| geneid | 5236 |
|---|---|
| ensemblid | ENSG00000079739.17 |
| hgncid | 8905 |
| symbol | PGM1 |
| name | phosphoglucomutase 1 |
| refseq_nuc | NM_002633.3 |
| refseq_prot | NP_002624.2 |
| ensembl_nuc | ENST00000371084.8 |
| ensembl_prot | ENSP00000360125.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 63593411 |
| end | 63660245 |
| strand | + |
| ver | v1.2 |
| region | chr1:63593411-63660245 |
| region5000 | chr1:63588411-63665245 |
| regionname0 | PGM1_chr1_63593411_63660245 |
| regionname5000 | PGM1_chr1_63588411_63665245 |
| 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 | 562 | 198 | 37 | 30 | 100 | 2 | 27 | 73 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0002 | 0/0 | 562 | 57 | 2 | 9 | 35 | 5 | 6 | 30 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0003 | 0/0 | 562 | 34 | 5 | 13 | 13 | 2 | 1 | 11 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0004 | 0/0 | 562 | 19 | 4 | 7 | 8 | 0 | 0 | 5 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0005 | 0/0 | 562 | 19 | 10 | 6 | 0 | 1 | 2 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0006 | 0/0 | 562 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0007 | 0/0 | 562 | 9 | 7 | 0 | 1 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0008 | 0/0 | 562 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0009 | 0/0 | 562 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0010 | 0/0 | 562 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0011 | 0/0 | 562 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0012 | 0/0 | 562 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0013 | 0/0 | 562 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0014 | 0/0 | 562 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0015 | 0/0 | 562 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| 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 | 1689 | 177 | 26 | 27 | 93 | 2 | 27 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0002 | 0/0 | 1689 | 57 | 2 | 9 | 35 | 5 | 6 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0003 | 0/0 | 1689 | 33 | 5 | 13 | 12 | 2 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0004 | 0/0 | 1689 | 19 | 4 | 7 | 8 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0005 | 0/0 | 1689 | 19 | 10 | 6 | 0 | 1 | 2 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0006 | 0/0 | 1689 | 10 | 7 | 3 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0007 | 0/0 | 1689 | 10 | 10 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0008 | 0/0 | 1689 | 7 | 0 | 0 | 7 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0009 | 0/0 | 1689 | 5 | 5 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0010 | 0/0 | 1689 | 5 | 5 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0011 | 0/0 | 1689 | 4 | 2 | 0 | 1 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0012 | 0/0 | 1689 | 4 | 0 | 0 | 4 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0013 | 0/0 | 1689 | 2 | 2 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0014 | 0/0 | 1689 | 2 | 2 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0015 | 0/0 | 1689 | 2 | 2 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0016 | 0/0 | 1689 | 2 | 1 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0017 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0018 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0019 | 0/0 | 1689 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0020 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0021 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0022 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0023 | 0/0 | 1689 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| c0024 | 0/0 | 1689 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| 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 | 649 | 256 | 44 | 45 | 130 | 4 | 31 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| t0002 | 0/0 | 649 | 48 | 6 | 13 | 25 | 2 | 2 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| t0003 | 0/0 | 649 | 45 | 31 | 6 | 2 | 3 | 3 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| t0004 | 0/0 | 649 | 4 | 0 | 0 | 4 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| t0005 | 0/0 | 649 | 4 | 4 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| t0006 | 0/0 | 649 | 3 | 0 | 2 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| t0007 | 0/0 | 649 | 2 | 0 | 1 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| t0008 | 0/0 | 649 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| t0009 | 0/0 | 649 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| t0010 | 0/0 | 649 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| t0011 | 0/0 | 649 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0008 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0022 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| 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 | 1689 | 177 | 26 | 27 | 93 | 2 | 27 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0006 | 0/0 | 1689 | 10 | 7 | 3 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0008 | 0/0 | 1689 | 7 | 0 | 0 | 7 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0014 | 0/0 | 1689 | 2 | 2 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0017 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0018 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0002c0002 | 0/0 | 1689 | 57 | 2 | 9 | 35 | 5 | 6 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0003c0003 | 0/0 | 1689 | 33 | 5 | 13 | 12 | 2 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0003c0020 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0004c0004 | 0/0 | 1689 | 19 | 4 | 7 | 8 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0005c0005 | 0/0 | 1689 | 19 | 10 | 6 | 0 | 1 | 2 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0006c0007 | 0/0 | 1689 | 10 | 10 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0006c0013 | 0/0 | 1689 | 2 | 2 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0007c0010 | 0/0 | 1689 | 5 | 5 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0007c0011 | 0/0 | 1689 | 4 | 2 | 0 | 1 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0008c0009 | 0/0 | 1689 | 5 | 5 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0009c0012 | 0/0 | 1689 | 4 | 0 | 0 | 4 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0010c0015 | 0/0 | 1689 | 2 | 2 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0010c0022 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0011c0016 | 0/0 | 1689 | 2 | 1 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0012c0021 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0013c0019 | 0/0 | 1689 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0014c0024 | 0/0 | 1689 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0015c0023 | 0/0 | 1689 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2337 | 144 | 15 | 24 | 79 | 1 | 23 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0001t0002 | 0/0 | 2337 | 12 | 0 | 0 | 11 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0001t0003 | 0/0 | 2337 | 14 | 11 | 1 | 0 | 0 | 2 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0001t0004 | 0/0 | 2337 | 3 | 0 | 0 | 3 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0001t0007 | 0/0 | 2337 | 2 | 0 | 1 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0001t0010 | 0/0 | 2337 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0001t0011 | 0/0 | 2337 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0006t0001 | 0/0 | 2337 | 4 | 2 | 2 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0006t0003 | 0/0 | 2337 | 6 | 5 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0008t0001 | 0/0 | 2337 | 6 | 0 | 0 | 6 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0008t0002 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0014t0003 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0014t0005 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0017t0001 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0001c0018t0003 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0002c0002t0001 | 0/0 | 2337 | 42 | 0 | 5 | 29 | 3 | 5 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0002c0002t0002 | 0/0 | 2337 | 6 | 0 | 3 | 3 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0002c0002t0003 | 0/0 | 2337 | 7 | 2 | 1 | 1 | 2 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0002c0002t0004 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0002c0002t0009 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0003c0003t0001 | 0/0 | 2337 | 11 | 1 | 4 | 6 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0003c0003t0002 | 0/0 | 2337 | 20 | 3 | 9 | 6 | 2 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0003c0003t0003 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0003c0003t0006 | 0/0 | 2337 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0003c0020t0002 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0004c0004t0001 | 0/0 | 2337 | 8 | 0 | 4 | 4 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0004c0004t0002 | 0/0 | 2337 | 6 | 2 | 1 | 3 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0004c0004t0003 | 0/0 | 2337 | 4 | 2 | 1 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0004c0004t0006 | 0/0 | 2337 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0005c0005t0001 | 0/0 | 2337 | 11 | 5 | 4 | 0 | 0 | 2 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0005c0005t0002 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0005c0005t0003 | 0/0 | 2337 | 7 | 4 | 2 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0006c0007t0001 | 0/0 | 2337 | 10 | 10 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0006c0013t0001 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0007c0010t0003 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0007c0010t0005 | 0/0 | 2337 | 3 | 3 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0007c0011t0001 | 0/0 | 2337 | 2 | 0 | 0 | 1 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0007c0011t0003 | 0/0 | 2337 | 2 | 2 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0008c0009t0001 | 0/0 | 2337 | 5 | 5 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0009c0012t0001 | 0/0 | 2337 | 4 | 0 | 0 | 4 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0010c0015t0001 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0010c0015t0008 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0010c0022t0001 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0011c0016t0001 | 0/0 | 2337 | 2 | 1 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0012c0021t0001 | 0/0 | 2337 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0013c0019t0001 | 0/0 | 2337 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0014c0024t0006 | 0/0 | 2337 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| a0015c0023t0002 | 0/0 | 2337 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | copy fasta | chr1 | 63588411 | 63665245 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0008 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0022 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0003g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0003g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0007g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0007g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0010g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0001t0011g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0006t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0006t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0006t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0006t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0006t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0006t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0006t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0006t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0006t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0006t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0008t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0008t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0008t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0008t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0008t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0008t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0014t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0014t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0017t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0001c0018t0003g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0002c0002t0009g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0002g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0003t0006g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0003c0020t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0004c0004t0006g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0005c0005t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0006c0007t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0006c0007t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0006c0007t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0006c0007t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0006c0007t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0006c0007t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0006c0007t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0006c0007t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0006c0007t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0006c0007t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0006c0013t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0006c0013t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0007c0010t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0007c0010t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0007c0010t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0007c0010t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0007c0010t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0007c0011t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0007c0011t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0007c0011t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0007c0011t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0008c0009t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0008c0009t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0008c0009t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0008c0009t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0008c0009t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0009c0012t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0009c0012t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0009c0012t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0009c0012t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0010c0015t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0010c0015t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0010c0022t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0011c0016t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0011c0016t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0012c0021t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0013c0019t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0014c0024t0006g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| a0015c0023t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0097 | EUR | GBR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00140 | hp2 | a0003 | c0003 | t0002 | g0340 | EUR | GBR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00408 | hp2 | a0002 | c0002 | t0003 | g0112 | EAS | CHS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00423 | hp1 | a0003 | c0003 | t0002 | g0241 | EAS | CHS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | CHS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00621 | hp1 | a0004 | c0004 | t0002 | g0205 | EAS | CHS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00621 | hp2 | a0002 | c0002 | t0004 | g0207 | EAS | CHS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00639 | hp1 | a0003 | c0003 | t0002 | g0293 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00642 | hp1 | a0003 | c0003 | t0001 | g0357 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | CHS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00733 | hp1 | a0005 | c0005 | t0001 | g0203 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00733 | hp2 | a0003 | c0003 | t0002 | g0316 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0260 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00738 | hp1 | a0001 | c0006 | t0001 | g0350 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00738 | hp2 | a0005 | c0005 | t0001 | g0056 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00741 | hp1 | a0003 | c0003 | t0001 | g0062 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG00741 | hp2 | a0005 | c0005 | t0001 | g0199 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01071 | hp2 | a0003 | c0003 | t0002 | g0040 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01074 | hp1 | a0004 | c0004 | t0002 | g0187 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01074 | hp2 | a0004 | c0004 | t0006 | g0255 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01167 | hp1 | a0002 | c0002 | t0003 | g0152 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01192 | hp1 | a0001 | c0006 | t0003 | g0145 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0232 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01243 | hp2 | a0011 | c0016 | t0001 | g0228 | AMR | PUR | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01255 | hp1 | a0001 | c0006 | t0001 | g0265 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0306 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01261 | hp2 | a0003 | c0003 | t0002 | g0033 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01346 | hp1 | a0003 | c0003 | t0002 | g0322 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01346 | hp2 | a0005 | c0005 | t0001 | g0259 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0362 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01358 | hp2 | a0003 | c0003 | t0001 | g0218 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01361 | hp1 | a0014 | c0024 | t0006 | g0236 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01361 | hp2 | a0005 | c0005 | t0003 | g0025 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01433 | hp2 | a0005 | c0005 | t0003 | g0275 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0099 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0017 | EUR | IBS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01515 | hp2 | a0005 | c0005 | t0003 | g0035 | EUR | IBS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01516 | hp1 | a0003 | c0003 | t0002 | g0021 | EUR | IBS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01516 | hp2 | a0002 | c0002 | t0003 | g0263 | EUR | IBS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01517 | hp1 | a0002 | c0002 | t0003 | g0264 | EUR | IBS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0016 | EUR | IBS | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01884 | hp2 | a0005 | c0005 | t0003 | g0197 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0353 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01891 | hp2 | a0006 | c0007 | t0001 | g0292 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01934 | hp1 | a0004 | c0004 | t0003 | g0083 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0133 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01952 | hp2 | a0004 | c0004 | t0001 | g0282 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01975 | hp1 | a0001 | c0001 | t0010 | g0283 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01975 | hp2 | a0004 | c0004 | t0001 | g0358 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01978 | hp1 | a0003 | c0003 | t0002 | g0364 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01978 | hp2 | a0003 | c0003 | t0001 | g0211 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01981 | hp1 | a0004 | c0004 | t0001 | g0215 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01981 | hp2 | a0003 | c0003 | t0002 | g0247 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG01993 | hp2 | a0003 | c0003 | t0002 | g0359 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02004 | hp1 | a0004 | c0004 | t0001 | g0286 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02004 | hp2 | a0003 | c0003 | t0002 | g0134 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02055 | hp2 | a0008 | c0009 | t0001 | g0164 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02129 | hp2 | a0007 | c0011 | t0001 | g0065 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CDX | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02155 | hp2 | a0004 | c0004 | t0002 | g0047 | EAS | CDX | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02165 | hp1 | a0004 | c0004 | t0001 | g0131 | EAS | CDX | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | CDX | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02257 | hp1 | a0010 | c0022 | t0001 | g0078 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0183 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02258 | hp1 | a0006 | c0007 | t0001 | g0166 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02258 | hp2 | a0003 | c0003 | t0002 | g0239 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02280 | hp1 | a0008 | c0009 | t0001 | g0139 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0209 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02293 | hp2 | a0013 | c0019 | t0001 | g0238 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02451 | hp2 | a0006 | c0007 | t0001 | g0252 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02523 | hp2 | a0003 | c0003 | t0002 | g0253 | EAS | KHV | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02572 | hp1 | a0006 | c0013 | t0001 | g0343 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02572 | hp2 | a0001 | c0006 | t0003 | g0141 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02602 | hp2 | a0005 | c0005 | t0001 | g0329 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0355 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02622 | hp1 | a0001 | c0006 | t0001 | g0347 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02622 | hp2 | a0008 | c0009 | t0001 | g0146 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02647 | hp1 | a0005 | c0005 | t0001 | g0349 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0363 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02717 | hp1 | a0003 | c0003 | t0002 | g0068 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02717 | hp2 | a0007 | c0010 | t0005 | g0144 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02735 | hp2 | a0002 | c0002 | t0003 | g0276 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02738 | hp1 | a0015 | c0023 | t0002 | g0191 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02809 | hp1 | a0001 | c0014 | t0005 | g0274 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02809 | hp2 | a0006 | c0007 | t0001 | g0206 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02818 | hp1 | a0004 | c0004 | t0002 | g0331 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02886 | hp2 | a0001 | c0006 | t0003 | g0342 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02895 | hp1 | a0007 | c0011 | t0003 | g0151 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02896 | hp1 | a0001 | c0006 | t0001 | g0162 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02896 | hp2 | a0004 | c0004 | t0003 | g0158 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02922 | hp1 | a0001 | c0006 | t0003 | g0170 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02922 | hp2 | a0002 | c0002 | t0003 | g0091 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02965 | hp1 | a0006 | c0007 | t0001 | g0249 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02965 | hp2 | a0001 | c0018 | t0003 | g0356 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02970 | hp1 | a0006 | c0013 | t0001 | g0237 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02970 | hp2 | a0007 | c0010 | t0003 | g0080 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02976 | hp2 | a0002 | c0002 | t0003 | g0150 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03098 | hp1 | a0010 | c0015 | t0008 | g0177 | AFR | MSL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03098 | hp2 | a0010 | c0015 | t0001 | g0079 | AFR | MSL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03130 | hp1 | a0003 | c0003 | t0002 | g0142 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03130 | hp2 | a0008 | c0009 | t0001 | g0318 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03139 | hp2 | a0006 | c0007 | t0001 | g0273 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03195 | hp1 | a0005 | c0005 | t0001 | g0348 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03209 | hp1 | a0003 | c0003 | t0003 | g0143 | AFR | MSL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03209 | hp2 | a0001 | c0006 | t0003 | g0346 | AFR | MSL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0360 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03453 | hp1 | a0001 | c0017 | t0001 | g0345 | AFR | MSL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03453 | hp2 | a0004 | c0004 | t0003 | g0159 | AFR | MSL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | MSL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | MSL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03490 | hp1 | a0005 | c0005 | t0001 | g0130 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0277 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0281 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03516 | hp1 | a0011 | c0016 | t0001 | g0057 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03516 | hp2 | a0001 | c0014 | t0003 | g0335 | AFR | ESN | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03540 | hp1 | a0007 | c0010 | t0005 | g0081 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | GWD | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03579 | hp1 | a0006 | c0007 | t0001 | g0354 | AFR | MSL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03579 | hp2 | a0006 | c0007 | t0001 | g0163 | AFR | MSL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03669 | hp1 | a0007 | c0011 | t0001 | g0175 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03704 | hp1 | a0003 | c0003 | t0006 | g0325 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0184 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0317 | SAS | BEB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | BEB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03927 | hp1 | a0001 | c0001 | t0011 | g0066 | SAS | BEB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0328 | SAS | BEB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | STU | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0116 | SAS | STU | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | STU | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0361 | SAS | STU | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0121 | SAS | STU | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18522 | hp1 | a0008 | c0009 | t0001 | g0086 | AFR | YRI | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18522 | hp2 | a0004 | c0004 | t0002 | g0043 | AFR | YRI | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18906 | hp1 | a0005 | c0005 | t0003 | g0044 | AFR | YRI | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18906 | hp2 | a0005 | c0005 | t0003 | g0242 | AFR | YRI | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18942 | hp2 | a0001 | c0008 | t0001 | g0339 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18947 | hp1 | a0002 | c0002 | t0009 | g0106 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18948 | hp1 | a0001 | c0008 | t0002 | g0058 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18949 | hp2 | a0003 | c0003 | t0002 | g0137 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18952 | hp1 | a0003 | c0003 | t0002 | g0179 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18973 | hp1 | a0009 | c0012 | t0001 | g0049 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18979 | hp1 | a0004 | c0004 | t0001 | g0219 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18980 | hp2 | a0004 | c0004 | t0001 | g0089 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18981 | hp1 | a0003 | c0003 | t0002 | g0172 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0341 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18989 | hp2 | a0003 | c0003 | t0002 | g0013 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18990 | hp1 | a0001 | c0008 | t0001 | g0338 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18994 | hp2 | a0012 | c0021 | t0001 | g0233 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19004 | hp2 | a0003 | c0003 | t0001 | g0071 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19006 | hp1 | a0004 | c0004 | t0002 | g0244 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19007 | hp2 | a0003 | c0003 | t0001 | g0279 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19010 | hp2 | a0001 | c0008 | t0001 | g0103 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19043 | hp1 | a0005 | c0005 | t0003 | g0149 | AFR | LWK | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19043 | hp2 | a0006 | c0007 | t0001 | g0157 | AFR | LWK | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19054 | hp2 | a0009 | c0012 | t0001 | g0050 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19055 | hp2 | a0003 | c0003 | t0001 | g0011 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0269 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19058 | hp2 | a0009 | c0012 | t0001 | g0070 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19062 | hp2 | a0003 | c0003 | t0001 | g0258 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19070 | hp1 | a0001 | c0008 | t0001 | g0001 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19072 | hp1 | a0004 | c0004 | t0001 | g0301 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19074 | hp1 | a0001 | c0008 | t0001 | g0001 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19075 | hp2 | a0009 | c0012 | t0001 | g0046 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19084 | hp2 | a0001 | c0008 | t0001 | g0337 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19087 | hp2 | a0003 | c0003 | t0001 | g0127 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19088 | hp2 | a0003 | c0020 | t0002 | g0336 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19091 | hp2 | a0004 | c0004 | t0003 | g0251 | EAS | JPT | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19240 | hp1 | a0006 | c0007 | t0001 | g0231 | AFR | YRI | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA19240 | hp2 | a0007 | c0011 | t0003 | g0272 | AFR | YRI | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA20129 | hp1 | a0005 | c0005 | t0001 | g0030 | AFR | ASW | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA20129 | hp2 | a0005 | c0005 | t0002 | g0314 | AFR | ASW | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA20805 | hp1 | a0001 | c0001 | t0007 | g0210 | EUR | TSI | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | GIH | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | GIH | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02109 | hp1 | a0007 | c0010 | t0005 | g0332 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG03471 | hp2 | a0007 | c0010 | t0003 | g0075 | AFR | MSL | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG06807 | hp1 | a0005 | c0005 | t0001 | g0344 | AFR | USA | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| HG06807 | hp2 | a0005 | c0005 | t0001 | g0171 | AFR | USA | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| NA20300 | hp2 | a0001 | c0006 | t0003 | g0148 | AFR | USA | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0022 | REF | REF | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0008 | REF | REF | PGM1_chr1_63588411_63665245 | PGM1 | chr1 | 63588411 | 63665245 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:63593691
|
A | T | 1 | a0009 | 4 | NA18973.hp1 NA19054.hp2 NA19058.hp2 others(1): Show |
missense_variant | MODERATE | c.203A>T | p.Lys68Met | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/11 | 281/2337 | 203/1689 | 68/562 | chr1 | 63593691 | ||
| chr1:63629440
|
A | G | 6 | a0005a0007a0010others(3): Show | 35 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(32): Show |
missense_variant | MODERATE | c.262A>G | p.Ile88Val | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 2/11 | 340/2337 | 262/1689 | 88/562 | chr1 | 63629440 | ||
| chr1:63631761
|
C | T | 5 | a0002a0004a0007others(2): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(84): Show |
missense_variant | MODERATE | c.661C>T | p.Arg221Cys | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/11 | 739/2337 | 661/1689 | 221/562 | chr1 | 63631761 | ||
| chr1:63634854
|
C | G | 1 | a0012 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.708C>G | p.Ile236Met | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 5/11 | 786/2337 | 708/1689 | 236/562 | chr1 | 63634854 | ||
| chr1:63648630
|
T | C | 6 | a0003a0004a0008others(3): Show | 63 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(60): Show |
missense_variant | MODERATE | c.1258T>C | p.Tyr420His | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/11 | 1336/2337 | 1258/1689 | 420/562 | chr1 | 63648630 | ||
| chr1:63654368
|
G | A | 4 | a0006a0008a0010others(1): Show | 22 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
missense_variant | MODERATE | c.1501G>A | p.Val501Ile | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/11 | 1579/2337 | 1501/1689 | 501/562 | chr1 | 63654368 | ||
| chr1:63659649
|
C | T | 1 | a0013 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.1663C>T | p.Arg555Cys | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 11/11 | 1741/2337 | 1663/1689 | 555/562 | chr1 | 63659649 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:63629577
|
T | C | 3 | a0001c0006a0001c0017a0006c0013 | 13 | HG00738.hp1 HG01192.hp1 HG01255.hp1 others(10): Show |
synonymous_variant | LOW | c.399T>C | p.Ile133Ile | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 2/11 | 477/2337 | 399/1689 | 133/562 | chr1 | 63629577 | ||
| chr1:63631673
|
G | A | 2 | a0001c0018a0010c0022 | 2 | HG02257.hp1 HG02965.hp2 |
synonymous_variant | LOW | c.573G>A | p.Ser191Ser | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/11 | 651/2337 | 573/1689 | 191/562 | chr1 | 63631673 | ||
| chr1:63636347
|
C | T | 2 | a0001c0008a0003c0020 | 8 | NA18942.hp2 NA18948.hp1 NA18990.hp1 others(5): Show |
synonymous_variant | LOW | c.987C>T | p.Arg329Arg | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/11 | 1065/2337 | 987/1689 | 329/562 | chr1 | 63636347 | ||
| chr1:63638799
|
C | T | 1 | a0001c0017 | 1 | HG03453.hp1 | splice_region_variant&synonymous_variant | LOW | c.1143C>T | p.Thr381Thr | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/11 | 1221/2337 | 1143/1689 | 381/562 | chr1 | 63638799 | ||
| chr1:63654367
|
C | T | 2 | a0001c0014a0007c0010 | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
synonymous_variant | LOW | c.1500C>T | p.Ile500Ile | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/11 | 1578/2337 | 1500/1689 | 500/562 | chr1 | 63654367 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:63593415
|
C | A | 1 | a0010c0015t0008 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-74C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/11 | 74 | chr1 | 63593415 | |||||
| chr1:63659697
|
C | T | 11 | a0001c0001t0002a0001c0008t0002a0002c0002t0002others(8): Show | 51 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*22C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 11/11 | 22 | chr1 | 63659697 | |||||
| chr1:63659712
|
G | A | 3 | a0003c0003t0006a0004c0004t0006a0014c0024t0006 | 3 | HG01074.hp2 HG01361.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*37G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 11/11 | 37 | chr1 | 63659712 | |||||
| chr1:63659768
|
A | C | 11 | a0001c0001t0002a0001c0008t0002a0002c0002t0002others(8): Show | 51 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*93A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 11/11 | 93 | chr1 | 63659768 | |||||
| chr1:63659805
|
C | T | 2 | a0001c0014t0005a0007c0010t0005 | 4 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*130C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 11/11 | 130 | chr1 | 63659805 | |||||
| chr1:63659873
|
C | T | 11 | a0001c0001t0003a0001c0001t0011a0001c0006t0003others(8): Show | 46 | HG00408.hp2 HG01167.hp1 HG01192.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*198C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 11/11 | 198 | chr1 | 63659873 | |||||
| chr1:63659924
|
C | T | 1 | a0001c0001t0010 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*249C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 11/11 | 249 | chr1 | 63659924 | |||||
| chr1:63660023
|
G | A | 1 | a0002c0002t0009 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*348G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 11/11 | 348 | chr1 | 63660023 | |||||
| chr1:63660039
|
G | T | 1 | a0001c0001t0011 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*364G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 11/11 | 364 | chr1 | 63660039 | |||||
| chr1:63660081
|
T | C | 1 | a0001c0001t0007 | 2 | HG01261.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*406T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 11/11 | 406 | chr1 | 63660081 | |||||
| chr1:63660122
|
G | A | 2 | a0001c0001t0004a0002c0002t0004 | 4 | HG00621.hp2 HG02129.hp1 NA19001.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*447G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 11/11 | 447 | chr1 | 63660122 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:63593801
|
C | T | 8 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0363others(5): Show | 8 | HG00642.hp1 HG01358.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.246+67C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63593801 | ||||||
| chr1:63593822
|
C | T | 5 | a0001c0001t0001g0352a0001c0001t0003g0353a0001c0001t0003g0355others(2): Show | 5 | HG01891.hp1 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+88C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63593822 | ||||||
| chr1:63593829
|
G | C | 1 | a0002c0002t0001g0003 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.246+95G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63593829 | ||||||
| chr1:63593866
|
C | G | 1 | a0001c0001t0001g0351 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.246+132C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63593866 | ||||||
| chr1:63593899
|
CCCGACGG others(6): Show |
C | 1 | a0001c0006t0001g0350 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.246+169_246+181del others(13): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63593899 | |||||
| chr1:63593907
|
A | G | 2 | a0005c0005t0001g0348a0005c0005t0001g0349 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.246+173A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63593907 | ||||||
| chr1:63593931
|
C | T | 6 | a0001c0006t0001g0347a0001c0006t0003g0342a0001c0006t0003g0346others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+197C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63593931 | ||||||
| chr1:63593953
|
T | C | 1 | a0001c0001t0001g0004 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.246+219T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63593953 | ||||||
| chr1:63593973
|
C | G | 291 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0085others(288): Show | 293 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.246+239C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63593973 | ||||||
| chr1:63594046
|
C | T | 6 | a0001c0006t0001g0347a0001c0006t0003g0342a0001c0006t0003g0346others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+312C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594046 | ||||||
| chr1:63594054
|
G | C | 7 | a0001c0001t0001g0077a0001c0001t0003g0082a0004c0004t0003g0083others(4): Show | 7 | HG01934.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+320G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594054 | ||||||
| chr1:63594100
|
A | C | 1 | a0003c0003t0002g0364 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.246+366A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594100 | ||||||
| chr1:63594101
|
A | C | 1 | a0002c0002t0001g0341 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.246+367A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594101 | ||||||
| chr1:63594118
|
A | T | 1 | a0003c0003t0002g0364 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.246+384A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594118 | ||||||
| chr1:63594176
|
C | T | 1 | a0003c0003t0002g0340 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.246+442C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594176 | ||||||
| chr1:63594192
|
T | A | 57 | a0001c0001t0001g0085a0001c0001t0001g0088a0001c0001t0001g0090others(54): Show | 58 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.246+458T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594192 | ||||||
| chr1:63594249
|
T | C | 22 | a0001c0001t0001g0352a0001c0001t0003g0140a0001c0001t0003g0147others(19): Show | 22 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.246+515T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594249 | ||||||
| chr1:63594280
|
CT | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(90): Show | 94 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.246+547delT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594280 | ||||||
| chr1:63594591
|
C | A | 30 | a0001c0001t0001g0077a0001c0001t0001g0154a0001c0001t0001g0155others(27): Show | 30 | HG01081.hp1 HG01167.hp1 HG01934.hp1 others(27): Show |
intron_variant | MODIFIER | c.246+857C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594591 | ||||||
| chr1:63594593
|
G | T | 1 | a0001c0001t0001g0076 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.246+859G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594593 | ||||||
| chr1:63594613
|
A | AT | 112 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(109): Show | 113 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.246+881dupT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63594613 | |||||
| chr1:63594616
|
A | T | 2 | a0001c0001t0001g0169a0001c0006t0003g0170 | 2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.246+882A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594616 | ||||||
| chr1:63594689
|
C | T | 4 | a0001c0008t0001g0337a0001c0008t0001g0338a0001c0008t0001g0339others(1): Show | 4 | NA18942.hp2 NA18990.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+955C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594689 | ||||||
| chr1:63594716
|
T | C | 2 | a0002c0002t0001g0232a0006c0007t0001g0231 | 2 | HG01192.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.246+982T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594716 | ||||||
| chr1:63594780
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0001g0138a0003c0003t0002g0137 | 3 | NA18940.hp1 NA18949.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.246+1046A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594780 | ||||||
| chr1:63594788
|
C | CA | 104 | a0001c0001t0001g0085a0001c0001t0001g0248a0001c0001t0001g0250others(101): Show | 104 | HG00408.hp1 HG00558.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.246+1077dupA | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63594788 | |||||
| chr1:63594788
|
C | CAA | 14 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0243others(11): Show | 14 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.246+1076_246+1077d others(4): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63594788 | |||||
| chr1:63594788
|
CA | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 136 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.246+1077delA | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63594788 | |||||
| chr1:63594788
|
CAA | C | 23 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0165others(20): Show | 23 | HG01081.hp1 HG01168.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.246+1076_246+1077d others(4): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63594788 | |||||
| chr1:63594788
|
CAAAAA | C | 9 | a0001c0001t0001g0352a0001c0001t0003g0140a0001c0001t0003g0353others(6): Show | 9 | HG01891.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.246+1073_246+1077d others(7): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63594788 | |||||
| chr1:63594788
|
CAAAAAA | C | 6 | a0001c0001t0003g0147a0001c0006t0003g0145a0001c0006t0003g0148others(3): Show | 6 | HG01192.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+1072_246+1077d others(8): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63594788 | |||||
| chr1:63594788
|
CAAAAAAA others(1): Show |
C | 16 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0128others(13): Show | 16 | HG00140.hp2 HG00438.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.246+1070_246+1077d others(10): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63594788 | |||||
| chr1:63594822
|
G | A | 1 | a0002c0002t0003g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.246+1088G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594822 | ||||||
| chr1:63594944
|
G | C | 1 | a0010c0015t0008g0177 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.246+1210G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594944 | ||||||
| chr1:63594960
|
C | CAAAA | 198 | a0001c0001t0001g0002a0001c0001t0001g0165a0001c0001t0001g0167others(195): Show | 199 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.246+1238_246+1241d others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63594960 | |||||
| chr1:63594960
|
C | CAAAAA | 31 | a0001c0001t0001g0077a0001c0001t0001g0154a0001c0001t0001g0155others(28): Show | 31 | HG00738.hp1 HG01167.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.246+1237_246+1241d others(7): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63594960 | |||||
| chr1:63594971
|
A | AAAAAG | 56 | a0001c0001t0001g0085a0001c0001t0001g0088a0001c0001t0001g0090others(53): Show | 57 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.246+1242_246+1246d others(7): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63594971 | |||||
| chr1:63594976
|
G | A | 2 | a0001c0001t0001g0178a0003c0003t0002g0179 | 2 | NA18940.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.246+1242G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63594976 | ||||||
| chr1:63595068
|
A | G | 1 | a0005c0005t0001g0349 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.246+1334A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63595068 | ||||||
| chr1:63595119
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0090a0004c0004t0001g0089 | 3 | HG00438.hp1 NA18747.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.246+1385T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63595119 | ||||||
| chr1:63595198
|
T | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(113): Show | 117 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.246+1464T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63595198 | ||||||
| chr1:63595335
|
G | A | 1 | a0001c0006t0001g0350 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.246+1601G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63595335 | ||||||
| chr1:63595351
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.246+1617A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63595351 | ||||||
| chr1:63595466
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(90): Show | 94 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.246+1732C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63595466 | ||||||
| chr1:63595604
|
A | ATCACT | 116 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(113): Show | 117 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.246+1873_246+1874i others(7): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63595604 | |||||
| chr1:63595654
|
CATTT | C | 4 | a0001c0001t0003g0140a0001c0006t0003g0141a0003c0003t0002g0142others(1): Show | 4 | HG02572.hp2 HG02886.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+1924_246+1927d others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63595654 | |||||
| chr1:63595741
|
G | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(113): Show | 117 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.246+2007G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63595741 | ||||||
| chr1:63595851
|
A | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(90): Show | 94 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.246+2117A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63595851 | ||||||
| chr1:63596002
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.246+2268A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63596002 | ||||||
| chr1:63596019
|
C | T | 1 | a0003c0003t0001g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.246+2285C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63596019 | ||||||
| chr1:63596226
|
CTTCT | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(115): Show | 119 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.246+2507_246+2510d others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63596226 | |||||
| chr1:63596254
|
C | CT | 23 | a0001c0001t0001g0010a0001c0001t0001g0060a0001c0001t0001g0061others(20): Show | 23 | HG00741.hp1 HG01192.hp2 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.246+2542dupT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63596254 | |||||
| chr1:63596254
|
CT | C | 21 | a0001c0001t0001g0077a0001c0001t0001g0092a0001c0001t0001g0093others(18): Show | 21 | HG01074.hp2 HG01256.hp1 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.246+2542delT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63596254 | |||||
| chr1:63596254
|
CTT | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0173a0001c0001t0001g0174others(70): Show | 74 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.246+2541_246+2542d others(4): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63596254 | |||||
| chr1:63596257
|
T | C | 1 | a0001c0001t0002g0245 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.246+2523T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63596257 | ||||||
| chr1:63596258
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.246+2524T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63596258 | ||||||
| chr1:63596259
|
T | C | 6 | a0001c0001t0003g0147a0001c0006t0003g0145a0001c0006t0003g0148others(3): Show | 6 | HG01192.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+2525T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63596259 | ||||||
| chr1:63596314
|
A | T | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.246+2580A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63596314 | ||||||
| chr1:63596558
|
A | G | 2 | a0005c0005t0001g0348a0005c0005t0001g0349 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.246+2824A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63596558 | ||||||
| chr1:63596562
|
C | A | 4 | a0003c0003t0001g0357a0003c0003t0002g0359a0003c0003t0002g0364others(1): Show | 4 | HG00642.hp1 HG01975.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+2828C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63596562 | ||||||
| chr1:63597178
|
GGAGGGAG others(8): Show |
G | 12 | a0001c0001t0003g0140a0001c0001t0003g0147a0001c0006t0001g0350others(9): Show | 12 | HG00738.hp1 HG01192.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+3450_246+3464d others(17): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63597178 | |||||
| chr1:63597207
|
C | T | 1 | a0001c0014t0003g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.246+3473C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63597207 | ||||||
| chr1:63597289
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.246+3555T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63597289 | ||||||
| chr1:63597436
|
C | T | 6 | a0001c0001t0003g0147a0001c0006t0003g0145a0001c0006t0003g0148others(3): Show | 6 | HG01192.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+3702C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63597436 | ||||||
| chr1:63597520
|
C | A | 1 | a0003c0003t0001g0011 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.246+3786C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63597520 | ||||||
| chr1:63597602
|
A | G | 1 | a0005c0005t0001g0348 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.246+3868A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63597602 | ||||||
| chr1:63597646
|
G | T | 6 | a0001c0006t0001g0347a0001c0006t0003g0342a0001c0006t0003g0346others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+3912G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63597646 | ||||||
| chr1:63597755
|
C | T | 1 | a0002c0002t0001g0009 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.246+4021C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63597755 | ||||||
| chr1:63597991
|
A | G | 1 | a0002c0002t0003g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.246+4257A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63597991 | ||||||
| chr1:63598121
|
G | A | 3 | a0001c0006t0003g0342a0005c0005t0001g0344a0006c0013t0001g0343 | 3 | HG02572.hp1 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.246+4387G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63598121 | ||||||
| chr1:63598141
|
G | A | 7 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0003g0168others(4): Show | 7 | HG01081.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+4407G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63598141 | ||||||
| chr1:63598209
|
A | C | 1 | a0001c0001t0002g0326 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.246+4475A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63598209 | ||||||
| chr1:63598273
|
C | T | 117 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0243others(114): Show | 117 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.246+4539C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63598273 | ||||||
| chr1:63598430
|
T | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0012 | 2 | NA19006.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.246+4696T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63598430 | ||||||
| chr1:63598504
|
A | C | 61 | a0001c0001t0001g0002a0001c0001t0001g0173a0001c0001t0001g0174others(58): Show | 62 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.246+4770A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63598504 | ||||||
| chr1:63598588
|
A | G | 11 | a0001c0001t0003g0140a0001c0001t0003g0147a0001c0006t0003g0141others(8): Show | 11 | HG01192.hp1 HG02280.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.246+4854A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63598588 | ||||||
| chr1:63598707
|
G | A | 134 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0243others(131): Show | 134 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.246+4973G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63598707 | ||||||
| chr1:63598919
|
T | G | 116 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0243others(113): Show | 116 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.246+5185T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63598919 | ||||||
| chr1:63599077
|
G | A | 3 | a0001c0006t0003g0342a0005c0005t0001g0344a0006c0013t0001g0343 | 3 | HG02572.hp1 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.246+5343G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63599077 | ||||||
| chr1:63599109
|
T | C | 291 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0085others(288): Show | 293 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.246+5375T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63599109 | ||||||
| chr1:63599273
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.246+5539C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63599273 | ||||||
| chr1:63599355
|
G | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.246+5621G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63599355 | ||||||
| chr1:63599400
|
A | G | 291 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0085others(288): Show | 293 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.246+5666A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63599400 | ||||||
| chr1:63599498
|
TA | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0059a0001c0001t0001g0165others(68): Show | 72 | HG00621.hp1 HG00621.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.246+5778delA | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63599498 | |||||
| chr1:63599498
|
TAA | T | 164 | a0001c0001t0001g0077a0001c0001t0001g0154a0001c0001t0001g0155others(161): Show | 164 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.246+5777_246+5778d others(4): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63599498 | |||||
| chr1:63599659
|
G | A | 3 | a0001c0006t0001g0162a0006c0007t0001g0163a0008c0009t0001g0164 | 3 | HG02055.hp2 HG02896.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.246+5925G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63599659 | ||||||
| chr1:63599662
|
C | T | 2 | a0001c0001t0001g0257a0003c0003t0006g0325 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.246+5928C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63599662 | ||||||
| chr1:63599989
|
A | G | 1 | a0002c0002t0003g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.246+6255A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63599989 | ||||||
| chr1:63600085
|
G | T | 2 | a0002c0002t0001g0133a0003c0003t0002g0134 | 2 | HG01952.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.246+6351G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63600085 | ||||||
| chr1:63600146
|
A | G | 234 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(231): Show | 235 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(232): Show |
intron_variant | MODIFIER | c.246+6412A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63600146 | ||||||
| chr1:63600273
|
A | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(97): Show | 101 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.246+6539A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63600273 | ||||||
| chr1:63600324
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.246+6590A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63600324 | ||||||
| chr1:63600407
|
T | C | 129 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0243others(126): Show | 129 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.246+6673T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63600407 | ||||||
| chr1:63600475
|
G | C | 1 | a0001c0001t0001g0060 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.246+6741G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63600475 | ||||||
| chr1:63600644
|
G | A | 2 | a0001c0001t0001g0061a0003c0003t0002g0013 | 2 | NA18989.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.246+6910G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63600644 | ||||||
| chr1:63600662
|
C | T | 6 | a0001c0001t0003g0147a0001c0006t0003g0145a0001c0006t0003g0148others(3): Show | 6 | HG01192.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+6928C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63600662 | ||||||
| chr1:63600679
|
G | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0173a0001c0001t0001g0174others(57): Show | 61 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.246+6945G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63600679 | ||||||
| chr1:63600734
|
G | A | 2 | a0001c0001t0001g0014a0002c0002t0001g0015 | 2 | HG00642.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.246+7000G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63600734 | ||||||
| chr1:63600776
|
T | G | 2 | a0002c0002t0001g0016a0002c0002t0001g0017 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.246+7042T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63600776 | ||||||
| chr1:63600824
|
G | A | 1 | a0002c0002t0003g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.246+7090G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63600824 | ||||||
| chr1:63600928
|
A | G | 129 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0243others(126): Show | 129 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.246+7194A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63600928 | ||||||
| chr1:63601008
|
G | A | 129 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0243others(126): Show | 129 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.246+7274G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63601008 | ||||||
| chr1:63601440
|
A | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0173a0001c0001t0001g0174others(58): Show | 62 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.246+7706A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63601440 | ||||||
| chr1:63601617
|
G | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0173a0001c0001t0001g0174others(58): Show | 62 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.246+7883G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63601617 | ||||||
| chr1:63601750
|
G | A | 7 | a0001c0001t0003g0147a0001c0006t0001g0350a0001c0006t0003g0145others(4): Show | 7 | HG00738.hp1 HG01192.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.246+8016G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63601750 | ||||||
| chr1:63601999
|
A | G | 7 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0003g0168others(4): Show | 7 | HG01081.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+8265A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63601999 | ||||||
| chr1:63602113
|
G | T | 1 | a0002c0002t0001g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.246+8379G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63602113 | ||||||
| chr1:63602245
|
A | C | 2 | a0001c0001t0001g0085a0008c0009t0001g0086 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.246+8511A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63602245 | ||||||
| chr1:63602349
|
T | G | 291 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0085others(288): Show | 293 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.246+8615T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63602349 | ||||||
| chr1:63602393
|
A | G | 1 | a0005c0005t0001g0348 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.246+8659A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63602393 | ||||||
| chr1:63602501
|
A | G | 6 | a0001c0001t0003g0082a0004c0004t0003g0083a0007c0010t0003g0080others(3): Show | 6 | HG01934.hp1 HG02257.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.246+8767A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63602501 | ||||||
| chr1:63602609
|
T | C | 234 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(231): Show | 235 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(232): Show |
intron_variant | MODIFIER | c.246+8875T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63602609 | ||||||
| chr1:63602610
|
G | A | 234 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(231): Show | 235 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(232): Show |
intron_variant | MODIFIER | c.246+8876G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63602610 | ||||||
| chr1:63602611
|
A | T | 234 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(231): Show | 235 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(232): Show |
intron_variant | MODIFIER | c.246+8877A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63602611 | ||||||
| chr1:63602612
|
A | C | 234 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(231): Show | 235 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(232): Show |
intron_variant | MODIFIER | c.246+8878A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63602612 | ||||||
| chr1:63602613
|
TTGAA | T | 234 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(231): Show | 235 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(232): Show |
intron_variant | MODIFIER | c.246+8880_246+8883d others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63602613 | ||||||
| chr1:63602618
|
A | C | 234 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0154others(231): Show | 235 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(232): Show |
intron_variant | MODIFIER | c.246+8884A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63602618 | ||||||
| chr1:63602665
|
G | A | 129 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0243others(126): Show | 129 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.246+8931G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63602665 | ||||||
| chr1:63602715
|
A | G | 116 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0243others(113): Show | 116 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.246+8981A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63602715 | ||||||
| chr1:63603127
|
C | A | 2 | a0001c0008t0001g0337a0003c0020t0002g0336 | 2 | NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.246+9393C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63603127 | ||||||
| chr1:63603186
|
G | C | 1 | a0003c0003t0001g0258 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.246+9452G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63603186 | ||||||
| chr1:63603191
|
A | G | 3 | a0001c0006t0001g0347a0001c0006t0003g0346a0001c0017t0001g0345 | 3 | HG02622.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.246+9457A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63603191 | ||||||
| chr1:63603285
|
G | A | 1 | a0003c0003t0002g0013 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.246+9551G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63603285 | ||||||
| chr1:63603542
|
C | T | 1 | a0003c0003t0001g0071 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.246+9808C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63603542 | ||||||
| chr1:63603570
|
C | T | 1 | a0001c0001t0007g0210 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.246+9836C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63603570 | ||||||
| chr1:63603666
|
A | G | 117 | a0001c0001t0001g0234a0001c0001t0001g0240a0001c0001t0001g0243others(114): Show | 117 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.246+9932A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63603666 | ||||||
| chr1:63603807
|
G | T | 2 | a0001c0008t0001g0337a0003c0020t0002g0336 | 2 | NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.246+10073G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63603807 | ||||||
| chr1:63603824
|
G | A | 291 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0085others(288): Show | 293 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.246+10090G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63603824 | ||||||
| chr1:63603857
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.246+10123A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63603857 | ||||||
| chr1:63603941
|
A | G | 116 | a0001c0001t0001g0161a0001c0001t0001g0234a0001c0001t0001g0240others(113): Show | 116 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.246+10207A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63603941 | ||||||
| chr1:63604226
|
A | C | 6 | a0001c0006t0001g0347a0001c0006t0003g0342a0001c0006t0003g0346others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+10492A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63604226 | ||||||
| chr1:63604414
|
C | T | 1 | a0001c0008t0002g0058 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.246+10680C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63604414 | ||||||
| chr1:63604623
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.246+10889T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63604623 | ||||||
| chr1:63604625
|
C | T | 1 | a0008c0009t0001g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.246+10891C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63604625 | ||||||
| chr1:63604673
|
C | T | 53 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0092others(50): Show | 54 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+10939C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63604673 | ||||||
| chr1:63604729
|
C | T | 24 | a0001c0001t0001g0077a0001c0001t0001g0154a0001c0001t0001g0155others(21): Show | 24 | HG01167.hp1 HG01243.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.246+10995C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63604729 | ||||||
| chr1:63604748
|
A | G | 7 | a0001c0001t0001g0351a0001c0006t0001g0347a0001c0006t0003g0342others(4): Show | 7 | HG02572.hp1 HG02622.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.246+11014A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63604748 | ||||||
| chr1:63604917
|
C | CG | 4 | a0001c0001t0001g0212a0002c0002t0001g0184a0002c0002t0001g0213others(1): Show | 4 | HG00558.hp1 HG03704.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+11183_246+1118 others(5): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63604917 | ||||||
| chr1:63604917
|
C | CGTG | 41 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0173others(38): Show | 42 | HG00609.hp1 HG00733.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.246+11183_246+1118 others(7): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63604917 | ||||||
| chr1:63604917
|
C | CGTGTG | 8 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG00621.hp1 HG00621.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.246+11183_246+1118 others(9): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63604917 | ||||||
| chr1:63604917
|
C | CTG | 23 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0045others(20): Show | 23 | HG01433.hp1 HG01515.hp1 HG01517.hp2 others(20): Show |
intron_variant | MODIFIER | c.246+11225_246+1122 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604917 | |||||
| chr1:63604917
|
C | CTGTCTGT others(3): Show |
1 | a0002c0002t0002g0261 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.246+11186_246+1118 others(14): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604917 | |||||
| chr1:63604917
|
C | CTGTG | 8 | a0001c0001t0001g0004a0001c0001t0001g0055a0001c0001t0001g0085others(5): Show | 8 | HG00738.hp2 HG03195.hp2 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.246+11223_246+1122 others(8): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604917 | |||||
| chr1:63604917
|
C | CTGTGTGT others(5): Show |
1 | a0005c0005t0001g0329 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.246+11215_246+1122 others(16): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604917 | |||||
| chr1:63604917
|
CT | C | 3 | a0001c0001t0003g0182a0003c0003t0001g0183a0003c0003t0001g0211 | 3 | HG01978.hp2 HG02257.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.246+11184delT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63604917 | ||||||
| chr1:63604917
|
CTG | C | 52 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0024others(49): Show | 53 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.246+11225_246+1122 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604917 | |||||
| chr1:63604917
|
CTGTG | C | 24 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0073others(21): Show | 24 | HG00741.hp1 HG01081.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.246+11223_246+1122 others(8): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604917 | |||||
| chr1:63604917
|
CTGTGTG | C | 18 | a0001c0001t0001g0006a0001c0001t0001g0096a0001c0001t0001g0098others(15): Show | 18 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.246+11221_246+1122 others(10): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604917 | |||||
| chr1:63604917
|
CTGTGTGT others(1): Show |
C | 20 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0128others(17): Show | 20 | HG00438.hp2 HG01952.hp1 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.246+11219_246+1122 others(12): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604917 | |||||
| chr1:63604917
|
CTGTGTGT others(3): Show |
C | 3 | a0001c0001t0003g0140a0002c0002t0003g0152a0004c0004t0003g0158 | 3 | HG01167.hp1 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.246+11217_246+1122 others(14): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604917 | |||||
| chr1:63604917
|
CTGTGTGT others(5): Show |
C | 4 | a0001c0006t0003g0141a0002c0002t0001g0124a0003c0003t0002g0142others(1): Show | 4 | HG02572.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+11215_246+1122 others(16): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604917 | |||||
| chr1:63604917
|
CTGTGTGT others(7): Show |
C | 4 | a0001c0001t0001g0005a0002c0002t0002g0018a0002c0002t0002g0019others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+11213_246+1122 others(18): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604917 | |||||
| chr1:63604959
|
G | GTGTGTGT others(4): Show |
2 | a0001c0001t0001g0333a0007c0011t0003g0272 | 2 | NA19012.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.246+11226_246+1122 others(15): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604959 | |||||
| chr1:63604959
|
G | GTGTGTGT others(6): Show |
1 | a0001c0006t0001g0265 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.246+11226_246+1122 others(17): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604959 | |||||
| chr1:63604959
|
G | GTGTGTGT others(11): Show |
1 | a0001c0001t0002g0245 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.246+11226_246+1122 others(22): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604959 | |||||
| chr1:63604959
|
G | GTGTGTGT others(9): Show |
3 | a0002c0002t0003g0263a0002c0002t0003g0264a0012c0021t0001g0233 | 3 | HG01516.hp2 HG01517.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.246+11226_246+1122 others(20): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604959 | |||||
| chr1:63604959
|
G | GTGTGTGT others(7): Show |
11 | a0001c0001t0001g0248a0001c0001t0001g0266a0001c0001t0001g0267others(8): Show | 11 | HG00735.hp2 HG01361.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.246+11226_246+1122 others(18): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604959 | |||||
| chr1:63604959
|
G | GTGTGTGT others(5): Show |
40 | a0001c0001t0001g0234a0001c0001t0001g0250a0001c0001t0001g0278others(37): Show | 40 | HG00642.hp1 HG00735.hp1 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.246+11226_246+1122 others(16): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604959 | |||||
| chr1:63604959
|
G | GTGTGTGT others(3): Show |
28 | a0001c0001t0001g0135a0001c0001t0001g0240a0001c0001t0001g0254others(25): Show | 28 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.246+11226_246+1122 others(14): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604959 | |||||
| chr1:63604959
|
G | GTGTGTGT others(1): Show |
21 | a0001c0001t0001g0243a0001c0001t0001g0257a0001c0001t0001g0310others(18): Show | 21 | HG00733.hp2 HG01192.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.246+11226_246+1122 others(12): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604959 | |||||
| chr1:63604959
|
G | GTGTGTT | 12 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321others(9): Show | 12 | HG01346.hp1 HG01934.hp2 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+11226_246+1122 others(10): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604959 | |||||
| chr1:63604959
|
G | GTGTT | 5 | a0001c0001t0001g0256a0001c0001t0001g0324a0001c0006t0003g0342others(2): Show | 5 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+11226_246+1122 others(8): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63604959 | |||||
| chr1:63604959
|
G | T | 9 | a0001c0001t0003g0140a0001c0006t0001g0350a0001c0006t0003g0141others(6): Show | 9 | HG00738.hp1 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.246+11225G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63604959 | ||||||
| chr1:63604993
|
T | C | 2 | a0001c0001t0001g0085a0008c0009t0001g0086 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.246+11259T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63604993 | ||||||
| chr1:63605328
|
C | G | 1 | a0001c0014t0003g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.246+11594C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63605328 | ||||||
| chr1:63605353
|
T | A | 3 | a0001c0006t0001g0347a0001c0006t0003g0346a0001c0017t0001g0345 | 3 | HG02622.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.246+11619T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63605353 | ||||||
| chr1:63605743
|
T | C | 28 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0067others(25): Show | 28 | HG00639.hp1 HG00642.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.246+12009T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63605743 | ||||||
| chr1:63605778
|
C | T | 1 | a0005c0005t0001g0203 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.246+12044C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63605778 | ||||||
| chr1:63605788
|
TCTCCAG | T | 7 | a0001c0001t0001g0351a0001c0006t0001g0347a0001c0006t0003g0342others(4): Show | 7 | HG02572.hp1 HG02622.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.246+12057_246+1206 others(10): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63605788 | |||||
| chr1:63605862
|
G | A | 2 | a0001c0001t0001g0085a0008c0009t0001g0086 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.246+12128G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63605862 | ||||||
| chr1:63606042
|
T | G | 1 | a0008c0009t0001g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.246+12308T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63606042 | ||||||
| chr1:63606443
|
G | A | 7 | a0001c0001t0001g0161a0001c0001t0003g0082a0004c0004t0003g0083others(4): Show | 7 | HG01934.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+12709G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63606443 | ||||||
| chr1:63606450
|
T | G | 1 | a0007c0010t0005g0144 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.246+12716T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63606450 | ||||||
| chr1:63606455
|
C | G | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | NA18985.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.246+12721C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63606455 | ||||||
| chr1:63606487
|
T | G | 5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0120others(2): Show | 5 | HG01243.hp1 HG01433.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+12753T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63606487 | ||||||
| chr1:63606497
|
C | T | 1 | a0002c0002t0003g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.246+12763C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63606497 | ||||||
| chr1:63606623
|
C | T | 2 | a0001c0001t0001g0014a0002c0002t0001g0015 | 2 | HG00642.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.246+12889C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63606623 | ||||||
| chr1:63606889
|
G | A | 1 | a0003c0003t0002g0340 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.246+13155G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63606889 | ||||||
| chr1:63606900
|
C | T | 6 | a0001c0001t0003g0147a0001c0006t0003g0145a0001c0006t0003g0148others(3): Show | 6 | HG01192.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+13166C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63606900 | ||||||
| chr1:63606975
|
A | T | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.246+13241A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63606975 | ||||||
| chr1:63607101
|
C | T | 1 | a0001c0006t0003g0170 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.246+13367C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63607101 | ||||||
| chr1:63607238
|
A | G | 2 | a0001c0001t0001g0085a0008c0009t0001g0086 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.246+13504A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63607238 | ||||||
| chr1:63607285
|
G | A | 1 | a0002c0002t0001g0204 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.246+13551G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63607285 | ||||||
| chr1:63607503
|
A | AGTGTGCT others(11): Show |
1 | a0001c0001t0001g0059 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.246+13775_246+1377 others(22): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63607503 | |||||
| chr1:63607511
|
T | C | 1 | a0001c0001t0001g0059 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.246+13777T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63607511 | ||||||
| chr1:63607539
|
G | A | 1 | a0004c0004t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.246+13805G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63607539 | ||||||
| chr1:63607630
|
T | A | 6 | a0001c0001t0003g0147a0001c0006t0003g0145a0001c0006t0003g0148others(3): Show | 6 | HG01192.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+13896T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63607630 | ||||||
| chr1:63607677
|
T | C | 5 | a0001c0001t0003g0140a0001c0006t0003g0141a0003c0003t0002g0142others(2): Show | 5 | HG02280.hp1 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+13943T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63607677 | ||||||
| chr1:63607716
|
C | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0173others(57): Show | 61 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.246+13982C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63607716 | ||||||
| chr1:63607743
|
A | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0088others(119): Show | 124 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.246+14009A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63607743 | ||||||
| chr1:63607849
|
C | T | 5 | a0001c0001t0003g0140a0001c0006t0003g0141a0003c0003t0002g0142others(2): Show | 5 | HG02280.hp1 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+14115C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63607849 | ||||||
| chr1:63608141
|
TCAA | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0077others(162): Show | 167 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.246+14409_246+1441 others(7): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63608141 | |||||
| chr1:63608148
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.246+14414G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63608148 | ||||||
| chr1:63608245
|
T | C | 296 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0060others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.246+14511T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63608245 | ||||||
| chr1:63608246
|
G | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0090a0004c0004t0001g0089 | 3 | HG00438.hp1 NA18747.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.246+14512G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63608246 | ||||||
| chr1:63608347
|
T | A | 1 | a0005c0005t0003g0275 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.246+14613T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63608347 | ||||||
| chr1:63608409
|
C | T | 298 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0060others(295): Show | 300 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(297): Show |
intron_variant | MODIFIER | c.246+14675C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63608409 | ||||||
| chr1:63608546
|
G | A | 122 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0088others(119): Show | 124 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.246+14812G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63608546 | ||||||
| chr1:63608766
|
C | T | 62 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0090others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.246+15032C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63608766 | ||||||
| chr1:63608874
|
G | A | 3 | a0001c0001t0001g0180a0001c0001t0001g0222a0001c0001t0001g0225 | 3 | NA18980.hp1 NA18991.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.246+15140G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63608874 | ||||||
| chr1:63609001
|
T | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0208 | 2 | NA18973.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.246+15267T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609001 | ||||||
| chr1:63609053
|
T | G | 1 | a0001c0001t0003g0099 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.246+15319T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609053 | ||||||
| chr1:63609060
|
G | A | 122 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0088others(119): Show | 124 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.246+15326G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609060 | ||||||
| chr1:63609292
|
G | A | 1 | a0001c0006t0001g0350 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.246+15558G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609292 | ||||||
| chr1:63609469
|
A | G | 1 | a0001c0001t0002g0202 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.246+15735A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609469 | ||||||
| chr1:63609479
|
G | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0060others(293): Show | 298 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(295): Show |
intron_variant | MODIFIER | c.246+15745G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609479 | ||||||
| chr1:63609485
|
C | T | 53 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0090others(50): Show | 54 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.246+15751C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609485 | ||||||
| chr1:63609509
|
C | T | 7 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0003g0168others(4): Show | 7 | HG01081.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+15775C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609509 | ||||||
| chr1:63609517
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0208 | 2 | NA18973.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.246+15783G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609517 | ||||||
| chr1:63609567
|
T | C | 2 | a0001c0001t0001g0243a0001c0001t0001g0319 | 2 | HG02135.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.246+15833T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609567 | ||||||
| chr1:63609713
|
C | T | 1 | a0001c0001t0001g0351 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.246+15979C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609713 | ||||||
| chr1:63609768
|
C | T | 2 | a0001c0001t0001g0248a0002c0002t0001g0271 | 2 | NA18981.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.246+16034C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609768 | ||||||
| chr1:63609788
|
T | A | 7 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0003g0168others(4): Show | 7 | HG01081.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.246+16054T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609788 | ||||||
| chr1:63609883
|
G | A | 31 | a0001c0001t0001g0077a0001c0001t0001g0154a0001c0001t0001g0155others(28): Show | 31 | HG01081.hp1 HG01167.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.246+16149G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609883 | ||||||
| chr1:63609886
|
TG | T | 3 | a0001c0006t0003g0342a0005c0005t0001g0344a0006c0013t0001g0343 | 3 | HG02572.hp1 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.246+16154delG | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63609886 | |||||
| chr1:63609926
|
A | G | 1 | a0001c0008t0002g0058 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.246+16192A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609926 | ||||||
| chr1:63609996
|
C | T | 2 | a0001c0006t0003g0342a0006c0013t0001g0343 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.246+16262C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63609996 | ||||||
| chr1:63610097
|
T | C | 60 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0173others(57): Show | 61 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.246+16363T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63610097 | ||||||
| chr1:63610451
|
A | T | 62 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0090others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.246+16717A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63610451 | ||||||
| chr1:63610585
|
G | A | 7 | a0001c0001t0001g0351a0001c0006t0001g0347a0001c0006t0003g0342others(4): Show | 7 | HG02572.hp1 HG02622.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.246+16851G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63610585 | ||||||
| chr1:63610691
|
T | A | 1 | a0002c0002t0003g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.246+16957T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63610691 | ||||||
| chr1:63610773
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.246+17039G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63610773 | ||||||
| chr1:63610823
|
G | A | 1 | a0003c0003t0002g0340 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.246+17089G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63610823 | ||||||
| chr1:63610884
|
T | C | 62 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0090others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.246+17150T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63610884 | ||||||
| chr1:63610973
|
G | A | 299 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0060others(296): Show | 301 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.246+17239G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63610973 | ||||||
| chr1:63611076
|
A | G | 2 | a0002c0002t0001g0213a0002c0002t0001g0221 | 2 | NA18966.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.246+17342A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63611076 | ||||||
| chr1:63611143
|
A | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0095a0001c0001t0001g0154others(81): Show | 85 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.246+17409A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63611143 | ||||||
| chr1:63611433
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.246+17699G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63611433 | ||||||
| chr1:63611444
|
A | G | 1 | a0001c0014t0003g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.246+17710A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63611444 | ||||||
| chr1:63611505
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0173a0001c0001t0001g0186others(1): Show | 5 | HG01074.hp1 HG01081.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+17771G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63611505 | ||||||
| chr1:63611554
|
A | G | 2 | a0001c0001t0001g0178a0003c0003t0002g0179 | 2 | NA18940.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.246+17820A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63611554 | ||||||
| chr1:63611589
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.247-17836G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63611589 | ||||||
| chr1:63611626
|
C | T | 4 | a0001c0001t0001g0351a0001c0006t0001g0347a0001c0006t0003g0346others(1): Show | 4 | HG02622.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-17799C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63611626 | ||||||
| chr1:63611628
|
G | T | 1 | a0002c0002t0001g0291 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.247-17797G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63611628 | ||||||
| chr1:63611924
|
G | A | 1 | a0002c0002t0001g0188 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.247-17501G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63611924 | ||||||
| chr1:63611930
|
G | A | 1 | a0003c0003t0002g0340 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.247-17495G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63611930 | ||||||
| chr1:63611989
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.247-17436C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63611989 | ||||||
| chr1:63612020
|
G | A | 2 | a0001c0006t0001g0350a0008c0009t0001g0139 | 2 | HG00738.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.247-17405G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63612020 | ||||||
| chr1:63612126
|
G | A | 2 | a0002c0002t0001g0084a0002c0002t0001g0100 | 2 | HG00423.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.247-17299G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63612126 | ||||||
| chr1:63612184
|
G | A | 7 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0003g0168others(4): Show | 7 | HG01081.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-17241G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63612184 | ||||||
| chr1:63612257
|
CA | C | 127 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0012others(124): Show | 128 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.247-17157delA | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63612257 | |||||
| chr1:63612430
|
T | G | 3 | a0001c0001t0001g0320a0002c0002t0001g0101a0004c0004t0002g0244 | 3 | NA18985.hp1 NA19006.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.247-16995T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63612430 | ||||||
| chr1:63612478
|
G | A | 1 | a0005c0005t0001g0348 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.247-16947G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63612478 | ||||||
| chr1:63612553
|
G | A | 59 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0095others(56): Show | 60 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.247-16872G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63612553 | ||||||
| chr1:63612572
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.247-16853T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63612572 | ||||||
| chr1:63612585
|
C | T | 5 | a0001c0001t0001g0256a0001c0001t0001g0324a0001c0001t0003g0246others(2): Show | 5 | HG00735.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-16840C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63612585 | ||||||
| chr1:63612617
|
A | G | 1 | a0003c0003t0002g0359 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.247-16808A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63612617 | ||||||
| chr1:63612683
|
C | T | 8 | a0001c0001t0001g0077a0001c0001t0001g0352a0001c0001t0003g0147others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.247-16742C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63612683 | ||||||
| chr1:63612754
|
A | G | 44 | a0001c0001t0001g0007a0001c0001t0001g0077a0001c0001t0001g0085others(41): Show | 44 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.247-16671A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63612754 | ||||||
| chr1:63612950
|
G | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0022a0002c0002t0001g0015 | 3 | HG00642.hp2 HG01069.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.247-16475G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63612950 | ||||||
| chr1:63613192
|
A | G | 136 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.247-16233A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63613192 | ||||||
| chr1:63613259
|
C | CT | 211 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 213 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(210): Show |
intron_variant | MODIFIER | c.247-16144dupT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63613259 | |||||
| chr1:63613259
|
C | CTT | 46 | a0001c0001t0001g0077a0001c0001t0001g0085a0001c0001t0001g0088others(43): Show | 46 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.247-16145_247-1614 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63613259 | |||||
| chr1:63613259
|
C | CTTTTTT | 61 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0034others(58): Show | 61 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.247-16149_247-1614 others(10): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63613259 | |||||
| chr1:63613259
|
C | CTTTTTTT | 11 | a0001c0001t0001g0053a0001c0001t0001g0161a0001c0001t0003g0082others(8): Show | 11 | HG01515.hp1 HG01517.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.247-16150_247-1614 others(11): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63613259 | |||||
| chr1:63613286
|
A | G | 1 | a0001c0001t0002g0317 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.247-16139A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63613286 | ||||||
| chr1:63613703
|
C | CT | 78 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0095others(75): Show | 79 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.247-15703dupT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63613703 | |||||
| chr1:63613703
|
C | CTT | 6 | a0001c0001t0001g0020a0001c0001t0001g0225a0001c0001t0003g0198others(3): Show | 6 | HG02145.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.247-15704_247-1570 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63613703 | |||||
| chr1:63613703
|
CT | C | 63 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0077others(60): Show | 63 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.247-15703delT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63613703 | |||||
| chr1:63613731
|
C | T | 46 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0034others(43): Show | 46 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.247-15694C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63613731 | ||||||
| chr1:63613815
|
T | C | 1 | a0002c0002t0003g0091 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.247-15610T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63613815 | ||||||
| chr1:63613936
|
C | T | 2 | a0003c0003t0002g0253a0004c0004t0003g0251 | 2 | HG02523.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.247-15489C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63613936 | ||||||
| chr1:63613937
|
G | A | 125 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0012others(122): Show | 125 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.247-15488G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63613937 | ||||||
| chr1:63613970
|
T | A | 44 | a0001c0001t0001g0007a0001c0001t0001g0077a0001c0001t0001g0085others(41): Show | 44 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.247-15455T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63613970 | ||||||
| chr1:63614006
|
G | A | 124 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0012others(121): Show | 124 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.247-15419G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63614006 | ||||||
| chr1:63614106
|
G | A | 4 | a0001c0001t0001g0069a0001c0006t0001g0350a0003c0003t0002g0068others(1): Show | 4 | HG00738.hp1 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-15319G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63614106 | ||||||
| chr1:63614116
|
T | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0022a0002c0002t0001g0015 | 3 | HG00642.hp2 HG01069.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.247-15309T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63614116 | ||||||
| chr1:63614328
|
G | T | 1 | a0001c0006t0001g0350 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.247-15097G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63614328 | ||||||
| chr1:63614388
|
C | T | 2 | a0006c0007t0001g0157a0008c0009t0001g0139 | 2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.247-15037C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63614388 | ||||||
| chr1:63614447
|
T | C | 192 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0010others(189): Show | 193 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.247-14978T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63614447 | ||||||
| chr1:63614464
|
A | C | 180 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0010others(177): Show | 181 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.247-14961A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63614464 | ||||||
| chr1:63614739
|
CA | C | 8 | a0001c0001t0001g0069a0001c0006t0003g0141a0001c0006t0003g0145others(5): Show | 8 | HG01192.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.247-14685delA | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63614739 | ||||||
| chr1:63614790
|
C | A | 10 | a0001c0001t0001g0069a0001c0006t0003g0141a0001c0006t0003g0145others(7): Show | 10 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.247-14635C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63614790 | ||||||
| chr1:63614800
|
T | G | 1 | a0015c0023t0002g0191 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.247-14625T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63614800 | ||||||
| chr1:63614953
|
G | GA | 141 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(138): Show | 142 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.247-14472_247-1447 others(5): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63614953 | ||||||
| chr1:63615004
|
G | A | 83 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0102others(80): Show | 84 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.247-14421G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615004 | ||||||
| chr1:63615010
|
G | A | 1 | a0007c0011t0003g0151 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.247-14415G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615010 | ||||||
| chr1:63615131
|
T | C | 3 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0321 | 3 | NA18945.hp1 NA19062.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.247-14294T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615131 | ||||||
| chr1:63615300
|
G | T | 12 | a0001c0001t0003g0140a0001c0001t0003g0160a0002c0002t0003g0150others(9): Show | 12 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.247-14125G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615300 | ||||||
| chr1:63615350
|
G | C | 8 | a0001c0001t0001g0077a0001c0001t0001g0352a0001c0001t0003g0147others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.247-14075G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615350 | ||||||
| chr1:63615411
|
G | A | 2 | a0007c0011t0003g0151a0008c0009t0001g0086 | 2 | HG02895.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.247-14014G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615411 | ||||||
| chr1:63615424
|
G | A | 1 | a0005c0005t0001g0056 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.247-14001G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615424 | ||||||
| chr1:63615478
|
A | G | 12 | a0001c0001t0003g0140a0001c0001t0003g0160a0002c0002t0003g0150others(9): Show | 12 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.247-13947A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615478 | ||||||
| chr1:63615547
|
CTTCTTTT | C | 7 | a0001c0006t0003g0141a0001c0006t0003g0145a0001c0006t0003g0148others(4): Show | 7 | HG01192.hp1 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-13875_247-1386 others(11): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63615547 | |||||
| chr1:63615550
|
C | CT | 44 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0102others(41): Show | 45 | HG00423.hp1 HG00423.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.247-13845dupT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63615550 | |||||
| chr1:63615550
|
C | CTT | 25 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0136others(22): Show | 25 | HG01074.hp1 HG01361.hp1 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.247-13846_247-1384 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63615550 | |||||
| chr1:63615550
|
C | CTTT | 27 | a0001c0001t0001g0010a0001c0001t0001g0069a0001c0001t0001g0138others(24): Show | 27 | HG00140.hp2 HG00673.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.247-13847_247-1384 others(7): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63615550 | |||||
| chr1:63615550
|
C | CTTTT | 17 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0052others(14): Show | 17 | HG00639.hp1 HG00738.hp2 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.247-13848_247-1384 others(8): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63615550 | |||||
| chr1:63615550
|
C | CTTTTT | 14 | a0001c0001t0001g0012a0001c0001t0001g0048a0001c0001t0001g0126others(11): Show | 14 | HG01515.hp1 HG02027.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.247-13849_247-1384 others(9): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63615550 | |||||
| chr1:63615550
|
C | CTTTTTT | 7 | a0001c0001t0001g0004a0001c0001t0001g0132a0001c0001t0001g0266others(4): Show | 7 | HG00438.hp2 HG01517.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.247-13850_247-1384 others(10): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63615550 | |||||
| chr1:63615550
|
C | CTTTTTTT others(3): Show |
6 | a0001c0001t0003g0153a0001c0006t0003g0170a0002c0002t0003g0152others(3): Show | 6 | HG01167.hp1 HG02109.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.247-13854_247-1384 others(14): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63615550 | |||||
| chr1:63615550
|
C | CTTTTTTT others(4): Show |
5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG02145.hp1 HG02647.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-13855_247-1384 others(15): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63615550 | |||||
| chr1:63615550
|
CT | C | 10 | a0001c0001t0001g0090a0001c0001t0001g0098a0001c0001t0001g0226others(7): Show | 10 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.247-13845delT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63615550 | |||||
| chr1:63615550
|
CTT | C | 28 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0092others(25): Show | 28 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(25): Show |
intron_variant | MODIFIER | c.247-13846_247-1384 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63615550 | |||||
| chr1:63615550
|
CTTTT | C | 9 | a0001c0001t0001g0077a0001c0001t0001g0352a0001c0001t0003g0147others(6): Show | 9 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-13848_247-1384 others(8): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63615550 | |||||
| chr1:63615550
|
CTTTTTT | C | 11 | a0001c0001t0003g0140a0001c0001t0003g0160a0003c0003t0003g0143others(8): Show | 11 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.247-13850_247-1384 others(10): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63615550 | |||||
| chr1:63615550
|
CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0001g0351a0001c0001t0003g0082a0001c0006t0003g0346others(4): Show | 7 | HG02559.hp1 HG02970.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.247-13854_247-1384 others(14): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63615550 | |||||
| chr1:63615550
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.247-13856_247-1384 others(16): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63615550 | |||||
| chr1:63615553
|
T | C | 1 | a0001c0001t0002g0023 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.247-13872T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615553 | ||||||
| chr1:63615565
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.247-13860T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615565 | ||||||
| chr1:63615578
|
T | G | 7 | a0001c0006t0003g0141a0001c0006t0003g0145a0001c0006t0003g0148others(4): Show | 7 | HG01192.hp1 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-13847T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615578 | ||||||
| chr1:63615649
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.247-13776G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615649 | ||||||
| chr1:63615656
|
G | A | 12 | a0001c0001t0003g0140a0001c0001t0003g0160a0002c0002t0003g0150others(9): Show | 12 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.247-13769G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615656 | ||||||
| chr1:63615718
|
T | C | 84 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0102others(81): Show | 85 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.247-13707T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615718 | ||||||
| chr1:63615774
|
G | A | 1 | a0005c0005t0001g0344 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.247-13651G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615774 | ||||||
| chr1:63615952
|
T | C | 1 | a0002c0002t0001g0295 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.247-13473T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615952 | ||||||
| chr1:63615953
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.247-13472G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615953 | ||||||
| chr1:63615959
|
A | G | 12 | a0001c0001t0003g0140a0001c0001t0003g0160a0002c0002t0003g0150others(9): Show | 12 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.247-13466A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63615959 | ||||||
| chr1:63616034
|
C | T | 7 | a0001c0006t0003g0141a0001c0006t0003g0145a0001c0006t0003g0148others(4): Show | 7 | HG01192.hp1 HG02055.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-13391C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63616034 | ||||||
| chr1:63616058
|
A | C | 20 | a0001c0001t0003g0082a0001c0001t0003g0140a0001c0001t0003g0160others(17): Show | 20 | HG01891.hp2 HG01934.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-13367A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63616058 | ||||||
| chr1:63616066
|
AC | A | 24 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0001g0181others(21): Show | 24 | HG00558.hp1 HG00621.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.247-13358delC | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63616066 | ||||||
| chr1:63616120
|
A | G | 1 | a0002c0002t0003g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.247-13305A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63616120 | ||||||
| chr1:63616507
|
A | C | 1 | a0005c0005t0001g0171 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-12918A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63616507 | ||||||
| chr1:63616608
|
A | G | 72 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(69): Show | 72 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.247-12817A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63616608 | ||||||
| chr1:63616693
|
TGAGGCA | T | 20 | a0001c0001t0003g0082a0001c0001t0003g0140a0001c0001t0003g0160others(17): Show | 20 | HG01891.hp2 HG01934.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-12724_247-1271 others(10): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63616693 | |||||
| chr1:63616853
|
A | G | 30 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0090others(27): Show | 30 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.247-12572A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63616853 | ||||||
| chr1:63616897
|
G | A | 1 | a0003c0003t0001g0127 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.247-12528G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63616897 | ||||||
| chr1:63617063
|
C | T | 82 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0102others(79): Show | 83 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.247-12362C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63617063 | ||||||
| chr1:63617155
|
G | T | 38 | a0001c0001t0001g0007a0001c0001t0001g0077a0001c0001t0001g0088others(35): Show | 38 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.247-12270G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63617155 | ||||||
| chr1:63617296
|
G | A | 2 | a0001c0008t0001g0337a0003c0020t0002g0336 | 2 | NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.247-12129G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63617296 | ||||||
| chr1:63617471
|
G | T | 9 | a0001c0006t0003g0141a0001c0006t0003g0145a0001c0006t0003g0148others(6): Show | 9 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-11954G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63617471 | ||||||
| chr1:63617606
|
TGAGGCTG others(16): Show |
T | 1 | a0001c0001t0001g0270 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.247-11800_247-1177 others(27): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63617606 | |||||
| chr1:63617730
|
C | CA | 65 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0024others(62): Show | 65 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.247-11666dupA | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63617730 | |||||
| chr1:63617730
|
C | CAA | 19 | a0001c0001t0001g0006a0001c0001t0001g0090a0001c0001t0001g0092others(16): Show | 19 | HG00438.hp1 HG00609.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.247-11667_247-1166 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63617730 | |||||
| chr1:63617730
|
CA | C | 99 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0048others(96): Show | 99 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.247-11666delA | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63617730 | |||||
| chr1:63617730
|
CAA | C | 47 | a0001c0001t0001g0020a0001c0001t0001g0055a0001c0001t0001g0059others(44): Show | 47 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.247-11667_247-1166 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63617730 | |||||
| chr1:63617730
|
CAAAAAAA others(8): Show |
C | 2 | a0006c0007t0001g0157a0008c0009t0001g0139 | 2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.247-11680_247-1166 others(19): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63617730 | |||||
| chr1:63617857
|
A | G | 85 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0085others(82): Show | 86 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.247-11568A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63617857 | ||||||
| chr1:63617879
|
G | GT | 52 | a0001c0001t0001g0007a0001c0001t0001g0077a0001c0001t0001g0085others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.247-11536dupT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63617879 | |||||
| chr1:63617946
|
G | A | 1 | a0001c0001t0002g0300 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.247-11479G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63617946 | ||||||
| chr1:63618205
|
A | C | 2 | a0001c0006t0003g0342a0006c0013t0001g0343 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.247-11220A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63618205 | ||||||
| chr1:63618495
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.247-10930A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63618495 | ||||||
| chr1:63618528
|
T | C | 54 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0102others(51): Show | 55 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.247-10897T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63618528 | ||||||
| chr1:63618548
|
T | C | 2 | a0001c0006t0003g0342a0006c0013t0001g0343 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.247-10877T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63618548 | ||||||
| chr1:63618551
|
T | C | 4 | a0001c0001t0001g0034a0002c0002t0001g0016a0002c0002t0001g0017others(1): Show | 4 | HG00738.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-10874T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63618551 | ||||||
| chr1:63618679
|
G | C | 1 | a0001c0001t0007g0210 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.247-10746G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63618679 | ||||||
| chr1:63618820
|
G | A | 72 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(69): Show | 72 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.247-10605G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63618820 | ||||||
| chr1:63618833
|
G | A | 30 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0090others(27): Show | 30 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.247-10592G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63618833 | ||||||
| chr1:63619160
|
G | A | 9 | a0001c0006t0003g0141a0001c0006t0003g0145a0001c0006t0003g0148others(6): Show | 9 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-10265G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63619160 | ||||||
| chr1:63619192
|
A | T | 67 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0102others(64): Show | 68 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.247-10233A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63619192 | ||||||
| chr1:63619201
|
T | C | 3 | a0001c0001t0001g0268a0002c0002t0003g0276a0014c0024t0006g0236 | 3 | HG00735.hp2 HG01361.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.247-10224T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63619201 | ||||||
| chr1:63619433
|
T | A | 1 | a0005c0005t0001g0349 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.247-9992T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63619433 | ||||||
| chr1:63619441
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.247-9984G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63619441 | ||||||
| chr1:63619463
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.247-9962A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63619463 | ||||||
| chr1:63619546
|
C | T | 1 | a0002c0002t0001g0232 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.247-9879C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63619546 | ||||||
| chr1:63619666
|
G | A | 38 | a0001c0001t0001g0007a0001c0001t0001g0077a0001c0001t0001g0088others(35): Show | 38 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.247-9759G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63619666 | ||||||
| chr1:63619740
|
C | T | 3 | a0001c0001t0001g0257a0003c0003t0006g0325a0007c0011t0001g0065 | 3 | HG02129.hp2 HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.247-9685C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63619740 | ||||||
| chr1:63619784
|
C | T | 3 | a0001c0014t0005g0274a0005c0005t0003g0242a0007c0011t0003g0272 | 3 | HG02809.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.247-9641C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63619784 | ||||||
| chr1:63619834
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.247-9591T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63619834 | ||||||
| chr1:63619916
|
G | T | 1 | a0001c0014t0003g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.247-9509G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63619916 | ||||||
| chr1:63620104
|
A | C | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.247-9321A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63620104 | ||||||
| chr1:63620224
|
G | A | 16 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0257others(13): Show | 16 | HG00642.hp1 HG01346.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.247-9201G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63620224 | ||||||
| chr1:63620263
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.247-9162A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63620263 | ||||||
| chr1:63620367
|
T | C | 7 | a0001c0001t0003g0082a0004c0004t0003g0083a0006c0007t0001g0157others(4): Show | 7 | HG01934.hp1 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-9058T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63620367 | ||||||
| chr1:63620548
|
C | T | 186 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0010others(183): Show | 187 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.247-8877C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63620548 | ||||||
| chr1:63620562
|
C | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0031 | 2 | HG00639.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.247-8863C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63620562 | ||||||
| chr1:63620722
|
G | C | 6 | a0006c0007t0001g0231a0006c0007t0001g0249a0006c0007t0001g0252others(3): Show | 6 | HG01891.hp2 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.247-8703G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63620722 | ||||||
| chr1:63620850
|
T | C | 2 | a0001c0001t0001g0069a0003c0003t0002g0068 | 2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.247-8575T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63620850 | ||||||
| chr1:63621068
|
A | G | 1 | a0002c0002t0001g0097 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.247-8357A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63621068 | ||||||
| chr1:63621091
|
A | G | 15 | a0001c0001t0001g0161a0001c0001t0003g0140a0001c0001t0003g0160others(12): Show | 15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.247-8334A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63621091 | ||||||
| chr1:63621178
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.247-8247A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63621178 | ||||||
| chr1:63621230
|
G | A | 76 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0102others(73): Show | 77 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.247-8195G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63621230 | ||||||
| chr1:63621305
|
A | G | 25 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0090others(22): Show | 25 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(22): Show |
intron_variant | MODIFIER | c.247-8120A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63621305 | ||||||
| chr1:63621364
|
C | T | 1 | a0001c0008t0001g0337 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.247-8061C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63621364 | ||||||
| chr1:63621428
|
C | G | 1 | a0003c0003t0002g0142 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.247-7997C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63621428 | ||||||
| chr1:63621486
|
G | A | 1 | a0001c0001t0001g0327 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.247-7939G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63621486 | ||||||
| chr1:63621522
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.247-7903A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63621522 | ||||||
| chr1:63621619
|
T | G | 2 | a0004c0004t0002g0331a0007c0010t0005g0332 | 2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.247-7806T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63621619 | ||||||
| chr1:63621773
|
A | G | 62 | a0001c0001t0001g0055a0001c0001t0001g0059a0001c0001t0001g0095others(59): Show | 62 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.247-7652A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63621773 | ||||||
| chr1:63621862
|
C | T | 37 | a0001c0001t0001g0061a0001c0001t0001g0102a0001c0001t0001g0105others(34): Show | 38 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.247-7563C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63621862 | ||||||
| chr1:63622088
|
G | A | 37 | a0001c0001t0001g0061a0001c0001t0001g0102a0001c0001t0001g0105others(34): Show | 38 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.247-7337G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63622088 | ||||||
| chr1:63622142
|
A | G | 72 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(69): Show | 72 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.247-7283A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63622142 | ||||||
| chr1:63622364
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.247-7061A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63622364 | ||||||
| chr1:63622587
|
T | C | 2 | a0001c0006t0003g0342a0006c0013t0001g0343 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.247-6838T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63622587 | ||||||
| chr1:63622601
|
G | A | 9 | a0001c0006t0003g0141a0001c0006t0003g0145a0001c0006t0003g0148others(6): Show | 9 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-6824G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63622601 | ||||||
| chr1:63622855
|
G | A | 1 | a0002c0002t0001g0100 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.247-6570G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63622855 | ||||||
| chr1:63622980
|
A | G | 20 | a0001c0001t0001g0077a0001c0001t0001g0161a0001c0001t0001g0352others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-6445A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63622980 | ||||||
| chr1:63622989
|
G | A | 9 | a0001c0006t0003g0141a0001c0006t0003g0145a0001c0006t0003g0148others(6): Show | 9 | HG01192.hp1 HG01243.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-6436G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63622989 | ||||||
| chr1:63623025
|
T | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0120 | 2 | HG01243.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.247-6400T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63623025 | ||||||
| chr1:63623123
|
A | G | 1 | a0002c0002t0001g0063 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.247-6302A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63623123 | ||||||
| chr1:63623150
|
G | A | 1 | a0003c0003t0002g0068 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.247-6275G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63623150 | ||||||
| chr1:63623338
|
T | G | 20 | a0001c0001t0001g0077a0001c0001t0001g0161a0001c0001t0001g0352others(17): Show | 20 | HG01891.hp1 HG01891.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-6087T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63623338 | ||||||
| chr1:63624064
|
T | C | 1 | a0002c0002t0003g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.247-5361T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63624064 | ||||||
| chr1:63624099
|
C | A | 12 | a0001c0001t0001g0161a0001c0001t0003g0140a0001c0001t0003g0160others(9): Show | 12 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.247-5326C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63624099 | ||||||
| chr1:63624182
|
T | C | 1 | a0002c0002t0003g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.247-5243T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63624182 | ||||||
| chr1:63624256
|
G | GA | 363 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(360): Show | 365 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(362): Show |
intron_variant | MODIFIER | c.247-5169_247-5168i others(3): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63624256 | ||||||
| chr1:63624364
|
C | T | 1 | a0002c0002t0002g0209 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.247-5061C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63624364 | ||||||
| chr1:63624469
|
T | C | 10 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0003g0168others(7): Show | 10 | HG00639.hp1 HG01081.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.247-4956T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63624469 | ||||||
| chr1:63624486
|
T | C | 8 | a0001c0001t0001g0077a0001c0001t0001g0352a0001c0001t0003g0147others(5): Show | 8 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.247-4939T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63624486 | ||||||
| chr1:63624506
|
A | G | 52 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0102others(49): Show | 53 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.247-4919A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63624506 | ||||||
| chr1:63624706
|
G | C | 146 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0012others(143): Show | 147 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.247-4719G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63624706 | ||||||
| chr1:63624991
|
A | G | 52 | a0001c0001t0001g0061a0001c0001t0001g0085a0001c0001t0001g0102others(49): Show | 53 | HG00423.hp1 HG00423.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.247-4434A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63624991 | ||||||
| chr1:63625211
|
G | A | 1 | a0005c0005t0001g0344 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.247-4214G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63625211 | ||||||
| chr1:63625271
|
G | A | 249 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0010others(246): Show | 250 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.247-4154G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63625271 | ||||||
| chr1:63625601
|
A | G | 9 | a0001c0001t0001g0077a0001c0001t0001g0352a0001c0001t0003g0147others(6): Show | 9 | HG01891.hp1 HG02451.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-3824A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63625601 | ||||||
| chr1:63625722
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.247-3703T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63625722 | ||||||
| chr1:63625844
|
G | C | 10 | a0001c0001t0001g0161a0001c0001t0003g0140a0001c0001t0003g0160others(7): Show | 10 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.247-3581G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63625844 | ||||||
| chr1:63626068
|
A | G | 191 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0061others(188): Show | 193 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(190): Show |
intron_variant | MODIFIER | c.247-3357A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63626068 | ||||||
| chr1:63626202
|
A | C | 1 | a0001c0001t0001g0222 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.247-3223A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63626202 | ||||||
| chr1:63626270
|
T | C | 3 | a0001c0001t0001g0248a0002c0002t0001g0271a0002c0002t0001g0298 | 3 | NA18979.hp2 NA18981.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.247-3155T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63626270 | ||||||
| chr1:63626618
|
GA | G | 221 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0052others(218): Show | 223 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.247-2797delA | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63626618 | |||||
| chr1:63626753
|
G | A | 95 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0077others(92): Show | 95 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.247-2672G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63626753 | ||||||
| chr1:63626848
|
G | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0052others(210): Show | 215 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.247-2577G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63626848 | ||||||
| chr1:63626893
|
C | A | 84 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0077others(81): Show | 84 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.247-2532C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63626893 | ||||||
| chr1:63627019
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.247-2406C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627019 | ||||||
| chr1:63627053
|
A | AC | 61 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0060others(58): Show | 61 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.247-2359dupC | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63627053 | |||||
| chr1:63627053
|
AC | A | 68 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0014others(65): Show | 68 | HG00558.hp2 HG00642.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.247-2359delC | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63627053 | |||||
| chr1:63627063
|
C | A | 3 | a0001c0006t0001g0162a0001c0006t0001g0347a0001c0006t0001g0350 | 3 | HG00738.hp1 HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.247-2362C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627063 | ||||||
| chr1:63627063
|
C | CA | 4 | a0001c0001t0001g0077a0001c0001t0003g0140a0001c0001t0003g0160others(1): Show | 4 | HG02451.hp1 HG02886.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-2362_247-2361i others(3): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627063 | ||||||
| chr1:63627064
|
CCCA | C | 40 | a0001c0001t0001g0085a0001c0001t0001g0154a0001c0001t0001g0155others(37): Show | 40 | HG00558.hp1 HG01074.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.247-2359_247-2357d others(5): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63627064 | |||||
| chr1:63627065
|
C | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0069a0001c0001t0001g0077others(25): Show | 29 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.247-2360C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627065 | ||||||
| chr1:63627065
|
C | CA | 5 | a0001c0006t0003g0342a0006c0013t0001g0237a0006c0013t0001g0343others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-2360_247-2359i others(3): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627065 | ||||||
| chr1:63627065
|
CCA | C | 46 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0067others(43): Show | 46 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.247-2346_247-2345d others(4): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr1 | 63627065 | |||||
| chr1:63627066
|
CA | C | 7 | a0001c0001t0001g0192a0001c0001t0001g0200a0001c0001t0003g0153others(4): Show | 7 | HG02615.hp2 HG03453.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.247-2358delA | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627066 | ||||||
| chr1:63627066
|
CACA | C | 12 | a0001c0001t0001g0052a0001c0001t0001g0059a0001c0001t0001g0061others(9): Show | 12 | HG00423.hp2 HG02922.hp1 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.247-2358_247-2356d others(5): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627066 | ||||||
| chr1:63627067
|
A | C | 26 | a0001c0001t0001g0007a0001c0001t0001g0092a0001c0001t0001g0096others(23): Show | 26 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(23): Show |
intron_variant | MODIFIER | c.247-2358A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627067 | ||||||
| chr1:63627069
|
A | C | 21 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0095others(18): Show | 21 | HG00609.hp1 HG00621.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.247-2356A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627069 | ||||||
| chr1:63627077
|
A | G | 78 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0154others(75): Show | 78 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.247-2348A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627077 | ||||||
| chr1:63627110
|
G | A | 3 | a0001c0001t0001g0178a0001c0001t0001g0192a0003c0003t0002g0179 | 3 | NA18940.hp2 NA18952.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.247-2315G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627110 | ||||||
| chr1:63627119
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0001g0138a0003c0003t0002g0137 | 3 | NA18940.hp1 NA18949.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.247-2306A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627119 | ||||||
| chr1:63627158
|
G | A | 1 | a0002c0002t0003g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.247-2267G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627158 | ||||||
| chr1:63627323
|
A | G | 1 | a0005c0005t0001g0344 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.247-2102A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627323 | ||||||
| chr1:63627367
|
G | A | 75 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0154others(72): Show | 75 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.247-2058G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627367 | ||||||
| chr1:63627388
|
G | A | 11 | a0001c0001t0001g0077a0001c0001t0003g0140a0001c0001t0003g0160others(8): Show | 11 | HG01243.hp2 HG02451.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.247-2037G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627388 | ||||||
| chr1:63627526
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.247-1899G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627526 | ||||||
| chr1:63627728
|
C | A | 4 | a0001c0001t0001g0278a0001c0001t0001g0304a0004c0004t0001g0282others(1): Show | 4 | HG01496.hp2 HG01952.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-1697C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627728 | ||||||
| chr1:63627809
|
T | C | 2 | a0001c0001t0001g0069a0003c0003t0002g0068 | 2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.247-1616T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627809 | ||||||
| chr1:63627834
|
G | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(37): Show | 41 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(38): Show |
intron_variant | MODIFIER | c.247-1591G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627834 | ||||||
| chr1:63627851
|
C | T | 1 | a0008c0009t0001g0086 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.247-1574C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627851 | ||||||
| chr1:63627925
|
C | G | 1 | a0006c0007t0001g0292 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.247-1500C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627925 | ||||||
| chr1:63627972
|
A | T | 1 | a0001c0001t0001g0352 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.247-1453A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63627972 | ||||||
| chr1:63628017
|
T | C | 75 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0154others(72): Show | 75 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.247-1408T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628017 | ||||||
| chr1:63628049
|
G | T | 74 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0154others(71): Show | 74 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.247-1376G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628049 | ||||||
| chr1:63628097
|
G | T | 74 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0154others(71): Show | 74 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.247-1328G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628097 | ||||||
| chr1:63628179
|
C | T | 1 | a0004c0004t0001g0301 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.247-1246C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628179 | ||||||
| chr1:63628180
|
G | A | 74 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0154others(71): Show | 74 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.247-1245G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628180 | ||||||
| chr1:63628183
|
T | A | 74 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0154others(71): Show | 74 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.247-1242T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628183 | ||||||
| chr1:63628317
|
C | T | 74 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0154others(71): Show | 74 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.247-1108C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628317 | ||||||
| chr1:63628369
|
T | C | 74 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0154others(71): Show | 74 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.247-1056T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628369 | ||||||
| chr1:63628393
|
G | A | 72 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0154others(69): Show | 72 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.247-1032G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628393 | ||||||
| chr1:63628394
|
G | T | 1 | a0005c0005t0001g0344 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.247-1031G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628394 | ||||||
| chr1:63628477
|
C | T | 2 | a0005c0005t0001g0344a0005c0005t0001g0348 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.247-948C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628477 | ||||||
| chr1:63628492
|
C | T | 94 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0077others(91): Show | 94 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.247-933C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628492 | ||||||
| chr1:63628496
|
A | G | 2 | a0010c0015t0008g0177a0011c0016t0001g0228 | 2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.247-929A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628496 | ||||||
| chr1:63628845
|
A | G | 1 | a0008c0009t0001g0164 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.247-580A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628845 | ||||||
| chr1:63628883
|
C | G | 2 | a0005c0005t0001g0344a0005c0005t0001g0348 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.247-542C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628883 | ||||||
| chr1:63628940
|
A | T | 81 | a0001c0001t0001g0067a0001c0001t0001g0077a0001c0001t0001g0085others(78): Show | 81 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.247-485A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63628940 | ||||||
| chr1:63629109
|
G | A | 66 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0154others(63): Show | 66 | HG00423.hp1 HG00621.hp2 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.247-316G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63629109 | ||||||
| chr1:63629204
|
C | T | 1 | a0001c0001t0001g0334 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.247-221C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63629204 | ||||||
| chr1:63629370
|
C | T | 1 | a0001c0001t0003g0153 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.247-55C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63629370 | ||||||
| chr1:63629371
|
G | T | 23 | a0001c0001t0001g0002a0001c0001t0001g0173a0001c0001t0003g0140others(20): Show | 24 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.247-54G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 1/10 | chr1 | 63629371 | ||||||
| chr1:63629722
|
G | T | 1 | a0002c0002t0003g0091 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.409+135G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 2/10 | chr1 | 63629722 | ||||||
| chr1:63629773
|
C | T | 1 | a0001c0001t0007g0306 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.410-169C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 2/10 | chr1 | 63629773 | ||||||
| chr1:63629822
|
T | C | 5 | a0001c0001t0001g0154a0001c0014t0003g0335a0005c0005t0001g0203others(2): Show | 5 | HG00733.hp1 HG02145.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.410-120T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 2/10 | chr1 | 63629822 | ||||||
| chr1:63630135
|
G | C | 5 | a0001c0001t0001g0085a0001c0001t0001g0156a0001c0001t0001g0169others(2): Show | 5 | HG01934.hp1 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.556+47G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 3/10 | chr1 | 63630135 | ||||||
| chr1:63630165
|
G | C | 28 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(25): Show | 28 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.556+77G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 3/10 | chr1 | 63630165 | ||||||
| chr1:63630191
|
G | A | 46 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0067others(43): Show | 47 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.556+103G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 3/10 | chr1 | 63630191 | ||||||
| chr1:63630285
|
G | A | 1 | a0002c0002t0001g0015 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.556+197G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 3/10 | chr1 | 63630285 | ||||||
| chr1:63630304
|
C | T | 1 | a0002c0002t0002g0209 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.556+216C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 3/10 | chr1 | 63630304 | ||||||
| chr1:63630376
|
A | G | 1 | a0005c0005t0001g0199 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.556+288A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 3/10 | chr1 | 63630376 | ||||||
| chr1:63630423
|
G | A | 114 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0024others(111): Show | 115 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.556+335G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 3/10 | chr1 | 63630423 | ||||||
| chr1:63630573
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.556+485T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 3/10 | chr1 | 63630573 | ||||||
| chr1:63630962
|
G | A | 1 | a0005c0005t0001g0199 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.557-695G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 3/10 | chr1 | 63630962 | ||||||
| chr1:63631271
|
C | T | 10 | a0001c0001t0003g0082a0001c0006t0001g0265a0001c0006t0001g0347others(7): Show | 10 | HG00639.hp1 HG01255.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.557-386C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 3/10 | chr1 | 63631271 | ||||||
| chr1:63631950
|
A | G | 4 | a0001c0001t0001g0351a0003c0003t0001g0183a0005c0005t0001g0171others(1): Show | 4 | HG02257.hp2 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+168A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63631950 | ||||||
| chr1:63631979
|
G | A | 4 | a0001c0001t0001g0351a0003c0003t0001g0183a0005c0005t0001g0171others(1): Show | 4 | HG02257.hp2 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+197G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63631979 | ||||||
| chr1:63632079
|
C | G | 4 | a0001c0001t0001g0351a0003c0003t0001g0183a0005c0005t0001g0171others(1): Show | 4 | HG02257.hp2 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+297C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63632079 | ||||||
| chr1:63632122
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.682+340G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63632122 | ||||||
| chr1:63632206
|
G | A | 1 | a0001c0001t0001g0361 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.682+424G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63632206 | ||||||
| chr1:63632271
|
G | A | 3 | a0002c0002t0001g0116a0002c0002t0001g0121a0002c0002t0001g0362 | 3 | HG01358.hp1 HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.682+489G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63632271 | ||||||
| chr1:63632394
|
T | C | 90 | a0001c0001t0001g0005a0001c0014t0003g0335a0002c0002t0001g0003others(87): Show | 90 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.682+612T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63632394 | ||||||
| chr1:63632517
|
C | T | 41 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0053others(38): Show | 41 | HG00558.hp2 HG01496.hp2 HG01934.hp2 others(38): Show |
intron_variant | MODIFIER | c.682+735C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63632517 | ||||||
| chr1:63632606
|
C | G | 1 | a0001c0001t0001g0006 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.682+824C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63632606 | ||||||
| chr1:63632734
|
C | T | 88 | a0001c0014t0003g0335a0002c0002t0001g0003a0002c0002t0001g0009others(85): Show | 88 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.682+952C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63632734 | ||||||
| chr1:63632802
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.682+1020G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63632802 | ||||||
| chr1:63632906
|
G | A | 10 | a0001c0001t0001g0069a0001c0001t0001g0085a0001c0001t0001g0155others(7): Show | 10 | HG00733.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.682+1124G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63632906 | ||||||
| chr1:63632919
|
A | G | 99 | a0001c0001t0003g0246a0001c0001t0003g0353a0001c0001t0003g0355others(96): Show | 99 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.682+1137A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63632919 | ||||||
| chr1:63633001
|
C | T | 1 | a0001c0001t0003g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.682+1219C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633001 | ||||||
| chr1:63633064
|
C | G | 1 | a0007c0011t0001g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.682+1282C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633064 | ||||||
| chr1:63633100
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.682+1318T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633100 | ||||||
| chr1:63633132
|
A | G | 4 | a0001c0001t0003g0246a0005c0005t0001g0344a0008c0009t0001g0086others(1): Show | 4 | HG01884.hp1 HG03098.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+1350A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633132 | ||||||
| chr1:63633239
|
T | C | 234 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 236 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(233): Show |
intron_variant | MODIFIER | c.682+1457T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633239 | ||||||
| chr1:63633364
|
C | A | 1 | a0002c0002t0001g0051 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.683-1465C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633364 | ||||||
| chr1:63633391
|
T | G | 1 | a0002c0002t0004g0207 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.683-1438T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633391 | ||||||
| chr1:63633409
|
A | G | 37 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(34): Show | 38 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.683-1420A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633409 | ||||||
| chr1:63633520
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.683-1309G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633520 | ||||||
| chr1:63633652
|
T | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 143 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.683-1177T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633652 | ||||||
| chr1:63633675
|
C | CT | 20 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(17): Show | 21 | HG00639.hp1 HG01069.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.683-1144dupT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633675 | |||||
| chr1:63633709
|
C | A | 87 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0024others(84): Show | 88 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.683-1120C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633709 | ||||||
| chr1:63633753
|
C | T | 8 | a0003c0003t0003g0143a0005c0005t0001g0348a0006c0007t0001g0231others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-1076C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633753 | ||||||
| chr1:63633866
|
CTG | C | 30 | a0001c0001t0001g0010a0001c0001t0001g0055a0001c0001t0001g0072others(27): Show | 30 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.683-911_683-910del others(2): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633866 | |||||
| chr1:63633866
|
CTGTG | C | 12 | a0001c0001t0001g0045a0001c0001t0001g0095a0001c0001t0001g0110others(9): Show | 12 | HG00609.hp1 HG01261.hp1 HG03239.hp2 others(9): Show |
intron_variant | MODIFIER | c.683-913_683-910del others(4): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633866 | |||||
| chr1:63633866
|
CTGTGTGT others(3): Show |
C | 9 | a0001c0001t0001g0032a0001c0001t0001g0229a0001c0001t0001g0270others(6): Show | 9 | HG00558.hp2 HG01993.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.683-919_683-910del others(10): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633866 | |||||
| chr1:63633866
|
CTGTGTGT others(5): Show |
C | 33 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0092others(30): Show | 34 | HG00609.hp2 HG01496.hp2 HG01934.hp2 others(31): Show |
intron_variant | MODIFIER | c.683-921_683-910del others(12): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633866 | |||||
| chr1:63633866
|
CTGTGTGT others(7): Show |
C | 36 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(33): Show | 36 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.683-923_683-910del others(14): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633866 | |||||
| chr1:63633866
|
CTGTGTGT others(9): Show |
C | 2 | a0001c0006t0003g0346a0001c0014t0005g0274 | 2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.683-925_683-910del others(16): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633866 | |||||
| chr1:63633866
|
CTGTGTGT others(11): Show |
C | 13 | a0002c0002t0001g0016a0002c0002t0001g0084a0002c0002t0001g0097others(10): Show | 13 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.683-927_683-910del others(18): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633866 | |||||
| chr1:63633866
|
CTGTGTGT others(13): Show |
C | 5 | a0002c0002t0001g0119a0002c0002t0001g0291a0004c0004t0001g0286others(2): Show | 5 | HG01975.hp2 HG02004.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-929_683-910del others(20): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633866 | |||||
| chr1:63633868
|
G | C | 70 | a0001c0014t0003g0335a0002c0002t0001g0003a0002c0002t0001g0009others(67): Show | 70 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.683-961G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633868 | ||||||
| chr1:63633875
|
T | G | 1 | a0002c0002t0001g0017 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.683-954T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633875 | ||||||
| chr1:63633886
|
G | C | 13 | a0002c0002t0001g0016a0002c0002t0001g0084a0002c0002t0001g0097others(10): Show | 13 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.683-943G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633886 | ||||||
| chr1:63633888
|
G | C | 5 | a0002c0002t0001g0119a0002c0002t0001g0291a0004c0004t0001g0286others(2): Show | 5 | HG01975.hp2 HG02004.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-941G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633888 | ||||||
| chr1:63633892
|
GTGTGTGT others(33): Show |
G | 1 | a0001c0006t0003g0170 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.683-935_683-896del others(40): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633892 | |||||
| chr1:63633893
|
T | G | 1 | a0002c0002t0001g0016 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.683-936T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633893 | ||||||
| chr1:63633898
|
GTGTGTGT others(15): Show |
G | 23 | a0001c0014t0003g0335a0002c0002t0001g0003a0002c0002t0001g0063others(20): Show | 23 | HG01361.hp1 HG01952.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.683-929_683-908del others(22): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633898 | |||||
| chr1:63633900
|
GTGTGTGT others(13): Show |
G | 45 | a0002c0002t0001g0009a0002c0002t0001g0015a0002c0002t0001g0017others(42): Show | 45 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.683-927_683-908del others(20): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633900 | |||||
| chr1:63633900
|
GTGTGTGT others(36): Show |
G | 1 | a0005c0005t0001g0348 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.683-927_683-885del others(43): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633900 | |||||
| chr1:63633902
|
G | A | 1 | a0001c0001t0003g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.683-927G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633902 | ||||||
| chr1:63633902
|
GTGTGTGT others(11): Show |
G | 2 | a0002c0002t0001g0116a0002c0002t0001g0232 | 2 | HG01192.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.683-925_683-908del others(18): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633902 | |||||
| chr1:63633902
|
GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0003g0153 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.683-925_683-904del others(22): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633902 | |||||
| chr1:63633902
|
GTGTGTGT others(33): Show |
G | 1 | a0011c0016t0001g0057 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.683-925_683-886del others(40): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633902 | |||||
| chr1:63633902
|
GTGTGTGT others(34): Show |
G | 5 | a0003c0003t0003g0143a0006c0007t0001g0231a0006c0007t0001g0249others(2): Show | 5 | HG02451.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-925_683-885del others(41): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633902 | |||||
| chr1:63633904
|
G | A | 4 | a0001c0001t0003g0168a0006c0007t0001g0157a0006c0013t0001g0237others(1): Show | 4 | HG01243.hp2 HG02970.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-925G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633904 | ||||||
| chr1:63633904
|
GTGTGTGT others(9): Show |
G | 1 | a0010c0022t0001g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.683-923_683-908del others(16): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633904 | |||||
| chr1:63633904
|
GTGTGTGT others(11): Show |
G | 1 | a0001c0018t0003g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.683-923_683-906del others(18): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633904 | |||||
| chr1:63633906
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(12): Show | 15 | HG00639.hp1 HG01069.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.683-923G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633906 | ||||||
| chr1:63633906
|
GTGTGTGT others(7): Show |
G | 3 | a0001c0001t0001g0012a0001c0001t0001g0102a0001c0001t0001g0176 | 3 | HG02300.hp1 NA18962.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.683-921_683-908del others(14): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633906 | |||||
| chr1:63633906
|
GTGTGTGT others(11): Show |
G | 2 | a0001c0006t0003g0141a0001c0006t0003g0145 | 2 | HG01192.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.683-921_683-904del others(18): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633906 | |||||
| chr1:63633906
|
GTGTGTGT others(13): Show |
G | 6 | a0001c0006t0001g0162a0001c0006t0001g0350a0001c0006t0003g0342others(3): Show | 6 | HG00738.hp1 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-921_683-902del others(20): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633906 | |||||
| chr1:63633906
|
GTGTGTGT others(30): Show |
G | 1 | a0006c0007t0001g0292 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.683-921_683-885del others(37): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633906 | |||||
| chr1:63633908
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(14): Show | 17 | HG00639.hp1 HG01069.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.683-921G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633908 | ||||||
| chr1:63633908
|
GTGTGTGT others(9): Show |
G | 1 | a0001c0006t0003g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.683-919_683-904del others(16): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633908 | |||||
| chr1:63633908
|
GTGTGTGT others(11): Show |
G | 1 | a0001c0001t0001g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.683-919_683-902del others(18): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633908 | |||||
| chr1:63633910
|
G | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(16): Show | 20 | HG00639.hp1 HG01069.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.683-919G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633910 | ||||||
| chr1:63633912
|
G | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(16): Show | 20 | HG00639.hp1 HG01069.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.683-917G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633912 | ||||||
| chr1:63633912
|
GTGTGTGT others(3): Show |
G | 1 | a0005c0005t0001g0203 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.683-915_683-906del others(10): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633912 | |||||
| chr1:63633912
|
GTGTGTGT others(5): Show |
G | 1 | a0005c0005t0003g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.683-915_683-904del others(12): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633912 | |||||
| chr1:63633912
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0001g0069 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.683-915_683-902del others(14): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633912 | |||||
| chr1:63633912
|
GTGTGTGT others(9): Show |
G | 1 | a0008c0009t0001g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.683-915_683-900del others(16): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633912 | |||||
| chr1:63633914
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 24 | HG00639.hp1 HG01069.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.683-915G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633914 | ||||||
| chr1:63633914
|
GTGTGTAT others(3): Show |
G | 6 | a0001c0001t0001g0085a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG02976.hp1 HG03195.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-913_683-904del others(10): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633914 | |||||
| chr1:63633916
|
G | A | 37 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(34): Show | 38 | HG00639.hp1 HG01069.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.683-913G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633916 | ||||||
| chr1:63633918
|
G | A | 117 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(114): Show | 118 | HG00140.hp2 HG00423.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.683-911G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633918 | ||||||
| chr1:63633918
|
G | GTA | 13 | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0001g0039others(10): Show | 13 | HG01071.hp2 HG01884.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.683-897_683-896dup others(2): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633918 | |||||
| chr1:63633918
|
G | GTGTA | 6 | a0001c0001t0001g0031a0001c0001t0001g0041a0003c0003t0002g0134others(3): Show | 6 | HG00639.hp2 HG00738.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-910_683-909ins others(4): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633918 | |||||
| chr1:63633918
|
G | GTGTGTA | 3 | a0001c0001t0003g0160a0006c0007t0001g0166a0010c0015t0008g0177 | 3 | HG02258.hp1 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.683-910_683-909ins others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633918 | |||||
| chr1:63633918
|
G | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(4): Show | 7 | HG01069.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-911G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633918 | ||||||
| chr1:63633920
|
A | G | 2 | a0001c0001t0001g0026a0006c0007t0001g0163 | 2 | HG01175.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.683-909A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633920 | ||||||
| chr1:63633920
|
A | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(14): Show | 17 | HG00639.hp1 HG01069.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.683-909A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633920 | ||||||
| chr1:63633922
|
A | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0173others(9): Show | 13 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.683-907A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633922 | ||||||
| chr1:63633924
|
A | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(6): Show | 10 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-905A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633924 | ||||||
| chr1:63633926
|
A | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0014others(14): Show | 17 | HG00639.hp1 HG01069.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.683-903A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633926 | ||||||
| chr1:63633928
|
A | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0173others(10): Show | 14 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.683-901A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633928 | ||||||
| chr1:63633929
|
TATA | T | 3 | a0001c0001t0001g0076a0001c0001t0001g0105a0001c0001t0001g0136 | 3 | NA18940.hp1 NA18945.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.683-899_683-897del others(3): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633929 | ||||||
| chr1:63633930
|
A | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(9): Show | 13 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.683-899A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633930 | ||||||
| chr1:63633931
|
TA | T | 7 | a0001c0001t0001g0118a0001c0001t0001g0154a0001c0001t0001g0161others(4): Show | 7 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-897delA | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633931 | ||||||
| chr1:63633932
|
A | ATAT | 7 | a0001c0001t0001g0067a0001c0001t0001g0178a0001c0001t0001g0305others(4): Show | 7 | HG00642.hp1 HG02145.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.683-896_683-895ins others(3): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633932 | |||||
| chr1:63633932
|
A | T | 26 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0167others(23): Show | 26 | HG00639.hp1 HG01243.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.683-897A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633932 | ||||||
| chr1:63633932
|
AT | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0053others(50): Show | 53 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.683-868delT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633932 | |||||
| chr1:63633932
|
ATT | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(4): Show | 7 | HG01069.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-869_683-868del others(2): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633932 | |||||
| chr1:63633932
|
ATTT | A | 12 | a0001c0001t0001g0069a0001c0001t0001g0174a0001c0001t0001g0229others(9): Show | 12 | HG00558.hp2 HG01074.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.683-870_683-868del others(3): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633932 | |||||
| chr1:63633932
|
ATTTTTT | A | 7 | a0001c0001t0001g0085a0001c0001t0001g0155a0001c0001t0001g0156others(4): Show | 7 | HG00733.hp1 HG02976.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.683-873_683-868del others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633932 | |||||
| chr1:63633932
|
ATTTTTTT others(6): Show |
A | 1 | a0005c0005t0003g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.683-880_683-868del others(13): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 63633932 | |||||
| chr1:63633933
|
T | TA | 4 | a0001c0001t0001g0036a0001c0001t0001g0093a0001c0001t0001g0227others(1): Show | 4 | HG02523.hp1 NA18957.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-896_683-895ins others(1): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633933 | ||||||
| chr1:63633934
|
T | A | 130 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0024others(127): Show | 131 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.683-895T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633934 | ||||||
| chr1:63633935
|
T | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0053others(35): Show | 38 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.683-894T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633935 | ||||||
| chr1:63633936
|
T | A | 76 | a0001c0001t0001g0102a0001c0001t0001g0176a0001c0001t0001g0224others(73): Show | 76 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.683-893T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633936 | ||||||
| chr1:63633937
|
T | A | 43 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0092others(40): Show | 43 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.683-892T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633937 | ||||||
| chr1:63633938
|
T | A | 55 | a0001c0001t0001g0102a0001c0001t0001g0176a0001c0001t0001g0330others(52): Show | 55 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.683-891T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633938 | ||||||
| chr1:63633939
|
T | A | 9 | a0002c0002t0001g0016a0002c0002t0001g0097a0002c0002t0001g0260others(6): Show | 9 | HG00140.hp1 HG00735.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.683-890T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633939 | ||||||
| chr1:63633940
|
T | A | 5 | a0002c0002t0003g0263a0002c0002t0003g0264a0004c0004t0002g0043others(2): Show | 5 | HG01516.hp2 HG01517.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-889T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633940 | ||||||
| chr1:63633944
|
T | A | 1 | a0011c0016t0001g0057 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.683-885T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633944 | ||||||
| chr1:63633945
|
T | A | 7 | a0003c0003t0003g0143a0005c0005t0001g0348a0006c0007t0001g0231others(4): Show | 7 | HG01891.hp2 HG02451.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-884T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633945 | ||||||
| chr1:63633947
|
T | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(17): Show | 21 | HG00639.hp1 HG01069.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.683-882T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63633947 | ||||||
| chr1:63634175
|
A | G | 4 | a0001c0001t0001g0351a0003c0003t0001g0183a0005c0005t0001g0171others(1): Show | 4 | HG02257.hp2 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-654A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63634175 | ||||||
| chr1:63634177
|
T | G | 1 | a0001c0001t0001g0334 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.683-652T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63634177 | ||||||
| chr1:63634406
|
A | C | 8 | a0003c0003t0003g0143a0005c0005t0001g0348a0006c0007t0001g0231others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-423A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63634406 | ||||||
| chr1:63634413
|
T | C | 12 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(9): Show | 12 | HG02027.hp1 HG02080.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.683-416T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63634413 | ||||||
| chr1:63634453
|
G | A | 3 | a0001c0001t0003g0168a0006c0007t0001g0157a0006c0013t0001g0237 | 3 | HG02970.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.683-376G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63634453 | ||||||
| chr1:63634469
|
A | C | 1 | a0001c0018t0003g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.683-360A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63634469 | ||||||
| chr1:63634552
|
G | A | 10 | a0002c0002t0001g0074a0002c0002t0001g0084a0002c0002t0001g0100others(7): Show | 10 | HG00423.hp2 NA18951.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.683-277G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63634552 | ||||||
| chr1:63634594
|
C | G | 37 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(34): Show | 38 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.683-235C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63634594 | ||||||
| chr1:63634806
|
C | T | 11 | a0001c0001t0003g0246a0001c0001t0003g0353a0001c0001t0003g0355others(8): Show | 11 | HG01255.hp1 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.683-23C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63634806 | ||||||
| chr1:63634807
|
A | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 210 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.683-22A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 4/10 | chr1 | 63634807 | ||||||
| chr1:63635210
|
C | T | 72 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0024others(69): Show | 73 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.873+191C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 5/10 | chr1 | 63635210 | ||||||
| chr1:63635213
|
A | G | 197 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(194): Show | 199 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.873+194A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 5/10 | chr1 | 63635213 | ||||||
| chr1:63635737
|
A | G | 11 | a0001c0001t0001g0077a0001c0001t0003g0153a0001c0006t0001g0162others(8): Show | 11 | HG00738.hp1 HG01192.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.874-497A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 5/10 | chr1 | 63635737 | ||||||
| chr1:63635961
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.874-273C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 5/10 | chr1 | 63635961 | ||||||
| chr1:63636029
|
T | C | 1 | a0005c0005t0001g0203 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.874-205T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 5/10 | chr1 | 63636029 | ||||||
| chr1:63636443
|
A | G | 207 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(204): Show | 209 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.1028+55A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63636443 | ||||||
| chr1:63636541
|
G | A | 1 | a0004c0004t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1028+153G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63636541 | ||||||
| chr1:63636599
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1028+211C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63636599 | ||||||
| chr1:63636662
|
A | T | 1 | a0001c0001t0001g0014 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1028+274A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63636662 | ||||||
| chr1:63636919
|
C | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(7): Show | 11 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1028+531C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63636919 | ||||||
| chr1:63637314
|
C | T | 1 | a0009c0012t0001g0046 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1028+926C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63637314 | ||||||
| chr1:63637361
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1028+973C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63637361 | ||||||
| chr1:63637378
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(19): Show | 23 | HG00639.hp1 HG01069.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.1028+990G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63637378 | ||||||
| chr1:63637514
|
G | GT | 4 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0226others(1): Show | 4 | HG00438.hp1 HG03834.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028+1133dupT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 63637514 | |||||
| chr1:63637531
|
A | G | 1 | a0002c0002t0001g0015 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1028+1143A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63637531 | ||||||
| chr1:63637573
|
G | A | 21 | a0001c0001t0001g0069a0001c0001t0001g0085a0001c0001t0001g0155others(18): Show | 21 | HG00733.hp1 HG01255.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1029-1112G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63637573 | ||||||
| chr1:63637650
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1029-1035C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63637650 | ||||||
| chr1:63637658
|
A | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 53 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.1029-1027A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63637658 | ||||||
| chr1:63637841
|
G | T | 2 | a0001c0001t0001g0267a0001c0001t0004g0109 | 2 | HG02040.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1029-844G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63637841 | ||||||
| chr1:63637900
|
G | T | 1 | a0001c0001t0001g0284 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1029-785G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63637900 | ||||||
| chr1:63638006
|
A | AT | 218 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(215): Show | 220 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.1029-670dupT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 63638006 | |||||
| chr1:63638110
|
A | T | 1 | a0001c0001t0001g0330 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1029-575A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63638110 | ||||||
| chr1:63638146
|
C | T | 1 | a0003c0003t0002g0241 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1029-539C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63638146 | ||||||
| chr1:63638255
|
C | T | 2 | a0001c0001t0003g0082a0008c0009t0001g0318 | 2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1029-430C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63638255 | ||||||
| chr1:63638424
|
T | C | 4 | a0001c0001t0003g0246a0005c0005t0001g0344a0008c0009t0001g0086others(1): Show | 4 | HG01884.hp1 HG03098.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029-261T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63638424 | ||||||
| chr1:63638428
|
A | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(15): Show | 19 | HG00639.hp1 HG01069.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.1029-257A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63638428 | ||||||
| chr1:63638429
|
C | T | 1 | a0005c0005t0002g0314 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1029-256C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63638429 | ||||||
| chr1:63638459
|
T | C | 1 | a0002c0002t0001g0097 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1029-226T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63638459 | ||||||
| chr1:63638495
|
GAATCCAC others(7): Show |
G | 9 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(6): Show | 10 | HG01069.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029-188_1029-175d others(16): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 63638495 | |||||
| chr1:63638573
|
G | C | 4 | a0001c0001t0001g0284a0002c0002t0001g0063a0002c0002t0001g0188others(1): Show | 4 | HG03834.hp1 NA18971.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1029-112G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63638573 | ||||||
| chr1:63638584
|
A | G | 5 | a0004c0004t0002g0043a0004c0004t0002g0331a0004c0004t0003g0083others(2): Show | 5 | HG01934.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1029-101A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63638584 | ||||||
| chr1:63638631
|
A | G | 1 | a0002c0002t0002g0209 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1029-54A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63638631 | ||||||
| chr1:63638636
|
C | T | 37 | a0001c0001t0001g0012a0001c0001t0001g0024a0001c0001t0001g0027others(34): Show | 37 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1029-49C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 6/10 | chr1 | 63638636 | ||||||
| chr1:63638863
|
G | A | 1 | a0001c0001t0001g0363 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1144+63G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63638863 | ||||||
| chr1:63638874
|
T | C | 10 | a0001c0006t0001g0162a0001c0006t0001g0350a0001c0006t0003g0141others(7): Show | 10 | HG00738.hp1 HG01192.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1144+74T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63638874 | ||||||
| chr1:63638898
|
C | T | 1 | a0001c0014t0005g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1144+98C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63638898 | ||||||
| chr1:63638959
|
GA | G | 36 | a0001c0001t0001g0053a0001c0001t0001g0077a0001c0001t0001g0156others(33): Show | 36 | HG00642.hp1 HG01081.hp1 HG01952.hp2 others(33): Show |
intron_variant | MODIFIER | c.1144+163delA | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63638959 | |||||
| chr1:63639036
|
G | A | 20 | a0001c0014t0003g0335a0001c0018t0003g0356a0002c0002t0003g0152others(17): Show | 20 | HG01167.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1144+236G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63639036 | ||||||
| chr1:63639329
|
G | A | 1 | a0002c0002t0001g0291 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1144+529G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63639329 | ||||||
| chr1:63639385
|
A | C | 66 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0059others(63): Show | 67 | HG00408.hp1 HG00438.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.1144+585A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63639385 | ||||||
| chr1:63639472
|
G | A | 1 | a0006c0007t0001g0163 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1144+672G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63639472 | ||||||
| chr1:63639505
|
C | T | 4 | a0001c0001t0001g0161a0002c0002t0001g0232a0004c0004t0003g0159others(1): Show | 4 | HG01192.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144+705C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63639505 | ||||||
| chr1:63639657
|
G | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0156others(30): Show | 34 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.1144+857G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63639657 | ||||||
| chr1:63639809
|
T | C | 3 | a0001c0001t0003g0140a0001c0001t0003g0168a0001c0001t0003g0246 | 3 | HG01884.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1144+1009T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63639809 | ||||||
| chr1:63639884
|
C | T | 2 | a0001c0001t0001g0161a0002c0002t0001g0232 | 2 | HG01192.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1144+1084C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63639884 | ||||||
| chr1:63640104
|
G | A | 240 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(237): Show | 242 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.1144+1304G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63640104 | ||||||
| chr1:63640128
|
T | C | 110 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(107): Show | 110 | HG00140.hp1 HG00408.hp2 HG00673.hp1 others(107): Show |
intron_variant | MODIFIER | c.1144+1328T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63640128 | ||||||
| chr1:63640377
|
A | G | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144+1577A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63640377 | ||||||
| chr1:63640409
|
C | T | 5 | a0001c0001t0001g0173a0001c0001t0001g0189a0001c0001t0001g0190others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1144+1609C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63640409 | ||||||
| chr1:63640496
|
T | C | 179 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(176): Show | 181 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.1144+1696T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63640496 | ||||||
| chr1:63640564
|
G | A | 2 | a0003c0003t0001g0127a0003c0003t0001g0269 | 2 | NA19056.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1144+1764G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63640564 | ||||||
| chr1:63640729
|
T | C | 1 | a0004c0004t0001g0282 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1144+1929T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63640729 | ||||||
| chr1:63640768
|
T | C | 2 | a0001c0018t0003g0356a0007c0011t0003g0151 | 2 | HG02895.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1144+1968T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63640768 | ||||||
| chr1:63640775
|
T | G | 3 | a0006c0007t0001g0354a0006c0013t0001g0343a0011c0016t0001g0228 | 3 | HG01243.hp2 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1144+1975T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63640775 | ||||||
| chr1:63641146
|
T | C | 56 | a0002c0002t0003g0263a0002c0002t0003g0264a0002c0002t0009g0106others(53): Show | 56 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1144+2346T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63641146 | ||||||
| chr1:63641195
|
C | T | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144+2395C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63641195 | ||||||
| chr1:63641357
|
A | G | 63 | a0001c0014t0003g0335a0001c0014t0005g0274a0002c0002t0003g0263others(60): Show | 63 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1144+2557A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63641357 | ||||||
| chr1:63641370
|
G | T | 4 | a0001c0001t0001g0360a0001c0017t0001g0345a0002c0002t0001g0116others(1): Show | 4 | HG03239.hp1 HG03453.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144+2570G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63641370 | ||||||
| chr1:63641418
|
T | A | 8 | a0001c0006t0003g0141a0001c0006t0003g0145a0001c0006t0003g0148others(5): Show | 8 | HG01192.hp1 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144+2618T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63641418 | ||||||
| chr1:63641613
|
C | T | 63 | a0002c0002t0009g0106a0003c0003t0001g0011a0003c0003t0001g0062others(60): Show | 63 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1144+2813C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63641613 | ||||||
| chr1:63641673
|
C | T | 1 | a0003c0003t0001g0218 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1144+2873C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63641673 | ||||||
| chr1:63641701
|
G | A | 1 | a0003c0003t0001g0279 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1144+2901G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63641701 | ||||||
| chr1:63641796
|
G | T | 1 | a0003c0003t0002g0142 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1144+2996G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63641796 | ||||||
| chr1:63641820
|
T | C | 65 | a0002c0002t0003g0263a0002c0002t0003g0264a0002c0002t0009g0106others(62): Show | 65 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1144+3020T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63641820 | ||||||
| chr1:63641924
|
A | G | 2 | a0005c0005t0003g0197a0005c0005t0003g0275 | 2 | HG01433.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1144+3124A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63641924 | ||||||
| chr1:63641958
|
C | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(30): Show | 35 | HG00438.hp2 HG01081.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.1144+3158C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63641958 | ||||||
| chr1:63642046
|
G | A | 1 | a0004c0004t0001g0215 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1144+3246G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63642046 | ||||||
| chr1:63642085
|
C | T | 3 | a0001c0001t0001g0154a0001c0006t0001g0350a0005c0005t0001g0349 | 3 | HG00738.hp1 HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1144+3285C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63642085 | ||||||
| chr1:63642109
|
C | T | 1 | a0001c0017t0001g0345 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1144+3309C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63642109 | ||||||
| chr1:63642222
|
G | A | 56 | a0002c0002t0003g0263a0002c0002t0003g0264a0002c0002t0009g0106others(53): Show | 56 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1144+3422G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63642222 | ||||||
| chr1:63642305
|
G | C | 1 | a0002c0002t0001g0074 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1144+3505G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63642305 | ||||||
| chr1:63642381
|
C | A | 9 | a0004c0004t0003g0159a0008c0009t0001g0086a0008c0009t0001g0139others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1144+3581C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63642381 | ||||||
| chr1:63642668
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1144+3868A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63642668 | ||||||
| chr1:63642736
|
G | A | 194 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(191): Show | 194 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.1144+3936G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63642736 | ||||||
| chr1:63642833
|
A | T | 217 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(214): Show | 218 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.1144+4033A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63642833 | ||||||
| chr1:63642873
|
C | A | 1 | a0001c0001t0001g0351 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1144+4073C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63642873 | ||||||
| chr1:63643011
|
G | A | 65 | a0002c0002t0003g0263a0002c0002t0003g0264a0002c0002t0009g0106others(62): Show | 65 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1144+4211G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63643011 | ||||||
| chr1:63643100
|
T | C | 72 | a0001c0014t0003g0335a0001c0014t0005g0274a0002c0002t0003g0263others(69): Show | 72 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1144+4300T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63643100 | ||||||
| chr1:63643303
|
C | T | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144+4503C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63643303 | ||||||
| chr1:63643309
|
G | A | 2 | a0001c0001t0001g0360a0002c0002t0001g0116 | 2 | HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1144+4509G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63643309 | ||||||
| chr1:63643590
|
A | C | 2 | a0008c0009t0001g0086a0010c0015t0001g0079 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1144+4790A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63643590 | ||||||
| chr1:63643593
|
T | C | 65 | a0002c0002t0003g0263a0002c0002t0003g0264a0002c0002t0009g0106others(62): Show | 65 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1144+4793T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63643593 | ||||||
| chr1:63643609
|
G | A | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144+4809G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63643609 | ||||||
| chr1:63643688
|
C | G | 64 | a0002c0002t0003g0263a0002c0002t0003g0264a0003c0003t0001g0011others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1145-4829C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63643688 | ||||||
| chr1:63643712
|
T | C | 1 | a0006c0007t0001g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1145-4805T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63643712 | ||||||
| chr1:63643965
|
C | G | 9 | a0004c0004t0003g0159a0008c0009t0001g0086a0008c0009t0001g0139others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1145-4552C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63643965 | ||||||
| chr1:63644012
|
C | T | 29 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0135others(26): Show | 29 | HG00408.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1145-4505C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63644012 | ||||||
| chr1:63644196
|
G | A | 30 | a0001c0014t0003g0335a0001c0014t0005g0274a0004c0004t0003g0159others(27): Show | 30 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1145-4321G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63644196 | ||||||
| chr1:63644209
|
C | T | 8 | a0001c0006t0003g0141a0001c0006t0003g0145a0001c0006t0003g0148others(5): Show | 8 | HG01192.hp1 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1145-4308C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63644209 | ||||||
| chr1:63644458
|
AAC | A | 95 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(92): Show | 95 | HG00408.hp2 HG00673.hp1 HG01069.hp1 others(92): Show |
intron_variant | MODIFIER | c.1145-4056_1145-405 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63644458 | |||||
| chr1:63644618
|
C | T | 14 | a0006c0007t0001g0157a0006c0007t0001g0163a0006c0007t0001g0166others(11): Show | 14 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1145-3899C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63644618 | ||||||
| chr1:63644681
|
C | T | 3 | a0001c0006t0003g0145a0001c0006t0003g0148a0007c0011t0003g0272 | 3 | HG01192.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1145-3836C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63644681 | ||||||
| chr1:63644682
|
G | T | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1145-3835G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63644682 | ||||||
| chr1:63644723
|
TTC | T | 5 | a0001c0001t0001g0036a0001c0001t0001g0090a0001c0001t0001g0110others(2): Show | 5 | HG00438.hp1 NA18950.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.1145-3792_1145-379 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63644723 | |||||
| chr1:63644984
|
C | G | 4 | a0001c0001t0001g0055a0001c0001t0001g0303a0001c0001t0001g0312others(1): Show | 4 | HG00558.hp2 HG02083.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-3533C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63644984 | ||||||
| chr1:63645192
|
C | A | 1 | a0001c0001t0001g0250 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1145-3325C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63645192 | ||||||
| chr1:63645633
|
T | A | 3 | a0001c0001t0001g0229a0002c0002t0001g0124a0005c0005t0002g0314 | 3 | NA18944.hp2 NA18957.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1145-2884T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63645633 | ||||||
| chr1:63645691
|
C | T | 1 | a0003c0003t0002g0359 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1145-2826C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63645691 | ||||||
| chr1:63645877
|
A | G | 53 | a0003c0003t0001g0011a0003c0003t0001g0062a0003c0003t0001g0071others(50): Show | 53 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1145-2640A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63645877 | ||||||
| chr1:63646195
|
C | T | 53 | a0003c0003t0001g0011a0003c0003t0001g0062a0003c0003t0001g0071others(50): Show | 53 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1145-2322C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63646195 | ||||||
| chr1:63646257
|
A | C | 4 | a0008c0009t0001g0146a0008c0009t0001g0164a0010c0015t0008g0177others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145-2260A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63646257 | ||||||
| chr1:63646498
|
A | C | 53 | a0003c0003t0001g0011a0003c0003t0001g0062a0003c0003t0001g0071others(50): Show | 53 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1145-2019A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63646498 | ||||||
| chr1:63646579
|
C | G | 97 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(94): Show | 97 | HG00408.hp2 HG00673.hp1 HG01069.hp1 others(94): Show |
intron_variant | MODIFIER | c.1145-1938C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63646579 | ||||||
| chr1:63646595
|
C | A | 3 | a0001c0001t0003g0140a0001c0001t0003g0168a0001c0001t0003g0246 | 3 | HG01884.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1145-1922C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63646595 | ||||||
| chr1:63646640
|
G | C | 1 | a0007c0011t0001g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1145-1877G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63646640 | ||||||
| chr1:63646909
|
A | T | 3 | a0001c0001t0002g0023a0002c0002t0002g0029a0002c0002t0002g0261 | 3 | NA18941.hp1 NA19058.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.1145-1608A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63646909 | ||||||
| chr1:63647063
|
C | G | 3 | a0006c0007t0001g0354a0006c0013t0001g0343a0011c0016t0001g0228 | 3 | HG01243.hp2 HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1145-1454C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647063 | ||||||
| chr1:63647107
|
G | T | 3 | a0001c0018t0003g0356a0005c0005t0002g0314a0007c0011t0003g0151 | 3 | HG02895.hp1 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1145-1410G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647107 | ||||||
| chr1:63647120
|
A | G | 21 | a0001c0014t0003g0335a0001c0014t0005g0274a0006c0007t0001g0157others(18): Show | 21 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1145-1397A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647120 | ||||||
| chr1:63647229
|
C | T | 5 | a0008c0009t0001g0146a0008c0009t0001g0164a0008c0009t0001g0318others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1145-1288C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647229 | ||||||
| chr1:63647230
|
G | A | 96 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(93): Show | 96 | HG00408.hp2 HG00673.hp1 HG01069.hp1 others(93): Show |
intron_variant | MODIFIER | c.1145-1287G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647230 | ||||||
| chr1:63647254
|
TTTTACAT others(17): Show |
T | 1 | a0005c0005t0002g0314 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1145-1261_1145-123 others(28): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647254 | |||||
| chr1:63647256
|
TTACATAT others(7): Show |
T | 1 | a0003c0003t0002g0247 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1145-1258_1145-124 others(18): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647256 | |||||
| chr1:63647256
|
TTACATAT others(9): Show |
T | 52 | a0003c0003t0001g0011a0003c0003t0001g0062a0003c0003t0001g0071others(49): Show | 52 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1145-1258_1145-124 others(20): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647256 | |||||
| chr1:63647256
|
TTACATAT others(15): Show |
T | 5 | a0008c0009t0001g0146a0008c0009t0001g0164a0008c0009t0001g0318others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1145-1258_1145-123 others(26): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647256 | |||||
| chr1:63647256
|
TTACATAT others(17): Show |
T | 9 | a0004c0004t0003g0159a0006c0007t0001g0157a0006c0007t0001g0206others(6): Show | 9 | HG02280.hp1 HG02451.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1145-1258_1145-123 others(28): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647256 | |||||
| chr1:63647256
|
TTACATAT others(19): Show |
T | 9 | a0006c0007t0001g0163a0006c0007t0001g0166a0006c0007t0001g0231others(6): Show | 9 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1145-1258_1145-123 others(30): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647256 | |||||
| chr1:63647256
|
TTACATAT others(23): Show |
T | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1145-1258_1145-122 others(34): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647256 | |||||
| chr1:63647256
|
TTACATAT others(25): Show |
T | 8 | a0001c0006t0003g0141a0001c0006t0003g0145a0001c0006t0003g0148others(5): Show | 8 | HG01192.hp1 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1145-1258_1145-122 others(36): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647256 | |||||
| chr1:63647256
|
TTACATAT others(31): Show |
T | 34 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(31): Show | 36 | HG00438.hp2 HG01081.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.1145-1258_1145-122 others(42): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647256 | |||||
| chr1:63647259
|
C | CAT | 10 | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0060others(7): Show | 10 | HG01069.hp2 HG01433.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1145-1210_1145-120 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
C | CATAT | 11 | a0001c0001t0001g0095a0001c0001t0001g0117a0001c0001t0001g0154others(8): Show | 11 | HG00609.hp1 HG00738.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1145-1212_1145-120 others(8): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
C | CATATAT | 30 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0067others(27): Show | 30 | HG00408.hp1 HG00733.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1145-1214_1145-120 others(10): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
C | CATATATA others(1): Show |
23 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0048others(20): Show | 23 | HG00621.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.1145-1216_1145-120 others(12): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
C | CATATATA others(12): Show |
1 | a0001c0001t0001g0107 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1145-1249_1145-124 others(23): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
C | CATATATA others(3): Show |
19 | a0001c0001t0001g0055a0001c0001t0001g0076a0001c0001t0001g0110others(16): Show | 19 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1145-1218_1145-120 others(14): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
C | CATATATA others(5): Show |
8 | a0001c0001t0001g0022a0001c0001t0001g0052a0001c0001t0001g0085others(5): Show | 8 | HG00735.hp2 HG03195.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1145-1220_1145-120 others(16): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
C | CATATATA others(7): Show |
11 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0031others(8): Show | 11 | HG00609.hp2 HG00639.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1145-1222_1145-120 others(18): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
C | CATATATA others(9): Show |
4 | a0001c0001t0001g0220a0002c0002t0001g0003a0002c0002t0001g0104others(1): Show | 4 | HG01167.hp1 NA18961.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1145-1224_1145-120 others(20): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
C | CATATATA others(11): Show |
11 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0096others(8): Show | 11 | HG00673.hp2 HG02083.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.1145-1226_1145-120 others(22): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
C | CATATATA others(13): Show |
3 | a0001c0001t0001g0032a0001c0001t0001g0108a0001c0001t0001g0333 | 3 | NA18950.hp2 NA18994.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1145-1228_1145-120 others(24): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
C | CATATATA others(15): Show |
1 | a0001c0001t0004g0290 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1145-1230_1145-120 others(26): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
C | CATATATA others(17): Show |
1 | a0001c0001t0001g0114 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1145-1232_1145-120 others(28): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
C | T | 2 | a0001c0018t0003g0356a0007c0011t0003g0151 | 2 | HG02895.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1145-1258C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647259 | ||||||
| chr1:63647259
|
CAT | C | 5 | a0001c0001t0001g0129a0001c0001t0003g0147a0001c0001t0003g0277others(2): Show | 5 | HG01891.hp1 HG02647.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1145-1210_1145-120 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
CATAT | C | 3 | a0001c0001t0001g0090a0001c0001t0011g0066a0002c0002t0001g0119 | 3 | HG00438.hp1 HG02027.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1145-1212_1145-120 others(8): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
CATATATA others(3): Show |
C | 4 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0185others(1): Show | 4 | HG02293.hp2 NA19080.hp2 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.1145-1218_1145-120 others(14): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
CATATATA others(5): Show |
C | 2 | a0001c0001t0001g0267a0009c0012t0001g0070 | 2 | HG02040.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1145-1220_1145-120 others(16): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
CATATATA others(7): Show |
C | 1 | a0002c0002t0001g0260 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1145-1222_1145-120 others(18): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
CATATATA others(9): Show |
C | 6 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0041others(3): Show | 6 | HG01258.hp1 NA18946.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1145-1224_1145-120 others(20): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
CATATATA others(11): Show |
C | 1 | a0001c0006t0001g0162 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1145-1226_1145-120 others(22): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
CATATATA others(15): Show |
C | 1 | a0007c0011t0001g0065 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1145-1230_1145-120 others(26): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
CATATATA others(17): Show |
C | 6 | a0001c0001t0001g0270a0002c0002t0001g0084a0002c0002t0001g0100others(3): Show | 6 | HG00423.hp2 HG02040.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.1145-1232_1145-120 others(28): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
CATATATA others(19): Show |
C | 1 | a0002c0002t0001g0121 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1145-1234_1145-120 others(30): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
CATATATA others(23): Show |
C | 31 | a0001c0001t0001g0053a0001c0001t0001g0102a0001c0001t0001g0105others(28): Show | 31 | HG00673.hp1 HG02015.hp1 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.1145-1238_1145-120 others(34): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647259
|
CATATATA others(25): Show |
C | 31 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0135others(28): Show | 31 | HG00408.hp2 HG00738.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.1145-1240_1145-120 others(36): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647259 | |||||
| chr1:63647272
|
A | T | 1 | a0003c0003t0002g0247 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1145-1245A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647272 | ||||||
| chr1:63647274
|
A | T | 50 | a0003c0003t0001g0011a0003c0003t0001g0062a0003c0003t0001g0071others(47): Show | 50 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1145-1243A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647274 | ||||||
| chr1:63647275
|
T | TATATATA others(3): Show |
2 | a0001c0001t0003g0099a0005c0005t0003g0035 | 2 | HG01496.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1145-1233_1145-123 others(14): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647275 | |||||
| chr1:63647280
|
A | G | 1 | a0005c0005t0002g0314 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1145-1237A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647280 | ||||||
| chr1:63647292
|
A | G | 1 | a0003c0003t0002g0247 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1145-1225A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647292 | ||||||
| chr1:63647294
|
A | G | 52 | a0003c0003t0001g0011a0003c0003t0001g0062a0003c0003t0001g0071others(49): Show | 52 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1145-1223A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647294 | ||||||
| chr1:63647304
|
A | ATATATAT others(5): Show |
1 | a0007c0011t0003g0151 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1145-1209_1145-120 others(16): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr1 | 63647304 | |||||
| chr1:63647408
|
T | C | 21 | a0001c0014t0003g0335a0001c0014t0005g0274a0006c0007t0001g0157others(18): Show | 21 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1145-1109T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647408 | ||||||
| chr1:63647417
|
A | G | 21 | a0001c0014t0003g0335a0001c0014t0005g0274a0006c0007t0001g0157others(18): Show | 21 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1145-1100A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647417 | ||||||
| chr1:63647710
|
T | C | 21 | a0001c0014t0003g0335a0001c0014t0005g0274a0006c0007t0001g0157others(18): Show | 21 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1145-807T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647710 | ||||||
| chr1:63647741
|
T | A | 227 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(224): Show | 229 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.1145-776T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647741 | ||||||
| chr1:63647788
|
A | G | 63 | a0003c0003t0001g0011a0003c0003t0001g0062a0003c0003t0001g0071others(60): Show | 63 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1145-729A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647788 | ||||||
| chr1:63647833
|
C | G | 8 | a0001c0006t0003g0141a0001c0006t0003g0145a0001c0006t0003g0148others(5): Show | 8 | HG01192.hp1 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1145-684C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63647833 | ||||||
| chr1:63648124
|
T | A | 9 | a0004c0004t0003g0159a0008c0009t0001g0086a0008c0009t0001g0139others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1145-393T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63648124 | ||||||
| chr1:63648125
|
A | T | 9 | a0004c0004t0003g0159a0008c0009t0001g0086a0008c0009t0001g0139others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1145-392A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63648125 | ||||||
| chr1:63648218
|
T | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(126): Show | 131 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1145-299T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63648218 | ||||||
| chr1:63648219
|
G | A | 8 | a0001c0006t0003g0141a0001c0006t0003g0145a0001c0006t0003g0148others(5): Show | 8 | HG01192.hp1 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1145-298G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63648219 | ||||||
| chr1:63648285
|
A | T | 84 | a0001c0014t0003g0335a0001c0014t0005g0274a0003c0003t0001g0011others(81): Show | 84 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.1145-232A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63648285 | ||||||
| chr1:63648410
|
C | T | 1 | a0002c0002t0003g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1145-107C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63648410 | ||||||
| chr1:63648510
|
C | G | 21 | a0001c0014t0003g0335a0001c0014t0005g0274a0006c0007t0001g0157others(18): Show | 21 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(18): Show |
splice_region_variant&intron_variant | LOW | c.1145-7C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 7/10 | chr1 | 63648510 | ||||||
| chr1:63648659
|
C | T | 14 | a0006c0007t0001g0157a0006c0007t0001g0163a0006c0007t0001g0166others(11): Show | 14 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.1280+7C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63648659 | ||||||
| chr1:63648758
|
G | T | 63 | a0003c0003t0001g0011a0003c0003t0001g0062a0003c0003t0001g0071others(60): Show | 63 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1280+106G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63648758 | ||||||
| chr1:63648866
|
A | C | 1 | a0001c0001t0002g0245 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1280+214A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63648866 | ||||||
| chr1:63648989
|
T | C | 84 | a0001c0014t0003g0335a0001c0014t0005g0274a0003c0003t0001g0011others(81): Show | 84 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.1280+337T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63648989 | ||||||
| chr1:63649010
|
C | G | 1 | a0001c0001t0001g0334 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1280+358C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649010 | ||||||
| chr1:63649010
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1280+358C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649010 | ||||||
| chr1:63649014
|
G | C | 2 | a0001c0001t0003g0182a0002c0002t0003g0152 | 2 | HG01167.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1280+362G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649014 | ||||||
| chr1:63649054
|
C | T | 14 | a0001c0001t0001g0045a0001c0001t0001g0095a0001c0001t0001g0111others(11): Show | 14 | HG00609.hp1 HG00673.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.1280+402C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649054 | ||||||
| chr1:63649106
|
T | C | 30 | a0001c0014t0003g0335a0001c0014t0005g0274a0004c0004t0003g0159others(27): Show | 30 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1280+454T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649106 | ||||||
| chr1:63649117
|
A | C | 1 | a0001c0001t0001g0032 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1280+465A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649117 | ||||||
| chr1:63649122
|
C | G | 1 | a0004c0004t0002g0187 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1280+470C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649122 | ||||||
| chr1:63649125
|
G | C | 12 | a0004c0004t0003g0159a0006c0007t0001g0354a0006c0013t0001g0343others(9): Show | 12 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1280+473G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649125 | ||||||
| chr1:63649172
|
C | T | 2 | a0001c0001t0001g0323a0002c0002t0001g0097 | 2 | HG00140.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1280+520C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649172 | ||||||
| chr1:63649173
|
G | A | 1 | a0005c0005t0002g0314 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1280+521G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649173 | ||||||
| chr1:63649327
|
C | T | 30 | a0001c0014t0003g0335a0001c0014t0005g0274a0004c0004t0003g0159others(27): Show | 30 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1280+675C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649327 | ||||||
| chr1:63649337
|
G | A | 1 | a0001c0001t0003g0246 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1280+685G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649337 | ||||||
| chr1:63649436
|
A | G | 3 | a0001c0001t0001g0154a0001c0006t0001g0350a0005c0005t0001g0349 | 3 | HG00738.hp1 HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1280+784A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649436 | ||||||
| chr1:63649520
|
G | A | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1280+868G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649520 | ||||||
| chr1:63649528
|
G | A | 1 | a0005c0005t0001g0130 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1280+876G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649528 | ||||||
| chr1:63649598
|
A | G | 1 | a0001c0001t0001g0250 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1280+946A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649598 | ||||||
| chr1:63649612
|
A | G | 5 | a0008c0009t0001g0146a0008c0009t0001g0164a0008c0009t0001g0318others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1280+960A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649612 | ||||||
| chr1:63649632
|
T | C | 1 | a0002c0002t0001g0063 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1280+980T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649632 | ||||||
| chr1:63649827
|
G | C | 8 | a0001c0001t0003g0099a0001c0001t0003g0277a0001c0001t0003g0281others(5): Show | 8 | HG01496.hp1 HG01515.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1280+1175G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649827 | ||||||
| chr1:63649965
|
T | A | 9 | a0004c0004t0003g0159a0008c0009t0001g0086a0008c0009t0001g0139others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1280+1313T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63649965 | ||||||
| chr1:63650298
|
T | C | 8 | a0001c0006t0003g0141a0001c0006t0003g0145a0001c0006t0003g0148others(5): Show | 8 | HG01192.hp1 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1281-1371T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63650298 | ||||||
| chr1:63650300
|
G | C | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1281-1369G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63650300 | ||||||
| chr1:63650448
|
C | A | 11 | a0006c0007t0001g0157a0006c0007t0001g0163a0006c0007t0001g0166others(8): Show | 11 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1281-1221C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63650448 | ||||||
| chr1:63650504
|
G | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0042others(1): Show | 4 | NA18946.hp1 NA18957.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281-1165G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63650504 | ||||||
| chr1:63650646
|
G | A | 9 | a0004c0004t0003g0159a0008c0009t0001g0086a0008c0009t0001g0139others(6): Show | 9 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1281-1023G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63650646 | ||||||
| chr1:63650914
|
T | A | 2 | a0008c0009t0001g0086a0010c0015t0001g0079 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1281-755T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63650914 | ||||||
| chr1:63650961
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1281-708G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63650961 | ||||||
| chr1:63651038
|
C | A | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1281-631C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63651038 | ||||||
| chr1:63651048
|
A | G | 14 | a0006c0007t0001g0157a0006c0007t0001g0163a0006c0007t0001g0166others(11): Show | 14 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1281-621A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63651048 | ||||||
| chr1:63651077
|
A | G | 21 | a0001c0014t0003g0335a0001c0014t0005g0274a0006c0007t0001g0157others(18): Show | 21 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1281-592A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63651077 | ||||||
| chr1:63651135
|
G | A | 8 | a0008c0009t0001g0086a0008c0009t0001g0139a0008c0009t0001g0146others(5): Show | 8 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281-534G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63651135 | ||||||
| chr1:63651156
|
A | G | 1 | a0001c0001t0002g0326 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1281-513A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63651156 | ||||||
| chr1:63651228
|
G | A | 21 | a0001c0014t0003g0335a0001c0014t0005g0274a0006c0007t0001g0157others(18): Show | 21 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1281-441G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63651228 | ||||||
| chr1:63651288
|
C | T | 1 | a0003c0003t0002g0179 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1281-381C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63651288 | ||||||
| chr1:63651303
|
A | C | 14 | a0006c0007t0001g0157a0006c0007t0001g0163a0006c0007t0001g0166others(11): Show | 14 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1281-366A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63651303 | ||||||
| chr1:63651345
|
A | G | 2 | a0003c0003t0002g0179a0003c0020t0002g0336 | 2 | NA18952.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1281-324A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63651345 | ||||||
| chr1:63651348
|
AT | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(30): Show | 35 | HG00438.hp2 HG01081.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.1281-320delT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63651348 | ||||||
| chr1:63651648
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0052a0001c0001t0001g0234others(3): Show | 6 | NA18990.hp2 NA18994.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.1281-21C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 8/10 | chr1 | 63651648 | ||||||
| chr1:63651866
|
G | T | 82 | a0001c0014t0003g0335a0001c0014t0005g0274a0003c0003t0001g0011others(79): Show | 82 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1464+14G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63651866 | ||||||
| chr1:63652067
|
G | A | 50 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0135others(47): Show | 50 | HG00408.hp2 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.1464+215G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63652067 | ||||||
| chr1:63652067
|
G | C | 11 | a0006c0007t0001g0354a0006c0013t0001g0343a0008c0009t0001g0086others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1464+215G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63652067 | ||||||
| chr1:63652242
|
A | G | 71 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(68): Show | 71 | HG00609.hp1 HG00673.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.1464+390A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63652242 | ||||||
| chr1:63652288
|
C | T | 1 | a0002c0002t0001g0260 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1464+436C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63652288 | ||||||
| chr1:63652541
|
A | C | 171 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(168): Show | 171 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.1464+689A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63652541 | ||||||
| chr1:63652572
|
C | CTGT | 179 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(176): Show | 179 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1464+724_1464+726d others(5): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 63652572 | |||||
| chr1:63652928
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1464+1076G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63652928 | ||||||
| chr1:63653130
|
T | C | 75 | a0003c0003t0001g0011a0003c0003t0001g0062a0003c0003t0001g0071others(72): Show | 75 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1465-1202T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63653130 | ||||||
| chr1:63653244
|
A | G | 84 | a0001c0014t0003g0335a0001c0014t0005g0274a0001c0018t0003g0356others(81): Show | 84 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.1465-1088A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63653244 | ||||||
| chr1:63653264
|
C | G | 1 | a0001c0001t0001g0022 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1465-1068C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63653264 | ||||||
| chr1:63653305
|
A | G | 84 | a0001c0014t0003g0335a0001c0014t0005g0274a0001c0018t0003g0356others(81): Show | 84 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.1465-1027A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63653305 | ||||||
| chr1:63653478
|
C | T | 22 | a0006c0007t0001g0157a0006c0007t0001g0163a0006c0007t0001g0166others(19): Show | 22 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1465-854C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63653478 | ||||||
| chr1:63653675
|
T | C | 77 | a0001c0018t0003g0356a0003c0003t0001g0011a0003c0003t0001g0062others(74): Show | 77 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1465-657T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63653675 | ||||||
| chr1:63653945
|
A | G | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1465-387A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63653945 | ||||||
| chr1:63654106
|
T | C | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1465-226T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63654106 | ||||||
| chr1:63654226
|
A | G | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1465-106A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63654226 | ||||||
| chr1:63654230
|
A | T | 29 | a0001c0014t0003g0335a0001c0014t0005g0274a0006c0007t0001g0157others(26): Show | 29 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1465-102A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63654230 | ||||||
| chr1:63654264
|
C | G | 1 | a0001c0001t0004g0290 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1465-68C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 9/10 | chr1 | 63654264 | ||||||
| chr1:63654475
|
C | T | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1599+9C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63654475 | ||||||
| chr1:63654511
|
G | A | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1599+45G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63654511 | ||||||
| chr1:63654543
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1599+77A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63654543 | ||||||
| chr1:63654683
|
G | C | 1 | a0008c0009t0001g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1599+217G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63654683 | ||||||
| chr1:63654687
|
T | C | 14 | a0006c0007t0001g0157a0006c0007t0001g0163a0006c0007t0001g0166others(11): Show | 14 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1599+221T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63654687 | ||||||
| chr1:63654788
|
A | G | 2 | a0003c0003t0006g0325a0014c0024t0006g0236 | 2 | HG01361.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1599+322A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63654788 | ||||||
| chr1:63654812
|
C | T | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1599+346C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63654812 | ||||||
| chr1:63654873
|
G | A | 29 | a0001c0014t0003g0335a0001c0014t0005g0274a0006c0007t0001g0157others(26): Show | 29 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1599+407G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63654873 | ||||||
| chr1:63654940
|
C | T | 14 | a0006c0007t0001g0157a0006c0007t0001g0163a0006c0007t0001g0166others(11): Show | 14 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1599+474C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63654940 | ||||||
| chr1:63654942
|
T | C | 75 | a0001c0001t0002g0054a0001c0001t0002g0113a0001c0001t0002g0122others(72): Show | 75 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1599+476T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63654942 | ||||||
| chr1:63654967
|
C | CT | 17 | a0001c0001t0001g0161a0001c0001t0001g0180a0001c0001t0001g0323others(14): Show | 17 | HG00140.hp1 HG00642.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1599+520dupT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63654967 | |||||
| chr1:63654967
|
C | CTT | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1599+519_1599+520d others(4): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63654967 | |||||
| chr1:63654967
|
CT | C | 22 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0135others(19): Show | 22 | HG01071.hp1 HG01074.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.1599+520delT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63654967 | |||||
| chr1:63654967
|
CTT | C | 23 | a0001c0001t0001g0190a0006c0007t0001g0157a0006c0007t0001g0163others(20): Show | 23 | HG01069.hp1 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1599+519_1599+520d others(4): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63654967 | |||||
| chr1:63654970
|
T | C | 1 | a0007c0011t0003g0151 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1599+504T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63654970 | ||||||
| chr1:63655003
|
C | G | 1 | a0001c0001t0001g0052 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1599+537C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63655003 | ||||||
| chr1:63655034
|
T | C | 2 | a0003c0003t0002g0134a0003c0003t0002g0359 | 2 | HG01993.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1599+568T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63655034 | ||||||
| chr1:63655115
|
C | T | 7 | a0001c0014t0003g0335a0001c0014t0005g0274a0007c0010t0003g0075others(4): Show | 7 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1599+649C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63655115 | ||||||
| chr1:63655140
|
CT | C | 24 | a0001c0001t0001g0190a0002c0002t0003g0152a0006c0007t0001g0157others(21): Show | 24 | HG01069.hp1 HG01167.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1599+688delT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63655140 | |||||
| chr1:63655460
|
T | C | 29 | a0001c0014t0003g0335a0001c0014t0005g0274a0006c0007t0001g0157others(26): Show | 29 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1599+994T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63655460 | ||||||
| chr1:63655632
|
C | G | 12 | a0001c0001t0003g0099a0001c0001t0003g0147a0001c0001t0003g0153others(9): Show | 12 | HG01496.hp1 HG01515.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.1599+1166C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63655632 | ||||||
| chr1:63655770
|
G | A | 155 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0135others(152): Show | 155 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1599+1304G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63655770 | ||||||
| chr1:63655892
|
C | T | 11 | a0006c0007t0001g0157a0006c0007t0001g0163a0006c0007t0001g0166others(8): Show | 11 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1599+1426C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63655892 | ||||||
| chr1:63655898
|
A | C | 98 | a0001c0001t0002g0054a0001c0001t0002g0113a0001c0001t0002g0122others(95): Show | 98 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.1599+1432A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63655898 | ||||||
| chr1:63655909
|
A | T | 14 | a0006c0007t0001g0157a0006c0007t0001g0163a0006c0007t0001g0166others(11): Show | 14 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1599+1443A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63655909 | ||||||
| chr1:63655910
|
C | T | 14 | a0006c0007t0001g0157a0006c0007t0001g0163a0006c0007t0001g0166others(11): Show | 14 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1599+1444C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63655910 | ||||||
| chr1:63656013
|
G | A | 100 | a0001c0001t0002g0054a0001c0001t0002g0113a0001c0001t0002g0122others(97): Show | 100 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.1599+1547G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63656013 | ||||||
| chr1:63656054
|
A | C | 1 | a0001c0001t0001g0315 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1599+1588A>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63656054 | ||||||
| chr1:63656168
|
G | A | 1 | a0008c0009t0001g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1599+1702G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63656168 | ||||||
| chr1:63656206
|
A | G | 99 | a0001c0001t0001g0303a0001c0001t0002g0054a0001c0001t0002g0113others(96): Show | 99 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1599+1740A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63656206 | ||||||
| chr1:63656285
|
G | A | 61 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0135others(58): Show | 61 | HG00408.hp2 HG01069.hp1 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.1599+1819G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63656285 | ||||||
| chr1:63656571
|
G | GGT | 54 | a0001c0001t0001g0022a0001c0001t0001g0154a0001c0001t0001g0192others(51): Show | 54 | HG00408.hp2 HG00642.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1599+2140_1599+214 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63656571 | |||||
| chr1:63656571
|
G | GGTGT | 52 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0052others(49): Show | 52 | HG01069.hp2 HG01361.hp2 HG01433.hp2 others(49): Show |
intron_variant | MODIFIER | c.1599+2138_1599+214 others(8): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63656571 | |||||
| chr1:63656571
|
G | GGTGTGT | 8 | a0001c0001t0001g0006a0001c0001t0001g0060a0001c0001t0001g0296others(5): Show | 8 | HG01496.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1599+2136_1599+214 others(10): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63656571 | |||||
| chr1:63656571
|
G | GGTGTGTG others(3): Show |
1 | a0007c0011t0003g0151 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1599+2132_1599+214 others(14): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63656571 | |||||
| chr1:63656571
|
GGT | G | 11 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0041others(8): Show | 11 | HG02572.hp2 HG02698.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1599+2140_1599+214 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63656571 | |||||
| chr1:63656571
|
GGTGT | G | 55 | a0001c0001t0001g0310a0001c0001t0002g0023a0001c0001t0002g0054others(52): Show | 55 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1599+2138_1599+214 others(8): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63656571 | |||||
| chr1:63656594
|
GTGTGTGT others(7): Show |
G | 17 | a0006c0007t0001g0157a0006c0007t0001g0163a0006c0007t0001g0166others(14): Show | 17 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1599+2130_1599+214 others(18): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63656594 | |||||
| chr1:63656596
|
GTGTGTGT others(5): Show |
G | 31 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0088others(28): Show | 33 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.1599+2132_1599+214 others(16): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63656596 | |||||
| chr1:63656598
|
GTGTGTGT others(3): Show |
G | 1 | a0005c0005t0001g0171 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1599+2134_1599+214 others(14): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63656598 | |||||
| chr1:63656690
|
A | G | 2 | a0001c0001t0007g0210a0001c0001t0007g0306 | 2 | HG01261.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1599+2224A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63656690 | ||||||
| chr1:63656722
|
C | T | 7 | a0006c0007t0001g0163a0006c0007t0001g0166a0006c0007t0001g0231others(4): Show | 7 | HG01891.hp2 HG02258.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1599+2256C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63656722 | ||||||
| chr1:63656834
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(100): Show | 105 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1599+2368A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63656834 | ||||||
| chr1:63656999
|
T | C | 1 | a0001c0001t0003g0246 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1599+2533T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63656999 | ||||||
| chr1:63657119
|
T | A | 4 | a0001c0014t0005g0274a0007c0010t0005g0081a0007c0010t0005g0144others(1): Show | 4 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-2467T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63657119 | ||||||
| chr1:63657212
|
A | T | 4 | a0001c0014t0005g0274a0007c0010t0005g0081a0007c0010t0005g0144others(1): Show | 4 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-2374A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63657212 | ||||||
| chr1:63657273
|
A | T | 4 | a0001c0006t0003g0170a0001c0006t0003g0346a0004c0004t0003g0159others(1): Show | 4 | HG02922.hp1 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1600-2313A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63657273 | ||||||
| chr1:63657376
|
AGTT | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(28): Show | 33 | HG00438.hp2 HG01081.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.1600-2206_1600-220 others(7): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63657376 | |||||
| chr1:63657487
|
C | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(100): Show | 105 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1600-2099C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63657487 | ||||||
| chr1:63657515
|
C | T | 1 | a0002c0002t0001g0271 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1600-2071C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63657515 | ||||||
| chr1:63657549
|
A | G | 51 | a0001c0001t0002g0023a0001c0001t0002g0054a0001c0001t0002g0113others(48): Show | 51 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1600-2037A>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63657549 | ||||||
| chr1:63657608
|
G | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(107): Show | 112 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1600-1978G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63657608 | ||||||
| chr1:63657789
|
GC | G | 4 | a0001c0014t0005g0274a0007c0010t0005g0081a0007c0010t0005g0144others(1): Show | 4 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-1793delC | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63657789 | |||||
| chr1:63658115
|
G | C | 3 | a0001c0001t0003g0147a0001c0001t0003g0353a0001c0001t0003g0355 | 3 | HG01891.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1600-1471G>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63658115 | ||||||
| chr1:63658197
|
G | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(105): Show | 110 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1600-1389G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63658197 | ||||||
| chr1:63658226
|
T | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(109): Show | 114 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1600-1360T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63658226 | ||||||
| chr1:63658331
|
C | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(105): Show | 110 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1600-1255C>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63658331 | ||||||
| chr1:63658345
|
G | GT | 108 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(105): Show | 110 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1600-1226dupT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63658345 | |||||
| chr1:63658345
|
G | GTT | 21 | a0001c0001t0001g0161a0001c0001t0002g0317a0001c0008t0001g0338others(18): Show | 21 | HG01192.hp2 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1600-1227_1600-122 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63658345 | |||||
| chr1:63658374
|
T | C | 22 | a0001c0001t0003g0082a0001c0001t0003g0160a0001c0001t0003g0198others(19): Show | 22 | HG00408.hp2 HG01192.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1600-1212T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63658374 | ||||||
| chr1:63658397
|
CT | C | 14 | a0001c0001t0003g0099a0001c0001t0003g0147a0001c0001t0003g0153others(11): Show | 14 | HG01496.hp1 HG01515.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.1600-1175delT | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63658397 | |||||
| chr1:63658397
|
CTT | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(104): Show | 109 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1600-1176_1600-117 others(6): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63658397 | |||||
| chr1:63658422
|
G | T | 1 | a0001c0001t0001g0053 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1600-1164G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63658422 | ||||||
| chr1:63658491
|
G | A | 4 | a0008c0009t0001g0146a0008c0009t0001g0164a0010c0015t0008g0177others(1): Show | 4 | HG02055.hp2 HG02257.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1600-1095G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63658491 | ||||||
| chr1:63658608
|
C | T | 4 | a0001c0014t0005g0274a0007c0010t0005g0081a0007c0010t0005g0144others(1): Show | 4 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-978C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63658608 | ||||||
| chr1:63658616
|
G | A | 22 | a0001c0001t0003g0082a0001c0001t0003g0160a0001c0001t0003g0198others(19): Show | 22 | HG00408.hp2 HG01192.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1600-970G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63658616 | ||||||
| chr1:63658639
|
T | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(38): Show | 43 | HG00438.hp2 HG01081.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.1600-947T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63658639 | ||||||
| chr1:63658752
|
CA | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(112): Show | 117 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.1600-818delA | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63658752 | |||||
| chr1:63658791
|
CACACTGC others(6): Show |
C | 8 | a0001c0001t0003g0099a0001c0001t0003g0277a0001c0001t0003g0281others(5): Show | 8 | HG01496.hp1 HG01515.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.1600-793_1600-781d others(15): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 63658791 | |||||
| chr1:63659068
|
C | T | 4 | a0001c0001t0001g0360a0002c0002t0001g0116a0003c0003t0001g0183others(1): Show | 4 | HG02257.hp2 HG03239.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1600-518C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63659068 | ||||||
| chr1:63659080
|
C | T | 51 | a0001c0001t0002g0023a0001c0001t0002g0054a0001c0001t0002g0113others(48): Show | 51 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1600-506C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63659080 | ||||||
| chr1:63659124
|
C | G | 13 | a0001c0001t0001g0059a0001c0001t0001g0123a0001c0001t0001g0136others(10): Show | 13 | HG00408.hp1 HG02015.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.1600-462C>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63659124 | ||||||
| chr1:63659153
|
A | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(109): Show | 114 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1600-433A>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63659153 | ||||||
| chr1:63659159
|
G | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(109): Show | 114 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1600-427G>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63659159 | ||||||
| chr1:63659205
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1600-381C>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63659205 | ||||||
| chr1:63659259
|
T | A | 54 | a0001c0001t0002g0023a0001c0001t0002g0054a0001c0001t0002g0113others(51): Show | 54 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.1600-327T>A | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63659259 | ||||||
| chr1:63659308
|
G | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(107): Show | 112 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1600-278G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63659308 | ||||||
| chr1:63659401
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(106): Show | 111 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1600-185T>C | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63659401 | ||||||
| chr1:63659449
|
CAT | C | 4 | a0001c0014t0005g0274a0007c0010t0005g0081a0007c0010t0005g0144others(1): Show | 4 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-136_1600-135d others(4): Show |
PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63659449 | ||||||
| chr1:63659477
|
T | G | 4 | a0001c0014t0005g0274a0007c0010t0005g0081a0007c0010t0005g0144others(1): Show | 4 | HG02109.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-109T>G | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63659477 | ||||||
| chr1:63659563
|
G | T | 108 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0027others(105): Show | 110 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1600-23G>T | PGM1 | ENSG00000079739.17 | transcript | ENST00000371084.8 | protein_coding | 10/10 | chr1 | 63659563 |