 48 | 5 | 12 | 16 | 3 | 11 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0004 | 0/0 | 6609 | 44 | 19 | 3 | 16 | 2 | 4 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0005 | 0/0 | 6609 | 42 | 0 | 8 | 29 | 0 | 5 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0006 | 0/0 | 6611 | 13 | 0 | 2 | 10 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0007 | 0/0 | 6611 | 11 | 0 | 0 | 11 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0008 | 0/0 | 6608 | 11 | 11 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0009 | 0/0 | 6606 | 9 | 9 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0010 | 0/0 | 6609 | 8 | 1 | 1 | 5 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0011 | 0/0 | 6614 | 5 | 1 | 2 | 0 | 2 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0012 | 0/0 | 6610 | 5 | 0 | 0 | 5 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0013 | 0/0 | 6608 | 5 | 5 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0014 | 0/0 | 6608 | 5 | 0 | 1 | 0 | 0 | 4 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0015 | 0/0 | 6608 | 4 | 4 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0016 | 0/0 | 6608 | 4 | 4 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0017 | 0/0 | 6609 | 4 | 3 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0018 | 0/0 | 6612 | 3 | 0 | 0 | 2 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0019 | 0/0 | 6607 | 3 | 2 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0020 | 0/0 | 6614 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0021 | 0/0 | 6612 | 2 | 0 | 0 | 1 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0022 | 0/0 | 6606 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0023 | 0/0 | 6608 | 2 | 1 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0024 | 0/0 | 6607 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0025 | 0/0 | 6609 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0026 | 0/0 | 6609 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0027 | 0/0 | 6609 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0028 | 0/0 | 6608 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0029 | 0/0 | 6609 | 2 | 1 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0030 | 0/0 | 6613 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0031 | 0/0 | 6609 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0032 | 0/0 | 6613 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0033 | 0/0 | 6613 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0034 | 0/0 | 6613 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0035 | 0/0 | 6609 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0036 | 0/0 | 6613 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0037 | 0/0 | 6613 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0038 | 0/0 | 6612 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0039 | 0/0 | 6607 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0040 | 0/0 | 6607 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0041 | 0/0 | 6611 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0042 | 0/0 | 6611 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0043 | 0/0 | 6607 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0044 | 0/0 | 6613 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0045 | 0/0 | 6608 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0046 | 0/0 | 6608 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0047 | 0/0 | 6608 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0048 | 0/0 | 6613 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0049 | 0/0 | 6608 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0050 | 0/0 | 6609 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0051 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0052 | 0/0 | 6608 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0053 | 0/0 | 6609 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0054 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0055 | 0/0 | 6609 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0056 | 0/0 | 6608 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0057 | 0/0 | 6609 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0058 | 0/0 | 6608 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0059 | 0/0 | 6609 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| t0060 | 1/0 | 6609 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| g0366 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1869 | 123 | 16 | 21 | 62 | 6 | 17 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004 | 0/0 | 1869 | 57 | 45 | 5 | 5 | 0 | 2 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0009 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0013 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0002c0002 | 1/0 | 1869 | 94 | 19 | 13 | 50 | 3 | 8 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0003 | 0/0 | 1869 | 86 | 5 | 7 | 63 | 3 | 8 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0006 | 0/0 | 1869 | 3 | 3 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0004c0005 | 0/0 | 1869 | 7 | 1 | 2 | 0 | 0 | 4 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0005c0007 | 0/0 | 1869 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0006c0014 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0007c0011 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0008c0010 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0009c0012 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0010c0008 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8481 | 52 | 1 | 6 | 41 | 1 | 3 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0001t0002 | 0/0 | 8479 | 7 | 3 | 1 | 1 | 0 | 2 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0001t0003 | 0/1 | 8481 | 46 | 5 | 12 | 16 | 3 | 9 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0001t0011 | 0/0 | 8482 | 4 | 1 | 1 | 0 | 2 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0001t0020 | 0/0 | 8482 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0001t0022 | 0/0 | 8474 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0001t0032 | 0/0 | 8481 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0001t0033 | 0/0 | 8481 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0001t0034 | 0/0 | 8481 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0001t0035 | 0/0 | 8477 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0001t0036 | 0/0 | 8481 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0001t0038 | 0/0 | 8480 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0001t0040 | 0/0 | 8475 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0001t0042 | 0/0 | 8479 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0001t0043 | 0/0 | 8475 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0001t0044 | 0/0 | 8481 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0008 | 0/0 | 8476 | 11 | 11 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0009 | 0/0 | 8474 | 9 | 9 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0010 | 0/0 | 8477 | 8 | 1 | 1 | 5 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0013 | 0/0 | 8476 | 4 | 4 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0015 | 0/0 | 8476 | 3 | 3 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0016 | 0/0 | 8476 | 3 | 3 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0017 | 0/0 | 8477 | 4 | 3 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0019 | 0/0 | 8475 | 3 | 2 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0023 | 0/0 | 8476 | 2 | 1 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0024 | 0/0 | 8475 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0025 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0026 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0029 | 0/0 | 8477 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0045 | 0/0 | 8476 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0048 | 0/0 | 8481 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0057 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0058 | 0/0 | 8476 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0004t0059 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0009t0029 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0001c0013t0031 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0002c0002t0004 | 0/0 | 8477 | 44 | 19 | 3 | 16 | 2 | 4 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0002c0002t0005 | 0/0 | 8477 | 39 | 0 | 8 | 27 | 0 | 4 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0002c0002t0027 | 0/0 | 8477 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0002c0002t0028 | 0/0 | 8476 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0002c0002t0050 | 0/0 | 8477 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0002c0002t0051 | 0/0 | 8477 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0002c0002t0052 | 0/0 | 8476 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0002c0002t0053 | 0/0 | 8477 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0002c0002t0055 | 0/0 | 8477 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0002c0002t0056 | 0/0 | 8476 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0002c0002t0060 | 1/0 | 8477 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0003t0001 | 0/0 | 8481 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0003t0002 | 0/0 | 8479 | 42 | 4 | 3 | 29 | 3 | 3 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0003t0003 | 0/0 | 8481 | 2 | 0 | 0 | 0 | 0 | 2 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0003t0006 | 0/0 | 8479 | 13 | 0 | 2 | 10 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0003t0007 | 0/0 | 8479 | 11 | 0 | 0 | 11 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0003t0011 | 0/0 | 8482 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0003t0012 | 0/0 | 8478 | 5 | 0 | 0 | 5 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0003t0018 | 0/0 | 8480 | 3 | 0 | 0 | 2 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0003t0021 | 0/0 | 8480 | 2 | 0 | 0 | 1 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0003t0030 | 0/0 | 8481 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0003t0037 | 0/0 | 8481 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0003t0039 | 0/0 | 8475 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0003t0041 | 0/0 | 8479 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0006t0013 | 0/0 | 8476 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0006t0015 | 0/0 | 8476 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0003c0006t0047 | 0/0 | 8476 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0004c0005t0014 | 0/0 | 8476 | 5 | 0 | 1 | 0 | 0 | 4 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0004c0005t0046 | 0/0 | 8476 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0004c0005t0049 | 0/0 | 8476 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0005c0007t0005 | 0/0 | 8477 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0005c0007t0054 | 0/0 | 8477 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0006c0014t0016 | 0/0 | 8476 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0007c0011t0026 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0008c0010t0025 | 0/0 | 8477 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0009c0012t0005 | 0/0 | 8477 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| a0010c0008t0001 | 0/0 | 8481 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | copy fasta | chr11 | 74325316 | 74403433 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0011g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0011g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0011g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0011g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0020g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0020g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0022g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0022g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0032g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0033g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0034g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0035g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0036g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0038g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0040g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0042g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0043g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0001t0044g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0009g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0010g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0010g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0010g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0010g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0010g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0010g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0010g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0013g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0013g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0013g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0013g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0015g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0015g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0015g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0016g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0016g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0016g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0017g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0017g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0017g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0017g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0019g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0019g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0019g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0023g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0023g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0024g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0024g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0025g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0026g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0029g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0045g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0048g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0057g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0058g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0004t0059g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0009t0029g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0001c0013t0031g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0027g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0027g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0028g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0028g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0050g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0051g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0052g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0053g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0055g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0056g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0002c0002t0060g0366 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0011g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0012g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0012g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0012g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0012g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0012g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0018g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0018g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0018g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0021g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0021g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0030g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0037g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0039g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0003t0041g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0006t0013g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0006t0015g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0003c0006t0047g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0004c0005t0014g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0004c0005t0014g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0004c0005t0014g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0004c0005t0014g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0004c0005t0014g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0004c0005t0046g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0004c0005t0049g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0005c0007t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0005c0007t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0005c0007t0054g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0006c0014t0016g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0007c0011t0026g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0008c0010t0025g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0009c0012t0005g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| a0010c0008t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0011 | g0220 | EUR | GBR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00140 | hp2 | a0002 | c0002 | t0004 | g0211 | EUR | GBR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00280 | hp1 | a0003 | c0003 | t0002 | g0025 | EUR | FIN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0224 | EUR | FIN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0178 | EUR | FIN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0284 | EUR | FIN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00408 | hp1 | a0003 | c0003 | t0001 | g0081 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00408 | hp2 | a0003 | c0003 | t0002 | g0037 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00423 | hp1 | a0003 | c0003 | t0012 | g0039 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00438 | hp2 | a0003 | c0003 | t0006 | g0045 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00544 | hp1 | a0003 | c0003 | t0002 | g0034 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00597 | hp1 | a0003 | c0003 | t0012 | g0062 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00597 | hp2 | a0002 | c0002 | t0005 | g0194 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00609 | hp2 | a0003 | c0003 | t0012 | g0050 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00621 | hp1 | a0003 | c0003 | t0002 | g0076 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00639 | hp2 | a0001 | c0004 | t0023 | g0095 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00642 | hp1 | a0003 | c0003 | t0002 | g0071 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00642 | hp2 | a0004 | c0005 | t0046 | g0126 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00673 | hp1 | a0003 | c0003 | t0001 | g0080 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00673 | hp2 | a0003 | c0003 | t0002 | g0041 | EAS | CHS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00733 | hp2 | a0002 | c0002 | t0005 | g0204 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00735 | hp1 | a0002 | c0002 | t0005 | g0225 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00738 | hp1 | a0003 | c0003 | t0041 | g0069 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00738 | hp2 | a0002 | c0002 | t0005 | g0199 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG00741 | hp2 | a0002 | c0002 | t0005 | g0202 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01069 | hp1 | a0002 | c0002 | t0005 | g0250 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01074 | hp1 | a0001 | c0004 | t0019 | g0350 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01074 | hp2 | a0002 | c0002 | t0004 | g0164 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01081 | hp1 | a0002 | c0002 | t0056 | g0148 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01081 | hp2 | a0001 | c0001 | t0035 | g0151 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01099 | hp1 | a0001 | c0004 | t0029 | g0361 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01099 | hp2 | a0001 | c0004 | t0010 | g0008 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01106 | hp1 | a0002 | c0002 | t0004 | g0267 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01106 | hp2 | a0001 | c0001 | t0011 | g0217 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01175 | hp1 | a0003 | c0003 | t0006 | g0073 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0154 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01243 | hp2 | a0001 | c0004 | t0017 | g0362 | AMR | PUR | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01257 | hp1 | a0003 | c0003 | t0002 | g0004 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0329 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01261 | hp1 | a0004 | c0005 | t0014 | g0122 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01261 | hp2 | a0002 | c0002 | t0005 | g0241 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01361 | hp1 | a0002 | c0002 | t0053 | g0253 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01433 | hp1 | a0002 | c0002 | t0005 | g0142 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0140 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01516 | hp1 | a0002 | c0002 | t0004 | g0252 | EUR | IBS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01516 | hp2 | a0003 | c0003 | t0002 | g0091 | EUR | IBS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01517 | hp1 | a0001 | c0001 | t0011 | g0240 | EUR | IBS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01517 | hp2 | a0003 | c0003 | t0002 | g0061 | EUR | IBS | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01884 | hp1 | a0001 | c0004 | t0008 | g0260 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01884 | hp2 | a0001 | c0004 | t0015 | g0247 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01891 | hp2 | a0002 | c0002 | t0004 | g0271 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02004 | hp1 | a0003 | c0003 | t0011 | g0089 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02015 | hp1 | a0005 | c0007 | t0005 | g0055 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02015 | hp2 | a0003 | c0003 | t0012 | g0048 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02027 | hp2 | a0002 | c0002 | t0004 | g0144 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02040 | hp1 | a0003 | c0003 | t0002 | g0066 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02040 | hp2 | a0002 | c0002 | t0005 | g0180 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02055 | hp1 | a0002 | c0002 | t0004 | g0251 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02055 | hp2 | a0002 | c0002 | t0004 | g0112 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02056 | hp1 | a0002 | c0002 | t0005 | g0207 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02074 | hp1 | a0003 | c0003 | t0021 | g0026 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02074 | hp2 | a0002 | c0002 | t0005 | g0153 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02080 | hp1 | a0003 | c0003 | t0002 | g0044 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02080 | hp2 | a0001 | c0001 | t0020 | g0294 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02129 | hp1 | a0003 | c0003 | t0002 | g0032 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02135 | hp1 | a0003 | c0003 | t0002 | g0043 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02145 | hp1 | a0002 | c0002 | t0004 | g0269 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02148 | hp2 | a0002 | c0002 | t0004 | g0168 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02165 | hp1 | a0005 | c0007 | t0005 | g0067 | EAS | CDX | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | CDX | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02257 | hp1 | a0001 | c0004 | t0008 | g0259 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0229 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02258 | hp1 | a0001 | c0004 | t0013 | g0108 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02258 | hp2 | a0001 | c0004 | t0008 | g0011 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02280 | hp1 | a0001 | c0004 | t0057 | g0357 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02280 | hp2 | a0002 | c0002 | t0004 | g0344 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02293 | hp1 | a0003 | c0003 | t0006 | g0053 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0192 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02300 | hp1 | a0002 | c0002 | t0005 | g0100 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02451 | hp1 | a0001 | c0004 | t0017 | g0359 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02451 | hp2 | a0002 | c0002 | t0004 | g0285 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02523 | hp1 | a0003 | c0003 | t0007 | g0019 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02572 | hp1 | a0001 | c0004 | t0025 | g0281 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02572 | hp2 | a0001 | c0013 | t0031 | g0343 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0221 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02602 | hp2 | a0002 | c0002 | t0005 | g0325 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02615 | hp1 | a0001 | c0001 | t0022 | g0356 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02615 | hp2 | a0001 | c0001 | t0040 | g0277 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02622 | hp1 | a0001 | c0001 | t0022 | g0355 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02622 | hp2 | a0001 | c0004 | t0009 | g0334 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02630 | hp1 | a0003 | c0003 | t0002 | g0090 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02630 | hp2 | a0001 | c0004 | t0013 | g0109 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02647 | hp1 | a0002 | c0002 | t0004 | g0226 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02647 | hp2 | a0001 | c0004 | t0009 | g0342 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02698 | hp2 | a0002 | c0002 | t0005 | g0332 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02717 | hp1 | a0001 | c0004 | t0008 | g0258 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02717 | hp2 | a0001 | c0004 | t0016 | g0262 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02723 | hp1 | a0001 | c0004 | t0008 | g0012 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02723 | hp2 | a0001 | c0004 | t0016 | g0263 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02735 | hp1 | a0004 | c0005 | t0014 | g0121 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02809 | hp1 | a0001 | c0004 | t0009 | g0340 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02809 | hp2 | a0003 | c0006 | t0047 | g0023 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02818 | hp1 | a0001 | c0004 | t0019 | g0351 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02818 | hp2 | a0003 | c0003 | t0002 | g0007 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02886 | hp1 | a0003 | c0006 | t0015 | g0022 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02886 | hp2 | a0002 | c0002 | t0004 | g0265 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02895 | hp1 | a0001 | c0009 | t0029 | g0365 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02895 | hp2 | a0001 | c0004 | t0009 | g0336 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02896 | hp1 | a0002 | c0002 | t0004 | g0013 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0327 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02897 | hp1 | a0001 | c0004 | t0009 | g0335 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02897 | hp2 | a0002 | c0002 | t0004 | g0013 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02922 | hp1 | a0002 | c0002 | t0004 | g0347 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02922 | hp2 | a0001 | c0004 | t0009 | g0337 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02965 | hp1 | a0001 | c0001 | t0038 | g0297 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02965 | hp2 | a0001 | c0004 | t0024 | g0106 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02970 | hp1 | a0002 | c0002 | t0004 | g0272 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02970 | hp2 | a0001 | c0004 | t0008 | g0256 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02976 | hp1 | a0001 | c0004 | t0008 | g0011 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02976 | hp2 | a0001 | c0004 | t0009 | g0338 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03017 | hp1 | a0003 | c0003 | t0003 | g0093 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03041 | hp1 | a0001 | c0001 | t0042 | g0326 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03041 | hp2 | a0001 | c0004 | t0008 | g0012 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03098 | hp1 | a0001 | c0004 | t0059 | g0364 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03098 | hp2 | a0001 | c0004 | t0026 | g0279 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03130 | hp1 | a0002 | c0002 | t0004 | g0268 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03130 | hp2 | a0001 | c0004 | t0015 | g0245 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03139 | hp2 | a0003 | c0003 | t0002 | g0092 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03195 | hp1 | a0001 | c0004 | t0008 | g0010 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03195 | hp2 | a0001 | c0004 | t0013 | g0107 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03209 | hp1 | a0001 | c0004 | t0015 | g0246 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03209 | hp2 | a0001 | c0004 | t0010 | g0008 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03225 | hp1 | a0001 | c0004 | t0008 | g0255 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03225 | hp2 | a0003 | c0003 | t0002 | g0007 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03239 | hp1 | a0009 | c0012 | t0005 | g0319 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03239 | hp2 | a0003 | c0003 | t0002 | g0087 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03453 | hp2 | a0001 | c0004 | t0009 | g0339 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03486 | hp2 | a0008 | c0010 | t0025 | g0282 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0186 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03490 | hp2 | a0001 | c0001 | t0043 | g0111 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03491 | hp1 | a0003 | c0003 | t0002 | g0049 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03491 | hp2 | a0004 | c0005 | t0014 | g0123 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03492 | hp2 | a0004 | c0005 | t0014 | g0125 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03516 | hp1 | a0002 | c0002 | t0004 | g0244 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03516 | hp2 | a0006 | c0014 | t0016 | g0257 | AFR | ESN | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03540 | hp2 | a0002 | c0002 | t0004 | g0270 | AFR | GWD | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03579 | hp1 | a0001 | c0004 | t0009 | g0341 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03579 | hp2 | a0001 | c0004 | t0017 | g0360 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03654 | hp1 | a0003 | c0003 | t0006 | g0005 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03669 | hp1 | a0002 | c0002 | t0004 | g0145 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03669 | hp2 | a0001 | c0001 | t0032 | g0147 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03710 | hp1 | a0003 | c0003 | t0003 | g0068 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03710 | hp2 | a0002 | c0002 | t0005 | g0303 | SAS | PJL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03831 | hp1 | a0001 | c0004 | t0048 | g0354 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03834 | hp1 | a0002 | c0002 | t0004 | g0212 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0209 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03927 | hp1 | a0003 | c0003 | t0021 | g0036 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03942 | hp1 | a0001 | c0001 | t0036 | g0237 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03942 | hp2 | a0002 | c0002 | t0004 | g0097 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0146 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04184 | hp2 | a0003 | c0003 | t0018 | g0040 | SAS | BEB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04199 | hp1 | a0003 | c0003 | t0002 | g0086 | SAS | STU | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0254 | SAS | STU | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04204 | hp1 | a0002 | c0002 | t0005 | g0323 | SAS | STU | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04204 | hp2 | a0004 | c0005 | t0014 | g0124 | SAS | STU | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04228 | hp1 | a0001 | c0004 | t0010 | g0116 | SAS | STU | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0195 | SAS | STU | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18522 | hp1 | a0003 | c0003 | t0039 | g0024 | AFR | YRI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18522 | hp2 | a0007 | c0011 | t0026 | g0280 | AFR | YRI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18612 | hp1 | a0002 | c0002 | t0005 | g0203 | EAS | CHB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18747 | hp1 | a0002 | c0002 | t0005 | g0177 | EAS | CHB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | CHB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18906 | hp1 | a0001 | c0004 | t0017 | g0363 | AFR | YRI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18906 | hp2 | a0002 | c0002 | t0004 | g0119 | AFR | YRI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18941 | hp1 | a0002 | c0002 | t0005 | g0205 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18941 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18942 | hp1 | a0002 | c0002 | t0005 | g0141 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18943 | hp2 | a0001 | c0004 | t0010 | g0117 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18944 | hp1 | a0003 | c0003 | t0006 | g0077 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18945 | hp2 | a0002 | c0002 | t0005 | g0172 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18946 | hp1 | a0002 | c0002 | t0005 | g0206 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18947 | hp1 | a0002 | c0002 | t0005 | g0104 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18947 | hp2 | a0003 | c0003 | t0001 | g0088 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18948 | hp1 | a0003 | c0003 | t0002 | g0029 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18948 | hp2 | a0002 | c0002 | t0005 | g0009 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18949 | hp2 | a0003 | c0003 | t0006 | g0078 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18950 | hp1 | a0003 | c0003 | t0002 | g0064 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18950 | hp2 | a0002 | c0002 | t0004 | g0167 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18952 | hp1 | a0005 | c0007 | t0054 | g0054 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18952 | hp2 | a0010 | c0008 | t0001 | g0079 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18953 | hp1 | a0002 | c0002 | t0004 | g0156 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18954 | hp1 | a0002 | c0002 | t0027 | g0197 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18956 | hp2 | a0002 | c0002 | t0004 | g0233 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18957 | hp1 | a0003 | c0003 | t0006 | g0070 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18957 | hp2 | a0002 | c0002 | t0005 | g0196 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18959 | hp1 | a0003 | c0003 | t0002 | g0072 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18959 | hp2 | a0003 | c0003 | t0030 | g0018 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18960 | hp1 | a0002 | c0002 | t0004 | g0102 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18960 | hp2 | a0002 | c0002 | t0005 | g0305 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18962 | hp1 | a0002 | c0002 | t0028 | g0174 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18962 | hp2 | a0003 | c0003 | t0006 | g0005 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18963 | hp1 | a0003 | c0003 | t0002 | g0030 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18963 | hp2 | a0002 | c0002 | t0004 | g0215 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18965 | hp1 | a0002 | c0002 | t0004 | g0232 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18965 | hp2 | a0001 | c0001 | t0044 | g0311 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18966 | hp2 | a0002 | c0002 | t0005 | g0227 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18969 | hp2 | a0003 | c0003 | t0037 | g0051 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18970 | hp1 | a0003 | c0003 | t0002 | g0084 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18970 | hp2 | a0002 | c0002 | t0004 | g0166 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18977 | hp1 | a0001 | c0004 | t0010 | g0118 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18977 | hp2 | a0003 | c0003 | t0007 | g0003 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18978 | hp1 | a0003 | c0003 | t0018 | g0083 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18978 | hp2 | a0002 | c0002 | t0005 | g0333 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18980 | hp1 | a0003 | c0003 | t0002 | g0074 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18981 | hp1 | a0002 | c0002 | t0005 | g0208 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18982 | hp1 | a0003 | c0003 | t0002 | g0028 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18982 | hp2 | a0002 | c0002 | t0005 | g0200 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18983 | hp1 | a0003 | c0003 | t0007 | g0003 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18984 | hp1 | a0001 | c0004 | t0010 | g0113 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18987 | hp1 | a0003 | c0003 | t0002 | g0058 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18988 | hp2 | a0003 | c0003 | t0002 | g0052 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18989 | hp2 | a0003 | c0003 | t0002 | g0075 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18991 | hp1 | a0003 | c0003 | t0002 | g0085 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18994 | hp1 | a0002 | c0002 | t0004 | g0216 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18997 | hp1 | a0003 | c0003 | t0002 | g0047 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18997 | hp2 | a0002 | c0002 | t0005 | g0210 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18998 | hp1 | a0003 | c0003 | t0002 | g0057 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18998 | hp2 | a0002 | c0002 | t0004 | g0162 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18999 | hp1 | a0001 | c0004 | t0010 | g0114 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19000 | hp2 | a0002 | c0002 | t0005 | g0213 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19001 | hp1 | a0001 | c0001 | t0020 | g0275 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19001 | hp2 | a0003 | c0003 | t0002 | g0031 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19002 | hp1 | a0002 | c0002 | t0005 | g0175 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19003 | hp1 | a0002 | c0002 | t0028 | g0149 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19003 | hp2 | a0001 | c0004 | t0010 | g0115 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19004 | hp2 | a0003 | c0003 | t0006 | g0033 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19005 | hp1 | a0003 | c0003 | t0007 | g0017 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19007 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19009 | hp1 | a0002 | c0002 | t0005 | g0171 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19010 | hp2 | a0003 | c0003 | t0002 | g0059 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19011 | hp1 | a0003 | c0003 | t0007 | g0016 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19043 | hp1 | a0002 | c0002 | t0004 | g0346 | AFR | LWK | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19043 | hp2 | a0002 | c0002 | t0004 | g0345 | AFR | LWK | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19058 | hp1 | a0002 | c0002 | t0005 | g0101 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19058 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19060 | hp1 | a0003 | c0003 | t0018 | g0042 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19060 | hp2 | a0002 | c0002 | t0055 | g0193 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19062 | hp1 | a0003 | c0003 | t0007 | g0015 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19062 | hp2 | a0002 | c0002 | t0004 | g0163 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19063 | hp1 | a0002 | c0002 | t0004 | g0234 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19063 | hp2 | a0001 | c0001 | t0034 | g0231 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19064 | hp1 | a0002 | c0002 | t0005 | g0173 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19066 | hp2 | a0003 | c0003 | t0007 | g0020 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19068 | hp1 | a0003 | c0003 | t0002 | g0046 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19070 | hp1 | a0003 | c0003 | t0006 | g0060 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19070 | hp2 | a0002 | c0002 | t0004 | g0214 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19074 | hp1 | a0003 | c0003 | t0007 | g0002 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19074 | hp2 | a0002 | c0002 | t0004 | g0161 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19075 | hp1 | a0002 | c0002 | t0004 | g0228 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19075 | hp2 | a0003 | c0003 | t0002 | g0035 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19076 | hp2 | a0003 | c0003 | t0007 | g0021 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19077 | hp1 | a0002 | c0002 | t0004 | g0159 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19077 | hp2 | a0003 | c0003 | t0002 | g0056 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19078 | hp1 | a0002 | c0002 | t0005 | g0201 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19079 | hp2 | a0003 | c0003 | t0006 | g0063 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19080 | hp1 | a0003 | c0003 | t0007 | g0014 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19080 | hp2 | a0002 | c0002 | t0005 | g0176 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19081 | hp1 | a0002 | c0002 | t0005 | g0009 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19081 | hp2 | a0003 | c0003 | t0006 | g0027 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19083 | hp1 | a0003 | c0003 | t0007 | g0002 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19085 | hp2 | a0002 | c0002 | t0051 | g0160 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19086 | hp1 | a0002 | c0002 | t0027 | g0198 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19088 | hp1 | a0003 | c0003 | t0006 | g0038 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19089 | hp1 | a0003 | c0003 | t0012 | g0065 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19240 | hp1 | a0001 | c0004 | t0019 | g0352 | AFR | YRI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA19240 | hp2 | a0001 | c0004 | t0008 | g0010 | AFR | YRI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0098 | EUR | TSI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA20752 | hp2 | a0002 | c0002 | t0050 | g0235 | EUR | TSI | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | GIH | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA20905 | hp2 | a0002 | c0002 | t0004 | g0304 | SAS | GIH | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01123 | hp1 | a0003 | c0003 | t0002 | g0082 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0218 | AMR | CLM | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02109 | hp1 | a0001 | c0004 | t0058 | g0358 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02109 | hp2 | a0001 | c0001 | t0011 | g0187 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02486 | hp1 | a0004 | c0005 | t0049 | g0120 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02486 | hp2 | a0001 | c0004 | t0013 | g0105 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02559 | hp1 | a0001 | c0004 | t0024 | g0261 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | ACB | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03471 | hp1 | a0003 | c0006 | t0013 | g0094 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| HG03471 | hp2 | a0002 | c0002 | t0004 | g0266 | AFR | MSL | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18955 | hp1 | a0002 | c0002 | t0052 | g0152 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA20300 | hp1 | a0001 | c0004 | t0023 | g0348 | AFR | USA | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA20300 | hp2 | a0001 | c0004 | t0016 | g0264 | AFR | USA | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA21309 | hp1 | a0001 | c0001 | t0033 | g0278 | AFR | LWK | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| NA21309 | hp2 | a0001 | c0004 | t0045 | g0349 | AFR | LWK | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0169 | REF | REF | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0060 | g0366 | REF | REF | PGM2L1_chr11_74325316_74403433 | PGM2L1 | chr11 | 74325316 | 74403433 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74336698
|
T | A | 1 | a0004 | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
missense_variant | MODERATE | c.1823A>T | p.Asn608Ile | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 2095/8477 | 1823/1869 | 608/622 | chr11 | 74336698 | ||
| chr11:74338592
|
C | T | 1 | a0010 | 1 | NA18952.hp2 | missense_variant | MODERATE | c.1642G>A | p.Val548Met | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/14 | 1914/8477 | 1642/1869 | 548/622 | chr11 | 74338592 | ||
| chr11:74342462
|
G | A | 1 | a0008 | 1 | HG03486.hp2 | missense_variant&splice_region_variant | MODERATE | c.1631C>T | p.Ser544Leu | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/14 | 1903/8477 | 1631/1869 | 544/622 | chr11 | 74342462 | ||
| chr11:74342502
|
C | T | 7 | a0001a0003a0004others(4): Show | 282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
missense_variant | MODERATE | c.1591G>A | p.Val531Ile | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/14 | 1863/8477 | 1591/1869 | 531/622 | chr11 | 74342502 | ||
| chr11:74342578
|
T | G | 1 | a0007 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.1515A>C | p.Glu505Asp | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/14 | 1787/8477 | 1515/1869 | 505/622 | chr11 | 74342578 | ||
| chr11:74342922
|
T | C | 1 | a0009 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.1405A>G | p.Ile469Val | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 11/14 | 1677/8477 | 1405/1869 | 469/622 | chr11 | 74342922 | ||
| chr11:74351455
|
G | A | 1 | a0006 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.677C>T | p.Pro226Leu | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/14 | 949/8477 | 677/1869 | 226/622 | chr11 | 74351455 | ||
| chr11:74398121
|
A | G | 3 | a0003a0005a0010 | 93 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(90): Show |
missense_variant | MODERATE | c.41T>C | p.Leu14Pro | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/14 | 313/8477 | 41/1869 | 14/622 | chr11 | 74398121 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74338524
|
A | G | 3 | a0001c0001a0003c0003a0010c0008 | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
synonymous_variant | LOW | c.1710T>C | p.Ser570Ser | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/14 | 1982/8477 | 1710/1869 | 570/622 | chr11 | 74338524 | ||
| chr11:74343336
|
A | G | 1 | a0001c0009 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.1299T>C | p.Phe433Phe | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 10/14 | 1571/8477 | 1299/1869 | 433/622 | chr11 | 74343336 | ||
| chr11:74346752
|
T | C | 1 | a0001c0013 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1017A>G | p.Ala339Ala | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/14 | 1289/8477 | 1017/1869 | 339/622 | chr11 | 74346752 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74330438
|
T | C | 2 | a0001c0001t0040a0003c0003t0039 | 2 | HG02615.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6214A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 6214 | chr11 | 74330438 | |||||
| chr11:74330539
|
A | C | 2 | a0001c0004t0016a0006c0014t0016 | 4 | HG02717.hp2 HG02723.hp2 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6113T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 6113 | chr11 | 74330539 | |||||
| chr11:74330547
|
A | T | 63 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(60): Show | 329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
3_prime_UTR_variant | MODIFIER | c.*6105T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 6105 | chr11 | 74330547 | |||||
| chr11:74330567
|
A | C | 1 | a0003c0003t0006 | 13 | HG00438.hp2 HG01175.hp1 HG02293.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*6085T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 6085 | chr11 | 74330567 | |||||
| chr11:74330873
|
C | G | 1 | a0002c0002t0051 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5779G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5779 | chr11 | 74330873 | |||||
| chr11:74331013
|
T | A | 1 | a0001c0001t0034 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5639A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5639 | chr11 | 74331013 | |||||
| chr11:74331123
|
G | A | 3 | a0004c0005t0014a0004c0005t0046a0004c0005t0049 | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5529C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5529 | chr11 | 74331123 | |||||
| chr11:74331196
|
A | G | 59 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(56): Show | 282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*5456T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5456 | chr11 | 74331196 | |||||
| chr11:74331241
|
G | A | 11 | a0001c0004t0009a0001c0004t0013a0001c0004t0016others(8): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5411C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5411 | chr11 | 74331241 | |||||
| chr11:74331263
|
C | CTTTT | 21 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | 194 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*5385_*5388dupAAAA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5388 | chr11 | 74331263 | |||||
| chr11:74331263
|
C | CTTTTT | 5 | a0001c0001t0011a0001c0001t0020a0001c0004t0048others(2): Show | 11 | HG00140.hp1 HG01106.hp2 HG01517.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5384_*5388dupAAAA others(1): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5388 | chr11 | 74331263 | |||||
| chr11:74331263
|
CT | C | 14 | a0001c0004t0009a0001c0004t0013a0001c0004t0016others(11): Show | 33 | HG00639.hp2 HG00642.hp2 HG01261.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*5388delA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5388 | chr11 | 74331263 | |||||
| chr11:74331284
|
T | C | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | 207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*5368A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5368 | chr11 | 74331284 | |||||
| chr11:74331285
|
G | A | 8 | a0001c0001t0003a0001c0001t0011a0001c0001t0032others(5): Show | 57 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*5367C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5367 | chr11 | 74331285 | |||||
| chr11:74331336
|
C | A | 11 | a0001c0004t0009a0001c0004t0013a0001c0004t0016others(8): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5316G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5316 | chr11 | 74331336 | |||||
| chr11:74331453
|
G | C | 1 | a0002c0002t0053 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5199C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5199 | chr11 | 74331453 | |||||
| chr11:74331489
|
C | T | 1 | a0001c0004t0019 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5163G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5163 | chr11 | 74331489 | |||||
| chr11:74331513
|
C | T | 2 | a0001c0004t0019a0001c0013t0031 | 4 | HG01074.hp1 HG02572.hp2 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5139G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5139 | chr11 | 74331513 | |||||
| chr11:74331622
|
G | C | 10 | a0001c0001t0002a0001c0001t0043a0003c0003t0002others(7): Show | 86 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*5030C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 5030 | chr11 | 74331622 | |||||
| chr11:74331672
|
G | C | 1 | a0001c0001t0036 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4980C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 4980 | chr11 | 74331672 | |||||
| chr11:74331742
|
A | G | 44 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(41): Show | 252 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*4910T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 4910 | chr11 | 74331742 | |||||
| chr11:74332085
|
G | A | 1 | a0005c0007t0054 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4567C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 4567 | chr11 | 74332085 | |||||
| chr11:74332126
|
A | G | 30 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*4526T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 4526 | chr11 | 74332126 | |||||
| chr11:74332205
|
A | G | 11 | a0001c0004t0009a0001c0004t0013a0001c0004t0016others(8): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4447T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 4447 | chr11 | 74332205 | |||||
| chr11:74332216
|
A | T | 1 | a0002c0002t0027 | 2 | NA18954.hp1 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4436T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 4436 | chr11 | 74332216 | |||||
| chr11:74332663
|
G | A | 59 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(56): Show | 282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*3989C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3989 | chr11 | 74332663 | |||||
| chr11:74332669
|
A | G | 1 | a0003c0003t0041 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3983T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3983 | chr11 | 74332669 | |||||
| chr11:74332727
|
T | C | 1 | a0001c0001t0040 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3925A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3925 | chr11 | 74332727 | |||||
| chr11:74332937
|
G | T | 2 | a0004c0005t0014a0004c0005t0046 | 6 | HG00642.hp2 HG01261.hp1 HG02735.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3715C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3715 | chr11 | 74332937 | |||||
| chr11:74332949
|
TAA | T | 1 | a0001c0004t0009 | 9 | HG02622.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3701_*3702delTT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3701 | chr11 | 74332949 | |||||
| chr11:74333094
|
G | A | 30 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*3558C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3558 | chr11 | 74333094 | |||||
| chr11:74333111
|
T | TA | 11 | a0001c0004t0009a0001c0004t0013a0001c0004t0016others(8): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3540dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3540 | chr11 | 74333111 | |||||
| chr11:74333188
|
TA | T | 1 | a0001c0004t0019 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3463delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3463 | chr11 | 74333188 | |||||
| chr11:74333420
|
C | T | 1 | a0001c0004t0019 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3232G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3232 | chr11 | 74333420 | |||||
| chr11:74333512
|
C | T | 30 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*3140G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3140 | chr11 | 74333512 | |||||
| chr11:74333646
|
T | C | 2 | a0001c0004t0029a0001c0009t0029 | 2 | HG01099.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3006A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 3006 | chr11 | 74333646 | |||||
| chr11:74333815
|
A | C | 1 | a0002c0002t0050 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2837T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 2837 | chr11 | 74333815 | |||||
| chr11:74333930
|
C | G | 11 | a0001c0004t0009a0001c0004t0013a0001c0004t0016others(8): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2722G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 2722 | chr11 | 74333930 | |||||
| chr11:74333931
|
C | T | 16 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(13): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*2721G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 2721 | chr11 | 74333931 | |||||
| chr11:74333982
|
C | G | 2 | a0001c0004t0025a0008c0010t0025 | 2 | HG02572.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2670G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 2670 | chr11 | 74333982 | |||||
| chr11:74334238
|
T | A | 5 | a0001c0004t0013a0001c0004t0024a0001c0004t0059others(2): Show | 9 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2414A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 2414 | chr11 | 74334238 | |||||
| chr11:74334359
|
C | G | 1 | a0001c0004t0008 | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2293G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 2293 | chr11 | 74334359 | |||||
| chr11:74334697
|
A | G | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(15): Show | 121 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*1955T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1955 | chr11 | 74334697 | |||||
| chr11:74334807
|
G | C | 1 | a0004c0005t0049 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1845C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1845 | chr11 | 74334807 | |||||
| chr11:74334907
|
CT | C | 20 | a0001c0001t0038a0001c0004t0008a0001c0004t0009others(17): Show | 52 | HG00639.hp2 HG00642.hp2 HG01074.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1744delA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1744 | chr11 | 74334907 | |||||
| chr11:74334907
|
CTT | C | 11 | a0001c0001t0002a0001c0001t0040a0001c0001t0042others(8): Show | 83 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1743_*1744delAA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1743 | chr11 | 74334907 | |||||
| chr11:74334907
|
CTTT | C | 2 | a0001c0001t0022a0003c0003t0012 | 7 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1742_*1744delAAA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1742 | chr11 | 74334907 | |||||
| chr11:74335005
|
G | A | 3 | a0004c0005t0014a0004c0005t0046a0004c0005t0049 | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1647C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1647 | chr11 | 74335005 | |||||
| chr11:74335061
|
G | A | 1 | a0002c0002t0055 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1591C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1591 | chr11 | 74335061 | |||||
| chr11:74335234
|
G | A | 1 | a0002c0002t0056 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1418C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1418 | chr11 | 74335234 | |||||
| chr11:74335237
|
T | C | 1 | a0003c0006t0047 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1415A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1415 | chr11 | 74335237 | |||||
| chr11:74335288
|
A | G | 2 | a0001c0004t0026a0007c0011t0026 | 2 | HG03098.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1364T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1364 | chr11 | 74335288 | |||||
| chr11:74335319
|
A | T | 1 | a0001c0001t0033 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1333T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1333 | chr11 | 74335319 | |||||
| chr11:74335321
|
C | A | 1 | a0001c0001t0033 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1331G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1331 | chr11 | 74335321 | |||||
| chr11:74335323
|
T | A | 1 | a0001c0001t0033 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1329A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1329 | chr11 | 74335323 | |||||
| chr11:74335324
|
A | C | 1 | a0001c0001t0033 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1328T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1328 | chr11 | 74335324 | |||||
| chr11:74335546
|
T | C | 1 | a0001c0001t0044 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1106A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1106 | chr11 | 74335546 | |||||
| chr11:74335638
|
C | CA | 3 | a0004c0005t0014a0004c0005t0046a0004c0005t0049 | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1013dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 1013 | chr11 | 74335638 | |||||
| chr11:74335713
|
A | T | 2 | a0001c0004t0025a0008c0010t0025 | 2 | HG02572.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*939T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 939 | chr11 | 74335713 | |||||
| chr11:74335816
|
C | T | 30 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
3_prime_UTR_variant | MODIFIER | c.*836G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 836 | chr11 | 74335816 | |||||
| chr11:74335930
|
C | T | 52 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(49): Show | 263 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*722G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 722 | chr11 | 74335930 | |||||
| chr11:74336181
|
C | G | 11 | a0001c0004t0009a0001c0004t0013a0001c0004t0016others(8): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*471G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 471 | chr11 | 74336181 | |||||
| chr11:74336198
|
A | C | 1 | a0004c0005t0046 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*454T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 454 | chr11 | 74336198 | |||||
| chr11:74336219
|
C | G | 2 | a0001c0004t0010a0001c0004t0057 | 9 | HG01099.hp2 HG02280.hp1 HG03209.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*433G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 433 | chr11 | 74336219 | |||||
| chr11:74336249
|
C | T | 1 | a0001c0013t0031 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*403G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 403 | chr11 | 74336249 | |||||
| chr11:74336311
|
C | T | 1 | a0001c0001t0032 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*341G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 341 | chr11 | 74336311 | |||||
| chr11:74336417
|
TA | T | 2 | a0001c0004t0015a0003c0006t0015 | 4 | HG01884.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*234delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 234 | chr11 | 74336417 | |||||
| chr11:74336453
|
C | T | 1 | a0001c0004t0045 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*199G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 199 | chr11 | 74336453 | |||||
| chr11:74336552
|
A | C | 1 | a0001c0013t0031 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 100 | chr11 | 74336552 | |||||
| chr11:74336638
|
A | G | 33 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(30): Show | 225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*14T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 14/14 | 14 | chr11 | 74336638 | |||||
| chr11:74398186
|
G | T | 2 | a0003c0003t0007a0003c0003t0030 | 12 | HG02523.hp1 NA18959.hp2 NA18977.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-25C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/14 | 25 | chr11 | 74398186 | |||||
| chr11:74398213
|
G | A | 6 | a0001c0004t0017a0001c0004t0029a0001c0004t0057others(3): Show | 9 | HG01099.hp1 HG01243.hp2 HG02109.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-52C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/14 | 52 | chr11 | 74398213 | |||||
| chr11:74398297
|
C | T | 72 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(69): Show | 379 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(376): Show |
5_prime_UTR_variant | MODIFIER | c.-136G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/14 | 136 | chr11 | 74398297 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:74336824
|
A | AT | 8 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1767-71dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74336824 | ||||||
| chr11:74336953
|
G | A | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1767-199C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74336953 | ||||||
| chr11:74336966
|
A | G | 2 | a0001c0004t0025g0281a0008c0010t0025g0282 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1767-212T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74336966 | ||||||
| chr11:74337177
|
G | A | 1 | a0001c0001t0003g0140 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1767-423C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337177 | ||||||
| chr11:74337243
|
C | T | 8 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(5): Show | 9 | HG01099.hp2 HG02280.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.1767-489G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337243 | ||||||
| chr11:74337262
|
A | G | 1 | a0003c0003t0002g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1767-508T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337262 | ||||||
| chr11:74337356
|
C | A | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1767-602G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337356 | ||||||
| chr11:74337428
|
C | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(114): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1767-674G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337428 | ||||||
| chr11:74337449
|
C | T | 1 | a0001c0004t0048g0354 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1767-695G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337449 | ||||||
| chr11:74337765
|
C | A | 2 | a0003c0003t0007g0015a0003c0003t0007g0019 | 2 | HG02523.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1766+703G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337765 | ||||||
| chr11:74337858
|
T | A | 2 | a0001c0001t0040g0277a0003c0003t0039g0024 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1766+610A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 13/13 | chr11 | 74337858 | ||||||
| chr11:74338763
|
G | A | 14 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(11): Show | 15 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1633-162C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74338763 | ||||||
| chr11:74338863
|
C | G | 1 | a0001c0001t0003g0140 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1633-262G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74338863 | ||||||
| chr11:74338997
|
A | G | 2 | a0001c0001t0003g0169a0001c0001t0003g0222 | 2 | HG00735.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1633-396T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74338997 | ||||||
| chr11:74338997
|
A | T | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1633-396T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74338997 | ||||||
| chr11:74339128
|
A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(232): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1633-527T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74339128 | ||||||
| chr11:74339164
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1633-563C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74339164 | ||||||
| chr11:74339204
|
G | A | 1 | a0003c0006t0015g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1633-603C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74339204 | ||||||
| chr11:74339217
|
C | A | 267 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(264): Show | 279 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.1633-616G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74339217 | ||||||
| chr11:74339321
|
C | T | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1633-720G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74339321 | ||||||
| chr11:74339694
|
C | G | 6 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0133others(3): Show | 6 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(3): Show |
intron_variant | MODIFIER | c.1633-1093G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74339694 | ||||||
| chr11:74339810
|
G | A | 2 | a0001c0001t0011g0240a0003c0003t0011g0089 | 2 | HG01517.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1633-1209C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74339810 | ||||||
| chr11:74340015
|
C | T | 8 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1633-1414G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74340015 | ||||||
| chr11:74340071
|
A | G | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1633-1470T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74340071 | ||||||
| chr11:74340340
|
A | G | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1633-1739T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74340340 | ||||||
| chr11:74340487
|
G | A | 1 | a0002c0002t0005g0203 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1633-1886C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74340487 | ||||||
| chr11:74340569
|
C | A | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1632+1892G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74340569 | ||||||
| chr11:74340639
|
T | C | 1 | a0001c0001t0003g0329 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1632+1822A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74340639 | ||||||
| chr11:74340999
|
G | C | 2 | a0001c0001t0003g0169a0001c0001t0003g0222 | 2 | HG00735.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1632+1462C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74340999 | ||||||
| chr11:74341154
|
T | C | 3 | a0002c0002t0004g0112a0002c0002t0004g0119a0002c0002t0004g0244 | 3 | HG02055.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1632+1307A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341154 | ||||||
| chr11:74341219
|
C | G | 15 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(12): Show | 16 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1632+1242G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341219 | ||||||
| chr11:74341312
|
T | G | 1 | a0001c0004t0058g0358 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1632+1149A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341312 | ||||||
| chr11:74341351
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0001g0291a0001c0001t0020g0275 | 3 | HG02004.hp2 HG02148.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1632+1110T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341351 | ||||||
| chr11:74341418
|
G | A | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1632+1043C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341418 | ||||||
| chr11:74341537
|
C | T | 2 | a0002c0002t0005g0225a0002c0002t0005g0250 | 2 | HG00735.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1632+924G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341537 | ||||||
| chr11:74341567
|
C | G | 5 | a0001c0004t0008g0011a0001c0004t0008g0256a0001c0004t0008g0258others(2): Show | 6 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1632+894G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341567 | ||||||
| chr11:74341651
|
C | G | 1 | a0001c0001t0003g0140 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1632+810G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341651 | ||||||
| chr11:74341695
|
G | GA | 122 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(119): Show | 129 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1632+765dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341695 | ||||||
| chr11:74341695
|
G | GAA | 11 | a0001c0001t0002g0273a0001c0004t0009g0334a0001c0004t0009g0341others(8): Show | 12 | HG02055.hp2 HG02074.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1632+764_1632+765d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341695 | ||||||
| chr11:74341695
|
GA | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(113): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1632+765delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341695 | ||||||
| chr11:74341825
|
T | A | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1632+636A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74341825 | ||||||
| chr11:74342151
|
T | C | 2 | a0003c0003t0002g0028a0003c0003t0002g0030 | 2 | NA18963.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1632+310A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 12/13 | chr11 | 74342151 | ||||||
| chr11:74342833
|
A | C | 9 | a0002c0002t0005g0009a0002c0002t0005g0141a0002c0002t0005g0200others(6): Show | 10 | NA18942.hp1 NA18946.hp1 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.1442+52T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 11/13 | chr11 | 74342833 | ||||||
| chr11:74343130
|
A | G | 13 | a0002c0002t0004g0102a0002c0002t0004g0156a0002c0002t0004g0211others(10): Show | 13 | HG00140.hp2 HG01081.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.1313-116T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 10/13 | chr11 | 74343130 | ||||||
| chr11:74343301
|
G | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(225): Show | 236 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1312+22C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 10/13 | chr11 | 74343301 | ||||||
| chr11:74343453
|
G | C | 2 | a0001c0001t0003g0185a0001c0001t0003g0218 | 2 | HG01123.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1219-37C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343453 | ||||||
| chr11:74343503
|
T | C | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-87A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343503 | ||||||
| chr11:74343572
|
A | G | 2 | a0001c0001t0040g0277a0003c0003t0039g0024 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1219-156T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343572 | ||||||
| chr11:74343769
|
C | CT | 51 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(48): Show | 55 | HG00639.hp2 HG01884.hp1 HG02027.hp2 others(52): Show |
intron_variant | MODIFIER | c.1219-354dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343769 | ||||||
| chr11:74343769
|
C | CTT | 10 | a0001c0004t0009g0339a0001c0004t0016g0262a0001c0004t0059g0364others(7): Show | 10 | HG01106.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1219-355_1219-354d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343769 | ||||||
| chr11:74343769
|
CT | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0130others(187): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1219-354delA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343769 | ||||||
| chr11:74343769
|
CTTTTTTT others(3): Show |
C | 1 | a0003c0003t0002g0090 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1219-363_1219-354d others(12): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343769 | ||||||
| chr11:74343769
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0013t0031g0343 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1219-365_1219-354d others(14): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343769 | ||||||
| chr11:74343802
|
G | A | 1 | a0003c0003t0002g0059 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1219-386C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343802 | ||||||
| chr11:74343831
|
T | A | 1 | a0003c0003t0002g0031 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1219-415A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343831 | ||||||
| chr11:74343934
|
G | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(232): Show | 243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1219-518C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74343934 | ||||||
| chr11:74344034
|
C | T | 1 | a0001c0001t0022g0355 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1219-618G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344034 | ||||||
| chr11:74344054
|
C | T | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1219-638G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344054 | ||||||
| chr11:74344066
|
C | T | 9 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(6): Show | 12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1219-650G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344066 | ||||||
| chr11:74344242
|
A | T | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1219-826T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344242 | ||||||
| chr11:74344253
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(113): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1219-837A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344253 | ||||||
| chr11:74344506
|
G | A | 1 | a0003c0003t0006g0063 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1218+963C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344506 | ||||||
| chr11:74344539
|
C | A | 1 | a0001c0001t0003g0223 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1218+930G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344539 | ||||||
| chr11:74344587
|
A | G | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1218+882T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344587 | ||||||
| chr11:74344760
|
T | C | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1218+709A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344760 | ||||||
| chr11:74344846
|
A | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(225): Show | 236 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1218+623T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74344846 | ||||||
| chr11:74345075
|
A | T | 1 | a0002c0002t0005g0153 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1218+394T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74345075 | ||||||
| chr11:74345284
|
C | T | 1 | a0001c0009t0029g0365 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1218+185G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74345284 | ||||||
| chr11:74345308
|
AG | A | 4 | a0001c0001t0011g0217a0001c0001t0011g0220a0001c0001t0011g0240others(1): Show | 4 | HG00140.hp1 HG01106.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218+160delC | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74345308 | ||||||
| chr11:74345341
|
T | C | 2 | a0001c0001t0040g0277a0003c0003t0039g0024 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1218+128A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74345341 | ||||||
| chr11:74345424
|
G | T | 1 | a0001c0004t0059g0364 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1218+45C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 9/13 | chr11 | 74345424 | ||||||
| chr11:74345677
|
A | G | 1 | a0007c0011t0026g0280 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1038-28T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74345677 | ||||||
| chr11:74345804
|
T | A | 1 | a0004c0005t0014g0121 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1038-155A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74345804 | ||||||
| chr11:74345812
|
G | A | 3 | a0002c0002t0004g0112a0002c0002t0004g0119a0002c0002t0004g0244 | 3 | HG02055.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1038-163C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74345812 | ||||||
| chr11:74345839
|
C | T | 1 | a0001c0013t0031g0343 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1038-190G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74345839 | ||||||
| chr11:74345986
|
G | A | 2 | a0001c0001t0001g0283a0001c0001t0001g0284 | 2 | HG00323.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1038-337C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74345986 | ||||||
| chr11:74346023
|
G | T | 8 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1038-374C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346023 | ||||||
| chr11:74346191
|
G | C | 3 | a0003c0003t0002g0007a0003c0003t0002g0090a0003c0003t0002g0092 | 4 | HG02630.hp1 HG02818.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037+541C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346191 | ||||||
| chr11:74346270
|
C | CA | 27 | a0002c0002t0004g0013a0002c0002t0004g0097a0002c0002t0004g0144others(24): Show | 28 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1037+461dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346270 | ||||||
| chr11:74346270
|
CA | C | 6 | a0001c0004t0025g0281a0002c0002t0004g0156a0002c0002t0005g0172others(3): Show | 6 | HG02572.hp1 HG03486.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037+461delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346270 | ||||||
| chr11:74346270
|
CAA | C | 15 | a0001c0001t0001g0129a0001c0001t0001g0133a0001c0001t0001g0289others(12): Show | 15 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.1037+460_1037+461d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346270 | ||||||
| chr11:74346270
|
CAAA | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0130others(58): Show | 63 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1037+459_1037+461d others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346270 | ||||||
| chr11:74346270
|
CAAAA | C | 141 | a0001c0001t0001g0299a0001c0001t0002g0110a0001c0001t0002g0127others(138): Show | 150 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1037+458_1037+461d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346270 | ||||||
| chr11:74346270
|
CAAAAA | C | 26 | a0001c0001t0040g0277a0001c0004t0009g0334a0001c0004t0009g0335others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02486.hp2 others(23): Show |
intron_variant | MODIFIER | c.1037+457_1037+461d others(7): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346270 | ||||||
| chr11:74346270
|
CAAAAAAA others(2): Show |
C | 14 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(11): Show | 15 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1037+453_1037+461d others(11): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346270 | ||||||
| chr11:74346310
|
A | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(113): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1037+422T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346310 | ||||||
| chr11:74346406
|
G | T | 1 | a0001c0001t0001g0312 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1037+326C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346406 | ||||||
| chr11:74346553
|
T | C | 1 | a0001c0001t0003g0223 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1037+179A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346553 | ||||||
| chr11:74346602
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(225): Show | 236 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1037+130A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346602 | ||||||
| chr11:74346693
|
A | G | 2 | a0002c0002t0004g0214a0002c0002t0004g0215 | 2 | NA18963.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1037+39T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 8/13 | chr11 | 74346693 | ||||||
| chr11:74346886
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.940-57G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 7/13 | chr11 | 74346886 | ||||||
| chr11:74347613
|
T | C | 2 | a0001c0001t0003g0186a0001c0001t0003g0254 | 2 | HG03490.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.750-276A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74347613 | ||||||
| chr11:74347665
|
T | G | 81 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(78): Show | 87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.750-328A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74347665 | ||||||
| chr11:74347793
|
C | G | 1 | a0003c0003t0002g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.750-456G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74347793 | ||||||
| chr11:74347822
|
C | A | 1 | a0001c0001t0003g0170 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.750-485G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74347822 | ||||||
| chr11:74347887
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(267): Show | 282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.750-550G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74347887 | ||||||
| chr11:74347924
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.750-587T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74347924 | ||||||
| chr11:74347945
|
C | A | 1 | a0001c0004t0048g0354 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.750-608G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74347945 | ||||||
| chr11:74348005
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(225): Show | 236 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.750-668A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348005 | ||||||
| chr11:74348053
|
C | T | 1 | a0002c0002t0004g0167 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.750-716G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348053 | ||||||
| chr11:74348126
|
T | C | 1 | a0001c0004t0017g0363 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.750-789A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348126 | ||||||
| chr11:74348206
|
C | G | 1 | a0002c0002t0005g0100 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.750-869G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348206 | ||||||
| chr11:74348209
|
C | T | 1 | a0001c0001t0003g0183 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.750-872G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348209 | ||||||
| chr11:74348303
|
C | G | 1 | a0001c0001t0001g0274 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.750-966G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348303 | ||||||
| chr11:74348744
|
C | T | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.750-1407G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348744 | ||||||
| chr11:74348953
|
T | C | 18 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(15): Show | 19 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.750-1616A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348953 | ||||||
| chr11:74348985
|
T | G | 10 | a0001c0001t0001g0130a0001c0001t0001g0135a0001c0001t0001g0288others(7): Show | 10 | HG01952.hp2 HG02056.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.750-1648A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74348985 | ||||||
| chr11:74349153
|
C | T | 7 | a0001c0001t0001g0136a0001c0001t0001g0289a0001c0001t0001g0291others(4): Show | 7 | HG02004.hp2 HG02148.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.750-1816G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74349153 | ||||||
| chr11:74349300
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.750-1963G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74349300 | ||||||
| chr11:74349359
|
G | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.750-2022C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74349359 | ||||||
| chr11:74349557
|
G | C | 1 | a0003c0003t0012g0050 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.749+1826C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74349557 | ||||||
| chr11:74349784
|
C | T | 1 | a0001c0001t0003g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.749+1599G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74349784 | ||||||
| chr11:74349960
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.749+1423G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74349960 | ||||||
| chr11:74350170
|
C | G | 1 | a0001c0004t0048g0354 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.749+1213G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350170 | ||||||
| chr11:74350171
|
T | G | 1 | a0001c0001t0001g0318 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.749+1212A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350171 | ||||||
| chr11:74350187
|
C | T | 4 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352others(1): Show | 4 | HG01074.hp1 HG02280.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.749+1196G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350187 | ||||||
| chr11:74350208
|
G | T | 1 | a0001c0009t0029g0365 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.749+1175C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350208 | ||||||
| chr11:74350421
|
T | C | 1 | a0002c0002t0005g0194 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.749+962A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350421 | ||||||
| chr11:74350608
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(225): Show | 236 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.749+775C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350608 | ||||||
| chr11:74350617
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(116): Show | 121 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.749+766G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350617 | ||||||
| chr11:74350889
|
AAGAAAGA others(3): Show |
A | 2 | a0002c0002t0004g0145a0002c0002t0004g0168 | 2 | HG02148.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.749+484_749+493del others(10): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350889 | ||||||
| chr11:74350897
|
AAG | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(200): Show | 211 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.749+484_749+485del others(2): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350897 | ||||||
| chr11:74350897
|
AAGAG | A | 5 | a0001c0001t0001g0135a0001c0001t0003g0103a0001c0001t0003g0154others(2): Show | 5 | HG00735.hp2 HG01175.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.749+482_749+485del others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350897 | ||||||
| chr11:74350903
|
GAGAGAGA others(9): Show |
G | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.749+464_749+479del others(16): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350903 | ||||||
| chr11:74350905
|
GAGAGAGA others(7): Show |
G | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.749+464_749+477del others(14): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350905 | ||||||
| chr11:74350935
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(237): Show | 251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.749+448C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74350935 | ||||||
| chr11:74351064
|
A | T | 15 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(12): Show | 16 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.749+319T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74351064 | ||||||
| chr11:74351146
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.749+237C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74351146 | ||||||
| chr11:74351303
|
ACACTTTT others(3): Show |
A | 8 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.749+70_749+79delAT others(8): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74351303 | ||||||
| chr11:74351307
|
T | C | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.749+76A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74351307 | ||||||
| chr11:74351335
|
T | C | 1 | a0001c0004t0013g0109 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.749+48A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74351335 | ||||||
| chr11:74351340
|
C | T | 8 | a0001c0001t0022g0355a0001c0001t0022g0356a0001c0004t0017g0359others(5): Show | 8 | HG01099.hp1 HG01243.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.749+43G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 6/13 | chr11 | 74351340 | ||||||
| chr11:74351643
|
T | A | 1 | a0003c0006t0015g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.556-67A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351643 | ||||||
| chr11:74351734
|
G | GGGCAGAT others(9): Show |
4 | a0001c0004t0015g0245a0001c0004t0015g0246a0001c0004t0015g0247others(1): Show | 4 | HG01884.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-174_556-159dup others(16): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351734 | ||||||
| chr11:74351776
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.556-200G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351776 | ||||||
| chr11:74351840
|
T | C | 13 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(10): Show | 13 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.556-264A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351840 | ||||||
| chr11:74351885
|
C | G | 1 | a0001c0004t0048g0354 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.556-309G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351885 | ||||||
| chr11:74351888
|
G | A | 4 | a0001c0004t0015g0245a0001c0004t0015g0246a0001c0004t0015g0247others(1): Show | 4 | HG01884.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.556-312C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351888 | ||||||
| chr11:74351961
|
C | CA | 16 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(13): Show | 16 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.556-386dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351961 | ||||||
| chr11:74351969
|
A | AT | 12 | a0001c0004t0013g0105a0001c0004t0013g0107a0001c0004t0013g0108others(9): Show | 12 | HG00639.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.556-394_556-393ins others(1): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351969 | ||||||
| chr11:74351971
|
A | T | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-395T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351971 | ||||||
| chr11:74351972
|
AT | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0130others(192): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.556-397delA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351972 | ||||||
| chr11:74351973
|
T | A | 6 | a0001c0001t0001g0099a0001c0001t0001g0328a0001c0004t0025g0281others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-397A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351973 | ||||||
| chr11:74351977
|
T | A | 2 | a0001c0001t0040g0277a0003c0003t0039g0024 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.556-401A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351977 | ||||||
| chr11:74351977
|
TAA | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(197): Show | 208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.556-403_556-402del others(2): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74351977 | ||||||
| chr11:74352119
|
T | C | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.556-543A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74352119 | ||||||
| chr11:74352338
|
A | C | 240 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(237): Show | 251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.556-762T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74352338 | ||||||
| chr11:74352440
|
G | T | 83 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(80): Show | 89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.556-864C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74352440 | ||||||
| chr11:74352599
|
G | A | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.556-1023C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74352599 | ||||||
| chr11:74352764
|
C | T | 4 | a0001c0004t0015g0245a0001c0004t0015g0246a0001c0004t0015g0247others(1): Show | 4 | HG01884.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-1188G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74352764 | ||||||
| chr11:74353029
|
T | C | 4 | a0001c0004t0016g0262a0001c0004t0016g0263a0001c0004t0016g0264others(1): Show | 4 | HG02717.hp2 HG02723.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-1453A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353029 | ||||||
| chr11:74353037
|
T | TAA | 14 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(11): Show | 15 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.556-1463_556-1462d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353037 | ||||||
| chr11:74353176
|
G | GT | 123 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(120): Show | 125 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.556-1601dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353176 | ||||||
| chr11:74353184
|
G | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(184): Show | 198 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.556-1608C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353184 | ||||||
| chr11:74353186
|
G | T | 27 | a0001c0001t0022g0355a0001c0001t0022g0356a0001c0004t0009g0334others(24): Show | 27 | HG00639.hp2 HG02258.hp1 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.556-1610C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353186 | ||||||
| chr11:74353263
|
CTTAAT | C | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.556-1692_556-1688d others(7): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353263 | ||||||
| chr11:74353335
|
A | ATT | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.556-1761_556-1760d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353335 | ||||||
| chr11:74353521
|
A | C | 3 | a0003c0003t0002g0043a0003c0003t0002g0082a0003c0003t0041g0069 | 3 | HG00738.hp1 HG01123.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.556-1945T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353521 | ||||||
| chr11:74353528
|
A | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(267): Show | 282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.556-1952T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353528 | ||||||
| chr11:74353627
|
A | G | 2 | a0002c0002t0004g0211a0002c0002t0004g0252 | 2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.556-2051T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353627 | ||||||
| chr11:74353722
|
CCA | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.556-2148_556-2147d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353722 | ||||||
| chr11:74353790
|
C | T | 2 | a0001c0001t0001g0286a0003c0003t0030g0018 | 2 | NA18959.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.556-2214G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353790 | ||||||
| chr11:74353811
|
G | A | 1 | a0002c0002t0053g0253 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.556-2235C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353811 | ||||||
| chr11:74353818
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.556-2242G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353818 | ||||||
| chr11:74353860
|
A | AGACGGGG others(71): Show |
1 | a0001c0001t0003g0096 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.556-2285_556-2284i others(80): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353860 | ||||||
| chr11:74353860
|
A | AGACGGGG others(70): Show |
3 | a0004c0005t0014g0123a0004c0005t0014g0125a0004c0005t0046g0126 | 3 | HG00642.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.556-2285_556-2284i others(79): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353860 | ||||||
| chr11:74353860
|
A | AGACGGGG others(70): Show |
264 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(261): Show | 276 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.556-2285_556-2284i others(79): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353860 | ||||||
| chr11:74353860
|
A | AGACGGGG others(71): Show |
1 | a0001c0001t0001g0307 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.556-2285_556-2284i others(80): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353860 | ||||||
| chr11:74353860
|
A | G | 1 | a0003c0003t0021g0026 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.556-2284T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353860 | ||||||
| chr11:74353863
|
T | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(264): Show | 279 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.556-2287A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353863 | ||||||
| chr11:74353863
|
T | TGGGGTGG others(70): Show |
95 | a0002c0002t0004g0013a0002c0002t0004g0097a0002c0002t0004g0102others(92): Show | 97 | HG00140.hp2 HG00597.hp2 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.556-2288_556-2287i others(79): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353863 | ||||||
| chr11:74353912
|
C | T | 1 | a0001c0004t0008g0012 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.556-2336G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74353912 | ||||||
| chr11:74354004
|
A | G | 1 | a0002c0002t0005g0177 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.556-2428T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354004 | ||||||
| chr11:74354069
|
C | T | 1 | a0003c0003t0002g0059 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.556-2493G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354069 | ||||||
| chr11:74354177
|
C | T | 1 | a0003c0003t0002g0043 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.556-2601G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354177 | ||||||
| chr11:74354181
|
C | T | 1 | a0001c0004t0058g0358 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.556-2605G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354181 | ||||||
| chr11:74354234
|
C | A | 14 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(11): Show | 15 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.556-2658G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354234 | ||||||
| chr11:74354366
|
G | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.556-2790C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354366 | ||||||
| chr11:74354367
|
T | C | 1 | a0001c0004t0048g0354 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.556-2791A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354367 | ||||||
| chr11:74354409
|
G | A | 2 | a0001c0001t0003g0096a0001c0001t0003g0223 | 2 | NA18949.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.556-2833C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354409 | ||||||
| chr11:74354442
|
C | T | 1 | a0002c0002t0005g0213 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.556-2866G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354442 | ||||||
| chr11:74354552
|
G | A | 2 | a0002c0002t0004g0285a0002c0002t0004g0344 | 2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.556-2976C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354552 | ||||||
| chr11:74354725
|
C | A | 1 | a0002c0002t0004g0228 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.556-3149G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354725 | ||||||
| chr11:74354806
|
G | T | 1 | a0002c0002t0004g0346 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.556-3230C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354806 | ||||||
| chr11:74354874
|
G | A | 5 | a0001c0004t0008g0011a0001c0004t0008g0256a0001c0004t0008g0258others(2): Show | 6 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.556-3298C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74354874 | ||||||
| chr11:74355012
|
C | T | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-3436G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355012 | ||||||
| chr11:74355063
|
G | A | 1 | a0002c0002t0005g0199 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.556-3487C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355063 | ||||||
| chr11:74355080
|
G | A | 8 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.556-3504C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355080 | ||||||
| chr11:74355142
|
T | C | 1 | a0001c0001t0003g0140 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.556-3566A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355142 | ||||||
| chr11:74355199
|
A | G | 1 | a0001c0004t0048g0354 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.556-3623T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355199 | ||||||
| chr11:74355279
|
C | A | 1 | a0001c0013t0031g0343 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.556-3703G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355279 | ||||||
| chr11:74355292
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.556-3716T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355292 | ||||||
| chr11:74355319
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.556-3743A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355319 | ||||||
| chr11:74355320
|
G | A | 1 | a0003c0003t0007g0003 | 2 | NA18977.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.556-3744C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355320 | ||||||
| chr11:74355382
|
G | A | 81 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(78): Show | 87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.556-3806C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355382 | ||||||
| chr11:74355425
|
T | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(241): Show | 255 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.556-3849A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355425 | ||||||
| chr11:74355427
|
G | A | 6 | a0001c0004t0017g0359a0001c0004t0017g0360a0001c0004t0017g0362others(3): Show | 6 | HG01099.hp1 HG01243.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.556-3851C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355427 | ||||||
| chr11:74355456
|
A | AG | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.556-3881dupC | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355456 | ||||||
| chr11:74355471
|
G | A | 3 | a0001c0001t0003g0186a0001c0001t0003g0254a0001c0004t0023g0095 | 3 | HG00639.hp2 HG03490.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.556-3895C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355471 | ||||||
| chr11:74355479
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.556-3903C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355479 | ||||||
| chr11:74355486
|
G | A | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.556-3910C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355486 | ||||||
| chr11:74355503
|
G | A | 2 | a0001c0001t0040g0277a0003c0003t0039g0024 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.556-3927C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355503 | ||||||
| chr11:74355541
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.556-3965C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355541 | ||||||
| chr11:74355553
|
C | CA | 20 | a0001c0004t0025g0281a0001c0004t0026g0279a0002c0002t0004g0156others(17): Show | 20 | HG00741.hp2 HG01361.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.556-3978dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355553
|
C | CAAAAAAA others(3): Show |
26 | a0001c0001t0003g0096a0001c0001t0003g0137a0001c0001t0003g0140others(23): Show | 26 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.556-3987_556-3978d others(12): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355553
|
C | CAAAAAAA others(4): Show |
20 | a0001c0001t0001g0132a0001c0001t0001g0290a0001c0001t0001g0320others(17): Show | 20 | HG00544.hp2 HG01069.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.556-3988_556-3978d others(13): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355553
|
C | CAAAAAAA others(5): Show |
41 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0135others(38): Show | 43 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.556-3989_556-3978d others(14): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355553
|
C | CAAAAAAA others(6): Show |
25 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(22): Show | 25 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.556-3990_556-3978d others(15): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355553
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0289a0001c0001t0001g0301a0001c0001t0001g0316others(1): Show | 4 | HG00423.hp2 HG02129.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-3991_556-3978d others(16): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355553
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0302 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.556-3994_556-3978d others(19): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355553
|
C | CAAAAAAA others(12): Show |
1 | a0004c0005t0014g0122 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.556-3996_556-3978d others(21): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355553
|
C | CAAAAAAA others(13): Show |
3 | a0001c0004t0015g0246a0004c0005t0014g0123a0004c0005t0014g0125 | 3 | HG03209.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.556-3997_556-3978d others(22): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355553
|
C | CAAAAAAA others(14): Show |
1 | a0004c0005t0046g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.556-3998_556-3978d others(23): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355553
|
C | CAAAAAAA others(16): Show |
1 | a0004c0005t0049g0120 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.556-4000_556-3978d others(25): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355553
|
C | CAAAAAAA others(17): Show |
1 | a0001c0004t0015g0247 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.556-4001_556-3978d others(26): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355553
|
C | CAAAAAAA others(18): Show |
1 | a0001c0004t0015g0245 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.556-4002_556-3978d others(27): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355553
|
CAA | C | 23 | a0001c0004t0009g0334a0001c0004t0009g0336a0001c0004t0009g0337others(20): Show | 23 | HG00639.hp2 HG02109.hp1 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.556-3979_556-3978d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355553
|
CAAA | C | 18 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(15): Show | 21 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.556-3980_556-3978d others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355553
|
CAAAA | C | 11 | a0001c0004t0010g0008a0001c0004t0017g0359a0001c0004t0017g0360others(8): Show | 12 | HG01074.hp1 HG01099.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.556-3981_556-3978d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355553 | ||||||
| chr11:74355569
|
AAAAAAAA others(4): Show |
A | 2 | a0001c0001t0002g0128a0003c0003t0002g0058 | 2 | HG00558.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.556-4004_556-3994d others(13): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355569 | ||||||
| chr11:74355570
|
AAAAAAAA others(3): Show |
A | 79 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0139others(76): Show | 85 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.556-4004_556-3995d others(12): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355570 | ||||||
| chr11:74355605
|
T | C | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-4029A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355605 | ||||||
| chr11:74355635
|
G | A | 5 | a0003c0003t0002g0035a0003c0003t0002g0041a0003c0003t0002g0052others(2): Show | 5 | HG00673.hp2 NA18978.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.556-4059C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355635 | ||||||
| chr11:74355730
|
T | C | 14 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(11): Show | 15 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.556-4154A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74355730 | ||||||
| chr11:74356106
|
G | A | 1 | a0001c0004t0013g0108 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.556-4530C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356106 | ||||||
| chr11:74356120
|
C | T | 1 | a0005c0007t0005g0055 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.556-4544G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356120 | ||||||
| chr11:74356144
|
G | C | 1 | a0001c0001t0003g0103 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.556-4568C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356144 | ||||||
| chr11:74356301
|
G | A | 1 | a0001c0013t0031g0343 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.556-4725C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356301 | ||||||
| chr11:74356418
|
A | C | 1 | a0001c0013t0031g0343 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.556-4842T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356418 | ||||||
| chr11:74356529
|
C | T | 7 | a0003c0003t0002g0034a0003c0003t0002g0035a0003c0003t0002g0041others(4): Show | 7 | HG00544.hp1 HG00673.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-4953G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356529 | ||||||
| chr11:74356814
|
T | C | 1 | a0003c0003t0002g0037 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.556-5238A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356814 | ||||||
| chr11:74356815
|
A | G | 8 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.556-5239T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356815 | ||||||
| chr11:74356839
|
CT | C | 83 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(80): Show | 89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.556-5264delA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356839 | ||||||
| chr11:74356937
|
G | A | 83 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(80): Show | 89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.556-5361C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74356937 | ||||||
| chr11:74357095
|
C | T | 8 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.556-5519G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357095 | ||||||
| chr11:74357298
|
C | T | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.556-5722G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357298 | ||||||
| chr11:74357469
|
CAAT | C | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.556-5896_556-5894d others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357469 | ||||||
| chr11:74357498
|
A | G | 6 | a0001c0001t0003g0146a0001c0001t0003g0165a0001c0001t0003g0178others(3): Show | 6 | HG00323.hp1 HG04184.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.556-5922T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357498 | ||||||
| chr11:74357698
|
C | G | 81 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(78): Show | 87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.556-6122G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357698 | ||||||
| chr11:74357722
|
C | T | 8 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(5): Show | 9 | HG01099.hp2 HG02280.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.556-6146G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357722 | ||||||
| chr11:74357748
|
A | G | 14 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(11): Show | 15 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.556-6172T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357748 | ||||||
| chr11:74357767
|
AG | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(114): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.556-6192delC | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357767 | ||||||
| chr11:74357874
|
T | A | 1 | a0001c0004t0023g0348 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.556-6298A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357874 | ||||||
| chr11:74357899
|
C | T | 2 | a0003c0003t0002g0058a0003c0003t0002g0084 | 2 | NA18970.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.556-6323G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357899 | ||||||
| chr11:74357926
|
A | G | 2 | a0003c0003t0007g0015a0003c0003t0007g0019 | 2 | HG02523.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.556-6350T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357926 | ||||||
| chr11:74357966
|
C | T | 1 | a0001c0001t0035g0151 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.556-6390G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74357966 | ||||||
| chr11:74358061
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.556-6485T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74358061 | ||||||
| chr11:74358072
|
G | C | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.556-6496C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74358072 | ||||||
| chr11:74358576
|
T | A | 2 | a0001c0004t0025g0281a0008c0010t0025g0282 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.556-7000A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74358576 | ||||||
| chr11:74358607
|
C | T | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-7031G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74358607 | ||||||
| chr11:74358653
|
C | T | 2 | a0001c0001t0001g0307a0003c0003t0001g0088 | 2 | NA18947.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.556-7077G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74358653 | ||||||
| chr11:74358950
|
A | G | 1 | a0001c0013t0031g0343 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.556-7374T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74358950 | ||||||
| chr11:74359056
|
A | T | 8 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.556-7480T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359056 | ||||||
| chr11:74359149
|
T | C | 2 | a0001c0001t0001g0299a0001c0001t0038g0297 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.556-7573A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359149 | ||||||
| chr11:74359315
|
T | C | 1 | a0002c0002t0005g0203 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.556-7739A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359315 | ||||||
| chr11:74359416
|
A | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(225): Show | 236 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.556-7840T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359416 | ||||||
| chr11:74359434
|
T | TAC | 8 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.556-7860_556-7859d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359434 | ||||||
| chr11:74359450
|
T | C | 1 | a0001c0001t0003g0329 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.556-7874A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359450 | ||||||
| chr11:74359564
|
C | CAT | 4 | a0001c0004t0048g0354a0002c0002t0005g0303a0002c0002t0005g0323others(1): Show | 4 | HG02602.hp2 HG03710.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.556-7990_556-7989d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359564 | ||||||
| chr11:74359564
|
C | CATATAT | 24 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(21): Show | 24 | HG00639.hp2 HG02258.hp1 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.556-7994_556-7989d others(8): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359564 | ||||||
| chr11:74359564
|
CAT | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(206): Show | 219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.556-7990_556-7989d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359564 | ||||||
| chr11:74359582
|
C | T | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-8006G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359582 | ||||||
| chr11:74359689
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0312 | 2 | NA18991.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.556-8113T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359689 | ||||||
| chr11:74359753
|
A | G | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-8177T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359753 | ||||||
| chr11:74359756
|
T | TGTGGACT others(1): Show |
8 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.556-8188_556-8181d others(10): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359756 | ||||||
| chr11:74359854
|
T | A | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.556-8278A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359854 | ||||||
| chr11:74359968
|
C | T | 1 | a0001c0001t0011g0217 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.556-8392G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74359968 | ||||||
| chr11:74360027
|
A | G | 81 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(78): Show | 87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.556-8451T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360027 | ||||||
| chr11:74360143
|
T | C | 1 | a0004c0005t0046g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.555+8349A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360143 | ||||||
| chr11:74360165
|
A | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(267): Show | 282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.555+8327T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360165 | ||||||
| chr11:74360272
|
A | AGAAG | 269 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(266): Show | 281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.555+8216_555+8219d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360272 | ||||||
| chr11:74360379
|
C | T | 3 | a0001c0001t0001g0307a0001c0001t0001g0310a0003c0003t0001g0088 | 3 | NA18942.hp2 NA18947.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.555+8113G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360379 | ||||||
| chr11:74360524
|
C | T | 1 | a0001c0013t0031g0343 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.555+7968G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360524 | ||||||
| chr11:74360532
|
T | A | 1 | a0001c0004t0059g0364 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.555+7960A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360532 | ||||||
| chr11:74360583
|
C | T | 4 | a0001c0004t0016g0262a0001c0004t0016g0263a0001c0004t0016g0264others(1): Show | 4 | HG02717.hp2 HG02723.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+7909G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360583 | ||||||
| chr11:74360610
|
A | G | 1 | a0001c0013t0031g0343 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.555+7882T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360610 | ||||||
| chr11:74360628
|
C | T | 1 | a0002c0002t0005g0153 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.555+7864G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360628 | ||||||
| chr11:74360640
|
T | C | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.555+7852A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360640 | ||||||
| chr11:74360680
|
G | A | 83 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(80): Show | 89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.555+7812C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360680 | ||||||
| chr11:74360711
|
G | A | 1 | a0001c0001t0011g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.555+7781C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360711 | ||||||
| chr11:74360762
|
C | A | 9 | a0001c0001t0040g0277a0003c0003t0039g0024a0004c0005t0014g0121others(6): Show | 9 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.555+7730G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360762 | ||||||
| chr11:74360847
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.555+7645G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360847 | ||||||
| chr11:74360848
|
G | A | 8 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.555+7644C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360848 | ||||||
| chr11:74360855
|
G | C | 1 | a0003c0003t0002g0074 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.555+7637C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360855 | ||||||
| chr11:74360900
|
G | C | 1 | a0001c0001t0001g0298 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.555+7592C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360900 | ||||||
| chr11:74360995
|
C | T | 1 | a0001c0004t0059g0364 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.555+7497G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74360995 | ||||||
| chr11:74361128
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(267): Show | 282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.555+7364A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361128 | ||||||
| chr11:74361148
|
C | A | 1 | a0001c0013t0031g0343 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.555+7344G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361148 | ||||||
| chr11:74361212
|
C | A | 1 | a0004c0005t0049g0120 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.555+7280G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361212 | ||||||
| chr11:74361247
|
C | T | 1 | a0001c0013t0031g0343 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.555+7245G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361247 | ||||||
| chr11:74361255
|
T | A | 1 | a0001c0004t0024g0261 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.555+7237A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361255 | ||||||
| chr11:74361288
|
G | T | 22 | a0002c0002t0005g0009a0002c0002t0005g0141a0002c0002t0005g0171others(19): Show | 23 | HG00733.hp2 HG02015.hp1 HG02165.hp1 others(20): Show |
intron_variant | MODIFIER | c.555+7204C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361288 | ||||||
| chr11:74361323
|
C | T | 3 | a0001c0004t0015g0245a0001c0004t0015g0246a0001c0004t0015g0247 | 3 | HG01884.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.555+7169G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361323 | ||||||
| chr11:74361560
|
C | G | 12 | a0001c0004t0013g0105a0001c0004t0013g0107a0001c0004t0013g0108others(9): Show | 12 | HG00639.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.555+6932G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361560 | ||||||
| chr11:74361668
|
G | A | 1 | a0002c0002t0005g0250 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.555+6824C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361668 | ||||||
| chr11:74361692
|
G | A | 1 | a0001c0004t0048g0354 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.555+6800C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361692 | ||||||
| chr11:74361726
|
A | T | 1 | a0002c0002t0004g0285 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.555+6766T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361726 | ||||||
| chr11:74361772
|
T | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(116): Show | 121 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.555+6720A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361772 | ||||||
| chr11:74361774
|
G | C | 8 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.555+6718C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361774 | ||||||
| chr11:74361846
|
GA | G | 13 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(10): Show | 13 | HG02622.hp2 HG02647.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.555+6645delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361846 | ||||||
| chr11:74361920
|
G | C | 2 | a0003c0003t0002g0043a0003c0003t0041g0069 | 2 | HG00738.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.555+6572C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74361920 | ||||||
| chr11:74362163
|
T | C | 315 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(312): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.555+6329A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362163 | ||||||
| chr11:74362279
|
T | C | 1 | a0001c0004t0015g0246 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.555+6213A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362279 | ||||||
| chr11:74362401
|
C | T | 1 | a0002c0002t0004g0345 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.555+6091G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362401 | ||||||
| chr11:74362417
|
C | T | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+6075G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362417 | ||||||
| chr11:74362442
|
T | C | 315 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(312): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.555+6050A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362442 | ||||||
| chr11:74362501
|
C | T | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.555+5991G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362501 | ||||||
| chr11:74362528
|
A | C | 10 | a0003c0003t0002g0028a0003c0003t0002g0029a0003c0003t0002g0030others(7): Show | 10 | NA18948.hp1 NA18950.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.555+5964T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362528 | ||||||
| chr11:74362651
|
C | T | 5 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0043g0111others(2): Show | 6 | HG00280.hp1 HG00733.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+5841G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362651 | ||||||
| chr11:74362751
|
A | C | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.555+5741T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362751 | ||||||
| chr11:74362914
|
C | G | 2 | a0002c0002t0004g0285a0002c0002t0004g0344 | 2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.555+5578G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362914 | ||||||
| chr11:74362954
|
T | C | 240 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(237): Show | 251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.555+5538A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362954 | ||||||
| chr11:74362955
|
G | A | 2 | a0001c0001t0001g0299a0001c0001t0038g0297 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.555+5537C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74362955 | ||||||
| chr11:74363009
|
G | A | 13 | a0001c0004t0013g0105a0001c0004t0013g0107a0001c0004t0013g0108others(10): Show | 13 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.555+5483C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363009 | ||||||
| chr11:74363031
|
A | G | 11 | a0001c0004t0013g0105a0001c0004t0013g0107a0001c0004t0013g0108others(8): Show | 11 | HG00639.hp2 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.555+5461T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363031 | ||||||
| chr11:74363141
|
G | A | 1 | a0003c0003t0007g0017 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.555+5351C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363141 | ||||||
| chr11:74363161
|
G | A | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+5331C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363161 | ||||||
| chr11:74363292
|
G | A | 1 | a0001c0001t0040g0277 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.555+5200C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363292 | ||||||
| chr11:74363349
|
C | T | 1 | a0001c0001t0003g0254 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.555+5143G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363349 | ||||||
| chr11:74363530
|
A | G | 4 | a0001c0004t0016g0262a0001c0004t0016g0263a0001c0004t0016g0264others(1): Show | 4 | HG02717.hp2 HG02723.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+4962T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363530 | ||||||
| chr11:74363687
|
C | A | 1 | a0001c0004t0023g0348 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.555+4805G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363687 | ||||||
| chr11:74363775
|
T | C | 13 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(10): Show | 16 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.555+4717A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363775 | ||||||
| chr11:74363828
|
T | C | 1 | a0001c0001t0003g0096 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.555+4664A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363828 | ||||||
| chr11:74363877
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(212): Show | 223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.555+4615G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363877 | ||||||
| chr11:74363893
|
G | A | 1 | a0001c0004t0048g0354 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.555+4599C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363893 | ||||||
| chr11:74363915
|
A | G | 9 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(6): Show | 9 | HG02622.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.555+4577T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363915 | ||||||
| chr11:74363965
|
A | G | 1 | a0001c0001t0032g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.555+4527T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74363965 | ||||||
| chr11:74364146
|
C | T | 2 | a0002c0002t0004g0097a0002c0002t0004g0304 | 2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.555+4346G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364146 | ||||||
| chr11:74364215
|
C | T | 11 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(8): Show | 14 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.555+4277G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364215 | ||||||
| chr11:74364305
|
A | C | 1 | a0003c0006t0015g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.555+4187T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364305 | ||||||
| chr11:74364333
|
C | T | 9 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(6): Show | 12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.555+4159G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364333 | ||||||
| chr11:74364393
|
G | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(116): Show | 121 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.555+4099C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364393 | ||||||
| chr11:74364470
|
C | T | 84 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(81): Show | 90 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.555+4022G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364470 | ||||||
| chr11:74364532
|
C | T | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+3960G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364532 | ||||||
| chr11:74364539
|
G | C | 1 | a0006c0014t0016g0257 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.555+3953C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364539 | ||||||
| chr11:74364696
|
T | C | 1 | a0001c0004t0023g0348 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.555+3796A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364696 | ||||||
| chr11:74364703
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.555+3789G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364703 | ||||||
| chr11:74364790
|
C | G | 1 | a0003c0006t0015g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.555+3702G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364790 | ||||||
| chr11:74364805
|
A | G | 1 | a0001c0001t0003g0219 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.555+3687T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364805 | ||||||
| chr11:74364858
|
A | G | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.555+3634T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364858 | ||||||
| chr11:74364927
|
G | A | 3 | a0002c0002t0004g0145a0002c0002t0004g0164a0002c0002t0004g0168 | 3 | HG01074.hp2 HG02148.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.555+3565C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74364927 | ||||||
| chr11:74365044
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.555+3448A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365044 | ||||||
| chr11:74365106
|
A | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.555+3386T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365106 | ||||||
| chr11:74365117
|
G | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.555+3375C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365117 | ||||||
| chr11:74365189
|
C | T | 1 | a0005c0007t0054g0054 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.555+3303G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365189 | ||||||
| chr11:74365296
|
T | C | 1 | a0001c0004t0048g0354 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.555+3196A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365296 | ||||||
| chr11:74365323
|
A | C | 1 | a0001c0004t0024g0261 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.555+3169T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365323 | ||||||
| chr11:74365388
|
T | C | 2 | a0001c0001t0040g0277a0003c0003t0039g0024 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.555+3104A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365388 | ||||||
| chr11:74365403
|
T | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(228): Show | 239 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.555+3089A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365403 | ||||||
| chr11:74365412
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(114): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.555+3080T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365412 | ||||||
| chr11:74365536
|
C | T | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.555+2956G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365536 | ||||||
| chr11:74365915
|
A | G | 1 | a0001c0001t0044g0311 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.555+2577T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74365915 | ||||||
| chr11:74366015
|
T | C | 8 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(5): Show | 9 | HG01099.hp2 HG02280.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.555+2477A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366015 | ||||||
| chr11:74366131
|
A | G | 1 | a0001c0001t0022g0356 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.555+2361T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366131 | ||||||
| chr11:74366253
|
C | T | 2 | a0002c0002t0005g0196a0002c0002t0052g0152 | 2 | NA18955.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.555+2239G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366253 | ||||||
| chr11:74366358
|
TA | T | 14 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0284others(11): Show | 14 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(11): Show |
intron_variant | MODIFIER | c.555+2133delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366358 | ||||||
| chr11:74366459
|
T | TA | 25 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(22): Show | 25 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.555+2032dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366459 | ||||||
| chr11:74366459
|
TA | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(201): Show | 212 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.555+2032delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366459 | ||||||
| chr11:74366464
|
A | T | 1 | a0001c0004t0045g0349 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.555+2028T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366464 | ||||||
| chr11:74366514
|
A | G | 2 | a0001c0001t0040g0277a0003c0003t0039g0024 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.555+1978T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366514 | ||||||
| chr11:74366699
|
T | A | 16 | a0002c0002t0004g0013a0002c0002t0004g0112a0002c0002t0004g0119others(13): Show | 17 | HG01106.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.555+1793A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74366699 | ||||||
| chr11:74367050
|
A | C | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+1442T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367050 | ||||||
| chr11:74367056
|
A | T | 9 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(6): Show | 9 | HG02622.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.555+1436T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367056 | ||||||
| chr11:74367086
|
T | C | 1 | a0001c0001t0003g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.555+1406A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367086 | ||||||
| chr11:74367108
|
A | G | 5 | a0001c0001t0003g0143a0001c0001t0003g0150a0001c0001t0003g0170others(2): Show | 5 | NA18944.hp2 NA18956.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.555+1384T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367108 | ||||||
| chr11:74367244
|
G | A | 1 | a0002c0002t0004g0212 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.555+1248C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367244 | ||||||
| chr11:74367317
|
T | G | 1 | a0001c0004t0019g0350 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.555+1175A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367317 | ||||||
| chr11:74367338
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.555+1154C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367338 | ||||||
| chr11:74367350
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.555+1142G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367350 | ||||||
| chr11:74367830
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(237): Show | 251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.555+662C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74367830 | ||||||
| chr11:74368108
|
C | A | 14 | a0002c0002t0004g0013a0002c0002t0004g0112a0002c0002t0004g0119others(11): Show | 15 | HG01106.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.555+384G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74368108 | ||||||
| chr11:74368231
|
G | A | 1 | a0001c0001t0001g0318 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.555+261C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74368231 | ||||||
| chr11:74368430
|
A | G | 86 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(83): Show | 92 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.555+62T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74368430 | ||||||
| chr11:74368455
|
C | T | 1 | a0002c0002t0005g0204 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.555+37G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 5/13 | chr11 | 74368455 | ||||||
| chr11:74368626
|
C | T | 1 | a0001c0004t0045g0349 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.472-51G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74368626 | ||||||
| chr11:74368709
|
T | C | 1 | a0002c0002t0005g0208 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.472-134A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74368709 | ||||||
| chr11:74368794
|
A | T | 1 | a0003c0006t0015g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.472-219T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74368794 | ||||||
| chr11:74368873
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.472-298T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74368873 | ||||||
| chr11:74368952
|
TC | T | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.472-378delG | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74368952 | ||||||
| chr11:74369032
|
G | A | 1 | a0001c0013t0031g0343 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.472-457C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369032 | ||||||
| chr11:74369062
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(237): Show | 251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.472-487C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369062 | ||||||
| chr11:74369077
|
A | G | 2 | a0003c0003t0002g0058a0003c0003t0002g0084 | 2 | NA18970.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.472-502T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369077 | ||||||
| chr11:74369191
|
A | T | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.472-616T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369191 | ||||||
| chr11:74369212
|
G | A | 4 | a0001c0004t0016g0262a0001c0004t0016g0263a0001c0004t0016g0264others(1): Show | 4 | HG02717.hp2 HG02723.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-637C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369212 | ||||||
| chr11:74369221
|
A | G | 1 | a0001c0004t0059g0364 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.472-646T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369221 | ||||||
| chr11:74369231
|
CAT | C | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.472-658_472-657del others(2): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369231 | ||||||
| chr11:74369265
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.472-690A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369265 | ||||||
| chr11:74369319
|
C | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(114): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.472-744G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369319 | ||||||
| chr11:74369366
|
GAAATTTG others(31): Show |
G | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.472-829_472-792del others(38): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369366 | ||||||
| chr11:74369687
|
G | A | 1 | a0003c0003t0002g0075 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.472-1112C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369687 | ||||||
| chr11:74369753
|
T | A | 9 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(6): Show | 12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.471+1149A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369753 | ||||||
| chr11:74369804
|
C | T | 5 | a0002c0002t0005g0171a0002c0002t0005g0172a0002c0002t0005g0173others(2): Show | 5 | NA18945.hp2 NA18962.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+1098G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369804 | ||||||
| chr11:74369805
|
G | A | 1 | a0001c0004t0008g0012 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.471+1097C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369805 | ||||||
| chr11:74369864
|
A | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(202): Show | 213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.471+1038T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369864 | ||||||
| chr11:74369898
|
C | T | 2 | a0001c0001t0003g0165a0001c0001t0003g0188 | 2 | NA19079.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.471+1004G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369898 | ||||||
| chr11:74369943
|
C | T | 1 | a0007c0011t0026g0280 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.471+959G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74369943 | ||||||
| chr11:74370049
|
C | A | 1 | a0003c0003t0037g0051 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.471+853G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74370049 | ||||||
| chr11:74370066
|
C | G | 11 | a0002c0002t0004g0013a0002c0002t0004g0265a0002c0002t0004g0266others(8): Show | 12 | HG01106.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+836G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74370066 | ||||||
| chr11:74370105
|
G | A | 1 | a0001c0004t0008g0012 | 2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.471+797C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74370105 | ||||||
| chr11:74370456
|
G | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(199): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.471+446C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74370456 | ||||||
| chr11:74370470
|
G | A | 18 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(15): Show | 19 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.471+432C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74370470 | ||||||
| chr11:74370605
|
G | A | 1 | a0001c0001t0022g0356 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.471+297C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 4/13 | chr11 | 74370605 | ||||||
| chr11:74371566
|
T | G | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.386+145A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 3/13 | chr11 | 74371566 | ||||||
| chr11:74371659
|
A | C | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.386+52T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 3/13 | chr11 | 74371659 | ||||||
| chr11:74371681
|
A | G | 9 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(6): Show | 12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.386+30T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 3/13 | chr11 | 74371681 | ||||||
| chr11:74371703
|
C | T | 12 | a0003c0003t0002g0034a0003c0003t0002g0035a0003c0003t0002g0037others(9): Show | 12 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.386+8G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 3/13 | chr11 | 74371703 | ||||||
| chr11:74371834
|
C | G | 2 | a0001c0004t0008g0256a0001c0004t0008g0260 | 2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.280-17G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74371834 | ||||||
| chr11:74372043
|
C | T | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-226G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74372043 | ||||||
| chr11:74372130
|
TA | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(245): Show | 259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.280-314delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74372130 | ||||||
| chr11:74372304
|
T | C | 2 | a0001c0004t0025g0281a0008c0010t0025g0282 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.280-487A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74372304 | ||||||
| chr11:74372503
|
TA | T | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.280-687delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74372503 | ||||||
| chr11:74372658
|
TA | T | 14 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(11): Show | 15 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.280-842delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74372658 | ||||||
| chr11:74372722
|
T | G | 37 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(34): Show | 40 | HG00639.hp2 HG01074.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.280-905A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74372722 | ||||||
| chr11:74372833
|
C | T | 16 | a0001c0001t0003g0098a0001c0001t0003g0182a0001c0001t0003g0183others(13): Show | 16 | HG00140.hp1 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.280-1016G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74372833 | ||||||
| chr11:74373025
|
T | TA | 131 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(128): Show | 133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.280-1209dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373025 | ||||||
| chr11:74373174
|
C | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(128): Show | 133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.279+1241G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373174 | ||||||
| chr11:74373532
|
T | A | 2 | a0001c0004t0026g0279a0007c0011t0026g0280 | 2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.279+883A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373532 | ||||||
| chr11:74373657
|
A | G | 2 | a0001c0001t0040g0277a0003c0003t0039g0024 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.279+758T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373657 | ||||||
| chr11:74373684
|
G | A | 252 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(249): Show | 263 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.279+731C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373684 | ||||||
| chr11:74373829
|
A | G | 1 | a0001c0013t0031g0343 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.279+586T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373829 | ||||||
| chr11:74373926
|
T | C | 11 | a0002c0002t0004g0013a0002c0002t0004g0265a0002c0002t0004g0266others(8): Show | 12 | HG01106.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.279+489A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373926 | ||||||
| chr11:74373956
|
T | C | 2 | a0001c0001t0040g0277a0003c0003t0039g0024 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.279+459A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74373956 | ||||||
| chr11:74374052
|
C | CA | 45 | a0001c0001t0001g0299a0001c0001t0003g0249a0001c0001t0038g0297others(42): Show | 48 | HG00642.hp2 HG00733.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.279+362dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374052 | ||||||
| chr11:74374052
|
C | CAA | 109 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(106): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.279+361_279+362dup others(2): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374052 | ||||||
| chr11:74374052
|
CA | C | 13 | a0001c0004t0010g0008a0001c0004t0010g0116a0001c0004t0015g0245others(10): Show | 14 | HG01099.hp1 HG01099.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.279+362delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374052 | ||||||
| chr11:74374071
|
AAC | A | 74 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(71): Show | 79 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.279+342_279+343del others(2): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374071 | ||||||
| chr11:74374072
|
AC | A | 7 | a0001c0001t0022g0356a0003c0003t0002g0031a0003c0003t0002g0041others(4): Show | 7 | HG00673.hp2 HG02615.hp1 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.279+342delG | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374072 | ||||||
| chr11:74374073
|
C | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(131): Show | 136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.279+342G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374073 | ||||||
| chr11:74374146
|
C | T | 2 | a0001c0004t0026g0279a0007c0011t0026g0280 | 2 | HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.279+269G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374146 | ||||||
| chr11:74374166
|
C | T | 9 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(6): Show | 9 | HG02622.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.279+249G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374166 | ||||||
| chr11:74374272
|
C | CGGGG | 32 | a0001c0001t0001g0001a0001c0001t0001g0130a0001c0001t0001g0135others(29): Show | 34 | HG00544.hp2 HG00621.hp2 HG01952.hp2 others(31): Show |
intron_variant | MODIFIER | c.279+139_279+142dup others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374272 | ||||||
| chr11:74374339
|
C | T | 81 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(78): Show | 87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.279+76G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374339 | ||||||
| chr11:74374375
|
T | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(214): Show | 225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.279+40A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 2/13 | chr11 | 74374375 | ||||||
| chr11:74374596
|
G | A | 1 | a0001c0004t0048g0354 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.112-14C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74374596 | ||||||
| chr11:74374796
|
A | C | 1 | a0003c0003t0003g0093 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.112-214T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74374796 | ||||||
| chr11:74374889
|
A | G | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-307T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74374889 | ||||||
| chr11:74375004
|
G | A | 2 | a0002c0002t0005g0241a0002c0002t0050g0235 | 2 | HG01261.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.112-422C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375004 | ||||||
| chr11:74375063
|
G | A | 3 | a0001c0004t0009g0337a0001c0004t0009g0338a0001c0004t0009g0341 | 3 | HG02922.hp2 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.112-481C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375063 | ||||||
| chr11:74375071
|
C | T | 3 | a0002c0002t0004g0112a0002c0002t0004g0119a0002c0002t0004g0244 | 3 | HG02055.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.112-489G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375071 | ||||||
| chr11:74375152
|
G | A | 1 | a0003c0003t0012g0048 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.112-570C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375152 | ||||||
| chr11:74375172
|
C | T | 1 | a0001c0013t0031g0343 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.112-590G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375172 | ||||||
| chr11:74375263
|
T | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(270): Show | 285 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.112-681A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375263 | ||||||
| chr11:74375315
|
A | G | 1 | a0004c0005t0049g0120 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.112-733T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375315 | ||||||
| chr11:74375597
|
T | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(214): Show | 225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.112-1015A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375597 | ||||||
| chr11:74375740
|
A | C | 1 | a0003c0006t0015g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.112-1158T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375740 | ||||||
| chr11:74375837
|
A | G | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.112-1255T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74375837 | ||||||
| chr11:74376108
|
C | G | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-1526G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376108 | ||||||
| chr11:74376203
|
A | G | 4 | a0001c0004t0015g0245a0001c0004t0015g0246a0001c0004t0015g0247others(1): Show | 4 | HG01884.hp2 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-1621T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376203 | ||||||
| chr11:74376234
|
C | T | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.112-1652G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376234 | ||||||
| chr11:74376459
|
ATATATAT others(6): Show |
A | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.112-1890_112-1878d others(15): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376459 | ||||||
| chr11:74376548
|
T | C | 2 | a0002c0002t0004g0112a0002c0002t0004g0244 | 2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.112-1966A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376548 | ||||||
| chr11:74376551
|
A | T | 1 | a0001c0001t0001g0308 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.112-1969T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376551 | ||||||
| chr11:74376579
|
T | G | 1 | a0003c0003t0039g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.112-1997A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376579 | ||||||
| chr11:74376655
|
A | G | 2 | a0002c0002t0027g0197a0002c0002t0027g0198 | 2 | NA18954.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.112-2073T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376655 | ||||||
| chr11:74376740
|
A | C | 6 | a0003c0003t0007g0002a0003c0003t0007g0003a0003c0003t0007g0014others(3): Show | 8 | NA18977.hp2 NA18983.hp1 NA19005.hp1 others(5): Show |
intron_variant | MODIFIER | c.112-2158T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376740 | ||||||
| chr11:74376771
|
T | C | 1 | a0001c0001t0003g0155 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.112-2189A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376771 | ||||||
| chr11:74376989
|
T | C | 2 | a0001c0001t0040g0277a0003c0003t0039g0024 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.112-2407A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74376989 | ||||||
| chr11:74377138
|
C | CT | 91 | a0001c0001t0001g0138a0001c0001t0002g0110a0001c0001t0002g0127others(88): Show | 97 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.112-2557dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377138 | ||||||
| chr11:74377228
|
G | A | 1 | a0001c0001t0003g0230 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.112-2646C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377228 | ||||||
| chr11:74377278
|
C | T | 3 | a0003c0003t0002g0043a0003c0003t0002g0082a0003c0003t0041g0069 | 3 | HG00738.hp1 HG01123.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.112-2696G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377278 | ||||||
| chr11:74377282
|
C | A | 83 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(80): Show | 89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.112-2700G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377282 | ||||||
| chr11:74377369
|
A | G | 1 | a0003c0003t0002g0056 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.112-2787T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377369 | ||||||
| chr11:74377496
|
G | T | 86 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(83): Show | 92 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.112-2914C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377496 | ||||||
| chr11:74377611
|
G | C | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-3029C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377611 | ||||||
| chr11:74377698
|
C | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(266): Show | 281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.112-3116G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377698 | ||||||
| chr11:74377947
|
G | GA | 7 | a0001c0004t0015g0245a0001c0004t0015g0246a0001c0004t0015g0247others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.112-3366dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74377947 | ||||||
| chr11:74378068
|
G | A | 1 | a0003c0003t0003g0068 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.112-3486C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74378068 | ||||||
| chr11:74378650
|
T | C | 26 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(23): Show | 26 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.112-4068A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74378650 | ||||||
| chr11:74378680
|
G | A | 10 | a0001c0001t0040g0277a0001c0004t0008g0010a0001c0004t0008g0011others(7): Show | 13 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.112-4098C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74378680 | ||||||
| chr11:74378692
|
A | T | 1 | a0001c0001t0001g0320 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.112-4110T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74378692 | ||||||
| chr11:74378771
|
T | C | 1 | a0006c0014t0016g0257 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.112-4189A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74378771 | ||||||
| chr11:74378853
|
C | T | 1 | a0001c0004t0048g0354 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.112-4271G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74378853 | ||||||
| chr11:74379024
|
C | T | 36 | a0001c0001t0040g0277a0001c0004t0008g0010a0001c0004t0008g0011others(33): Show | 39 | HG00639.hp2 HG01884.hp1 HG02109.hp1 others(36): Show |
intron_variant | MODIFIER | c.112-4442G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74379024 | ||||||
| chr11:74379181
|
T | C | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.112-4599A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74379181 | ||||||
| chr11:74379188
|
C | T | 2 | a0002c0002t0005g0196a0002c0002t0052g0152 | 2 | NA18955.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.112-4606G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74379188 | ||||||
| chr11:74379294
|
C | T | 83 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(80): Show | 89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.112-4712G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74379294 | ||||||
| chr11:74379651
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(114): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.112-5069G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74379651 | ||||||
| chr11:74379817
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(114): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.112-5235G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74379817 | ||||||
| chr11:74379883
|
A | C | 269 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(266): Show | 281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.112-5301T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74379883 | ||||||
| chr11:74380003
|
A | G | 9 | a0001c0001t0040g0277a0001c0004t0008g0010a0001c0004t0008g0011others(6): Show | 12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.112-5421T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380003 | ||||||
| chr11:74380027
|
T | C | 1 | a0002c0002t0004g0269 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.112-5445A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380027 | ||||||
| chr11:74380201
|
C | A | 2 | a0002c0002t0005g0303a0002c0002t0005g0325 | 2 | HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.112-5619G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380201 | ||||||
| chr11:74380292
|
T | G | 29 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(26): Show | 29 | HG00639.hp2 HG01074.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.112-5710A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380292 | ||||||
| chr11:74380367
|
TTTCC | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(209): Show | 220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.112-5789_112-5786d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380367 | ||||||
| chr11:74380412
|
T | C | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-5830A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380412 | ||||||
| chr11:74380464
|
T | C | 1 | a0003c0003t0039g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.112-5882A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380464 | ||||||
| chr11:74380497
|
GATTT | G | 3 | a0001c0004t0015g0245a0001c0004t0015g0246a0001c0004t0015g0247 | 3 | HG01884.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.112-5919_112-5916d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380497 | ||||||
| chr11:74380678
|
T | A | 83 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(80): Show | 89 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.112-6096A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380678 | ||||||
| chr11:74380754
|
C | G | 3 | a0001c0004t0015g0245a0001c0004t0015g0246a0001c0004t0015g0247 | 3 | HG01884.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.112-6172G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380754 | ||||||
| chr11:74380777
|
A | G | 2 | a0001c0004t0009g0339a0001c0004t0009g0340 | 2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.112-6195T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380777 | ||||||
| chr11:74380909
|
C | T | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.112-6327G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74380909 | ||||||
| chr11:74381139
|
A | G | 2 | a0001c0001t0003g0103a0001c0001t0003g0154 | 2 | HG01175.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.112-6557T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381139 | ||||||
| chr11:74381177
|
C | T | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-6595G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381177 | ||||||
| chr11:74381358
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(209): Show | 220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.112-6776A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381358 | ||||||
| chr11:74381361
|
A | G | 1 | a0001c0013t0031g0343 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.112-6779T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381361 | ||||||
| chr11:74381420
|
A | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(212): Show | 223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.112-6838T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381420 | ||||||
| chr11:74381515
|
T | C | 1 | a0001c0013t0031g0343 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.112-6933A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381515 | ||||||
| chr11:74381571
|
C | CT | 18 | a0001c0001t0001g0324a0001c0004t0015g0245a0001c0004t0015g0246others(15): Show | 18 | HG01081.hp1 HG01884.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.112-6990dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381571 | ||||||
| chr11:74381571
|
CT | C | 38 | a0001c0001t0040g0277a0001c0004t0008g0010a0001c0004t0008g0011others(35): Show | 43 | HG01099.hp1 HG01099.hp2 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.112-6990delA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381571 | ||||||
| chr11:74381571
|
CTTT | C | 98 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(95): Show | 104 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.112-6992_112-6990d others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381571 | ||||||
| chr11:74381571
|
CTTTT | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(108): Show | 113 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.112-6993_112-6990d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381571 | ||||||
| chr11:74381576
|
T | C | 2 | a0003c0003t0006g0073a0003c0003t0007g0021 | 2 | HG01175.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.112-6994A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381576 | ||||||
| chr11:74381577
|
T | C | 81 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(78): Show | 87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.112-6995A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381577 | ||||||
| chr11:74381663
|
G | A | 1 | a0003c0006t0047g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.112-7081C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381663 | ||||||
| chr11:74381889
|
C | G | 5 | a0002c0002t0004g0159a0002c0002t0004g0161a0002c0002t0004g0162others(2): Show | 5 | NA18998.hp2 NA19062.hp2 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-7307G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381889 | ||||||
| chr11:74381901
|
TC | T | 10 | a0002c0002t0004g0144a0002c0002t0004g0159a0002c0002t0004g0161others(7): Show | 10 | HG02027.hp2 NA18950.hp2 NA18956.hp2 others(7): Show |
intron_variant | MODIFIER | c.112-7320delG | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381901 | ||||||
| chr11:74381902
|
C | T | 1 | a0001c0004t0048g0354 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.112-7320G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381902 | ||||||
| chr11:74381906
|
C | A | 1 | a0002c0002t0004g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.112-7324G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381906 | ||||||
| chr11:74381911
|
C | G | 1 | a0001c0004t0024g0261 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.112-7329G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74381911 | ||||||
| chr11:74382108
|
G | A | 2 | a0002c0002t0005g0241a0002c0002t0050g0235 | 2 | HG01261.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.112-7526C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382108 | ||||||
| chr11:74382140
|
G | A | 3 | a0001c0004t0015g0245a0001c0004t0015g0246a0001c0004t0015g0247 | 3 | HG01884.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.112-7558C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382140 | ||||||
| chr11:74382176
|
G | A | 10 | a0001c0001t0040g0277a0001c0004t0008g0010a0001c0004t0008g0011others(7): Show | 13 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.112-7594C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382176 | ||||||
| chr11:74382216
|
T | C | 2 | a0003c0003t0002g0041a0003c0003t0002g0052 | 2 | HG00673.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.112-7634A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382216 | ||||||
| chr11:74382223
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(113): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.112-7641C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382223 | ||||||
| chr11:74382365
|
G | A | 3 | a0001c0004t0016g0263a0001c0004t0016g0264a0006c0014t0016g0257 | 3 | HG02723.hp2 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.112-7783C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382365 | ||||||
| chr11:74382453
|
C | T | 3 | a0002c0002t0004g0251a0002c0002t0004g0347a0002c0002t0053g0253 | 3 | HG01361.hp1 HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.112-7871G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382453 | ||||||
| chr11:74382947
|
C | T | 216 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(213): Show | 224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.112-8365G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74382947 | ||||||
| chr11:74383085
|
C | T | 1 | a0007c0011t0026g0280 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.112-8503G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383085 | ||||||
| chr11:74383093
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(213): Show | 224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.112-8511A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383093 | ||||||
| chr11:74383298
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(213): Show | 224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.112-8716T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383298 | ||||||
| chr11:74383408
|
G | A | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-8826C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383408 | ||||||
| chr11:74383453
|
T | G | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-8871A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383453 | ||||||
| chr11:74383693
|
C | T | 5 | a0001c0004t0016g0262a0001c0004t0016g0263a0001c0004t0016g0264others(2): Show | 5 | HG02572.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-9111G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383693 | ||||||
| chr11:74383820
|
A | AATATATA others(21): Show |
1 | a0002c0002t0004g0344 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.112-9239_112-9238i others(30): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383820 | ||||||
| chr11:74383820
|
A | AATATATA others(23): Show |
1 | a0002c0002t0004g0285 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.112-9239_112-9238i others(32): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383820 | ||||||
| chr11:74383824
|
A | AAT | 105 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0001t0002g0128others(102): Show | 111 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.112-9244_112-9243d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATAAATA others(31): Show |
1 | a0003c0003t0039g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.112-9243_112-9242i others(40): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATAAATA others(7): Show |
2 | a0001c0004t0009g0339a0001c0004t0009g0340 | 2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.112-9243_112-9242i others(16): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATAAATA others(25): Show |
5 | a0002c0002t0004g0267a0002c0002t0004g0268a0002c0002t0004g0269others(2): Show | 5 | HG01106.hp1 HG01891.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(34): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATAAATA others(27): Show |
4 | a0001c0004t0048g0354a0002c0002t0004g0013a0002c0002t0004g0266others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(36): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATAAATA others(26): Show |
1 | a0002c0002t0004g0265 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.112-9243_112-9242i others(35): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATAAATA others(7): Show |
14 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(11): Show | 14 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(16): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATAAATA others(9): Show |
1 | a0001c0001t0003g0195 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.112-9243_112-9242i others(18): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATAAATA others(11): Show |
3 | a0001c0001t0003g0181a0001c0001t0022g0355a0001c0004t0023g0095 | 3 | HG00639.hp2 HG02622.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.112-9243_112-9242i others(20): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATAAATA others(17): Show |
1 | a0007c0011t0026g0280 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.112-9243_112-9242i others(26): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATAAATA others(19): Show |
3 | a0001c0004t0025g0281a0003c0006t0015g0022a0008c0010t0025g0282 | 3 | HG02572.hp1 HG02886.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.112-9243_112-9242i others(28): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATAAATA others(21): Show |
1 | a0001c0004t0026g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.112-9243_112-9242i others(30): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATAAATA others(23): Show |
1 | a0002c0002t0004g0272 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.112-9243_112-9242i others(32): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATAAATA others(27): Show |
1 | a0002c0002t0004g0345 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.112-9243_112-9242i others(36): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATATATA others(1): Show |
10 | a0001c0001t0003g0209a0001c0001t0022g0356a0001c0004t0008g0010others(7): Show | 13 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.112-9250_112-9243d others(10): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATATATA others(3): Show |
30 | a0001c0001t0003g0143a0002c0002t0005g0009a0002c0002t0005g0100others(27): Show | 31 | HG00733.hp2 HG00738.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.112-9252_112-9243d others(12): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATATATA others(5): Show |
44 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(41): Show | 44 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.112-9254_112-9243d others(14): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATATATA others(7): Show |
15 | a0001c0001t0003g0140a0001c0001t0003g0178a0001c0001t0003g0179others(12): Show | 15 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.112-9256_112-9243d others(16): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATATATA others(9): Show |
13 | a0001c0001t0003g0146a0001c0001t0003g0150a0001c0001t0003g0249others(10): Show | 13 | HG01069.hp2 HG02027.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.112-9258_112-9243d others(18): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATATATA others(11): Show |
4 | a0001c0001t0003g0157a0001c0004t0013g0109a0002c0002t0004g0159others(1): Show | 4 | HG02630.hp2 NA18950.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-9260_112-9243d others(20): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATATATA others(13): Show |
7 | a0001c0001t0011g0240a0002c0002t0004g0166a0002c0002t0004g0232others(4): Show | 7 | HG01517.hp1 HG02004.hp1 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(22): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATATATA others(15): Show |
6 | a0001c0001t0003g0158a0002c0002t0004g0216a0002c0002t0005g0175others(3): Show | 6 | NA18747.hp2 NA18962.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(24): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATATATA others(17): Show |
6 | a0001c0004t0024g0261a0002c0002t0004g0102a0002c0002t0004g0214others(3): Show | 6 | HG01516.hp1 HG02559.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(26): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATATATA others(19): Show |
5 | a0001c0004t0013g0108a0002c0002t0004g0212a0002c0002t0005g0172others(2): Show | 5 | HG01081.hp1 HG02258.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(28): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATATATA others(21): Show |
3 | a0001c0004t0013g0107a0002c0002t0004g0156a0002c0002t0004g0228 | 3 | HG03195.hp2 NA18953.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.112-9243_112-9242i others(30): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATATATA others(23): Show |
2 | a0001c0004t0015g0247a0002c0002t0053g0253 | 2 | HG01361.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.112-9243_112-9242i others(32): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATATATA others(25): Show |
4 | a0001c0004t0015g0245a0001c0004t0015g0246a0002c0002t0004g0251others(1): Show | 4 | HG02055.hp1 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.112-9243_112-9242i others(34): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATATATA others(27): Show |
1 | a0002c0002t0004g0211 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.112-9243_112-9242i others(36): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | AATATATA others(29): Show |
1 | a0002c0002t0004g0347 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.112-9243_112-9242i others(38): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383824
|
A | T | 2 | a0002c0002t0004g0285a0002c0002t0004g0344 | 2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.112-9242T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383824 | ||||||
| chr11:74383860
|
G | C | 1 | a0002c0002t0004g0269 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.112-9278C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383860 | ||||||
| chr11:74383868
|
C | T | 1 | a0003c0003t0002g0090 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.112-9286G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383868 | ||||||
| chr11:74383869
|
C | T | 1 | a0003c0006t0015g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.112-9287G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74383869 | ||||||
| chr11:74384138
|
C | T | 2 | a0001c0001t0003g0170a0001c0004t0010g0116 | 2 | HG04228.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.112-9556G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384138 | ||||||
| chr11:74384329
|
T | C | 2 | a0002c0002t0004g0285a0002c0002t0004g0344 | 2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.112-9747A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384329 | ||||||
| chr11:74384333
|
T | C | 1 | a0002c0002t0053g0253 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.112-9751A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384333 | ||||||
| chr11:74384394
|
T | A | 3 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352 | 3 | HG01074.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.112-9812A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384394 | ||||||
| chr11:74384467
|
C | T | 2 | a0001c0001t0001g0307a0003c0003t0001g0088 | 2 | NA18947.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.112-9885G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384467 | ||||||
| chr11:74384505
|
G | C | 9 | a0001c0001t0040g0277a0001c0004t0008g0010a0001c0004t0008g0011others(6): Show | 12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.112-9923C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384505 | ||||||
| chr11:74384514
|
G | C | 1 | a0003c0006t0015g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.112-9932C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384514 | ||||||
| chr11:74384778
|
T | C | 2 | a0003c0003t0002g0006a0003c0003t0002g0066 | 3 | HG02040.hp1 NA18941.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.112-10196A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384778 | ||||||
| chr11:74384817
|
T | C | 1 | a0003c0003t0039g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.112-10235A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384817 | ||||||
| chr11:74384908
|
C | T | 1 | a0001c0001t0032g0147 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.112-10326G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74384908 | ||||||
| chr11:74385089
|
T | C | 108 | a0001c0001t0001g0286a0001c0001t0002g0110a0001c0001t0002g0127others(105): Show | 115 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.112-10507A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385089 | ||||||
| chr11:74385302
|
T | C | 1 | a0001c0004t0045g0349 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.112-10720A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385302 | ||||||
| chr11:74385424
|
G | T | 1 | a0001c0001t0022g0356 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.112-10842C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385424 | ||||||
| chr11:74385425
|
ACAATTTA others(3): Show |
A | 1 | a0001c0001t0022g0356 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.112-10853_112-1084 others(14): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385425 | ||||||
| chr11:74385494
|
C | A | 1 | a0003c0003t0039g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.112-10912G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385494 | ||||||
| chr11:74385549
|
T | C | 1 | a0003c0003t0006g0053 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.112-10967A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385549 | ||||||
| chr11:74385633
|
A | G | 7 | a0001c0004t0017g0359a0001c0004t0017g0360a0001c0004t0017g0362others(4): Show | 7 | HG01099.hp1 HG01243.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.112-11051T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385633 | ||||||
| chr11:74385797
|
A | T | 11 | a0002c0002t0004g0013a0002c0002t0004g0265a0002c0002t0004g0266others(8): Show | 12 | HG01106.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.112-11215T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385797 | ||||||
| chr11:74385950
|
G | C | 299 | a0001c0001t0001g0099a0001c0001t0001g0286a0001c0001t0002g0110others(296): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.112-11368C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74385950 | ||||||
| chr11:74386002
|
G | T | 108 | a0001c0001t0001g0286a0001c0001t0002g0110a0001c0001t0002g0127others(105): Show | 115 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.112-11420C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386002 | ||||||
| chr11:74386081
|
G | A | 298 | a0001c0001t0001g0099a0001c0001t0001g0286a0001c0001t0002g0110others(295): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.112-11499C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386081 | ||||||
| chr11:74386141
|
A | G | 185 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(182): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.112-11559T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386141 | ||||||
| chr11:74386170
|
A | C | 9 | a0001c0001t0040g0277a0001c0004t0008g0010a0001c0004t0008g0011others(6): Show | 12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.112-11588T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386170 | ||||||
| chr11:74386421
|
T | G | 188 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(185): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.111+11630A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386421 | ||||||
| chr11:74386478
|
A | C | 1 | a0001c0001t0003g0169 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.111+11573T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386478 | ||||||
| chr11:74386480
|
C | CT | 9 | a0001c0001t0001g0298a0001c0001t0001g0307a0001c0001t0001g0330others(6): Show | 9 | HG02572.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.111+11570dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386480 | ||||||
| chr11:74386920
|
G | A | 185 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(182): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.111+11131C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386920 | ||||||
| chr11:74386998
|
G | C | 1 | a0003c0003t0039g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111+11053C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74386998 | ||||||
| chr11:74387044
|
T | C | 9 | a0001c0001t0040g0277a0001c0004t0008g0010a0001c0004t0008g0011others(6): Show | 12 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.111+11007A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387044 | ||||||
| chr11:74387212
|
G | A | 1 | a0003c0003t0039g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111+10839C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387212 | ||||||
| chr11:74387237
|
T | C | 25 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(22): Show | 26 | HG00642.hp2 HG01099.hp2 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.111+10814A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387237 | ||||||
| chr11:74387437
|
C | T | 108 | a0001c0001t0001g0286a0001c0001t0002g0110a0001c0001t0002g0127others(105): Show | 115 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.111+10614G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387437 | ||||||
| chr11:74387600
|
G | T | 299 | a0001c0001t0001g0099a0001c0001t0001g0286a0001c0001t0002g0110others(296): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.111+10451C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387600 | ||||||
| chr11:74387651
|
T | C | 1 | a0003c0003t0039g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111+10400A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387651 | ||||||
| chr11:74387688
|
C | T | 147 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(144): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.111+10363G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387688 | ||||||
| chr11:74387793
|
T | C | 1 | a0001c0001t0022g0356 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.111+10258A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387793 | ||||||
| chr11:74387849
|
G | A | 1 | a0001c0001t0040g0277 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.111+10202C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74387849 | ||||||
| chr11:74388305
|
C | T | 185 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(182): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.111+9746G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388305 | ||||||
| chr11:74388335
|
TA | T | 299 | a0001c0001t0001g0099a0001c0001t0001g0286a0001c0001t0002g0110others(296): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.111+9715delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388335 | ||||||
| chr11:74388497
|
C | G | 1 | a0001c0001t0001g0274 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.111+9554G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388497 | ||||||
| chr11:74388516
|
A | C | 108 | a0001c0001t0001g0286a0001c0001t0002g0110a0001c0001t0002g0127others(105): Show | 115 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.111+9535T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388516 | ||||||
| chr11:74388583
|
T | C | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+9468A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388583 | ||||||
| chr11:74388591
|
G | A | 185 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(182): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.111+9460C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388591 | ||||||
| chr11:74388652
|
T | C | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+9399A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388652 | ||||||
| chr11:74388682
|
C | T | 2 | a0002c0002t0004g0285a0002c0002t0004g0344 | 2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.111+9369G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388682 | ||||||
| chr11:74388785
|
T | C | 1 | a0003c0006t0015g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.111+9266A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388785 | ||||||
| chr11:74388847
|
T | C | 299 | a0001c0001t0001g0099a0001c0001t0001g0286a0001c0001t0002g0110others(296): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.111+9204A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74388847 | ||||||
| chr11:74389062
|
T | A | 5 | a0001c0004t0025g0281a0001c0004t0026g0279a0001c0004t0048g0354others(2): Show | 5 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+8989A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389062 | ||||||
| chr11:74389282
|
C | G | 108 | a0001c0001t0001g0286a0001c0001t0002g0110a0001c0001t0002g0127others(105): Show | 115 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.111+8769G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389282 | ||||||
| chr11:74389495
|
G | A | 185 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(182): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.111+8556C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389495 | ||||||
| chr11:74389601
|
T | C | 185 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(182): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.111+8450A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389601 | ||||||
| chr11:74389621
|
G | A | 10 | a0001c0004t0015g0245a0001c0004t0015g0246a0001c0004t0015g0247others(7): Show | 10 | HG00642.hp2 HG01261.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.111+8430C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389621 | ||||||
| chr11:74389720
|
G | C | 4 | a0001c0004t0019g0350a0001c0004t0019g0351a0001c0004t0019g0352others(1): Show | 4 | HG01074.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+8331C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389720 | ||||||
| chr11:74389947
|
C | CA | 11 | a0001c0001t0001g0129a0001c0001t0001g0134a0001c0001t0001g0296others(8): Show | 11 | HG00438.hp1 HG00673.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+8103dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | ||||||
| chr11:74389947
|
C | CAAAAA | 88 | a0001c0001t0001g0099a0001c0001t0003g0098a0001c0001t0003g0140others(85): Show | 89 | HG00323.hp1 HG00597.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.111+8099_111+8103d others(7): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | ||||||
| chr11:74389947
|
C | CAAAAAA | 62 | a0001c0001t0003g0096a0001c0001t0003g0103a0001c0001t0003g0146others(59): Show | 65 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.111+8098_111+8103d others(8): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | ||||||
| chr11:74389947
|
C | CAAAAAAA | 9 | a0001c0001t0003g0229a0001c0001t0003g0230a0001c0001t0040g0277others(6): Show | 9 | HG01891.hp1 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.111+8097_111+8103d others(9): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | ||||||
| chr11:74389947
|
C | CAAAAAAA others(3): Show |
32 | a0001c0001t0001g0286a0001c0001t0002g0110a0001c0001t0002g0127others(29): Show | 35 | HG00280.hp1 HG00609.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.111+8094_111+8103d others(12): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | ||||||
| chr11:74389947
|
C | CAAAAAAA others(4): Show |
44 | a0001c0001t0002g0128a0001c0001t0002g0306a0001c0004t0017g0360others(41): Show | 47 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.111+8093_111+8103d others(13): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | ||||||
| chr11:74389947
|
C | CAAAAAAA others(5): Show |
16 | a0001c0001t0002g0273a0001c0004t0010g0008a0001c0004t0010g0113others(13): Show | 17 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.111+8092_111+8103d others(14): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | ||||||
| chr11:74389947
|
C | CAAAAAAA others(6): Show |
8 | a0001c0004t0010g0116a0001c0004t0010g0117a0001c0004t0010g0118others(5): Show | 8 | HG01175.hp1 HG02135.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.111+8091_111+8103d others(15): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | ||||||
| chr11:74389947
|
C | CAAAAAAA others(7): Show |
2 | a0001c0013t0031g0343a0002c0002t0004g0112 | 2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.111+8090_111+8103d others(16): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | ||||||
| chr11:74389947
|
C | CAAAAAAA others(8): Show |
1 | a0004c0005t0014g0121 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.111+8089_111+8103d others(17): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | ||||||
| chr11:74389947
|
C | CAAAAAAA others(9): Show |
6 | a0001c0004t0016g0262a0001c0004t0016g0263a0004c0005t0014g0122others(3): Show | 6 | HG01261.hp1 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+8088_111+8103d others(18): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | ||||||
| chr11:74389947
|
C | CAAAAAAA others(10): Show |
4 | a0001c0004t0016g0264a0004c0005t0014g0124a0004c0005t0014g0125others(1): Show | 4 | HG00642.hp2 HG03492.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+8087_111+8103d others(19): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | ||||||
| chr11:74389947
|
CA | C | 5 | a0001c0001t0038g0297a0002c0002t0004g0013a0002c0002t0004g0268others(2): Show | 6 | HG02145.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+8103delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | ||||||
| chr11:74389947
|
CAA | C | 8 | a0002c0002t0004g0265a0002c0002t0004g0266a0002c0002t0004g0267others(5): Show | 8 | HG01106.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+8102_111+8103d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389947 | ||||||
| chr11:74389968
|
A | AAAAAAAA others(6): Show |
1 | a0003c0003t0002g0082 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.111+8082_111+8083i others(15): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389968 | ||||||
| chr11:74389974
|
C | G | 1 | a0001c0001t0003g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.111+8077G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389974 | ||||||
| chr11:74389976
|
A | G | 300 | a0001c0001t0001g0099a0001c0001t0001g0286a0001c0001t0002g0110others(297): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.111+8075T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74389976 | ||||||
| chr11:74390033
|
G | A | 3 | a0001c0004t0015g0245a0001c0004t0015g0246a0001c0004t0015g0247 | 3 | HG01884.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.111+8018C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390033 | ||||||
| chr11:74390035
|
C | T | 156 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(153): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.111+8016G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390035 | ||||||
| chr11:74390118
|
CA | C | 161 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(158): Show | 163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.111+7932delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390118 | ||||||
| chr11:74390118
|
CAA | C | 16 | a0001c0001t0003g0165a0002c0002t0004g0097a0002c0002t0004g0144others(13): Show | 16 | HG01074.hp2 HG02027.hp2 HG02148.hp2 others(13): Show |
intron_variant | MODIFIER | c.111+7931_111+7932d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390118 | ||||||
| chr11:74390170
|
G | GA | 250 | a0001c0001t0001g0099a0001c0001t0001g0286a0001c0001t0002g0110others(247): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.111+7880dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390170 | ||||||
| chr11:74390170
|
G | GAA | 35 | a0001c0001t0003g0158a0001c0001t0034g0231a0001c0004t0010g0008others(32): Show | 36 | HG00438.hp2 HG00642.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.111+7879_111+7880d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390170 | ||||||
| chr11:74390372
|
C | A | 1 | a0001c0004t0023g0095 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.111+7679G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390372 | ||||||
| chr11:74390752
|
A | C | 4 | a0001c0004t0025g0281a0001c0004t0026g0279a0007c0011t0026g0280others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.111+7299T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390752 | ||||||
| chr11:74390941
|
G | A | 3 | a0002c0002t0004g0232a0002c0002t0004g0233a0002c0002t0004g0234 | 3 | NA18956.hp2 NA18965.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.111+7110C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74390941 | ||||||
| chr11:74391176
|
C | T | 3 | a0001c0001t0003g0157a0001c0001t0003g0158a0002c0002t0004g0156 | 3 | NA18747.hp2 NA18953.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.111+6875G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74391176 | ||||||
| chr11:74391274
|
C | T | 44 | a0001c0001t0001g0001a0001c0001t0001g0130a0001c0001t0001g0135others(41): Show | 47 | HG00544.hp2 HG00621.hp2 HG01106.hp1 others(44): Show |
intron_variant | MODIFIER | c.111+6777G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74391274 | ||||||
| chr11:74391333
|
T | C | 21 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(18): Show | 22 | HG00639.hp2 HG00642.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.111+6718A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74391333 | ||||||
| chr11:74391726
|
T | A | 1 | a0002c0002t0050g0235 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.111+6325A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74391726 | ||||||
| chr11:74391828
|
TGGTATG | T | 104 | a0001c0001t0001g0286a0001c0001t0002g0110a0001c0001t0002g0127others(101): Show | 111 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.111+6217_111+6222d others(8): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74391828 | ||||||
| chr11:74391834
|
G | T | 1 | a0001c0004t0057g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.111+6217C>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74391834 | ||||||
| chr11:74391929
|
T | C | 1 | a0003c0006t0015g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.111+6122A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74391929 | ||||||
| chr11:74392348
|
G | A | 1 | a0002c0002t0053g0253 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.111+5703C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74392348 | ||||||
| chr11:74392356
|
T | G | 1 | a0002c0002t0053g0253 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.111+5695A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74392356 | ||||||
| chr11:74392365
|
A | G | 1 | a0001c0001t0001g0274 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.111+5686T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74392365 | ||||||
| chr11:74392669
|
G | A | 5 | a0001c0004t0016g0262a0001c0004t0016g0263a0001c0004t0016g0264others(2): Show | 5 | HG02572.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+5382C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74392669 | ||||||
| chr11:74392735
|
C | T | 188 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(185): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.111+5316G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74392735 | ||||||
| chr11:74392791
|
C | T | 1 | a0003c0003t0039g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111+5260G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74392791 | ||||||
| chr11:74392836
|
G | A | 1 | a0001c0004t0017g0363 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.111+5215C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74392836 | ||||||
| chr11:74393022
|
T | C | 146 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(143): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.111+5029A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393022 | ||||||
| chr11:74393043
|
T | C | 5 | a0001c0004t0016g0262a0001c0004t0016g0263a0001c0004t0016g0264others(2): Show | 5 | HG02572.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+5008A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393043 | ||||||
| chr11:74393266
|
A | C | 2 | a0003c0003t0002g0029a0003c0003t0002g0046 | 2 | NA18948.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.111+4785T>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393266 | ||||||
| chr11:74393328
|
C | T | 1 | a0003c0006t0015g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.111+4723G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393328 | ||||||
| chr11:74393463
|
T | C | 185 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(182): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.111+4588A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393463 | ||||||
| chr11:74393630
|
A | G | 1 | a0003c0003t0002g0028 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.111+4421T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393630 | ||||||
| chr11:74393679
|
C | A | 1 | a0001c0001t0003g0236 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.111+4372G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393679 | ||||||
| chr11:74393784
|
G | C | 365 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0129others(362): Show | 379 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.111+4267C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393784 | ||||||
| chr11:74393977
|
GA | G | 292 | a0001c0001t0001g0099a0001c0001t0001g0286a0001c0001t0002g0110others(289): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.111+4073delT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74393977 | ||||||
| chr11:74394060
|
C | T | 156 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(153): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.111+3991G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74394060 | ||||||
| chr11:74394318
|
A | G | 8 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(5): Show | 11 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+3733T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74394318 | ||||||
| chr11:74394444
|
C | T | 1 | a0001c0009t0029g0365 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.111+3607G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74394444 | ||||||
| chr11:74394804
|
T | C | 10 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(7): Show | 11 | HG01099.hp2 HG02055.hp2 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.111+3247A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74394804 | ||||||
| chr11:74394950
|
C | CTA | 294 | a0001c0001t0001g0099a0001c0001t0001g0286a0001c0001t0002g0110others(291): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.111+3100_111+3101i others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74394950 | ||||||
| chr11:74394954
|
T | G | 1 | a0003c0003t0039g0024 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.111+3097A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74394954 | ||||||
| chr11:74395532
|
C | T | 1 | a0001c0001t0003g0143 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.111+2519G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395532 | ||||||
| chr11:74395549
|
C | CT | 28 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(25): Show | 28 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.111+2501dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | ||||||
| chr11:74395549
|
C | CTT | 6 | a0001c0001t0001g0129a0001c0001t0001g0287a0001c0001t0002g0273others(3): Show | 7 | HG00438.hp1 HG02145.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+2500_111+2501d others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | ||||||
| chr11:74395549
|
C | CTTT | 66 | a0001c0001t0001g0286a0001c0001t0002g0128a0001c0001t0022g0355others(63): Show | 71 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.111+2499_111+2501d others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | ||||||
| chr11:74395549
|
C | CTTTT | 32 | a0001c0001t0002g0110a0001c0001t0002g0127a0001c0004t0017g0359others(29): Show | 33 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.111+2498_111+2501d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | ||||||
| chr11:74395549
|
CTTT | C | 7 | a0001c0001t0003g0143a0001c0004t0008g0259a0001c0004t0016g0262others(4): Show | 7 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+2499_111+2501d others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | ||||||
| chr11:74395549
|
CTTTT | C | 47 | a0001c0001t0003g0096a0001c0001t0003g0146a0001c0001t0003g0150others(44): Show | 51 | HG00639.hp2 HG00642.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.111+2498_111+2501d others(6): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | ||||||
| chr11:74395549
|
CTTTTT | C | 128 | a0001c0001t0001g0099a0001c0001t0003g0098a0001c0001t0003g0103others(125): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.111+2497_111+2501d others(7): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | ||||||
| chr11:74395549
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0003g0236 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.111+2490_111+2501d others(14): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395549 | ||||||
| chr11:74395550
|
T | C | 1 | a0001c0004t0048g0354 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.111+2501A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395550 | ||||||
| chr11:74395553
|
T | C | 1 | a0002c0002t0004g0112 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.111+2498A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395553 | ||||||
| chr11:74395554
|
T | C | 9 | a0001c0004t0010g0008a0001c0004t0010g0113a0001c0004t0010g0114others(6): Show | 10 | HG01099.hp2 HG03209.hp2 HG03516.hp1 others(7): Show |
intron_variant | MODIFIER | c.111+2497A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395554 | ||||||
| chr11:74395597
|
G | A | 7 | a0004c0005t0014g0121a0004c0005t0014g0122a0004c0005t0014g0123others(4): Show | 7 | HG00642.hp2 HG01261.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+2454C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395597 | ||||||
| chr11:74395613
|
G | A | 9 | a0001c0004t0009g0334a0001c0004t0009g0335a0001c0004t0009g0336others(6): Show | 9 | HG02622.hp2 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.111+2438C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395613 | ||||||
| chr11:74395650
|
G | A | 11 | a0001c0004t0015g0245a0001c0004t0015g0246a0001c0004t0015g0247others(8): Show | 11 | HG00639.hp2 HG00642.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.111+2401C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395650 | ||||||
| chr11:74395714
|
A | G | 12 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(9): Show | 15 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+2337T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395714 | ||||||
| chr11:74395793
|
C | T | 294 | a0001c0001t0001g0099a0001c0001t0001g0286a0001c0001t0002g0110others(291): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.111+2258G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395793 | ||||||
| chr11:74395810
|
C | T | 1 | a0001c0004t0008g0258 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.111+2241G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395810 | ||||||
| chr11:74395973
|
C | T | 103 | a0001c0001t0001g0286a0001c0001t0002g0110a0001c0001t0002g0127others(100): Show | 110 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.111+2078G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74395973 | ||||||
| chr11:74396025
|
G | C | 1 | a0001c0001t0036g0237 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.111+2026C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396025 | ||||||
| chr11:74396086
|
T | TA | 7 | a0001c0001t0003g0254a0001c0004t0016g0262a0001c0004t0016g0263others(4): Show | 7 | HG02572.hp2 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.111+1964dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396086 | ||||||
| chr11:74396099
|
A | T | 97 | a0001c0001t0001g0286a0001c0001t0002g0110a0001c0001t0002g0127others(94): Show | 103 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.111+1952T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396099 | ||||||
| chr11:74396152
|
G | A | 3 | a0001c0001t0001g0328a0001c0001t0002g0139a0001c0001t0003g0329 | 3 | HG01257.hp2 HG01258.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.111+1899C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396152 | ||||||
| chr11:74396206
|
T | A | 1 | a0003c0003t0002g0082 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.111+1845A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396206 | ||||||
| chr11:74396221
|
T | C | 2 | a0001c0001t0003g0238a0001c0001t0003g0239 | 2 | NA18954.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.111+1830A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396221 | ||||||
| chr11:74396266
|
T | TA | 8 | a0001c0001t0001g0330a0001c0001t0001g0331a0003c0003t0001g0088others(5): Show | 8 | HG03239.hp2 HG04199.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.111+1784dupT | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396266 | ||||||
| chr11:74396266
|
TAAA | T | 182 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(179): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.111+1782_111+1784d others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396266 | ||||||
| chr11:74396359
|
G | C | 1 | a0003c0006t0015g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.111+1692C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396359 | ||||||
| chr11:74396440
|
A | T | 1 | a0001c0004t0045g0349 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.111+1611T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396440 | ||||||
| chr11:74396449
|
C | T | 12 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(9): Show | 15 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+1602G>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396449 | ||||||
| chr11:74396454
|
G | A | 12 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(9): Show | 15 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+1597C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396454 | ||||||
| chr11:74396484
|
C | G | 2 | a0001c0001t0003g0140a0001c0001t0003g0249 | 2 | HG01069.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.111+1567G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396484 | ||||||
| chr11:74396560
|
G | C | 5 | a0001c0004t0016g0262a0001c0004t0016g0263a0001c0004t0016g0264others(2): Show | 5 | HG02572.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+1491C>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396560 | ||||||
| chr11:74396609
|
T | C | 12 | a0001c0004t0008g0010a0001c0004t0008g0011a0001c0004t0008g0012others(9): Show | 15 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+1442A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396609 | ||||||
| chr11:74396706
|
G | A | 146 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(143): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.111+1345C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396706 | ||||||
| chr11:74396710
|
G | A | 6 | a0001c0004t0013g0105a0001c0004t0013g0107a0001c0004t0013g0108others(3): Show | 6 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+1341C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396710 | ||||||
| chr11:74396976
|
T | A | 5 | a0001c0004t0016g0262a0001c0004t0016g0263a0001c0004t0016g0264others(2): Show | 5 | HG02572.hp2 HG02717.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.111+1075A>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396976 | ||||||
| chr11:74396983
|
T | C | 1 | a0003c0003t0002g0031 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.111+1068A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74396983 | ||||||
| chr11:74397369
|
T | C | 16 | a0001c0001t0022g0356a0001c0004t0008g0010a0001c0004t0008g0011others(13): Show | 19 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.111+682A>G | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397369 | ||||||
| chr11:74397526
|
C | G | 198 | a0001c0001t0001g0099a0001c0001t0001g0129a0001c0001t0001g0130others(195): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.111+525G>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397526 | ||||||
| chr11:74397536
|
T | G | 1 | a0001c0004t0045g0349 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.111+515A>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397536 | ||||||
| chr11:74397568
|
G | A | 199 | a0001c0001t0001g0099a0001c0001t0001g0129a0001c0001t0001g0130others(196): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.111+483C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397568 | ||||||
| chr11:74397586
|
A | G | 4 | a0001c0004t0015g0245a0001c0004t0015g0246a0001c0004t0015g0247others(1): Show | 4 | HG01884.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.111+465T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397586 | ||||||
| chr11:74397734
|
C | A | 1 | a0001c0004t0058g0358 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.111+317G>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397734 | ||||||
| chr11:74397745
|
A | AT | 25 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0002g0273others(22): Show | 26 | HG00609.hp1 HG01099.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.111+305dupA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397745 | ||||||
| chr11:74397745
|
A | ATT | 79 | a0001c0004t0008g0011a0001c0004t0008g0012a0001c0004t0008g0258others(76): Show | 86 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.111+304_111+305dup others(2): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397745 | ||||||
| chr11:74397745
|
A | ATTT | 24 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0254others(21): Show | 25 | HG00280.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.111+303_111+305dup others(3): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397745 | ||||||
| chr11:74397745
|
A | ATTTT | 137 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(134): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.111+302_111+305dup others(4): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397745 | ||||||
| chr11:74397745
|
A | ATTTTT | 15 | a0001c0001t0001g0099a0001c0001t0003g0096a0001c0001t0003g0098others(12): Show | 15 | HG00639.hp2 HG01243.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.111+301_111+305dup others(5): Show |
PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397745 | ||||||
| chr11:74397745
|
A | T | 9 | a0002c0002t0004g0013a0002c0002t0004g0265a0002c0002t0004g0266others(6): Show | 10 | HG01106.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.111+306T>A | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397745 | ||||||
| chr11:74397745
|
AT | A | 6 | a0001c0001t0001g0353a0001c0001t0022g0356a0001c0004t0019g0350others(3): Show | 6 | HG01074.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.111+305delA | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397745 | ||||||
| chr11:74397769
|
A | G | 1 | a0001c0004t0057g0357 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.111+282T>C | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397769 | ||||||
| chr11:74397905
|
G | A | 86 | a0001c0001t0022g0355a0001c0001t0022g0356a0003c0003t0001g0080others(83): Show | 92 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.111+146C>T | PGM2L1 | ENSG00000165434.8 | transcript | ENST00000298198.5 | protein_coding | 1/13 | chr11 | 74397905 |