Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 669 |
| ensemblid | ENSG00000172331.12 |
| hgncid | 1093 |
| symbol | BPGM |
| name | bisphosphoglycerate mutase |
| refseq_nuc | NM_001724.5 |
| refseq_prot | NP_001715.1 |
| ensembl_nuc | ENST00000344924.8 |
| ensembl_prot | ENSP00000342032.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 134646853 |
| end | 134679816 |
| strand | + |
| ver | v1.2 |
| region | chr7:134646853-134679816 |
| region5000 | chr7:134641853-134684816 |
| regionname0 | BPGM_chr7_134646853_134679816 |
| regionname5000 | BPGM_chr7_134641853_134684816 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 259 | 359 | 81 | 68 | 155 | 16 | 37 | 125 | BPGM_chr7_134641853_134684816 | BPGM | MSKYK others(254): Show |
chr7 | 134641853 | 134684816 |
| a0002 | 0/0 | 259 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | MSKYK others(254): Show |
chr7 | 134641853 | 134684816 |
| a0003 | 0/0 | 259 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | MSKYK others(254): Show |
chr7 | 134641853 | 134684816 |
| a0004 | 0/0 | 259 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | MSKYK others(254): Show |
chr7 | 134641853 | 134684816 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 777 | 357 | 81 | 68 | 153 | 16 | 37 | BPGM_chr7_134641853_134684816 | BPGM | ATGTC others(772): Show |
chr7 | 134641853 | 134684816 | ||
| a0001c0002 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | ATGTC others(772): Show |
chr7 | 134641853 | 134684816 | ||
| a0001c0005 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | ATGTC others(772): Show |
chr7 | 134641853 | 134684816 | ||
| a0002c0003 | 0/0 | 777 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | ATGTC others(772): Show |
chr7 | 134641853 | 134684816 | ||
| a0003c0004 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | ATGTC others(772): Show |
chr7 | 134641853 | 134684816 | ||
| a0004c0006 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | ATGTC others(772): Show |
chr7 | 134641853 | 134684816 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1711 | 325 | 65 | 65 | 150 | 16 | 27 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1706): Show |
chr7 | 134641853 | 134684816 |
| a0001c0001t0002 | 0/0 | 1714 | 11 | 5 | 2 | 0 | 0 | 4 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1709): Show |
chr7 | 134641853 | 134684816 |
| a0001c0001t0003 | 0/0 | 1714 | 4 | 2 | 0 | 1 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1709): Show |
chr7 | 134641853 | 134684816 |
| a0001c0001t0004 | 0/0 | 1711 | 4 | 4 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1706): Show |
chr7 | 134641853 | 134684816 |
| a0001c0001t0005 | 0/0 | 1711 | 3 | 0 | 0 | 0 | 0 | 3 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1706): Show |
chr7 | 134641853 | 134684816 |
| a0001c0001t0006 | 0/0 | 1708 | 3 | 2 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1703): Show |
chr7 | 134641853 | 134684816 |
| a0001c0001t0007 | 0/0 | 1711 | 2 | 0 | 0 | 0 | 0 | 2 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1706): Show |
chr7 | 134641853 | 134684816 |
| a0001c0001t0008 | 0/0 | 1729 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1724): Show |
chr7 | 134641853 | 134684816 |
| a0001c0001t0009 | 0/0 | 1711 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1706): Show |
chr7 | 134641853 | 134684816 |
| a0001c0001t0010 | 0/0 | 1711 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1706): Show |
chr7 | 134641853 | 134684816 |
| a0001c0001t0011 | 0/0 | 1711 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1706): Show |
chr7 | 134641853 | 134684816 |
| a0001c0001t0012 | 0/0 | 1711 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1706): Show |
chr7 | 134641853 | 134684816 |
| a0001c0002t0001 | 0/0 | 1711 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1706): Show |
chr7 | 134641853 | 134684816 |
| a0001c0005t0001 | 0/0 | 1711 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1706): Show |
chr7 | 134641853 | 134684816 |
| a0002c0003t0001 | 0/0 | 1711 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1706): Show |
chr7 | 134641853 | 134684816 |
| a0003c0004t0013 | 0/0 | 1711 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1706): Show |
chr7 | 134641853 | 134684816 |
| a0004c0006t0001 | 0/0 | 1711 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | GATGA others(1706): Show |
chr7 | 134641853 | 134684816 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 45 | 1 | 7 | 29 | 1 | 7 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0002 | 0/0 | 20 | 0 | 0 | 20 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0003 | 0/0 | 21 | 0 | 8 | 11 | 0 | 2 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0004 | 0/0 | 9 | 1 | 0 | 8 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 2 | 4 | 1 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0006 | 0/0 | 7 | 1 | 3 | 0 | 2 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0008 | 0/0 | 6 | 1 | 0 | 4 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0011 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0012 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0013 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0017 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0042 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0002g0007 | 0/0 | 4 | 1 | 0 | 0 | 0 | 3 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0005g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0007g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0009g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0010g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0011g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0001t0012g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0001c0005t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0003c0004t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| a0004c0006t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | FIN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | FIN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00639 | hp1 | a0001 | c0001 | t0012 | g0084 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0040 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0098 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0097 | AFR | ESN | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03239 | hp1 | a0002 | c0003 | t0001 | g0149 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03490 | hp1 | a0001 | c0001 | t0007 | g0001 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0001 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0144 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0093 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0040 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | STU | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0085 | AFR | YRI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | YRI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18960 | hp1 | a0003 | c0004 | t0013 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19009 | hp1 | a0001 | c0005 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19009 | hp2 | a0001 | c0001 | t0009 | g0023 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | LWK | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19030 | hp2 | a0001 | c0001 | t0010 | g0054 | AFR | LWK | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19043 | hp2 | a0004 | c0006 | t0001 | g0137 | AFR | LWK | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19070 | hp2 | a0001 | c0001 | t0006 | g0136 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0055 | AFR | YRI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | YRI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ASW | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | TSI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | GIH | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | USA | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | USA | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0051 | REF | REF | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0042 | REF | REF | BPGM_chr7_134641853_134684816 | BPGM | chr7 | 134641853 | 134684816 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:134661925 | C | T | 1 | a0004 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.418C>T | p.Arg140Trp | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/3 | 564/1711 | 418/780 | 140/259 | chr7 | 134661925 | |||
| chr7:134678885 | C | G | 1 | a0003 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.634C>G | p.Leu212Val | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 780/1711 | 634/780 | 212/259 | chr7 | 134678885 | |||
| chr7:134678930 | C | T | 1 | a0002 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.679C>T | p.Arg227Cys | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 825/1711 | 679/780 | 227/259 | chr7 | 134678930 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:134661942 | C | T | 1 | a0001c0005 | 1 | NA19009.hp1 | synonymous_variant | LOW | c.435C>T | p.Cys145Cys | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/3 | 581/1711 | 435/780 | 145/259 | chr7 | 134661942 | |||
| chr7:134678971 | G | A | 1 | a0001c0002 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.720G>A | p.Ala240Ala | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 866/1711 | 720/780 | 240/259 | chr7 | 134678971 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:134646875 | C | G | 1 | a0003c0004t0013 | 1 | NA18960.hp1 | 5_prime_UTR_variant | MODIFIER | c.-124C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/3 | 14633 | chr7 | 134646875 | ||||||
| chr7:134646885 | G | T | 1 | a0001c0001t0007 | 2 | HG03490.hp1 HG03492.hp1 |
5_prime_UTR_variant | MODIFIER | c.-114G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/3 | 14623 | chr7 | 134646885 | ||||||
| chr7:134646886 | C | T | 1 | a0001c0001t0012 | 1 | HG00639.hp1 | 5_prime_UTR_variant | MODIFIER | c.-113C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/3 | 14622 | chr7 | 134646886 | ||||||
| chr7:134646897 | G | GGCT | 2 | a0001c0001t0002 a0001c0001t0003 |
15 | HG01099.hp1 HG01358.hp2 HG02257.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-79_-77dupCTG | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/3 | 14585 | INFO_REALIGN_3_PRIME | chr7 | 134646897 | |||||
| chr7:134646897 | G | GGCTGCTG others(11): Show |
1 | a0001c0001t0008 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-94_-77dupCTGCTGCT others(10): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/3 | 14585 | INFO_REALIGN_3_PRIME | chr7 | 134646897 | |||||
| chr7:134646897 | GGCT | G | 1 | a0001c0001t0006 | 3 | HG02970.hp1 HG03195.hp2 NA19070.hp2 |
5_prime_UTR_variant | MODIFIER | c.-79_-77delCTG | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/3 | 14586 | INFO_REALIGN_3_PRIME | chr7 | 134646897 | |||||
| chr7:134679118 | G | A | 2 | a0001c0001t0002 a0001c0001t0004 |
15 | HG01099.hp1 HG01358.hp2 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*87G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 87 | chr7 | 134679118 | ||||||
| chr7:134679406 | C | T | 2 | a0001c0001t0011 a0001c0001t0012 |
2 | HG00639.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*375C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 375 | chr7 | 134679406 | ||||||
| chr7:134679463 | G | A | 1 | a0001c0001t0009 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*432G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 432 | chr7 | 134679463 | ||||||
| chr7:134679569 | C | A | 2 | a0001c0001t0005 a0001c0001t0010 |
4 | HG02735.hp2 HG04199.hp2 HG04228.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*538C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 538 | chr7 | 134679569 | ||||||
| chr7:134679662 | T | C | 1 | a0001c0001t0010 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*631T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 3/3 | 631 | chr7 | 134679662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:134646971 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-62+34G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134646971 | |||||||
| chr7:134647085 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-62+148C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647085 | |||||||
| chr7:134647342 | A | G | 1 | a0001c0001t0001g0047 | 2 | HG00544.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.-62+405A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647342 | |||||||
| chr7:134647355 | TATCA | T | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-62+419_-62+422del others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647355 | |||||||
| chr7:134647408 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-62+471G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647408 | |||||||
| chr7:134647423 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+486G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647423 | |||||||
| chr7:134647835 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+898C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647835 | |||||||
| chr7:134647888 | A | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-62+951A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647888 | |||||||
| chr7:134647891 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-62+954G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134647891 | |||||||
| chr7:134648003 | G | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0049 a0001c0001t0001g0145 others(1): Show |
6 | HG01071.hp1 HG01943.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-62+1066G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648003 | |||||||
| chr7:134648069 | A | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+1132A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648069 | |||||||
| chr7:134648070 | T | TCC | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+1133_-62+1134i others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648070 | |||||||
| chr7:134648071 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+1134T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648071 | |||||||
| chr7:134648073 | C | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+1136C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648073 | |||||||
| chr7:134648117 | C | CT | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-62+1183dupT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134648117 | ||||||
| chr7:134648121 | C | G | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-62+1184C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648121 | |||||||
| chr7:134648130 | TGG | T | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-62+1194_-62+1195d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648130 | |||||||
| chr7:134648131 | G | GC | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-62+1194_-62+1195i others(3): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648131 | |||||||
| chr7:134648131 | G | GTTT | 23 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0027 others(20): Show |
47 | HG00597.hp1 HG01099.hp1 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.-62+1194_-62+1195i others(5): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648131 | |||||||
| chr7:134648131 | G | GTTTT | 3 | a0001c0001t0001g0092 a0001c0001t0011g0085 a0001c0001t0012g0084 |
3 | HG00639.hp1 NA18522.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.-62+1194_-62+1195i others(6): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648131 | |||||||
| chr7:134648131 | G | GTTTTT | 19 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0026 others(16): Show |
24 | HG00280.hp1 HG00642.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-62+1194_-62+1195i others(7): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648131 | |||||||
| chr7:134648131 | G | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0086 others(1): Show |
6 | NA18960.hp2 NA18967.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.-62+1194G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648131 | |||||||
| chr7:134648132 | G | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(138): Show |
267 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.-62+1195G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648132 | |||||||
| chr7:134648137 | T | G | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-62+1200T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648137 | |||||||
| chr7:134648143 | G | T | 1 | a0001c0001t0001g0143 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-62+1206G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648143 | |||||||
| chr7:134648148 | G | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+1211G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648148 | |||||||
| chr7:134648153 | C | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+1216C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648153 | |||||||
| chr7:134648166 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-62+1229G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648166 | |||||||
| chr7:134648321 | G | T | 1 | a0001c0001t0001g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-62+1384G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648321 | |||||||
| chr7:134648427 | G | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0156 a0001c0001t0001g0157 others(1): Show |
5 | HG02896.hp1 HG02897.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-62+1490G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648427 | |||||||
| chr7:134648438 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-62+1501T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648438 | |||||||
| chr7:134648445 | T | C | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-62+1508T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648445 | |||||||
| chr7:134648687 | A | AT | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(129): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.-62+1760dupT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134648687 | ||||||
| chr7:134648687 | A | ATT | 5 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0048 others(2): Show |
10 | HG02055.hp1 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-62+1759_-62+1760d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134648687 | ||||||
| chr7:134648925 | T | G | 1 | a0001c0001t0010g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-62+1988T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134648925 | |||||||
| chr7:134649134 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-62+2197A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649134 | |||||||
| chr7:134649137 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-62+2200G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649137 | |||||||
| chr7:134649171 | A | AT | 11 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
32 | HG00597.hp1 HG02074.hp2 NA18942.hp2 others(29): Show |
intron_variant | MODIFIER | c.-62+2236dupT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134649171 | ||||||
| chr7:134649173 | TG | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
6 | HG03453.hp2 NA19012.hp2 NA19043.hp1 others(3): Show |
intron_variant | MODIFIER | c.-62+2237delG | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649173 | |||||||
| chr7:134649174 | G | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(130): Show |
259 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-62+2237G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649174 | |||||||
| chr7:134649174 | GT | G | 31 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(28): Show |
58 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.-62+2248delT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134649174 | ||||||
| chr7:134649198 | C | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(9): Show |
33 | HG00597.hp1 HG02074.hp2 NA18942.hp2 others(30): Show |
intron_variant | MODIFIER | c.-62+2261C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649198 | |||||||
| chr7:134649273 | T | C | 1 | a0001c0001t0008g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-62+2336T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649273 | |||||||
| chr7:134649280 | T | G | 1 | a0001c0001t0001g0044 | 2 | HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-62+2343T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649280 | |||||||
| chr7:134649388 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+2451G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649388 | |||||||
| chr7:134649489 | G | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): Show |
36 | HG00597.hp1 HG00639.hp1 HG02074.hp2 others(33): Show |
intron_variant | MODIFIER | c.-62+2552G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649489 | |||||||
| chr7:134649534 | TG | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-62+2599delG | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134649534 | ||||||
| chr7:134649639 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-62+2702A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649639 | |||||||
| chr7:134649692 | A | G | 1 | a0001c0001t0006g0136 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-62+2755A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649692 | |||||||
| chr7:134649886 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-62+2949C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649886 | |||||||
| chr7:134649905 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+2968C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134649905 | |||||||
| chr7:134650002 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+3065A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650002 | |||||||
| chr7:134650010 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+3073G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650010 | |||||||
| chr7:134650060 | G | C | 2 | a0001c0001t0001g0094 a0001c0001t0003g0093 |
2 | HG02738.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-62+3123G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650060 | |||||||
| chr7:134650088 | G | T | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-62+3151G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650088 | |||||||
| chr7:134650170 | C | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+3233C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650170 | |||||||
| chr7:134650237 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+3300C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650237 | |||||||
| chr7:134650355 | G | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(20): Show |
50 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.-62+3418G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650355 | |||||||
| chr7:134650411 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-62+3474G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650411 | |||||||
| chr7:134650421 | G | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
324 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.-62+3484G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650421 | |||||||
| chr7:134650457 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+3520A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650457 | |||||||
| chr7:134650646 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-62+3709A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650646 | |||||||
| chr7:134650786 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+3849G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650786 | |||||||
| chr7:134650794 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-62+3857G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650794 | |||||||
| chr7:134650798 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+3861A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650798 | |||||||
| chr7:134650805 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-62+3868G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650805 | |||||||
| chr7:134650856 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-62+3919C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650856 | |||||||
| chr7:134650869 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+3932G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650869 | |||||||
| chr7:134650903 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-62+3966C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650903 | |||||||
| chr7:134650915 | A | T | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-62+3978A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650915 | |||||||
| chr7:134650945 | T | C | 2 | a0001c0001t0006g0097 a0001c0001t0006g0098 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-62+4008T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650945 | |||||||
| chr7:134650981 | C | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+4044C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134650981 | |||||||
| chr7:134651593 | A | T | 1 | a0001c0001t0011g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-62+4656A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134651593 | |||||||
| chr7:134652015 | T | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0099 |
6 | HG02109.hp2 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-62+5078T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652015 | |||||||
| chr7:134652016 | A | G | 1 | a0001c0001t0002g0082 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-62+5079A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652016 | |||||||
| chr7:134652045 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-62+5108A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652045 | |||||||
| chr7:134652120 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-62+5183C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652120 | |||||||
| chr7:134652225 | G | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0158 others(3): Show |
10 | HG00280.hp2 HG01074.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.-62+5288G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652225 | |||||||
| chr7:134652441 | C | T | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-62+5504C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652441 | |||||||
| chr7:134652457 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0133 |
2 | NA18747.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.-62+5520A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652457 | |||||||
| chr7:134652463 | T | G | 2 | a0001c0001t0006g0097 a0001c0001t0006g0098 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-62+5526T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652463 | |||||||
| chr7:134652625 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0100 a0001c0001t0001g0101 |
7 | HG01069.hp1 HG01074.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.-62+5688G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652625 | |||||||
| chr7:134652670 | T | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(51): Show |
93 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-62+5733T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652670 | |||||||
| chr7:134652706 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-62+5769C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652706 | |||||||
| chr7:134652720 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-62+5783C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652720 | |||||||
| chr7:134652947 | G | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(181): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-62+6010G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652947 | |||||||
| chr7:134652960 | A | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(51): Show |
93 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-62+6023A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652960 | |||||||
| chr7:134652989 | C | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(51): Show |
93 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-62+6052C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134652989 | |||||||
| chr7:134653098 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-62+6161T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134653098 | |||||||
| chr7:134653172 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-62+6235T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134653172 | |||||||
| chr7:134653201 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0155 |
4 | NA18944.hp2 NA18986.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.-62+6264A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134653201 | |||||||
| chr7:134654127 | T | TAC | 40 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0024 others(37): Show |
73 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.-62+7207_-62+7208d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134654127 | ||||||
| chr7:134654146 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-62+7209G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654146 | |||||||
| chr7:134654147 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-62+7210T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654147 | |||||||
| chr7:134654149 | CTGAAGA | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(51): Show |
93 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-62+7219_-62+7224d others(8): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134654149 | ||||||
| chr7:134654150 | T | A | 1 | a0001c0001t0001g0001 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-62+7213T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654150 | |||||||
| chr7:134654150 | T | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
171 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-62+7213T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654150 | |||||||
| chr7:134654151 | G | C | 1 | a0001c0001t0001g0001 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-62+7214G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654151 | |||||||
| chr7:134654151 | G | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
171 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-62+7214G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654151 | |||||||
| chr7:134654152 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-62+7215A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654152 | |||||||
| chr7:134654152 | AAG | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
171 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-62+7217_-62+7218d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134654152 | ||||||
| chr7:134654153 | A | T | 1 | a0001c0001t0001g0001 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-62+7216A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654153 | |||||||
| chr7:134654154 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-62+7217G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654154 | |||||||
| chr7:134654155 | A | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-62+7218A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654155 | |||||||
| chr7:134654319 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-61-7128A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654319 | |||||||
| chr7:134654327 | G | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-61-7120G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654327 | |||||||
| chr7:134654498 | A | G | 1 | a0001c0001t0010g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-61-6949A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654498 | |||||||
| chr7:134654688 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-61-6759G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654688 | |||||||
| chr7:134654890 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-61-6557A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654890 | |||||||
| chr7:134654988 | C | G | 1 | a0001c0001t0006g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-61-6459C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134654988 | |||||||
| chr7:134655238 | T | C | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-61-6209T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655238 | |||||||
| chr7:134655406 | A | C | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61-6041A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655406 | |||||||
| chr7:134655551 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-61-5896T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655551 | |||||||
| chr7:134655561 | A | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(20): Show |
50 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.-61-5886A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655561 | |||||||
| chr7:134655581 | T | A | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61-5866T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655581 | |||||||
| chr7:134655608 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-61-5839A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655608 | |||||||
| chr7:134655661 | C | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(13): Show |
27 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.-61-5786C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655661 | |||||||
| chr7:134655661 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-61-5786C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655661 | |||||||
| chr7:134655666 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-61-5781G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655666 | |||||||
| chr7:134655738 | T | A | 1 | a0001c0001t0001g0103 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-61-5709T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655738 | |||||||
| chr7:134655789 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-61-5658G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655789 | |||||||
| chr7:134655928 | G | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-61-5519G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655928 | |||||||
| chr7:134655956 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02129.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-61-5491G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134655956 | |||||||
| chr7:134656009 | G | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(51): Show |
93 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-61-5438G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656009 | |||||||
| chr7:134656204 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-61-5243C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656204 | |||||||
| chr7:134656210 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-61-5237G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656210 | |||||||
| chr7:134656486 | T | G | 32 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(29): Show |
60 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.-61-4961T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656486 | |||||||
| chr7:134656602 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-61-4845A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656602 | |||||||
| chr7:134656615 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-61-4832C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656615 | |||||||
| chr7:134656677 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-61-4770T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656677 | |||||||
| chr7:134656717 | C | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-61-4730C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656717 | |||||||
| chr7:134656895 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-61-4552G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134656895 | |||||||
| chr7:134657002 | G | T | 3 | a0001c0001t0005g0040 a0001c0001t0005g0144 a0001c0001t0010g0054 |
4 | HG02735.hp2 HG04199.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-61-4445G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657002 | |||||||
| chr7:134657050 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.-61-4397A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657050 | |||||||
| chr7:134657058 | A | G | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0139 others(1): Show |
4 | HG00408.hp2 HG00423.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-61-4389A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657058 | |||||||
| chr7:134657317 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-61-4130A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657317 | |||||||
| chr7:134657359 | G | A | 2 | a0001c0001t0002g0073 a0001c0001t0002g0074 |
2 | HG01099.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-61-4088G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657359 | |||||||
| chr7:134657423 | T | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-61-4024T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657423 | |||||||
| chr7:134657469 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-61-3978G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657469 | |||||||
| chr7:134657524 | A | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-61-3923A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657524 | |||||||
| chr7:134657775 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
172 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-61-3672T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657775 | |||||||
| chr7:134657979 | A | C | 1 | a0001c0001t0001g0140 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-61-3468A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657979 | |||||||
| chr7:134657996 | A | G | 1 | a0001c0001t0001g0045 | 2 | HG00280.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-61-3451A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134657996 | |||||||
| chr7:134658097 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
171 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-61-3350G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658097 | |||||||
| chr7:134658174 | T | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(19): Show |
33 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.-61-3273T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658174 | |||||||
| chr7:134658176 | G | C | 2 | a0001c0001t0011g0085 a0001c0001t0012g0084 |
2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-61-3271G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658176 | |||||||
| chr7:134658190 | G | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-61-3257G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658190 | |||||||
| chr7:134658313 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-61-3134G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658313 | |||||||
| chr7:134658480 | G | C | 1 | a0001c0001t0002g0073 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-61-2967G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658480 | |||||||
| chr7:134658573 | G | T | 1 | a0001c0001t0001g0037 | 2 | NA18992.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.-61-2874G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658573 | |||||||
| chr7:134658575 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(52): Show |
94 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-61-2872G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658575 | |||||||
| chr7:134658582 | G | A | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-61-2865G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658582 | |||||||
| chr7:134658691 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-61-2756G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658691 | |||||||
| chr7:134658701 | G | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(20): Show |
50 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.-61-2746G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658701 | |||||||
| chr7:134658732 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-61-2715G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658732 | |||||||
| chr7:134658739 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-61-2708T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658739 | |||||||
| chr7:134658848 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0002c0003t0001g0149 |
3 | HG01993.hp1 HG03239.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-61-2599G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658848 | |||||||
| chr7:134658890 | G | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-61-2557G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658890 | |||||||
| chr7:134658892 | A | ATTTTTTT others(9): Show |
54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(51): Show |
93 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-61-2547_-61-2546i others(18): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | ||||||
| chr7:134658892 | A | ATTTTTTT others(10): Show |
82 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(79): Show |
170 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.-61-2547_-61-2546i others(19): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | ||||||
| chr7:134658892 | A | ATTTTTTT others(9): Show |
1 | a0001c0001t0001g0128 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-61-2547_-61-2546i others(18): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | ||||||
| chr7:134658892 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0163 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-61-2545_-61-2544i others(17): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | ||||||
| chr7:134658892 | A | ATTTTTTT others(9): Show |
17 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0044 others(14): Show |
41 | HG00280.hp2 HG00733.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.-61-2545_-61-2544i others(18): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | ||||||
| chr7:134658892 | A | ATTTTTTT others(10): Show |
5 | a0001c0001t0001g0015 a0001c0001t0001g0157 a0001c0001t0001g0160 others(2): Show |
8 | HG01074.hp2 HG01123.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.-61-2545_-61-2544i others(19): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | ||||||
| chr7:134658892 | A | ATTTTTTT others(11): Show |
4 | a0001c0001t0001g0043 a0001c0001t0001g0156 a0001c0001t0001g0171 others(1): Show |
5 | HG02896.hp1 HG02897.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61-2545_-61-2544i others(20): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | ||||||
| chr7:134658892 | A | ATTTTTTT others(12): Show |
2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01255.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-61-2545_-61-2544i others(21): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | ||||||
| chr7:134658892 | A | ATTTTTTT others(13): Show |
2 | a0001c0001t0001g0176 a0001c0001t0001g0178 |
2 | HG02895.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-61-2545_-61-2544i others(22): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | ||||||
| chr7:134658892 | A | ATTTTTTT others(14): Show |
1 | a0001c0001t0001g0177 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-61-2545_-61-2544i others(23): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658892 | ||||||
| chr7:134658895 | T | TTTTTTAT others(8): Show |
1 | a0001c0001t0010g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-61-2547_-61-2546i others(17): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134658895 | ||||||
| chr7:134658952 | G | T | 1 | a0001c0001t0010g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-61-2495G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658952 | |||||||
| chr7:134658977 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-61-2470G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134658977 | |||||||
| chr7:134659174 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-61-2273G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659174 | |||||||
| chr7:134659178 | C | T | 1 | a0001c0001t0010g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-61-2269C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659178 | |||||||
| chr7:134659235 | A | G | 1 | a0001c0001t0010g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-61-2212A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659235 | |||||||
| chr7:134659372 | C | CGT | 11 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0052 others(8): Show |
19 | HG02145.hp2 HG02615.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.-61-2036_-61-2035d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | ||||||
| chr7:134659372 | C | CGTGT | 6 | a0001c0001t0001g0020 a0001c0001t0001g0048 a0001c0001t0001g0069 others(3): Show |
8 | HG02055.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-61-2038_-61-2035d others(6): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | ||||||
| chr7:134659372 | C | CGTGTGT | 4 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0096 others(1): Show |
5 | HG00408.hp1 HG00423.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-61-2040_-61-2035d others(8): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | ||||||
| chr7:134659372 | CGT | C | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(16): Show |
42 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-61-2036_-61-2035d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | ||||||
| chr7:134659372 | CGTGT | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0016 others(30): Show |
56 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.-61-2038_-61-2035d others(6): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | ||||||
| chr7:134659372 | CGTGTGT | C | 10 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0066 others(7): Show |
11 | HG01358.hp2 HG02683.hp2 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.-61-2040_-61-2035d others(8): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | ||||||
| chr7:134659372 | CGTGTGTG others(1): Show |
C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0086 others(12): Show |
36 | HG00597.hp1 HG02074.hp2 HG02615.hp1 others(33): Show |
intron_variant | MODIFIER | c.-61-2042_-61-2035d others(10): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | ||||||
| chr7:134659372 | CGTGTGTG others(11): Show |
C | 9 | a0001c0001t0001g0043 a0001c0001t0001g0156 a0001c0001t0001g0157 others(6): Show |
10 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-61-2052_-61-2035d others(20): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | ||||||
| chr7:134659372 | CGTGTGTG others(13): Show |
C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(20): Show |
50 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.-61-2054_-61-2035d others(22): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134659372 | ||||||
| chr7:134659418 | A | T | 1 | a0001c0001t0002g0082 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-61-2029A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659418 | |||||||
| chr7:134659438 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-61-2009G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659438 | |||||||
| chr7:134659466 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.-61-1981T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659466 | |||||||
| chr7:134659475 | A | G | 2 | a0001c0001t0002g0078 a0001c0001t0002g0081 |
2 | HG01358.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-61-1972A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659475 | |||||||
| chr7:134659662 | C | T | 1 | a0001c0001t0006g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-61-1785C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659662 | |||||||
| chr7:134659764 | C | T | 1 | a0001c0001t0001g0046 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-61-1683C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659764 | |||||||
| chr7:134659791 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(49): Show |
90 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.-61-1656C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659791 | |||||||
| chr7:134659835 | T | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(52): Show |
94 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-61-1612T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659835 | |||||||
| chr7:134659892 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-61-1555C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134659892 | |||||||
| chr7:134660004 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-61-1443A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660004 | |||||||
| chr7:134660026 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-61-1421G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660026 | |||||||
| chr7:134660061 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-61-1386C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660061 | |||||||
| chr7:134660138 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-61-1309T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660138 | |||||||
| chr7:134660259 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0173 |
2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-61-1188A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660259 | |||||||
| chr7:134660275 | T | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-61-1172T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660275 | |||||||
| chr7:134660316 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-61-1131T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660316 | |||||||
| chr7:134660387 | A | C | 1 | a0004c0006t0001g0137 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-61-1060A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660387 | |||||||
| chr7:134660579 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-61-868C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660579 | |||||||
| chr7:134660608 | G | T | 1 | a0001c0001t0001g0034 | 2 | NA18972.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-61-839G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660608 | |||||||
| chr7:134660714 | G | A | 14 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
20 | HG01099.hp1 HG01358.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-61-733G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660714 | |||||||
| chr7:134660784 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-61-663C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660784 | |||||||
| chr7:134660791 | T | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(22): Show |
52 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.-61-656T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660791 | |||||||
| chr7:134660796 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-61-651G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134660796 | |||||||
| chr7:134661145 | T | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.-61-302T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | chr7 | 134661145 | |||||||
| chr7:134661146 | AAATTGCC others(12): Show |
A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.-61-299_-61-281del others(19): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | 134661146 | ||||||
| chr7:134662256 | A | G | 15 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): Show |
36 | HG00597.hp1 HG00639.hp1 HG02074.hp2 others(33): Show |
intron_variant | MODIFIER | c.601+148A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134662256 | |||||||
| chr7:134662325 | C | G | 1 | a0001c0001t0001g0064 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.601+217C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134662325 | |||||||
| chr7:134662382 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.601+274C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134662382 | |||||||
| chr7:134662463 | T | G | 1 | a0001c0001t0001g0164 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.601+355T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134662463 | |||||||
| chr7:134662637 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.601+529A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134662637 | |||||||
| chr7:134662854 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.601+746A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134662854 | |||||||
| chr7:134663039 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.601+931G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663039 | |||||||
| chr7:134663111 | C | T | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.601+1003C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663111 | |||||||
| chr7:134663140 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG01496.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.601+1032G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663140 | |||||||
| chr7:134663170 | G | T | 2 | a0001c0001t0011g0085 a0001c0001t0012g0084 |
2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.601+1062G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663170 | |||||||
| chr7:134663285 | C | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0173 |
2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601+1177C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663285 | |||||||
| chr7:134663368 | A | ATG | 81 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(78): Show |
169 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.601+1276_601+1277d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134663368 | ||||||
| chr7:134663368 | A | ATGTG | 39 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0024 others(36): Show |
72 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.601+1274_601+1277d others(6): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134663368 | ||||||
| chr7:134663368 | A | ATGTGTG | 16 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0075 others(13): Show |
22 | HG01358.hp2 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.601+1272_601+1277d others(8): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134663368 | ||||||
| chr7:134663524 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01255.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.601+1416C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663524 | |||||||
| chr7:134663629 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.601+1521G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663629 | |||||||
| chr7:134663654 | G | T | 1 | a0001c0001t0001g0028 | 2 | NA18969.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.601+1546G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663654 | |||||||
| chr7:134663663 | T | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(52): Show |
94 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.601+1555T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663663 | |||||||
| chr7:134663663 | T | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.601+1555T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663663 | |||||||
| chr7:134663711 | T | C | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+1603T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663711 | |||||||
| chr7:134663724 | C | G | 14 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0076 others(11): Show |
20 | HG01099.hp1 HG01358.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.601+1616C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663724 | |||||||
| chr7:134663762 | G | C | 30 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(27): Show |
57 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.601+1654G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663762 | |||||||
| chr7:134663923 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.601+1815C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134663923 | |||||||
| chr7:134664013 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.601+1905A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664013 | |||||||
| chr7:134664043 | T | C | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+1935T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664043 | |||||||
| chr7:134664214 | A | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.601+2106A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664214 | |||||||
| chr7:134664303 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601+2195G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664303 | |||||||
| chr7:134664318 | C | G | 1 | a0001c0001t0001g0034 | 2 | NA18972.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.601+2210C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664318 | |||||||
| chr7:134664326 | C | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.601+2218C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664326 | |||||||
| chr7:134664338 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.601+2230T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664338 | |||||||
| chr7:134664437 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.601+2329C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664437 | |||||||
| chr7:134664468 | G | A | 13 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0076 others(10): Show |
19 | HG01099.hp1 HG01358.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.601+2360G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664468 | |||||||
| chr7:134664548 | A | AGGTATT | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.601+2442_601+2443i others(8): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134664548 | ||||||
| chr7:134664569 | G | A | 30 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(27): Show |
57 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.601+2461G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664569 | |||||||
| chr7:134664611 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.601+2503A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664611 | |||||||
| chr7:134664649 | C | G | 2 | a0001c0001t0011g0085 a0001c0001t0012g0084 |
2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.601+2541C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664649 | |||||||
| chr7:134664708 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.601+2600C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664708 | |||||||
| chr7:134664728 | C | T | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+2620C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664728 | |||||||
| chr7:134664790 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.601+2682A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664790 | |||||||
| chr7:134664849 | A | T | 1 | a0001c0001t0001g0092 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.601+2741A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664849 | |||||||
| chr7:134664894 | C | A | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.601+2786C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664894 | |||||||
| chr7:134664914 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(52): Show |
94 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.601+2806G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134664914 | |||||||
| chr7:134665016 | T | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): Show |
36 | HG00597.hp1 HG00639.hp1 HG02074.hp2 others(33): Show |
intron_variant | MODIFIER | c.601+2908T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665016 | |||||||
| chr7:134665146 | G | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0039 others(7): Show |
16 | HG01099.hp2 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.601+3038G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665146 | |||||||
| chr7:134665172 | G | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.601+3064G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665172 | |||||||
| chr7:134665185 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.601+3077C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665185 | |||||||
| chr7:134665189 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(138): Show |
273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.601+3081C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665189 | |||||||
| chr7:134665247 | CAAAGTGC others(416): Show |
C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.601+3148_601+3570d others(2): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134665247 | ||||||
| chr7:134665381 | G | A | 1 | a0001c0001t0001g0015 | 3 | HG01074.hp2 HG01123.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.601+3273G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665381 | |||||||
| chr7:134665623 | T | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0154 |
3 | HG00558.hp2 NA18966.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.601+3515T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665623 | |||||||
| chr7:134665645 | T | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(42): Show |
92 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.601+3537T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665645 | |||||||
| chr7:134665649 | G | GAAAAA | 3 | a0001c0001t0001g0003 a0001c0001t0001g0160 a0001c0001t0001g0165 |
6 | HG00733.hp2 HG01109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+3561_601+3565d others(7): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134665649 | ||||||
| chr7:134665649 | G | GAAAAAA | 15 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(12): Show |
31 | HG00280.hp2 HG01074.hp2 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.601+3560_601+3565d others(8): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134665649 | ||||||
| chr7:134665649 | G | GAAAAAAA | 7 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0044 others(4): Show |
10 | HG01175.hp2 HG01346.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.601+3559_601+3565d others(9): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134665649 | ||||||
| chr7:134665649 | GAAAAAAA others(3): Show |
G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01255.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.601+3556_601+3565d others(12): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134665649 | ||||||
| chr7:134665811 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.601+3703A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134665811 | |||||||
| chr7:134665865 | A | ATTTTCTT others(3): Show |
1 | a0001c0001t0001g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.601+3777_601+3786d others(12): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134665865 | ||||||
| chr7:134665865 | ATTTTC | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
151 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.601+3782_601+3786d others(7): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134665865 | ||||||
| chr7:134666022 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.601+3914T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666022 | |||||||
| chr7:134666023 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.601+3915G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666023 | |||||||
| chr7:134666081 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.601+3973C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666081 | |||||||
| chr7:134666155 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0109 |
4 | HG00140.hp1 HG02698.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+4047G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666155 | |||||||
| chr7:134666170 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0059 |
5 | HG00323.hp1 HG01081.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+4062G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666170 | |||||||
| chr7:134666180 | A | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG02129.hp1 NA18956.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.601+4072A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666180 | |||||||
| chr7:134666516 | G | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(20): Show |
50 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.601+4408G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666516 | |||||||
| chr7:134666598 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.601+4490G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666598 | |||||||
| chr7:134666616 | G | A | 52 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(49): Show |
90 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.601+4508G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666616 | |||||||
| chr7:134666668 | G | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0155 |
4 | NA18944.hp2 NA18986.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+4560G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666668 | |||||||
| chr7:134666762 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.601+4654A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666762 | |||||||
| chr7:134666802 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.601+4694T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666802 | |||||||
| chr7:134666958 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.601+4850T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134666958 | |||||||
| chr7:134667005 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
235 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.601+4897A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667005 | |||||||
| chr7:134667104 | T | C | 52 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(49): Show |
90 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.601+4996T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667104 | |||||||
| chr7:134667126 | C | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.601+5018C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667126 | |||||||
| chr7:134667156 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.601+5048T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667156 | |||||||
| chr7:134667232 | T | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(19): Show |
33 | HG00280.hp1 HG00544.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.601+5124T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667232 | |||||||
| chr7:134667396 | T | TTATGTGG others(36): Show |
1 | a0001c0001t0001g0069 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601+5290_601+5332d others(45): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134667396 | ||||||
| chr7:134667492 | G | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
235 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.601+5384G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667492 | |||||||
| chr7:134667533 | C | G | 1 | a0001c0001t0001g0135 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.601+5425C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667533 | |||||||
| chr7:134667567 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0173 |
2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601+5459C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667567 | |||||||
| chr7:134667677 | T | C | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.601+5569T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667677 | |||||||
| chr7:134667844 | C | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.601+5736C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134667844 | |||||||
| chr7:134668068 | T | TA | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
235 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.601+5961dupA | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134668068 | ||||||
| chr7:134668350 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
235 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.601+6242T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134668350 | |||||||
| chr7:134668525 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.601+6417A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134668525 | |||||||
| chr7:134668673 | T | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
235 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.601+6565T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134668673 | |||||||
| chr7:134668879 | C | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0120 a0001c0001t0001g0156 |
4 | HG02717.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+6771C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134668879 | |||||||
| chr7:134668891 | A | AAC | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
235 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.601+6785_601+6786d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134668891 | ||||||
| chr7:134669059 | G | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
235 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.601+6951G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669059 | |||||||
| chr7:134669277 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.601+7169C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669277 | |||||||
| chr7:134669321 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0173 |
2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601+7213T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669321 | |||||||
| chr7:134669506 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601+7398G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669506 | |||||||
| chr7:134669512 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.601+7404A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669512 | |||||||
| chr7:134669545 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.601+7437G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669545 | |||||||
| chr7:134669776 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
235 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.601+7668A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669776 | |||||||
| chr7:134669890 | C | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0027 others(27): Show |
57 | HG00597.hp1 HG00639.hp1 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.601+7782C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134669890 | |||||||
| chr7:134670089 | C | G | 23 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(20): Show |
50 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.601+7981C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670089 | |||||||
| chr7:134670132 | T | A | 1 | a0001c0001t0001g0160 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.601+8024T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670132 | |||||||
| chr7:134670233 | G | C | 1 | a0001c0001t0010g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.601+8125G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670233 | |||||||
| chr7:134670297 | G | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(20): Show |
50 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.601+8189G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670297 | |||||||
| chr7:134670312 | G | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0171 |
2 | NA18995.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.601+8204G>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670312 | |||||||
| chr7:134670396 | A | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(116): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.601+8288A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670396 | |||||||
| chr7:134670535 | A | G | 1 | a0001c0001t0001g0037 | 2 | NA18992.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.602-8318A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670535 | |||||||
| chr7:134670627 | A | AATAG | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(116): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.602-8223_602-8220d others(6): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134670627 | ||||||
| chr7:134670657 | A | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(116): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.602-8196A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670657 | |||||||
| chr7:134670674 | G | T | 26 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(23): Show |
37 | HG00544.hp1 HG00642.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.602-8179G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670674 | |||||||
| chr7:134670729 | A | G | 1 | a0001c0001t0010g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.602-8124A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670729 | |||||||
| chr7:134670879 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
264 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.602-7974G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134670879 | |||||||
| chr7:134671105 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(116): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.602-7748A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671105 | |||||||
| chr7:134671188 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.602-7665T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671188 | |||||||
| chr7:134671278 | G | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0169 a0001c0001t0009g0023 |
4 | NA18994.hp1 NA18997.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.602-7575G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671278 | |||||||
| chr7:134671285 | C | T | 1 | a0001c0001t0008g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.602-7568C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671285 | |||||||
| chr7:134671363 | C | CT | 33 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0018 others(30): Show |
67 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.602-7474dupT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134671363 | ||||||
| chr7:134671363 | C | CTT | 26 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0027 others(23): Show |
53 | HG00597.hp1 HG00639.hp1 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.602-7475_602-7474d others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134671363 | ||||||
| chr7:134671392 | C | T | 3 | a0001c0001t0005g0040 a0001c0001t0005g0144 a0001c0001t0010g0054 |
4 | HG02735.hp2 HG04199.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-7461C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671392 | |||||||
| chr7:134671488 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.602-7365A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671488 | |||||||
| chr7:134671511 | G | A | 3 | a0001c0001t0005g0040 a0001c0001t0005g0144 a0001c0001t0010g0054 |
4 | HG02735.hp2 HG04199.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-7342G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671511 | |||||||
| chr7:134671639 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.602-7214T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671639 | |||||||
| chr7:134671890 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.602-6963C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134671890 | |||||||
| chr7:134672068 | T | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.602-6785T>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672068 | |||||||
| chr7:134672243 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.602-6610G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672243 | |||||||
| chr7:134672257 | A | T | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-6596A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672257 | |||||||
| chr7:134672276 | TAACACAG others(13): Show |
T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
322 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.602-6561_602-6542d others(22): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134672276 | ||||||
| chr7:134672414 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-6439T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672414 | |||||||
| chr7:134672436 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.602-6417G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672436 | |||||||
| chr7:134672437 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
265 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.602-6416A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672437 | |||||||
| chr7:134672546 | A | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(9): Show |
33 | HG00597.hp1 HG02074.hp2 NA18942.hp2 others(30): Show |
intron_variant | MODIFIER | c.602-6307A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672546 | |||||||
| chr7:134672651 | A | AT | 5 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(2): Show |
5 | HG01255.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.602-6196dupT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134672651 | ||||||
| chr7:134672661 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0173 |
2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.602-6192A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672661 | |||||||
| chr7:134672903 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG01516.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.602-5950G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134672903 | |||||||
| chr7:134673019 | A | G | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-5834A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673019 | |||||||
| chr7:134673025 | G | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.602-5828G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673025 | |||||||
| chr7:134673043 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.602-5810G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673043 | |||||||
| chr7:134673060 | A | G | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-5793A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673060 | |||||||
| chr7:134673123 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.602-5730G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673123 | |||||||
| chr7:134673128 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.602-5725C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673128 | |||||||
| chr7:134673190 | T | TAATAAAA others(13): Show |
2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-5646_602-5645i others(22): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134673190 | ||||||
| chr7:134673289 | T | C | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-5564T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673289 | |||||||
| chr7:134673290 | G | A | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-5563G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673290 | |||||||
| chr7:134673466 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.602-5387A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673466 | |||||||
| chr7:134673532 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.602-5321A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673532 | |||||||
| chr7:134673583 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-5270A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673583 | |||||||
| chr7:134673903 | C | CT | 26 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0022 others(23): Show |
45 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.602-4928dupT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134673903 | ||||||
| chr7:134673903 | CT | C | 15 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0088 others(12): Show |
15 | HG00099.hp1 HG01099.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.602-4928delT | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134673903 | ||||||
| chr7:134673926 | A | T | 1 | a0001c0001t0001g0154 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.602-4927A>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134673926 | |||||||
| chr7:134674165 | A | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(101): Show |
209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.602-4688A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674165 | |||||||
| chr7:134674396 | C | T | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-4457C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674396 | |||||||
| chr7:134674401 | C | A | 1 | a0001c0001t0008g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.602-4452C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674401 | |||||||
| chr7:134674423 | A | C | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-4430A>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674423 | |||||||
| chr7:134674428 | T | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0022 others(5): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.602-4425T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674428 | |||||||
| chr7:134674449 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.602-4404T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674449 | |||||||
| chr7:134674451 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.602-4402T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674451 | |||||||
| chr7:134674452 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.602-4401G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674452 | |||||||
| chr7:134674499 | T | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(21): Show |
52 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.602-4354T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674499 | |||||||
| chr7:134674759 | C | T | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-4094C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674759 | |||||||
| chr7:134674844 | C | T | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-4009C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134674844 | |||||||
| chr7:134675178 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(115): Show |
234 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.602-3675A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134675178 | |||||||
| chr7:134675298 | T | A | 1 | a0001c0001t0001g0025 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.602-3555T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134675298 | |||||||
| chr7:134675466 | A | G | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-3387A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134675466 | |||||||
| chr7:134676433 | A | G | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.602-2420A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134676433 | |||||||
| chr7:134676585 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.602-2268T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134676585 | |||||||
| chr7:134676707 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG00642.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.602-2146C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134676707 | |||||||
| chr7:134677122 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.602-1731A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134677122 | |||||||
| chr7:134677251 | T | TTTTC | 25 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
36 | HG00544.hp1 HG00642.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.602-1586_602-1583d others(6): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134677251 | ||||||
| chr7:134677532 | G | T | 1 | a0001c0001t0001g0155 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.602-1321G>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134677532 | |||||||
| chr7:134677632 | T | C | 2 | a0001c0001t0005g0040 a0001c0001t0005g0144 |
3 | HG02735.hp2 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.602-1221T>C | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134677632 | |||||||
| chr7:134677696 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(86): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.602-1157A>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134677696 | |||||||
| chr7:134677744 | AAAG | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0023 others(21): Show |
52 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.602-1108_602-1106d others(5): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134677744 | |||||||
| chr7:134677840 | T | A | 1 | a0001c0001t0010g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.602-1013T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134677840 | |||||||
| chr7:134677934 | T | A | 1 | a0001c0001t0001g0114 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.602-919T>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134677934 | |||||||
| chr7:134678076 | C | CTGTT | 21 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(18): Show |
32 | HG00544.hp1 HG00642.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.602-775_602-772dup others(4): Show |
BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr7 | 134678076 | ||||||
| chr7:134678132 | C | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0022 others(5): Show |
21 | HG00558.hp2 HG00673.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.602-721C>G | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134678132 | |||||||
| chr7:134678218 | C | T | 2 | a0001c0001t0011g0085 a0001c0001t0012g0084 |
2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.602-635C>T | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134678218 | |||||||
| chr7:134678315 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-538C>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134678315 | |||||||
| chr7:134678330 | G | A | 1 | a0001c0001t0010g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.602-523G>A | BPGM | ENSG00000172331.12 | transcript | ENST00000344924.8 | protein_coding | 2/2 | chr7 | 134678330 |