Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55276 |
| ensemblid | ENSG00000169299.14 |
| hgncid | 8906 |
| symbol | PGM2 |
| name | phosphoglucomutase 2 |
| refseq_nuc | NM_018290.4 |
| refseq_prot | NP_060760.2 |
| ensembl_nuc | ENST00000381967.9 |
| ensembl_prot | ENSP00000371393.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 37826686 |
| end | 37862937 |
| strand | + |
| ver | v1.2 |
| region | chr4:37826686-37862937 |
| region5000 | chr4:37821686-37867937 |
| regionname0 | PGM2_chr4_37826686_37862937 |
| regionname5000 | PGM2_chr4_37821686_37867937 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 612 | 374 | 66 | 55 | 195 | 18 | 38 | 162 | PGM2_chr4_37821686_37867937 | PGM2 | MAAPE others(607): Show |
chr4 | 37821686 | 37867937 |
| a0002 | 0/0 | 612 | 61 | 20 | 11 | 29 | 0 | 1 | 16 | PGM2_chr4_37821686_37867937 | PGM2 | MAAPE others(607): Show |
chr4 | 37821686 | 37867937 |
| a0003 | 0/0 | 612 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | MAAPE others(607): Show |
chr4 | 37821686 | 37867937 |
| a0004 | 0/0 | 612 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | MAAPE others(607): Show |
chr4 | 37821686 | 37867937 |
| a0005 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | MAAPE others(607): Show |
chr4 | 37821686 | 37867937 |
| a0006 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | MAAPE others(607): Show |
chr4 | 37821686 | 37867937 |
| a0007 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | MAAPE others(607): Show |
chr4 | 37821686 | 37867937 |
| a0008 | 0/0 | 612 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | MAAPE others(607): Show |
chr4 | 37821686 | 37867937 |
| a0009 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | MAAPE others(607): Show |
chr4 | 37821686 | 37867937 |
| a0010 | 0/0 | 258 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | MAAPE others(253): Show |
chr4 | 37821686 | 37867937 |
| a0011 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | MAAPE others(607): Show |
chr4 | 37821686 | 37867937 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1836 | 285 | 24 | 43 | 169 | 16 | 31 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0001c0002 | 0/0 | 1836 | 55 | 20 | 6 | 25 | 2 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0001c0004 | 0/0 | 1836 | 27 | 21 | 3 | 0 | 0 | 3 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0001c0005 | 0/0 | 1836 | 6 | 1 | 3 | 1 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0001c0019 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0002c0003 | 0/0 | 1836 | 43 | 16 | 9 | 17 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0002c0006 | 0/0 | 1836 | 6 | 1 | 0 | 5 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0002c0007 | 0/0 | 1836 | 5 | 3 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0002c0008 | 0/0 | 1836 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0002c0009 | 0/0 | 1836 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0002c0012 | 0/0 | 1836 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0003c0010 | 0/0 | 1836 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0004c0011 | 0/0 | 1836 | 2 | 0 | 0 | 0 | 0 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0005c0015 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0006c0016 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0007c0013 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0008c0020 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0009c0014 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 | ||
| a0010c0017 | 0/0 | 1801 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1796): Show |
chr4 | 37821686 | 37867937 | ||
| a0011c0018 | 0/0 | 1836 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | ATGGC others(1831): Show |
chr4 | 37821686 | 37867937 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3211 | 229 | 18 | 41 | 126 | 15 | 27 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0001t0002 | 0/0 | 3211 | 4 | 4 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0001t0003 | 0/0 | 3211 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0001t0004 | 0/0 | 3211 | 33 | 0 | 1 | 31 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0001t0005 | 0/0 | 3205 | 9 | 0 | 0 | 9 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3200): Show |
chr4 | 37821686 | 37867937 |
| a0001c0001t0006 | 0/0 | 3211 | 4 | 0 | 1 | 0 | 1 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0001t0007 | 0/0 | 3211 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0001t0011 | 0/0 | 3211 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0002t0001 | 0/0 | 3211 | 3 | 1 | 1 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0002t0002 | 0/0 | 3211 | 44 | 12 | 4 | 24 | 2 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0002t0003 | 0/0 | 3211 | 6 | 6 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0002t0009 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0002t0010 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3241): Show |
chr4 | 37821686 | 37867937 |
| a0001c0004t0001 | 0/0 | 3211 | 26 | 20 | 3 | 0 | 0 | 3 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0004t0007 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0005t0001 | 0/0 | 3211 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0005t0002 | 0/0 | 3211 | 3 | 1 | 1 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0005t0003 | 0/0 | 3211 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0005t0012 | 0/0 | 3211 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0001c0019t0001 | 0/0 | 3211 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0002c0003t0001 | 0/0 | 3211 | 18 | 12 | 2 | 4 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0002c0003t0003 | 0/0 | 3211 | 23 | 2 | 7 | 13 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0002c0003t0006 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0002c0003t0008 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0002c0006t0003 | 0/0 | 3211 | 6 | 1 | 0 | 5 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0002c0007t0001 | 0/0 | 3211 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0002c0007t0002 | 0/0 | 3211 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0002c0007t0003 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0002c0008t0001 | 0/0 | 3211 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0002c0009t0003 | 0/0 | 3211 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0002c0012t0002 | 0/0 | 3211 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0003c0010t0001 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0003c0010t0003 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0004c0011t0004 | 0/0 | 3211 | 2 | 0 | 0 | 0 | 0 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0005c0015t0001 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0006c0016t0002 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0007c0013t0003 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0008c0020t0001 | 0/0 | 3211 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0009c0014t0001 | 0/0 | 3211 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3206): Show |
chr4 | 37821686 | 37867937 |
| a0010c0017t0005 | 0/0 | 3170 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3165): Show |
chr4 | 37821686 | 37867937 |
| a0011c0018t0005 | 0/0 | 3205 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | AGATC others(3200): Show |
chr4 | 37821686 | 37867937 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0009 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0373 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0002g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0006g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0007g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0001t0011g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0002t0010g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0001g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0004t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0005t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0005t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0005t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0005t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0005t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0005t0012g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0001c0019t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0003t0008g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0006t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0006t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0006t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0006t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0006t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0006t0003g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0007t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0007t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0007t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0007t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0007t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0008t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0008t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0008t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0009t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0009t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0012t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0002c0012t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0003c0010t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0003c0010t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0004c0011t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0004c0011t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0005c0015t0001g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0006c0016t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0007c0013t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0008c0020t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0009c0014t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0010c0017t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| a0011c0018t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0167 | EUR | GBR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0353 | EUR | GBR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0315 | EUR | GBR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0379 | EUR | FIN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00408 | hp2 | a0002 | c0003 | t0001 | g0217 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00597 | hp1 | a0002 | c0007 | t0001 | g0229 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00609 | hp1 | a0002 | c0003 | t0001 | g0216 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00609 | hp2 | a0002 | c0003 | t0003 | g0208 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00639 | hp2 | a0001 | c0004 | t0001 | g0017 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0372 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00733 | hp1 | a0002 | c0003 | t0003 | g0023 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0078 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0388 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00738 | hp1 | a0001 | c0002 | t0010 | g0115 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0106 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0022 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01106 | hp2 | a0002 | c0003 | t0001 | g0236 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0382 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01167 | hp1 | a0001 | c0005 | t0002 | g0202 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01167 | hp2 | a0002 | c0012 | t0002 | g0299 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01168 | hp1 | a0001 | c0004 | t0001 | g0091 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01169 | hp1 | a0002 | c0012 | t0002 | g0300 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01192 | hp1 | a0002 | c0003 | t0003 | g0023 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0237 | AMR | PUR | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01255 | hp1 | a0001 | c0004 | t0001 | g0017 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01258 | hp1 | a0001 | c0005 | t0003 | g0169 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0380 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0354 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0102 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01361 | hp2 | a0001 | c0005 | t0001 | g0168 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0063 | EUR | IBS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0374 | EUR | IBS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0067 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0239 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0114 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01952 | hp2 | a0002 | c0003 | t0003 | g0025 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01975 | hp2 | a0002 | c0003 | t0003 | g0206 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01978 | hp1 | a0002 | c0003 | t0003 | g0227 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0387 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0062 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02015 | hp2 | a0002 | c0003 | t0003 | g0223 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0284 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0279 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02040 | hp2 | a0002 | c0003 | t0003 | g0209 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0117 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02080 | hp1 | a0002 | c0003 | t0003 | g0210 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02083 | hp1 | a0002 | c0006 | t0003 | g0164 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02129 | hp1 | a0002 | c0003 | t0003 | g0244 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02132 | hp2 | a0002 | c0008 | t0001 | g0245 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02135 | hp1 | a0002 | c0003 | t0001 | g0024 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CDX | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0365 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02257 | hp2 | a0002 | c0003 | t0006 | g0213 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0101 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02280 | hp1 | a0002 | c0003 | t0001 | g0037 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02280 | hp2 | a0001 | c0004 | t0001 | g0026 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02293 | hp1 | a0002 | c0003 | t0003 | g0243 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0051 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02451 | hp1 | a0001 | c0004 | t0001 | g0258 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02451 | hp2 | a0002 | c0003 | t0001 | g0238 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02523 | hp1 | a0002 | c0006 | t0003 | g0266 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | KHV | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0257 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0039 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0133 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02602 | hp2 | a0001 | c0004 | t0001 | g0089 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02615 | hp1 | a0002 | c0007 | t0002 | g0212 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0256 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02622 | hp1 | a0001 | c0004 | t0001 | g0254 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02622 | hp2 | a0002 | c0007 | t0003 | g0207 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0384 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02647 | hp1 | a0003 | c0010 | t0003 | g0264 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0220 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02717 | hp1 | a0001 | c0004 | t0001 | g0255 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02723 | hp1 | a0001 | c0004 | t0001 | g0005 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02723 | hp2 | a0005 | c0015 | t0001 | g0383 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0059 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02735 | hp2 | a0004 | c0011 | t0004 | g0285 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0082 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02886 | hp1 | a0001 | c0002 | t0002 | g0084 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0111 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0201 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0109 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0043 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0080 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0116 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0219 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0250 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02965 | hp2 | a0001 | c0004 | t0001 | g0110 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02970 | hp1 | a0006 | c0016 | t0002 | g0108 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02970 | hp2 | a0002 | c0003 | t0003 | g0248 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0005 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03041 | hp2 | a0002 | c0003 | t0001 | g0204 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0261 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0079 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03130 | hp1 | a0001 | c0002 | t0009 | g0112 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03130 | hp2 | a0002 | c0007 | t0002 | g0214 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03139 | hp1 | a0002 | c0006 | t0003 | g0378 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03195 | hp1 | a0002 | c0003 | t0001 | g0218 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0081 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03209 | hp2 | a0002 | c0003 | t0003 | g0035 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03225 | hp1 | a0007 | c0013 | t0003 | g0249 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03225 | hp2 | a0001 | c0004 | t0007 | g0260 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0385 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03239 | hp2 | a0001 | c0005 | t0002 | g0203 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03453 | hp1 | a0003 | c0010 | t0001 | g0005 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03453 | hp2 | a0001 | c0002 | t0003 | g0113 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0107 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0252 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0233 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0211 | AFR | ESN | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0105 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0263 | AFR | GWD | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0366 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0005 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03654 | hp1 | a0001 | c0001 | t0011 | g0293 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03669 | hp1 | a0001 | c0004 | t0001 | g0100 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0291 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03831 | hp1 | a0008 | c0020 | t0001 | g0362 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0377 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0371 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03834 | hp2 | a0004 | c0011 | t0004 | g0286 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0376 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04184 | hp2 | a0002 | c0003 | t0003 | g0215 | SAS | BEB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0022 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04204 | hp2 | a0001 | c0019 | t0001 | g0303 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0083 | AFR | YRI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18522 | hp2 | a0009 | c0014 | t0001 | g0166 | AFR | YRI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | CHB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18747 | hp1 | a0002 | c0006 | t0003 | g0265 | EAS | CHB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | CHB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18906 | hp2 | a0002 | c0003 | t0001 | g0234 | AFR | YRI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18944 | hp2 | a0002 | c0003 | t0001 | g0024 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18949 | hp1 | a0002 | c0003 | t0003 | g0222 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18951 | hp1 | a0002 | c0008 | t0001 | g0240 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18953 | hp1 | a0002 | c0003 | t0003 | g0232 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18961 | hp2 | a0001 | c0005 | t0012 | g0047 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18964 | hp1 | a0002 | c0003 | t0003 | g0247 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0280 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0282 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18974 | hp1 | a0002 | c0009 | t0003 | g0246 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18982 | hp2 | a0002 | c0003 | t0003 | g0224 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18984 | hp2 | a0002 | c0003 | t0003 | g0228 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18987 | hp2 | a0002 | c0003 | t0003 | g0230 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18994 | hp2 | a0002 | c0006 | t0003 | g0267 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0375 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18997 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0370 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19006 | hp2 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0381 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | LWK | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | LWK | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19056 | hp2 | a0002 | c0009 | t0003 | g0225 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19062 | hp2 | a0002 | c0003 | t0003 | g0226 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19063 | hp2 | a0002 | c0007 | t0001 | g0221 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19064 | hp1 | a0002 | c0003 | t0003 | g0242 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19065 | hp2 | a0002 | c0006 | t0003 | g0268 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19075 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19076 | hp2 | a0010 | c0017 | t0005 | g0272 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19084 | hp2 | a0011 | c0018 | t0005 | g0281 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19085 | hp2 | a0002 | c0008 | t0001 | g0241 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19087 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0262 | AFR | YRI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0076 | AFR | ASW | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ASW | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | TSI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0075 | EUR | TSI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0355 | EUR | TSI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | GIH | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20905 | hp2 | a0001 | c0004 | t0001 | g0074 | SAS | GIH | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG01123 | hp2 | a0002 | c0003 | t0003 | g0025 | AMR | CLM | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0235 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0259 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0251 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02559 | hp1 | a0002 | c0003 | t0008 | g0038 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG02559 | hp2 | a0001 | c0004 | t0001 | g0386 | AFR | ACB | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03471 | hp1 | a0001 | c0002 | t0003 | g0077 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0064 | AFR | MSL | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | USA | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0231 | AFR | USA | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18955 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20300 | hp1 | a0001 | c0005 | t0002 | g0173 | AFR | USA | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | USA | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA21309 | hp1 | a0001 | c0004 | t0001 | g0253 | AFR | LWK | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0026 | AFR | LWK | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0373 | REF | REF | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0065 | REF | REF | PGM2_chr4_37821686_37867937 | PGM2 | chr4 | 37821686 | 37867937 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37829982 | G | A | 1 | a0007 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.100G>A | p.Ala34Thr | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/14 | 147/3211 | 100/1839 | 34/612 | chr4 | 37829982 | |||
| chr4:37830097 | G | A | 1 | a0009 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.215G>A | p.Arg72His | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/14 | 262/3211 | 215/1839 | 72/612 | chr4 | 37830097 | |||
| chr4:37840093 | A | G | 1 | a0003 | 2 | HG02647.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.553A>G | p.Ile185Val | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/14 | 600/3211 | 553/1839 | 185/612 | chr4 | 37840093 | |||
| chr4:37844412 | TGGGGTGG others(28): Show |
T | 1 | a0010 | 1 | NA19076.hp2 | frameshift_variant | HIGH | c.771_805delGGTGGGTC others(27): Show |
p.Val258fs | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/14 | 818/3211 | 771/1839 | 257/612 | INFO_REALIGN_3_PRIME | chr4 | 37844412 | ||
| chr4:37848522 | G | T | 1 | a0006 | 1 | HG02970.hp1 | missense_variant&splice_region_variant | MODERATE | c.1283G>T | p.Gly428Val | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/14 | 1330/3211 | 1283/1839 | 428/612 | chr4 | 37848522 | |||
| chr4:37848551 | A | G | 1 | a0008 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.1312A>G | p.Lys438Glu | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/14 | 1359/3211 | 1312/1839 | 438/612 | chr4 | 37848551 | |||
| chr4:37850235 | A | C | 1 | a0002 | 61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
missense_variant | MODERATE | c.1464A>C | p.Glu488Asp | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/14 | 1511/3211 | 1464/1839 | 488/612 | chr4 | 37850235 | |||
| chr4:37855628 | C | G | 1 | a0004 | 2 | HG02735.hp2 HG03834.hp2 |
missense_variant | MODERATE | c.1623C>G | p.Ser541Arg | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/14 | 1670/3211 | 1623/1839 | 541/612 | chr4 | 37855628 | |||
| chr4:37861527 | A | G | 1 | a0011 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.1754A>G | p.Lys585Arg | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 1801/3211 | 1754/1839 | 585/612 | chr4 | 37861527 | |||
| chr4:37861583 | A | G | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1810A>G | p.Lys604Glu | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 1857/3211 | 1810/1839 | 604/612 | chr4 | 37861583 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37834680 | T | C | 10 | a0001c0002 a0001c0004 a0002c0003 others(7): Show |
140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
synonymous_variant | LOW | c.312T>C | p.Ser104Ser | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/14 | 359/3211 | 312/1839 | 104/612 | chr4 | 37834680 | |||
| chr4:37845689 | C | T | 1 | a0002c0012 | 2 | HG01167.hp2 HG01169.hp1 |
synonymous_variant | LOW | c.966C>T | p.Asp322Asp | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/14 | 1013/3211 | 966/1839 | 322/612 | chr4 | 37845689 | |||
| chr4:37847039 | G | A | 1 | a0002c0008 | 3 | HG02132.hp2 NA18951.hp1 NA19085.hp2 |
synonymous_variant | LOW | c.1116G>A | p.Thr372Thr | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 9/14 | 1163/3211 | 1116/1839 | 372/612 | chr4 | 37847039 | |||
| chr4:37855721 | G | C | 5 | a0001c0002 a0001c0005 a0002c0007 others(2): Show |
68 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(65): Show |
synonymous_variant | LOW | c.1716G>C | p.Leu572Leu | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/14 | 1763/3211 | 1716/1839 | 572/612 | chr4 | 37855721 | |||
| chr4:37855727 | C | T | 1 | a0001c0019 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.1722C>T | p.Ala574Ala | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/14 | 1769/3211 | 1722/1839 | 574/612 | chr4 | 37855727 | |||
| chr4:37855733 | T | A | 1 | a0002c0009 | 2 | NA18974.hp1 NA19056.hp2 |
synonymous_variant | LOW | c.1728T>A | p.Pro576Pro | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/14 | 1775/3211 | 1728/1839 | 576/612 | chr4 | 37855733 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37826714 | C | T | 7 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0011 others(4): Show |
48 | HG00408.hp1 HG00423.hp1 HG02027.hp1 others(45): Show |
5_prime_UTR_variant | MODIFIER | c.-19C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/14 | 19 | chr4 | 37826714 | ||||||
| chr4:37861617 | G | A | 3 | a0001c0001t0007 a0001c0004t0007 a0002c0003t0008 |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 5 | chr4 | 37861617 | ||||||
| chr4:37861764 | C | T | 7 | a0001c0001t0002 a0001c0002t0002 a0001c0005t0002 others(4): Show |
57 | HG00733.hp2 HG01069.hp1 HG01167.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*152C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 152 | chr4 | 37861764 | ||||||
| chr4:37861835 | T | G | 3 | a0001c0001t0007 a0001c0004t0007 a0002c0003t0008 |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*223T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 223 | chr4 | 37861835 | ||||||
| chr4:37861904 | C | T | 1 | a0002c0003t0008 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*292C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 292 | chr4 | 37861904 | ||||||
| chr4:37862142 | G | C | 3 | a0001c0001t0006 a0001c0001t0011 a0002c0003t0006 |
6 | HG00099.hp1 HG01081.hp2 HG02257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*530G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 530 | chr4 | 37862142 | ||||||
| chr4:37862225 | G | A | 1 | a0001c0002t0009 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*613G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 613 | chr4 | 37862225 | ||||||
| chr4:37862244 | A | G | 3 | a0001c0001t0007 a0001c0004t0007 a0002c0003t0008 |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*632A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 632 | chr4 | 37862244 | ||||||
| chr4:37862326 | G | A | 14 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0011 others(11): Show |
52 | HG00099.hp1 HG00609.hp2 HG00733.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*714G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 714 | chr4 | 37862326 | ||||||
| chr4:37862531 | A | G | 3 | a0001c0001t0007 a0001c0004t0007 a0002c0003t0008 |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*919A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 919 | chr4 | 37862531 | ||||||
| chr4:37862561 | C | CTCATAAT others(28): Show |
1 | a0001c0002t0010 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*973_*974insCCCATC others(29): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 974 | INFO_REALIGN_3_PRIME | chr4 | 37862561 | |||||
| chr4:37862685 | GCCATTA | G | 3 | a0001c0001t0005 a0010c0017t0005 a0011c0018t0005 |
11 | HG02027.hp1 HG02040.hp1 NA18955.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1074_*1079delCCAT others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 1074 | chr4 | 37862685 | ||||||
| chr4:37862794 | C | T | 3 | a0001c0001t0007 a0001c0004t0007 a0002c0003t0008 |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1182C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 1182 | chr4 | 37862794 | ||||||
| chr4:37862824 | A | G | 3 | a0001c0001t0007 a0001c0004t0007 a0002c0003t0008 |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1212A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 1212 | chr4 | 37862824 | ||||||
| chr4:37862916 | A | G | 3 | a0001c0001t0007 a0001c0004t0007 a0002c0003t0008 |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1304A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 14/14 | 1304 | chr4 | 37862916 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37826848 | C | T | 1 | a0001c0001t0001g0388 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.81+35C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37826848 | |||||||
| chr4:37826887 | T | C | 1 | a0002c0003t0003g0035 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.81+74T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37826887 | |||||||
| chr4:37826952 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.81+139G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37826952 | |||||||
| chr4:37827100 | G | A | 1 | a0002c0003t0001g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.81+287G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827100 | |||||||
| chr4:37827121 | T | C | 1 | a0002c0003t0008g0038 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.81+308T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827121 | |||||||
| chr4:37827139 | G | T | 1 | a0002c0003t0008g0038 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.81+326G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827139 | |||||||
| chr4:37827208 | G | C | 1 | a0001c0002t0002g0039 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.81+395G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827208 | |||||||
| chr4:37827510 | C | T | 1 | a0001c0001t0001g0387 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.81+697C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827510 | |||||||
| chr4:37827551 | CGTTGTGA others(9): Show |
C | 1 | a0001c0004t0001g0386 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.81+739_81+754delGT others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827551 | |||||||
| chr4:37827608 | C | T | 1 | a0001c0001t0001g0385 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.81+795C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827608 | |||||||
| chr4:37827621 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.81+808G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827621 | |||||||
| chr4:37827629 | A | C | 3 | a0001c0002t0001g0040 a0002c0003t0003g0035 a0002c0003t0008g0038 |
3 | HG01255.hp2 HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.81+816A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827629 | |||||||
| chr4:37827660 | A | G | 3 | a0001c0002t0001g0040 a0002c0003t0003g0035 a0002c0003t0008g0038 |
3 | HG01255.hp2 HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.81+847A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827660 | |||||||
| chr4:37827966 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.81+1153G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37827966 | |||||||
| chr4:37828348 | CT | C | 19 | a0001c0001t0001g0058 a0001c0001t0004g0006 a0001c0001t0004g0016 others(16): Show |
22 | HG00408.hp1 HG02293.hp2 HG02897.hp1 others(19): Show |
intron_variant | MODIFIER | c.81+1547delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 37828348 | ||||||
| chr4:37828360 | TA | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0384 |
4 | HG02630.hp2 HG02809.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+1549delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 37828360 | ||||||
| chr4:37828637 | C | G | 1 | a0005c0015t0001g0383 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.82-1327C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828637 | |||||||
| chr4:37828647 | T | G | 1 | a0001c0002t0002g0059 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.82-1317T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828647 | |||||||
| chr4:37828666 | A | G | 326 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(323): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.82-1298A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828666 | |||||||
| chr4:37828674 | A | G | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.82-1290A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828674 | |||||||
| chr4:37828736 | G | A | 103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(100): Show |
125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.82-1228G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828736 | |||||||
| chr4:37828759 | C | T | 1 | a0001c0001t0001g0382 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.82-1205C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828759 | |||||||
| chr4:37828761 | A | G | 336 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(333): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.82-1203A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828761 | |||||||
| chr4:37828840 | T | C | 1 | a0002c0003t0001g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82-1124T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828840 | |||||||
| chr4:37828930 | C | G | 1 | a0001c0001t0001g0381 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.82-1034C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37828930 | |||||||
| chr4:37829006 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.82-958G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829006 | |||||||
| chr4:37829049 | G | T | 1 | a0001c0004t0001g0117 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.82-915G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829049 | |||||||
| chr4:37829185 | C | CAA | 51 | a0001c0002t0001g0040 a0002c0003t0001g0024 a0002c0003t0001g0037 others(48): Show |
54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.82-770_82-769dupAA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 37829185 | ||||||
| chr4:37829235 | G | A | 1 | a0002c0003t0003g0206 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-729G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829235 | |||||||
| chr4:37829295 | T | G | 1 | a0002c0003t0008g0038 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.82-669T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829295 | |||||||
| chr4:37829430 | CA | C | 49 | a0001c0002t0001g0040 a0002c0003t0001g0024 a0002c0003t0001g0037 others(46): Show |
52 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.82-530delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 37829430 | ||||||
| chr4:37829435 | G | T | 49 | a0001c0002t0001g0040 a0002c0003t0001g0024 a0002c0003t0001g0037 others(46): Show |
52 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.82-529G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829435 | |||||||
| chr4:37829647 | G | A | 51 | a0001c0002t0001g0040 a0002c0003t0001g0024 a0002c0003t0001g0037 others(48): Show |
54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.82-317G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829647 | |||||||
| chr4:37829716 | T | C | 16 | a0001c0001t0004g0006 a0001c0001t0004g0016 a0001c0001t0004g0044 others(13): Show |
19 | HG00408.hp1 HG02293.hp2 NA18942.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-248T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829716 | |||||||
| chr4:37829748 | G | A | 51 | a0001c0002t0001g0040 a0002c0003t0001g0024 a0002c0003t0001g0037 others(48): Show |
54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.82-216G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829748 | |||||||
| chr4:37829756 | C | T | 2 | a0001c0001t0001g0379 a0001c0001t0001g0380 |
2 | HG00323.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.82-208C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829756 | |||||||
| chr4:37829847 | C | CAT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(94): Show |
118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.82-105_82-104dupTA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 37829847 | ||||||
| chr4:37829859 | T | C | 51 | a0001c0002t0001g0040 a0002c0003t0001g0024 a0002c0003t0001g0037 others(48): Show |
54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.82-105T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829859 | |||||||
| chr4:37829861 | C | CAT | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG02074.hp1 HG02080.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.82-92_82-91dupAT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 37829861 | ||||||
| chr4:37829861 | C | T | 51 | a0001c0002t0001g0040 a0002c0003t0001g0024 a0002c0003t0001g0037 others(48): Show |
54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.82-103C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829861 | |||||||
| chr4:37829861 | CAT | C | 9 | a0001c0002t0003g0113 a0001c0002t0003g0114 a0001c0002t0003g0116 others(6): Show |
9 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-92_82-91delAT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 37829861 | ||||||
| chr4:37829870 | A | T | 48 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(45): Show |
51 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.82-94A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829870 | |||||||
| chr4:37829872 | A | T | 48 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(45): Show |
51 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.82-92A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 1/13 | chr4 | 37829872 | |||||||
| chr4:37830198 | C | A | 1 | a0002c0007t0003g0207 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.249+67C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37830198 | |||||||
| chr4:37830228 | C | T | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(304): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.249+97C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37830228 | |||||||
| chr4:37830237 | C | G | 1 | a0002c0006t0003g0378 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.249+106C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37830237 | |||||||
| chr4:37830240 | G | A | 48 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(45): Show |
51 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.249+109G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37830240 | |||||||
| chr4:37830245 | A | T | 51 | a0001c0002t0001g0040 a0002c0003t0001g0024 a0002c0003t0001g0037 others(48): Show |
54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.249+114A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37830245 | |||||||
| chr4:37830367 | A | C | 3 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 |
3 | HG02165.hp2 NA18988.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.249+236A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37830367 | |||||||
| chr4:37830919 | C | T | 1 | a0003c0010t0003g0264 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.249+788C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37830919 | |||||||
| chr4:37831131 | C | T | 2 | a0001c0001t0001g0376 a0001c0001t0001g0377 |
2 | HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.249+1000C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831131 | |||||||
| chr4:37831184 | C | T | 4 | a0001c0004t0001g0026 a0001c0004t0001g0261 a0001c0004t0001g0262 others(1): Show |
5 | HG02280.hp2 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+1053C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831184 | |||||||
| chr4:37831192 | C | CA | 60 | a0001c0001t0001g0031 a0001c0001t0001g0301 a0001c0001t0001g0302 others(57): Show |
64 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.249+1082dupA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 37831192 | ||||||
| chr4:37831192 | C | CAAAAAAA | 49 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(46): Show |
59 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.249+1076_249+1082d others(9): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 37831192 | ||||||
| chr4:37831192 | C | CAAAAAAA others(1): Show |
46 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(43): Show |
58 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.249+1075_249+1082d others(10): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 37831192 | ||||||
| chr4:37831192 | C | CAAAAAAA others(2): Show |
7 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG00438.hp1 HG00597.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.249+1074_249+1082d others(11): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 37831192 | ||||||
| chr4:37831192 | CA | C | 56 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0292 others(53): Show |
61 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.249+1082delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 37831192 | ||||||
| chr4:37831438 | G | T | 103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(100): Show |
125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.249+1307G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831438 | |||||||
| chr4:37831454 | T | C | 7 | a0002c0003t0003g0208 a0002c0003t0003g0209 a0002c0003t0003g0210 others(4): Show |
7 | HG00609.hp2 HG02040.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+1323T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831454 | |||||||
| chr4:37831491 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(80): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.249+1360C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831491 | |||||||
| chr4:37831538 | G | C | 1 | a0002c0003t0001g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.249+1407G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831538 | |||||||
| chr4:37831749 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.249+1618C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831749 | |||||||
| chr4:37831839 | G | A | 51 | a0001c0002t0001g0040 a0002c0003t0001g0024 a0002c0003t0001g0037 others(48): Show |
54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.249+1708G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831839 | |||||||
| chr4:37831855 | A | G | 1 | a0002c0003t0001g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.249+1724A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831855 | |||||||
| chr4:37831863 | G | A | 7 | a0001c0001t0004g0016 a0001c0001t0004g0046 a0001c0001t0004g0048 others(4): Show |
8 | HG00408.hp1 HG02293.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+1732G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831863 | |||||||
| chr4:37831968 | G | C | 1 | a0001c0002t0002g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.249+1837G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37831968 | |||||||
| chr4:37832238 | A | G | 1 | a0001c0001t0001g0372 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.249+2107A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37832238 | |||||||
| chr4:37832311 | C | T | 2 | a0001c0001t0007g0043 a0001c0001t0007g0201 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.249+2180C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37832311 | |||||||
| chr4:37832702 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(91): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.250-1916C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37832702 | |||||||
| chr4:37832844 | T | C | 53 | a0001c0002t0001g0040 a0002c0003t0001g0024 a0002c0003t0001g0037 others(50): Show |
56 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.250-1774T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37832844 | |||||||
| chr4:37833238 | G | A | 1 | a0001c0019t0001g0303 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.250-1380G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833238 | |||||||
| chr4:37833305 | G | A | 1 | a0001c0001t0004g0269 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.250-1313G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833305 | |||||||
| chr4:37833314 | A | G | 51 | a0001c0002t0001g0040 a0002c0003t0001g0024 a0002c0003t0001g0037 others(48): Show |
54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.250-1304A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833314 | |||||||
| chr4:37833370 | A | G | 51 | a0001c0002t0001g0040 a0002c0003t0001g0024 a0002c0003t0001g0037 others(48): Show |
54 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.250-1248A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833370 | |||||||
| chr4:37833432 | G | C | 52 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0292 others(49): Show |
57 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.250-1186G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833432 | |||||||
| chr4:37833515 | C | T | 1 | a0001c0001t0001g0371 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.250-1103C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833515 | |||||||
| chr4:37833633 | A | G | 2 | a0001c0002t0002g0250 a0001c0004t0007g0260 |
2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.250-985A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833633 | |||||||
| chr4:37833651 | A | G | 1 | a0001c0001t0001g0370 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.250-967A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833651 | |||||||
| chr4:37833708 | G | A | 1 | a0002c0003t0001g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.250-910G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833708 | |||||||
| chr4:37833732 | G | A | 1 | a0002c0003t0001g0211 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.250-886G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833732 | |||||||
| chr4:37833897 | C | A | 2 | a0001c0001t0001g0304 a0001c0001t0001g0372 |
2 | HG00673.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.250-721C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37833897 | |||||||
| chr4:37833902 | AT | A | 48 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(45): Show |
51 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.250-714delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 37833902 | ||||||
| chr4:37834046 | G | C | 4 | a0002c0003t0006g0213 a0002c0007t0002g0212 a0002c0007t0002g0214 others(1): Show |
4 | HG02257.hp2 HG02615.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-572G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834046 | |||||||
| chr4:37834180 | A | T | 1 | a0001c0001t0001g0165 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.250-438A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834180 | |||||||
| chr4:37834201 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.250-417G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834201 | |||||||
| chr4:37834239 | TA | T | 132 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(129): Show |
139 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.250-378delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834239 | |||||||
| chr4:37834240 | A | G | 1 | a0002c0003t0003g0215 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.250-378A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834240 | |||||||
| chr4:37834249 | T | C | 2 | a0002c0012t0002g0299 a0002c0012t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.250-369T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834249 | |||||||
| chr4:37834285 | A | G | 31 | a0001c0001t0001g0030 a0001c0001t0001g0292 a0001c0001t0001g0294 others(28): Show |
35 | HG00408.hp1 HG00438.hp2 HG02083.hp1 others(32): Show |
intron_variant | MODIFIER | c.250-333A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834285 | |||||||
| chr4:37834339 | GA | G | 71 | a0001c0002t0001g0040 a0001c0002t0002g0039 a0001c0002t0002g0250 others(68): Show |
77 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.250-266delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 37834339 | ||||||
| chr4:37834536 | C | T | 1 | a0002c0003t0001g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.250-82C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834536 | |||||||
| chr4:37834564 | G | A | 1 | a0001c0002t0002g0250 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.250-54G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834564 | |||||||
| chr4:37834579 | T | C | 1 | a0001c0002t0002g0066 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.250-39T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 2/13 | chr4 | 37834579 | |||||||
| chr4:37834794 | A | G | 1 | a0002c0007t0003g0207 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.356+70A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37834794 | |||||||
| chr4:37834999 | A | T | 133 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(130): Show |
140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.356+275A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37834999 | |||||||
| chr4:37835104 | C | T | 1 | a0002c0008t0001g0245 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.356+380C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835104 | |||||||
| chr4:37835108 | T | C | 1 | a0009c0014t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.356+384T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835108 | |||||||
| chr4:37835228 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.356+504G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835228 | |||||||
| chr4:37835229 | T | C | 1 | a0001c0004t0007g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.356+505T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835229 | |||||||
| chr4:37835245 | T | C | 1 | a0001c0004t0001g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.356+521T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835245 | |||||||
| chr4:37835414 | A | G | 1 | a0001c0004t0007g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.356+690A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835414 | |||||||
| chr4:37835443 | A | G | 133 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(130): Show |
140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.356+719A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835443 | |||||||
| chr4:37835510 | C | T | 1 | a0002c0006t0003g0378 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.356+786C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835510 | |||||||
| chr4:37835596 | G | A | 133 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(130): Show |
140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.356+872G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835596 | |||||||
| chr4:37835626 | T | C | 1 | a0001c0001t0001g0009 | 3 | HG00323.hp1 HG01123.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.356+902T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835626 | |||||||
| chr4:37835636 | G | A | 133 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(130): Show |
140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.356+912G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835636 | |||||||
| chr4:37835774 | C | T | 5 | a0001c0001t0001g0367 a0001c0001t0001g0368 a0001c0001t0001g0369 others(2): Show |
5 | HG02074.hp2 HG02735.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.356+1050C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835774 | |||||||
| chr4:37835945 | T | C | 131 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(128): Show |
138 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.356+1221T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37835945 | |||||||
| chr4:37836043 | A | T | 1 | a0001c0002t0002g0059 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.356+1319A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836043 | |||||||
| chr4:37836056 | G | A | 48 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(45): Show |
51 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.356+1332G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836056 | |||||||
| chr4:37836197 | G | A | 293 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(290): Show |
327 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.357-1332G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836197 | |||||||
| chr4:37836296 | C | CT | 3 | a0001c0001t0001g0364 a0001c0001t0001g0365 a0001c0001t0001g0366 |
3 | HG02257.hp1 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.357-1232dupT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 37836296 | ||||||
| chr4:37836310 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.357-1219G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836310 | |||||||
| chr4:37836426 | G | A | 58 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0292 others(55): Show |
63 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.357-1103G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836426 | |||||||
| chr4:37836513 | C | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0021 others(32): Show |
41 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.357-1016C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836513 | |||||||
| chr4:37836514 | G | C | 9 | a0001c0001t0004g0287 a0001c0001t0004g0288 a0001c0001t0004g0289 others(6): Show |
9 | HG02083.hp1 HG02523.hp1 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.357-1015G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836514 | |||||||
| chr4:37836600 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.357-929C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836600 | |||||||
| chr4:37836615 | C | T | 133 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(130): Show |
140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.357-914C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836615 | |||||||
| chr4:37836697 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0175 |
4 | NA18948.hp1 NA18970.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.357-832C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836697 | |||||||
| chr4:37836761 | C | T | 133 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(130): Show |
140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.357-768C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836761 | |||||||
| chr4:37836862 | G | GGTGTGT | 149 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(146): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.357-652_357-647dup others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 37836862 | ||||||
| chr4:37836862 | G | GGTGTGTG others(1): Show |
78 | a0001c0001t0001g0009 a0001c0001t0001g0157 a0001c0001t0001g0165 others(75): Show |
82 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.357-654_357-647dup others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 37836862 | ||||||
| chr4:37836862 | G | GGTGTGTG others(3): Show |
37 | a0001c0001t0001g0027 a0001c0001t0004g0027 a0001c0001t0004g0028 others(34): Show |
40 | HG00423.hp1 HG01069.hp1 HG02027.hp1 others(37): Show |
intron_variant | MODIFIER | c.357-656_357-647dup others(10): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 37836862 | ||||||
| chr4:37836862 | G | GGTGTGTG others(5): Show |
26 | a0001c0001t0001g0030 a0001c0001t0001g0292 a0001c0001t0001g0294 others(23): Show |
30 | HG00408.hp1 HG00438.hp2 HG02083.hp1 others(27): Show |
intron_variant | MODIFIER | c.357-658_357-647dup others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 37836862 | ||||||
| chr4:37836862 | G | GGTGTGTG others(7): Show |
3 | a0001c0001t0001g0295 a0001c0001t0004g0050 a0001c0001t0004g0051 |
3 | HG02293.hp2 NA18968.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.357-660_357-647dup others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 37836862 | ||||||
| chr4:37836862 | G | GTGTGTGT others(4): Show |
1 | a0001c0001t0004g0045 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.357-667_357-666ins others(11): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836862 | |||||||
| chr4:37836895 | G | A | 3 | a0001c0002t0002g0067 a0002c0003t0001g0216 a0002c0003t0001g0217 |
3 | HG00408.hp2 HG00609.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.357-634G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37836895 | |||||||
| chr4:37837092 | C | T | 1 | a0001c0004t0001g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.357-437C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37837092 | |||||||
| chr4:37837110 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.357-419A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37837110 | |||||||
| chr4:37837502 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.357-27T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 3/13 | chr4 | 37837502 | |||||||
| chr4:37837737 | G | A | 2 | a0002c0003t0001g0218 a0002c0003t0001g0219 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.441+124G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37837737 | |||||||
| chr4:37837744 | A | G | 133 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(130): Show |
140 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.441+131A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37837744 | |||||||
| chr4:37837887 | AT | A | 134 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(131): Show |
141 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.441+285delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 37837887 | ||||||
| chr4:37837966 | C | T | 4 | a0001c0004t0001g0026 a0001c0004t0001g0261 a0001c0004t0001g0262 others(1): Show |
5 | HG02280.hp2 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+353C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37837966 | |||||||
| chr4:37837976 | G | A | 1 | a0001c0004t0001g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.441+363G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37837976 | |||||||
| chr4:37838139 | C | T | 3 | a0002c0003t0003g0035 a0002c0003t0003g0244 a0002c0003t0008g0038 |
3 | HG02129.hp1 HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.441+526C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838139 | |||||||
| chr4:37838148 | T | G | 1 | a0001c0001t0004g0271 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.441+535T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838148 | |||||||
| chr4:37838173 | G | A | 2 | a0002c0003t0003g0035 a0002c0003t0008g0038 |
2 | HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.441+560G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838173 | |||||||
| chr4:37838251 | G | A | 1 | a0001c0001t0004g0269 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.441+638G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838251 | |||||||
| chr4:37838399 | A | G | 2 | a0002c0003t0003g0035 a0002c0003t0008g0038 |
2 | HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.441+786A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838399 | |||||||
| chr4:37838547 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.441+934A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838547 | |||||||
| chr4:37838660 | ACT | A | 52 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0292 others(49): Show |
57 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.441+1050_441+1051d others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 37838660 | ||||||
| chr4:37838742 | T | C | 7 | a0001c0002t0002g0060 a0001c0002t0002g0068 a0001c0002t0002g0069 others(4): Show |
7 | NA18949.hp2 NA18954.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-1106T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838742 | |||||||
| chr4:37838780 | A | G | 9 | a0001c0001t0001g0163 a0001c0001t0001g0194 a0001c0001t0001g0195 others(6): Show |
9 | HG00735.hp1 HG01109.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-1068A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838780 | |||||||
| chr4:37838806 | C | T | 2 | a0002c0003t0001g0218 a0002c0003t0001g0219 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.442-1042C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838806 | |||||||
| chr4:37838908 | G | C | 1 | a0001c0004t0001g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.442-940G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838908 | |||||||
| chr4:37838984 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(99): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.442-864G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37838984 | |||||||
| chr4:37839031 | A | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(99): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.442-817A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839031 | |||||||
| chr4:37839045 | A | G | 1 | a0005c0015t0001g0383 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.442-803A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839045 | |||||||
| chr4:37839111 | A | AT | 20 | a0001c0001t0001g0058 a0001c0001t0001g0296 a0001c0001t0001g0297 others(17): Show |
20 | HG01952.hp1 HG01978.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.442-713dupT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 37839111 | ||||||
| chr4:37839111 | AT | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(95): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.442-713delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 37839111 | ||||||
| chr4:37839111 | ATT | A | 15 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0175 others(12): Show |
16 | HG00558.hp1 HG01167.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.442-714_442-713del others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 37839111 | ||||||
| chr4:37839111 | ATTT | A | 119 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(116): Show |
125 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.442-715_442-713del others(3): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 37839111 | ||||||
| chr4:37839161 | C | T | 1 | a0001c0004t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-687C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839161 | |||||||
| chr4:37839249 | G | A | 1 | a0001c0002t0003g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.442-599G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839249 | |||||||
| chr4:37839250 | C | T | 1 | a0004c0011t0004g0286 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.442-598C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839250 | |||||||
| chr4:37839262 | G | C | 138 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(135): Show |
145 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.442-586G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839262 | |||||||
| chr4:37839279 | A | C | 1 | a0002c0003t0008g0038 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.442-569A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839279 | |||||||
| chr4:37839289 | A | G | 1 | a0001c0004t0007g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.442-559A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839289 | |||||||
| chr4:37839459 | G | A | 1 | a0001c0001t0006g0167 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.442-389G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839459 | |||||||
| chr4:37839511 | T | C | 2 | a0002c0012t0002g0299 a0002c0012t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.442-337T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839511 | |||||||
| chr4:37839558 | G | A | 1 | a0001c0004t0007g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.442-290G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839558 | |||||||
| chr4:37839687 | A | C | 1 | a0002c0003t0008g0038 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.442-161A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839687 | |||||||
| chr4:37839732 | A | G | 1 | a0001c0004t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-116A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839732 | |||||||
| chr4:37839808 | C | T | 138 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(135): Show |
145 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.442-40C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 4/13 | chr4 | 37839808 | |||||||
| chr4:37839956 | C | T | 2 | a0004c0011t0004g0285 a0004c0011t0004g0286 |
2 | HG02735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.525+25C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 5/13 | chr4 | 37839956 | |||||||
| chr4:37840041 | C | T | 2 | a0001c0002t0002g0103 a0001c0002t0002g0104 |
2 | NA18747.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.526-25C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 5/13 | chr4 | 37840041 | |||||||
| chr4:37840320 | T | C | 138 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(135): Show |
145 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.719+61T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840320 | |||||||
| chr4:37840353 | C | G | 1 | a0001c0002t0002g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.719+94C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840353 | |||||||
| chr4:37840365 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.719+106C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840365 | |||||||
| chr4:37840632 | A | G | 138 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(135): Show |
145 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.719+373A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840632 | |||||||
| chr4:37840916 | T | A | 138 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(135): Show |
145 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.719+657T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840916 | |||||||
| chr4:37840947 | A | AGT | 54 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0292 others(51): Show |
60 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.719+705_719+706dup others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37840947 | ||||||
| chr4:37840947 | A | AGTGT | 11 | a0001c0001t0005g0029 a0001c0001t0005g0278 a0001c0001t0005g0279 others(8): Show |
12 | HG02027.hp1 HG02040.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.719+703_719+706dup others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37840947 | ||||||
| chr4:37840960 | G | GTA | 85 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(82): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.719+702_719+703ins others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37840960 | ||||||
| chr4:37840960 | G | GTATA | 11 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(8): Show |
11 | HG01258.hp1 HG01361.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.719+702_719+703ins others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37840960 | ||||||
| chr4:37840960 | G | GTATATA | 3 | a0001c0001t0001g0127 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG00597.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.719+702_719+703ins others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37840960 | ||||||
| chr4:37840962 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(99): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.719+703G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840962 | |||||||
| chr4:37840964 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(99): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.719+705G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840964 | |||||||
| chr4:37840964 | GTA | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(100): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.719+723_719+724del others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37840964 | ||||||
| chr4:37840966 | A | G | 132 | a0001c0001t0004g0049 a0001c0002t0001g0040 a0001c0002t0001g0092 others(129): Show |
139 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.719+707A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840966 | |||||||
| chr4:37840968 | A | G | 88 | a0001c0001t0001g0371 a0001c0002t0001g0040 a0001c0002t0001g0092 others(85): Show |
92 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(89): Show |
intron_variant | MODIFIER | c.719+709A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840968 | |||||||
| chr4:37840970 | A | G | 1 | a0001c0004t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.719+711A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840970 | |||||||
| chr4:37840982 | A | G | 136 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(133): Show |
143 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.719+723A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37840982 | |||||||
| chr4:37841039 | A | G | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.719+780A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841039 | |||||||
| chr4:37841070 | G | A | 2 | a0002c0008t0001g0240 a0002c0008t0001g0241 |
2 | NA18951.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.719+811G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841070 | |||||||
| chr4:37841071 | C | CGT | 3 | a0001c0001t0001g0296 a0001c0001t0001g0298 a0001c0001t0001g0381 |
3 | HG02165.hp2 NA18989.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.719+813_719+814dup others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841071 | ||||||
| chr4:37841072 | G | GTATATAT others(1): Show |
5 | a0001c0001t0001g0031 a0001c0001t0001g0350 a0001c0001t0001g0351 others(2): Show |
6 | HG01109.hp2 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.719+835_719+842dup others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841072 | G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0034 a0001c0001t0001g0301 |
3 | HG00280.hp1 NA18940.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.719+833_719+842dup others(10): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841072 | G | GTATATAT others(5): Show |
4 | a0001c0001t0001g0305 a0001c0001t0001g0348 a0001c0001t0001g0349 others(1): Show |
4 | HG00621.hp1 HG02257.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.719+831_719+842dup others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841072 | G | GTATATAT others(7): Show |
10 | a0001c0001t0001g0342 a0001c0001t0001g0343 a0001c0001t0001g0344 others(7): Show |
10 | HG03139.hp2 HG03239.hp1 HG03579.hp1 others(7): Show |
intron_variant | MODIFIER | c.719+829_719+842dup others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841072 | G | GTATATAT others(9): Show |
13 | a0001c0001t0001g0013 a0001c0001t0001g0306 a0001c0001t0001g0307 others(10): Show |
15 | HG00544.hp2 HG01074.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.719+827_719+842dup others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841072 | G | GTATATAT others(11): Show |
14 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0058 others(11): Show |
19 | HG00673.hp1 HG00673.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.719+825_719+842dup others(18): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841072 | G | GTATATAT others(13): Show |
10 | a0001c0001t0001g0012 a0001c0001t0001g0317 a0001c0001t0001g0318 others(7): Show |
12 | HG01516.hp2 NA18968.hp1 NA18983.hp2 others(9): Show |
intron_variant | MODIFIER | c.719+823_719+842dup others(20): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841072 | G | GTATATAT others(15): Show |
4 | a0001c0001t0001g0011 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
6 | HG00140.hp1 HG01167.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.719+821_719+842dup others(22): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841072 | G | GTATATAT others(17): Show |
6 | a0001c0001t0001g0033 a0001c0001t0001g0313 a0001c0001t0001g0314 others(3): Show |
7 | HG01169.hp1 HG02273.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.719+819_719+842dup others(24): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841072 | G | GTATATAT others(19): Show |
2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | HG02300.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.719+817_719+842dup others(26): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841072 | G | GTATATAT others(23): Show |
1 | a0001c0001t0001g0308 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.719+842_719+843ins others(30): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841072 | G | GTATATAT others(27): Show |
1 | a0001c0001t0001g0369 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.719+842_719+843ins others(34): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841072 | GTA | G | 46 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0178 others(43): Show |
51 | HG00423.hp1 HG00438.hp2 HG02027.hp1 others(48): Show |
intron_variant | MODIFIER | c.719+841_719+842del others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841072 | GTATA | G | 20 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0163 others(17): Show |
21 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.719+839_719+842del others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841072 | GTATATA | G | 70 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(67): Show |
89 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.719+837_719+842del others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841072 | GTATATAT others(1): Show |
G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0125 a0001c0001t0001g0126 others(9): Show |
14 | NA18939.hp1 NA18947.hp2 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.719+835_719+842del others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841072 | ||||||
| chr4:37841084 | A | G | 1 | a0002c0006t0003g0378 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.719+825A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841084 | |||||||
| chr4:37841094 | A | ATGTG | 52 | a0001c0002t0001g0092 a0001c0002t0001g0251 a0001c0002t0002g0042 others(49): Show |
53 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.719+836_719+837ins others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841094 | ||||||
| chr4:37841094 | A | G | 2 | a0001c0002t0002g0101 a0001c0002t0002g0102 |
2 | HG01361.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.719+835A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841094 | |||||||
| chr4:37841096 | A | ATGTGTG | 3 | a0001c0002t0002g0068 a0001c0002t0009g0112 a0001c0004t0001g0110 |
3 | HG02965.hp2 HG03130.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.719+838_719+839ins others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841096 | ||||||
| chr4:37841096 | A | G | 56 | a0001c0002t0001g0092 a0001c0002t0001g0251 a0001c0002t0002g0042 others(53): Show |
57 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.719+837A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841096 | |||||||
| chr4:37841098 | A | ATGTGTGT others(1): Show |
5 | a0001c0002t0001g0040 a0001c0002t0003g0259 a0001c0004t0001g0026 others(2): Show |
6 | HG01255.hp2 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.719+840_719+841ins others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841098 | ||||||
| chr4:37841098 | A | ATGTGTGT others(3): Show |
2 | a0001c0002t0002g0039 a0001c0004t0001g0252 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.719+840_719+841ins others(10): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841098 | ||||||
| chr4:37841098 | A | G | 74 | a0001c0001t0001g0019 a0001c0001t0001g0120 a0001c0001t0001g0123 others(71): Show |
76 | HG00621.hp2 HG00639.hp2 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.719+839A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841098 | |||||||
| chr4:37841100 | A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0032 | 2 | NA18964.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.719+842_719+843ins others(32): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATAT others(21): Show |
2 | a0001c0001t0001g0309 a0002c0003t0003g0206 |
2 | HG01975.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.719+842_719+843ins others(28): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0312 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.719+842_719+843ins others(26): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0356 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.719+842_719+843ins others(24): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0321 a0001c0001t0004g0051 |
2 | HG01106.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.719+842_719+843ins others(20): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATAT others(11): Show |
10 | a0001c0001t0001g0302 a0001c0001t0001g0329 a0001c0001t0001g0330 others(7): Show |
11 | HG00609.hp2 HG00733.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.719+842_719+843ins others(18): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATAT others(9): Show |
9 | a0001c0001t0001g0003 a0001c0001t0001g0304 a0001c0001t0001g0341 others(6): Show |
13 | HG00609.hp1 HG02293.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.719+842_719+843ins others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATAT others(7): Show |
18 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0003g0025 others(15): Show |
20 | HG00597.hp1 HG01123.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.719+842_719+843ins others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATAT others(9): Show |
3 | a0002c0003t0003g0222 a0002c0003t0003g0223 a0002c0003t0003g0224 |
3 | HG02015.hp2 NA18949.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.719+842_719+843ins others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATAT others(5): Show |
1 | a0002c0003t0003g0244 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.719+842_719+843ins others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATAT others(7): Show |
1 | a0002c0003t0001g0217 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.719+842_719+843ins others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATAT others(3): Show |
2 | a0002c0003t0001g0231 a0002c0008t0001g0240 |
2 | HG06807.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.719+842_719+843ins others(10): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATAT others(1): Show |
3 | a0002c0003t0001g0233 a0002c0008t0001g0241 a0002c0008t0001g0245 |
3 | HG02132.hp2 HG03516.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.719+842_719+843ins others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATAT others(3): Show |
1 | a0002c0003t0003g0232 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.719+842_719+843ins others(10): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATG | 9 | a0002c0003t0001g0204 a0002c0003t0001g0218 a0002c0003t0001g0219 others(6): Show |
9 | HG01106.hp2 HG01192.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.719+842_719+843ins others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATGT others(1): Show |
5 | a0002c0003t0001g0211 a0002c0003t0003g0248 a0002c0007t0002g0212 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.719+842_719+843ins others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATATGT others(9): Show |
1 | a0001c0004t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.719+842_719+843ins others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATGTGT others(5): Show |
1 | a0002c0003t0003g0035 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.719+842_719+843ins others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATATGTGT others(7): Show |
1 | a0007c0013t0003g0249 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.719+842_719+843ins others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATGTGTGT others(5): Show |
7 | a0001c0002t0002g0256 a0001c0004t0001g0005 a0001c0004t0001g0255 others(4): Show |
9 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.719+845_719+856dup others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | ATGTGTGT others(7): Show |
1 | a0001c0004t0001g0254 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.719+843_719+856dup others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841100 | ||||||
| chr4:37841100 | A | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(226): Show |
258 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.719+841A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841100 | |||||||
| chr4:37841102 | G | A | 4 | a0001c0001t0001g0301 a0001c0001t0001g0328 a0001c0001t0001g0350 others(1): Show |
4 | HG01934.hp1 HG02258.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.719+843G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841102 | |||||||
| chr4:37841104 | G | A | 1 | a0001c0001t0001g0363 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.719+845G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841104 | |||||||
| chr4:37841116 | T | G | 2 | a0001c0002t0002g0250 a0001c0004t0007g0260 |
2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.719+857T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841116 | |||||||
| chr4:37841143 | C | T | 1 | a0009c0014t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.719+884C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841143 | |||||||
| chr4:37841158 | T | TGTGTGTG others(10): Show |
1 | a0005c0015t0001g0383 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.719+899_719+900ins others(17): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841158 | |||||||
| chr4:37841158 | T | TGTGTGTG others(12): Show |
1 | a0003c0010t0003g0264 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.719+899_719+900ins others(19): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841158 | |||||||
| chr4:37841158 | T | TTGTG | 3 | a0001c0001t0001g0179 a0001c0001t0001g0183 a0008c0020t0001g0362 |
3 | HG01074.hp2 HG03491.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.719+926_719+929dup others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | ||||||
| chr4:37841158 | T | TTGTGTGT others(1): Show |
35 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
43 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.719+922_719+929dup others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | ||||||
| chr4:37841158 | T | TTGTGTGT others(3): Show |
51 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(48): Show |
61 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.719+920_719+929dup others(10): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | ||||||
| chr4:37841158 | T | TTGTGTGT others(5): Show |
17 | a0001c0001t0001g0008 a0001c0001t0001g0126 a0001c0001t0001g0131 others(14): Show |
19 | HG00558.hp1 HG01106.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.719+918_719+929dup others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | ||||||
| chr4:37841158 | T | TTGTGTGT others(7): Show |
42 | a0001c0001t0001g0145 a0001c0001t0001g0174 a0001c0001t0002g0015 others(39): Show |
47 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.719+916_719+929dup others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | ||||||
| chr4:37841158 | T | TTGTGTGT others(9): Show |
5 | a0001c0001t0001g0155 a0002c0003t0001g0217 a0002c0003t0001g0218 others(2): Show |
5 | HG00408.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.719+914_719+929dup others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | ||||||
| chr4:37841158 | T | TTGTGTGT others(11): Show |
1 | a0002c0003t0003g0210 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.719+912_719+929dup others(18): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | ||||||
| chr4:37841158 | TTGTG | T | 52 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0292 others(49): Show |
57 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.719+926_719+929del others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841158 | ||||||
| chr4:37841173 | T | TGTGTGTG others(7): Show |
1 | a0002c0006t0003g0266 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.719+927_719+928ins others(14): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37841173 | ||||||
| chr4:37841188 | G | GTGTGTGT others(2): Show |
5 | a0001c0002t0002g0078 a0001c0002t0002g0101 a0001c0002t0002g0250 others(2): Show |
5 | HG00733.hp2 HG02055.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.719+929_719+930ins others(9): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841188 | |||||||
| chr4:37841188 | G | GTGTGTGT others(4): Show |
2 | a0001c0004t0001g0110 a0007c0013t0003g0249 |
2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.719+929_719+930ins others(11): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841188 | |||||||
| chr4:37841188 | G | GTGTGTGT others(6): Show |
33 | a0001c0002t0001g0251 a0001c0002t0002g0063 a0001c0002t0002g0067 others(30): Show |
36 | HG01069.hp1 HG01361.hp1 HG01515.hp1 others(33): Show |
intron_variant | MODIFIER | c.719+929_719+930ins others(13): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841188 | |||||||
| chr4:37841188 | G | GTGTGTGT others(8): Show |
18 | a0001c0002t0001g0092 a0001c0002t0002g0039 a0001c0002t0002g0066 others(15): Show |
19 | HG00639.hp2 HG01168.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.719+929_719+930ins others(15): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841188 | |||||||
| chr4:37841188 | G | GTGTGTGT others(10): Show |
15 | a0001c0002t0002g0042 a0001c0002t0002g0059 a0001c0002t0002g0070 others(12): Show |
15 | HG00738.hp1 HG02559.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.719+929_719+930ins others(17): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841188 | |||||||
| chr4:37841188 | G | GTGTGTGT others(12): Show |
6 | a0001c0002t0002g0060 a0001c0002t0002g0061 a0001c0002t0002g0062 others(3): Show |
6 | HG01981.hp2 NA19000.hp1 NA19066.hp1 others(3): Show |
intron_variant | MODIFIER | c.719+929_719+930ins others(19): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841188 | |||||||
| chr4:37841189 | G | T | 4 | a0001c0002t0002g0064 a0001c0002t0003g0077 a0003c0010t0003g0264 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.719+930G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841189 | |||||||
| chr4:37841190 | T | G | 4 | a0001c0002t0002g0064 a0001c0002t0003g0077 a0003c0010t0003g0264 others(1): Show |
4 | HG02647.hp1 HG02723.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.719+931T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841190 | |||||||
| chr4:37841190 | T | TG | 82 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(79): Show |
86 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.719+931_719+932ins others(1): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841190 | |||||||
| chr4:37841191 | T | G | 1 | a0001c0004t0001g0074 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.719+932T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841191 | |||||||
| chr4:37841192 | T | G | 86 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(83): Show |
90 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.719+933T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841192 | |||||||
| chr4:37841202 | A | G | 87 | a0001c0002t0001g0040 a0001c0002t0001g0092 a0001c0002t0001g0251 others(84): Show |
91 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.719+943A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841202 | |||||||
| chr4:37841318 | G | A | 48 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0292 others(45): Show |
53 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.719+1059G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841318 | |||||||
| chr4:37841334 | A | G | 1 | a0002c0003t0003g0248 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.719+1075A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841334 | |||||||
| chr4:37841401 | T | G | 53 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(50): Show |
56 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.719+1142T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841401 | |||||||
| chr4:37841540 | G | A | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(292): Show |
329 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.719+1281G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841540 | |||||||
| chr4:37841646 | C | T | 57 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(54): Show |
60 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.719+1387C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841646 | |||||||
| chr4:37841771 | A | G | 1 | a0002c0003t0001g0237 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.719+1512A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841771 | |||||||
| chr4:37841815 | T | G | 1 | a0001c0004t0001g0253 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.719+1556T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841815 | |||||||
| chr4:37841841 | C | T | 1 | a0001c0001t0004g0048 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.719+1582C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841841 | |||||||
| chr4:37841848 | G | C | 1 | a0001c0001t0005g0278 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.719+1589G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841848 | |||||||
| chr4:37841851 | C | T | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.719+1592C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37841851 | |||||||
| chr4:37842064 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.719+1805G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842064 | |||||||
| chr4:37842090 | T | C | 2 | a0002c0003t0003g0035 a0002c0003t0008g0038 |
2 | HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.719+1831T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842090 | |||||||
| chr4:37842106 | T | A | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.719+1847T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842106 | |||||||
| chr4:37842197 | T | G | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.719+1938T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842197 | |||||||
| chr4:37842199 | CTATA | C | 54 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(51): Show |
57 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.719+1947_719+1950d others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37842199 | ||||||
| chr4:37842199 | CTATATA | C | 4 | a0002c0003t0003g0035 a0002c0003t0008g0038 a0002c0012t0002g0299 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.719+1945_719+1950d others(8): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37842199 | ||||||
| chr4:37842211 | A | T | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.719+1952A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842211 | |||||||
| chr4:37842251 | C | T | 294 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(291): Show |
328 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.719+1992C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842251 | |||||||
| chr4:37842332 | A | G | 2 | a0002c0012t0002g0299 a0002c0012t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.720-2032A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842332 | |||||||
| chr4:37842374 | TA | T | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-1989delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842374 | |||||||
| chr4:37842520 | G | C | 1 | a0002c0003t0001g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.720-1844G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842520 | |||||||
| chr4:37842556 | TTC | T | 58 | a0001c0001t0001g0154 a0001c0001t0004g0056 a0001c0002t0001g0092 others(55): Show |
59 | HG00639.hp2 HG00733.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.720-1806_720-1805d others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37842556 | ||||||
| chr4:37842557 | TC | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(174): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.720-1806delC | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842557 | |||||||
| chr4:37842558 | C | T | 65 | a0001c0001t0001g0350 a0001c0001t0001g0363 a0001c0001t0001g0364 others(62): Show |
69 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.720-1806C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842558 | |||||||
| chr4:37842605 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.720-1759A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842605 | |||||||
| chr4:37842668 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.720-1696C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842668 | |||||||
| chr4:37842668 | CT | C | 293 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(290): Show |
327 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.720-1686delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37842668 | ||||||
| chr4:37842669 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.720-1695T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842669 | |||||||
| chr4:37842687 | T | G | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-1677T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842687 | |||||||
| chr4:37842731 | G | T | 1 | a0001c0001t0001g0381 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.720-1633G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842731 | |||||||
| chr4:37842773 | G | C | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-1591G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842773 | |||||||
| chr4:37842883 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(99): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.720-1481G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842883 | |||||||
| chr4:37842958 | C | T | 3 | a0001c0002t0002g0075 a0001c0002t0002g0076 a0001c0002t0002g0106 |
3 | HG01069.hp1 NA20129.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.720-1406C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842958 | |||||||
| chr4:37842983 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(99): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.720-1381C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37842983 | |||||||
| chr4:37843120 | A | C | 2 | a0002c0012t0002g0299 a0002c0012t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.720-1244A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843120 | |||||||
| chr4:37843121 | C | T | 2 | a0002c0012t0002g0299 a0002c0012t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.720-1243C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843121 | |||||||
| chr4:37843229 | T | C | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-1135T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843229 | |||||||
| chr4:37843257 | G | A | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-1107G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843257 | |||||||
| chr4:37843315 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.720-1049T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843315 | |||||||
| chr4:37843368 | T | G | 1 | a0001c0001t0001g0165 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.720-996T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843368 | |||||||
| chr4:37843422 | A | C | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | HG02165.hp2 NA18988.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.720-942A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843422 | |||||||
| chr4:37843578 | C | A | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-786C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843578 | |||||||
| chr4:37843591 | T | C | 4 | a0002c0003t0001g0218 a0002c0003t0001g0219 a0002c0003t0001g0236 others(1): Show |
4 | HG01106.hp2 HG01192.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.720-773T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843591 | |||||||
| chr4:37843610 | A | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0001g0193 others(1): Show |
4 | HG01943.hp1 HG01975.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.720-754A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843610 | |||||||
| chr4:37843612 | T | TA | 56 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(53): Show |
59 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.720-752_720-751ins others(1): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843612 | |||||||
| chr4:37843613 | T | A | 32 | a0001c0001t0001g0030 a0001c0001t0001g0292 a0001c0001t0001g0294 others(29): Show |
36 | HG00408.hp1 HG00438.hp2 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.720-751T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843613 | |||||||
| chr4:37843615 | T | A | 2 | a0002c0003t0008g0038 a0002c0006t0003g0378 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.720-749T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843615 | |||||||
| chr4:37843632 | G | A | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-732G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843632 | |||||||
| chr4:37843679 | G | A | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG02074.hp1 HG02080.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.720-685G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843679 | |||||||
| chr4:37843845 | A | G | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-519A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843845 | |||||||
| chr4:37843881 | T | C | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.720-483T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843881 | |||||||
| chr4:37843967 | G | A | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | HG02165.hp2 NA18988.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.720-397G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37843967 | |||||||
| chr4:37844010 | A | G | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-354A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37844010 | |||||||
| chr4:37844026 | C | T | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-338C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37844026 | |||||||
| chr4:37844056 | G | A | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.720-308G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37844056 | |||||||
| chr4:37844069 | T | C | 1 | a0001c0001t0001g0304 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.720-295T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37844069 | |||||||
| chr4:37844212 | A | AAT | 103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(100): Show |
125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.720-143_720-142dup others(2): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 37844212 | ||||||
| chr4:37844290 | A | T | 2 | a0002c0012t0002g0299 a0002c0012t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.720-74A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 6/13 | chr4 | 37844290 | |||||||
| chr4:37844558 | C | A | 1 | a0001c0001t0001g0335 | 1 | NA18971.hp2 | splice_region_variant&intron_variant | LOW | c.909+5C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37844558 | |||||||
| chr4:37844682 | G | A | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.909+129G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37844682 | |||||||
| chr4:37844684 | T | A | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.909+131T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37844684 | |||||||
| chr4:37844699 | G | A | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.909+146G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37844699 | |||||||
| chr4:37844874 | G | A | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(292): Show |
329 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.909+321G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37844874 | |||||||
| chr4:37844969 | T | C | 296 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(293): Show |
330 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.909+416T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37844969 | |||||||
| chr4:37844975 | C | CA | 15 | a0001c0001t0001g0205 a0001c0001t0001g0322 a0001c0001t0001g0374 others(12): Show |
15 | HG01255.hp2 HG01516.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.909+442dupA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr4 | 37844975 | ||||||
| chr4:37844975 | CA | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(158): Show |
184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.909+442delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr4 | 37844975 | ||||||
| chr4:37844988 | A | C | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.909+435A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37844988 | |||||||
| chr4:37845016 | T | C | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.909+463T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37845016 | |||||||
| chr4:37845022 | T | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(181): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.909+469T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37845022 | |||||||
| chr4:37845130 | G | A | 1 | a0001c0001t0001g0352 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.910-503G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37845130 | |||||||
| chr4:37845218 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.910-415G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37845218 | |||||||
| chr4:37845318 | A | C | 25 | a0001c0001t0001g0030 a0001c0001t0001g0292 a0001c0001t0001g0294 others(22): Show |
29 | HG00408.hp1 HG00438.hp2 HG03654.hp1 others(26): Show |
intron_variant | MODIFIER | c.910-315A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37845318 | |||||||
| chr4:37845589 | C | G | 1 | a0001c0002t0002g0078 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.910-44C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 7/13 | chr4 | 37845589 | |||||||
| chr4:37845849 | G | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1007+119G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37845849 | |||||||
| chr4:37845909 | TG | T | 54 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(51): Show |
57 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1007+185delG | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 37845909 | ||||||
| chr4:37845923 | G | A | 4 | a0001c0001t0001g0317 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | NA18950.hp1 NA18956.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007+193G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37845923 | |||||||
| chr4:37846040 | A | T | 1 | a0001c0004t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1007+310A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846040 | |||||||
| chr4:37846076 | T | C | 2 | a0001c0002t0002g0250 a0001c0004t0007g0260 |
2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1007+346T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846076 | |||||||
| chr4:37846206 | T | C | 50 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(47): Show |
53 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1007+476T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846206 | |||||||
| chr4:37846214 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1007+484G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846214 | |||||||
| chr4:37846321 | GA | G | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1007+594delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | 37846321 | ||||||
| chr4:37846399 | C | T | 2 | a0001c0001t0007g0043 a0001c0001t0007g0201 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1008-532C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846399 | |||||||
| chr4:37846464 | T | G | 103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(100): Show |
125 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1008-467T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846464 | |||||||
| chr4:37846677 | C | T | 47 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0292 others(44): Show |
52 | HG00408.hp1 HG00438.hp2 HG02027.hp1 others(49): Show |
intron_variant | MODIFIER | c.1008-254C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846677 | |||||||
| chr4:37846834 | T | G | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1008-97T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846834 | |||||||
| chr4:37846846 | T | C | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1008-85T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846846 | |||||||
| chr4:37846909 | T | G | 79 | a0001c0001t0005g0280 a0001c0002t0001g0092 a0001c0002t0001g0251 others(76): Show |
82 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.1008-22T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846909 | |||||||
| chr4:37846914 | T | G | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1008-17T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 8/13 | chr4 | 37846914 | |||||||
| chr4:37847328 | C | T | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1282+33C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847328 | |||||||
| chr4:37847383 | C | T | 54 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(51): Show |
57 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1282+88C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847383 | |||||||
| chr4:37847392 | T | G | 1 | a0001c0001t0001g0145 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1282+97T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847392 | |||||||
| chr4:37847424 | C | G | 1 | a0001c0001t0001g0309 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1282+129C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847424 | |||||||
| chr4:37847488 | T | C | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1282+193T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847488 | |||||||
| chr4:37847548 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1282+253G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847548 | |||||||
| chr4:37847675 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(182): Show |
211 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.1282+380G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847675 | |||||||
| chr4:37847731 | TACTC | T | 4 | a0002c0003t0003g0035 a0002c0003t0008g0038 a0002c0012t0002g0299 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282+439_1282+442d others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 37847731 | ||||||
| chr4:37847761 | C | A | 1 | a0002c0003t0003g0232 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1282+466C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847761 | |||||||
| chr4:37847889 | T | C | 4 | a0001c0002t0002g0080 a0001c0002t0002g0081 a0001c0002t0002g0109 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282+594T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37847889 | |||||||
| chr4:37848034 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1283-488G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37848034 | |||||||
| chr4:37848034 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1283-488G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37848034 | |||||||
| chr4:37848045 | A | G | 2 | a0001c0002t0002g0087 a0001c0002t0002g0088 |
2 | NA18945.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1283-477A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37848045 | |||||||
| chr4:37848249 | G | C | 1 | a0001c0001t0006g0167 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1283-273G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37848249 | |||||||
| chr4:37848268 | G | A | 1 | a0002c0006t0003g0378 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1283-254G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37848268 | |||||||
| chr4:37848402 | A | G | 1 | a0002c0006t0003g0378 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1283-120A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37848402 | |||||||
| chr4:37848421 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1283-101G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 10/13 | chr4 | 37848421 | |||||||
| chr4:37848691 | TG | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(99): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1412+41delG | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37848691 | |||||||
| chr4:37848780 | T | C | 82 | a0001c0002t0001g0092 a0001c0002t0001g0251 a0001c0002t0002g0039 others(79): Show |
86 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.1412+129T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37848780 | |||||||
| chr4:37848846 | G | A | 1 | a0002c0003t0003g0035 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1412+195G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37848846 | |||||||
| chr4:37849070 | C | CA | 15 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0001c0001t0001g0184 others(12): Show |
15 | HG01255.hp2 HG01261.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1412+437dupA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849070 | ||||||
| chr4:37849070 | C | CAAAAAAA others(294): Show |
2 | a0002c0012t0002g0299 a0002c0012t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1412+433_1412+434i others(303): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849070 | ||||||
| chr4:37849070 | CA | C | 14 | a0001c0001t0001g0007 a0001c0001t0001g0058 a0001c0001t0001g0119 others(11): Show |
16 | HG00558.hp1 HG01884.hp1 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.1412+437delA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849070 | ||||||
| chr4:37849070 | CAA | C | 53 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(50): Show |
56 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1412+436_1412+437d others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849070 | ||||||
| chr4:37849088 | A | T | 2 | a0001c0002t0003g0114 a0001c0002t0003g0116 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1412+437A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849088 | |||||||
| chr4:37849091 | T | A | 1 | a0010c0017t0005g0272 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1412+440T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849091 | |||||||
| chr4:37849133 | A | G | 1 | a0002c0006t0003g0378 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1412+482A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849133 | |||||||
| chr4:37849154 | G | A | 7 | a0001c0002t0002g0250 a0001c0004t0007g0260 a0002c0003t0003g0035 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1412+503G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849154 | |||||||
| chr4:37849210 | G | A | 294 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(291): Show |
328 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.1412+559G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849210 | |||||||
| chr4:37849264 | C | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(240): Show |
272 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1412+613C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849264 | |||||||
| chr4:37849309 | A | G | 2 | a0002c0003t0003g0035 a0002c0003t0008g0038 |
2 | HG02559.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1412+658A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849309 | |||||||
| chr4:37849324 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1412+673G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849324 | |||||||
| chr4:37849404 | C | CT | 22 | a0001c0001t0001g0120 a0001c0001t0001g0301 a0001c0001t0001g0311 others(19): Show |
22 | HG00544.hp2 HG01255.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1413-754dupT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849404 | ||||||
| chr4:37849404 | CT | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(175): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1413-754delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849404 | ||||||
| chr4:37849404 | CTT | C | 11 | a0001c0001t0001g0131 a0001c0001t0001g0143 a0001c0001t0001g0176 others(8): Show |
11 | HG00558.hp1 HG01069.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1413-755_1413-754d others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849404 | ||||||
| chr4:37849404 | CTTTTT | C | 55 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(52): Show |
58 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1413-758_1413-754d others(7): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr4 | 37849404 | ||||||
| chr4:37849405 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1412+754T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849405 | |||||||
| chr4:37849468 | G | A | 1 | a0001c0002t0010g0115 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1413-716G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849468 | |||||||
| chr4:37849504 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1413-680T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849504 | |||||||
| chr4:37849624 | G | T | 2 | a0001c0001t0001g0307 a0001c0001t0001g0375 |
2 | NA18995.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1413-560G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849624 | |||||||
| chr4:37849632 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1413-552C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849632 | |||||||
| chr4:37849687 | G | A | 54 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(51): Show |
57 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1413-497G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849687 | |||||||
| chr4:37849689 | G | A | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1413-495G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849689 | |||||||
| chr4:37849710 | A | G | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1413-474A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849710 | |||||||
| chr4:37849769 | C | T | 47 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0292 others(44): Show |
52 | HG00408.hp1 HG00438.hp2 HG02027.hp1 others(49): Show |
intron_variant | MODIFIER | c.1413-415C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849769 | |||||||
| chr4:37849785 | T | C | 1 | a0001c0001t0001g0385 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1413-399T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849785 | |||||||
| chr4:37849823 | G | A | 62 | a0001c0004t0001g0026 a0001c0004t0001g0261 a0001c0004t0001g0262 others(59): Show |
66 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1413-361G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849823 | |||||||
| chr4:37849843 | A | G | 2 | a0001c0002t0002g0250 a0001c0004t0007g0260 |
2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1413-341A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849843 | |||||||
| chr4:37849948 | C | T | 1 | a0001c0004t0007g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1413-236C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849948 | |||||||
| chr4:37849949 | G | A | 1 | a0001c0001t0001g0356 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1413-235G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849949 | |||||||
| chr4:37849971 | A | G | 1 | a0001c0001t0001g0360 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1413-213A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37849971 | |||||||
| chr4:37850003 | G | C | 1 | a0009c0014t0001g0166 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1413-181G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37850003 | |||||||
| chr4:37850010 | A | G | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1413-174A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 11/13 | chr4 | 37850010 | |||||||
| chr4:37850522 | C | T | 47 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0292 others(44): Show |
52 | HG00408.hp1 HG00438.hp2 HG02027.hp1 others(49): Show |
intron_variant | MODIFIER | c.1602+149C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850522 | |||||||
| chr4:37850523 | G | A | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1602+150G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850523 | |||||||
| chr4:37850618 | C | T | 1 | a0001c0001t0006g0133 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1602+245C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850618 | |||||||
| chr4:37850680 | G | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(240): Show |
272 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1602+307G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850680 | |||||||
| chr4:37850701 | C | T | 58 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(55): Show |
61 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1602+328C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850701 | |||||||
| chr4:37850705 | A | G | 55 | a0001c0001t0001g0296 a0002c0003t0001g0024 a0002c0003t0001g0037 others(52): Show |
58 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1602+332A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850705 | |||||||
| chr4:37850868 | A | G | 3 | a0001c0001t0001g0351 a0001c0001t0001g0382 a0002c0006t0003g0378 |
3 | HG01109.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1602+495A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850868 | |||||||
| chr4:37850886 | G | A | 1 | a0001c0004t0001g0257 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1602+513G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850886 | |||||||
| chr4:37850889 | C | G | 294 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(291): Show |
328 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.1602+516C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850889 | |||||||
| chr4:37850916 | A | G | 244 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(241): Show |
273 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.1602+543A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850916 | |||||||
| chr4:37850943 | A | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(99): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1602+570A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37850943 | |||||||
| chr4:37850990 | C | CA | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1602+636dupA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37850990 | ||||||
| chr4:37850990 | C | CAA | 82 | a0001c0001t0001g0121 a0001c0001t0001g0320 a0001c0001t0005g0282 others(79): Show |
86 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.1602+635_1602+636d others(4): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37850990 | ||||||
| chr4:37850990 | C | CAAA | 53 | a0001c0002t0002g0090 a0002c0003t0001g0024 a0002c0003t0001g0037 others(50): Show |
56 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1602+634_1602+636d others(5): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37850990 | ||||||
| chr4:37851135 | T | C | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1602+762T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851135 | |||||||
| chr4:37851470 | G | T | 2 | a0001c0002t0002g0250 a0001c0004t0007g0260 |
2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1602+1097G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851470 | |||||||
| chr4:37851487 | T | TCA | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1114_1602+111 others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851487 | |||||||
| chr4:37851488 | T | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1115T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851488 | |||||||
| chr4:37851537 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1602+1164G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851537 | |||||||
| chr4:37851551 | T | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1178T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851551 | |||||||
| chr4:37851622 | C | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1249C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851622 | |||||||
| chr4:37851647 | T | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1274T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851647 | |||||||
| chr4:37851664 | G | A | 1 | a0002c0003t0001g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1602+1291G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851664 | |||||||
| chr4:37851665 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1292T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851665 | |||||||
| chr4:37851754 | T | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1381T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851754 | |||||||
| chr4:37851771 | C | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1398C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851771 | |||||||
| chr4:37851786 | A | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1413A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851786 | |||||||
| chr4:37851936 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1563A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851936 | |||||||
| chr4:37851961 | G | GTTTTCTT others(4): Show |
3 | a0001c0001t0001g0123 a0001c0001t0001g0176 a0001c0001t0001g0198 |
3 | HG01069.hp2 HG01515.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1602+1591_1602+159 others(15): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37851961 | ||||||
| chr4:37851961 | G | GTTTTCTT others(5): Show |
96 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(93): Show |
118 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1602+1591_1602+159 others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37851961 | ||||||
| chr4:37851961 | G | GTTTTCTT others(6): Show |
7 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0159 others(4): Show |
7 | HG01074.hp2 HG02896.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602+1591_1602+159 others(17): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37851961 | ||||||
| chr4:37851965 | G | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(103): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1602+1592G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851965 | |||||||
| chr4:37851970 | C | CTTTCTTT others(5): Show |
6 | a0002c0003t0003g0222 a0002c0003t0003g0223 a0002c0003t0006g0213 others(3): Show |
6 | HG02015.hp2 HG02257.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+1600_1602+160 others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37851970 | ||||||
| chr4:37851970 | C | CTTTCTTT others(5): Show |
45 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(42): Show |
48 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1602+1600_1602+160 others(16): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37851970 | ||||||
| chr4:37851970 | C | CTTTCTTT others(6): Show |
3 | a0002c0008t0001g0240 a0002c0008t0001g0241 a0002c0008t0001g0245 |
3 | HG02132.hp2 NA18951.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1602+1600_1602+160 others(17): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37851970 | ||||||
| chr4:37851970 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(103): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1602+1597C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37851970 | |||||||
| chr4:37852040 | G | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1667G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852040 | |||||||
| chr4:37852043 | C | A | 5 | a0002c0003t0001g0218 a0002c0003t0001g0219 a0002c0003t0001g0233 others(2): Show |
5 | HG01106.hp2 HG01192.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602+1670C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852043 | |||||||
| chr4:37852052 | T | C | 2 | a0002c0012t0002g0299 a0002c0012t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1602+1679T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852052 | |||||||
| chr4:37852066 | T | C | 294 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(291): Show |
328 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.1602+1693T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852066 | |||||||
| chr4:37852075 | T | C | 5 | a0001c0002t0002g0064 a0001c0002t0002g0067 a0001c0002t0002g0079 others(2): Show |
5 | HG01884.hp1 HG03098.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602+1702T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852075 | |||||||
| chr4:37852133 | C | CT | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(112): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1602+1786dupT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37852133 | ||||||
| chr4:37852133 | C | CTT | 22 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0123 others(19): Show |
22 | HG00621.hp2 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1602+1785_1602+178 others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37852133 | ||||||
| chr4:37852133 | CT | C | 79 | a0001c0001t0001g0030 a0001c0001t0001g0160 a0001c0001t0001g0292 others(76): Show |
88 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1602+1786delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37852133 | ||||||
| chr4:37852133 | CTTTTTTT others(1): Show |
C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0329 a0001c0001t0001g0341 |
7 | HG02132.hp1 NA18947.hp1 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.1602+1779_1602+178 others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37852133 | ||||||
| chr4:37852163 | G | A | 3 | a0001c0001t0001g0306 a0001c0001t0001g0340 a0001c0001t0001g0343 |
3 | HG00544.hp2 NA18612.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1602+1790G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852163 | |||||||
| chr4:37852168 | G | A | 1 | a0001c0004t0007g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1602+1795G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852168 | |||||||
| chr4:37852180 | A | G | 1 | a0001c0001t0001g0018 | 2 | HG00558.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1602+1807A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852180 | |||||||
| chr4:37852227 | A | G | 1 | a0001c0002t0010g0115 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1602+1854A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852227 | |||||||
| chr4:37852261 | T | A | 12 | a0001c0002t0002g0256 a0001c0002t0003g0259 a0001c0004t0001g0005 others(9): Show |
14 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1602+1888T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852261 | |||||||
| chr4:37852301 | T | C | 2 | a0001c0001t0007g0043 a0001c0001t0007g0201 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1602+1928T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852301 | |||||||
| chr4:37852318 | T | TA | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+1945_1602+194 others(5): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852318 | |||||||
| chr4:37852329 | G | T | 2 | a0001c0002t0002g0250 a0001c0004t0007g0260 |
2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1602+1956G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852329 | |||||||
| chr4:37852397 | T | TGGTTCCT others(28): Show |
160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+2028_1602+202 others(39): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37852397 | ||||||
| chr4:37852512 | T | A | 1 | a0002c0008t0001g0245 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1602+2139T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852512 | |||||||
| chr4:37852561 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+2188A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852561 | |||||||
| chr4:37852599 | A | T | 1 | a0001c0001t0001g0186 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1602+2226A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852599 | |||||||
| chr4:37852631 | G | A | 1 | a0001c0002t0002g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1602+2258G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852631 | |||||||
| chr4:37852686 | T | C | 1 | a0001c0004t0001g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1602+2313T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852686 | |||||||
| chr4:37852706 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+2333T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852706 | |||||||
| chr4:37852969 | C | A | 1 | a0001c0002t0003g0113 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1602+2596C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852969 | |||||||
| chr4:37852986 | C | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1602+2613C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37852986 | |||||||
| chr4:37853072 | C | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1603-2536C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853072 | |||||||
| chr4:37853135 | T | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1603-2473T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853135 | |||||||
| chr4:37853167 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1603-2441T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853167 | |||||||
| chr4:37853206 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1603-2402T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853206 | |||||||
| chr4:37853228 | C | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1603-2380C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853228 | |||||||
| chr4:37853290 | G | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1603-2318G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853290 | |||||||
| chr4:37853299 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1603-2309A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853299 | |||||||
| chr4:37853340 | G | A | 1 | a0005c0015t0001g0383 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1603-2268G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853340 | |||||||
| chr4:37853359 | CT | C | 78 | a0001c0001t0001g0031 a0001c0001t0001g0306 a0001c0001t0001g0323 others(75): Show |
82 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.1603-2226delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37853359 | ||||||
| chr4:37853359 | CTT | C | 17 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(14): Show |
18 | HG02165.hp2 HG02280.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1603-2227_1603-222 others(6): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37853359 | ||||||
| chr4:37853359 | CTTT | C | 45 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0292 others(42): Show |
50 | HG00408.hp1 HG00438.hp2 HG02027.hp1 others(47): Show |
intron_variant | MODIFIER | c.1603-2228_1603-222 others(7): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37853359 | ||||||
| chr4:37853359 | CTTTTTTT | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(148): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1603-2232_1603-222 others(11): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37853359 | ||||||
| chr4:37853359 | CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0001g0130 a0001c0001t0001g0198 a0001c0002t0010g0115 others(6): Show |
9 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1603-2233_1603-222 others(12): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37853359 | ||||||
| chr4:37853386 | G | A | 54 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(51): Show |
57 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1603-2222G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853386 | |||||||
| chr4:37853422 | T | C | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | HG02165.hp2 NA18988.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1603-2186T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853422 | |||||||
| chr4:37853445 | A | G | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1603-2163A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853445 | |||||||
| chr4:37853699 | C | T | 2 | a0002c0003t0003g0222 a0002c0003t0003g0223 |
2 | HG02015.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1603-1909C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853699 | |||||||
| chr4:37853718 | G | C | 46 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(43): Show |
49 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1603-1890G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853718 | |||||||
| chr4:37853739 | T | C | 1 | a0002c0003t0001g0220 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1603-1869T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853739 | |||||||
| chr4:37853929 | T | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1603-1679T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853929 | |||||||
| chr4:37853980 | C | T | 12 | a0001c0002t0002g0256 a0001c0002t0003g0259 a0001c0004t0001g0005 others(9): Show |
14 | HG02109.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1603-1628C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37853980 | |||||||
| chr4:37854152 | G | A | 1 | a0001c0001t0001g0381 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1603-1456G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854152 | |||||||
| chr4:37854370 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1603-1238A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854370 | |||||||
| chr4:37854393 | C | G | 78 | a0001c0002t0001g0092 a0001c0002t0001g0251 a0001c0002t0002g0039 others(75): Show |
81 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.1603-1215C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854393 | |||||||
| chr4:37854647 | C | T | 54 | a0002c0003t0001g0024 a0002c0003t0001g0037 a0002c0003t0001g0204 others(51): Show |
57 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1603-961C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854647 | |||||||
| chr4:37854649 | C | T | 4 | a0001c0001t0001g0313 a0001c0001t0001g0333 a0001c0001t0001g0334 others(1): Show |
4 | HG03491.hp2 HG03492.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603-959C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854649 | |||||||
| chr4:37854671 | T | TA | 7 | a0001c0001t0001g0187 a0001c0004t0001g0026 a0001c0004t0001g0261 others(4): Show |
8 | HG02280.hp2 HG03098.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.1603-925dupA | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr4 | 37854671 | ||||||
| chr4:37854684 | C | A | 4 | a0001c0002t0002g0059 a0001c0002t0002g0075 a0001c0002t0002g0076 others(1): Show |
4 | HG01069.hp1 HG02735.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1603-924C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854684 | |||||||
| chr4:37854694 | T | G | 1 | a0001c0001t0003g0150 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1603-914T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854694 | |||||||
| chr4:37854742 | A | T | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG02165.hp2 HG02523.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.1603-866A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854742 | |||||||
| chr4:37854927 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(89): Show |
113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1603-681G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37854927 | |||||||
| chr4:37855014 | A | T | 2 | a0001c0002t0002g0087 a0001c0002t0002g0088 |
2 | NA18945.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1603-594A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855014 | |||||||
| chr4:37855075 | A | G | 1 | a0002c0003t0003g0232 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1603-533A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855075 | |||||||
| chr4:37855122 | C | T | 1 | a0001c0001t0001g0010 | 3 | HG01071.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1603-486C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855122 | |||||||
| chr4:37855156 | A | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(267): Show |
302 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.1603-452A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855156 | |||||||
| chr4:37855181 | A | G | 1 | a0001c0004t0001g0386 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1603-427A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855181 | |||||||
| chr4:37855417 | C | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(278): Show |
314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.1603-191C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855417 | |||||||
| chr4:37855440 | G | A | 281 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(278): Show |
314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.1603-168G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855440 | |||||||
| chr4:37855485 | G | A | 281 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(278): Show |
314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.1603-123G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855485 | |||||||
| chr4:37855545 | A | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(278): Show |
314 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.1603-63A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855545 | |||||||
| chr4:37855553 | T | C | 1 | a0005c0015t0001g0383 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1603-55T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 12/13 | chr4 | 37855553 | |||||||
| chr4:37855846 | A | G | 2 | a0002c0012t0002g0299 a0002c0012t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1736+105A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37855846 | |||||||
| chr4:37855894 | T | G | 1 | a0001c0001t0001g0363 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1736+153T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37855894 | |||||||
| chr4:37856025 | GTAGCTAA others(4): Show |
G | 1 | a0001c0001t0001g0058 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1736+285_1736+295d others(13): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856025 | |||||||
| chr4:37856103 | G | A | 4 | a0001c0004t0001g0026 a0001c0004t0001g0261 a0001c0004t0001g0262 others(1): Show |
5 | HG02280.hp2 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1736+362G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856103 | |||||||
| chr4:37856107 | C | T | 2 | a0001c0001t0007g0043 a0001c0001t0007g0201 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1736+366C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856107 | |||||||
| chr4:37856108 | G | A | 5 | a0001c0004t0001g0026 a0001c0004t0001g0261 a0001c0004t0001g0262 others(2): Show |
6 | HG02280.hp2 HG02723.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1736+367G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856108 | |||||||
| chr4:37856160 | C | T | 2 | a0001c0004t0001g0386 a0002c0006t0003g0378 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1736+419C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856160 | |||||||
| chr4:37856181 | T | C | 239 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(236): Show |
272 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1736+440T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856181 | |||||||
| chr4:37856201 | C | T | 30 | a0001c0002t0001g0040 a0001c0002t0001g0251 a0001c0002t0002g0039 others(27): Show |
30 | HG00738.hp1 HG01167.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1736+460C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856201 | |||||||
| chr4:37856202 | G | A | 55 | a0001c0001t0003g0149 a0001c0001t0003g0150 a0001c0001t0003g0325 others(52): Show |
60 | HG00609.hp2 HG00733.hp1 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1736+461G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856202 | |||||||
| chr4:37856204 | T | C | 385 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(382): Show |
440 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(437): Show |
intron_variant | MODIFIER | c.1736+463T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856204 | |||||||
| chr4:37856212 | C | G | 30 | a0001c0002t0001g0040 a0001c0002t0001g0251 a0001c0002t0002g0039 others(27): Show |
30 | HG00738.hp1 HG01167.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1736+471C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856212 | |||||||
| chr4:37856274 | A | G | 1 | a0001c0002t0002g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1736+533A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856274 | |||||||
| chr4:37856316 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(117): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1736+575C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856316 | |||||||
| chr4:37856321 | C | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(112): Show |
136 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1736+580C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856321 | |||||||
| chr4:37856337 | A | G | 2 | a0001c0002t0002g0067 a0001c0002t0002g0079 |
2 | HG01884.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1736+596A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856337 | |||||||
| chr4:37856363 | C | T | 1 | a0002c0003t0001g0231 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1736+622C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856363 | |||||||
| chr4:37856372 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1736+631G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856372 | |||||||
| chr4:37856378 | C | T | 2 | a0001c0001t0001g0351 a0001c0001t0001g0382 |
2 | HG01109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1736+637C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856378 | |||||||
| chr4:37856460 | A | G | 30 | a0001c0002t0001g0040 a0001c0002t0001g0251 a0001c0002t0002g0039 others(27): Show |
30 | HG00738.hp1 HG01167.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1736+719A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856460 | |||||||
| chr4:37856575 | AG | A | 61 | a0001c0001t0003g0149 a0001c0001t0003g0150 a0001c0001t0003g0325 others(58): Show |
67 | HG00099.hp1 HG00609.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1736+835delG | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856575 | |||||||
| chr4:37856636 | G | A | 2 | a0002c0012t0002g0299 a0002c0012t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1736+895G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856636 | |||||||
| chr4:37856649 | G | A | 1 | a0002c0003t0003g0035 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1736+908G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856649 | |||||||
| chr4:37856682 | C | T | 1 | a0002c0007t0002g0214 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1736+941C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856682 | |||||||
| chr4:37856689 | C | G | 30 | a0001c0002t0001g0040 a0001c0002t0001g0251 a0001c0002t0002g0039 others(27): Show |
30 | HG00738.hp1 HG01167.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1736+948C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856689 | |||||||
| chr4:37856699 | C | T | 30 | a0001c0002t0001g0040 a0001c0002t0001g0251 a0001c0002t0002g0039 others(27): Show |
30 | HG00738.hp1 HG01167.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1736+958C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856699 | |||||||
| chr4:37856700 | T | G | 30 | a0001c0002t0001g0040 a0001c0002t0001g0251 a0001c0002t0002g0039 others(27): Show |
30 | HG00738.hp1 HG01167.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1736+959T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856700 | |||||||
| chr4:37856764 | T | C | 154 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0148 others(151): Show |
166 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.1736+1023T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856764 | |||||||
| chr4:37856828 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0152 |
2 | HG01934.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1736+1087G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856828 | |||||||
| chr4:37856956 | C | T | 29 | a0001c0002t0001g0251 a0001c0002t0002g0039 a0001c0002t0002g0062 others(26): Show |
29 | HG00738.hp1 HG01167.hp1 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.1736+1215C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856956 | |||||||
| chr4:37856999 | C | T | 2 | a0001c0001t0007g0043 a0001c0001t0007g0201 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1736+1258C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37856999 | |||||||
| chr4:37857167 | G | C | 148 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0148 others(145): Show |
160 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.1736+1426G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857167 | |||||||
| chr4:37857194 | T | G | 148 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0148 others(145): Show |
160 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.1736+1453T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857194 | |||||||
| chr4:37857250 | G | A | 2 | a0004c0011t0004g0285 a0004c0011t0004g0286 |
2 | HG02735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1736+1509G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857250 | |||||||
| chr4:37857269 | A | G | 151 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0148 others(148): Show |
163 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.1736+1528A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857269 | |||||||
| chr4:37857333 | C | T | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(235): Show |
271 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.1736+1592C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857333 | |||||||
| chr4:37857347 | G | T | 1 | a0010c0017t0005g0272 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1736+1606G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857347 | |||||||
| chr4:37857400 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1736+1659A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857400 | |||||||
| chr4:37857444 | A | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(111): Show |
135 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1736+1703A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857444 | |||||||
| chr4:37857573 | T | C | 51 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0148 others(48): Show |
56 | HG00408.hp1 HG00438.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1736+1832T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857573 | |||||||
| chr4:37857583 | C | T | 1 | a0002c0008t0001g0245 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1736+1842C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857583 | |||||||
| chr4:37857620 | C | T | 1 | a0001c0001t0001g0381 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1736+1879C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857620 | |||||||
| chr4:37857927 | T | C | 2 | a0001c0002t0002g0078 a0001c0002t0002g0102 |
2 | HG00733.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1736+2186T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37857927 | |||||||
| chr4:37858054 | C | T | 148 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0148 others(145): Show |
160 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.1736+2313C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858054 | |||||||
| chr4:37858110 | G | A | 2 | a0001c0004t0001g0253 a0002c0003t0008g0038 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1736+2369G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858110 | |||||||
| chr4:37858223 | G | T | 2 | a0002c0007t0002g0212 a0002c0007t0002g0214 |
2 | HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1736+2482G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858223 | |||||||
| chr4:37858280 | C | G | 185 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0148 others(182): Show |
197 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.1736+2539C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858280 | |||||||
| chr4:37858294 | C | T | 66 | a0001c0002t0001g0251 a0001c0002t0002g0039 a0001c0002t0002g0042 others(63): Show |
66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1736+2553C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858294 | |||||||
| chr4:37858304 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1736+2563C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858304 | |||||||
| chr4:37858325 | A | C | 1 | a0001c0001t0001g0318 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1736+2584A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858325 | |||||||
| chr4:37858330 | T | C | 1 | a0001c0004t0001g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1736+2589T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858330 | |||||||
| chr4:37858344 | T | TG | 66 | a0001c0002t0001g0251 a0001c0002t0002g0039 a0001c0002t0002g0042 others(63): Show |
66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1736+2603_1736+260 others(5): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858344 | |||||||
| chr4:37858347 | G | T | 66 | a0001c0002t0001g0251 a0001c0002t0002g0039 a0001c0002t0002g0042 others(63): Show |
66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1736+2606G>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858347 | |||||||
| chr4:37858349 | T | G | 66 | a0001c0002t0001g0251 a0001c0002t0002g0039 a0001c0002t0002g0042 others(63): Show |
66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1736+2608T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858349 | |||||||
| chr4:37858424 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0384 |
4 | HG02630.hp2 HG02809.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1736+2683C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858424 | |||||||
| chr4:37858429 | T | A | 1 | a0001c0002t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1736+2688T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858429 | |||||||
| chr4:37858470 | G | A | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(273): Show |
309 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.1736+2729G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858470 | |||||||
| chr4:37858495 | C | G | 119 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0148 others(116): Show |
131 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1736+2754C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858495 | |||||||
| chr4:37858513 | G | GT | 187 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0030 others(184): Show |
200 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1736+2788dupT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 37858513 | ||||||
| chr4:37858659 | G | C | 2 | a0002c0012t0002g0299 a0002c0012t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1737-2851G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858659 | |||||||
| chr4:37858730 | A | T | 1 | a0005c0015t0001g0383 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1737-2780A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858730 | |||||||
| chr4:37858732 | T | A | 1 | a0005c0015t0001g0383 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1737-2778T>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858732 | |||||||
| chr4:37858744 | T | C | 5 | a0001c0004t0001g0026 a0001c0004t0001g0261 a0001c0004t0001g0262 others(2): Show |
6 | HG02280.hp2 HG02723.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737-2766T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858744 | |||||||
| chr4:37858805 | T | C | 119 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0148 others(116): Show |
131 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1737-2705T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858805 | |||||||
| chr4:37858860 | A | T | 1 | a0002c0003t0001g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1737-2650A>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858860 | |||||||
| chr4:37858972 | C | A | 66 | a0001c0002t0001g0251 a0001c0002t0002g0039 a0001c0002t0002g0042 others(63): Show |
66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-2538C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37858972 | |||||||
| chr4:37859207 | C | A | 2 | a0002c0012t0002g0299 a0002c0012t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1737-2303C>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859207 | |||||||
| chr4:37859282 | A | G | 2 | a0001c0004t0001g0253 a0002c0003t0008g0038 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1737-2228A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859282 | |||||||
| chr4:37859346 | C | T | 66 | a0001c0002t0001g0251 a0001c0002t0002g0039 a0001c0002t0002g0042 others(63): Show |
66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-2164C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859346 | |||||||
| chr4:37859575 | T | C | 2 | a0002c0012t0002g0299 a0002c0012t0002g0300 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1737-1935T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859575 | |||||||
| chr4:37859604 | AT | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0179 |
4 | HG00280.hp2 HG01993.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737-1905delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859604 | |||||||
| chr4:37859616 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(275): Show |
311 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.1737-1894G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859616 | |||||||
| chr4:37859720 | TC | T | 66 | a0001c0002t0001g0251 a0001c0002t0002g0039 a0001c0002t0002g0042 others(63): Show |
66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-1786delC | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 37859720 | ||||||
| chr4:37859722 | C | G | 5 | a0001c0004t0001g0026 a0001c0004t0001g0261 a0001c0004t0001g0262 others(2): Show |
6 | HG02280.hp2 HG02723.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737-1788C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859722 | |||||||
| chr4:37859772 | A | G | 66 | a0001c0002t0001g0251 a0001c0002t0002g0039 a0001c0002t0002g0042 others(63): Show |
66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-1738A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859772 | |||||||
| chr4:37859826 | C | G | 66 | a0001c0002t0001g0251 a0001c0002t0002g0039 a0001c0002t0002g0042 others(63): Show |
66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-1684C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859826 | |||||||
| chr4:37859901 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1737-1609T>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37859901 | |||||||
| chr4:37860005 | A | C | 2 | a0002c0003t0001g0218 a0002c0003t0001g0219 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1737-1505A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860005 | |||||||
| chr4:37860030 | C | G | 66 | a0001c0002t0001g0251 a0001c0002t0002g0039 a0001c0002t0002g0042 others(63): Show |
66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-1480C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860030 | |||||||
| chr4:37860072 | A | G | 2 | a0002c0003t0001g0218 a0002c0003t0001g0219 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1737-1438A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860072 | |||||||
| chr4:37860093 | G | C | 66 | a0001c0002t0001g0251 a0001c0002t0002g0039 a0001c0002t0002g0042 others(63): Show |
66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-1417G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860093 | |||||||
| chr4:37860097 | CGTAATGT others(29): Show |
C | 1 | a0001c0002t0010g0115 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1737-1412_1737-137 others(40): Show |
PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860097 | |||||||
| chr4:37860098 | G | A | 65 | a0001c0002t0001g0251 a0001c0002t0002g0039 a0001c0002t0002g0042 others(62): Show |
65 | HG00597.hp1 HG00733.hp2 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.1737-1412G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860098 | |||||||
| chr4:37860142 | A | G | 10 | a0001c0001t0001g0008 a0001c0001t0001g0125 a0001c0001t0001g0126 others(7): Show |
12 | NA18939.hp1 NA18947.hp2 NA18956.hp2 others(9): Show |
intron_variant | MODIFIER | c.1737-1368A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860142 | |||||||
| chr4:37860267 | C | G | 66 | a0001c0002t0001g0251 a0001c0002t0002g0039 a0001c0002t0002g0042 others(63): Show |
66 | HG00597.hp1 HG00733.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1737-1243C>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860267 | |||||||
| chr4:37860450 | A | G | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(152): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1737-1060A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860450 | |||||||
| chr4:37860563 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1737-947C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860563 | |||||||
| chr4:37860680 | A | G | 63 | a0001c0001t0003g0149 a0001c0001t0003g0150 a0001c0001t0003g0325 others(60): Show |
68 | HG00099.hp1 HG00609.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.1737-830A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860680 | |||||||
| chr4:37860870 | G | C | 1 | a0001c0004t0001g0091 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1737-640G>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860870 | |||||||
| chr4:37860901 | C | T | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(273): Show |
309 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.1737-609C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37860901 | |||||||
| chr4:37861001 | T | G | 5 | a0001c0001t0007g0043 a0001c0001t0007g0201 a0001c0004t0001g0386 others(2): Show |
5 | HG02559.hp1 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737-509T>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37861001 | |||||||
| chr4:37861068 | A | G | 54 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0148 others(51): Show |
59 | HG00408.hp1 HG00438.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1737-442A>G | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37861068 | |||||||
| chr4:37861230 | G | A | 1 | a0001c0002t0002g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1737-280G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37861230 | |||||||
| chr4:37861267 | C | T | 2 | a0002c0003t0003g0209 a0002c0003t0003g0210 |
2 | HG02040.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1737-243C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37861267 | |||||||
| chr4:37861392 | C | T | 66 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
77 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1737-118C>T | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37861392 | |||||||
| chr4:37861424 | AT | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(121): Show |
146 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1737-84delT | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 37861424 | ||||||
| chr4:37861459 | G | A | 23 | a0001c0001t0001g0030 a0001c0001t0001g0148 a0001c0001t0001g0292 others(20): Show |
27 | HG00408.hp1 HG00438.hp2 NA18942.hp2 others(24): Show |
intron_variant | MODIFIER | c.1737-51G>A | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37861459 | |||||||
| chr4:37861468 | A | C | 1 | a0001c0001t0001g0319 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1737-42A>C | PGM2 | ENSG00000169299.14 | transcript | ENST00000381967.9 | protein_coding | 13/13 | chr4 | 37861468 |