| geneid | 55276 |
|---|---|
| ensemblid | ENSG00000169299.14 |
| hgncid | 8906 |
| symbol | PGM2 |
| name | phosphoglucomutase 2 |
| refseq_nuc | NM_018290.4 |
| refseq_prot | NP_060760.2 |
| ensembl_nuc | ENST00000381967.9 |
| ensembl_prot | ENSP00000371393.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 37826686 |
| end | 37862937 |
| strand | + |
| ver | v1.2 |
| region | chr4:37826686-37862937 |
| region5000 | chr4:37821686-37867937 |
| regionname0 | PGM2_chr4_37826686_37862937 |
| regionname5000 | PGM2_chr4_37821686_37867937 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 612 | 374 | 66 | 55 | 195 | 18 | 38 | 162 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002 | 0/0 | 612 | 61 | 20 | 11 | 29 | 0 | 1 | 16 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0003 | 0/0 | 612 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0004 | 0/0 | 612 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0005 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0006 | 0/0 | 258 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0007 | 0/0 | 612 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0008 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0009 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0010 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0011 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1839 | 285 | 24 | 43 | 169 | 16 | 31 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0002 | 0/0 | 1839 | 55 | 20 | 6 | 25 | 2 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0003 | 0/0 | 1839 | 43 | 16 | 9 | 17 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0004 | 0/0 | 1839 | 27 | 21 | 3 | 0 | 0 | 3 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0005 | 0/0 | 1839 | 6 | 1 | 3 | 1 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0006 | 0/0 | 1839 | 6 | 1 | 0 | 5 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0007 | 0/0 | 1839 | 5 | 3 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0008 | 0/0 | 1839 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0009 | 0/0 | 1839 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0010 | 0/0 | 1839 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0011 | 0/0 | 1839 | 2 | 0 | 0 | 0 | 0 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0012 | 0/0 | 1839 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0013 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0014 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0015 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0016 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0017 | 0/0 | 1804 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0018 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0019 | 0/0 | 1839 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| c0020 | 0/0 | 1839 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1373 | 287 | 54 | 48 | 136 | 15 | 32 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| t0002 | 0/0 | 1373 | 56 | 20 | 7 | 24 | 2 | 3 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| t0003 | 0/0 | 1373 | 44 | 12 | 8 | 23 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| t0004 | 0/0 | 1373 | 35 | 0 | 1 | 31 | 0 | 3 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| t0005 | 0/0 | 1367 | 11 | 0 | 0 | 11 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| t0006 | 0/0 | 1373 | 5 | 1 | 1 | 0 | 1 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| t0007 | 0/0 | 1373 | 3 | 3 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| t0008 | 0/0 | 1373 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| t0009 | 0/0 | 1373 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| t0010 | 0/0 | 1408 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| t0011 | 0/0 | 1373 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| t0012 | 0/0 | 1373 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| 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 | 5 | 0 | 0 | 5 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0004 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0009 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0010 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0329 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0376 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0381 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1839 | 285 | 24 | 43 | 169 | 16 | 31 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0002 | 0/0 | 1839 | 55 | 20 | 6 | 25 | 2 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0004 | 0/0 | 1839 | 27 | 21 | 3 | 0 | 0 | 3 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0005 | 0/0 | 1839 | 6 | 1 | 3 | 1 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0019 | 0/0 | 1839 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0003 | 0/0 | 1839 | 43 | 16 | 9 | 17 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0006 | 0/0 | 1839 | 6 | 1 | 0 | 5 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0007 | 0/0 | 1839 | 5 | 3 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0008 | 0/0 | 1839 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0009 | 0/0 | 1839 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0012 | 0/0 | 1839 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0003c0011 | 0/0 | 1839 | 2 | 0 | 0 | 0 | 0 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0004c0010 | 0/0 | 1839 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0005c0014 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0006c0017 | 0/0 | 1804 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0007c0020 | 0/0 | 1839 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0008c0015 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0009c0018 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0010c0016 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0011c0013 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3211 | 229 | 18 | 41 | 126 | 15 | 27 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0001t0002 | 0/0 | 3211 | 4 | 4 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0001t0003 | 0/0 | 3211 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0001t0004 | 0/0 | 3211 | 33 | 0 | 1 | 31 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0001t0005 | 0/0 | 3205 | 9 | 0 | 0 | 9 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0001t0006 | 0/0 | 3211 | 4 | 0 | 1 | 0 | 1 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0001t0007 | 0/0 | 3211 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0001t0011 | 0/0 | 3211 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0002t0001 | 0/0 | 3211 | 3 | 1 | 1 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0002t0002 | 0/0 | 3211 | 44 | 12 | 4 | 24 | 2 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0002t0003 | 0/0 | 3211 | 6 | 6 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0002t0009 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0002t0010 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0004t0001 | 0/0 | 3211 | 26 | 20 | 3 | 0 | 0 | 3 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0004t0007 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0005t0001 | 0/0 | 3211 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0005t0002 | 0/0 | 3211 | 3 | 1 | 1 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0005t0003 | 0/0 | 3211 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0005t0012 | 0/0 | 3211 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0001c0019t0001 | 0/0 | 3211 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0003t0001 | 0/0 | 3211 | 18 | 12 | 2 | 4 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0003t0003 | 0/0 | 3211 | 23 | 2 | 7 | 13 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0003t0006 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0003t0008 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0006t0003 | 0/0 | 3211 | 6 | 1 | 0 | 5 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0007t0001 | 0/0 | 3211 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0007t0002 | 0/0 | 3211 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0007t0003 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0008t0001 | 0/0 | 3211 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0009t0003 | 0/0 | 3211 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0002c0012t0002 | 0/0 | 3211 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0003c0011t0004 | 0/0 | 3211 | 2 | 0 | 0 | 0 | 0 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0004c0010t0001 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0004c0010t0003 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0005c0014t0001 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0006c0017t0005 | 0/0 | 3170 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0007c0020t0001 | 0/0 | 3211 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0008c0015t0001 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0009c0018t0005 | 0/0 | 3205 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0010c0016t0002 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| a0011c0013t0003 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | copy fasta | chr4 | 37821686 | 37867937 |
| 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 | 5 | 0 | 0 | 5 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0009 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0329 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0002g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0006g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0011g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0010g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0005t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0005t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0005t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0005t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0005t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0005t0012g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0019t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0008g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0006t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0006t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0006t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0006t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0006t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0006t0003g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0007t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0007t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0007t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0007t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0007t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0008t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0008t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0008t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0009t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0009t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0012t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0012t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0003c0011t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0003c0011t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0004c0010t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0004c0010t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0005c0014t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0006c0017t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0007c0020t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0008c0015t0001g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0009c0018t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0010c0016t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0011c0013t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0167 | EUR | GBR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0362 | EUR | GBR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0325 | EUR | GBR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0381 | EUR | FIN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00408 | hp2 | a0002 | c0003 | t0001 | g0216 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00597 | hp1 | a0002 | c0007 | t0001 | g0228 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00609 | hp1 | a0002 | c0003 | t0001 | g0215 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00609 | hp2 | a0002 | c0003 | t0003 | g0208 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00639 | hp2 | a0001 | c0004 | t0001 | g0016 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0375 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00733 | hp1 | a0002 | c0003 | t0003 | g0022 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0078 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0390 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00738 | hp1 | a0001 | c0002 | t0010 | g0115 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0106 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01106 | hp2 | a0002 | c0003 | t0001 | g0235 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0384 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01167 | hp1 | a0001 | c0005 | t0002 | g0202 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01167 | hp2 | a0002 | c0012 | t0002 | g0299 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01168 | hp1 | a0001 | c0004 | t0001 | g0091 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01169 | hp1 | a0002 | c0012 | t0002 | g0300 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01192 | hp1 | a0002 | c0003 | t0003 | g0022 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0236 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01255 | hp1 | a0001 | c0004 | t0001 | g0016 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01258 | hp1 | a0001 | c0005 | t0003 | g0169 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0382 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0363 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0102 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01361 | hp2 | a0001 | c0005 | t0001 | g0168 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0063 | EUR | IBS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0376 | EUR | IBS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0067 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0238 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0114 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0367 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01952 | hp2 | a0002 | c0003 | t0003 | g0024 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01975 | hp2 | a0002 | c0003 | t0003 | g0206 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01978 | hp1 | a0002 | c0003 | t0003 | g0226 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0366 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0389 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0062 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02015 | hp2 | a0002 | c0003 | t0003 | g0222 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0284 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0279 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02040 | hp2 | a0002 | c0003 | t0003 | g0209 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0117 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0371 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02080 | hp1 | a0002 | c0003 | t0003 | g0210 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02083 | hp1 | a0002 | c0006 | t0003 | g0164 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02129 | hp1 | a0002 | c0003 | t0003 | g0243 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02132 | hp2 | a0002 | c0008 | t0001 | g0244 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02135 | hp1 | a0002 | c0003 | t0001 | g0023 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CDX | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02257 | hp2 | a0002 | c0003 | t0006 | g0213 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0101 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02280 | hp1 | a0002 | c0003 | t0001 | g0037 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02280 | hp2 | a0001 | c0004 | t0001 | g0025 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02293 | hp1 | a0002 | c0003 | t0003 | g0242 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0051 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02451 | hp1 | a0001 | c0004 | t0001 | g0258 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02451 | hp2 | a0002 | c0003 | t0001 | g0237 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02523 | hp1 | a0002 | c0006 | t0003 | g0266 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0257 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0039 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0133 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02602 | hp2 | a0001 | c0004 | t0001 | g0089 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02615 | hp1 | a0002 | c0007 | t0002 | g0212 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0256 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02622 | hp1 | a0001 | c0004 | t0001 | g0254 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02622 | hp2 | a0002 | c0007 | t0003 | g0207 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0386 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02647 | hp1 | a0004 | c0010 | t0003 | g0264 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0219 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02717 | hp1 | a0001 | c0004 | t0001 | g0255 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02723 | hp1 | a0001 | c0004 | t0001 | g0005 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02723 | hp2 | a0008 | c0015 | t0001 | g0385 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0059 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02735 | hp2 | a0003 | c0011 | t0004 | g0285 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0082 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0084 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0111 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0201 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0109 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0043 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0080 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0116 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0218 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0250 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0110 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02970 | hp1 | a0010 | c0016 | t0002 | g0108 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02970 | hp2 | a0002 | c0003 | t0003 | g0248 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0005 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03041 | hp2 | a0002 | c0003 | t0001 | g0204 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0261 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0079 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03130 | hp1 | a0001 | c0002 | t0009 | g0112 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03130 | hp2 | a0002 | c0007 | t0002 | g0214 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03139 | hp1 | a0002 | c0006 | t0003 | g0380 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03195 | hp1 | a0002 | c0003 | t0001 | g0217 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0081 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03209 | hp2 | a0002 | c0003 | t0003 | g0035 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03225 | hp1 | a0011 | c0013 | t0003 | g0249 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03225 | hp2 | a0001 | c0004 | t0007 | g0260 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0387 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03239 | hp2 | a0001 | c0005 | t0002 | g0203 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03453 | hp1 | a0004 | c0010 | t0001 | g0005 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03453 | hp2 | a0001 | c0002 | t0003 | g0113 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0107 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0252 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0232 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0211 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0105 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0263 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0005 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03654 | hp1 | a0001 | c0001 | t0011 | g0293 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03669 | hp1 | a0001 | c0004 | t0001 | g0100 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0355 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0350 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0291 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03831 | hp1 | a0007 | c0020 | t0001 | g0369 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0379 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0374 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03834 | hp2 | a0003 | c0011 | t0004 | g0286 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0378 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04184 | hp2 | a0002 | c0003 | t0003 | g0245 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0021 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04204 | hp2 | a0001 | c0019 | t0001 | g0313 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0083 | AFR | YRI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18522 | hp2 | a0005 | c0014 | t0001 | g0166 | AFR | YRI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | CHB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18747 | hp1 | a0002 | c0006 | t0003 | g0265 | EAS | CHB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | CHB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18906 | hp2 | a0002 | c0003 | t0001 | g0233 | AFR | YRI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18944 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18949 | hp1 | a0002 | c0003 | t0003 | g0221 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18951 | hp1 | a0002 | c0008 | t0001 | g0239 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18953 | hp1 | a0002 | c0003 | t0003 | g0231 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18961 | hp2 | a0001 | c0005 | t0012 | g0047 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18964 | hp1 | a0002 | c0003 | t0003 | g0247 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0280 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0370 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0282 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18974 | hp1 | a0002 | c0009 | t0003 | g0246 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18982 | hp2 | a0002 | c0003 | t0003 | g0223 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18984 | hp2 | a0002 | c0003 | t0003 | g0227 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18987 | hp2 | a0002 | c0003 | t0003 | g0229 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18994 | hp2 | a0002 | c0006 | t0003 | g0267 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0377 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19006 | hp2 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0383 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | LWK | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | LWK | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19056 | hp2 | a0002 | c0009 | t0003 | g0224 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19062 | hp2 | a0002 | c0003 | t0003 | g0225 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19063 | hp2 | a0002 | c0007 | t0001 | g0220 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19064 | hp1 | a0002 | c0003 | t0003 | g0241 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19065 | hp2 | a0002 | c0006 | t0003 | g0268 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19075 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19076 | hp2 | a0006 | c0017 | t0005 | g0272 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19084 | hp2 | a0009 | c0018 | t0005 | g0281 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19085 | hp2 | a0002 | c0008 | t0001 | g0240 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0262 | AFR | YRI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0076 | AFR | ASW | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ASW | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | TSI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0075 | EUR | TSI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0307 | EUR | TSI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | GIH | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20905 | hp2 | a0001 | c0004 | t0001 | g0074 | SAS | GIH | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01123 | hp2 | a0002 | c0003 | t0003 | g0024 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0234 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0259 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0251 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02559 | hp1 | a0002 | c0003 | t0008 | g0038 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02559 | hp2 | a0001 | c0004 | t0001 | g0388 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0077 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0064 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | USA | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0230 | AFR | USA | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18955 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20300 | hp1 | a0001 | c0005 | t0002 | g0173 | AFR | USA | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | USA | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA21309 | hp1 | a0001 | c0004 | t0001 | g0253 | AFR | LWK | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0025 | AFR | LWK | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0329 | REF | REF | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0065 | REF | REF | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37829982
|
G | A | 1 | a0011 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.100G>A | p.Ala34Thr | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/14 | 147/3211 | 100/1839 | 34/612 | chr4 | 37829982 | ||
| chr4:37830097
|
G | A | 1 | a0005 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.215G>A | p.Arg72His | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/14 | 262/3211 | 215/1839 | 72/612 | chr4 | 37830097 | ||
| chr4:37840093
|
A | G | 1 | a0004 | 2 | HG02647.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.553A>G | p.Ile185Val | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/14 | 600/3211 | 553/1839 | 185/612 | chr4 | 37840093 | ||
| chr4:37844412
|
TGGGGTGG others(28): Show |
T | 1 | a0006 | 1 | NA19076.hp2 | frameshift_variant | HIGH | c.771_805delGGTGGGTC others(27): Show |
p.Val258fs | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/14 | 818/3211 | 771/1839 | 257/612 | INFO_REALIGN_3_PRIME | chr4 | 37844412 | |
| chr4:37848522
|
G | T | 1 | a0010 | 1 | HG02970.hp1 | missense_variant&splice_region_variant | MODERATE | c.1283G>T | p.Gly428Val | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/14 | 1330/3211 | 1283/1839 | 428/612 | chr4 | 37848522 | ||
| chr4:37848551
|
A | G | 1 | a0007 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.1312A>G | p.Lys438Glu | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/14 | 1359/3211 | 1312/1839 | 438/612 | chr4 | 37848551 | ||
| chr4:37850235
|
A | C | 1 | a0002 | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
missense_variant | MODERATE | c.1464A>C | p.Glu488Asp | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/14 | 1511/3211 | 1464/1839 | 488/612 | chr4 | 37850235 | ||
| chr4:37855628
|
C | G | 1 | a0003 | 2 | HG02735.hp2 HG03834.hp2 |
missense_variant | MODERATE | c.1623C>G | p.Ser541Arg | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/14 | 1670/3211 | 1623/1839 | 541/612 | chr4 | 37855628 | ||
| chr4:37861527
|
A | G | 1 | a0009 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.1754A>G | p.Lys585Arg | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 1801/3211 | 1754/1839 | 585/612 | chr4 | 37861527 | ||
| chr4:37861583
|
A | G | 1 | a0008 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1810A>G | p.Lys604Glu | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 1857/3211 | 1810/1839 | 604/612 | chr4 | 37861583 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37834680
|
T | C | 10 | a0001c0002a0001c0004a0002c0003others(7): Show | 140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
synonymous_variant | LOW | c.312T>C | p.Ser104Ser | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/14 | 359/3211 | 312/1839 | 104/612 | chr4 | 37834680 | ||
| chr4:37845689
|
C | T | 1 | a0002c0012 | 2 | HG01167.hp2 HG01169.hp1 |
synonymous_variant | LOW | c.966C>T | p.Asp322Asp | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/14 | 1013/3211 | 966/1839 | 322/612 | chr4 | 37845689 | ||
| chr4:37847039
|
G | A | 1 | a0002c0008 | 3 | HG02132.hp2 NA18951.hp1 NA19085.hp2 |
synonymous_variant | LOW | c.1116G>A | p.Thr372Thr | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 9/14 | 1163/3211 | 1116/1839 | 372/612 | chr4 | 37847039 | ||
| chr4:37855721
|
G | C | 5 | a0001c0002a0001c0005a0002c0007others(2): Show | 68 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(65): Show |
synonymous_variant | LOW | c.1716G>C | p.Leu572Leu | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/14 | 1763/3211 | 1716/1839 | 572/612 | chr4 | 37855721 | ||
| chr4:37855727
|
C | T | 1 | a0001c0019 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.1722C>T | p.Ala574Ala | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/14 | 1769/3211 | 1722/1839 | 574/612 | chr4 | 37855727 | ||
| chr4:37855733
|
T | A | 1 | a0002c0009 | 2 | NA18974.hp1 NA19056.hp2 |
synonymous_variant | LOW | c.1728T>A | p.Pro576Pro | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/14 | 1775/3211 | 1728/1839 | 576/612 | chr4 | 37855733 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37826714
|
C | T | 7 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(4): Show | 48 | HG00408.hp1 HG00423.hp1 HG02027.hp1 others(45): Show |
5_prime_UTR_variant | MODIFIER | c.-19C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/14 | 19 | chr4 | 37826714 | |||||
| chr4:37861617
|
G | A | 3 | a0001c0001t0007a0001c0004t0007a0002c0003t0008 | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 5 | chr4 | 37861617 | |||||
| chr4:37861764
|
C | T | 7 | a0001c0001t0002a0001c0002t0002a0001c0005t0002others(4): Show | 57 | HG00733.hp2 HG01069.hp1 HG01167.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*152C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 152 | chr4 | 37861764 | |||||
| chr4:37861835
|
T | G | 3 | a0001c0001t0007a0001c0004t0007a0002c0003t0008 | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*223T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 223 | chr4 | 37861835 | |||||
| chr4:37861904
|
C | T | 1 | a0002c0003t0008 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*292C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 292 | chr4 | 37861904 | |||||
| chr4:37862142
|
G | C | 3 | a0001c0001t0006a0001c0001t0011a0002c0003t0006 | 6 | HG00099.hp1 HG01081.hp2 HG02257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*530G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 530 | chr4 | 37862142 | |||||
| chr4:37862225
|
G | A | 1 | a0001c0002t0009 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*613G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 613 | chr4 | 37862225 | |||||
| chr4:37862244
|
A | G | 3 | a0001c0001t0007a0001c0004t0007a0002c0003t0008 | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*632A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 632 | chr4 | 37862244 | |||||
| chr4:37862326
|
G | A | 14 | a0001c0001t0003a0001c0001t0006a0001c0001t0011others(11): Show | 52 | HG00099.hp1 HG00609.hp2 HG00733.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*714G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 714 | chr4 | 37862326 | |||||
| chr4:37862531
|
A | G | 3 | a0001c0001t0007a0001c0004t0007a0002c0003t0008 | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*919A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 919 | chr4 | 37862531 | |||||
| chr4:37862561
|
C | CTCATAAT others(28): Show |
1 | a0001c0002t0010 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*973_*974insCCCATC others(29): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 974 | INFO_REALIGN_3_PRIME | chr4 | 37862561 | ||||
| chr4:37862685
|
GCCATTA | G | 3 | a0001c0001t0005a0006c0017t0005a0009c0018t0005 | 11 | HG02027.hp1 HG02040.hp1 NA18955.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1074_*1079delCCAT others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 1074 | chr4 | 37862685 | |||||
| chr4:37862794
|
C | T | 3 | a0001c0001t0007a0001c0004t0007a0002c0003t0008 | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1182C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 1182 | chr4 | 37862794 | |||||
| chr4:37862824
|
A | G | 3 | a0001c0001t0007a0001c0004t0007a0002c0003t0008 | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1212A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 1212 | chr4 | 37862824 | |||||
| chr4:37862916
|
A | G | 3 | a0001c0001t0007a0001c0004t0007a0002c0003t0008 | 4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1304A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 1304 | chr4 | 37862916 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37826848
|
C | T | 1 | a0001c0001t0001g0390 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.81+35C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37826848 | ||||||
| chr4:37826887
|
T | C | 1 | a0002c0003t0003g0035 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.81+74T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37826887 | ||||||
| chr4:37826952
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.81+139G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37826952 | ||||||
| chr4:37827100
|
G | A | 1 | a0002c0003t0001g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.81+287G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827100 | ||||||
| chr4:37827121
|
T | C | 1 | a0002c0003t0008g0038 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.81+308T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827121 | ||||||
| chr4:37827139
|
G | T | 1 | a0002c0003t0008g0038 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.81+326G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827139 | ||||||
| chr4:37827208
|
G | C | 1 | a0001c0002t0002g0039 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.81+395G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827208 | ||||||
| chr4:37827510
|
C | T | 1 | a0001c0001t0001g0389 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.81+697C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827510 | ||||||
| chr4:37827551
|
CGTTGTGA others(9): Show |
C | 1 | a0001c0004t0001g0388 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.81+739_81+754delGT others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827551 | ||||||
| chr4:37827608
|
C | T | 1 | a0001c0001t0001g0387 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.81+795C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827608 | ||||||
| chr4:37827621
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.81+808G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827621 | ||||||
| chr4:37827629
|
A | C | 3 | a0001c0002t0001g0040a0002c0003t0003g0035a0002c0003t0008g0038 | 3 | HG01255.hp2 HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.81+816A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827629 | ||||||
| chr4:37827660
|
A | G | 3 | a0001c0002t0001g0040a0002c0003t0003g0035a0002c0003t0008g0038 | 3 | HG01255.hp2 HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.81+847A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827660 | ||||||
| chr4:37827966
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.81+1153G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827966 | ||||||
| chr4:37828348
|
CT | C | 19 | a0001c0001t0001g0058a0001c0001t0004g0006a0001c0001t0004g0015others(16): Show | 22 | HG00408.hp1 HG02293.hp2 HG02897.hp1 others(19): Show |
intron_variant | MODIFIER | c.81+1547delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 37828348 | |||||
| chr4:37828360
|
TA | T | 2 | a0001c0001t0002g0014a0001c0001t0002g0386 | 4 | HG02630.hp2 HG02809.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+1549delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 37828360 | |||||
| chr4:37828637
|
C | G | 1 | a0008c0015t0001g0385 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.82-1327C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828637 | ||||||
| chr4:37828647
|
T | G | 1 | a0001c0002t0002g0059 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.82-1317T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828647 | ||||||
| chr4:37828666
|
A | G | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(326): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.82-1298A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828666 | ||||||
| chr4:37828674
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.82-1290A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828674 | ||||||
| chr4:37828736
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(100): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.82-1228G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828736 | ||||||
| chr4:37828759
|
C | T | 1 | a0001c0001t0001g0384 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.82-1205C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828759 | ||||||
| chr4:37828761
|
A | G | 339 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(336): Show | 391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.82-1203A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828761 | ||||||
| chr4:37828840
|
T | C | 1 | a0002c0003t0001g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82-1124T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828840 | ||||||
| chr4:37828930
|
C | G | 1 | a0001c0001t0001g0383 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.82-1034C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828930 | ||||||
| chr4:37829006
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.82-958G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829006 | ||||||
| chr4:37829049
|
G | T | 1 | a0001c0004t0001g0117 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.82-915G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829049 | ||||||
| chr4:37829185
|
C | CAA | 51 | a0001c0002t0001g0040a0002c0003t0001g0023a0002c0003t0001g0037others(48): Show | 54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.82-770_82-769dupAA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 37829185 | |||||
| chr4:37829235
|
G | A | 1 | a0002c0003t0003g0206 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-729G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829235 | ||||||
| chr4:37829295
|
T | G | 1 | a0002c0003t0008g0038 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.82-669T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829295 | ||||||
| chr4:37829430
|
CA | C | 49 | a0001c0002t0001g0040a0002c0003t0001g0023a0002c0003t0001g0037others(46): Show | 52 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.82-530delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 37829430 | |||||
| chr4:37829435
|
G | T | 49 | a0001c0002t0001g0040a0002c0003t0001g0023a0002c0003t0001g0037others(46): Show | 52 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.82-529G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829435 | ||||||
| chr4:37829647
|
G | A | 51 | a0001c0002t0001g0040a0002c0003t0001g0023a0002c0003t0001g0037others(48): Show | 54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.82-317G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829647 | ||||||
| chr4:37829716
|
T | C | 16 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0044others(13): Show | 19 | HG00408.hp1 HG02293.hp2 NA18942.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-248T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829716 | ||||||
| chr4:37829748
|
G | A | 51 | a0001c0002t0001g0040a0002c0003t0001g0023a0002c0003t0001g0037others(48): Show | 54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.82-216G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829748 | ||||||
| chr4:37829756
|
C | T | 2 | a0001c0001t0001g0381a0001c0001t0001g0382 | 2 | HG00323.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.82-208C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829756 | ||||||
| chr4:37829847
|
C | CAT | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(97): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.82-105_82-104dupTA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 37829847 | |||||
| chr4:37829859
|
T | C | 51 | a0001c0002t0001g0040a0002c0003t0001g0023a0002c0003t0001g0037others(48): Show | 54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.82-105T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829859 | ||||||
| chr4:37829861
|
C | CAT | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG02074.hp1 HG02080.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.82-92_82-91dupAT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 37829861 | |||||
| chr4:37829861
|
C | T | 51 | a0001c0002t0001g0040a0002c0003t0001g0023a0002c0003t0001g0037others(48): Show | 54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.82-103C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829861 | ||||||
| chr4:37829861
|
CAT | C | 9 | a0001c0002t0003g0113a0001c0002t0003g0114a0001c0002t0003g0116others(6): Show | 9 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-92_82-91delAT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 37829861 | |||||
| chr4:37829870
|
A | T | 48 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(45): Show | 51 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.82-94A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829870 | ||||||
| chr4:37829872
|
A | T | 48 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(45): Show | 51 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.82-92A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829872 | ||||||
| chr4:37830198
|
C | A | 1 | a0002c0007t0003g0207 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.249+67C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37830198 | ||||||
| chr4:37830228
|
C | T | 310 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(307): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.249+97C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37830228 | ||||||
| chr4:37830237
|
C | G | 1 | a0002c0006t0003g0380 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.249+106C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37830237 | ||||||
| chr4:37830240
|
G | A | 48 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(45): Show | 51 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.249+109G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37830240 | ||||||
| chr4:37830245
|
A | T | 51 | a0001c0002t0001g0040a0002c0003t0001g0023a0002c0003t0001g0037others(48): Show | 54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.249+114A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37830245 | ||||||
| chr4:37830367
|
A | C | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG02165.hp2 NA18988.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.249+236A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37830367 | ||||||
| chr4:37830919
|
C | T | 1 | a0004c0010t0003g0264 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.249+788C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37830919 | ||||||
| chr4:37831131
|
C | T | 2 | a0001c0001t0001g0378a0001c0001t0001g0379 | 2 | HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.249+1000C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831131 | ||||||
| chr4:37831184
|
C | T | 4 | a0001c0004t0001g0025a0001c0004t0001g0261a0001c0004t0001g0262others(1): Show | 5 | HG02280.hp2 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+1053C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831184 | ||||||
| chr4:37831192
|
C | CA | 60 | a0001c0001t0001g0030a0001c0001t0001g0301a0001c0001t0001g0302others(57): Show | 64 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.249+1082dupA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 37831192 | |||||
| chr4:37831192
|
C | CAAAAAAA | 49 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(46): Show | 59 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.249+1076_249+1082d others(9): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 37831192 | |||||
| chr4:37831192
|
C | CAAAAAAA others(1): Show |
46 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(43): Show | 58 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.249+1075_249+1082d others(10): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 37831192 | |||||
| chr4:37831192
|
C | CAAAAAAA others(2): Show |
7 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(4): Show | 7 | HG00438.hp1 HG00597.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.249+1074_249+1082d others(11): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 37831192 | |||||
| chr4:37831192
|
CA | C | 56 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0292others(53): Show | 61 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.249+1082delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 37831192 | |||||
| chr4:37831438
|
G | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(100): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.249+1307G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831438 | ||||||
| chr4:37831454
|
T | C | 7 | a0002c0003t0003g0208a0002c0003t0003g0209a0002c0003t0003g0210others(4): Show | 7 | HG00609.hp2 HG02040.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+1323T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831454 | ||||||
| chr4:37831491
|
C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(81): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.249+1360C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831491 | ||||||
| chr4:37831538
|
G | C | 1 | a0002c0003t0001g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.249+1407G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831538 | ||||||
| chr4:37831749
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.249+1618C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831749 | ||||||
| chr4:37831839
|
G | A | 51 | a0001c0002t0001g0040a0002c0003t0001g0023a0002c0003t0001g0037others(48): Show | 54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.249+1708G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831839 | ||||||
| chr4:37831855
|
A | G | 1 | a0002c0003t0001g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.249+1724A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831855 | ||||||
| chr4:37831863
|
G | A | 7 | a0001c0001t0004g0015a0001c0001t0004g0046a0001c0001t0004g0048others(4): Show | 8 | HG00408.hp1 HG02293.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+1732G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831863 | ||||||
| chr4:37831968
|
G | C | 1 | a0001c0002t0002g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.249+1837G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831968 | ||||||
| chr4:37832238
|
A | G | 1 | a0001c0001t0001g0375 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.249+2107A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37832238 | ||||||
| chr4:37832311
|
C | T | 2 | a0001c0001t0007g0043a0001c0001t0007g0201 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.249+2180C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37832311 | ||||||
| chr4:37832702
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(94): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.250-1916C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37832702 | ||||||
| chr4:37832844
|
T | C | 53 | a0001c0002t0001g0040a0002c0003t0001g0023a0002c0003t0001g0037others(50): Show | 56 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.250-1774T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37832844 | ||||||
| chr4:37833238
|
G | A | 1 | a0001c0019t0001g0313 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.250-1380G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833238 | ||||||
| chr4:37833305
|
G | A | 1 | a0001c0001t0004g0269 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.250-1313G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833305 | ||||||
| chr4:37833314
|
A | G | 51 | a0001c0002t0001g0040a0002c0003t0001g0023a0002c0003t0001g0037others(48): Show | 54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.250-1304A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833314 | ||||||
| chr4:37833370
|
A | G | 51 | a0001c0002t0001g0040a0002c0003t0001g0023a0002c0003t0001g0037others(48): Show | 54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.250-1248A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833370 | ||||||
| chr4:37833432
|
G | C | 52 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0292others(49): Show | 57 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.250-1186G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833432 | ||||||
| chr4:37833515
|
C | T | 1 | a0001c0001t0001g0374 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.250-1103C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833515 | ||||||
| chr4:37833633
|
A | G | 2 | a0001c0002t0002g0250a0001c0004t0007g0260 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.250-985A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833633 | ||||||
| chr4:37833651
|
A | G | 1 | a0001c0001t0001g0373 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.250-967A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833651 | ||||||
| chr4:37833708
|
G | A | 1 | a0002c0003t0001g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.250-910G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833708 | ||||||
| chr4:37833732
|
G | A | 1 | a0002c0003t0001g0211 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.250-886G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833732 | ||||||
| chr4:37833897
|
C | A | 2 | a0001c0001t0001g0314a0001c0001t0001g0375 | 2 | HG00673.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.250-721C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833897 | ||||||
| chr4:37833902
|
AT | A | 48 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(45): Show | 51 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.250-714delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 37833902 | |||||
| chr4:37834046
|
G | C | 4 | a0002c0003t0006g0213a0002c0007t0002g0212a0002c0007t0002g0214others(1): Show | 4 | HG02257.hp2 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-572G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834046 | ||||||
| chr4:37834180
|
A | T | 1 | a0001c0001t0001g0165 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.250-438A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834180 | ||||||
| chr4:37834201
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.250-417G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834201 | ||||||
| chr4:37834239
|
TA | T | 132 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(129): Show | 139 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.250-378delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834239 | ||||||
| chr4:37834240
|
A | G | 1 | a0002c0003t0003g0245 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.250-378A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834240 | ||||||
| chr4:37834249
|
T | C | 2 | a0002c0012t0002g0299a0002c0012t0002g0300 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.250-369T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834249 | ||||||
| chr4:37834285
|
A | G | 31 | a0001c0001t0001g0029a0001c0001t0001g0292a0001c0001t0001g0294others(28): Show | 35 | HG00408.hp1 HG00438.hp2 HG02083.hp1 others(32): Show |
intron_variant | MODIFIER | c.250-333A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834285 | ||||||
| chr4:37834339
|
GA | G | 71 | a0001c0002t0001g0040a0001c0002t0002g0039a0001c0002t0002g0250others(68): Show | 77 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.250-266delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 37834339 | |||||
| chr4:37834536
|
C | T | 1 | a0002c0003t0001g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.250-82C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834536 | ||||||
| chr4:37834564
|
G | A | 1 | a0001c0002t0002g0250 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.250-54G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834564 | ||||||
| chr4:37834579
|
T | C | 1 | a0001c0002t0002g0066 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.250-39T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834579 | ||||||
| chr4:37834794
|
A | G | 1 | a0002c0007t0003g0207 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.356+70A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37834794 | ||||||
| chr4:37834999
|
A | T | 133 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(130): Show | 140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.356+275A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37834999 | ||||||
| chr4:37835104
|
C | T | 1 | a0002c0008t0001g0244 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.356+380C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835104 | ||||||
| chr4:37835108
|
T | C | 1 | a0005c0014t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.356+384T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835108 | ||||||
| chr4:37835228
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.356+504G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835228 | ||||||
| chr4:37835229
|
T | C | 1 | a0001c0004t0007g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.356+505T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835229 | ||||||
| chr4:37835245
|
T | C | 1 | a0001c0004t0001g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.356+521T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835245 | ||||||
| chr4:37835414
|
A | G | 1 | a0001c0004t0007g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.356+690A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835414 | ||||||
| chr4:37835443
|
A | G | 133 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(130): Show | 140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.356+719A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835443 | ||||||
| chr4:37835510
|
C | T | 1 | a0002c0006t0003g0380 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.356+786C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835510 | ||||||
| chr4:37835596
|
G | A | 133 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(130): Show | 140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.356+872G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835596 | ||||||
| chr4:37835626
|
T | C | 1 | a0001c0001t0001g0009 | 3 | HG00323.hp1 HG01123.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.356+902T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835626 | ||||||
| chr4:37835636
|
G | A | 133 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(130): Show | 140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.356+912G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835636 | ||||||
| chr4:37835774
|
C | T | 5 | a0001c0001t0001g0370a0001c0001t0001g0371a0001c0001t0001g0372others(2): Show | 5 | HG02074.hp2 HG02735.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.356+1050C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835774 | ||||||
| chr4:37835945
|
T | C | 131 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(128): Show | 138 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.356+1221T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835945 | ||||||
| chr4:37836043
|
A | T | 1 | a0001c0002t0002g0059 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.356+1319A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836043 | ||||||
| chr4:37836056
|
G | A | 48 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(45): Show | 51 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.356+1332G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836056 | ||||||
| chr4:37836197
|
G | A | 293 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(290): Show | 327 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.357-1332G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836197 | ||||||
| chr4:37836296
|
C | CT | 3 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312 | 3 | HG02257.hp1 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.357-1232dupT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 37836296 | |||||
| chr4:37836310
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.357-1219G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836310 | ||||||
| chr4:37836426
|
G | A | 58 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0292others(55): Show | 63 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.357-1103G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836426 | ||||||
| chr4:37836513
|
C | T | 35 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0020others(32): Show | 41 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.357-1016C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836513 | ||||||
| chr4:37836514
|
G | C | 9 | a0001c0001t0004g0287a0001c0001t0004g0288a0001c0001t0004g0289others(6): Show | 9 | HG02083.hp1 HG02523.hp1 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.357-1015G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836514 | ||||||
| chr4:37836600
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.357-929C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836600 | ||||||
| chr4:37836615
|
C | T | 133 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(130): Show | 140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.357-914C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836615 | ||||||
| chr4:37836697
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0158a0001c0001t0001g0175 | 4 | NA18948.hp1 NA18970.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.357-832C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836697 | ||||||
| chr4:37836761
|
C | T | 133 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(130): Show | 140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.357-768C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836761 | ||||||
| chr4:37836862
|
G | GGTGTGT | 149 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(146): Show | 172 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.357-652_357-647dup others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 37836862 | |||||
| chr4:37836862
|
G | GGTGTGTG others(1): Show |
78 | a0001c0001t0001g0009a0001c0001t0001g0157a0001c0001t0001g0165others(75): Show | 82 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.357-654_357-647dup others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 37836862 | |||||
| chr4:37836862
|
G | GGTGTGTG others(3): Show |
37 | a0001c0001t0001g0026a0001c0001t0004g0026a0001c0001t0004g0027others(34): Show | 40 | HG00423.hp1 HG01069.hp1 HG02027.hp1 others(37): Show |
intron_variant | MODIFIER | c.357-656_357-647dup others(10): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 37836862 | |||||
| chr4:37836862
|
G | GGTGTGTG others(5): Show |
26 | a0001c0001t0001g0029a0001c0001t0001g0292a0001c0001t0001g0294others(23): Show | 30 | HG00408.hp1 HG00438.hp2 HG02083.hp1 others(27): Show |
intron_variant | MODIFIER | c.357-658_357-647dup others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 37836862 | |||||
| chr4:37836862
|
G | GGTGTGTG others(7): Show |
3 | a0001c0001t0001g0295a0001c0001t0004g0050a0001c0001t0004g0051 | 3 | HG02293.hp2 NA18968.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.357-660_357-647dup others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 37836862 | |||||
| chr4:37836862
|
G | GTGTGTGT others(4): Show |
1 | a0001c0001t0004g0045 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.357-667_357-666ins others(11): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836862 | ||||||
| chr4:37836895
|
G | A | 3 | a0001c0002t0002g0067a0002c0003t0001g0215a0002c0003t0001g0216 | 3 | HG00408.hp2 HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.357-634G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836895 | ||||||
| chr4:37837092
|
C | T | 1 | a0001c0004t0001g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.357-437C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37837092 | ||||||
| chr4:37837110
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.357-419A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37837110 | ||||||
| chr4:37837502
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.357-27T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37837502 | ||||||
| chr4:37837737
|
G | A | 2 | a0002c0003t0001g0217a0002c0003t0001g0218 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.441+124G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37837737 | ||||||
| chr4:37837744
|
A | G | 133 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(130): Show | 140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.441+131A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37837744 | ||||||
| chr4:37837887
|
AT | A | 134 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(131): Show | 141 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.441+285delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 37837887 | |||||
| chr4:37837966
|
C | T | 4 | a0001c0004t0001g0025a0001c0004t0001g0261a0001c0004t0001g0262others(1): Show | 5 | HG02280.hp2 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+353C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37837966 | ||||||
| chr4:37837976
|
G | A | 1 | a0001c0004t0001g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.441+363G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37837976 | ||||||
| chr4:37838139
|
C | T | 3 | a0002c0003t0003g0035a0002c0003t0003g0243a0002c0003t0008g0038 | 3 | HG02129.hp1 HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.441+526C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838139 | ||||||
| chr4:37838148
|
T | G | 1 | a0001c0001t0004g0271 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.441+535T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838148 | ||||||
| chr4:37838173
|
G | A | 2 | a0002c0003t0003g0035a0002c0003t0008g0038 | 2 | HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.441+560G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838173 | ||||||
| chr4:37838251
|
G | A | 1 | a0001c0001t0004g0269 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.441+638G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838251 | ||||||
| chr4:37838399
|
A | G | 2 | a0002c0003t0003g0035a0002c0003t0008g0038 | 2 | HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.441+786A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838399 | ||||||
| chr4:37838547
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.441+934A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838547 | ||||||
| chr4:37838660
|
ACT | A | 52 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0292others(49): Show | 57 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.441+1050_441+1051d others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 37838660 | |||||
| chr4:37838742
|
T | C | 7 | a0001c0002t0002g0060a0001c0002t0002g0068a0001c0002t0002g0069others(4): Show | 7 | NA18949.hp2 NA18954.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-1106T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838742 | ||||||
| chr4:37838780
|
A | G | 9 | a0001c0001t0001g0163a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG00735.hp1 HG01109.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-1068A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838780 | ||||||
| chr4:37838806
|
C | T | 2 | a0002c0003t0001g0217a0002c0003t0001g0218 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.442-1042C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838806 | ||||||
| chr4:37838908
|
G | C | 1 | a0001c0004t0001g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.442-940G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838908 | ||||||
| chr4:37838984
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(99): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.442-864G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838984 | ||||||
| chr4:37839031
|
A | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(99): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.442-817A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839031 | ||||||
| chr4:37839045
|
A | G | 1 | a0008c0015t0001g0385 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.442-803A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839045 | ||||||
| chr4:37839111
|
A | AT | 20 | a0001c0001t0001g0058a0001c0001t0001g0296a0001c0001t0001g0297others(17): Show | 20 | HG01952.hp1 HG01978.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.442-713dupT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 37839111 | |||||
| chr4:37839111
|
AT | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(95): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.442-713delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 37839111 | |||||
| chr4:37839111
|
ATT | A | 15 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0175others(12): Show | 16 | HG00558.hp1 HG01167.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-714_442-713del others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 37839111 | |||||
| chr4:37839111
|
ATTT | A | 119 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(116): Show | 125 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.442-715_442-713del others(3): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 37839111 | |||||
| chr4:37839161
|
C | T | 1 | a0001c0004t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-687C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839161 | ||||||
| chr4:37839249
|
G | A | 1 | a0001c0002t0003g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.442-599G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839249 | ||||||
| chr4:37839250
|
C | T | 1 | a0003c0011t0004g0286 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.442-598C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839250 | ||||||
| chr4:37839262
|
G | C | 138 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(135): Show | 145 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.442-586G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839262 | ||||||
| chr4:37839279
|
A | C | 1 | a0002c0003t0008g0038 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.442-569A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839279 | ||||||
| chr4:37839289
|
A | G | 1 | a0001c0004t0007g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.442-559A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839289 | ||||||
| chr4:37839459
|
G | A | 1 | a0001c0001t0006g0167 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.442-389G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839459 | ||||||
| chr4:37839511
|
T | C | 2 | a0002c0012t0002g0299a0002c0012t0002g0300 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.442-337T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839511 | ||||||
| chr4:37839558
|
G | A | 1 | a0001c0004t0007g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.442-290G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839558 | ||||||
| chr4:37839687
|
A | C | 1 | a0002c0003t0008g0038 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.442-161A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839687 | ||||||
| chr4:37839732
|
A | G | 1 | a0001c0004t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-116A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839732 | ||||||
| chr4:37839808
|
C | T | 138 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(135): Show | 145 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.442-40C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839808 | ||||||
| chr4:37839956
|
C | T | 2 | a0003c0011t0004g0285a0003c0011t0004g0286 | 2 | HG02735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.525+25C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 5/13 | chr4 | 37839956 | ||||||
| chr4:37840041
|
C | T | 2 | a0001c0002t0002g0103a0001c0002t0002g0104 | 2 | NA18747.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.526-25C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 5/13 | chr4 | 37840041 | ||||||
| chr4:37840320
|
T | C | 138 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(135): Show | 145 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.719+61T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840320 | ||||||
| chr4:37840353
|
C | G | 1 | a0001c0002t0002g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.719+94C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840353 | ||||||
| chr4:37840365
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.719+106C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840365 | ||||||
| chr4:37840632
|
A | G | 138 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(135): Show | 145 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.719+373A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840632 | ||||||
| chr4:37840916
|
T | A | 138 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(135): Show | 145 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.719+657T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840916 | ||||||
| chr4:37840947
|
A | AGT | 54 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0292others(51): Show | 60 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.719+705_719+706dup others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37840947 | |||||
| chr4:37840947
|
A | AGTGT | 11 | a0001c0001t0005g0028a0001c0001t0005g0278a0001c0001t0005g0279others(8): Show | 12 | HG02027.hp1 HG02040.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.719+703_719+706dup others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37840947 | |||||
| chr4:37840960
|
G | GTA | 85 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(82): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.719+702_719+703ins others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37840960 | |||||
| chr4:37840960
|
G | GTATA | 11 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(8): Show | 11 | HG01258.hp1 HG01361.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.719+702_719+703ins others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37840960 | |||||
| chr4:37840960
|
G | GTATATA | 3 | a0001c0001t0001g0127a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG00597.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.719+702_719+703ins others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37840960 | |||||
| chr4:37840962
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(99): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.719+703G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840962 | ||||||
| chr4:37840964
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(99): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.719+705G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840964 | ||||||
| chr4:37840964
|
GTA | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(103): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.719+723_719+724del others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37840964 | |||||
| chr4:37840966
|
A | G | 132 | a0001c0001t0004g0049a0001c0002t0001g0040a0001c0002t0001g0092others(129): Show | 139 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.719+707A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840966 | ||||||
| chr4:37840968
|
A | G | 88 | a0001c0001t0001g0374a0001c0002t0001g0040a0001c0002t0001g0092others(85): Show | 92 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(89): Show |
intron_variant | MODIFIER | c.719+709A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840968 | ||||||
| chr4:37840970
|
A | G | 1 | a0001c0004t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.719+711A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840970 | ||||||
| chr4:37840982
|
A | G | 136 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(133): Show | 143 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.719+723A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840982 | ||||||
| chr4:37841039
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.719+780A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841039 | ||||||
| chr4:37841070
|
G | A | 2 | a0002c0008t0001g0239a0002c0008t0001g0240 | 2 | NA18951.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.719+811G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841070 | ||||||
| chr4:37841071
|
C | CGT | 3 | a0001c0001t0001g0296a0001c0001t0001g0298a0001c0001t0001g0383 | 3 | HG02165.hp2 NA18989.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.719+813_719+814dup others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841071 | |||||
| chr4:37841072
|
G | GTATATAT others(1): Show |
5 | a0001c0001t0001g0030a0001c0001t0001g0305a0001c0001t0001g0306others(2): Show | 6 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.719+835_719+842dup others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841072
|
G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0034a0001c0001t0001g0301 | 3 | HG00280.hp1 NA18940.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.719+833_719+842dup others(10): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841072
|
G | GTATATAT others(5): Show |
4 | a0001c0001t0001g0311a0001c0001t0001g0315a0001c0001t0001g0359others(1): Show | 4 | HG00621.hp1 HG02257.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.719+831_719+842dup others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841072
|
G | GTATATAT others(7): Show |
10 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0353others(7): Show | 10 | HG03139.hp2 HG03239.hp1 HG03579.hp1 others(7): Show |
intron_variant | MODIFIER | c.719+829_719+842dup others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841072
|
G | GTATATAT others(9): Show |
13 | a0001c0001t0001g0012a0001c0001t0001g0316a0001c0001t0001g0317others(10): Show | 15 | HG00544.hp2 HG01074.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.719+827_719+842dup others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841072
|
G | GTATATAT others(11): Show |
15 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0058others(12): Show | 19 | HG00673.hp1 HG00673.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.719+825_719+842dup others(18): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841072
|
G | GTATATAT others(13): Show |
11 | a0001c0001t0001g0011a0001c0001t0001g0327a0001c0001t0001g0328others(8): Show | 13 | HG01516.hp2 NA18968.hp1 NA18983.hp2 others(10): Show |
intron_variant | MODIFIER | c.719+823_719+842dup others(20): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841072
|
G | GTATATAT others(15): Show |
5 | a0001c0001t0001g0033a0001c0001t0001g0303a0001c0001t0001g0325others(2): Show | 6 | HG00140.hp1 HG01167.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.719+821_719+842dup others(22): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841072
|
G | GTATATAT others(17): Show |
6 | a0001c0001t0001g0032a0001c0001t0001g0323a0001c0001t0001g0324others(3): Show | 7 | HG01169.hp1 HG02273.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.719+819_719+842dup others(24): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841072
|
G | GTATATAT others(19): Show |
2 | a0001c0001t0001g0320a0001c0001t0001g0321 | 2 | HG02300.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.719+817_719+842dup others(26): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841072
|
G | GTATATAT others(23): Show |
1 | a0001c0001t0001g0318 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.719+842_719+843ins others(30): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841072
|
G | GTATATAT others(27): Show |
1 | a0001c0001t0001g0372 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.719+842_719+843ins others(34): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841072
|
GTA | G | 46 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0178others(43): Show | 51 | HG00423.hp1 HG00438.hp2 HG02027.hp1 others(48): Show |
intron_variant | MODIFIER | c.719+841_719+842del others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841072
|
GTATA | G | 20 | a0001c0001t0001g0020a0001c0001t0001g0160a0001c0001t0001g0163others(17): Show | 21 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.719+839_719+842del others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841072
|
GTATATA | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(67): Show | 89 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.719+837_719+842del others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841072
|
GTATATAT others(1): Show |
G | 12 | a0001c0001t0001g0008a0001c0001t0001g0125a0001c0001t0001g0126others(9): Show | 14 | NA18939.hp1 NA18947.hp2 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.719+835_719+842del others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | |||||
| chr4:37841084
|
A | G | 1 | a0002c0006t0003g0380 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.719+825A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841084 | ||||||
| chr4:37841094
|
A | ATGTG | 52 | a0001c0002t0001g0092a0001c0002t0001g0251a0001c0002t0002g0042others(49): Show | 53 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.719+836_719+837ins others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841094 | |||||
| chr4:37841094
|
A | G | 2 | a0001c0002t0002g0101a0001c0002t0002g0102 | 2 | HG01361.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.719+835A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841094 | ||||||
| chr4:37841096
|
A | ATGTGTG | 3 | a0001c0002t0002g0068a0001c0002t0009g0112a0001c0004t0001g0110 | 3 | HG02965.hp2 HG03130.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.719+838_719+839ins others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841096 | |||||
| chr4:37841096
|
A | G | 56 | a0001c0002t0001g0092a0001c0002t0001g0251a0001c0002t0002g0042others(53): Show | 57 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.719+837A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841096 | ||||||
| chr4:37841098
|
A | ATGTGTGT others(1): Show |
5 | a0001c0002t0001g0040a0001c0002t0003g0259a0001c0004t0001g0025others(2): Show | 6 | HG01255.hp2 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.719+840_719+841ins others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841098 | |||||
| chr4:37841098
|
A | ATGTGTGT others(3): Show |
2 | a0001c0002t0002g0039a0001c0004t0001g0252 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.719+840_719+841ins others(10): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841098 | |||||
| chr4:37841098
|
A | G | 74 | a0001c0001t0001g0018a0001c0001t0001g0120a0001c0001t0001g0123others(71): Show | 76 | HG00621.hp2 HG00639.hp2 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.719+839A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841098 | ||||||
| chr4:37841100
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0031 | 2 | NA18964.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.719+842_719+843ins others(32): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATAT others(21): Show |
2 | a0001c0001t0001g0319a0002c0003t0003g0206 | 2 | HG01975.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.719+842_719+843ins others(28): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0322 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.719+842_719+843ins others(26): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0308 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.719+842_719+843ins others(24): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0332a0001c0001t0004g0051 | 2 | HG01106.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.719+842_719+843ins others(20): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATAT others(11): Show |
10 | a0001c0001t0001g0302a0001c0001t0001g0340a0001c0001t0001g0341others(7): Show | 11 | HG00609.hp2 HG00733.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.719+842_719+843ins others(18): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATAT others(9): Show |
9 | a0001c0001t0001g0003a0001c0001t0001g0314a0001c0001t0001g0352others(6): Show | 13 | HG00609.hp1 HG02293.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.719+842_719+843ins others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATAT others(7): Show |
18 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0003g0024others(15): Show | 20 | HG00597.hp1 HG01123.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.719+842_719+843ins others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATAT others(9): Show |
3 | a0002c0003t0003g0221a0002c0003t0003g0222a0002c0003t0003g0223 | 3 | HG02015.hp2 NA18949.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.719+842_719+843ins others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATAT others(5): Show |
1 | a0002c0003t0003g0243 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.719+842_719+843ins others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATAT others(7): Show |
1 | a0002c0003t0001g0216 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.719+842_719+843ins others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATAT others(3): Show |
2 | a0002c0003t0001g0230a0002c0008t0001g0239 | 2 | HG06807.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.719+842_719+843ins others(10): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATAT others(1): Show |
3 | a0002c0003t0001g0232a0002c0008t0001g0240a0002c0008t0001g0244 | 3 | HG02132.hp2 HG03516.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.719+842_719+843ins others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATAT others(3): Show |
1 | a0002c0003t0003g0231 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.719+842_719+843ins others(10): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATG | 9 | a0002c0003t0001g0204a0002c0003t0001g0217a0002c0003t0001g0218others(6): Show | 9 | HG01106.hp2 HG01192.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.719+842_719+843ins others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATGT others(1): Show |
5 | a0002c0003t0001g0211a0002c0003t0003g0248a0002c0007t0002g0212others(2): Show | 5 | HG02615.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.719+842_719+843ins others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATATGT others(9): Show |
1 | a0001c0004t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.719+842_719+843ins others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATGTGT others(5): Show |
1 | a0002c0003t0003g0035 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.719+842_719+843ins others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATATGTGT others(7): Show |
1 | a0011c0013t0003g0249 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.719+842_719+843ins others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATGTGTGT others(5): Show |
7 | a0001c0002t0002g0256a0001c0004t0001g0005a0001c0004t0001g0255others(4): Show | 9 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.719+845_719+856dup others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | ATGTGTGT others(7): Show |
1 | a0001c0004t0001g0254 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.719+843_719+856dup others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | |||||
| chr4:37841100
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(226): Show | 258 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.719+841A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841100 | ||||||
| chr4:37841102
|
G | A | 4 | a0001c0001t0001g0301a0001c0001t0001g0305a0001c0001t0001g0309others(1): Show | 4 | HG01934.hp1 HG02258.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.719+843G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841102 | ||||||
| chr4:37841104
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.719+845G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841104 | ||||||
| chr4:37841116
|
T | G | 2 | a0001c0002t0002g0250a0001c0004t0007g0260 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.719+857T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841116 | ||||||
| chr4:37841143
|
C | T | 1 | a0005c0014t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.719+884C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841143 | ||||||
| chr4:37841158
|
T | TGTGTGTG others(10): Show |
1 | a0008c0015t0001g0385 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.719+899_719+900ins others(17): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841158 | ||||||
| chr4:37841158
|
T | TGTGTGTG others(12): Show |
1 | a0004c0010t0003g0264 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.719+899_719+900ins others(19): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841158 | ||||||
| chr4:37841158
|
T | TTGTG | 3 | a0001c0001t0001g0179a0001c0001t0001g0183a0007c0020t0001g0369 | 3 | HG01074.hp2 HG03491.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.719+926_719+929dup others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | |||||
| chr4:37841158
|
T | TTGTGTGT others(1): Show |
35 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 43 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.719+922_719+929dup others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | |||||
| chr4:37841158
|
T | TTGTGTGT others(3): Show |
51 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0017others(48): Show | 61 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.719+920_719+929dup others(10): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | |||||
| chr4:37841158
|
T | TTGTGTGT others(5): Show |
17 | a0001c0001t0001g0008a0001c0001t0001g0126a0001c0001t0001g0131others(14): Show | 19 | HG00558.hp1 HG01106.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.719+918_719+929dup others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | |||||
| chr4:37841158
|
T | TTGTGTGT others(7): Show |
42 | a0001c0001t0001g0145a0001c0001t0001g0174a0001c0001t0002g0014others(39): Show | 47 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.719+916_719+929dup others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | |||||
| chr4:37841158
|
T | TTGTGTGT others(9): Show |
5 | a0001c0001t0001g0155a0002c0003t0001g0216a0002c0003t0001g0217others(2): Show | 5 | HG00408.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.719+914_719+929dup others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | |||||
| chr4:37841158
|
T | TTGTGTGT others(11): Show |
1 | a0002c0003t0003g0210 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.719+912_719+929dup others(18): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | |||||
| chr4:37841158
|
TTGTG | T | 52 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0292others(49): Show | 57 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.719+926_719+929del others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | |||||
| chr4:37841173
|
T | TGTGTGTG others(7): Show |
1 | a0002c0006t0003g0266 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.719+927_719+928ins others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841173 | |||||
| chr4:37841188
|
G | GTGTGTGT others(2): Show |
5 | a0001c0002t0002g0078a0001c0002t0002g0101a0001c0002t0002g0250others(2): Show | 5 | HG00733.hp2 HG02055.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.719+929_719+930ins others(9): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841188 | ||||||
| chr4:37841188
|
G | GTGTGTGT others(4): Show |
2 | a0001c0004t0001g0110a0011c0013t0003g0249 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.719+929_719+930ins others(11): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841188 | ||||||
| chr4:37841188
|
G | GTGTGTGT others(6): Show |
33 | a0001c0002t0001g0251a0001c0002t0002g0063a0001c0002t0002g0067others(30): Show | 36 | HG01069.hp1 HG01361.hp1 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.719+929_719+930ins others(13): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841188 | ||||||
| chr4:37841188
|
G | GTGTGTGT others(8): Show |
18 | a0001c0002t0001g0092a0001c0002t0002g0039a0001c0002t0002g0066others(15): Show | 19 | HG00639.hp2 HG01168.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.719+929_719+930ins others(15): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841188 | ||||||
| chr4:37841188
|
G | GTGTGTGT others(10): Show |
15 | a0001c0002t0002g0042a0001c0002t0002g0059a0001c0002t0002g0070others(12): Show | 15 | HG00738.hp1 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.719+929_719+930ins others(17): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841188 | ||||||
| chr4:37841188
|
G | GTGTGTGT others(12): Show |
6 | a0001c0002t0002g0060a0001c0002t0002g0061a0001c0002t0002g0062others(3): Show | 6 | HG01981.hp2 NA19000.hp1 NA19066.hp1 others(3): Show |
intron_variant | MODIFIER | c.719+929_719+930ins others(19): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841188 | ||||||
| chr4:37841189
|
G | T | 4 | a0001c0002t0002g0064a0001c0002t0003g0077a0004c0010t0003g0264others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.719+930G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841189 | ||||||
| chr4:37841190
|
T | G | 4 | a0001c0002t0002g0064a0001c0002t0003g0077a0004c0010t0003g0264others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.719+931T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841190 | ||||||
| chr4:37841190
|
T | TG | 82 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(79): Show | 86 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.719+931_719+932ins others(1): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841190 | ||||||
| chr4:37841191
|
T | G | 1 | a0001c0004t0001g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.719+932T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841191 | ||||||
| chr4:37841192
|
T | G | 86 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(83): Show | 90 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.719+933T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841192 | ||||||
| chr4:37841202
|
A | G | 87 | a0001c0002t0001g0040a0001c0002t0001g0092a0001c0002t0001g0251others(84): Show | 91 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.719+943A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841202 | ||||||
| chr4:37841318
|
G | A | 48 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0292others(45): Show | 53 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.719+1059G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841318 | ||||||
| chr4:37841334
|
A | G | 1 | a0002c0003t0003g0248 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.719+1075A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841334 | ||||||
| chr4:37841401
|
T | G | 53 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(50): Show | 56 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.719+1142T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841401 | ||||||
| chr4:37841540
|
G | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(292): Show | 329 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.719+1281G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841540 | ||||||
| chr4:37841646
|
C | T | 57 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(54): Show | 60 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.719+1387C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841646 | ||||||
| chr4:37841771
|
A | G | 1 | a0002c0003t0001g0236 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.719+1512A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841771 | ||||||
| chr4:37841815
|
T | G | 1 | a0001c0004t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.719+1556T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841815 | ||||||
| chr4:37841841
|
C | T | 1 | a0001c0001t0004g0048 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.719+1582C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841841 | ||||||
| chr4:37841848
|
G | C | 1 | a0001c0001t0005g0278 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.719+1589G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841848 | ||||||
| chr4:37841851
|
C | T | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.719+1592C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841851 | ||||||
| chr4:37842064
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.719+1805G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842064 | ||||||
| chr4:37842090
|
T | C | 2 | a0002c0003t0003g0035a0002c0003t0008g0038 | 2 | HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.719+1831T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842090 | ||||||
| chr4:37842106
|
T | A | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.719+1847T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842106 | ||||||
| chr4:37842197
|
T | G | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.719+1938T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842197 | ||||||
| chr4:37842199
|
CTATA | C | 54 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(51): Show | 57 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.719+1947_719+1950d others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37842199 | |||||
| chr4:37842199
|
CTATATA | C | 4 | a0002c0003t0003g0035a0002c0003t0008g0038a0002c0012t0002g0299others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.719+1945_719+1950d others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37842199 | |||||
| chr4:37842211
|
A | T | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.719+1952A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842211 | ||||||
| chr4:37842251
|
C | T | 294 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(291): Show | 328 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.719+1992C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842251 | ||||||
| chr4:37842332
|
A | G | 2 | a0002c0012t0002g0299a0002c0012t0002g0300 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.720-2032A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842332 | ||||||
| chr4:37842374
|
TA | T | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-1989delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842374 | ||||||
| chr4:37842520
|
G | C | 1 | a0002c0003t0001g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.720-1844G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842520 | ||||||
| chr4:37842556
|
TTC | T | 58 | a0001c0001t0001g0154a0001c0001t0004g0053a0001c0002t0001g0092others(55): Show | 59 | HG00639.hp2 HG00733.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.720-1806_720-1805d others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37842556 | |||||
| chr4:37842557
|
TC | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(174): Show | 206 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.720-1806delC | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842557 | ||||||
| chr4:37842558
|
C | T | 65 | a0001c0001t0001g0305a0001c0001t0001g0309a0001c0001t0001g0310others(62): Show | 69 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.720-1806C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842558 | ||||||
| chr4:37842605
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.720-1759A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842605 | ||||||
| chr4:37842668
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.720-1696C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842668 | ||||||
| chr4:37842668
|
CT | C | 293 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(290): Show | 327 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.720-1686delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37842668 | |||||
| chr4:37842669
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.720-1695T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842669 | ||||||
| chr4:37842687
|
T | G | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-1677T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842687 | ||||||
| chr4:37842731
|
G | T | 1 | a0001c0001t0001g0383 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.720-1633G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842731 | ||||||
| chr4:37842773
|
G | C | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-1591G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842773 | ||||||
| chr4:37842883
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(99): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.720-1481G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842883 | ||||||
| chr4:37842958
|
C | T | 3 | a0001c0002t0002g0075a0001c0002t0002g0076a0001c0002t0002g0106 | 3 | HG01069.hp1 NA20129.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.720-1406C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842958 | ||||||
| chr4:37842983
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(99): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.720-1381C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842983 | ||||||
| chr4:37843120
|
A | C | 2 | a0002c0012t0002g0299a0002c0012t0002g0300 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.720-1244A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843120 | ||||||
| chr4:37843121
|
C | T | 2 | a0002c0012t0002g0299a0002c0012t0002g0300 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.720-1243C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843121 | ||||||
| chr4:37843229
|
T | C | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-1135T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843229 | ||||||
| chr4:37843257
|
G | A | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-1107G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843257 | ||||||
| chr4:37843315
|
T | C | 1 | a0001c0001t0001g0340 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.720-1049T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843315 | ||||||
| chr4:37843368
|
T | G | 1 | a0001c0001t0001g0165 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.720-996T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843368 | ||||||
| chr4:37843422
|
A | C | 4 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(1): Show | 4 | HG02165.hp2 NA18988.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.720-942A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843422 | ||||||
| chr4:37843578
|
C | A | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-786C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843578 | ||||||
| chr4:37843591
|
T | C | 4 | a0002c0003t0001g0217a0002c0003t0001g0218a0002c0003t0001g0235others(1): Show | 4 | HG01106.hp2 HG01192.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.720-773T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843591 | ||||||
| chr4:37843610
|
A | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0143a0001c0001t0001g0193others(1): Show | 4 | HG01943.hp1 HG01975.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.720-754A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843610 | ||||||
| chr4:37843612
|
T | TA | 56 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(53): Show | 59 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.720-752_720-751ins others(1): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843612 | ||||||
| chr4:37843613
|
T | A | 32 | a0001c0001t0001g0029a0001c0001t0001g0292a0001c0001t0001g0294others(29): Show | 36 | HG00408.hp1 HG00438.hp2 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.720-751T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843613 | ||||||
| chr4:37843615
|
T | A | 2 | a0002c0003t0008g0038a0002c0006t0003g0380 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.720-749T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843615 | ||||||
| chr4:37843632
|
G | A | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-732G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843632 | ||||||
| chr4:37843679
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | HG02074.hp1 HG02080.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.720-685G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843679 | ||||||
| chr4:37843845
|
A | G | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-519A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843845 | ||||||
| chr4:37843881
|
T | C | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.720-483T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843881 | ||||||
| chr4:37843967
|
G | A | 4 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(1): Show | 4 | HG02165.hp2 NA18988.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.720-397G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843967 | ||||||
| chr4:37844010
|
A | G | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-354A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37844010 | ||||||
| chr4:37844026
|
C | T | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-338C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37844026 | ||||||
| chr4:37844056
|
G | A | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-308G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37844056 | ||||||
| chr4:37844069
|
T | C | 1 | a0001c0001t0001g0314 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.720-295T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37844069 | ||||||
| chr4:37844212
|
A | AAT | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(100): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.720-143_720-142dup others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37844212 | |||||
| chr4:37844290
|
A | T | 2 | a0002c0012t0002g0299a0002c0012t0002g0300 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.720-74A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37844290 | ||||||
| chr4:37844558
|
C | A | 1 | a0001c0001t0001g0346 | 1 | NA18971.hp2 | splice_region_variant&intron_variant | LOW | c.909+5C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37844558 | ||||||
| chr4:37844682
|
G | A | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.909+129G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37844682 | ||||||
| chr4:37844684
|
T | A | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.909+131T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37844684 | ||||||
| chr4:37844699
|
G | A | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.909+146G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37844699 | ||||||
| chr4:37844874
|
G | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(292): Show | 329 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.909+321G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37844874 | ||||||
| chr4:37844969
|
T | C | 296 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(293): Show | 330 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.909+416T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37844969 | ||||||
| chr4:37844975
|
C | CA | 15 | a0001c0001t0001g0205a0001c0001t0001g0333a0001c0001t0001g0376others(12): Show | 15 | HG01255.hp2 HG01516.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.909+442dupA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr4 | 37844975 | |||||
| chr4:37844975
|
CA | C | 161 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(158): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.909+442delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr4 | 37844975 | |||||
| chr4:37844988
|
A | C | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.909+435A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37844988 | ||||||
| chr4:37845016
|
T | C | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.909+463T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37845016 | ||||||
| chr4:37845022
|
T | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(181): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.909+469T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37845022 | ||||||
| chr4:37845130
|
G | A | 1 | a0001c0001t0001g0361 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.910-503G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37845130 | ||||||
| chr4:37845218
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.910-415G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37845218 | ||||||
| chr4:37845318
|
A | C | 25 | a0001c0001t0001g0029a0001c0001t0001g0292a0001c0001t0001g0294others(22): Show | 29 | HG00408.hp1 HG00438.hp2 HG03654.hp1 others(26): Show |
intron_variant | MODIFIER | c.910-315A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37845318 | ||||||
| chr4:37845589
|
C | G | 1 | a0001c0002t0002g0078 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.910-44C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37845589 | ||||||
| chr4:37845849
|
G | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1007+119G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37845849 | ||||||
| chr4:37845909
|
TG | T | 54 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(51): Show | 57 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1007+185delG | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 37845909 | |||||
| chr4:37845923
|
G | A | 4 | a0001c0001t0001g0327a0001c0001t0001g0347a0001c0001t0001g0348others(1): Show | 4 | NA18950.hp1 NA18956.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007+193G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37845923 | ||||||
| chr4:37846040
|
A | T | 1 | a0001c0004t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1007+310A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846040 | ||||||
| chr4:37846076
|
T | C | 2 | a0001c0002t0002g0250a0001c0004t0007g0260 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1007+346T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846076 | ||||||
| chr4:37846206
|
T | C | 50 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(47): Show | 53 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1007+476T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846206 | ||||||
| chr4:37846214
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1007+484G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846214 | ||||||
| chr4:37846321
|
GA | G | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1007+594delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 37846321 | |||||
| chr4:37846399
|
C | T | 2 | a0001c0001t0007g0043a0001c0001t0007g0201 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1008-532C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846399 | ||||||
| chr4:37846464
|
T | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(100): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1008-467T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846464 | ||||||
| chr4:37846677
|
C | T | 47 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0292others(44): Show | 52 | HG00408.hp1 HG00438.hp2 HG02027.hp1 others(49): Show |
intron_variant | MODIFIER | c.1008-254C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846677 | ||||||
| chr4:37846834
|
T | G | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1008-97T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846834 | ||||||
| chr4:37846846
|
T | C | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1008-85T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846846 | ||||||
| chr4:37846909
|
T | G | 79 | a0001c0001t0005g0280a0001c0002t0001g0092a0001c0002t0001g0251others(76): Show | 82 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.1008-22T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846909 | ||||||
| chr4:37846914
|
T | G | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1008-17T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846914 | ||||||
| chr4:37847328
|
C | T | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1282+33C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847328 | ||||||
| chr4:37847383
|
C | T | 54 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(51): Show | 57 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1282+88C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847383 | ||||||
| chr4:37847392
|
T | G | 1 | a0001c0001t0001g0145 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1282+97T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847392 | ||||||
| chr4:37847424
|
C | G | 1 | a0001c0001t0001g0319 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1282+129C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847424 | ||||||
| chr4:37847488
|
T | C | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1282+193T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847488 | ||||||
| chr4:37847548
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1282+253G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847548 | ||||||
| chr4:37847675
|
G | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(182): Show | 211 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.1282+380G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847675 | ||||||
| chr4:37847731
|
TACTC | T | 4 | a0002c0003t0003g0035a0002c0003t0008g0038a0002c0012t0002g0299others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282+439_1282+442d others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 37847731 | |||||
| chr4:37847761
|
C | A | 1 | a0002c0003t0003g0231 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1282+466C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847761 | ||||||
| chr4:37847889
|
T | C | 4 | a0001c0002t0002g0080a0001c0002t0002g0081a0001c0002t0002g0109others(1): Show | 4 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282+594T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847889 | ||||||
| chr4:37848034
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1283-488G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37848034 | ||||||
| chr4:37848034
|
G | T | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1283-488G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37848034 | ||||||
| chr4:37848045
|
A | G | 2 | a0001c0002t0002g0087a0001c0002t0002g0088 | 2 | NA18945.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1283-477A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37848045 | ||||||
| chr4:37848249
|
G | C | 1 | a0001c0001t0006g0167 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1283-273G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37848249 | ||||||
| chr4:37848268
|
G | A | 1 | a0002c0006t0003g0380 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1283-254G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37848268 | ||||||
| chr4:37848402
|
A | G | 1 | a0002c0006t0003g0380 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1283-120A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37848402 | ||||||
| chr4:37848421
|
G | A | 1 | a0001c0001t0001g0328 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1283-101G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37848421 | ||||||
| chr4:37848691
|
TG | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(99): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1412+41delG | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37848691 | ||||||
| chr4:37848780
|
T | C | 82 | a0001c0002t0001g0092a0001c0002t0001g0251a0001c0002t0002g0039others(79): Show | 86 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.1412+129T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37848780 | ||||||
| chr4:37848846
|
G | A | 1 | a0002c0003t0003g0035 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1412+195G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37848846 | ||||||
| chr4:37849070
|
C | CA | 15 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0001t0001g0184others(12): Show | 15 | HG01255.hp2 HG01261.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1412+437dupA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849070 | |||||
| chr4:37849070
|
C | CAAAAAAA others(294): Show |
2 | a0002c0012t0002g0299a0002c0012t0002g0300 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1412+433_1412+434i others(303): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849070 | |||||
| chr4:37849070
|
CA | C | 14 | a0001c0001t0001g0007a0001c0001t0001g0058a0001c0001t0001g0119others(11): Show | 16 | HG00558.hp1 HG01884.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.1412+437delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849070 | |||||
| chr4:37849070
|
CAA | C | 53 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(50): Show | 56 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1412+436_1412+437d others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849070 | |||||
| chr4:37849088
|
A | T | 2 | a0001c0002t0003g0114a0001c0002t0003g0116 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1412+437A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849088 | ||||||
| chr4:37849091
|
T | A | 1 | a0006c0017t0005g0272 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1412+440T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849091 | ||||||
| chr4:37849133
|
A | G | 1 | a0002c0006t0003g0380 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1412+482A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849133 | ||||||
| chr4:37849154
|
G | A | 7 | a0001c0002t0002g0250a0001c0004t0007g0260a0002c0003t0003g0035others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412+503G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849154 | ||||||
| chr4:37849210
|
G | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(291): Show | 328 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.1412+559G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849210 | ||||||
| chr4:37849264
|
C | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(240): Show | 272 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1412+613C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849264 | ||||||
| chr4:37849309
|
A | G | 2 | a0002c0003t0003g0035a0002c0003t0008g0038 | 2 | HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1412+658A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849309 | ||||||
| chr4:37849310
|
G | T | 392 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(389): Show | 445 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(442): Show |
intron_variant | MODIFIER | c.1412+659G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849310 | ||||||
| chr4:37849324
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1412+673G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849324 | ||||||
| chr4:37849404
|
C | CT | 22 | a0001c0001t0001g0120a0001c0001t0001g0301a0001c0001t0001g0321others(19): Show | 22 | HG00544.hp2 HG01255.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1413-754dupT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849404 | |||||
| chr4:37849404
|
CT | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(175): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1413-754delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849404 | |||||
| chr4:37849404
|
CTT | C | 11 | a0001c0001t0001g0131a0001c0001t0001g0143a0001c0001t0001g0176others(8): Show | 11 | HG00558.hp1 HG01069.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1413-755_1413-754d others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849404 | |||||
| chr4:37849404
|
CTTTTT | C | 55 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(52): Show | 58 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1413-758_1413-754d others(7): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849404 | |||||
| chr4:37849405
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1412+754T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849405 | ||||||
| chr4:37849468
|
G | A | 1 | a0001c0002t0010g0115 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1413-716G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849468 | ||||||
| chr4:37849504
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1413-680T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849504 | ||||||
| chr4:37849624
|
G | T | 2 | a0001c0001t0001g0317a0001c0001t0001g0377 | 2 | NA18995.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1413-560G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849624 | ||||||
| chr4:37849632
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1413-552C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849632 | ||||||
| chr4:37849687
|
G | A | 54 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(51): Show | 57 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1413-497G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849687 | ||||||
| chr4:37849689
|
G | A | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1413-495G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849689 | ||||||
| chr4:37849710
|
A | G | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1413-474A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849710 | ||||||
| chr4:37849769
|
C | T | 47 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0292others(44): Show | 52 | HG00408.hp1 HG00438.hp2 HG02027.hp1 others(49): Show |
intron_variant | MODIFIER | c.1413-415C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849769 | ||||||
| chr4:37849785
|
T | C | 1 | a0001c0001t0001g0387 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1413-399T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849785 | ||||||
| chr4:37849823
|
G | A | 62 | a0001c0004t0001g0025a0001c0004t0001g0261a0001c0004t0001g0262others(59): Show | 66 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1413-361G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849823 | ||||||
| chr4:37849843
|
A | G | 2 | a0001c0002t0002g0250a0001c0004t0007g0260 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1413-341A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849843 | ||||||
| chr4:37849948
|
C | T | 1 | a0001c0004t0007g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1413-236C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849948 | ||||||
| chr4:37849949
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1413-235G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849949 | ||||||
| chr4:37849971
|
A | G | 1 | a0001c0001t0001g0367 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1413-213A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849971 | ||||||
| chr4:37850003
|
G | C | 1 | a0005c0014t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1413-181G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37850003 | ||||||
| chr4:37850010
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1413-174A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37850010 | ||||||
| chr4:37850522
|
C | T | 47 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0292others(44): Show | 52 | HG00408.hp1 HG00438.hp2 HG02027.hp1 others(49): Show |
intron_variant | MODIFIER | c.1602+149C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850522 | ||||||
| chr4:37850523
|
G | A | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1602+150G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850523 | ||||||
| chr4:37850618
|
C | T | 1 | a0001c0001t0006g0133 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1602+245C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850618 | ||||||
| chr4:37850680
|
G | A | 243 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(240): Show | 272 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1602+307G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850680 | ||||||
| chr4:37850701
|
C | T | 58 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(55): Show | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1602+328C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850701 | ||||||
| chr4:37850705
|
A | G | 55 | a0001c0001t0001g0296a0002c0003t0001g0023a0002c0003t0001g0037others(52): Show | 58 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1602+332A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850705 | ||||||
| chr4:37850868
|
A | G | 3 | a0001c0001t0001g0306a0001c0001t0001g0384a0002c0006t0003g0380 | 3 | HG01109.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1602+495A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850868 | ||||||
| chr4:37850886
|
G | A | 1 | a0001c0004t0001g0257 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1602+513G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850886 | ||||||
| chr4:37850889
|
C | G | 294 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(291): Show | 328 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.1602+516C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850889 | ||||||
| chr4:37850916
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(241): Show | 273 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.1602+543A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850916 | ||||||
| chr4:37850943
|
A | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(99): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1602+570A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850943 | ||||||
| chr4:37850990
|
C | CA | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1602+636dupA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37850990 | |||||
| chr4:37850990
|
C | CAA | 82 | a0001c0001t0001g0121a0001c0001t0001g0331a0001c0001t0005g0282others(79): Show | 86 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.1602+635_1602+636d others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37850990 | |||||
| chr4:37850990
|
C | CAAA | 53 | a0001c0002t0002g0090a0002c0003t0001g0023a0002c0003t0001g0037others(50): Show | 56 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1602+634_1602+636d others(5): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37850990 | |||||
| chr4:37851135
|
T | C | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1602+762T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851135 | ||||||
| chr4:37851470
|
G | T | 2 | a0001c0002t0002g0250a0001c0004t0007g0260 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1602+1097G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851470 | ||||||
| chr4:37851487
|
T | TCA | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1114_1602+111 others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851487 | ||||||
| chr4:37851488
|
T | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1115T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851488 | ||||||
| chr4:37851537
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1602+1164G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851537 | ||||||
| chr4:37851551
|
T | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1178T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851551 | ||||||
| chr4:37851622
|
C | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1249C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851622 | ||||||
| chr4:37851647
|
T | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1274T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851647 | ||||||
| chr4:37851664
|
G | A | 1 | a0002c0003t0001g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1602+1291G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851664 | ||||||
| chr4:37851665
|
T | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1292T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851665 | ||||||
| chr4:37851754
|
T | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1381T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851754 | ||||||
| chr4:37851771
|
C | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1398C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851771 | ||||||
| chr4:37851786
|
A | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1413A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851786 | ||||||
| chr4:37851936
|
A | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1563A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851936 | ||||||
| chr4:37851961
|
G | GTTTTCTT others(4): Show |
3 | a0001c0001t0001g0123a0001c0001t0001g0176a0001c0001t0001g0198 | 3 | HG01069.hp2 HG01515.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1602+1591_1602+159 others(15): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37851961 | |||||
| chr4:37851961
|
G | GTTTTCTT others(5): Show |
96 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(93): Show | 118 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1602+1591_1602+159 others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37851961 | |||||
| chr4:37851961
|
G | GTTTTCTT others(6): Show |
7 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0159others(4): Show | 7 | HG01074.hp2 HG02896.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602+1591_1602+159 others(17): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37851961 | |||||
| chr4:37851965
|
G | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(103): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1602+1592G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851965 | ||||||
| chr4:37851970
|
C | CTTTCTTT others(5): Show |
6 | a0002c0003t0003g0221a0002c0003t0003g0222a0002c0003t0006g0213others(3): Show | 6 | HG02015.hp2 HG02257.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+1600_1602+160 others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37851970 | |||||
| chr4:37851970
|
C | CTTTCTTT others(5): Show |
45 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(42): Show | 48 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1602+1600_1602+160 others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37851970 | |||||
| chr4:37851970
|
C | CTTTCTTT others(6): Show |
3 | a0002c0008t0001g0239a0002c0008t0001g0240a0002c0008t0001g0244 | 3 | HG02132.hp2 NA18951.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1602+1600_1602+160 others(17): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37851970 | |||||
| chr4:37851970
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(103): Show | 128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1602+1597C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851970 | ||||||
| chr4:37852040
|
G | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1667G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852040 | ||||||
| chr4:37852043
|
C | A | 5 | a0002c0003t0001g0217a0002c0003t0001g0218a0002c0003t0001g0232others(2): Show | 5 | HG01106.hp2 HG01192.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602+1670C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852043 | ||||||
| chr4:37852052
|
T | C | 2 | a0002c0012t0002g0299a0002c0012t0002g0300 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1602+1679T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852052 | ||||||
| chr4:37852066
|
T | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(291): Show | 328 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.1602+1693T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852066 | ||||||
| chr4:37852075
|
T | C | 5 | a0001c0002t0002g0064a0001c0002t0002g0067a0001c0002t0002g0079others(2): Show | 5 | HG01884.hp1 HG03098.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602+1702T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852075 | ||||||
| chr4:37852133
|
C | CT | 115 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(112): Show | 138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1602+1786dupT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37852133 | |||||
| chr4:37852133
|
C | CTT | 22 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0123others(19): Show | 22 | HG00621.hp2 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1602+1785_1602+178 others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37852133 | |||||
| chr4:37852133
|
CT | C | 79 | a0001c0001t0001g0029a0001c0001t0001g0160a0001c0001t0001g0292others(76): Show | 88 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1602+1786delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37852133 | |||||
| chr4:37852133
|
CTTTTTTT others(1): Show |
C | 3 | a0001c0001t0001g0003a0001c0001t0001g0340a0001c0001t0001g0352 | 7 | HG02132.hp1 NA18947.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.1602+1779_1602+178 others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37852133 | |||||
| chr4:37852163
|
G | A | 3 | a0001c0001t0001g0316a0001c0001t0001g0351a0001c0001t0001g0354 | 3 | HG00544.hp2 NA18612.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1602+1790G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852163 | ||||||
| chr4:37852168
|
G | A | 1 | a0001c0004t0007g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1602+1795G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852168 | ||||||
| chr4:37852180
|
A | G | 1 | a0001c0001t0001g0017 | 2 | HG00558.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1602+1807A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852180 | ||||||
| chr4:37852227
|
A | G | 1 | a0001c0002t0010g0115 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1602+1854A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852227 | ||||||
| chr4:37852261
|
T | A | 12 | a0001c0002t0002g0256a0001c0002t0003g0259a0001c0004t0001g0005others(9): Show | 14 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1602+1888T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852261 | ||||||
| chr4:37852301
|
T | C | 2 | a0001c0001t0007g0043a0001c0001t0007g0201 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1602+1928T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852301 | ||||||
| chr4:37852318
|
T | TA | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1945_1602+194 others(5): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852318 | ||||||
| chr4:37852329
|
G | T | 2 | a0001c0002t0002g0250a0001c0004t0007g0260 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1602+1956G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852329 | ||||||
| chr4:37852397
|
T | TGGTTCCT others(28): Show |
160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+2028_1602+202 others(39): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37852397 | |||||
| chr4:37852512
|
T | A | 1 | a0002c0008t0001g0244 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1602+2139T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852512 | ||||||
| chr4:37852561
|
A | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+2188A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852561 | ||||||
| chr4:37852599
|
A | T | 1 | a0001c0001t0001g0186 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1602+2226A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852599 | ||||||
| chr4:37852631
|
G | A | 1 | a0001c0002t0002g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1602+2258G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852631 | ||||||
| chr4:37852686
|
T | C | 1 | a0001c0004t0001g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1602+2313T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852686 | ||||||
| chr4:37852706
|
T | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+2333T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852706 | ||||||
| chr4:37852969
|
C | A | 1 | a0001c0002t0003g0113 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1602+2596C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852969 | ||||||
| chr4:37852986
|
C | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+2613C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852986 | ||||||
| chr4:37853072
|
C | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1603-2536C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853072 | ||||||
| chr4:37853135
|
T | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1603-2473T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853135 | ||||||
| chr4:37853167
|
T | C | 1 | a0001c0001t0001g0325 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1603-2441T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853167 | ||||||
| chr4:37853206
|
T | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1603-2402T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853206 | ||||||
| chr4:37853228
|
C | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1603-2380C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853228 | ||||||
| chr4:37853290
|
G | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1603-2318G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853290 | ||||||
| chr4:37853299
|
A | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1603-2309A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853299 | ||||||
| chr4:37853340
|
G | A | 1 | a0008c0015t0001g0385 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1603-2268G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853340 | ||||||
| chr4:37853359
|
CT | C | 78 | a0001c0001t0001g0030a0001c0001t0001g0306a0001c0001t0001g0316others(75): Show | 82 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.1603-2226delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37853359 | |||||
| chr4:37853359
|
CTT | C | 17 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(14): Show | 18 | HG02165.hp2 HG02280.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1603-2227_1603-222 others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37853359 | |||||
| chr4:37853359
|
CTTT | C | 45 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0292others(42): Show | 50 | HG00408.hp1 HG00438.hp2 HG02027.hp1 others(47): Show |
intron_variant | MODIFIER | c.1603-2228_1603-222 others(7): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37853359 | |||||
| chr4:37853359
|
CTTTTTTT | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(148): Show | 176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1603-2232_1603-222 others(11): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37853359 | |||||
| chr4:37853359
|
CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0001g0130a0001c0001t0001g0198a0001c0002t0010g0115others(6): Show | 9 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1603-2233_1603-222 others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37853359 | |||||
| chr4:37853386
|
G | A | 54 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(51): Show | 57 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1603-2222G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853386 | ||||||
| chr4:37853422
|
T | C | 4 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(1): Show | 4 | HG02165.hp2 NA18988.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603-2186T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853422 | ||||||
| chr4:37853445
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1603-2163A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853445 | ||||||
| chr4:37853699
|
C | T | 2 | a0002c0003t0003g0221a0002c0003t0003g0222 | 2 | HG02015.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1603-1909C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853699 | ||||||
| chr4:37853718
|
G | C | 46 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(43): Show | 49 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1603-1890G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853718 | ||||||
| chr4:37853739
|
T | C | 1 | a0002c0003t0001g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1603-1869T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853739 | ||||||
| chr4:37853929
|
T | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(157): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1603-1679T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853929 | ||||||
| chr4:37853980
|
C | T | 12 | a0001c0002t0002g0256a0001c0002t0003g0259a0001c0004t0001g0005others(9): Show | 14 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1603-1628C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853980 | ||||||
| chr4:37854152
|
G | A | 1 | a0001c0001t0001g0383 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1603-1456G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854152 | ||||||
| chr4:37854370
|
A | G | 1 | a0001c0001t0001g0350 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1603-1238A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854370 | ||||||
| chr4:37854393
|
C | G | 78 | a0001c0002t0001g0092a0001c0002t0001g0251a0001c0002t0002g0039others(75): Show | 81 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.1603-1215C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854393 | ||||||
| chr4:37854647
|
C | T | 54 | a0002c0003t0001g0023a0002c0003t0001g0037a0002c0003t0001g0204others(51): Show | 57 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1603-961C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854647 | ||||||
| chr4:37854649
|
C | T | 4 | a0001c0001t0001g0323a0001c0001t0001g0344a0001c0001t0001g0345others(1): Show | 4 | HG03491.hp2 HG03492.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603-959C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854649 | ||||||
| chr4:37854671
|
T | TA | 7 | a0001c0001t0001g0187a0001c0004t0001g0025a0001c0004t0001g0261others(4): Show | 8 | HG02280.hp2 HG03098.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.1603-925dupA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37854671 | |||||
| chr4:37854684
|
C | A | 4 | a0001c0002t0002g0059a0001c0002t0002g0075a0001c0002t0002g0076others(1): Show | 4 | HG01069.hp1 HG02735.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603-924C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854684 | ||||||
| chr4:37854694
|
T | G | 1 | a0001c0001t0003g0150 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1603-914T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854694 | ||||||
| chr4:37854742
|
A | T | 5 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(2): Show | 5 | HG02165.hp2 HG02523.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603-866A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854742 | ||||||
| chr4:37854927
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(89): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1603-681G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854927 | ||||||
| chr4:37855014
|
A | T | 2 | a0001c0002t0002g0087a0001c0002t0002g0088 | 2 | NA18945.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1603-594A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855014 | ||||||
| chr4:37855075
|
A | G | 1 | a0002c0003t0003g0231 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1603-533A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855075 | ||||||
| chr4:37855122
|
C | T | 1 | a0001c0001t0001g0010 | 3 | HG01071.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1603-486C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855122 | ||||||
| chr4:37855156
|
A | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(267): Show | 302 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.1603-452A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855156 | ||||||
| chr4:37855181
|
A | G | 1 | a0001c0004t0001g0388 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1603-427A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855181 | ||||||
| chr4:37855417
|
C | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(278): Show | 314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.1603-191C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855417 | ||||||
| chr4:37855440
|
G | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(278): Show | 314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.1603-168G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855440 | ||||||
| chr4:37855485
|
G | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(278): Show | 314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.1603-123G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855485 | ||||||
| chr4:37855545
|
A | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(278): Show | 314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.1603-63A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855545 | ||||||
| chr4:37855553
|
T | C | 1 | a0008c0015t0001g0385 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1603-55T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855553 | ||||||
| chr4:37855846
|
A | G | 2 | a0002c0012t0002g0299a0002c0012t0002g0300 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1736+105A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37855846 | ||||||
| chr4:37855894
|
T | G | 1 | a0001c0001t0001g0309 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1736+153T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37855894 | ||||||
| chr4:37856025
|
GTAGCTAA others(4): Show |
G | 1 | a0001c0001t0001g0058 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1736+285_1736+295d others(13): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856025 | ||||||
| chr4:37856103
|
G | A | 4 | a0001c0004t0001g0025a0001c0004t0001g0261a0001c0004t0001g0262others(1): Show | 5 | HG02280.hp2 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1736+362G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856103 | ||||||
| chr4:37856107
|
C | T | 2 | a0001c0001t0007g0043a0001c0001t0007g0201 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1736+366C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856107 | ||||||
| chr4:37856108
|
G | A | 5 | a0001c0004t0001g0025a0001c0004t0001g0261a0001c0004t0001g0262others(2): Show | 6 | HG02280.hp2 HG02723.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1736+367G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856108 | ||||||
| chr4:37856160
|
C | T | 2 | a0001c0004t0001g0388a0002c0006t0003g0380 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1736+419C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856160 | ||||||
| chr4:37856181
|
T | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(236): Show | 272 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1736+440T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856181 | ||||||
| chr4:37856201
|
C | T | 30 | a0001c0002t0001g0040a0001c0002t0001g0251a0001c0002t0002g0039others(27): Show | 30 | HG00738.hp1 HG01167.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1736+460C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856201 | ||||||
| chr4:37856202
|
G | A | 55 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0001t0003g0336others(52): Show | 60 | HG00609.hp2 HG00733.hp1 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1736+461G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856202 | ||||||
| chr4:37856204
|
T | C | 388 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(385): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.1736+463T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856204 | ||||||
| chr4:37856212
|
C | G | 30 | a0001c0002t0001g0040a0001c0002t0001g0251a0001c0002t0002g0039others(27): Show | 30 | HG00738.hp1 HG01167.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1736+471C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856212 | ||||||
| chr4:37856253
|
C | G | 392 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(389): Show | 445 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(442): Show |
intron_variant | MODIFIER | c.1736+512C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856253 | ||||||
| chr4:37856256
|
G | A | 392 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(389): Show | 445 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(442): Show |
intron_variant | MODIFIER | c.1736+515G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856256 | ||||||
| chr4:37856257
|
C | T | 392 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(389): Show | 445 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(442): Show |
intron_variant | MODIFIER | c.1736+516C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856257 | ||||||
| chr4:37856274
|
A | G | 1 | a0001c0002t0002g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1736+533A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856274 | ||||||
| chr4:37856316
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(117): Show | 141 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1736+575C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856316 | ||||||
| chr4:37856321
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(112): Show | 136 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1736+580C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856321 | ||||||
| chr4:37856337
|
A | G | 2 | a0001c0002t0002g0067a0001c0002t0002g0079 | 2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1736+596A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856337 | ||||||
| chr4:37856363
|
C | T | 1 | a0002c0003t0001g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1736+622C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856363 | ||||||
| chr4:37856372
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1736+631G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856372 | ||||||
| chr4:37856378
|
C | T | 2 | a0001c0001t0001g0306a0001c0001t0001g0384 | 2 | HG01109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1736+637C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856378 | ||||||
| chr4:37856460
|
A | G | 30 | a0001c0002t0001g0040a0001c0002t0001g0251a0001c0002t0002g0039others(27): Show | 30 | HG00738.hp1 HG01167.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1736+719A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856460 | ||||||
| chr4:37856575
|
AG | A | 61 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0001t0003g0336others(58): Show | 67 | HG00099.hp1 HG00609.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1736+835delG | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856575 | ||||||
| chr4:37856636
|
G | A | 2 | a0002c0012t0002g0299a0002c0012t0002g0300 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1736+895G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856636 | ||||||
| chr4:37856649
|
G | A | 1 | a0002c0003t0003g0035 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1736+908G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856649 | ||||||
| chr4:37856682
|
C | T | 1 | a0002c0007t0002g0214 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1736+941C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856682 | ||||||
| chr4:37856689
|
C | G | 30 | a0001c0002t0001g0040a0001c0002t0001g0251a0001c0002t0002g0039others(27): Show | 30 | HG00738.hp1 HG01167.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1736+948C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856689 | ||||||
| chr4:37856699
|
C | T | 30 | a0001c0002t0001g0040a0001c0002t0001g0251a0001c0002t0002g0039others(27): Show | 30 | HG00738.hp1 HG01167.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1736+958C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856699 | ||||||
| chr4:37856700
|
T | G | 30 | a0001c0002t0001g0040a0001c0002t0001g0251a0001c0002t0002g0039others(27): Show | 30 | HG00738.hp1 HG01167.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1736+959T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856700 | ||||||
| chr4:37856764
|
T | C | 154 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0148others(151): Show | 166 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.1736+1023T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856764 | ||||||
| chr4:37856828
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0152 | 2 | HG01934.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1736+1087G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856828 | ||||||
| chr4:37856956
|
C | T | 29 | a0001c0002t0001g0251a0001c0002t0002g0039a0001c0002t0002g0062others(26): Show | 29 | HG00738.hp1 HG01167.hp1 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.1736+1215C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856956 | ||||||
| chr4:37856999
|
C | T | 2 | a0001c0001t0007g0043a0001c0001t0007g0201 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1736+1258C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856999 | ||||||
| chr4:37857167
|
G | C | 148 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0148others(145): Show | 160 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.1736+1426G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857167 | ||||||
| chr4:37857194
|
T | G | 148 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0148others(145): Show | 160 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.1736+1453T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857194 | ||||||
| chr4:37857250
|
G | A | 2 | a0003c0011t0004g0285a0003c0011t0004g0286 | 2 | HG02735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1736+1509G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857250 | ||||||
| chr4:37857269
|
A | G | 151 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0148others(148): Show | 163 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.1736+1528A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857269 | ||||||
| chr4:37857333
|
C | T | 238 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(235): Show | 271 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.1736+1592C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857333 | ||||||
| chr4:37857347
|
G | T | 1 | a0006c0017t0005g0272 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1736+1606G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857347 | ||||||
| chr4:37857400
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1736+1659A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857400 | ||||||
| chr4:37857444
|
A | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(111): Show | 135 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1736+1703A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857444 | ||||||
| chr4:37857573
|
T | C | 51 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0148others(48): Show | 56 | HG00408.hp1 HG00438.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1736+1832T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857573 | ||||||
| chr4:37857583
|
C | T | 1 | a0002c0008t0001g0244 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1736+1842C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857583 | ||||||
| chr4:37857620
|
C | T | 1 | a0001c0001t0001g0383 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1736+1879C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857620 | ||||||
| chr4:37857927
|
T | C | 2 | a0001c0002t0002g0078a0001c0002t0002g0102 | 2 | HG00733.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1736+2186T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857927 | ||||||
| chr4:37858054
|
C | T | 148 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0148others(145): Show | 160 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.1736+2313C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858054 | ||||||
| chr4:37858110
|
G | A | 2 | a0001c0004t0001g0253a0002c0003t0008g0038 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1736+2369G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858110 | ||||||
| chr4:37858223
|
G | T | 2 | a0002c0007t0002g0212a0002c0007t0002g0214 | 2 | HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1736+2482G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858223 | ||||||
| chr4:37858280
|
C | G | 185 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0148others(182): Show | 197 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.1736+2539C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858280 | ||||||
| chr4:37858294
|
C | T | 66 | a0001c0002t0001g0251a0001c0002t0002g0039a0001c0002t0002g0042others(63): Show | 66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1736+2553C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858294 | ||||||
| chr4:37858304
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1736+2563C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858304 | ||||||
| chr4:37858325
|
A | C | 1 | a0001c0001t0001g0328 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1736+2584A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858325 | ||||||
| chr4:37858330
|
T | C | 1 | a0001c0004t0001g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1736+2589T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858330 | ||||||
| chr4:37858344
|
T | TG | 66 | a0001c0002t0001g0251a0001c0002t0002g0039a0001c0002t0002g0042others(63): Show | 66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1736+2603_1736+260 others(5): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858344 | ||||||
| chr4:37858347
|
G | T | 66 | a0001c0002t0001g0251a0001c0002t0002g0039a0001c0002t0002g0042others(63): Show | 66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1736+2606G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858347 | ||||||
| chr4:37858349
|
T | G | 66 | a0001c0002t0001g0251a0001c0002t0002g0039a0001c0002t0002g0042others(63): Show | 66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1736+2608T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858349 | ||||||
| chr4:37858424
|
C | T | 2 | a0001c0001t0002g0014a0001c0001t0002g0386 | 4 | HG02630.hp2 HG02809.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1736+2683C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858424 | ||||||
| chr4:37858429
|
T | A | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1736+2688T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858429 | ||||||
| chr4:37858470
|
G | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(273): Show | 309 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.1736+2729G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858470 | ||||||
| chr4:37858495
|
C | G | 119 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0148others(116): Show | 131 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1736+2754C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858495 | ||||||
| chr4:37858513
|
G | GT | 187 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0029others(184): Show | 200 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1736+2788dupT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 37858513 | |||||
| chr4:37858659
|
G | C | 2 | a0002c0012t0002g0299a0002c0012t0002g0300 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1737-2851G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858659 | ||||||
| chr4:37858730
|
A | T | 1 | a0008c0015t0001g0385 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1737-2780A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858730 | ||||||
| chr4:37858732
|
T | A | 1 | a0008c0015t0001g0385 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1737-2778T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858732 | ||||||
| chr4:37858744
|
T | C | 5 | a0001c0004t0001g0025a0001c0004t0001g0261a0001c0004t0001g0262others(2): Show | 6 | HG02280.hp2 HG02723.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737-2766T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858744 | ||||||
| chr4:37858805
|
T | C | 119 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0148others(116): Show | 131 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1737-2705T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858805 | ||||||
| chr4:37858860
|
A | T | 1 | a0002c0003t0001g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1737-2650A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858860 | ||||||
| chr4:37858972
|
C | A | 66 | a0001c0002t0001g0251a0001c0002t0002g0039a0001c0002t0002g0042others(63): Show | 66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-2538C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858972 | ||||||
| chr4:37859061
|
C | A | 1 | a0001c0001t0001g0329 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1737-2449C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859061 | ||||||
| chr4:37859207
|
C | A | 2 | a0002c0012t0002g0299a0002c0012t0002g0300 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1737-2303C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859207 | ||||||
| chr4:37859282
|
A | G | 2 | a0001c0004t0001g0253a0002c0003t0008g0038 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1737-2228A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859282 | ||||||
| chr4:37859346
|
C | T | 66 | a0001c0002t0001g0251a0001c0002t0002g0039a0001c0002t0002g0042others(63): Show | 66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-2164C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859346 | ||||||
| chr4:37859575
|
T | C | 2 | a0002c0012t0002g0299a0002c0012t0002g0300 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1737-1935T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859575 | ||||||
| chr4:37859604
|
AT | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0160a0001c0001t0001g0179 | 4 | HG00280.hp2 HG01993.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737-1905delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859604 | ||||||
| chr4:37859616
|
G | A | 278 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(275): Show | 311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.1737-1894G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859616 | ||||||
| chr4:37859720
|
TC | T | 66 | a0001c0002t0001g0251a0001c0002t0002g0039a0001c0002t0002g0042others(63): Show | 66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-1786delC | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 37859720 | |||||
| chr4:37859722
|
C | G | 5 | a0001c0004t0001g0025a0001c0004t0001g0261a0001c0004t0001g0262others(2): Show | 6 | HG02280.hp2 HG02723.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737-1788C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859722 | ||||||
| chr4:37859772
|
A | G | 66 | a0001c0002t0001g0251a0001c0002t0002g0039a0001c0002t0002g0042others(63): Show | 66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-1738A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859772 | ||||||
| chr4:37859826
|
C | G | 66 | a0001c0002t0001g0251a0001c0002t0002g0039a0001c0002t0002g0042others(63): Show | 66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-1684C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859826 | ||||||
| chr4:37859901
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1737-1609T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859901 | ||||||
| chr4:37860005
|
A | C | 2 | a0002c0003t0001g0217a0002c0003t0001g0218 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1737-1505A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860005 | ||||||
| chr4:37860030
|
C | G | 66 | a0001c0002t0001g0251a0001c0002t0002g0039a0001c0002t0002g0042others(63): Show | 66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-1480C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860030 | ||||||
| chr4:37860072
|
A | G | 2 | a0002c0003t0001g0217a0002c0003t0001g0218 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1737-1438A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860072 | ||||||
| chr4:37860093
|
G | C | 66 | a0001c0002t0001g0251a0001c0002t0002g0039a0001c0002t0002g0042others(63): Show | 66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-1417G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860093 | ||||||
| chr4:37860097
|
CGTAATGT others(29): Show |
C | 1 | a0001c0002t0010g0115 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1737-1412_1737-137 others(40): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860097 | ||||||
| chr4:37860098
|
G | A | 65 | a0001c0002t0001g0251a0001c0002t0002g0039a0001c0002t0002g0042others(62): Show | 65 | HG00597.hp1 HG00733.hp2 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.1737-1412G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860098 | ||||||
| chr4:37860142
|
A | G | 10 | a0001c0001t0001g0008a0001c0001t0001g0125a0001c0001t0001g0126others(7): Show | 12 | NA18939.hp1 NA18947.hp2 NA18956.hp2 others(9): Show |
intron_variant | MODIFIER | c.1737-1368A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860142 | ||||||
| chr4:37860267
|
C | G | 66 | a0001c0002t0001g0251a0001c0002t0002g0039a0001c0002t0002g0042others(63): Show | 66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-1243C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860267 | ||||||
| chr4:37860450
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(152): Show | 176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1737-1060A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860450 | ||||||
| chr4:37860563
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1737-947C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860563 | ||||||
| chr4:37860680
|
A | G | 63 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0001t0003g0336others(60): Show | 68 | HG00099.hp1 HG00609.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.1737-830A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860680 | ||||||
| chr4:37860870
|
G | C | 1 | a0001c0004t0001g0091 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1737-640G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860870 | ||||||
| chr4:37860901
|
C | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(273): Show | 309 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.1737-609C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860901 | ||||||
| chr4:37861001
|
T | G | 5 | a0001c0001t0007g0043a0001c0001t0007g0201a0001c0004t0001g0388others(2): Show | 5 | HG02559.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737-509T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37861001 | ||||||
| chr4:37861068
|
A | G | 54 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0148others(51): Show | 59 | HG00408.hp1 HG00438.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1737-442A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37861068 | ||||||
| chr4:37861230
|
G | A | 1 | a0001c0002t0002g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1737-280G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37861230 | ||||||
| chr4:37861267
|
C | T | 2 | a0002c0003t0003g0209a0002c0003t0003g0210 | 2 | HG02040.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1737-243C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37861267 | ||||||
| chr4:37861392
|
C | T | 66 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(63): Show | 77 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1737-118C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37861392 | ||||||
| chr4:37861424
|
AT | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(121): Show | 146 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1737-84delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 37861424 | |||||
| chr4:37861459
|
G | A | 23 | a0001c0001t0001g0029a0001c0001t0001g0148a0001c0001t0001g0292others(20): Show | 27 | HG00408.hp1 HG00438.hp2 NA18942.hp2 others(24): Show |
intron_variant | MODIFIER | c.1737-51G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37861459 | ||||||
| chr4:37861468
|
A | C | 1 | a0001c0001t0001g0330 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1737-42A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37861468 |