Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 100506374 |
| ensemblid | ENSG00000267710.9 |
| hgncid | 53168 |
| symbol | EDDM13 |
| name | epididymal protein 13 |
| refseq_nuc | NM_001354658.2 |
| refseq_prot | NP_001341587.1 |
| ensembl_nuc | ENST00000649256.2 |
| ensembl_prot | ENSP00000497858.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 56272748 |
| end | 56310454 |
| strand | + |
| ver | v1.2 |
| region | chr19:56272748-56310454 |
| region5000 | chr19:56267748-56315454 |
| regionname0 | EDDM13_chr19_56272748_56310454 |
| regionname5000 | EDDM13_chr19_56267748_56315454 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 161 | 390 | 91 | 76 | 163 | 14 | 44 | 129 | EDDM13_chr19_56267748_56315454 | EDDM13 | MHRSE others(156): Show |
chr19 | 56267748 | 56315454 |
| a0002 | 0/0 | 161 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | MHRSE others(156): Show |
chr19 | 56267748 | 56315454 |
| a0003 | 0/0 | 152 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | MSLLI others(147): Show |
chr19 | 56267748 | 56315454 |
| a0004 | 0/0 | 39 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | MHRSE others(34): Show |
chr19 | 56267748 | 56315454 |
| a0005 | 0/0 | 161 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | MHRSE others(156): Show |
chr19 | 56267748 | 56315454 |
| a0006 | 0/0 | 159 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | MHRSE others(154): Show |
chr19 | 56267748 | 56315454 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 483 | 385 | 87 | 76 | 162 | 14 | 44 | EDDM13_chr19_56267748_56315454 | EDDM13 | ATGCA others(478): Show |
chr19 | 56267748 | 56315454 | ||
| a0001c0002 | 0/0 | 483 | 2 | 2 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | ATGCA others(478): Show |
chr19 | 56267748 | 56315454 | ||
| a0001c0003 | 0/0 | 483 | 2 | 2 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | ATGCA others(478): Show |
chr19 | 56267748 | 56315454 | ||
| a0001c0007 | 0/0 | 483 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | ATGCA others(478): Show |
chr19 | 56267748 | 56315454 | ||
| a0002c0004 | 0/0 | 483 | 2 | 2 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | ATGCA others(478): Show |
chr19 | 56267748 | 56315454 | ||
| a0003c0009 | 0/0 | 483 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | TTGCA others(478): Show |
chr19 | 56267748 | 56315454 | ||
| a0004c0008 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | ATGCA others(471): Show |
chr19 | 56267748 | 56315454 | ||
| a0005c0005 | 0/0 | 483 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | ATGCA others(478): Show |
chr19 | 56267748 | 56315454 | ||
| a0006c0006 | 0/0 | 477 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | ATGCA others(472): Show |
chr19 | 56267748 | 56315454 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 879 | 241 | 67 | 34 | 117 | 5 | 17 | EDDM13_chr19_56267748_56315454 | EDDM13 | GTCCC others(874): Show |
chr19 | 56267748 | 56315454 |
| a0001c0001t0002 | 0/0 | 879 | 111 | 9 | 36 | 36 | 7 | 23 | EDDM13_chr19_56267748_56315454 | EDDM13 | GTCCC others(874): Show |
chr19 | 56267748 | 56315454 |
| a0001c0001t0003 | 0/1 | 879 | 23 | 6 | 4 | 8 | 2 | 2 | EDDM13_chr19_56267748_56315454 | EDDM13 | GTCCC others(874): Show |
chr19 | 56267748 | 56315454 |
| a0001c0001t0004 | 0/0 | 879 | 4 | 3 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | GTCCC others(874): Show |
chr19 | 56267748 | 56315454 |
| a0001c0001t0005 | 0/0 | 879 | 3 | 0 | 1 | 0 | 0 | 2 | EDDM13_chr19_56267748_56315454 | EDDM13 | GTCCC others(874): Show |
chr19 | 56267748 | 56315454 |
| a0001c0001t0006 | 0/0 | 879 | 2 | 2 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | GTCCC others(874): Show |
chr19 | 56267748 | 56315454 |
| a0001c0001t0007 | 0/0 | 879 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | GTCCC others(874): Show |
chr19 | 56267748 | 56315454 |
| a0001c0002t0001 | 0/0 | 879 | 2 | 2 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | GTCCC others(874): Show |
chr19 | 56267748 | 56315454 |
| a0001c0003t0001 | 0/0 | 879 | 2 | 2 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | GTCCC others(874): Show |
chr19 | 56267748 | 56315454 |
| a0001c0007t0001 | 0/0 | 879 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | GTCCC others(874): Show |
chr19 | 56267748 | 56315454 |
| a0002c0004t0001 | 0/0 | 879 | 2 | 2 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | GTCCC others(874): Show |
chr19 | 56267748 | 56315454 |
| a0003c0009t0004 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | GTCCC others(874): Show |
chr19 | 56267748 | 56315454 |
| a0004c0008t0001 | 0/0 | 872 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | GTCCC others(867): Show |
chr19 | 56267748 | 56315454 |
| a0005c0005t0001 | 0/0 | 879 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | GTCCC others(874): Show |
chr19 | 56267748 | 56315454 |
| a0006c0006t0001 | 0/0 | 873 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | GTCCC others(868): Show |
chr19 | 56267748 | 56315454 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0239 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 0 | 1 | 5 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0001t0007g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0001c0007t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0002c0004t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0003c0009t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0004c0008t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0005c0005t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| a0006c0006t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | GBR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | GBR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0019 | EUR | GBR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | FIN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | FIN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0162 | EUR | FIN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0320 | EUR | FIN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | CHS | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | CHS | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0174 | AMR | CLM | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | CLM | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0142 | EUR | IBS | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0271 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0294 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CDX | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CDX | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02257 | hp1 | a0003 | c0009 | t0004 | g0062 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02258 | hp2 | a0001 | c0003 | t0001 | g0193 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PEL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0289 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0304 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02976 | hp2 | a0002 | c0004 | t0001 | g0031 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | MSL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03098 | hp2 | a0002 | c0004 | t0001 | g0031 | AFR | MSL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | MSL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0213 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0109 | AFR | MSL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0270 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | STU | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | STU | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | BEB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0114 | SAS | BEB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0178 | SAS | STU | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | BEB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | BEB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | STU | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | STU | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | STU | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | STU | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | STU | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | YRI | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18956 | hp2 | a0004 | c0008 | t0001 | g0277 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18992 | hp2 | a0001 | c0001 | t0007 | g0290 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19002 | hp2 | a0005 | c0005 | t0001 | g0261 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19004 | hp2 | a0006 | c0006 | t0001 | g0105 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | LWK | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19085 | hp1 | a0001 | c0007 | t0001 | g0284 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | YRI | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ASW | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0309 | EUR | TSI | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | TSI | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0198 | EUR | TSI | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0111 | EUR | TSI | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | GIH | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | MSL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | USA | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | USA | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | LWK | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | LWK | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0196 | REF | REF | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0239 | REF | REF | EDDM13_chr19_56267748_56315454 | EDDM13 | chr19 | 56267748 | 56315454 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:56272835 | A | T | 1 | a0003 | 1 | HG02257.hp1 | initiator_codon_variant | LOW | c.1A>T | p.Met1? | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/15 | 88/879 | 1/486 | 1/161 | chr19 | 56272835 | |||
| chr19:56272914 | G | A | 1 | a0005 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.80G>A | p.Arg27His | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/15 | 167/879 | 80/486 | 27/161 | chr19 | 56272914 | |||
| chr19:56282492 | GCTGAAAG others(294): Show |
G | 1 | a0004 | 1 | NA18956.hp2 | splice_donor_variant&disruptive_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.116_118+298del | p.Lys39_Gly40delinsA others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/15 | 203/879 | 116/486 | 39/161 | INFO_REALIGN_3_PRIME | chr19 | 56282492 | ||
| chr19:56285019 | C | T | 1 | a0002 | 2 | HG02976.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.149C>T | p.Pro50Leu | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/15 | 236/879 | 149/486 | 50/161 | chr19 | 56285019 | |||
| chr19:56290059 | GTGGTTTC others(4278): Show |
G | 1 | a0006 | 1 | NA19004.hp2 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.227-778_233-1612de others(1): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr19 | 56290059 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:56288434 | G | A | 1 | a0001c0002 | 2 | HG03130.hp2 NA18522.hp2 |
synonymous_variant | LOW | c.204G>A | p.Pro68Pro | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 7/15 | 291/879 | 204/486 | 68/161 | chr19 | 56288434 | |||
| chr19:56302008 | C | A | 1 | a0001c0007 | 1 | NA19085.hp1 | synonymous_variant | LOW | c.336C>A | p.Leu112Leu | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/15 | 423/879 | 336/486 | 112/161 | chr19 | 56302008 | |||
| chr19:56302044 | C | T | 1 | a0001c0003 | 2 | HG02258.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.372C>T | p.Cys124Cys | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/15 | 459/879 | 372/486 | 124/161 | chr19 | 56302044 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:56272755 | G | A | 1 | a0001c0001t0007 | 1 | NA18992.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/15 | 80 | chr19 | 56272755 | ||||||
| chr19:56272792 | C | A | 3 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
5_prime_UTR_variant | MODIFIER | c.-43C>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/15 | 43 | chr19 | 56272792 | ||||||
| chr19:56310299 | T | C | 1 | a0001c0001t0006 | 2 | HG02630.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*151T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 15/15 | 151 | chr19 | 56310299 | ||||||
| chr19:56310304 | A | G | 2 | a0001c0001t0003 a0001c0001t0005 |
25 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*156A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 15/15 | 156 | chr19 | 56310304 | ||||||
| chr19:56310349 | C | T | 2 | a0001c0001t0004 a0003c0009t0004 |
5 | HG02004.hp1 HG02257.hp1 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*201C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 15/15 | 201 | chr19 | 56310349 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:56272936 | T | C | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.85+17T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56272936 | |||||||
| chr19:56272980 | T | C | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.85+61T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56272980 | |||||||
| chr19:56273044 | C | T | 1 | a0001c0001t0001g0336 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.85+125C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273044 | |||||||
| chr19:56273062 | T | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(159): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.85+143T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273062 | |||||||
| chr19:56273069 | A | G | 99 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0004 others(96): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.85+150A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273069 | |||||||
| chr19:56273169 | C | T | 98 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(95): Show |
118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.85+250C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273169 | |||||||
| chr19:56273254 | G | A | 1 | a0001c0001t0006g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.85+335G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273254 | |||||||
| chr19:56273325 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0192 others(2): Show |
7 | HG02258.hp2 HG02559.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.85+406T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273325 | |||||||
| chr19:56273405 | C | G | 1 | a0001c0001t0001g0335 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.85+486C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273405 | |||||||
| chr19:56273461 | T | G | 18 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(15): Show |
22 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.85+542T>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273461 | |||||||
| chr19:56273466 | A | AAAAAGAC others(6): Show |
96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.85+550_85+551insAG others(11): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56273466 | ||||||
| chr19:56273468 | A | G | 18 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(15): Show |
22 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.85+549A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273468 | |||||||
| chr19:56273470 | T | C | 96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.85+551T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273470 | |||||||
| chr19:56273486 | G | A | 4 | a0001c0001t0002g0016 a0001c0001t0002g0110 a0001c0001t0002g0111 others(1): Show |
5 | HG01099.hp2 HG01346.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+567G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273486 | |||||||
| chr19:56273518 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.85+599T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273518 | |||||||
| chr19:56273525 | T | G | 97 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0004 others(94): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.85+606T>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273525 | |||||||
| chr19:56273532 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.85+613T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273532 | |||||||
| chr19:56273659 | C | T | 97 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(94): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.85+740C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273659 | |||||||
| chr19:56273713 | G | A | 1 | a0001c0001t0003g0211 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.85+794G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273713 | |||||||
| chr19:56273852 | T | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0005g0114 |
3 | HG02615.hp2 HG03471.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.85+933T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273852 | |||||||
| chr19:56273862 | C | T | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(251): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.85+943C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273862 | |||||||
| chr19:56273998 | G | C | 1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.85+1079G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56273998 | |||||||
| chr19:56274039 | C | T | 20 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(17): Show |
24 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.85+1120C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274039 | |||||||
| chr19:56274061 | T | C | 1 | a0001c0001t0002g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.85+1142T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274061 | |||||||
| chr19:56274179 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.85+1260C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274179 | |||||||
| chr19:56274216 | A | C | 1 | a0001c0001t0001g0107 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.85+1297A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274216 | |||||||
| chr19:56274230 | G | C | 2 | a0001c0001t0001g0214 a0001c0001t0004g0213 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.85+1311G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274230 | |||||||
| chr19:56274275 | G | A | 2 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
2 | NA18956.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.85+1356G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274275 | |||||||
| chr19:56274318 | G | T | 94 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(91): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.85+1399G>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274318 | |||||||
| chr19:56274319 | T | C | 94 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(91): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.85+1400T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274319 | |||||||
| chr19:56274327 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.85+1408G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274327 | |||||||
| chr19:56274372 | T | G | 95 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(92): Show |
115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.85+1453T>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274372 | |||||||
| chr19:56274402 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.85+1483C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274402 | |||||||
| chr19:56274440 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.85+1521C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274440 | |||||||
| chr19:56274467 | GA | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0025 others(69): Show |
85 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.85+1561delA | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56274467 | ||||||
| chr19:56274467 | GAA | G | 93 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(90): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.85+1560_85+1561del others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56274467 | ||||||
| chr19:56274536 | A | G | 96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.86-1556A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274536 | |||||||
| chr19:56274537 | G | A | 96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.86-1555G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274537 | |||||||
| chr19:56274579 | G | A | 18 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(15): Show |
22 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.86-1513G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274579 | |||||||
| chr19:56274703 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.86-1389T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274703 | |||||||
| chr19:56274762 | GT | G | 96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.86-1324delT | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | 56274762 | ||||||
| chr19:56274769 | G | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(63): Show |
71 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.86-1323G>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274769 | |||||||
| chr19:56274819 | T | C | 1 | a0001c0007t0001g0284 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.86-1273T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56274819 | |||||||
| chr19:56275030 | G | A | 2 | a0001c0001t0001g0285 a0001c0001t0001g0336 |
2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.86-1062G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56275030 | |||||||
| chr19:56275074 | G | A | 94 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(91): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.86-1018G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56275074 | |||||||
| chr19:56275226 | C | T | 96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.86-866C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56275226 | |||||||
| chr19:56275466 | C | T | 3 | a0001c0001t0002g0118 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG01891.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.86-626C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56275466 | |||||||
| chr19:56275681 | G | C | 1 | a0001c0001t0001g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.86-411G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56275681 | |||||||
| chr19:56275922 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.86-170T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56275922 | |||||||
| chr19:56275980 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.86-112C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56275980 | |||||||
| chr19:56276057 | G | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02056.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.86-35G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 1/14 | chr19 | 56276057 | |||||||
| chr19:56276317 | C | T | 96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.103+208C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56276317 | |||||||
| chr19:56276319 | C | T | 1 | a0006c0006t0001g0105 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.103+210C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56276319 | |||||||
| chr19:56276321 | C | T | 96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.103+212C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56276321 | |||||||
| chr19:56276385 | C | T | 1 | a0001c0001t0006g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.103+276C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56276385 | |||||||
| chr19:56276496 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0003g0282 |
2 | HG02129.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.103+387C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56276496 | |||||||
| chr19:56276506 | C | CTTTTT | 93 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(90): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.103+406_103+410dup others(5): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56276506 | ||||||
| chr19:56276534 | T | TTTTA | 94 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(91): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.103+441_103+444dup others(4): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56276534 | ||||||
| chr19:56276567 | C | T | 1 | a0001c0001t0006g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.103+458C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56276567 | |||||||
| chr19:56276589 | T | C | 2 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.103+480T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56276589 | |||||||
| chr19:56276591 | T | A | 1 | a0001c0001t0002g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.103+482T>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56276591 | |||||||
| chr19:56276685 | G | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0123 a0001c0001t0002g0124 |
4 | HG01070.hp2 HG03669.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+576G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56276685 | |||||||
| chr19:56276716 | C | T | 96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.103+607C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56276716 | |||||||
| chr19:56276752 | G | C | 2 | a0001c0001t0002g0004 a0001c0001t0002g0125 |
4 | NA18939.hp2 NA18960.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.103+643G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56276752 | |||||||
| chr19:56276760 | C | T | 96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.103+651C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56276760 | |||||||
| chr19:56276789 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.103+680G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56276789 | |||||||
| chr19:56277016 | T | C | 2 | a0001c0001t0001g0283 a0001c0001t0003g0282 |
2 | HG02129.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.103+907T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56277016 | |||||||
| chr19:56277023 | C | A | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.103+914C>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56277023 | |||||||
| chr19:56277075 | C | G | 4 | a0001c0001t0001g0103 a0001c0001t0003g0101 a0001c0001t0003g0102 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+966C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56277075 | |||||||
| chr19:56277175 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.103+1066C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56277175 | |||||||
| chr19:56277207 | G | T | 1 | a0001c0001t0002g0188 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.103+1098G>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56277207 | |||||||
| chr19:56277394 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.103+1285A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56277394 | |||||||
| chr19:56277458 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0192 others(2): Show |
7 | HG02258.hp2 HG02559.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.103+1349C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56277458 | |||||||
| chr19:56277532 | T | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(60): Show |
68 | HG00733.hp1 HG01109.hp1 HG01109.hp2 others(65): Show |
intron_variant | MODIFIER | c.103+1423T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56277532 | |||||||
| chr19:56277612 | T | C | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.103+1503T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56277612 | |||||||
| chr19:56277623 | G | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0123 a0001c0001t0002g0124 |
4 | HG01070.hp2 HG03669.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.103+1514G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56277623 | |||||||
| chr19:56277815 | A | C | 96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.103+1706A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56277815 | |||||||
| chr19:56277968 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0003g0282 |
2 | HG02129.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.103+1859G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56277968 | |||||||
| chr19:56277985 | AC | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0212 a0001c0001t0005g0114 |
3 | HG02615.hp2 HG03471.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.103+1878delC | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56277985 | ||||||
| chr19:56278101 | A | AT | 96 | a0001c0001t0001g0278 a0001c0001t0002g0001 a0001c0001t0002g0004 others(93): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.103+2006dupT | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56278101 | ||||||
| chr19:56278101 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0003g0098 |
2 | HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.103+1992A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56278101 | |||||||
| chr19:56278101 | AT | A | 22 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(19): Show |
26 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.103+2006delT | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56278101 | ||||||
| chr19:56278190 | C | T | 95 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(92): Show |
115 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.103+2081C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56278190 | |||||||
| chr19:56278200 | T | C | 96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.103+2091T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56278200 | |||||||
| chr19:56278242 | A | C | 96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.103+2133A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56278242 | |||||||
| chr19:56278246 | G | C | 96 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.103+2137G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56278246 | |||||||
| chr19:56278256 | C | T | 94 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(91): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.103+2147C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56278256 | |||||||
| chr19:56278271 | C | T | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(252): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.103+2162C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56278271 | |||||||
| chr19:56278305 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.103+2196T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56278305 | |||||||
| chr19:56278426 | G | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0188 |
2 | HG01943.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.103+2317G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56278426 | |||||||
| chr19:56278461 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.103+2352T>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56278461 | |||||||
| chr19:56278614 | T | G | 1 | a0001c0001t0003g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.103+2505T>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56278614 | |||||||
| chr19:56278660 | G | A | 1 | a0001c0001t0003g0289 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.103+2551G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56278660 | |||||||
| chr19:56278770 | T | A | 12 | a0001c0001t0002g0018 a0001c0001t0002g0116 a0001c0001t0002g0117 others(9): Show |
13 | HG01261.hp2 HG01496.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.103+2661T>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56278770 | |||||||
| chr19:56278808 | C | G | 91 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.103+2699C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56278808 | |||||||
| chr19:56278808 | C | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0047 others(8): Show |
13 | HG01109.hp2 HG01192.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.103+2699C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56278808 | |||||||
| chr19:56279108 | A | T | 1 | a0001c0001t0002g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.104-2585A>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56279108 | |||||||
| chr19:56279239 | C | T | 86 | a0001c0001t0001g0214 a0001c0001t0002g0001 a0001c0001t0002g0004 others(83): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.104-2454C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56279239 | |||||||
| chr19:56279487 | T | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0025 others(189): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.104-2206T>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56279487 | |||||||
| chr19:56279805 | T | A | 3 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0007g0290 |
3 | HG01074.hp1 NA18992.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.104-1888T>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56279805 | |||||||
| chr19:56280060 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.104-1633C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56280060 | |||||||
| chr19:56280291 | G | A | 87 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(84): Show |
107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.104-1402G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56280291 | |||||||
| chr19:56280305 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.104-1388A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56280305 | |||||||
| chr19:56280478 | G | C | 1 | a0001c0001t0007g0290 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.104-1215G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56280478 | |||||||
| chr19:56280538 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.104-1155C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56280538 | |||||||
| chr19:56280541 | G | C | 1 | a0001c0001t0002g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.104-1152G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56280541 | |||||||
| chr19:56280556 | G | A | 1 | a0001c0001t0002g0138 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.104-1137G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56280556 | |||||||
| chr19:56280652 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0004g0213 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.104-1041C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56280652 | |||||||
| chr19:56280729 | G | C | 10 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(7): Show |
10 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.104-964G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56280729 | |||||||
| chr19:56280803 | T | C | 2 | a0001c0001t0001g0293 a0001c0001t0004g0294 |
2 | HG02004.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.104-890T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56280803 | |||||||
| chr19:56280920 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.104-773C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56280920 | |||||||
| chr19:56281083 | A | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG02886.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.104-610A>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56281083 | |||||||
| chr19:56281120 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0192 others(2): Show |
7 | HG02258.hp2 HG02559.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.104-573G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56281120 | |||||||
| chr19:56281130 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.104-563T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56281130 | |||||||
| chr19:56281179 | A | T | 7 | a0001c0001t0001g0050 a0001c0001t0001g0084 a0001c0001t0001g0085 others(4): Show |
7 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.104-514A>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56281179 | |||||||
| chr19:56281216 | T | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0025 others(196): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.104-477T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56281216 | |||||||
| chr19:56281279 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0025 others(66): Show |
82 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.104-414G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56281279 | |||||||
| chr19:56281291 | G | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0025 others(189): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.104-402G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56281291 | |||||||
| chr19:56281357 | T | TGTGA | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(251): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.104-334_104-333ins others(4): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | 56281357 | ||||||
| chr19:56281451 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.104-242C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56281451 | |||||||
| chr19:56281520 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.104-173G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 2/14 | chr19 | 56281520 | |||||||
| chr19:56281841 | C | A | 1 | a0001c0001t0005g0114 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.109+143C>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 3/14 | chr19 | 56281841 | |||||||
| chr19:56282127 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.110-364G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 3/14 | chr19 | 56282127 | |||||||
| chr19:56282159 | C | T | 1 | a0001c0001t0006g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.110-332C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 3/14 | chr19 | 56282159 | |||||||
| chr19:56282555 | G | C | 1 | a0001c0001t0002g0120 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.118+56G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56282555 | |||||||
| chr19:56282660 | T | C | 1 | a0001c0001t0001g0042 | 2 | HG01069.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.118+161T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56282660 | |||||||
| chr19:56283204 | T | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(251): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.118+705T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283204 | |||||||
| chr19:56283261 | CATT | C | 7 | a0001c0001t0001g0051 a0001c0001t0001g0103 a0001c0001t0001g0333 others(4): Show |
7 | HG02258.hp1 HG02886.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+773_118+775del others(3): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 56283261 | ||||||
| chr19:56283276 | G | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0025 others(189): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.118+777G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283276 | |||||||
| chr19:56283394 | A | G | 1 | a0001c0001t0002g0186 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.119-804A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283394 | |||||||
| chr19:56283439 | C | T | 192 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0025 others(189): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.119-759C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283439 | |||||||
| chr19:56283475 | C | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
5 | NA18612.hp2 NA18948.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-723C>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283475 | |||||||
| chr19:56283610 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.119-588A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283610 | |||||||
| chr19:56283682 | CAG | C | 2 | a0001c0001t0002g0006 a0001c0001t0002g0024 |
5 | HG00099.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-510_119-509del others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | 56283682 | ||||||
| chr19:56283705 | C | T | 1 | a0001c0001t0003g0332 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.119-493C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283705 | |||||||
| chr19:56283746 | CG | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0192 others(2): Show |
7 | HG02258.hp2 HG02559.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-451delG | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283746 | |||||||
| chr19:56283769 | G | A | 90 | a0001c0001t0001g0283 a0001c0001t0002g0001 a0001c0001t0002g0004 others(87): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.119-429G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283769 | |||||||
| chr19:56283870 | T | C | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.119-328T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283870 | |||||||
| chr19:56283878 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.119-320T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283878 | |||||||
| chr19:56283894 | T | C | 1 | a0001c0001t0001g0295 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.119-304T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283894 | |||||||
| chr19:56283901 | A | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-297A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283901 | |||||||
| chr19:56283902 | G | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-296G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283902 | |||||||
| chr19:56283903 | A | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-295A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283903 | |||||||
| chr19:56283904 | A | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-294A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283904 | |||||||
| chr19:56283906 | G | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-292G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283906 | |||||||
| chr19:56283907 | G | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-291G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283907 | |||||||
| chr19:56283908 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-290T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283908 | |||||||
| chr19:56283909 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-289T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283909 | |||||||
| chr19:56283912 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-286T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283912 | |||||||
| chr19:56283913 | G | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-285G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283913 | |||||||
| chr19:56283914 | A | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-284A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283914 | |||||||
| chr19:56283915 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-283T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283915 | |||||||
| chr19:56283916 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-282T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283916 | |||||||
| chr19:56283917 | A | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-281A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283917 | |||||||
| chr19:56283919 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-279T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283919 | |||||||
| chr19:56283920 | G | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-278G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283920 | |||||||
| chr19:56283921 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-277T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283921 | |||||||
| chr19:56283925 | A | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-273A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283925 | |||||||
| chr19:56283926 | A | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-272A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283926 | |||||||
| chr19:56283929 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-269T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283929 | |||||||
| chr19:56283931 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-267T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283931 | |||||||
| chr19:56283932 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-266T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283932 | |||||||
| chr19:56283933 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-265T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283933 | |||||||
| chr19:56283935 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-263T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283935 | |||||||
| chr19:56283938 | A | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-260A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283938 | |||||||
| chr19:56283940 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-258T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283940 | |||||||
| chr19:56283941 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-257T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283941 | |||||||
| chr19:56283942 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-256T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283942 | |||||||
| chr19:56283943 | G | T | 1 | a0001c0001t0001g0274 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-255G>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283943 | |||||||
| chr19:56283948 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.119-250C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56283948 | |||||||
| chr19:56284127 | G | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0025 others(189): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.119-71G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56284127 | |||||||
| chr19:56284147 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.119-51C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 4/14 | chr19 | 56284147 | |||||||
| chr19:56284206 | G | GGTAA | 3 | a0001c0001t0002g0118 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG01891.hp2 HG02818.hp1 NA20300.hp2 |
splice_region_variant&intron_variant | LOW | c.127+4_127+7dupAGTA | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 56284206 | ||||||
| chr19:56284481 | AATTAG | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0025 others(180): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.127+282_127+286del others(5): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 56284481 | ||||||
| chr19:56284491 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.127+285G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | chr19 | 56284491 | |||||||
| chr19:56284505 | T | G | 90 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(87): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.127+299T>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | chr19 | 56284505 | |||||||
| chr19:56284513 | A | AT | 38 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0026 others(35): Show |
43 | HG00099.hp1 HG00639.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.127+328dupT | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 56284513 | ||||||
| chr19:56284513 | A | ATT | 7 | a0001c0001t0001g0029 a0001c0001t0001g0083 a0001c0001t0001g0205 others(4): Show |
8 | HG00280.hp1 HG01496.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.127+327_127+328dup others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 56284513 | ||||||
| chr19:56284513 | A | ATTT | 79 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(76): Show |
99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.127+326_127+328dup others(3): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 56284513 | ||||||
| chr19:56284513 | A | ATTTT | 8 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0179 others(5): Show |
8 | HG00738.hp1 HG00738.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.127+325_127+328dup others(4): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 56284513 | ||||||
| chr19:56284513 | AT | A | 9 | a0001c0001t0001g0060 a0001c0001t0001g0217 a0001c0001t0001g0219 others(6): Show |
9 | HG01168.hp2 HG02132.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.127+328delT | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 56284513 | ||||||
| chr19:56284513 | ATTTTTTT | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(54): Show |
68 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.127+322_127+328del others(7): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 56284513 | ||||||
| chr19:56284513 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.127+317_127+328del others(12): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr19 | 56284513 | ||||||
| chr19:56284608 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG02886.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.128-390G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | chr19 | 56284608 | |||||||
| chr19:56284673 | T | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(251): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.128-325T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | chr19 | 56284673 | |||||||
| chr19:56284785 | T | C | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02056.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.128-213T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | chr19 | 56284785 | |||||||
| chr19:56284803 | G | A | 5 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0140 others(2): Show |
7 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.128-195G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | chr19 | 56284803 | |||||||
| chr19:56284822 | T | C | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG02015.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.128-176T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 5/14 | chr19 | 56284822 | |||||||
| chr19:56285071 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0003g0282 |
2 | HG02129.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.154+47G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56285071 | |||||||
| chr19:56285202 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0003g0282 |
2 | HG02129.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.154+178C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56285202 | |||||||
| chr19:56285696 | G | C | 2 | a0001c0001t0001g0230 a0001c0001t0002g0185 |
2 | HG03831.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.154+672G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56285696 | |||||||
| chr19:56285714 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.154+690C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56285714 | |||||||
| chr19:56285719 | T | C | 2 | a0001c0001t0002g0142 a0001c0001t0002g0143 |
2 | HG01081.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.154+695T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56285719 | |||||||
| chr19:56285759 | A | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(77): Show |
91 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.154+735A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56285759 | |||||||
| chr19:56285777 | C | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0274 |
2 | NA18982.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.154+753C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56285777 | |||||||
| chr19:56285807 | A | C | 2 | a0001c0001t0001g0283 a0001c0001t0003g0282 |
2 | HG02129.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.154+783A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56285807 | |||||||
| chr19:56285945 | C | G | 1 | a0001c0001t0001g0269 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.154+921C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56285945 | |||||||
| chr19:56285957 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.154+933T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56285957 | |||||||
| chr19:56286114 | C | T | 1 | a0001c0001t0006g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.154+1090C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56286114 | |||||||
| chr19:56286149 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0003g0282 |
2 | HG02129.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.154+1125G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56286149 | |||||||
| chr19:56286176 | C | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.154+1152C>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56286176 | |||||||
| chr19:56286271 | C | T | 3 | a0001c0001t0001g0285 a0001c0001t0001g0336 a0001c0001t0006g0109 |
3 | HG02965.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.154+1247C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56286271 | |||||||
| chr19:56286382 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.154+1358A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56286382 | |||||||
| chr19:56286383 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0004g0213 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.154+1359C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56286383 | |||||||
| chr19:56286473 | CCTT | C | 17 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(14): Show |
21 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.154+1450_154+1452d others(5): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56286473 | |||||||
| chr19:56286510 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0056 others(104): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.154+1486G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56286510 | |||||||
| chr19:56286535 | A | C | 1 | a0001c0001t0001g0007 | 3 | HG02965.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.154+1511A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56286535 | |||||||
| chr19:56286577 | G | A | 152 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0025 others(149): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.154+1553G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56286577 | |||||||
| chr19:56286638 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.154+1614G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56286638 | |||||||
| chr19:56286791 | G | C | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(254): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.155-1594G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56286791 | |||||||
| chr19:56286861 | T | C | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(253): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.155-1524T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56286861 | |||||||
| chr19:56286951 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.155-1434C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56286951 | |||||||
| chr19:56287015 | A | G | 2 | a0001c0001t0001g0283 a0001c0001t0003g0282 |
2 | HG02129.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.155-1370A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56287015 | |||||||
| chr19:56287049 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0096 |
3 | HG02615.hp1 HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.155-1336A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56287049 | |||||||
| chr19:56287059 | T | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(76): Show |
90 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.155-1326T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56287059 | |||||||
| chr19:56287093 | T | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0192 others(2): Show |
7 | HG02258.hp2 HG02559.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.155-1292T>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56287093 | |||||||
| chr19:56287144 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.155-1241T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56287144 | |||||||
| chr19:56287257 | T | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0056 others(103): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.155-1128T>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56287257 | |||||||
| chr19:56287404 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.155-981G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56287404 | |||||||
| chr19:56287465 | A | G | 3 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 |
3 | NA19001.hp2 NA19057.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.155-920A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56287465 | |||||||
| chr19:56287497 | A | C | 16 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(13): Show |
19 | HG01109.hp2 HG01192.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.155-888A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56287497 | |||||||
| chr19:56287672 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.155-713G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56287672 | |||||||
| chr19:56287935 | A | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(77): Show |
91 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.155-450A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56287935 | |||||||
| chr19:56288097 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.155-288G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56288097 | |||||||
| chr19:56288216 | T | C | 5 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-169T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56288216 | |||||||
| chr19:56288241 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.155-144C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56288241 | |||||||
| chr19:56288276 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0056 others(104): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.155-109A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56288276 | |||||||
| chr19:56288282 | C | T | 4 | a0001c0001t0001g0103 a0001c0001t0003g0101 a0001c0001t0003g0102 others(1): Show |
4 | HG02258.hp1 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-103C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56288282 | |||||||
| chr19:56288299 | C | T | 5 | a0001c0001t0001g0060 a0001c0001t0001g0103 a0001c0001t0003g0101 others(2): Show |
5 | HG02258.hp1 HG02735.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-86C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 6/14 | chr19 | 56288299 | |||||||
| chr19:56288453 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.208+15C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 7/14 | chr19 | 56288453 | |||||||
| chr19:56288561 | A | T | 1 | a0001c0001t0002g0188 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.208+123A>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 7/14 | chr19 | 56288561 | |||||||
| chr19:56288765 | G | C | 34 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(31): Show |
39 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.209-109G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 7/14 | chr19 | 56288765 | |||||||
| chr19:56288833 | C | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0056 others(103): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.209-41C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 7/14 | chr19 | 56288833 | |||||||
| chr19:56289056 | C | G | 22 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(19): Show |
27 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.226+165C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56289056 | |||||||
| chr19:56289089 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.226+198C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56289089 | |||||||
| chr19:56289318 | G | A | 1 | a0001c0001t0002g0120 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.226+427G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56289318 | |||||||
| chr19:56289461 | T | C | 3 | a0001c0001t0001g0285 a0001c0001t0001g0336 a0001c0001t0006g0109 |
3 | HG02965.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.226+570T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56289461 | |||||||
| chr19:56289466 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0210 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.226+575C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56289466 | |||||||
| chr19:56289574 | A | G | 1 | a0001c0001t0005g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.226+683A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56289574 | |||||||
| chr19:56289760 | C | G | 1 | a0001c0001t0006g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.226+869C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56289760 | |||||||
| chr19:56289770 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.226+879T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56289770 | |||||||
| chr19:56289779 | A | G | 1 | a0001c0001t0003g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.226+888A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56289779 | |||||||
| chr19:56289836 | A | T | 1 | a0001c0001t0007g0290 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.226+945A>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56289836 | |||||||
| chr19:56289870 | T | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG02886.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.227-971T>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56289870 | |||||||
| chr19:56289969 | T | C | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | NA18612.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.227-872T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56289969 | |||||||
| chr19:56289979 | C | T | 4 | a0001c0001t0001g0283 a0001c0001t0001g0326 a0001c0001t0001g0327 others(1): Show |
4 | HG01884.hp1 HG02129.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-862C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56289979 | |||||||
| chr19:56290066 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0003g0282 |
2 | HG02129.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.227-775C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56290066 | |||||||
| chr19:56290097 | C | A | 1 | a0001c0001t0001g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.227-744C>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56290097 | |||||||
| chr19:56290136 | A | G | 1 | a0001c0007t0001g0284 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.227-705A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56290136 | |||||||
| chr19:56290385 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0004g0213 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.227-456C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56290385 | |||||||
| chr19:56290803 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.227-38A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 8/14 | chr19 | 56290803 | |||||||
| chr19:56291065 | G | A | 1 | a0001c0001t0006g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232+219G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56291065 | |||||||
| chr19:56291180 | T | C | 1 | a0001c0001t0002g0022 | 2 | NA18985.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.232+334T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56291180 | |||||||
| chr19:56291325 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.232+479C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56291325 | |||||||
| chr19:56291455 | C | A | 2 | a0001c0001t0001g0283 a0001c0001t0003g0282 |
2 | HG02129.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.232+609C>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56291455 | |||||||
| chr19:56291522 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.232+676G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56291522 | |||||||
| chr19:56291626 | A | G | 8 | a0001c0001t0001g0050 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
8 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.232+780A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56291626 | |||||||
| chr19:56291903 | T | C | 24 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(21): Show |
27 | HG01109.hp2 HG01192.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.232+1057T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56291903 | |||||||
| chr19:56291915 | G | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0034 a0001c0001t0001g0249 others(6): Show |
9 | HG01934.hp2 HG01978.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.232+1069G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56291915 | |||||||
| chr19:56292004 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0056 others(105): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.232+1158G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292004 | |||||||
| chr19:56292019 | G | C | 6 | a0001c0001t0001g0231 a0001c0001t0001g0331 a0001c0001t0003g0232 others(3): Show |
6 | HG01106.hp2 HG01952.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.232+1173G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292019 | |||||||
| chr19:56292052 | T | C | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(224): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.232+1206T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292052 | |||||||
| chr19:56292221 | T | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0039 others(56): Show |
72 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.232+1375T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292221 | |||||||
| chr19:56292278 | A | G | 2 | a0001c0001t0001g0283 a0001c0001t0003g0282 |
2 | HG02129.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.232+1432A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292278 | |||||||
| chr19:56292448 | T | C | 24 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(21): Show |
27 | HG01109.hp2 HG01192.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.232+1602T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292448 | |||||||
| chr19:56292451 | G | GTTTTTAC others(10): Show |
1 | a0001c0001t0001g0042 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.232+1609_232+1625d others(19): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56292451 | ||||||
| chr19:56292451 | G | GTTTTTAC others(11): Show |
57 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0039 others(54): Show |
68 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.232+1608_232+1625d others(20): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56292451 | ||||||
| chr19:56292451 | G | GTTTTTAC others(12): Show |
1 | a0001c0001t0003g0321 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.232+1607_232+1625d others(21): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56292451 | ||||||
| chr19:56292458 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0307 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.232+1625_232+1626i others(21): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56292458 | ||||||
| chr19:56292512 | T | G | 1 | a0001c0001t0002g0138 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.232+1666T>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292512 | |||||||
| chr19:56292514 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0039 others(62): Show |
77 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.232+1668C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292514 | |||||||
| chr19:56292532 | C | T | 1 | a0001c0001t0002g0006 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.232+1686C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292532 | |||||||
| chr19:56292610 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0004g0213 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.232+1764T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292610 | |||||||
| chr19:56292684 | A | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0039 others(52): Show |
67 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.232+1838A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292684 | |||||||
| chr19:56292703 | T | C | 7 | a0001c0001t0002g0001 a0001c0001t0002g0021 a0001c0001t0002g0115 others(4): Show |
9 | HG01256.hp2 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.232+1857T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292703 | |||||||
| chr19:56292743 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0039 others(56): Show |
71 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.232+1897G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292743 | |||||||
| chr19:56292811 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.232+1965G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292811 | |||||||
| chr19:56292817 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.232+1971G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292817 | |||||||
| chr19:56292928 | T | C | 1 | a0001c0001t0001g0309 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.232+2082T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56292928 | |||||||
| chr19:56293058 | C | T | 6 | a0001c0001t0001g0293 a0001c0001t0001g0299 a0001c0001t0001g0300 others(3): Show |
6 | HG00741.hp2 HG02004.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.232+2212C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56293058 | |||||||
| chr19:56293104 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0091 a0001c0001t0001g0095 |
3 | HG02109.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.232+2258T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56293104 | |||||||
| chr19:56293120 | G | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0192 others(2): Show |
7 | HG02258.hp2 HG02559.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.232+2274G>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56293120 | |||||||
| chr19:56293395 | C | A | 8 | a0001c0001t0002g0021 a0001c0001t0002g0120 a0001c0001t0002g0121 others(5): Show |
9 | HG01256.hp2 HG01361.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.232+2549C>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56293395 | |||||||
| chr19:56293408 | C | T | 16 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(13): Show |
19 | HG00738.hp1 HG01109.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.233-2551C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56293408 | |||||||
| chr19:56293416 | C | T | 8 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0024 others(5): Show |
11 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.233-2543C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56293416 | |||||||
| chr19:56293575 | C | T | 6 | a0001c0001t0001g0293 a0001c0001t0001g0299 a0001c0001t0001g0300 others(3): Show |
6 | HG00741.hp2 HG02004.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.233-2384C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56293575 | |||||||
| chr19:56293631 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.233-2328T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56293631 | |||||||
| chr19:56293738 | A | C | 4 | a0001c0001t0004g0213 a0001c0002t0001g0045 a0001c0002t0001g0046 others(1): Show |
5 | HG02976.hp2 HG03098.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-2221A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56293738 | |||||||
| chr19:56293843 | C | T | 4 | a0001c0001t0004g0213 a0001c0002t0001g0045 a0001c0002t0001g0046 others(1): Show |
5 | HG02976.hp2 HG03098.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-2116C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56293843 | |||||||
| chr19:56293855 | C | CA | 6 | a0001c0001t0001g0293 a0001c0001t0001g0299 a0001c0001t0001g0300 others(3): Show |
6 | HG00741.hp2 HG02004.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.233-2097dupA | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr19 | 56293855 | ||||||
| chr19:56293903 | C | A | 2 | a0001c0001t0001g0283 a0001c0001t0003g0282 |
2 | HG02129.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.233-2056C>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56293903 | |||||||
| chr19:56293951 | T | G | 23 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0051 others(20): Show |
26 | HG01070.hp2 HG01261.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.233-2008T>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56293951 | |||||||
| chr19:56293991 | C | T | 6 | a0001c0001t0001g0293 a0001c0001t0001g0299 a0001c0001t0001g0300 others(3): Show |
6 | HG00741.hp2 HG02004.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.233-1968C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56293991 | |||||||
| chr19:56294103 | C | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG02015.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.233-1856C>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56294103 | |||||||
| chr19:56294676 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0003g0282 |
2 | HG02129.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.233-1283C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56294676 | |||||||
| chr19:56294694 | C | T | 2 | a0001c0001t0003g0271 a0001c0001t0005g0174 |
2 | HG01261.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.233-1265C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56294694 | |||||||
| chr19:56294957 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0050 others(105): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.233-1002G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56294957 | |||||||
| chr19:56294979 | G | T | 179 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(176): Show |
208 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.233-980G>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56294979 | |||||||
| chr19:56294981 | G | C | 5 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0148 others(2): Show |
5 | HG01257.hp2 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-978G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56294981 | |||||||
| chr19:56295110 | G | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(18): Show |
24 | HG01109.hp2 HG01192.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.233-849G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56295110 | |||||||
| chr19:56295266 | G | A | 1 | a0002c0004t0001g0031 | 2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.233-693G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56295266 | |||||||
| chr19:56295550 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
5 | NA18612.hp2 NA18948.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.233-409G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56295550 | |||||||
| chr19:56295868 | G | A | 1 | a0001c0007t0001g0284 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.233-91G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56295868 | |||||||
| chr19:56295885 | T | C | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(314): Show |
372 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(369): Show |
intron_variant | MODIFIER | c.233-74T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 9/14 | chr19 | 56295885 | |||||||
| chr19:56296129 | G | A | 1 | a0001c0001t0003g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.241+162G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 10/14 | chr19 | 56296129 | |||||||
| chr19:56296129 | G | T | 1 | a0001c0001t0002g0138 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.241+162G>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 10/14 | chr19 | 56296129 | |||||||
| chr19:56296212 | G | A | 1 | a0001c0001t0002g0128 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.242-124G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 10/14 | chr19 | 56296212 | |||||||
| chr19:56296422 | G | GT | 152 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(149): Show |
179 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.268+66dupT | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56296422 | ||||||
| chr19:56296615 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.268+253A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 11/14 | chr19 | 56296615 | |||||||
| chr19:56296669 | T | C | 1 | a0001c0001t0003g0271 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.268+307T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 11/14 | chr19 | 56296669 | |||||||
| chr19:56296696 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG02886.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.268+334A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 11/14 | chr19 | 56296696 | |||||||
| chr19:56296776 | G | C | 1 | a0001c0001t0006g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.268+414G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 11/14 | chr19 | 56296776 | |||||||
| chr19:56296791 | T | G | 23 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0056 others(20): Show |
25 | HG01109.hp1 HG01884.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.268+429T>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 11/14 | chr19 | 56296791 | |||||||
| chr19:56296862 | C | T | 1 | a0001c0001t0003g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.268+500C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 11/14 | chr19 | 56296862 | |||||||
| chr19:56297069 | C | CA | 109 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0027 others(106): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.269-425dupA | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr19 | 56297069 | ||||||
| chr19:56297093 | C | T | 6 | a0001c0001t0001g0293 a0001c0001t0001g0299 a0001c0001t0001g0300 others(3): Show |
6 | HG00741.hp2 HG02004.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.269-412C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 11/14 | chr19 | 56297093 | |||||||
| chr19:56297279 | C | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0195 |
5 | HG01074.hp2 HG01256.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.269-226C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 11/14 | chr19 | 56297279 | |||||||
| chr19:56297606 | TAGAAGAG others(29): Show |
T | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.295+76_295+111delA others(35): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56297606 | |||||||
| chr19:56297742 | A | G | 2 | a0001c0001t0001g0264 a0001c0001t0001g0273 |
2 | HG02080.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.295+211A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56297742 | |||||||
| chr19:56297968 | G | A | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.295+437G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56297968 | |||||||
| chr19:56298067 | C | CA | 32 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(29): Show |
35 | HG00438.hp1 HG00642.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.295+552dupA | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr19 | 56298067 | ||||||
| chr19:56298153 | C | T | 310 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(307): Show |
363 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.295+622C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56298153 | |||||||
| chr19:56298249 | T | A | 1 | a0001c0001t0001g0084 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.295+718T>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56298249 | |||||||
| chr19:56298366 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.295+835G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56298366 | |||||||
| chr19:56298428 | G | C | 3 | a0001c0001t0004g0213 a0001c0002t0001g0045 a0001c0002t0001g0046 |
3 | HG03130.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.295+897G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56298428 | |||||||
| chr19:56298608 | G | A | 5 | a0001c0001t0001g0050 a0001c0001t0001g0085 a0001c0001t0001g0086 others(2): Show |
5 | HG02451.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.295+1077G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56298608 | |||||||
| chr19:56298635 | G | C | 1 | a0001c0001t0001g0273 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.295+1104G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56298635 | |||||||
| chr19:56298651 | CA | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0025 others(115): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.295+1136delA | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr19 | 56298651 | ||||||
| chr19:56298651 | CAA | C | 64 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(61): Show |
69 | HG00642.hp2 HG00733.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.295+1135_295+1136d others(4): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr19 | 56298651 | ||||||
| chr19:56298684 | T | G | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG03130.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.295+1153T>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56298684 | |||||||
| chr19:56298749 | A | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG02886.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.295+1218A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56298749 | |||||||
| chr19:56298969 | C | G | 1 | a0001c0001t0001g0262 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.295+1438C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56298969 | |||||||
| chr19:56298984 | T | A | 4 | a0001c0001t0002g0004 a0001c0001t0002g0125 a0001c0001t0002g0151 others(1): Show |
6 | HG00558.hp2 NA18939.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.295+1453T>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56298984 | |||||||
| chr19:56299163 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.295+1632G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56299163 | |||||||
| chr19:56299214 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.295+1683C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56299214 | |||||||
| chr19:56299444 | T | TA | 46 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(43): Show |
49 | HG00642.hp2 HG00733.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.295+1927dupA | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr19 | 56299444 | ||||||
| chr19:56299445 | A | T | 1 | a0001c0001t0003g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.295+1914A>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56299445 | |||||||
| chr19:56299595 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.295+2064G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56299595 | |||||||
| chr19:56299663 | G | T | 1 | a0001c0001t0001g0214 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.295+2132G>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56299663 | |||||||
| chr19:56299762 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.296-2206T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56299762 | |||||||
| chr19:56299937 | C | T | 1 | a0005c0005t0001g0261 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.296-2031C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56299937 | |||||||
| chr19:56299982 | A | G | 1 | a0001c0001t0002g0170 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.296-1986A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56299982 | |||||||
| chr19:56300068 | A | C | 18 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0058 others(15): Show |
18 | HG00642.hp2 HG00733.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.296-1900A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56300068 | |||||||
| chr19:56300078 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG02886.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.296-1890G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56300078 | |||||||
| chr19:56300153 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.296-1815A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56300153 | |||||||
| chr19:56300254 | A | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0061 a0003c0009t0004g0062 |
5 | HG01884.hp2 HG02257.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.296-1714A>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56300254 | |||||||
| chr19:56300606 | C | T | 1 | a0001c0001t0003g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.296-1362C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56300606 | |||||||
| chr19:56300802 | TA | T | 23 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0058 others(20): Show |
23 | HG00642.hp2 HG00733.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.296-1156delA | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr19 | 56300802 | ||||||
| chr19:56300815 | A | C | 1 | a0001c0001t0001g0044 | 2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.296-1153A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56300815 | |||||||
| chr19:56300873 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0215 a0001c0001t0002g0118 |
3 | HG01891.hp2 NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.296-1095C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56300873 | |||||||
| chr19:56301042 | G | A | 42 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(39): Show |
46 | HG01109.hp1 HG01109.hp2 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.296-926G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301042 | |||||||
| chr19:56301081 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.296-887G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301081 | |||||||
| chr19:56301090 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.296-878C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301090 | |||||||
| chr19:56301155 | A | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0060 others(84): Show |
106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.296-813A>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301155 | |||||||
| chr19:56301215 | G | C | 1 | a0001c0001t0001g0291 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.296-753G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301215 | |||||||
| chr19:56301221 | C | T | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
106 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.296-747C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301221 | |||||||
| chr19:56301273 | G | A | 1 | a0001c0001t0005g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.296-695G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301273 | |||||||
| chr19:56301383 | A | G | 1 | a0001c0001t0002g0169 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.296-585A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301383 | |||||||
| chr19:56301403 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0202 |
2 | HG01516.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.296-565C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301403 | |||||||
| chr19:56301517 | G | A | 156 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(153): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.296-451G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301517 | |||||||
| chr19:56301545 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01192.hp2 HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.296-423C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301545 | |||||||
| chr19:56301647 | C | G | 13 | a0001c0001t0001g0044 a0001c0001t0001g0063 a0001c0001t0001g0064 others(10): Show |
14 | HG01109.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.296-321C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301647 | |||||||
| chr19:56301744 | T | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG02886.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.296-224T>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301744 | |||||||
| chr19:56301824 | T | C | 45 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0048 others(42): Show |
48 | HG00642.hp2 HG00733.hp1 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.296-144T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301824 | |||||||
| chr19:56301919 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.296-49G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301919 | |||||||
| chr19:56301955 | C | T | 1 | a0001c0001t0006g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.296-13C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 12/14 | chr19 | 56301955 | |||||||
| chr19:56302151 | G | C | 9 | a0001c0001t0001g0050 a0001c0001t0001g0066 a0001c0001t0001g0085 others(6): Show |
9 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.423+56G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302151 | |||||||
| chr19:56302159 | G | A | 4 | a0001c0001t0001g0092 a0001c0001t0002g0138 a0001c0001t0002g0189 others(1): Show |
4 | HG02257.hp2 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+64G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302159 | |||||||
| chr19:56302179 | A | G | 7 | a0001c0001t0001g0066 a0001c0001t0001g0100 a0001c0001t0001g0210 others(4): Show |
7 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.423+84A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302179 | |||||||
| chr19:56302252 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0002g0137 |
2 | HG02080.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.423+157C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302252 | |||||||
| chr19:56302254 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.423+159C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302254 | |||||||
| chr19:56302258 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.423+163C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302258 | |||||||
| chr19:56302272 | A | G | 16 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0055 others(13): Show |
16 | HG02080.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.423+177A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302272 | |||||||
| chr19:56302309 | TCTCC | T | 36 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0204 others(33): Show |
43 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.423+228_423+231del others(4): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302309 | ||||||
| chr19:56302312 | C | T | 14 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(11): Show |
14 | HG01109.hp1 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.423+217C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302312 | |||||||
| chr19:56302323 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(187): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.423+228T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302323 | |||||||
| chr19:56302324 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(187): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.423+229C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302324 | |||||||
| chr19:56302325 | C | T | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(188): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.423+230C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302325 | |||||||
| chr19:56302329 | T | C | 1 | a0001c0001t0003g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.423+234T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302329 | |||||||
| chr19:56302397 | A | G | 7 | a0001c0001t0001g0011 a0001c0001t0001g0240 a0001c0001t0001g0258 others(4): Show |
9 | HG02040.hp2 HG02129.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.423+302A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302397 | |||||||
| chr19:56302430 | CCCTT | C | 39 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0027 others(36): Show |
46 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.423+344_423+347del others(4): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302430 | ||||||
| chr19:56302430 | CCCTTCCT others(1): Show |
C | 8 | a0001c0001t0001g0011 a0001c0001t0001g0238 a0001c0001t0001g0258 others(5): Show |
10 | HG02040.hp2 HG02129.hp1 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.423+340_423+347del others(8): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302430 | ||||||
| chr19:56302439 | C | T | 10 | a0001c0001t0001g0051 a0001c0001t0001g0067 a0001c0001t0001g0106 others(7): Show |
10 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.423+344C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302439 | |||||||
| chr19:56302484 | C | CCATCCTT others(21): Show |
1 | a0001c0001t0004g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.423+404_423+405ins others(28): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302484 | ||||||
| chr19:56302484 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(203): Show |
240 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(237): Show |
intron_variant | MODIFIER | c.423+389C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302484 | |||||||
| chr19:56302510 | TTTCC | T | 36 | a0001c0001t0001g0015 a0001c0001t0001g0051 a0001c0001t0001g0052 others(33): Show |
38 | HG00323.hp2 HG00438.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.423+421_423+424del others(4): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302510 | ||||||
| chr19:56302516 | T | C | 3 | a0001c0001t0001g0214 a0001c0001t0001g0327 a0001c0001t0003g0282 |
3 | HG01884.hp1 HG02129.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.423+421T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302516 | |||||||
| chr19:56302516 | TCCTC | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
106 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.423+434_423+437del others(4): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302516 | ||||||
| chr19:56302522 | C | CTCCCTCT others(207): Show |
1 | a0001c0001t0001g0291 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.423+433_423+434ins others(214): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302522 | ||||||
| chr19:56302529 | CCTCT | C | 98 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0027 others(95): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.423+435_423+438del others(4): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302529 | |||||||
| chr19:56302530 | CTCT | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0195 a0001c0001t0003g0304 |
4 | HG01074.hp2 HG01346.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+441_423+443del others(3): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302530 | ||||||
| chr19:56302532 | C | T | 1 | a0001c0001t0003g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.423+437C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302532 | |||||||
| chr19:56302533 | T | C | 5 | a0001c0001t0001g0214 a0001c0001t0001g0327 a0001c0001t0002g0119 others(2): Show |
5 | HG00438.hp2 HG01884.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.423+438T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302533 | |||||||
| chr19:56302545 | G | GTTCCTCC others(17): Show |
1 | a0001c0001t0003g0227 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.423+462_423+463ins others(24): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302545 | ||||||
| chr19:56302545 | G | GTTCCTCC others(21): Show |
30 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(27): Show |
34 | HG01175.hp1 HG01978.hp1 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.423+459_423+486dup others(28): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302545 | ||||||
| chr19:56302545 | G | GTTCCTCC others(49): Show |
2 | a0001c0001t0001g0058 a0001c0001t0002g0117 |
2 | NA19082.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.423+486_423+487ins others(56): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302545 | ||||||
| chr19:56302545 | G | GTTCCTCC others(104): Show |
1 | a0001c0001t0001g0071 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.423+486_423+487ins others(111): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302545 | ||||||
| chr19:56302545 | G | GTTCCTCC others(133): Show |
1 | a0001c0001t0001g0069 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.423+486_423+487ins others(140): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302545 | ||||||
| chr19:56302545 | G | GTTCCTCC others(21): Show |
1 | a0001c0001t0001g0255 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.423+467_423+468ins others(28): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302545 | ||||||
| chr19:56302545 | G | T | 1 | a0001c0001t0003g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.423+450G>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302545 | |||||||
| chr19:56302547 | T | TCCTCCCT others(68): Show |
3 | a0001c0001t0001g0050 a0001c0001t0001g0085 a0001c0001t0001g0099 |
3 | HG02896.hp2 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.423+467_423+468ins others(75): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302547 | ||||||
| chr19:56302547 | TCCTC | T | 73 | a0001c0001t0001g0048 a0001c0001t0001g0060 a0001c0001t0001g0080 others(70): Show |
90 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.423+463_423+466del others(4): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302547 | ||||||
| chr19:56302551 | C | CCCTCCCC others(136): Show |
1 | a0001c0001t0002g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.423+462_423+463ins others(143): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302551 | ||||||
| chr19:56302555 | C | CCCCCCTT others(47): Show |
1 | a0001c0001t0002g0184 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.423+462_423+463ins others(54): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302555 | ||||||
| chr19:56302558 | T | C | 1 | a0001c0001t0005g0114 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.423+463T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302558 | |||||||
| chr19:56302561 | C | T | 2 | a0001c0001t0002g0184 a0001c0001t0005g0114 |
2 | HG01175.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.423+466C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302561 | |||||||
| chr19:56302562 | C | T | 1 | a0001c0001t0005g0114 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.423+467C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302562 | |||||||
| chr19:56302563 | C | CCTTCCTT others(122): Show |
1 | a0001c0001t0001g0335 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.423+486_423+487ins others(129): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302563 | ||||||
| chr19:56302563 | C | CT | 9 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0089 others(6): Show |
9 | HG01081.hp1 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.423+468_423+469ins others(1): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302563 | |||||||
| chr19:56302563 | C | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(51): Show |
69 | HG00438.hp1 HG00673.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.423+468C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302563 | |||||||
| chr19:56302563 | CCTTCCTT others(1): Show |
C | 15 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0001g0214 others(12): Show |
16 | HG00642.hp1 HG01081.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.423+469_423+476del others(8): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302563 | |||||||
| chr19:56302566 | T | TTTCTTCC others(4): Show |
1 | a0001c0001t0005g0114 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.423+471_423+472ins others(11): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302566 | |||||||
| chr19:56302566 | TCCTTTTC others(8): Show |
T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0278 others(5): Show |
11 | HG03710.hp2 HG04184.hp1 HG04199.hp1 others(8): Show |
intron_variant | MODIFIER | c.423+485_423+499del others(15): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302566 | ||||||
| chr19:56302575 | TCCTCCC | T | 15 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0001g0214 others(12): Show |
16 | HG00642.hp1 HG01081.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.423+484_423+489del others(6): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302575 | ||||||
| chr19:56302580 | CCCCTTTT others(8): Show |
C | 62 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(59): Show |
76 | HG00438.hp1 HG00673.hp1 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.423+490_423+504del others(15): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302580 | ||||||
| chr19:56302581 | C | CCCTCTT | 4 | a0001c0001t0001g0051 a0001c0001t0001g0210 a0001c0001t0001g0323 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+489_423+490ins others(6): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302581 | ||||||
| chr19:56302581 | C | CCCTCTTC others(56): Show |
2 | a0001c0001t0001g0212 a0001c0001t0001g0298 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.423+489_423+490ins others(63): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302581 | ||||||
| chr19:56302581 | C | CCCTCTTC others(134): Show |
1 | a0001c0001t0001g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.423+489_423+490ins others(141): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302581 | ||||||
| chr19:56302581 | C | CCCTTTTC others(13): Show |
1 | a0001c0001t0001g0231 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.423+499_423+500ins others(20): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302581 | ||||||
| chr19:56302581 | C | CCTCTT | 9 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0001g0090 others(6): Show |
9 | HG01243.hp2 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.423+487_423+488ins others(5): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302581 | ||||||
| chr19:56302581 | C | CTCCCTCC others(6): Show |
24 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(21): Show |
29 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.423+486_423+487ins others(13): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(104): Show |
1 | a0001c0001t0001g0077 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.423+486_423+487ins others(111): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(27): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0061 |
3 | HG01884.hp2 HG02486.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.423+486_423+487ins others(34): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(177): Show |
1 | a0001c0001t0001g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.423+486_423+487ins others(184): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(255): Show |
1 | a0001c0001t0001g0028 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.423+486_423+487ins others(262): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(61): Show |
1 | a0001c0001t0001g0322 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.423+486_423+487ins others(68): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(146): Show |
1 | a0001c0001t0001g0250 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.423+486_423+487ins others(153): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(84): Show |
5 | a0001c0001t0001g0029 a0001c0001t0001g0076 a0001c0001t0001g0199 others(2): Show |
5 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.423+486_423+487ins others(91): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(198): Show |
1 | a0001c0001t0001g0204 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.423+486_423+487ins others(205): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(162): Show |
1 | a0001c0001t0001g0207 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.423+486_423+487ins others(169): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(189): Show |
1 | a0001c0001t0001g0237 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.423+486_423+487ins others(196): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(69): Show |
1 | a0001c0001t0003g0282 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.423+486_423+487ins others(76): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(34): Show |
5 | a0001c0001t0001g0026 a0001c0001t0001g0195 a0001c0001t0001g0215 others(2): Show |
6 | HG00642.hp2 HG01074.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.423+486_423+487ins others(41): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(112): Show |
1 | a0001c0001t0001g0029 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.423+486_423+487ins others(119): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(62): Show |
1 | a0001c0007t0001g0284 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.423+486_423+487ins others(69): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(90): Show |
1 | a0001c0001t0001g0075 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.423+486_423+487ins others(97): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(244): Show |
1 | a0001c0001t0001g0217 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.423+486_423+487ins others(251): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(63): Show |
1 | a0001c0001t0003g0012 | 2 | NA18952.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.423+486_423+487ins others(70): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(62): Show |
1 | a0001c0001t0003g0211 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.423+486_423+487ins others(69): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(35): Show |
2 | a0001c0001t0002g0191 a0001c0001t0003g0012 |
2 | HG04228.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.423+486_423+487ins others(42): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(34): Show |
2 | a0001c0001t0001g0229 a0001c0001t0001g0281 |
2 | HG02523.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.423+486_423+487ins others(41): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(58): Show |
1 | a0001c0001t0001g0003 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.423+486_423+487ins others(65): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(7): Show |
1 | a0001c0001t0001g0219 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.423+486_423+487ins others(14): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302581 | C | CTCCCTCC others(6): Show |
5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0070 others(2): Show |
5 | NA18994.hp1 NA19002.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+486_423+487ins others(13): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302581 | |||||||
| chr19:56302585 | T | C | 4 | a0001c0001t0001g0305 a0001c0001t0001g0313 a0001c0001t0002g0143 others(1): Show |
4 | HG00639.hp1 HG01081.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+490T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302585 | |||||||
| chr19:56302585 | TTTCTTCC others(8): Show |
T | 24 | a0001c0001t0001g0015 a0001c0001t0001g0055 a0001c0001t0001g0057 others(21): Show |
25 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.423+509_423+523del others(15): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302585 | ||||||
| chr19:56302595 | T | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(95): Show |
110 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.423+500T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302595 | |||||||
| chr19:56302595 | T | TCCCTCTT others(36): Show |
1 | a0001c0001t0001g0194 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.423+508_423+509ins others(43): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302595 | ||||||
| chr19:56302595 | T | TCCCTCTT others(56): Show |
2 | a0001c0001t0001g0248 a0001c0001t0003g0232 |
2 | HG01943.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.423+508_423+509ins others(63): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302595 | ||||||
| chr19:56302595 | T | TCCCTCTT others(76): Show |
1 | a0001c0001t0005g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.423+508_423+509ins others(83): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302595 | ||||||
| chr19:56302595 | T | TCCCTCTT others(60): Show |
3 | a0001c0001t0001g0025 a0001c0003t0001g0025 a0001c0003t0001g0193 |
3 | HG02258.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.423+508_423+509ins others(67): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302595 | ||||||
| chr19:56302595 | T | TCCCTCTT others(8): Show |
2 | a0001c0001t0001g0066 a0001c0001t0001g0313 |
2 | NA18906.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.423+514_423+515ins others(15): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302595 | ||||||
| chr19:56302600 | C | CTTCCTCC others(64): Show |
1 | a0001c0001t0001g0295 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.423+508_423+509ins others(71): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302600 | ||||||
| chr19:56302600 | C | T | 36 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(33): Show |
42 | HG00280.hp1 HG00642.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.423+505C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302600 | |||||||
| chr19:56302604 | T | C | 4 | a0001c0001t0001g0058 a0001c0001t0001g0068 a0001c0001t0002g0143 others(1): Show |
4 | HG01081.hp1 HG02698.hp1 NA19091.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+509T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302604 | |||||||
| chr19:56302607 | CT | C | 4 | a0001c0001t0001g0058 a0001c0001t0001g0068 a0001c0001t0002g0143 others(1): Show |
4 | HG01081.hp1 HG02698.hp1 NA19091.hp2 others(1): Show |
intron_variant | MODIFIER | c.423+513delT | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302607 | |||||||
| chr19:56302608 | TCTCCCTC others(7): Show |
T | 1 | a0001c0001t0001g0276 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.423+521_423+534del others(14): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302608 | ||||||
| chr19:56302616 | T | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0068 a0001c0001t0002g0143 others(2): Show |
5 | HG01081.hp1 HG02698.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.423+521T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302616 | |||||||
| chr19:56302654 | CCT | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0026 others(18): Show |
26 | HG00733.hp1 HG01074.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.423+561_423+562del others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302654 | ||||||
| chr19:56302660 | T | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0026 others(24): Show |
32 | HG00733.hp1 HG01074.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.423+565T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302660 | |||||||
| chr19:56302675 | CCTTCCCT others(28): Show |
C | 1 | a0001c0001t0003g0234 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.423+590_423+624del others(35): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56302675 | ||||||
| chr19:56302710 | T | C | 174 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(171): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.423+615T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302710 | |||||||
| chr19:56302820 | G | A | 1 | a0001c0001t0001g0322 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.423+725G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302820 | |||||||
| chr19:56302960 | C | T | 1 | a0001c0001t0001g0044 | 2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.423+865C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56302960 | |||||||
| chr19:56303071 | C | G | 17 | a0001c0001t0001g0051 a0001c0001t0001g0087 a0001c0001t0001g0272 others(14): Show |
19 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.423+976C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56303071 | |||||||
| chr19:56303107 | G | A | 8 | a0001c0001t0001g0103 a0001c0001t0003g0101 a0001c0001t0003g0102 others(5): Show |
9 | HG02129.hp1 HG02258.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.423+1012G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56303107 | |||||||
| chr19:56303202 | G | A | 6 | a0001c0001t0001g0103 a0001c0001t0003g0101 a0001c0001t0003g0102 others(3): Show |
7 | HG02258.hp1 HG02818.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.423+1107G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56303202 | |||||||
| chr19:56303208 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0192 |
2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.423+1113G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56303208 | |||||||
| chr19:56303218 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.423+1123G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56303218 | |||||||
| chr19:56303251 | G | A | 5 | a0001c0001t0001g0047 a0001c0001t0001g0083 a0001c0001t0004g0294 others(2): Show |
5 | HG02004.hp1 HG02109.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.423+1156G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56303251 | |||||||
| chr19:56303659 | G | A | 3 | a0001c0001t0003g0227 a0001c0001t0003g0282 a0001c0001t0005g0178 |
3 | HG02129.hp1 HG04115.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.424-1134G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56303659 | |||||||
| chr19:56303828 | TA | T | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(246): Show |
293 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.424-963delA | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr19 | 56303828 | ||||||
| chr19:56303885 | C | T | 2 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.424-908C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56303885 | |||||||
| chr19:56303963 | G | A | 114 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0028 others(111): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.424-830G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56303963 | |||||||
| chr19:56304058 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.424-735A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304058 | |||||||
| chr19:56304067 | T | C | 10 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0092 others(7): Show |
10 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.424-726T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304067 | |||||||
| chr19:56304148 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.424-645G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304148 | |||||||
| chr19:56304162 | C | G | 26 | a0001c0001t0001g0087 a0001c0001t0001g0092 a0001c0001t0001g0093 others(23): Show |
28 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.424-631C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304162 | |||||||
| chr19:56304199 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.424-594T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304199 | |||||||
| chr19:56304200 | G | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0047 others(8): Show |
13 | HG01109.hp2 HG02004.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.424-593G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304200 | |||||||
| chr19:56304228 | C | G | 1 | a0001c0001t0001g0259 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.424-565C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304228 | |||||||
| chr19:56304306 | A | G | 1 | a0001c0001t0002g0138 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.424-487A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304306 | |||||||
| chr19:56304431 | A | C | 1 | a0001c0001t0002g0024 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.424-362A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304431 | |||||||
| chr19:56304470 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.424-323G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304470 | |||||||
| chr19:56304489 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0002g0163 |
2 | NA18971.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.424-304C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304489 | |||||||
| chr19:56304494 | A | G | 1 | a0001c0001t0002g0168 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.424-299A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304494 | |||||||
| chr19:56304554 | G | A | 77 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(74): Show |
83 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.424-239G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304554 | |||||||
| chr19:56304594 | G | A | 80 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(77): Show |
86 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.424-199G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304594 | |||||||
| chr19:56304600 | A | T | 8 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0100 others(5): Show |
8 | HG01891.hp2 HG02129.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.424-193A>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304600 | |||||||
| chr19:56304707 | G | C | 3 | a0001c0001t0003g0227 a0001c0001t0003g0282 a0001c0001t0005g0178 |
3 | HG02129.hp1 HG04115.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.424-86G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304707 | |||||||
| chr19:56304791 | A | C | 3 | a0001c0001t0003g0227 a0001c0001t0003g0282 a0001c0001t0005g0178 |
3 | HG02129.hp1 HG04115.hp2 NA18960.hp2 |
splice_acceptor_variant&intron_variant | HIGH | c.424-2A>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 13/14 | chr19 | 56304791 | |||||||
| chr19:56304863 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.461+33C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56304863 | |||||||
| chr19:56305046 | T | C | 93 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(90): Show |
101 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.461+216T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56305046 | |||||||
| chr19:56305120 | C | G | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.461+290C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56305120 | |||||||
| chr19:56305208 | C | A | 1 | a0001c0001t0001g0245 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.461+378C>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56305208 | |||||||
| chr19:56305245 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.461+415G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56305245 | |||||||
| chr19:56305255 | CCT | C | 51 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(48): Show |
57 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.461+426_461+427del others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56305255 | |||||||
| chr19:56305308 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0052 others(4): Show |
9 | HG02145.hp2 HG02258.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.461+478T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56305308 | |||||||
| chr19:56305384 | C | G | 8 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0075 others(5): Show |
8 | HG02135.hp2 NA18942.hp2 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.461+554C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56305384 | |||||||
| chr19:56305439 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.461+609C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56305439 | |||||||
| chr19:56305447 | G | A | 2 | a0001c0001t0001g0257 a0001c0001t0002g0189 |
2 | HG02818.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.461+617G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56305447 | |||||||
| chr19:56305491 | G | A | 1 | a0001c0001t0002g0138 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.461+661G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56305491 | |||||||
| chr19:56305571 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.461+741C>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56305571 | |||||||
| chr19:56305666 | G | A | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(186): Show |
225 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.461+836G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56305666 | |||||||
| chr19:56305743 | G | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(187): Show |
226 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.461+913G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56305743 | |||||||
| chr19:56305875 | G | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.461+1045G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56305875 | |||||||
| chr19:56306107 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.461+1277T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306107 | |||||||
| chr19:56306146 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(156): Show |
193 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(190): Show |
intron_variant | MODIFIER | c.461+1316T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306146 | |||||||
| chr19:56306178 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.461+1348C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306178 | |||||||
| chr19:56306218 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.461+1388C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306218 | |||||||
| chr19:56306220 | G | T | 50 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(47): Show |
56 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.461+1390G>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306220 | |||||||
| chr19:56306297 | CATCGCCA others(161): Show |
C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(135): Show |
170 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.461+1468_461+1635d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306297 | |||||||
| chr19:56306298 | A | G | 16 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0078 others(13): Show |
18 | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.461+1468A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306298 | |||||||
| chr19:56306298 | ATCGCCAG others(245): Show |
A | 58 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0034 others(55): Show |
64 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.461+1850_461+2101d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306298 | ||||||
| chr19:56306300 | C | T | 1 | a0001c0001t0001g0333 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.461+1470C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306300 | |||||||
| chr19:56306300 | CGCCAGAG others(161): Show |
C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0192 others(8): Show |
12 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.461+1543_461+1710d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306300 | ||||||
| chr19:56306300 | CGCCAGAG others(749): Show |
C | 1 | a0001c0001t0001g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.461+1586_461+2341d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306300 | ||||||
| chr19:56306311 | GTACTAAG others(160): Show |
G | 1 | a0001c0001t0001g0078 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.461+1482_461+1648d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306311 | |||||||
| chr19:56306366 | CCCTGGCC others(160): Show |
C | 1 | a0001c0001t0002g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.461+1539_461+1705d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306366 | ||||||
| chr19:56306373 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0214 a0001c0001t0001g0327 |
4 | HG01070.hp1 HG01071.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.461+1543C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306373 | |||||||
| chr19:56306373 | CTCTCCCA others(161): Show |
C | 3 | a0001c0001t0003g0234 a0001c0001t0003g0304 a0001c0001t0003g0320 |
3 | HG00323.hp2 HG00642.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.461+1586_461+1753d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306373 | ||||||
| chr19:56306373 | CTCTCCCA others(413): Show |
C | 12 | a0001c0001t0001g0272 a0001c0001t0003g0012 a0001c0001t0003g0198 others(9): Show |
14 | HG00544.hp2 HG00741.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.461+1586_461+2005d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306373 | ||||||
| chr19:56306384 | CGCCAGAG others(77): Show |
C | 5 | a0001c0001t0003g0098 a0001c0001t0003g0101 a0001c0001t0003g0102 others(2): Show |
5 | HG01109.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.461+1586_461+1669d others(86): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306384 | ||||||
| chr19:56306384 | CGCCAGAG others(329): Show |
C | 1 | a0001c0001t0001g0028 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.461+1586_461+1921d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306384 | ||||||
| chr19:56306395 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.461+1565G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306395 | |||||||
| chr19:56306416 | C | T | 5 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0214 others(2): Show |
5 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+1586C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306416 | |||||||
| chr19:56306428 | C | T | 5 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0214 others(2): Show |
5 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+1598C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306428 | |||||||
| chr19:56306430 | G | A | 5 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0214 others(2): Show |
5 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+1600G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306430 | |||||||
| chr19:56306433 | T | G | 5 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0214 others(2): Show |
5 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+1603T>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306433 | |||||||
| chr19:56306436 | G | A | 5 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0214 others(2): Show |
5 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+1606G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306436 | |||||||
| chr19:56306445 | G | C | 5 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0214 others(2): Show |
5 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+1615G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306445 | |||||||
| chr19:56306447 | C | G | 1 | a0001c0001t0002g0018 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.461+1617C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306447 | |||||||
| chr19:56306449 | C | T | 5 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0214 others(2): Show |
5 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+1619C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306449 | |||||||
| chr19:56306453 | C | T | 5 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0214 others(2): Show |
5 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+1623C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306453 | |||||||
| chr19:56306464 | C | A | 5 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0214 others(2): Show |
5 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+1634C>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306464 | |||||||
| chr19:56306465 | T | C | 5 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0214 others(2): Show |
5 | HG01884.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+1635T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306465 | |||||||
| chr19:56306466 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0327 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.461+1636G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306466 | |||||||
| chr19:56306468 | T | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(140): Show |
175 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.461+1638T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306468 | |||||||
| chr19:56306515 | T | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0291 |
2 | HG01074.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.461+1685T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306515 | |||||||
| chr19:56306537 | TGGCTTCT others(497): Show |
T | 3 | a0001c0001t0003g0227 a0001c0001t0003g0282 a0001c0001t0005g0178 |
3 | HG02129.hp1 HG04115.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.461+1711_461+2214d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306537 | ||||||
| chr19:56306541 | T | C | 13 | a0001c0001t0001g0066 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG01109.hp1 HG01891.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.461+1711T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306541 | |||||||
| chr19:56306541 | TTCTCCCA others(581): Show |
T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0106 others(2): Show |
5 | HG02572.hp2 HG02886.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+1810_461+2397d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306541 | ||||||
| chr19:56306552 | CGCCAGAG others(497): Show |
C | 1 | a0001c0001t0001g0087 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.461+1838_461+2341d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306552 | ||||||
| chr19:56306584 | T | TTTCTCTT others(77): Show |
1 | a0001c0001t0002g0001 | 2 | HG02683.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.461+1766_461+1849d others(86): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306584 | ||||||
| chr19:56306621 | T | C | 11 | a0001c0001t0001g0009 a0001c0001t0001g0108 a0001c0001t0001g0216 others(8): Show |
13 | HG00738.hp1 HG01106.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.461+1791T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306621 | |||||||
| chr19:56306625 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0100 a0001c0001t0001g0286 others(1): Show |
4 | HG01891.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.461+1795C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306625 | |||||||
| chr19:56306634 | G | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(125): Show |
156 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.461+1804G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306634 | |||||||
| chr19:56306636 | CGCCAGAG others(77): Show |
C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(161): Show |
197 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.461+1838_461+1921d others(86): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306636 | ||||||
| chr19:56306636 | CGCCAGAG others(413): Show |
C | 4 | a0001c0001t0001g0088 a0001c0001t0001g0100 a0001c0001t0001g0286 others(1): Show |
4 | HG01891.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.461+1838_461+2257d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306636 | ||||||
| chr19:56306705 | C | T | 1 | a0001c0001t0004g0213 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.461+1875C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306705 | |||||||
| chr19:56306793 | T | C | 13 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0210 others(10): Show |
14 | HG00323.hp2 HG00642.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.461+1963T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306793 | |||||||
| chr19:56306802 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0055 |
3 | HG03139.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.461+1972G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306802 | |||||||
| chr19:56306836 | T | C | 1 | a0001c0002t0001g0046 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.461+2006T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306836 | |||||||
| chr19:56306836 | TTTCTCTT others(77): Show |
T | 1 | a0001c0001t0006g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.461+2102_461+2185d others(86): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306836 | ||||||
| chr19:56306877 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(139): Show |
174 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.461+2047C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306877 | |||||||
| chr19:56306886 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0327 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.461+2056G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306886 | |||||||
| chr19:56306888 | CGCCAGAG others(161): Show |
C | 12 | a0001c0001t0001g0272 a0001c0001t0003g0012 a0001c0001t0003g0198 others(9): Show |
14 | HG00544.hp2 HG00741.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.461+2090_461+2257d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306888 | ||||||
| chr19:56306920 | C | T | 14 | a0001c0001t0001g0028 a0001c0001t0001g0066 a0001c0001t0001g0210 others(11): Show |
15 | HG00323.hp2 HG00642.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.461+2090C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306920 | |||||||
| chr19:56306961 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0214 a0001c0001t0001g0327 |
4 | HG01070.hp1 HG01071.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.461+2131C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56306961 | |||||||
| chr19:56306972 | CGCCAGAG others(77): Show |
C | 11 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0323 others(8): Show |
11 | HG00323.hp2 HG00642.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.461+2174_461+2257d others(86): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306972 | ||||||
| chr19:56306980 | AAAGTACT others(160): Show |
A | 1 | a0001c0001t0002g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.461+2153_461+2319d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56306980 | ||||||
| chr19:56307004 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0327 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.461+2174C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307004 | |||||||
| chr19:56307004 | CTTCTCTT others(77): Show |
C | 1 | a0001c0001t0001g0028 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.461+2186_461+2269d others(86): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56307004 | ||||||
| chr19:56307004 | CTTCTCTT others(161): Show |
C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(147): Show |
183 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.461+2186_461+2353d others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56307004 | ||||||
| chr19:56307016 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0327 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.461+2186C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307016 | |||||||
| chr19:56307018 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0327 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.461+2188G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307018 | |||||||
| chr19:56307021 | T | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0327 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.461+2191T>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307021 | |||||||
| chr19:56307024 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0327 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.461+2194G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307024 | |||||||
| chr19:56307033 | G | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0327 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.461+2203G>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307033 | |||||||
| chr19:56307037 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0327 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.461+2207C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307037 | |||||||
| chr19:56307041 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0327 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.461+2211C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307041 | |||||||
| chr19:56307045 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0327 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.461+2215C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307045 | |||||||
| chr19:56307052 | C | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0327 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.461+2222C>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307052 | |||||||
| chr19:56307053 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0327 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.461+2223T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307053 | |||||||
| chr19:56307056 | T | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0327 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.461+2226T>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307056 | |||||||
| chr19:56307088 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0327 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.461+2258T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307088 | |||||||
| chr19:56307129 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.461+2299C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307129 | |||||||
| chr19:56307138 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.461+2308G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307138 | |||||||
| chr19:56307172 | T | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0214 a0001c0001t0001g0315 others(2): Show |
6 | HG01070.hp1 HG01071.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.461+2342T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307172 | |||||||
| chr19:56307293 | T | C | 1 | a0001c0001t0001g0269 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.461+2463T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307293 | |||||||
| chr19:56307294 | A | G | 31 | a0001c0001t0001g0066 a0001c0001t0001g0087 a0001c0001t0001g0088 others(28): Show |
33 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.461+2464A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307294 | |||||||
| chr19:56307360 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0002g0168 a0001c0001t0002g0172 |
3 | NA18945.hp1 NA19006.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.461+2530T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307360 | |||||||
| chr19:56307572 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.462-2552T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307572 | |||||||
| chr19:56307635 | C | T | 3 | a0001c0001t0003g0227 a0001c0001t0003g0282 a0001c0001t0005g0178 |
3 | HG02129.hp1 HG04115.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.462-2489C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307635 | |||||||
| chr19:56307879 | G | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(149): Show |
186 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(183): Show |
intron_variant | MODIFIER | c.462-2245G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56307879 | |||||||
| chr19:56308223 | G | A | 3 | a0001c0001t0003g0227 a0001c0001t0003g0282 a0001c0001t0005g0178 |
3 | HG02129.hp1 HG04115.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.462-1901G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56308223 | |||||||
| chr19:56308231 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG02886.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.462-1893A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56308231 | |||||||
| chr19:56308248 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG02886.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.462-1876G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56308248 | |||||||
| chr19:56308252 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.462-1872T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56308252 | |||||||
| chr19:56308267 | T | C | 26 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0272 others(23): Show |
28 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.462-1857T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56308267 | |||||||
| chr19:56308311 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0106 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.462-1813C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56308311 | |||||||
| chr19:56308313 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.462-1811T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56308313 | |||||||
| chr19:56308331 | C | CTTTTTTT others(1): Show |
22 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0323 others(19): Show |
24 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.462-1790_462-1783d others(10): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56308331 | ||||||
| chr19:56308390 | C | A | 13 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(10): Show |
13 | HG00733.hp1 HG01243.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.462-1734C>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56308390 | |||||||
| chr19:56308544 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.462-1580G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56308544 | |||||||
| chr19:56308672 | G | A | 3 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG02451.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.462-1452G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56308672 | |||||||
| chr19:56308826 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.462-1298G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56308826 | |||||||
| chr19:56309096 | C | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(159): Show |
196 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(193): Show |
intron_variant | MODIFIER | c.462-1028C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56309096 | |||||||
| chr19:56309100 | G | T | 1 | a0001c0001t0001g0248 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.462-1024G>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56309100 | |||||||
| chr19:56309142 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG02886.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.462-982C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56309142 | |||||||
| chr19:56309178 | C | T | 22 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0323 others(19): Show |
24 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.462-946C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56309178 | |||||||
| chr19:56309221 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.462-903G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56309221 | |||||||
| chr19:56309300 | G | A | 24 | a0001c0001t0001g0056 a0001c0001t0001g0066 a0001c0001t0001g0106 others(21): Show |
26 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.462-824G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56309300 | |||||||
| chr19:56309323 | CTT | C | 26 | a0001c0001t0001g0056 a0001c0001t0001g0087 a0001c0001t0001g0088 others(23): Show |
28 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.462-798_462-797del others(2): Show |
EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr19 | 56309323 | ||||||
| chr19:56309342 | T | C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0323 |
3 | HG02559.hp2 HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.462-782T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56309342 | |||||||
| chr19:56309380 | T | C | 25 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0323 others(22): Show |
27 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.462-744T>C | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56309380 | |||||||
| chr19:56309483 | A | G | 22 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0323 others(19): Show |
24 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.462-641A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56309483 | |||||||
| chr19:56309644 | T | G | 22 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0323 others(19): Show |
24 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.462-480T>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56309644 | |||||||
| chr19:56309684 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.462-440A>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56309684 | |||||||
| chr19:56309775 | C | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0210 a0001c0001t0001g0323 |
3 | HG02559.hp2 HG02615.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.462-349C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56309775 | |||||||
| chr19:56309796 | C | G | 5 | a0001c0001t0001g0056 a0001c0001t0001g0106 a0001c0001t0003g0227 others(2): Show |
5 | HG02129.hp1 HG02572.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.462-328C>G | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56309796 | |||||||
| chr19:56309927 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.462-197C>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56309927 | |||||||
| chr19:56309933 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0192 |
2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.462-191G>A | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56309933 | |||||||
| chr19:56310066 | A | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(170): Show |
209 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.462-58A>T | EDDM13 | ENSG00000267710.9 | transcript | ENST00000649256.2 | protein_coding | 14/14 | chr19 | 56310066 |