| geneid | 57724 |
|---|---|
| ensemblid | ENSG00000152223.16 |
| hgncid | 29331 |
| symbol | EPG5 |
| name | ectopic P-granules 5 autophagy tethering factor |
| refseq_nuc | NM_020964.3 |
| refseq_prot | NP_066015.2 |
| ensembl_nuc | ENST00000282041.11 |
| ensembl_prot | ENSP00000282041.4 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 45847609 |
| end | 45967329 |
| strand | - |
| ver | v1.2 |
| region | chr18:45847609-45967329 |
| region5000 | chr18:45842609-45972329 |
| regionname0 | EPG5_chr18_45847609_45967329 |
| regionname5000 | EPG5_chr18_45842609_45972329 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 2579 | 106 | 14 | 22 | 49 | 5 | 15 | 39 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002 | 0/0 | 2579 | 76 | 14 | 15 | 35 | 3 | 9 | 29 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0003 | 0/0 | 2579 | 26 | 4 | 1 | 16 | 0 | 5 | 16 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0004 | 0/0 | 2579 | 16 | 12 | 1 | 1 | 1 | 1 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0005 | 1/0 | 2579 | 16 | 2 | 7 | 1 | 0 | 5 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0006 | 0/0 | 2579 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0007 | 0/0 | 2579 | 7 | 1 | 1 | 1 | 1 | 3 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0008 | 0/0 | 2579 | 6 | 0 | 2 | 3 | 0 | 1 | 2 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0009 | 0/0 | 2579 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0010 | 0/0 | 2579 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0011 | 0/0 | 2579 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0012 | 0/0 | 2579 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0013 | 0/0 | 2579 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0014 | 0/0 | 2579 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0015 | 0/0 | 2579 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0016 | 0/0 | 2579 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0017 | 0/0 | 2579 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0018 | 0/0 | 2579 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0019 | 0/0 | 2579 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0020 | 0/0 | 2579 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0021 | 0/0 | 2579 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0022 | 0/0 | 87 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0023 | 0/0 | 2579 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0024 | 0/0 | 2579 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0025 | 0/0 | 2579 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0026 | 0/0 | 2579 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0027 | 0/0 | 2579 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0028 | 0/0 | 2579 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0029 | 0/0 | 2579 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0030 | 0/0 | 2579 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0031 | 0/0 | 2579 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0032 | 0/0 | 2579 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 7740 | 100 | 14 | 20 | 45 | 5 | 15 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0002 | 0/0 | 7740 | 68 | 13 | 14 | 30 | 2 | 9 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0003 | 0/0 | 7740 | 22 | 1 | 1 | 16 | 0 | 4 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0004 | 0/0 | 7740 | 14 | 10 | 1 | 1 | 1 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0005 | 1/0 | 7740 | 11 | 1 | 5 | 1 | 0 | 3 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0006 | 0/0 | 7740 | 7 | 1 | 1 | 1 | 1 | 3 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0007 | 0/0 | 7740 | 6 | 6 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0008 | 0/0 | 7740 | 6 | 0 | 2 | 3 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0009 | 0/0 | 7740 | 5 | 0 | 0 | 5 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0010 | 0/0 | 7740 | 4 | 0 | 0 | 4 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0011 | 0/0 | 7740 | 4 | 4 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0012 | 0/0 | 7740 | 4 | 4 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0013 | 0/0 | 7740 | 3 | 3 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0014 | 0/0 | 7740 | 3 | 1 | 1 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0015 | 0/0 | 7740 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0016 | 0/0 | 7740 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0017 | 0/0 | 7740 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0018 | 0/0 | 7740 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0019 | 0/0 | 7740 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0020 | 0/0 | 7740 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0021 | 0/0 | 7740 | 2 | 0 | 2 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0022 | 0/0 | 7740 | 2 | 1 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0023 | 0/0 | 7740 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0024 | 0/0 | 7740 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0025 | 0/0 | 7740 | 2 | 0 | 1 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0026 | 0/0 | 7740 | 2 | 0 | 0 | 0 | 2 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0027 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0028 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0029 | 0/0 | 7740 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0030 | 0/0 | 7740 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0031 | 0/0 | 7740 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0032 | 0/0 | 7740 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0033 | 0/0 | 7740 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0034 | 0/0 | 7740 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0035 | 0/0 | 7740 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0036 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0037 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0038 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0039 | 0/0 | 7740 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0040 | 0/0 | 7740 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0041 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0042 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0043 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0044 | 0/0 | 7740 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0045 | 0/0 | 7740 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0046 | 0/0 | 7740 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0047 | 0/0 | 7740 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0048 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| c0049 | 0/0 | 7740 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 4949 | 93 | 15 | 16 | 46 | 6 | 9 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0002 | 0/0 | 4948 | 58 | 1 | 13 | 37 | 1 | 6 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0003 | 1/0 | 4949 | 40 | 4 | 8 | 10 | 2 | 15 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0004 | 0/0 | 4948 | 24 | 6 | 6 | 6 | 1 | 5 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0005 | 0/0 | 4955 | 14 | 10 | 1 | 1 | 2 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0006 | 0/0 | 4953 | 10 | 10 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0007 | 0/0 | 4952 | 8 | 8 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0008 | 0/0 | 4949 | 6 | 1 | 0 | 3 | 0 | 2 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0009 | 0/0 | 4950 | 5 | 0 | 2 | 3 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0010 | 0/0 | 4955 | 4 | 4 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0011 | 0/0 | 4951 | 3 | 0 | 2 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0012 | 0/0 | 4950 | 3 | 0 | 0 | 3 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0013 | 0/0 | 4954 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0014 | 0/0 | 4952 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0015 | 0/0 | 4948 | 2 | 1 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0016 | 0/0 | 4949 | 2 | 0 | 1 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0017 | 0/0 | 4955 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0018 | 0/0 | 4952 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0019 | 0/0 | 4952 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0020 | 0/0 | 4950 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0021 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0022 | 0/0 | 4951 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0023 | 0/0 | 4953 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0024 | 0/0 | 4948 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0025 | 0/0 | 4948 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0026 | 0/0 | 4948 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0027 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0028 | 0/0 | 4948 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0029 | 0/0 | 4949 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0030 | 0/0 | 4948 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0031 | 0/0 | 4948 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0032 | 0/0 | 4949 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0033 | 0/0 | 4949 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0034 | 0/0 | 4951 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0035 | 0/0 | 4949 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0036 | 0/0 | 4949 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0037 | 0/0 | 4949 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0038 | 0/0 | 4949 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0039 | 0/0 | 4949 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0040 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0041 | 0/0 | 4949 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0042 | 0/0 | 4950 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0043 | 0/0 | 4948 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| t0044 | 0/0 | 4950 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0004 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| g0296 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 7740 | 100 | 14 | 20 | 45 | 5 | 15 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0021 | 0/0 | 7740 | 2 | 0 | 2 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0024 | 0/0 | 7740 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0030 | 0/0 | 7740 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0034 | 0/0 | 7740 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002 | 0/0 | 7740 | 68 | 13 | 14 | 30 | 2 | 9 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0009 | 0/0 | 7740 | 5 | 0 | 0 | 5 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0033 | 0/0 | 7740 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0038 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0040 | 0/0 | 7740 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0003c0003 | 0/0 | 7740 | 22 | 1 | 1 | 16 | 0 | 4 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0003c0013 | 0/0 | 7740 | 3 | 3 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0003c0044 | 0/0 | 7740 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0004c0004 | 0/0 | 7740 | 14 | 10 | 1 | 1 | 1 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0004c0027 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0004c0048 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0005c0005 | 1/0 | 7740 | 11 | 1 | 5 | 1 | 0 | 3 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0005c0014 | 0/0 | 7740 | 3 | 1 | 1 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0005c0025 | 0/0 | 7740 | 2 | 0 | 1 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0006c0011 | 0/0 | 7740 | 4 | 4 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0006c0012 | 0/0 | 7740 | 4 | 4 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0006c0037 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0007c0006 | 0/0 | 7740 | 7 | 1 | 1 | 1 | 1 | 3 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0008c0008 | 0/0 | 7740 | 6 | 0 | 2 | 3 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0009c0007 | 0/0 | 7740 | 6 | 6 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0010c0010 | 0/0 | 7740 | 4 | 0 | 0 | 4 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0011c0015 | 0/0 | 7740 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0012c0026 | 0/0 | 7740 | 2 | 0 | 0 | 0 | 2 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0013c0018 | 0/0 | 7740 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0014c0019 | 0/0 | 7740 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0015c0020 | 0/0 | 7740 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0016c0022 | 0/0 | 7740 | 2 | 1 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0017c0023 | 0/0 | 7740 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0018c0042 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0018c0043 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0019c0016 | 0/0 | 7740 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0020c0017 | 0/0 | 7740 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0021c0028 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0022c0029 | 0/0 | 7740 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0023c0046 | 0/0 | 7740 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0024c0035 | 0/0 | 7740 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0025c0036 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0026c0039 | 0/0 | 7740 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0027c0041 | 0/0 | 7740 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0028c0045 | 0/0 | 7740 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0029c0032 | 0/0 | 7740 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0030c0047 | 0/0 | 7740 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0031c0031 | 0/0 | 7740 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0032c0049 | 0/0 | 7740 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 12688 | 63 | 7 | 10 | 33 | 4 | 8 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0001t0002 | 0/0 | 12687 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0001t0003 | 0/0 | 12688 | 5 | 1 | 2 | 0 | 0 | 2 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0001t0004 | 0/0 | 12687 | 16 | 4 | 5 | 2 | 1 | 4 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0001t0005 | 0/0 | 12694 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0001t0009 | 0/0 | 12689 | 4 | 0 | 1 | 3 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0001t0011 | 0/0 | 12690 | 3 | 0 | 2 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0001t0012 | 0/0 | 12689 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0001t0032 | 0/0 | 12688 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0001t0036 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0001t0039 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0001t0040 | 0/0 | 12689 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0001t0043 | 0/0 | 12687 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0021t0001 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0021t0004 | 0/0 | 12687 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0024t0001 | 0/0 | 12688 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0030t0001 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0001c0034t0001 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0001 | 0/0 | 12688 | 4 | 2 | 1 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0002 | 0/0 | 12687 | 41 | 1 | 11 | 23 | 1 | 5 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0003 | 0/0 | 12688 | 2 | 0 | 0 | 0 | 0 | 2 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0004 | 0/0 | 12687 | 4 | 2 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0008 | 0/0 | 12688 | 6 | 1 | 0 | 3 | 0 | 2 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0014 | 0/0 | 12691 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0017 | 0/0 | 12694 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0024 | 0/0 | 12687 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0025 | 0/0 | 12687 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0026 | 0/0 | 12687 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0027 | 0/0 | 12689 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0029 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0030 | 0/0 | 12687 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0031 | 0/0 | 12687 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0037 | 0/0 | 12688 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0002t0038 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0009t0002 | 0/0 | 12687 | 5 | 0 | 0 | 5 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0033t0001 | 0/0 | 12688 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0038t0007 | 0/0 | 12691 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0002c0040t0002 | 0/0 | 12687 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0003c0003t0001 | 0/0 | 12688 | 4 | 1 | 0 | 3 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0003c0003t0002 | 0/0 | 12687 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0003c0003t0003 | 0/0 | 12688 | 12 | 0 | 1 | 9 | 0 | 2 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0003c0003t0012 | 0/0 | 12689 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0003c0003t0015 | 0/0 | 12687 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0003c0003t0016 | 0/0 | 12688 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0003c0003t0042 | 0/0 | 12689 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0003c0013t0001 | 0/0 | 12688 | 3 | 3 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0003c0044t0003 | 0/0 | 12688 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0004c0004t0001 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0004c0004t0003 | 0/0 | 12688 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0004c0004t0004 | 0/0 | 12687 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0004c0004t0005 | 0/0 | 12694 | 8 | 8 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0004c0004t0009 | 0/0 | 12689 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0004c0004t0015 | 0/0 | 12687 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0004c0004t0044 | 0/0 | 12689 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0004c0027t0005 | 0/0 | 12694 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0004c0048t0003 | 0/0 | 12688 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0005c0005t0003 | 1/0 | 12688 | 6 | 0 | 3 | 0 | 0 | 2 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0005c0005t0005 | 0/0 | 12694 | 2 | 0 | 1 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0005c0005t0016 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0005c0005t0033 | 0/0 | 12688 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0005c0005t0034 | 0/0 | 12690 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0005c0014t0003 | 0/0 | 12688 | 2 | 1 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0005c0014t0035 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0005c0025t0003 | 0/0 | 12688 | 2 | 0 | 1 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0006c0011t0006 | 0/0 | 12692 | 3 | 3 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0006c0011t0013 | 0/0 | 12693 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0006c0012t0006 | 0/0 | 12692 | 4 | 4 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0006c0037t0006 | 0/0 | 12692 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0007c0006t0003 | 0/0 | 12688 | 7 | 1 | 1 | 1 | 1 | 3 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0008c0008t0001 | 0/0 | 12688 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0008c0008t0002 | 0/0 | 12687 | 4 | 0 | 1 | 3 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0008c0008t0028 | 0/0 | 12687 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0009c0007t0007 | 0/0 | 12691 | 6 | 6 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0010c0010t0001 | 0/0 | 12688 | 4 | 0 | 0 | 4 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0011c0015t0014 | 0/0 | 12691 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0011c0015t0019 | 0/0 | 12691 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0012c0026t0005 | 0/0 | 12694 | 2 | 0 | 0 | 0 | 2 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0013c0018t0001 | 0/0 | 12688 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0014c0019t0006 | 0/0 | 12692 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0015c0020t0004 | 0/0 | 12687 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0016c0022t0020 | 0/0 | 12689 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0016c0022t0021 | 0/0 | 12689 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0017c0023t0002 | 0/0 | 12687 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0018c0042t0022 | 0/0 | 12690 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0018c0043t0023 | 0/0 | 12692 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0019c0016t0010 | 0/0 | 12694 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0020c0017t0010 | 0/0 | 12694 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0021c0028t0018 | 0/0 | 12691 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0022c0029t0001 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0023c0046t0003 | 0/0 | 12688 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0024c0035t0001 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0025c0036t0013 | 0/0 | 12693 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0026c0039t0002 | 0/0 | 12687 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0027c0041t0007 | 0/0 | 12691 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0028c0045t0001 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0029c0032t0041 | 0/0 | 12688 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0030c0047t0002 | 0/0 | 12687 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0031c0031t0001 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| a0032c0049t0001 | 0/0 | 12688 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | copy fasta | chr18 | 45842609 | 45972329 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0009g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0009g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0009g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0009g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0011g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0011g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0011g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0012g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0032g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0036g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0039g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0040g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0001t0043g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0021t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0021t0004g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0024t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0024t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0030t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0001c0034t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0008g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0008g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0008g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0008g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0008g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0008g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0014g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0017g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0024g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0025g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0026g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0027g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0029g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0030g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0031g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0037g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0002t0038g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0009t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0009t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0009t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0009t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0009t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0033t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0038t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0002c0040t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0012g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0012g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0015g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0016g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0003t0042g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0013t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0013t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0013t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0003c0044t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0004t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0004t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0004t0004g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0004t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0004t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0004t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0004t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0004t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0004t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0004t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0004t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0004t0009g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0004t0015g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0004t0044g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0027t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0004c0048t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0005t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0005t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0005t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0005t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0005t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0005t0003g0296 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0005t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0005t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0005t0016g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0005t0033g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0005t0034g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0014t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0014t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0014t0035g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0025t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0005c0025t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0006c0011t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0006c0011t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0006c0011t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0006c0011t0013g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0006c0012t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0006c0012t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0006c0012t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0006c0012t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0006c0037t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0007c0006t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0007c0006t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0007c0006t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0007c0006t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0007c0006t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0007c0006t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0007c0006t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0008c0008t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0008c0008t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0008c0008t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0008c0008t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0008c0008t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0008c0008t0028g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0009c0007t0007g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0009c0007t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0009c0007t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0009c0007t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0009c0007t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0010c0010t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0010c0010t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0010c0010t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0010c0010t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0011c0015t0014g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0011c0015t0019g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0012c0026t0005g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0012c0026t0005g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0013c0018t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0013c0018t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0014c0019t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0014c0019t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0015c0020t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0015c0020t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0016c0022t0020g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0016c0022t0021g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0017c0023t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0017c0023t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0018c0042t0022g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0018c0043t0023g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0019c0016t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0019c0016t0010g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0020c0017t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0020c0017t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0021c0028t0018g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0022c0029t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0023c0046t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0024c0035t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0025c0036t0013g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0026c0039t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0027c0041t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0028c0045t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0029c0032t0041g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0030c0047t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0031c0031t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| a0032c0049t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | GBR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0281 | EUR | GBR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00140 | hp1 | a0004 | c0004 | t0003 | g0030 | EUR | GBR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | GBR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0063 | EUR | FIN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00323 | hp1 | a0007 | c0006 | t0003 | g0214 | EUR | FIN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00323 | hp2 | a0002 | c0033 | t0001 | g0061 | EUR | FIN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00438 | hp1 | a0001 | c0001 | t0009 | g0218 | EAS | CHS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00609 | hp1 | a0029 | c0032 | t0041 | g0139 | EAS | CHS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00609 | hp2 | a0002 | c0002 | t0004 | g0285 | EAS | CHS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00621 | hp1 | a0002 | c0009 | t0002 | g0280 | EAS | CHS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00621 | hp2 | a0015 | c0020 | t0004 | g0217 | EAS | CHS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0253 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0271 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00733 | hp2 | a0005 | c0005 | t0016 | g0106 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0132 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00741 | hp1 | a0031 | c0031 | t0001 | g0172 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG00741 | hp2 | a0005 | c0005 | t0003 | g0104 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0117 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0273 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01074 | hp1 | a0002 | c0002 | t0025 | g0067 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0064 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0256 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01106 | hp1 | a0005 | c0025 | t0003 | g0109 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0065 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01109 | hp1 | a0002 | c0002 | t0029 | g0228 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01109 | hp2 | a0032 | c0049 | t0001 | g0178 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01169 | hp1 | a0022 | c0029 | t0001 | g0059 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0108 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01175 | hp2 | a0001 | c0001 | t0009 | g0169 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0274 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0251 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01258 | hp2 | a0028 | c0045 | t0001 | g0115 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01261 | hp1 | a0001 | c0001 | t0011 | g0181 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0263 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01346 | hp1 | a0001 | c0021 | t0001 | g0135 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01346 | hp2 | a0007 | c0006 | t0003 | g0212 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0071 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01358 | hp2 | a0008 | c0008 | t0002 | g0018 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01361 | hp1 | a0005 | c0005 | t0003 | g0084 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01361 | hp2 | a0004 | c0004 | t0009 | g0036 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01496 | hp1 | a0016 | c0022 | t0020 | g0044 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0118 | EUR | IBS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01516 | hp2 | a0012 | c0026 | t0005 | g0022 | EUR | IBS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01517 | hp2 | a0012 | c0026 | t0005 | g0021 | EUR | IBS | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01884 | hp1 | a0006 | c0011 | t0006 | g0041 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01884 | hp2 | a0011 | c0015 | t0014 | g0290 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01891 | hp1 | a0018 | c0043 | t0023 | g0046 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01891 | hp2 | a0027 | c0041 | t0007 | g0219 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01928 | hp1 | a0002 | c0040 | t0002 | g0267 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01928 | hp2 | a0003 | c0003 | t0003 | g0186 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01943 | hp1 | a0005 | c0005 | t0003 | g0099 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0246 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01975 | hp1 | a0001 | c0021 | t0004 | g0136 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0070 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0249 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02055 | hp1 | a0002 | c0038 | t0007 | g0008 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0098 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02071 | hp2 | a0008 | c0008 | t0002 | g0020 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02074 | hp1 | a0002 | c0009 | t0002 | g0278 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02074 | hp2 | a0001 | c0001 | t0012 | g0157 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02083 | hp2 | a0002 | c0009 | t0002 | g0279 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02145 | hp1 | a0005 | c0014 | t0003 | g0089 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02145 | hp2 | a0013 | c0018 | t0001 | g0206 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02155 | hp1 | a0015 | c0020 | t0004 | g0170 | EAS | CDX | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02165 | hp1 | a0001 | c0001 | t0036 | g0167 | EAS | CDX | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0245 | EAS | CDX | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02257 | hp1 | a0004 | c0004 | t0005 | g0025 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02273 | hp1 | a0005 | c0005 | t0005 | g0107 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02273 | hp2 | a0008 | c0008 | t0028 | g0017 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02280 | hp2 | a0009 | c0007 | t0007 | g0009 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0248 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02293 | hp2 | a0001 | c0001 | t0011 | g0180 | AMR | PEL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02523 | hp2 | a0001 | c0024 | t0001 | g0177 | EAS | KHV | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02572 | hp2 | a0025 | c0036 | t0013 | g0286 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0254 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02602 | hp2 | a0003 | c0044 | t0003 | g0182 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02615 | hp1 | a0002 | c0002 | t0004 | g0230 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02615 | hp2 | a0002 | c0002 | t0031 | g0048 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0294 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02622 | hp2 | a0004 | c0004 | t0005 | g0031 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02630 | hp1 | a0006 | c0011 | t0013 | g0042 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02630 | hp2 | a0002 | c0002 | t0024 | g0265 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02647 | hp1 | a0002 | c0002 | t0008 | g0275 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02647 | hp2 | a0002 | c0002 | t0017 | g0229 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02683 | hp1 | a0003 | c0003 | t0016 | g0055 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02683 | hp2 | a0005 | c0005 | t0003 | g0105 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02723 | hp1 | a0020 | c0017 | t0010 | g0224 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02723 | hp2 | a0002 | c0002 | t0014 | g0220 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02735 | hp1 | a0002 | c0002 | t0003 | g0183 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02735 | hp2 | a0005 | c0025 | t0003 | g0016 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02809 | hp1 | a0004 | c0004 | t0005 | g0032 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02809 | hp2 | a0006 | c0012 | t0006 | g0221 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02818 | hp1 | a0006 | c0012 | t0006 | g0272 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02818 | hp2 | a0020 | c0017 | t0010 | g0223 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02886 | hp1 | a0018 | c0042 | t0022 | g0043 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02886 | hp2 | a0021 | c0028 | t0018 | g0292 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02897 | hp1 | a0004 | c0027 | t0005 | g0007 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02897 | hp2 | a0006 | c0012 | t0006 | g0227 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02922 | hp1 | a0011 | c0015 | t0019 | g0291 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02922 | hp2 | a0003 | c0013 | t0001 | g0207 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02970 | hp1 | a0009 | c0007 | t0007 | g0006 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02970 | hp2 | a0004 | c0004 | t0005 | g0023 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0264 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03017 | hp2 | a0001 | c0001 | t0043 | g0057 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03041 | hp1 | a0009 | c0007 | t0007 | g0010 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03130 | hp1 | a0004 | c0004 | t0005 | g0033 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03130 | hp2 | a0003 | c0013 | t0001 | g0204 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03139 | hp1 | a0004 | c0004 | t0005 | g0026 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03139 | hp2 | a0002 | c0002 | t0030 | g0049 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03209 | hp1 | a0004 | c0004 | t0005 | g0027 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03209 | hp2 | a0019 | c0016 | t0010 | g0225 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0094 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03239 | hp2 | a0007 | c0006 | t0003 | g0211 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03453 | hp1 | a0019 | c0016 | t0010 | g0226 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03453 | hp2 | a0006 | c0011 | t0006 | g0038 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03486 | hp1 | a0013 | c0018 | t0001 | g0205 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03486 | hp2 | a0004 | c0048 | t0003 | g0015 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03490 | hp2 | a0007 | c0006 | t0003 | g0288 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0074 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03491 | hp2 | a0005 | c0014 | t0003 | g0091 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03492 | hp1 | a0007 | c0006 | t0003 | g0289 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0075 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03516 | hp1 | a0004 | c0004 | t0005 | g0024 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03516 | hp2 | a0002 | c0002 | t0004 | g0053 | AFR | ESN | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03540 | hp1 | a0006 | c0012 | t0006 | g0222 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03579 | hp2 | a0009 | c0007 | t0007 | g0006 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03654 | hp1 | a0002 | c0002 | t0003 | g0237 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03704 | hp1 | a0005 | c0005 | t0034 | g0086 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03704 | hp2 | a0002 | c0002 | t0008 | g0066 | SAS | PJL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03831 | hp1 | a0023 | c0046 | t0003 | g0200 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03927 | hp1 | a0002 | c0002 | t0008 | g0062 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03942 | hp1 | a0005 | c0005 | t0003 | g0092 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0081 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0257 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG04184 | hp1 | a0003 | c0003 | t0003 | g0191 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0250 | SAS | BEB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0176 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0056 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG04204 | hp2 | a0004 | c0004 | t0004 | g0012 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG04228 | hp1 | a0008 | c0008 | t0001 | g0034 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0255 | SAS | STU | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18522 | hp1 | a0002 | c0002 | t0026 | g0235 | AFR | YRI | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18522 | hp2 | a0001 | c0001 | t0032 | g0113 | AFR | YRI | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18747 | hp1 | a0002 | c0002 | t0038 | g0236 | EAS | CHB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18906 | hp1 | a0003 | c0013 | t0001 | g0203 | AFR | YRI | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18939 | hp1 | a0007 | c0006 | t0003 | g0210 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18940 | hp1 | a0024 | c0035 | t0001 | g0133 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18942 | hp2 | a0002 | c0002 | t0027 | g0233 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18944 | hp2 | a0003 | c0003 | t0012 | g0198 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18945 | hp1 | a0030 | c0047 | t0002 | g0268 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18945 | hp2 | a0003 | c0003 | t0003 | g0185 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18947 | hp1 | a0003 | c0003 | t0003 | g0187 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18947 | hp2 | a0001 | c0034 | t0001 | g0088 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18948 | hp1 | a0003 | c0003 | t0003 | g0197 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18948 | hp2 | a0001 | c0030 | t0001 | g0138 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18952 | hp1 | a0008 | c0008 | t0002 | g0035 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18957 | hp1 | a0003 | c0003 | t0003 | g0208 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18960 | hp2 | a0001 | c0001 | t0011 | g0151 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18963 | hp1 | a0002 | c0002 | t0008 | g0243 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18963 | hp2 | a0001 | c0001 | t0040 | g0140 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18964 | hp1 | a0002 | c0009 | t0002 | g0277 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18966 | hp2 | a0003 | c0003 | t0003 | g0195 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18967 | hp2 | a0002 | c0002 | t0008 | g0244 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18970 | hp1 | a0003 | c0003 | t0003 | g0209 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18971 | hp1 | a0002 | c0002 | t0008 | g0050 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18971 | hp2 | a0003 | c0003 | t0012 | g0199 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18973 | hp2 | a0001 | c0001 | t0009 | g0153 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18992 | hp1 | a0003 | c0003 | t0015 | g0196 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18994 | hp1 | a0002 | c0009 | t0002 | g0276 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18994 | hp2 | a0001 | c0001 | t0009 | g0161 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18998 | hp1 | a0005 | c0005 | t0005 | g0103 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18999 | hp1 | a0008 | c0008 | t0002 | g0019 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19002 | hp1 | a0026 | c0039 | t0002 | g0242 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19003 | hp1 | a0002 | c0002 | t0004 | g0234 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19003 | hp2 | a0010 | c0010 | t0001 | g0174 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19004 | hp1 | a0010 | c0010 | t0001 | g0129 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19004 | hp2 | a0003 | c0003 | t0003 | g0193 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19006 | hp1 | a0003 | c0003 | t0042 | g0194 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19006 | hp2 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19009 | hp2 | a0001 | c0024 | t0001 | g0163 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19011 | hp2 | a0001 | c0001 | t0039 | g0097 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19030 | hp1 | a0004 | c0004 | t0015 | g0014 | AFR | LWK | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19030 | hp2 | a0009 | c0007 | t0007 | g0011 | AFR | LWK | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19043 | hp1 | a0006 | c0011 | t0006 | g0040 | AFR | LWK | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19043 | hp2 | a0009 | c0007 | t0007 | g0013 | AFR | LWK | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19058 | hp2 | a0017 | c0023 | t0002 | g0259 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19063 | hp1 | a0004 | c0004 | t0001 | g0028 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19065 | hp1 | a0010 | c0010 | t0001 | g0130 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19072 | hp2 | a0003 | c0003 | t0003 | g0189 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19080 | hp1 | a0017 | c0023 | t0002 | g0258 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19080 | hp2 | a0003 | c0003 | t0003 | g0283 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19083 | hp1 | a0003 | c0003 | t0001 | g0192 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19083 | hp2 | a0010 | c0010 | t0001 | g0145 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19088 | hp2 | a0003 | c0003 | t0001 | g0184 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0079 | AFR | YRI | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0202 | AFR | YRI | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0247 | AFR | ASW | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA20129 | hp2 | a0002 | c0002 | t0037 | g0295 | AFR | ASW | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA20905 | hp1 | a0003 | c0003 | t0003 | g0201 | SAS | GIH | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA20905 | hp2 | a0003 | c0003 | t0002 | g0287 | SAS | GIH | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01123 | hp1 | a0005 | c0014 | t0035 | g0100 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0076 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02559 | hp1 | a0014 | c0019 | t0006 | g0082 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG02559 | hp2 | a0004 | c0004 | t0044 | g0029 | AFR | ACB | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0293 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG03471 | hp2 | a0005 | c0005 | t0033 | g0047 | AFR | MSL | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0072 | AFR | USA | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| HG06807 | hp2 | a0006 | c0037 | t0006 | g0039 | AFR | USA | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA18955 | hp2 | a0003 | c0003 | t0001 | g0188 | EAS | JPT | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA20300 | hp1 | a0016 | c0022 | t0021 | g0045 | AFR | USA | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA20300 | hp2 | a0007 | c0006 | t0003 | g0213 | AFR | USA | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| NA21309 | hp2 | a0014 | c0019 | t0006 | g0110 | AFR | LWK | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0127 | REF | REF | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| homoSapiens_grch38 | hp1 | a0005 | c0005 | t0003 | g0296 | REF | REF | EPG5_chr18_45842609_45972329 | EPG5 | chr18 | 45842609 | 45972329 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:45867602
|
C | A | 1 | a0015 | 2 | HG00621.hp2 HG02155.hp1 |
missense_variant | MODERATE | c.6372G>T | p.Met2124Ile | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 37/44 | 6462/12688 | 6372/7740 | 2124/2579 | chr18 | 45867602 | ||
| chr18:45876331
|
C | T | 3 | a0016a0019a0020 | 6 | HG01496.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
missense_variant | MODERATE | c.5954G>A | p.Arg1985Gln | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/44 | 6044/12688 | 5954/7740 | 1985/2579 | chr18 | 45876331 | ||
| chr18:45876332
|
G | A | 1 | a0026 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.5953C>T | p.Arg1985Trp | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/44 | 6043/12688 | 5953/7740 | 1985/2579 | chr18 | 45876332 | ||
| chr18:45879202
|
T | C | 1 | a0021 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.5680A>G | p.Ile1894Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 33/44 | 5770/12688 | 5680/7740 | 1894/2579 | chr18 | 45879202 | ||
| chr18:45880124
|
T | A | 1 | a0010 | 4 | NA19003.hp2 NA19004.hp1 NA19065.hp1 others(1): Show |
missense_variant | MODERATE | c.5618A>T | p.Glu1873Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/44 | 5708/12688 | 5618/7740 | 1873/2579 | chr18 | 45880124 | ||
| chr18:45880151
|
C | T | 3 | a0006a0014a0025 | 12 | HG01884.hp1 HG02559.hp1 HG02572.hp2 others(9): Show |
missense_variant | MODERATE | c.5591G>A | p.Ser1864Asn | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/44 | 5681/12688 | 5591/7740 | 1864/2579 | chr18 | 45880151 | ||
| chr18:45884648
|
T | C | 1 | a0017 | 2 | NA19058.hp2 NA19080.hp1 |
missense_variant | MODERATE | c.5273A>G | p.Asn1758Ser | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/44 | 5363/12688 | 5273/7740 | 1758/2579 | chr18 | 45884648 | ||
| chr18:45889889
|
G | A | 1 | a0027 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.4861C>T | p.Arg1621Trp | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/44 | 4951/12688 | 4861/7740 | 1621/2579 | chr18 | 45889889 | ||
| chr18:45901110
|
G | A | 13 | a0002a0006a0009others(10): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
missense_variant | MODERATE | c.4532C>T | p.Ala1511Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/44 | 4622/12688 | 4532/7740 | 1511/2579 | chr18 | 45901110 | ||
| chr18:45915596
|
C | T | 1 | a0019 | 2 | HG03209.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.3608G>A | p.Arg1203Gln | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/44 | 3698/12688 | 3608/7740 | 1203/2579 | chr18 | 45915596 | ||
| chr18:45916098
|
T | C | 1 | a0013 | 2 | HG02145.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.3493A>G | p.Ile1165Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 19/44 | 3583/12688 | 3493/7740 | 1165/2579 | chr18 | 45916098 | ||
| chr18:45916200
|
T | C | 1 | a0024 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.3391A>G | p.Ile1131Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 19/44 | 3481/12688 | 3391/7740 | 1131/2579 | chr18 | 45916200 | ||
| chr18:45916574
|
G | A | 1 | a0007 | 7 | HG00323.hp1 HG01346.hp2 HG03239.hp2 others(4): Show |
missense_variant | MODERATE | c.3248C>T | p.Ser1083Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 18/44 | 3338/12688 | 3248/7740 | 1083/2579 | chr18 | 45916574 | ||
| chr18:45917745
|
A | G | 10 | a0001a0010a0014others(7): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
missense_variant | MODERATE | c.3173T>C | p.Val1058Ala | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/44 | 3263/12688 | 3173/7740 | 1058/2579 | chr18 | 45917745 | ||
| chr18:45922441
|
T | C | 1 | a0018 | 2 | HG01891.hp1 HG02886.hp1 |
missense_variant | MODERATE | c.2998A>G | p.Met1000Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/44 | 3088/12688 | 2998/7740 | 1000/2579 | chr18 | 45922441 | ||
| chr18:45922528
|
A | C | 1 | a0011 | 2 | HG01884.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.2911T>G | p.Leu971Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/44 | 3001/12688 | 2911/7740 | 971/2579 | chr18 | 45922528 | ||
| chr18:45928890
|
C | G | 4 | a0003a0007a0013others(1): Show | 36 | HG00323.hp1 HG01346.hp2 HG01928.hp2 others(33): Show |
missense_variant | MODERATE | c.2532G>C | p.Glu844Asp | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/44 | 2622/12688 | 2532/7740 | 844/2579 | chr18 | 45928890 | ||
| chr18:45939636
|
A | G | 2 | a0019a0020 | 4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
missense_variant | MODERATE | c.2063T>C | p.Phe688Ser | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/44 | 2153/12688 | 2063/7740 | 688/2579 | chr18 | 45939636 | ||
| chr18:45944031
|
T | C | 1 | a0028 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.1766A>G | p.Gln589Arg | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/44 | 1856/12688 | 1766/7740 | 589/2579 | chr18 | 45944031 | ||
| chr18:45946731
|
C | T | 1 | a0029 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.1609G>A | p.Glu537Lys | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/44 | 1699/12688 | 1609/7740 | 537/2579 | chr18 | 45946731 | ||
| chr18:45949563
|
G | A | 1 | a0023 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.1418C>T | p.Pro473Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 5/44 | 1508/12688 | 1418/7740 | 473/2579 | chr18 | 45949563 | ||
| chr18:45951220
|
C | T | 1 | a0012 | 2 | HG01516.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.1271G>A | p.Ser424Asn | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/44 | 1361/12688 | 1271/7740 | 424/2579 | chr18 | 45951220 | ||
| chr18:45954632
|
T | C | 1 | a0030 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.770A>G | p.Lys257Arg | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 860/12688 | 770/7740 | 257/2579 | chr18 | 45954632 | ||
| chr18:45954662
|
G | A | 1 | a0008 | 6 | HG01358.hp2 HG02071.hp2 HG02273.hp2 others(3): Show |
missense_variant | MODERATE | c.740C>T | p.Pro247Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 830/12688 | 740/7740 | 247/2579 | chr18 | 45954662 | ||
| chr18:45954858
|
T | C | 4 | a0004a0008a0009others(1): Show | 30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
missense_variant | MODERATE | c.544A>G | p.Lys182Glu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 634/12688 | 544/7740 | 182/2579 | chr18 | 45954858 | ||
| chr18:45954978
|
C | T | 1 | a0031 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.424G>A | p.Glu142Lys | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 514/12688 | 424/7740 | 142/2579 | chr18 | 45954978 | ||
| chr18:45955139
|
A | C | 1 | a0022 | 1 | HG01169.hp1 | stop_gained | HIGH | c.263T>G | p.Leu88* | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 353/12688 | 263/7740 | 88/2579 | chr18 | 45955139 | ||
| chr18:45955251
|
G | C | 1 | a0032 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.151C>G | p.Leu51Val | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 241/12688 | 151/7740 | 51/2579 | chr18 | 45955251 | ||
| chr18:45955298
|
C | T | 2 | a0011a0021 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.104G>A | p.Ser35Asn | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 194/12688 | 104/7740 | 35/2579 | chr18 | 45955298 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:45852586
|
A | G | 1 | a0006c0037 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.7621T>C | p.Leu2541Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 7711/12688 | 7621/7740 | 2541/2579 | chr18 | 45852586 | ||
| chr18:45857927
|
G | A | 1 | a0001c0034 | 1 | NA18947.hp2 | synonymous_variant | LOW | c.7368C>T | p.Leu2456Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/44 | 7458/12688 | 7368/7740 | 2456/2579 | chr18 | 45857927 | ||
| chr18:45866897
|
C | T | 1 | a0005c0014 | 3 | HG01123.hp1 HG02145.hp1 HG03491.hp2 |
synonymous_variant | LOW | c.6522G>A | p.Pro2174Pro | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/44 | 6612/12688 | 6522/7740 | 2174/2579 | chr18 | 45866897 | ||
| chr18:45866903
|
G | A | 2 | a0016c0022a0018c0043 | 3 | HG01496.hp1 HG01891.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.6516C>T | p.Tyr2172Tyr | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/44 | 6606/12688 | 6516/7740 | 2172/2579 | chr18 | 45866903 | ||
| chr18:45879182
|
A | G | 2 | a0003c0013a0013c0018 | 5 | HG02145.hp2 HG02922.hp2 HG03130.hp2 others(2): Show |
synonymous_variant | LOW | c.5700T>C | p.Phe1900Phe | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 33/44 | 5790/12688 | 5700/7740 | 1900/2579 | chr18 | 45879182 | ||
| chr18:45880126
|
G | A | 1 | a0010c0010 | 4 | NA19003.hp2 NA19004.hp1 NA19065.hp1 others(1): Show |
synonymous_variant | LOW | c.5616C>T | p.Thr1872Thr | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/44 | 5706/12688 | 5616/7740 | 1872/2579 | chr18 | 45880126 | ||
| chr18:45880159
|
G | A | 1 | a0016c0022 | 2 | HG01496.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.5583C>T | p.Cys1861Cys | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/44 | 5673/12688 | 5583/7740 | 1861/2579 | chr18 | 45880159 | ||
| chr18:45880198
|
G | C | 1 | a0002c0040 | 1 | HG01928.hp1 | synonymous_variant | LOW | c.5544C>G | p.Pro1848Pro | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/44 | 5634/12688 | 5544/7740 | 1848/2579 | chr18 | 45880198 | ||
| chr18:45884692
|
G | A | 1 | a0002c0009 | 5 | HG00621.hp1 HG02074.hp1 HG02083.hp2 others(2): Show |
synonymous_variant | LOW | c.5229C>T | p.Phe1743Phe | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/44 | 5319/12688 | 5229/7740 | 1743/2579 | chr18 | 45884692 | ||
| chr18:45901013
|
C | T | 1 | a0016c0022 | 2 | HG01496.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.4629G>A | p.Leu1543Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/44 | 4719/12688 | 4629/7740 | 1543/2579 | chr18 | 45901013 | ||
| chr18:45910637
|
G | A | 12 | a0002c0002a0002c0009a0002c0033others(9): Show | 92 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(89): Show |
synonymous_variant | LOW | c.4089C>T | p.His1363His | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/44 | 4179/12688 | 4089/7740 | 1363/2579 | chr18 | 45910637 | ||
| chr18:45916155
|
A | G | 3 | a0016c0022a0018c0042a0018c0043 | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
synonymous_variant | LOW | c.3436T>C | p.Leu1146Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 19/44 | 3526/12688 | 3436/7740 | 1146/2579 | chr18 | 45916155 | ||
| chr18:45916543
|
G | A | 1 | a0001c0021 | 2 | HG01346.hp1 HG01975.hp1 |
synonymous_variant | LOW | c.3279C>T | p.Ser1093Ser | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 18/44 | 3369/12688 | 3279/7740 | 1093/2579 | chr18 | 45916543 | ||
| chr18:45930715
|
G | A | 1 | a0003c0044 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.2373C>T | p.Asp791Asp | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/44 | 2463/12688 | 2373/7740 | 791/2579 | chr18 | 45930715 | ||
| chr18:45943175
|
A | G | 1 | a0002c0033 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.1929T>C | p.Ile643Ile | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/44 | 2019/12688 | 1929/7740 | 643/2579 | chr18 | 45943175 | ||
| chr18:45949520
|
G | A | 1 | a0001c0024 | 2 | HG02523.hp2 NA19009.hp2 |
synonymous_variant | LOW | c.1461C>T | p.Pro487Pro | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 5/44 | 1551/12688 | 1461/7740 | 487/2579 | chr18 | 45949520 | ||
| chr18:45949582
|
G | A | 1 | a0005c0025 | 2 | HG01106.hp1 HG02735.hp2 |
synonymous_variant | LOW | c.1399C>T | p.Leu467Leu | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 5/44 | 1489/12688 | 1399/7740 | 467/2579 | chr18 | 45949582 | ||
| chr18:45955021
|
A | G | 1 | a0001c0030 | 1 | NA18948.hp2 | synonymous_variant | LOW | c.381T>C | p.Asn127Asn | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 471/12688 | 381/7740 | 127/2579 | chr18 | 45955021 | ||
| chr18:45955096
|
G | A | 1 | a0004c0048 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.306C>T | p.Pro102Pro | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/44 | 396/12688 | 306/7740 | 102/2579 | chr18 | 45955096 | ||
| chr18:45967222
|
C | T | 1 | a0004c0027 | 1 | HG02897.hp1 | synonymous_variant | LOW | c.18G>A | p.Lys6Lys | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/44 | 108/12688 | 18/7740 | 6/2579 | chr18 | 45967222 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:45847656
|
T | C | 1 | a0029c0032t0041 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4811A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 4811 | chr18 | 45847656 | |||||
| chr18:45847658
|
G | A | 25 | a0001c0001t0002a0001c0001t0012a0002c0002t0002others(22): Show | 85 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*4809C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 4809 | chr18 | 45847658 | |||||
| chr18:45847953
|
G | A | 9 | a0001c0001t0005a0001c0001t0032a0002c0002t0017others(6): Show | 20 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4514C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 4514 | chr18 | 45847953 | |||||
| chr18:45847979
|
C | T | 1 | a0011c0015t0019 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4488G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 4488 | chr18 | 45847979 | |||||
| chr18:45847992
|
A | AT | 45 | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(42): Show | 122 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*4474dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 4474 | chr18 | 45847992 | |||||
| chr18:45848500
|
T | C | 1 | a0016c0022t0021 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3967A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3967 | chr18 | 45848500 | |||||
| chr18:45848584
|
C | T | 4 | a0016c0022t0020a0016c0022t0021a0018c0042t0022others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3883G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3883 | chr18 | 45848584 | |||||
| chr18:45848647
|
C | T | 1 | a0001c0001t0039 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3820G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3820 | chr18 | 45848647 | |||||
| chr18:45848971
|
T | C | 42 | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(39): Show | 119 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*3496A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3496 | chr18 | 45848971 | |||||
| chr18:45849061
|
G | A | 1 | a0002c0002t0029 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3406C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3406 | chr18 | 45849061 | |||||
| chr18:45849081
|
C | CA | 8 | a0001c0001t0009a0003c0003t0042a0004c0004t0009others(5): Show | 11 | HG00438.hp1 HG01175.hp2 HG01361.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3385dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3385 | chr18 | 45849081 | |||||
| chr18:45849081
|
CA | C | 23 | a0001c0001t0004a0001c0001t0005a0001c0001t0032others(20): Show | 64 | HG00609.hp2 HG00621.hp2 HG01071.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*3385delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3385 | chr18 | 45849081 | |||||
| chr18:45849081
|
CAA | C | 15 | a0001c0001t0002a0002c0002t0002a0002c0002t0024others(12): Show | 64 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*3384_*3385delTT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3384 | chr18 | 45849081 | |||||
| chr18:45849107
|
T | G | 1 | a0002c0002t0017 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3360A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3360 | chr18 | 45849107 | |||||
| chr18:45849218
|
T | A | 80 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(77): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*3249A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3249 | chr18 | 45849218 | |||||
| chr18:45849222
|
C | T | 1 | a0002c0002t0026 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3245G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3245 | chr18 | 45849222 | |||||
| chr18:45849298
|
A | C | 1 | a0002c0002t0025 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3169T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3169 | chr18 | 45849298 | |||||
| chr18:45849315
|
G | A | 1 | a0008c0008t0028 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3152C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3152 | chr18 | 45849315 | |||||
| chr18:45849335
|
C | T | 2 | a0019c0016t0010a0020c0017t0010 | 4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3132G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3132 | chr18 | 45849335 | |||||
| chr18:45849372
|
A | G | 45 | a0001c0001t0002a0001c0001t0005a0001c0001t0032others(42): Show | 121 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*3095T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 3095 | chr18 | 45849372 | |||||
| chr18:45849523
|
T | C | 1 | a0002c0002t0031 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2944A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2944 | chr18 | 45849523 | |||||
| chr18:45849607
|
A | G | 1 | a0002c0002t0037 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2860T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2860 | chr18 | 45849607 | |||||
| chr18:45849741
|
C | G | 2 | a0016c0022t0020a0016c0022t0021 | 2 | HG01496.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2726G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2726 | chr18 | 45849741 | |||||
| chr18:45850001
|
C | T | 36 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(33): Show | 136 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*2466G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2466 | chr18 | 45850001 | |||||
| chr18:45850174
|
G | A | 40 | a0001c0001t0002a0001c0001t0005a0001c0001t0032others(37): Show | 116 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*2293C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2293 | chr18 | 45850174 | |||||
| chr18:45850225
|
C | A | 40 | a0001c0001t0002a0001c0001t0005a0001c0001t0032others(37): Show | 116 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*2242G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2242 | chr18 | 45850225 | |||||
| chr18:45850238
|
G | A | 1 | a0002c0002t0029 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2229C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2229 | chr18 | 45850238 | |||||
| chr18:45850357
|
C | T | 1 | a0001c0001t0036 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2110G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2110 | chr18 | 45850357 | |||||
| chr18:45850383
|
G | A | 3 | a0001c0001t0043a0003c0003t0016a0005c0005t0016 | 3 | HG00733.hp2 HG02683.hp1 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2084C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2084 | chr18 | 45850383 | |||||
| chr18:45850444
|
C | A | 40 | a0001c0001t0002a0001c0001t0005a0001c0001t0032others(37): Show | 116 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*2023G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 2023 | chr18 | 45850444 | |||||
| chr18:45850878
|
A | G | 1 | a0002c0002t0024 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1589T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 1589 | chr18 | 45850878 | |||||
| chr18:45850951
|
C | T | 1 | a0005c0014t0035 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1516G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 1516 | chr18 | 45850951 | |||||
| chr18:45851468
|
T | C | 1 | a0004c0004t0044 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*999A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 999 | chr18 | 45851468 | |||||
| chr18:45851602
|
G | A | 1 | a0002c0002t0029 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*865C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 865 | chr18 | 45851602 | |||||
| chr18:45851772
|
G | C | 2 | a0002c0002t0030a0002c0002t0031 | 2 | HG02615.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*695C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 695 | chr18 | 45851772 | |||||
| chr18:45851835
|
C | T | 8 | a0001c0001t0005a0002c0002t0017a0004c0004t0005others(5): Show | 19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*632G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 632 | chr18 | 45851835 | |||||
| chr18:45851885
|
C | T | 1 | a0021c0028t0018 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*582G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 582 | chr18 | 45851885 | |||||
| chr18:45852068
|
G | A | 1 | a0001c0001t0032 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*399C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 399 | chr18 | 45852068 | |||||
| chr18:45852197
|
C | T | 4 | a0016c0022t0020a0016c0022t0021a0018c0042t0022others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*270G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 270 | chr18 | 45852197 | |||||
| chr18:45852280
|
A | AAC | 10 | a0001c0001t0011a0002c0002t0014a0002c0038t0007others(7): Show | 17 | HG01261.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*185_*186dupGT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 186 | chr18 | 45852280 | |||||
| chr18:45852280
|
A | AACAC | 6 | a0006c0011t0006a0006c0011t0013a0006c0012t0006others(3): Show | 12 | HG01884.hp1 HG02559.hp1 HG02572.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*183_*186dupGTGT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 186 | chr18 | 45852280 | |||||
| chr18:45852280
|
A | AACACAC | 8 | a0001c0001t0005a0002c0002t0017a0004c0004t0005others(5): Show | 19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*181_*186dupGTGTGT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 186 | chr18 | 45852280 | |||||
| chr18:45852301
|
A | C | 3 | a0016c0022t0020a0016c0022t0021a0018c0042t0022 | 3 | HG01496.hp1 HG02886.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*166T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 166 | chr18 | 45852301 | |||||
| chr18:45852303
|
A | C | 4 | a0005c0005t0033a0016c0022t0020a0016c0022t0021others(1): Show | 4 | HG01496.hp1 HG02886.hp1 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*164T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 164 | chr18 | 45852303 | |||||
| chr18:45852327
|
C | T | 44 | a0001c0001t0002a0001c0001t0005a0001c0001t0032others(41): Show | 120 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*140G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 140 | chr18 | 45852327 | |||||
| chr18:45852393
|
A | C | 21 | a0001c0001t0005a0002c0002t0014a0002c0002t0017others(18): Show | 43 | HG01516.hp2 HG01517.hp2 HG01884.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*74T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 44/44 | 74 | chr18 | 45852393 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:45852660
|
C | T | 29 | a0001c0001t0001g0068a0001c0001t0001g0085a0001c0001t0001g0087others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.7558-11G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45852660 | ||||||
| chr18:45852781
|
G | A | 1 | a0004c0004t0044g0029 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7558-132C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45852781 | ||||||
| chr18:45852854
|
G | A | 11 | a0002c0002t0014g0220a0002c0038t0007g0008a0009c0007t0007g0006others(8): Show | 12 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.7558-205C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45852854 | ||||||
| chr18:45853005
|
G | A | 2 | a0001c0001t0001g0060a0022c0029t0001g0059 | 2 | HG01169.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.7558-356C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853005 | ||||||
| chr18:45853138
|
G | C | 1 | a0008c0008t0002g0018 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.7558-489C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853138 | ||||||
| chr18:45853264
|
C | G | 11 | a0002c0002t0014g0220a0002c0038t0007g0008a0009c0007t0007g0006others(8): Show | 12 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.7558-615G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853264 | ||||||
| chr18:45853436
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.7558-787T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853436 | ||||||
| chr18:45853581
|
C | T | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0166others(2): Show | 5 | NA18948.hp2 NA18967.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.7558-932G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853581 | ||||||
| chr18:45853582
|
C | G | 69 | a0001c0001t0002g0173a0001c0001t0002g0190a0001c0001t0032g0113others(66): Show | 72 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.7558-933G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853582 | ||||||
| chr18:45853709
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.7558-1060C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853709 | ||||||
| chr18:45853787
|
G | A | 4 | a0002c0002t0014g0220a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 4 | HG01884.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.7558-1138C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45853787 | ||||||
| chr18:45854000
|
A | G | 1 | a0010c0010t0001g0174 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.7558-1351T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854000 | ||||||
| chr18:45854013
|
C | T | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.7558-1364G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854013 | ||||||
| chr18:45854029
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0168 | 2 | NA19010.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.7558-1380T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854029 | ||||||
| chr18:45854190
|
T | G | 2 | a0003c0003t0012g0198a0003c0003t0012g0199 | 2 | NA18944.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.7557+1383A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854190 | ||||||
| chr18:45854218
|
G | T | 1 | a0004c0004t0044g0029 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7557+1355C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854218 | ||||||
| chr18:45854282
|
G | A | 1 | a0001c0001t0032g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.7557+1291C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854282 | ||||||
| chr18:45854338
|
T | C | 1 | a0004c0004t0044g0029 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.7557+1235A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854338 | ||||||
| chr18:45854559
|
CA | C | 6 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(3): Show | 6 | HG01109.hp2 NA18747.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.7557+1013delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854559 | ||||||
| chr18:45854642
|
T | C | 1 | a0010c0010t0001g0174 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.7557+931A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854642 | ||||||
| chr18:45854703
|
A | T | 1 | a0021c0028t0018g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.7557+870T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854703 | ||||||
| chr18:45854705
|
T | A | 2 | a0002c0002t0004g0053a0002c0002t0004g0230 | 2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.7557+868A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854705 | ||||||
| chr18:45854791
|
T | C | 2 | a0002c0002t0001g0063a0002c0033t0001g0061 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.7557+782A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854791 | ||||||
| chr18:45854926
|
C | T | 1 | a0003c0013t0001g0203 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7557+647G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854926 | ||||||
| chr18:45854956
|
T | C | 76 | a0001c0001t0002g0173a0001c0001t0002g0190a0001c0001t0012g0157others(73): Show | 79 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.7557+617A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45854956 | ||||||
| chr18:45855162
|
G | A | 3 | a0002c0002t0002g0249a0002c0002t0002g0250a0002c0002t0002g0263 | 3 | HG01261.hp2 HG01981.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.7557+411C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45855162 | ||||||
| chr18:45855558
|
A | G | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0137others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.7557+15T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 43/43 | chr18 | 45855558 | ||||||
| chr18:45855701
|
G | A | 3 | a0002c0002t0014g0220a0011c0015t0014g0290a0011c0015t0019g0291 | 3 | HG01884.hp2 HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.7443-14C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45855701 | ||||||
| chr18:45855768
|
C | T | 1 | a0008c0008t0002g0020 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.7443-81G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45855768 | ||||||
| chr18:45855773
|
A | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.7443-86T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45855773 | ||||||
| chr18:45856094
|
T | C | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.7443-407A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856094 | ||||||
| chr18:45856190
|
C | A | 19 | a0001c0001t0005g0098a0002c0002t0017g0229a0004c0004t0005g0023others(16): Show | 19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.7443-503G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856190 | ||||||
| chr18:45856256
|
T | C | 42 | a0001c0001t0005g0098a0002c0002t0014g0220a0002c0002t0017g0229others(39): Show | 43 | HG01516.hp2 HG01517.hp2 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.7443-569A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856256 | ||||||
| chr18:45856666
|
T | C | 1 | a0010c0010t0001g0174 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.7443-979A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856666 | ||||||
| chr18:45856699
|
C | T | 1 | a0005c0005t0033g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.7443-1012G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856699 | ||||||
| chr18:45856735
|
A | G | 17 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0090others(14): Show | 17 | HG00438.hp1 HG01081.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.7443-1048T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856735 | ||||||
| chr18:45856792
|
A | AT | 19 | a0001c0001t0005g0098a0002c0002t0017g0229a0004c0004t0005g0023others(16): Show | 19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.7442+1060dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856792 | ||||||
| chr18:45856992
|
G | A | 1 | a0001c0001t0004g0069 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.7442+861C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856992 | ||||||
| chr18:45856997
|
C | T | 17 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0090others(14): Show | 17 | HG00438.hp1 HG01081.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.7442+856G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45856997 | ||||||
| chr18:45857021
|
C | G | 9 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0156others(6): Show | 12 | HG02083.hp1 HG02523.hp2 HG03834.hp1 others(9): Show |
intron_variant | MODIFIER | c.7442+832G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857021 | ||||||
| chr18:45857099
|
G | GTTTA | 3 | a0008c0008t0001g0034a0012c0026t0005g0021a0012c0026t0005g0022 | 3 | HG01516.hp2 HG01517.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.7442+750_7442+753d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857099 | ||||||
| chr18:45857099
|
GTTTA | G | 75 | a0001c0001t0002g0173a0001c0001t0002g0190a0001c0001t0012g0157others(72): Show | 78 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.7442+750_7442+753d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857099 | ||||||
| chr18:45857281
|
T | C | 70 | a0001c0001t0002g0173a0001c0001t0002g0190a0001c0001t0012g0157others(67): Show | 73 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.7442+572A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857281 | ||||||
| chr18:45857403
|
G | A | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.7442+450C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857403 | ||||||
| chr18:45857529
|
C | A | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.7442+324G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857529 | ||||||
| chr18:45857587
|
C | A | 1 | a0018c0042t0022g0043 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.7442+266G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857587 | ||||||
| chr18:45857661
|
A | G | 1 | a0002c0002t0001g0064 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.7442+192T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857661 | ||||||
| chr18:45857760
|
C | T | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.7442+93G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 42/43 | chr18 | 45857760 | ||||||
| chr18:45858191
|
C | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.7227-123G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 41/43 | chr18 | 45858191 | ||||||
| chr18:45858196
|
G | C | 7 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0004g0058others(4): Show | 7 | HG01175.hp1 HG01243.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.7227-128C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 41/43 | chr18 | 45858196 | ||||||
| chr18:45858228
|
G | A | 1 | a0002c0002t0003g0237 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.7227-160C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 41/43 | chr18 | 45858228 | ||||||
| chr18:45858250
|
C | T | 1 | a0002c0002t0002g0239 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.7227-182G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 41/43 | chr18 | 45858250 | ||||||
| chr18:45858471
|
T | A | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.7226+95A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 41/43 | chr18 | 45858471 | ||||||
| chr18:45858871
|
A | AT | 22 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(19): Show | 23 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.7010-90dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45858871 | ||||||
| chr18:45858873
|
T | C | 1 | a0004c0004t0005g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.7010-91A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45858873 | ||||||
| chr18:45859145
|
T | A | 2 | a0002c0002t0004g0053a0002c0002t0004g0230 | 2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.7010-363A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45859145 | ||||||
| chr18:45859318
|
C | T | 1 | a0006c0012t0006g0272 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7010-536G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45859318 | ||||||
| chr18:45859469
|
A | G | 2 | a0012c0026t0005g0021a0012c0026t0005g0022 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.7009+635T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45859469 | ||||||
| chr18:45859933
|
ATC | A | 7 | a0007c0006t0003g0210a0007c0006t0003g0211a0007c0006t0003g0212others(4): Show | 7 | HG00323.hp1 HG01346.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.7009+169_7009+170d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45859933 | ||||||
| chr18:45859937
|
T | G | 7 | a0007c0006t0003g0210a0007c0006t0003g0211a0007c0006t0003g0212others(4): Show | 7 | HG00323.hp1 HG01346.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.7009+167A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45859937 | ||||||
| chr18:45859963
|
C | T | 2 | a0001c0001t0004g0074a0001c0001t0004g0075 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.7009+141G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 40/43 | chr18 | 45859963 | ||||||
| chr18:45860521
|
G | T | 1 | a0001c0001t0005g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6767-175C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860521 | ||||||
| chr18:45860527
|
G | A | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6767-181C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860527 | ||||||
| chr18:45860584
|
G | A | 3 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043 | 3 | HG01496.hp1 HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6767-238C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860584 | ||||||
| chr18:45860597
|
ATACT | A | 19 | a0001c0001t0005g0098a0002c0002t0017g0229a0004c0004t0005g0023others(16): Show | 19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.6767-255_6767-252d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860597 | ||||||
| chr18:45860641
|
C | T | 1 | a0006c0011t0013g0042 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.6767-295G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860641 | ||||||
| chr18:45860703
|
G | A | 71 | a0001c0001t0002g0173a0001c0001t0002g0190a0001c0001t0032g0113others(68): Show | 74 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.6767-357C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860703 | ||||||
| chr18:45860711
|
C | T | 1 | a0002c0002t0002g0239 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.6767-365G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860711 | ||||||
| chr18:45860720
|
T | C | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.6767-374A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860720 | ||||||
| chr18:45860762
|
C | T | 3 | a0002c0002t0014g0220a0011c0015t0014g0290a0011c0015t0019g0291 | 3 | HG01884.hp2 HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.6767-416G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860762 | ||||||
| chr18:45860900
|
C | T | 1 | a0005c0014t0003g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.6767-554G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860900 | ||||||
| chr18:45860907
|
G | C | 1 | a0021c0028t0018g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6767-561C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45860907 | ||||||
| chr18:45861353
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6767-1007G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45861353 | ||||||
| chr18:45861435
|
T | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.6767-1089A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45861435 | ||||||
| chr18:45861613
|
T | C | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.6767-1267A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45861613 | ||||||
| chr18:45861793
|
G | C | 1 | a0027c0041t0007g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.6767-1447C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45861793 | ||||||
| chr18:45861910
|
A | G | 1 | a0003c0044t0003g0182 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.6767-1564T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45861910 | ||||||
| chr18:45862111
|
G | A | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0137others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.6767-1765C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45862111 | ||||||
| chr18:45862156
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.6767-1810A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45862156 | ||||||
| chr18:45862319
|
T | C | 2 | a0002c0002t0030g0049a0002c0002t0031g0048 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.6767-1973A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45862319 | ||||||
| chr18:45862366
|
C | T | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6767-2020G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45862366 | ||||||
| chr18:45862604
|
TC | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.6767-2259delG | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45862604 | ||||||
| chr18:45862688
|
C | T | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6767-2342G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45862688 | ||||||
| chr18:45862877
|
C | T | 1 | a0004c0004t0044g0029 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.6767-2531G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45862877 | ||||||
| chr18:45862920
|
T | C | 76 | a0001c0001t0002g0173a0001c0001t0002g0190a0001c0001t0012g0157others(73): Show | 79 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.6767-2574A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45862920 | ||||||
| chr18:45863000
|
T | G | 1 | a0006c0012t0006g0222 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.6766+2615A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45863000 | ||||||
| chr18:45863242
|
C | G | 2 | a0002c0002t0029g0228a0018c0042t0022g0043 | 2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.6766+2373G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45863242 | ||||||
| chr18:45863253
|
T | C | 3 | a0001c0001t0001g0122a0001c0021t0001g0135a0001c0021t0004g0136 | 3 | HG01346.hp1 HG01975.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.6766+2362A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45863253 | ||||||
| chr18:45863816
|
G | C | 1 | a0001c0034t0001g0088 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.6766+1799C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45863816 | ||||||
| chr18:45863888
|
T | G | 1 | a0030c0047t0002g0268 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.6766+1727A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45863888 | ||||||
| chr18:45864067
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0123a0001c0001t0001g0126others(1): Show | 5 | HG00140.hp2 HG00639.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.6766+1548A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864067 | ||||||
| chr18:45864099
|
A | C | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6766+1516T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864099 | ||||||
| chr18:45864169
|
C | A | 1 | a0002c0002t0026g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6766+1446G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864169 | ||||||
| chr18:45864197
|
C | T | 4 | a0001c0001t0003g0093a0005c0025t0003g0016a0005c0025t0003g0109others(1): Show | 4 | HG01106.hp1 HG02280.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.6766+1418G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864197 | ||||||
| chr18:45864332
|
C | T | 19 | a0001c0001t0005g0098a0002c0002t0017g0229a0004c0004t0005g0023others(16): Show | 19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.6766+1283G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864332 | ||||||
| chr18:45864337
|
G | C | 7 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(4): Show | 7 | HG01884.hp1 HG02559.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.6766+1278C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864337 | ||||||
| chr18:45864654
|
C | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.6766+961G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864654 | ||||||
| chr18:45864892
|
T | G | 70 | a0001c0001t0002g0173a0001c0001t0002g0190a0001c0001t0012g0157others(67): Show | 73 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.6766+723A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864892 | ||||||
| chr18:45864921
|
T | C | 16 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0004g0056others(13): Show | 16 | HG00609.hp2 HG00621.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.6766+694A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864921 | ||||||
| chr18:45864989
|
C | T | 1 | a0001c0001t0012g0157 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.6766+626G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45864989 | ||||||
| chr18:45865242
|
T | G | 1 | a0002c0002t0029g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.6766+373A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45865242 | ||||||
| chr18:45865267
|
G | A | 1 | a0002c0002t0008g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6766+348C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45865267 | ||||||
| chr18:45865293
|
G | A | 19 | a0001c0001t0005g0098a0002c0002t0017g0229a0004c0004t0005g0023others(16): Show | 19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.6766+322C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45865293 | ||||||
| chr18:45865377
|
C | T | 72 | a0001c0001t0002g0173a0001c0001t0002g0190a0001c0001t0012g0157others(69): Show | 75 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.6766+238G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 39/43 | chr18 | 45865377 | ||||||
| chr18:45865765
|
C | CA | 13 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0080others(10): Show | 13 | HG00735.hp1 HG01175.hp1 HG01243.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.6622-7dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45865765 | ||||||
| chr18:45865765
|
C | CAAAAAAA others(3): Show |
1 | a0018c0043t0023g0046 | 1 | HG01891.hp1 | splice_region_variant&intron_variant | LOW | c.6622-16_6622-7dupT others(9): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45865765 | ||||||
| chr18:45865765
|
C | CAAAAAAA others(5): Show |
2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
splice_region_variant&intron_variant | LOW | c.6622-18_6622-7dupT others(11): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45865765 | ||||||
| chr18:45865765
|
CA | C | 72 | a0001c0001t0002g0173a0001c0001t0002g0190a0001c0001t0004g0074others(69): Show | 75 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
splice_region_variant&intron_variant | LOW | c.6622-7delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45865765 | ||||||
| chr18:45865851
|
G | C | 72 | a0001c0001t0002g0173a0001c0001t0002g0190a0001c0001t0012g0157others(69): Show | 75 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.6622-92C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45865851 | ||||||
| chr18:45866006
|
A | G | 2 | a0002c0002t0029g0228a0018c0042t0022g0043 | 2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.6622-247T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866006 | ||||||
| chr18:45866122
|
C | CT | 113 | a0001c0001t0001g0096a0001c0001t0002g0173a0001c0001t0005g0098others(110): Show | 117 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.6622-364dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866122 | ||||||
| chr18:45866177
|
T | C | 1 | a0021c0028t0018g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.6622-418A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866177 | ||||||
| chr18:45866183
|
G | A | 7 | a0002c0038t0007g0008a0009c0007t0007g0006a0009c0007t0007g0009others(4): Show | 8 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6622-424C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866183 | ||||||
| chr18:45866322
|
T | C | 10 | a0002c0002t0002g0246a0002c0002t0002g0248a0002c0002t0002g0251others(7): Show | 10 | HG00639.hp2 HG01074.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.6621+476A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866322 | ||||||
| chr18:45866364
|
G | A | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.6621+434C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866364 | ||||||
| chr18:45866467
|
C | T | 1 | a0001c0024t0001g0163 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.6621+331G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866467 | ||||||
| chr18:45866541
|
T | C | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.6621+257A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866541 | ||||||
| chr18:45866769
|
T | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.6621+29A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 38/43 | chr18 | 45866769 | ||||||
| chr18:45867257
|
C | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.6412-250G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 37/43 | chr18 | 45867257 | ||||||
| chr18:45867497
|
G | A | 1 | a0002c0002t0004g0285 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.6411+66C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 37/43 | chr18 | 45867497 | ||||||
| chr18:45868324
|
C | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.6226-576G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868324 | ||||||
| chr18:45868339
|
C | CTT | 7 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(4): Show | 7 | HG01884.hp1 HG02559.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.6226-593_6226-592d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868339 | ||||||
| chr18:45868390
|
C | T | 1 | a0003c0003t0003g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.6226-642G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868390 | ||||||
| chr18:45868391
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.6226-643C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868391 | ||||||
| chr18:45868400
|
C | T | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.6226-652G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868400 | ||||||
| chr18:45868423
|
C | T | 1 | a0004c0048t0003g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6226-675G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868423 | ||||||
| chr18:45868424
|
G | T | 1 | a0001c0001t0001g0083 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6226-676C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868424 | ||||||
| chr18:45868660
|
C | T | 19 | a0001c0001t0005g0098a0002c0002t0017g0229a0004c0004t0005g0023others(16): Show | 19 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.6226-912G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868660 | ||||||
| chr18:45868665
|
G | A | 1 | a0008c0008t0002g0020 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.6226-917C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868665 | ||||||
| chr18:45868671
|
T | C | 4 | a0019c0016t0010g0225a0019c0016t0010g0226a0020c0017t0010g0223others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.6226-923A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868671 | ||||||
| chr18:45868935
|
G | A | 68 | a0001c0001t0002g0173a0001c0001t0002g0190a0002c0002t0002g0002others(65): Show | 71 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.6226-1187C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868935 | ||||||
| chr18:45868954
|
C | T | 1 | a0002c0002t0029g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.6226-1206G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45868954 | ||||||
| chr18:45869047
|
T | A | 1 | a0004c0004t0015g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6226-1299A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45869047 | ||||||
| chr18:45869054
|
C | CA | 20 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(17): Show | 21 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.6226-1307dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45869054 | ||||||
| chr18:45869183
|
T | C | 7 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(4): Show | 7 | HG01884.hp1 HG02559.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.6225+1384A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45869183 | ||||||
| chr18:45869266
|
G | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0073others(72): Show | 78 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.6225+1301C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45869266 | ||||||
| chr18:45869353
|
T | C | 1 | a0005c0005t0033g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6225+1214A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45869353 | ||||||
| chr18:45869741
|
T | A | 1 | a0018c0043t0023g0046 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6225+826A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45869741 | ||||||
| chr18:45869928
|
TA | T | 82 | a0001c0001t0001g0122a0001c0001t0001g0143a0001c0001t0001g0155others(79): Show | 85 | HG00099.hp2 HG00438.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.6225+638delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45869928 | ||||||
| chr18:45870082
|
C | T | 1 | a0001c0001t0003g0132 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.6225+485G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45870082 | ||||||
| chr18:45870104
|
T | A | 8 | a0002c0002t0017g0229a0004c0004t0005g0023a0004c0004t0005g0024others(5): Show | 8 | HG02257.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.6225+463A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45870104 | ||||||
| chr18:45870242
|
T | A | 1 | a0001c0001t0039g0097 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.6225+325A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45870242 | ||||||
| chr18:45870386
|
T | C | 73 | a0001c0001t0002g0173a0001c0001t0002g0190a0001c0001t0012g0157others(70): Show | 76 | HG00099.hp2 HG00438.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.6225+181A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45870386 | ||||||
| chr18:45870393
|
G | A | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.6225+174C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 36/43 | chr18 | 45870393 | ||||||
| chr18:45870776
|
T | C | 1 | a0002c0002t0008g0244 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-34A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45870776 | ||||||
| chr18:45870779
|
G | T | 1 | a0002c0002t0008g0244 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-37C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45870779 | ||||||
| chr18:45870780
|
G | T | 1 | a0004c0004t0005g0024 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.6050-38C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45870780 | ||||||
| chr18:45870788
|
T | TA | 7 | a0002c0038t0007g0008a0009c0007t0007g0006a0009c0007t0007g0009others(4): Show | 8 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6050-47dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45870788 | ||||||
| chr18:45870788
|
TA | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.6050-47delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45870788 | ||||||
| chr18:45871002
|
C | T | 1 | a0004c0048t0003g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6050-260G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871002 | ||||||
| chr18:45871419
|
C | G | 1 | a0001c0001t0001g0146 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.6050-677G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871419 | ||||||
| chr18:45871431
|
T | C | 5 | a0001c0001t0001g0164a0016c0022t0020g0044a0016c0022t0021g0045others(2): Show | 5 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.6050-689A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871431 | ||||||
| chr18:45871537
|
T | C | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.6050-795A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871537 | ||||||
| chr18:45871645
|
T | A | 1 | a0002c0002t0008g0244 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-903A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871645 | ||||||
| chr18:45871646
|
G | C | 1 | a0002c0002t0008g0244 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-904C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871646 | ||||||
| chr18:45871647
|
G | T | 1 | a0002c0002t0008g0244 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-905C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871647 | ||||||
| chr18:45871651
|
A | T | 1 | a0002c0002t0008g0244 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-909T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871651 | ||||||
| chr18:45871653
|
T | G | 1 | a0002c0002t0008g0244 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-911A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871653 | ||||||
| chr18:45871655
|
A | G | 1 | a0002c0002t0008g0244 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-913T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871655 | ||||||
| chr18:45871658
|
C | T | 1 | a0002c0002t0008g0244 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6050-916G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871658 | ||||||
| chr18:45871891
|
A | AG | 14 | a0002c0002t0002g0246a0002c0002t0002g0248a0002c0002t0002g0251others(11): Show | 14 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.6050-1150_6050-114 others(5): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871891 | ||||||
| chr18:45871892
|
C | G | 14 | a0002c0002t0002g0246a0002c0002t0002g0248a0002c0002t0002g0251others(11): Show | 14 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.6050-1150G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871892 | ||||||
| chr18:45871966
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.6050-1224C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45871966 | ||||||
| chr18:45872074
|
A | AT | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.6050-1333dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872074 | ||||||
| chr18:45872331
|
T | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(125): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.6050-1589A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872331 | ||||||
| chr18:45872499
|
T | A | 1 | a0005c0014t0003g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.6050-1757A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872499 | ||||||
| chr18:45872502
|
G | A | 2 | a0005c0014t0003g0089a0005c0014t0035g0100 | 2 | HG01123.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.6050-1760C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872502 | ||||||
| chr18:45872602
|
G | A | 4 | a0019c0016t0010g0225a0019c0016t0010g0226a0020c0017t0010g0223others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.6050-1860C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872602 | ||||||
| chr18:45872831
|
G | A | 1 | a0001c0001t0004g0108 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.6050-2089C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872831 | ||||||
| chr18:45872971
|
C | T | 3 | a0002c0002t0014g0220a0011c0015t0014g0290a0011c0015t0019g0291 | 3 | HG01884.hp2 HG02723.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.6050-2229G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872971 | ||||||
| chr18:45872972
|
G | C | 1 | a0005c0005t0033g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6050-2230C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45872972 | ||||||
| chr18:45874059
|
C | T | 2 | a0002c0002t0029g0228a0018c0042t0022g0043 | 2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.6049+2177G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874059 | ||||||
| chr18:45874198
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0123 | 3 | HG00639.hp1 HG01074.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.6049+2038A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874198 | ||||||
| chr18:45874236
|
G | A | 6 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0121others(3): Show | 6 | HG00280.hp1 HG00741.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.6049+2000C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874236 | ||||||
| chr18:45874350
|
A | T | 2 | a0001c0001t0001g0146a0001c0001t0039g0097 | 2 | NA18990.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.6049+1886T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874350 | ||||||
| chr18:45874363
|
CA | C | 7 | a0002c0002t0002g0239a0002c0002t0002g0269a0008c0008t0002g0018others(4): Show | 7 | HG01358.hp2 HG02071.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.6049+1872delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874363 | ||||||
| chr18:45874365
|
A | G | 2 | a0002c0002t0002g0260a0002c0002t0002g0261 | 2 | NA18968.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.6049+1871T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874365 | ||||||
| chr18:45874658
|
G | A | 4 | a0019c0016t0010g0225a0019c0016t0010g0226a0020c0017t0010g0223others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.6049+1578C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874658 | ||||||
| chr18:45874821
|
T | C | 16 | a0001c0001t0003g0132a0001c0001t0005g0098a0002c0002t0017g0229others(13): Show | 16 | HG00735.hp1 HG01516.hp2 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.6049+1415A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874821 | ||||||
| chr18:45874889
|
C | T | 1 | a0003c0003t0016g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.6049+1347G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45874889 | ||||||
| chr18:45875088
|
G | C | 2 | a0012c0026t0005g0021a0012c0026t0005g0022 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.6049+1148C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875088 | ||||||
| chr18:45875221
|
G | C | 1 | a0005c0005t0003g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.6049+1015C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875221 | ||||||
| chr18:45875264
|
C | A | 72 | a0001c0001t0002g0173a0001c0001t0002g0190a0001c0001t0032g0113others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.6049+972G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875264 | ||||||
| chr18:45875461
|
T | C | 16 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0004g0058others(13): Show | 16 | HG00609.hp2 HG00621.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.6049+775A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875461 | ||||||
| chr18:45875597
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.6049+639G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875597 | ||||||
| chr18:45875667
|
A | C | 1 | a0002c0002t0003g0237 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.6049+569T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875667 | ||||||
| chr18:45875764
|
A | G | 7 | a0002c0038t0007g0008a0009c0007t0007g0006a0009c0007t0007g0009others(4): Show | 8 | HG01891.hp2 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6049+472T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875764 | ||||||
| chr18:45875863
|
T | A | 3 | a0002c0002t0029g0228a0018c0042t0022g0043a0018c0043t0023g0046 | 3 | HG01109.hp1 HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.6049+373A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875863 | ||||||
| chr18:45875992
|
G | C | 6 | a0016c0022t0020g0044a0016c0022t0021g0045a0019c0016t0010g0225others(3): Show | 6 | HG01496.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.6049+244C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45875992 | ||||||
| chr18:45876035
|
C | T | 1 | a0001c0001t0032g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6049+201G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45876035 | ||||||
| chr18:45876062
|
GA | G | 6 | a0016c0022t0020g0044a0016c0022t0021g0045a0019c0016t0010g0225others(3): Show | 6 | HG01496.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.6049+173delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45876062 | ||||||
| chr18:45876110
|
C | T | 38 | a0001c0001t0005g0098a0002c0002t0014g0220a0002c0002t0017g0229others(35): Show | 39 | HG01516.hp2 HG01517.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.6049+126G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 35/43 | chr18 | 45876110 | ||||||
| chr18:45876546
|
A | C | 6 | a0016c0022t0020g0044a0016c0022t0021g0045a0019c0016t0010g0225others(3): Show | 6 | HG01496.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.5943-204T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45876546 | ||||||
| chr18:45876588
|
T | C | 11 | a0002c0002t0014g0220a0002c0038t0007g0008a0009c0007t0007g0006others(8): Show | 12 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.5943-246A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45876588 | ||||||
| chr18:45876710
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5943-368C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45876710 | ||||||
| chr18:45876780
|
A | C | 8 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(5): Show | 8 | HG01496.hp1 HG01891.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.5943-438T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45876780 | ||||||
| chr18:45876846
|
C | T | 72 | a0001c0001t0002g0173a0001c0001t0002g0190a0001c0001t0012g0157others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.5943-504G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45876846 | ||||||
| chr18:45876874
|
C | A | 1 | a0002c0002t0002g0247 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5943-532G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45876874 | ||||||
| chr18:45877031
|
G | A | 1 | a0002c0002t0029g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5943-689C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877031 | ||||||
| chr18:45877258
|
T | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.5943-916A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877258 | ||||||
| chr18:45877264
|
T | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.5943-922A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877264 | ||||||
| chr18:45877265
|
G | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.5943-923C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877265 | ||||||
| chr18:45877297
|
T | C | 1 | a0001c0001t0004g0079 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5943-955A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877297 | ||||||
| chr18:45877355
|
G | T | 1 | a0001c0001t0009g0218 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5943-1013C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877355 | ||||||
| chr18:45877639
|
A | G | 1 | a0003c0003t0002g0287 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.5942+737T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877639 | ||||||
| chr18:45877691
|
T | C | 76 | a0001c0001t0002g0173a0001c0001t0002g0190a0001c0001t0012g0157others(73): Show | 79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.5942+685A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877691 | ||||||
| chr18:45877702
|
G | A | 4 | a0019c0016t0010g0225a0019c0016t0010g0226a0020c0017t0010g0223others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.5942+674C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877702 | ||||||
| chr18:45877886
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.5942+490G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 34/43 | chr18 | 45877886 | ||||||
| chr18:45878505
|
G | A | 3 | a0001c0001t0003g0093a0005c0025t0003g0016a0005c0025t0003g0109 | 3 | HG01106.hp1 HG02280.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.5870-57C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 33/43 | chr18 | 45878505 | ||||||
| chr18:45878593
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0123 | 3 | HG00639.hp1 HG01074.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.5870-145A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 33/43 | chr18 | 45878593 | ||||||
| chr18:45878620
|
C | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.5870-172G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 33/43 | chr18 | 45878620 | ||||||
| chr18:45878720
|
C | T | 6 | a0016c0022t0020g0044a0016c0022t0021g0045a0019c0016t0010g0225others(3): Show | 6 | HG01496.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.5870-272G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 33/43 | chr18 | 45878720 | ||||||
| chr18:45879306
|
C | A | 4 | a0002c0002t0002g0247a0002c0002t0002g0252a0002c0002t0008g0050others(1): Show | 4 | NA18945.hp1 NA18971.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.5668-92G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879306 | ||||||
| chr18:45879395
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.5668-181A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879395 | ||||||
| chr18:45879398
|
T | C | 31 | a0001c0001t0005g0098a0002c0002t0014g0220a0002c0002t0017g0229others(28): Show | 32 | HG01496.hp1 HG01516.hp2 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.5668-184A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879398 | ||||||
| chr18:45879399
|
G | A | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5668-185C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879399 | ||||||
| chr18:45879453
|
C | T | 1 | a0002c0040t0002g0267 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.5668-239G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879453 | ||||||
| chr18:45879454
|
G | A | 1 | a0002c0002t0002g0051 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.5668-240C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879454 | ||||||
| chr18:45879516
|
C | G | 15 | a0001c0001t0005g0098a0002c0002t0017g0229a0004c0004t0005g0023others(12): Show | 15 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.5668-302G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879516 | ||||||
| chr18:45879589
|
G | A | 1 | a0001c0001t0004g0071 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.5668-375C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879589 | ||||||
| chr18:45879778
|
C | T | 1 | a0031c0031t0001g0172 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5667+297G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45879778 | ||||||
| chr18:45880025
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.5667+50C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 32/43 | chr18 | 45880025 | ||||||
| chr18:45880302
|
C | A | 1 | a0001c0001t0001g0159 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.5519-79G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45880302 | ||||||
| chr18:45880530
|
G | C | 1 | a0021c0028t0018g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.5519-307C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45880530 | ||||||
| chr18:45880786
|
T | A | 16 | a0001c0001t0005g0098a0002c0002t0017g0229a0004c0004t0005g0023others(13): Show | 16 | HG01516.hp2 HG01517.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.5519-563A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45880786 | ||||||
| chr18:45880872
|
G | A | 1 | a0010c0010t0001g0174 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.5519-649C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45880872 | ||||||
| chr18:45880928
|
C | T | 2 | a0003c0003t0012g0198a0003c0003t0012g0199 | 2 | NA18944.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.5519-705G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45880928 | ||||||
| chr18:45881039
|
C | T | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5519-816G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45881039 | ||||||
| chr18:45881042
|
A | T | 12 | a0002c0002t0014g0220a0009c0007t0007g0006a0009c0007t0007g0009others(9): Show | 13 | HG01496.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.5519-819T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45881042 | ||||||
| chr18:45881162
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5519-939A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45881162 | ||||||
| chr18:45881186
|
T | G | 9 | a0002c0002t0017g0229a0002c0002t0029g0228a0004c0048t0003g0015others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.5519-963A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45881186 | ||||||
| chr18:45881400
|
T | C | 2 | a0002c0002t0004g0053a0002c0002t0004g0230 | 2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5518+874A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45881400 | ||||||
| chr18:45881698
|
T | C | 2 | a0011c0015t0014g0290a0011c0015t0019g0291 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5518+576A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45881698 | ||||||
| chr18:45881855
|
C | T | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5518+419G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45881855 | ||||||
| chr18:45882048
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5518+226G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 31/43 | chr18 | 45882048 | ||||||
| chr18:45882757
|
C | T | 1 | a0001c0034t0001g0088 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.5305-270G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45882757 | ||||||
| chr18:45882884
|
G | T | 1 | a0006c0012t0006g0272 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5305-397C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45882884 | ||||||
| chr18:45882921
|
A | G | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5305-434T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45882921 | ||||||
| chr18:45882964
|
G | A | 1 | a0021c0028t0018g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.5305-477C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45882964 | ||||||
| chr18:45883012
|
C | CA | 80 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0002others(77): Show | 84 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.5305-526dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883012 | ||||||
| chr18:45883012
|
C | CAA | 7 | a0002c0002t0001g0293a0002c0002t0002g0241a0002c0002t0002g0257others(4): Show | 7 | HG02818.hp1 HG03471.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.5305-527_5305-526d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883012 | ||||||
| chr18:45883012
|
C | CAAAAA | 8 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(5): Show | 8 | HG01884.hp1 HG02723.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.5305-530_5305-526d others(7): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883012 | ||||||
| chr18:45883015
|
A | C | 1 | a0001c0001t0043g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.5305-528T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883015 | ||||||
| chr18:45883031
|
A | AG | 9 | a0001c0001t0001g0073a0001c0001t0001g0096a0001c0001t0001g0156others(6): Show | 9 | HG01175.hp2 HG01243.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.5305-545dupC | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883031 | ||||||
| chr18:45883031
|
A | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(130): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.5305-544T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883031 | ||||||
| chr18:45883069
|
G | A | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.5305-582C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883069 | ||||||
| chr18:45883347
|
A | G | 1 | a0002c0002t0002g0266 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.5305-860T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883347 | ||||||
| chr18:45883361
|
A | C | 3 | a0002c0002t0004g0053a0002c0002t0004g0230a0002c0002t0026g0235 | 3 | HG02615.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.5305-874T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883361 | ||||||
| chr18:45883461
|
C | CTT | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.5305-976_5305-975d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883461 | ||||||
| chr18:45883461
|
CT | C | 14 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(11): Show | 14 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.5305-975delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883461 | ||||||
| chr18:45883491
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.5305-1004G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883491 | ||||||
| chr18:45883507
|
T | C | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5305-1020A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883507 | ||||||
| chr18:45883614
|
G | GT | 59 | a0001c0001t0003g0114a0002c0002t0001g0293a0002c0002t0002g0002others(56): Show | 61 | HG00621.hp1 HG00733.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.5304+1002dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883614 | ||||||
| chr18:45883614
|
G | GTT | 9 | a0001c0001t0003g0176a0002c0002t0002g0240a0002c0038t0007g0008others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.5304+1001_5304+100 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883614 | ||||||
| chr18:45883614
|
GT | G | 25 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0005g0023others(22): Show | 25 | HG00140.hp1 HG00323.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.5304+1002delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883614 | ||||||
| chr18:45883619
|
T | TTG | 22 | a0001c0001t0001g0068a0001c0001t0001g0077a0001c0001t0001g0143others(19): Show | 22 | HG00735.hp1 HG01109.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.5304+997_5304+998i others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883619 | ||||||
| chr18:45883620
|
T | TG | 98 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.5304+996_5304+997i others(3): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883620 | ||||||
| chr18:45883621
|
T | G | 5 | a0004c0004t0004g0012a0004c0004t0009g0036a0005c0005t0033g0047others(2): Show | 5 | HG01361.hp2 HG02071.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.5304+996A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883621 | ||||||
| chr18:45883622
|
T | G | 21 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0005g0023others(18): Show | 21 | HG00140.hp1 HG01358.hp2 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.5304+995A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883622 | ||||||
| chr18:45883629
|
T | G | 2 | a0001c0001t0004g0074a0001c0001t0004g0075 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.5304+988A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883629 | ||||||
| chr18:45883630
|
T | G | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5304+987A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883630 | ||||||
| chr18:45883631
|
T | G | 2 | a0001c0021t0001g0135a0001c0021t0004g0136 | 2 | HG01346.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.5304+986A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883631 | ||||||
| chr18:45883635
|
T | G | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.5304+982A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883635 | ||||||
| chr18:45883659
|
G | GT | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5304+957dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883659 | ||||||
| chr18:45883694
|
A | T | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5304+923T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45883694 | ||||||
| chr18:45884521
|
A | G | 1 | a0003c0003t0003g0283 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.5304+96T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 30/43 | chr18 | 45884521 | ||||||
| chr18:45884860
|
C | A | 1 | a0003c0003t0003g0185 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.5110-49G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45884860 | ||||||
| chr18:45884946
|
A | C | 1 | a0004c0048t0003g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5110-135T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45884946 | ||||||
| chr18:45885060
|
C | T | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5110-249G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45885060 | ||||||
| chr18:45885063
|
G | A | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG01109.hp2 NA18747.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.5110-252C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45885063 | ||||||
| chr18:45885359
|
T | C | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5110-548A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45885359 | ||||||
| chr18:45885379
|
A | T | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5110-568T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45885379 | ||||||
| chr18:45885675
|
C | T | 3 | a0004c0004t0005g0027a0004c0004t0005g0031a0025c0036t0013g0286 | 3 | HG02572.hp2 HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.5110-864G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45885675 | ||||||
| chr18:45886185
|
G | C | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5110-1374C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886185 | ||||||
| chr18:45886186
|
C | G | 1 | a0003c0003t0003g0201 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.5110-1375G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886186 | ||||||
| chr18:45886343
|
G | A | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5109+1408C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886343 | ||||||
| chr18:45886369
|
A | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.5109+1382T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886369 | ||||||
| chr18:45886520
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.5109+1231A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886520 | ||||||
| chr18:45886568
|
C | T | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.5109+1183G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886568 | ||||||
| chr18:45886571
|
T | C | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5109+1180A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886571 | ||||||
| chr18:45886585
|
C | T | 77 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0002others(74): Show | 80 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.5109+1166G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886585 | ||||||
| chr18:45886763
|
A | G | 1 | a0001c0001t0009g0218 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5109+988T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886763 | ||||||
| chr18:45886805
|
C | T | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5109+946G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886805 | ||||||
| chr18:45886912
|
C | T | 1 | a0002c0002t0002g0257 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5109+839G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886912 | ||||||
| chr18:45886953
|
G | C | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5109+798C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45886953 | ||||||
| chr18:45887170
|
C | T | 1 | a0002c0002t0002g0238 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.5109+581G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45887170 | ||||||
| chr18:45887519
|
G | C | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.5109+232C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 29/43 | chr18 | 45887519 | ||||||
| chr18:45888038
|
T | C | 3 | a0002c0002t0017g0229a0002c0002t0029g0228a0006c0012t0006g0227 | 3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4953-131A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888038 | ||||||
| chr18:45888108
|
T | C | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4953-201A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888108 | ||||||
| chr18:45888116
|
G | C | 1 | a0002c0002t0008g0066 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.4953-209C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888116 | ||||||
| chr18:45888182
|
C | T | 1 | a0005c0005t0033g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4953-275G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888182 | ||||||
| chr18:45888191
|
C | T | 5 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(2): Show | 5 | HG01109.hp2 NA18747.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.4953-284G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888191 | ||||||
| chr18:45888256
|
C | T | 2 | a0002c0002t0002g0249a0002c0002t0002g0250 | 2 | HG01981.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.4953-349G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888256 | ||||||
| chr18:45888313
|
A | AT | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4953-407dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888313 | ||||||
| chr18:45888317
|
A | T | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4953-410T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888317 | ||||||
| chr18:45888327
|
G | A | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4953-420C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888327 | ||||||
| chr18:45888846
|
GT | G | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4953-940delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888846 | ||||||
| chr18:45888982
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.4952+816G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45888982 | ||||||
| chr18:45889423
|
T | C | 1 | a0005c0005t0033g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4952+375A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45889423 | ||||||
| chr18:45889482
|
G | A | 1 | a0002c0002t0026g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4952+316C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45889482 | ||||||
| chr18:45889614
|
G | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.4952+184C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45889614 | ||||||
| chr18:45889630
|
T | G | 1 | a0004c0004t0003g0030 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4952+168A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 28/43 | chr18 | 45889630 | ||||||
| chr18:45889992
|
C | T | 1 | a0025c0036t0013g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4810-52G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45889992 | ||||||
| chr18:45890169
|
C | T | 2 | a0001c0021t0001g0135a0001c0021t0004g0136 | 2 | HG01346.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.4810-229G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45890169 | ||||||
| chr18:45890381
|
G | T | 1 | a0001c0001t0009g0218 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4810-441C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45890381 | ||||||
| chr18:45890580
|
T | TA | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.4810-641dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45890580 | ||||||
| chr18:45890717
|
T | A | 1 | a0001c0001t0001g0037 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4810-777A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45890717 | ||||||
| chr18:45890799
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.4810-859T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45890799 | ||||||
| chr18:45891047
|
T | C | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4810-1107A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891047 | ||||||
| chr18:45891142
|
T | C | 2 | a0015c0020t0004g0170a0015c0020t0004g0217 | 2 | HG00621.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.4810-1202A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891142 | ||||||
| chr18:45891163
|
C | T | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4810-1223G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891163 | ||||||
| chr18:45891170
|
G | A | 44 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(41): Show | 47 | HG00609.hp1 HG01109.hp2 HG01169.hp2 others(44): Show |
intron_variant | MODIFIER | c.4810-1230C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891170 | ||||||
| chr18:45891236
|
C | T | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.4810-1296G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891236 | ||||||
| chr18:45891376
|
G | A | 2 | a0004c0004t0005g0027a0004c0004t0005g0031 | 2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4810-1436C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891376 | ||||||
| chr18:45891498
|
C | CA | 27 | a0001c0001t0001g0077a0002c0002t0002g0257a0002c0002t0004g0285others(24): Show | 27 | HG00609.hp2 HG00621.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.4810-1559dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891498 | ||||||
| chr18:45891498
|
CA | C | 18 | a0001c0001t0001g0147a0002c0002t0001g0064a0002c0002t0002g0002others(15): Show | 21 | HG00733.hp1 HG01081.hp2 NA18747.hp2 others(18): Show |
intron_variant | MODIFIER | c.4810-1559delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891498 | ||||||
| chr18:45891962
|
C | T | 1 | a0021c0028t0018g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4810-2022G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45891962 | ||||||
| chr18:45892070
|
A | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.4810-2130T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892070 | ||||||
| chr18:45892088
|
G | A | 2 | a0002c0002t0030g0049a0002c0002t0031g0048 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4810-2148C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892088 | ||||||
| chr18:45892181
|
G | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.4810-2241C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892181 | ||||||
| chr18:45892191
|
C | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.4810-2251G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892191 | ||||||
| chr18:45892209
|
C | CA | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4810-2270dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892209 | ||||||
| chr18:45892302
|
T | A | 2 | a0001c0001t0004g0056a0001c0001t0004g0081 | 2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.4810-2362A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892302 | ||||||
| chr18:45892359
|
T | C | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4810-2419A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892359 | ||||||
| chr18:45892427
|
T | C | 5 | a0001c0001t0001g0120a0001c0001t0001g0158a0001c0001t0002g0190others(2): Show | 5 | HG04199.hp2 NA18973.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.4810-2487A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892427 | ||||||
| chr18:45892548
|
T | A | 1 | a0005c0025t0003g0016 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4810-2608A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892548 | ||||||
| chr18:45892613
|
C | T | 2 | a0007c0006t0003g0213a0007c0006t0003g0214 | 2 | HG00323.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4810-2673G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892613 | ||||||
| chr18:45892670
|
C | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.4810-2730G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892670 | ||||||
| chr18:45892708
|
C | T | 65 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0002others(62): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.4810-2768G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892708 | ||||||
| chr18:45892752
|
A | G | 1 | a0005c0005t0033g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4810-2812T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892752 | ||||||
| chr18:45892867
|
T | C | 1 | a0002c0002t0002g0257 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4810-2927A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45892867 | ||||||
| chr18:45893024
|
T | C | 5 | a0002c0002t0017g0229a0002c0002t0029g0228a0006c0012t0006g0227others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.4810-3084A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893024 | ||||||
| chr18:45893164
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.4810-3224A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893164 | ||||||
| chr18:45893254
|
T | A | 1 | a0004c0048t0003g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4810-3314A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893254 | ||||||
| chr18:45893410
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.4810-3470G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893410 | ||||||
| chr18:45893458
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.4810-3518T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893458 | ||||||
| chr18:45893505
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.4810-3565T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893505 | ||||||
| chr18:45893551
|
T | TA | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.4810-3612dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893551 | ||||||
| chr18:45893654
|
A | G | 4 | a0002c0002t0014g0220a0006c0012t0006g0221a0006c0012t0006g0222others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4810-3714T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893654 | ||||||
| chr18:45893792
|
T | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.4810-3852A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893792 | ||||||
| chr18:45893909
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.4810-3969C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45893909 | ||||||
| chr18:45894034
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4810-4094C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894034 | ||||||
| chr18:45894275
|
C | G | 85 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0002others(82): Show | 89 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.4810-4335G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894275 | ||||||
| chr18:45894430
|
G | A | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.4810-4490C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894430 | ||||||
| chr18:45894476
|
A | T | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4810-4536T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894476 | ||||||
| chr18:45894479
|
T | A | 2 | a0001c0001t0004g0056a0002c0009t0002g0276 | 2 | HG04204.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.4810-4539A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894479 | ||||||
| chr18:45894502
|
C | T | 2 | a0005c0005t0003g0104a0005c0005t0034g0086 | 2 | HG00741.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.4810-4562G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894502 | ||||||
| chr18:45894712
|
G | A | 75 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0002others(72): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.4809+4692C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894712 | ||||||
| chr18:45894830
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.4809+4574A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894830 | ||||||
| chr18:45894858
|
G | A | 4 | a0019c0016t0010g0225a0019c0016t0010g0226a0020c0017t0010g0223others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4809+4546C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894858 | ||||||
| chr18:45894958
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.4809+4446G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45894958 | ||||||
| chr18:45895023
|
G | A | 9 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4809+4381C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895023 | ||||||
| chr18:45895067
|
G | A | 1 | a0018c0042t0022g0043 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4809+4337C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895067 | ||||||
| chr18:45895077
|
C | G | 294 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.4809+4327G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895077 | ||||||
| chr18:45895306
|
G | A | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4809+4098C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895306 | ||||||
| chr18:45895424
|
T | C | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4809+3980A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895424 | ||||||
| chr18:45895437
|
C | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.4809+3967G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895437 | ||||||
| chr18:45895444
|
GA | G | 86 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(83): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.4809+3959delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895444 | ||||||
| chr18:45895587
|
T | C | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4809+3817A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895587 | ||||||
| chr18:45895772
|
G | A | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4809+3632C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895772 | ||||||
| chr18:45895842
|
A | C | 1 | a0001c0001t0001g0149 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.4809+3562T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45895842 | ||||||
| chr18:45896043
|
A | C | 1 | a0001c0001t0001g0152 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4809+3361T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896043 | ||||||
| chr18:45896137
|
C | A | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4809+3267G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896137 | ||||||
| chr18:45896145
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.4809+3259T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896145 | ||||||
| chr18:45896155
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4809+3249A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896155 | ||||||
| chr18:45896156
|
A | G | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4809+3248T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896156 | ||||||
| chr18:45896178
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.4809+3226A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896178 | ||||||
| chr18:45896363
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.4809+3041C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896363 | ||||||
| chr18:45896421
|
G | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 121 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.4809+2983C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896421 | ||||||
| chr18:45896499
|
A | G | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4809+2905T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896499 | ||||||
| chr18:45896631
|
ACCTCCTG others(12): Show |
A | 1 | a0001c0001t0003g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4809+2754_4809+277 others(23): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896631 | ||||||
| chr18:45896706
|
G | A | 1 | a0001c0001t0003g0094 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4809+2698C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896706 | ||||||
| chr18:45896827
|
G | A | 1 | a0030c0047t0002g0268 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4809+2577C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896827 | ||||||
| chr18:45896836
|
C | A | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.4809+2568G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896836 | ||||||
| chr18:45896839
|
G | C | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4809+2565C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45896839 | ||||||
| chr18:45897063
|
A | G | 2 | a0001c0001t0001g0144a0010c0010t0001g0145 | 2 | NA18968.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.4809+2341T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897063 | ||||||
| chr18:45897259
|
T | G | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4809+2145A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897259 | ||||||
| chr18:45897285
|
T | A | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4809+2119A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897285 | ||||||
| chr18:45897428
|
G | A | 4 | a0002c0002t0014g0220a0006c0012t0006g0221a0006c0012t0006g0222others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4809+1976C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897428 | ||||||
| chr18:45897431
|
T | C | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4809+1973A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897431 | ||||||
| chr18:45897442
|
T | TA | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4809+1961_4809+196 others(5): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897442 | ||||||
| chr18:45897447
|
T | C | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4809+1957A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897447 | ||||||
| chr18:45897475
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4809+1929A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897475 | ||||||
| chr18:45897497
|
T | G | 2 | a0011c0015t0014g0290a0011c0015t0019g0291 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4809+1907A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897497 | ||||||
| chr18:45897513
|
C | T | 3 | a0002c0002t0017g0229a0002c0002t0029g0228a0006c0012t0006g0227 | 3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4809+1891G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897513 | ||||||
| chr18:45897640
|
G | A | 2 | a0002c0002t0002g0260a0002c0002t0002g0261 | 2 | NA18968.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.4809+1764C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897640 | ||||||
| chr18:45897712
|
T | C | 1 | a0021c0028t0018g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4809+1692A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897712 | ||||||
| chr18:45897793
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4809+1611T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45897793 | ||||||
| chr18:45898138
|
T | C | 2 | a0004c0004t0004g0012a0004c0004t0009g0036 | 2 | HG01361.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.4809+1266A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898138 | ||||||
| chr18:45898209
|
T | C | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4809+1195A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898209 | ||||||
| chr18:45898246
|
C | A | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.4809+1158G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898246 | ||||||
| chr18:45898277
|
G | A | 3 | a0003c0003t0003g0193a0003c0003t0003g0195a0003c0003t0042g0194 | 3 | NA18966.hp2 NA19004.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.4809+1127C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898277 | ||||||
| chr18:45898603
|
A | G | 103 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(100): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.4809+801T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898603 | ||||||
| chr18:45898823
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4809+581G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898823 | ||||||
| chr18:45898848
|
C | T | 2 | a0011c0015t0014g0290a0011c0015t0019g0291 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4809+556G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898848 | ||||||
| chr18:45898865
|
G | A | 2 | a0004c0004t0005g0032a0004c0004t0005g0033 | 2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4809+539C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898865 | ||||||
| chr18:45898892
|
C | A | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4809+512G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898892 | ||||||
| chr18:45898977
|
T | A | 1 | a0002c0009t0002g0280 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4809+427A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45898977 | ||||||
| chr18:45899018
|
G | A | 87 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0002others(84): Show | 91 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.4809+386C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45899018 | ||||||
| chr18:45899099
|
T | C | 75 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0002others(72): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.4809+305A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45899099 | ||||||
| chr18:45899339
|
T | C | 2 | a0001c0001t0004g0072a0002c0038t0007g0008 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4809+65A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 27/43 | chr18 | 45899339 | ||||||
| chr18:45899798
|
T | C | 1 | a0002c0002t0002g0247 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4647-232A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45899798 | ||||||
| chr18:45899855
|
G | C | 1 | a0003c0003t0001g0184 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4647-289C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45899855 | ||||||
| chr18:45899903
|
T | C | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4647-337A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45899903 | ||||||
| chr18:45899975
|
C | G | 103 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(100): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.4647-409G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45899975 | ||||||
| chr18:45900102
|
T | C | 103 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(100): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.4647-536A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900102 | ||||||
| chr18:45900103
|
G | A | 1 | a0002c0002t0030g0049 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4647-537C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900103 | ||||||
| chr18:45900105
|
T | C | 1 | a0008c0008t0001g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4647-539A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900105 | ||||||
| chr18:45900130
|
T | C | 103 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(100): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.4647-564A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900130 | ||||||
| chr18:45900404
|
C | CA | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.4646+591dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900404 | ||||||
| chr18:45900404
|
C | CAA | 8 | a0001c0001t0001g0152a0001c0001t0001g0168a0002c0002t0002g0269others(5): Show | 8 | HG01192.hp2 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.4646+590_4646+591d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900404 | ||||||
| chr18:45900495
|
C | T | 78 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0002others(75): Show | 81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.4646+501G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900495 | ||||||
| chr18:45900564
|
G | A | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4646+432C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900564 | ||||||
| chr18:45900590
|
C | T | 5 | a0002c0002t0014g0220a0006c0012t0006g0221a0006c0012t0006g0222others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4646+406G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900590 | ||||||
| chr18:45900806
|
C | A | 91 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(88): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.4646+190G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900806 | ||||||
| chr18:45900818
|
G | A | 1 | a0019c0016t0010g0226 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4646+178C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900818 | ||||||
| chr18:45900856
|
A | C | 9 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4646+140T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900856 | ||||||
| chr18:45900961
|
A | G | 91 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(88): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.4646+35T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 26/43 | chr18 | 45900961 | ||||||
| chr18:45901268
|
T | G | 1 | a0005c0005t0033g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4475-101A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901268 | ||||||
| chr18:45901290
|
G | C | 1 | a0004c0048t0003g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4475-123C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901290 | ||||||
| chr18:45901405
|
C | T | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.4475-238G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901405 | ||||||
| chr18:45901625
|
G | A | 1 | a0002c0002t0008g0243 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4475-458C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901625 | ||||||
| chr18:45901649
|
T | G | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4475-482A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901649 | ||||||
| chr18:45901765
|
C | CCA | 13 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0002others(10): Show | 16 | HG00609.hp2 HG00741.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.4475-600_4475-599d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901765 | ||||||
| chr18:45901765
|
C | CCACA | 7 | a0004c0004t0015g0014a0004c0048t0003g0015a0009c0007t0007g0006others(4): Show | 8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.4475-602_4475-599d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901765 | ||||||
| chr18:45901765
|
C | CCACACA | 9 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4475-604_4475-599d others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901765 | ||||||
| chr18:45901765
|
C | CCACACAC others(1): Show |
3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4475-606_4475-599d others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901765 | ||||||
| chr18:45901765
|
CCA | C | 5 | a0002c0002t0002g0263a0002c0002t0014g0220a0006c0012t0006g0221others(2): Show | 5 | HG01261.hp2 HG01891.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.4475-600_4475-599d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901765 | ||||||
| chr18:45901765
|
CCACA | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0159others(7): Show | 13 | HG02083.hp1 HG02523.hp2 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.4475-602_4475-599d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901765 | ||||||
| chr18:45901790
|
C | CAT | 5 | a0001c0001t0001g0003a0001c0001t0001g0123a0001c0001t0001g0158others(2): Show | 6 | HG00438.hp2 HG00639.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.4475-624_4475-623i others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901790 | ||||||
| chr18:45901790
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(108): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.4475-623G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901790 | ||||||
| chr18:45901803
|
G | C | 1 | a0001c0001t0032g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4475-636C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901803 | ||||||
| chr18:45901833
|
T | G | 1 | a0001c0001t0005g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4475-666A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901833 | ||||||
| chr18:45901920
|
T | C | 1 | a0025c0036t0013g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4475-753A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901920 | ||||||
| chr18:45901959
|
T | A | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.4475-792A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45901959 | ||||||
| chr18:45902128
|
T | C | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4475-961A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45902128 | ||||||
| chr18:45902138
|
A | G | 1 | a0004c0004t0003g0030 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4475-971T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45902138 | ||||||
| chr18:45902280
|
C | T | 3 | a0002c0002t0017g0229a0002c0002t0029g0228a0006c0012t0006g0227 | 3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4475-1113G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45902280 | ||||||
| chr18:45902295
|
T | G | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.4475-1128A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45902295 | ||||||
| chr18:45902681
|
CTCTTA | C | 3 | a0001c0001t0001g0154a0001c0001t0001g0175a0001c0030t0001g0138 | 3 | NA18948.hp2 NA18967.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.4474+1287_4474+129 others(9): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45902681 | ||||||
| chr18:45902743
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0095others(36): Show | 42 | HG00609.hp1 HG01109.hp2 HG02074.hp2 others(39): Show |
intron_variant | MODIFIER | c.4474+1230C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45902743 | ||||||
| chr18:45903021
|
G | A | 5 | a0002c0002t0002g0054a0002c0002t0002g0239a0002c0002t0002g0269others(2): Show | 5 | NA18940.hp2 NA18942.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.4474+952C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903021 | ||||||
| chr18:45903059
|
T | A | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.4474+914A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903059 | ||||||
| chr18:45903078
|
G | A | 5 | a0001c0001t0001g0128a0009c0007t0007g0006a0009c0007t0007g0010others(2): Show | 6 | HG02109.hp1 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4474+895C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903078 | ||||||
| chr18:45903113
|
AT | A | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.4474+859delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903113 | ||||||
| chr18:45903184
|
C | T | 1 | a0005c0014t0003g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4474+789G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903184 | ||||||
| chr18:45903186
|
T | C | 1 | a0001c0001t0043g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4474+787A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903186 | ||||||
| chr18:45903213
|
C | A | 18 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0120others(15): Show | 18 | HG00609.hp1 HG02074.hp2 HG04199.hp2 others(15): Show |
intron_variant | MODIFIER | c.4474+760G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903213 | ||||||
| chr18:45903360
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.4474+613C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903360 | ||||||
| chr18:45903414
|
G | A | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.4474+559C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903414 | ||||||
| chr18:45903487
|
T | G | 1 | a0021c0028t0018g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4474+486A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903487 | ||||||
| chr18:45903514
|
G | A | 1 | a0002c0002t0002g0256 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4474+459C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 25/43 | chr18 | 45903514 | ||||||
| chr18:45904160
|
T | G | 2 | a0001c0001t0005g0098a0001c0001t0032g0113 | 2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.4330-43A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45904160 | ||||||
| chr18:45904326
|
T | C | 10 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(7): Show | 10 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.4330-209A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45904326 | ||||||
| chr18:45904376
|
C | T | 1 | a0001c0001t0004g0081 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4330-259G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45904376 | ||||||
| chr18:45904552
|
G | A | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4330-435C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45904552 | ||||||
| chr18:45904630
|
G | A | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4330-513C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45904630 | ||||||
| chr18:45904701
|
C | A | 4 | a0001c0001t0004g0216a0001c0001t0009g0218a0015c0020t0004g0170others(1): Show | 4 | HG00438.hp1 HG00621.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.4330-584G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45904701 | ||||||
| chr18:45904737
|
TA | T | 91 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(88): Show | 95 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.4330-621delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45904737 | ||||||
| chr18:45905054
|
A | G | 80 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0002others(77): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.4330-937T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45905054 | ||||||
| chr18:45905184
|
T | C | 1 | a0018c0043t0023g0046 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4330-1067A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45905184 | ||||||
| chr18:45905384
|
A | G | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4330-1267T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45905384 | ||||||
| chr18:45905558
|
C | A | 2 | a0011c0015t0014g0290a0011c0015t0019g0291 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4330-1441G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45905558 | ||||||
| chr18:45905745
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.4330-1628T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45905745 | ||||||
| chr18:45905975
|
C | T | 1 | a0027c0041t0007g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4330-1858G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45905975 | ||||||
| chr18:45905996
|
G | C | 103 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(100): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.4330-1879C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45905996 | ||||||
| chr18:45906009
|
A | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0143 | 2 | NA18964.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.4330-1892T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906009 | ||||||
| chr18:45906168
|
C | A | 1 | a0003c0003t0003g0185 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.4329+1790G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906168 | ||||||
| chr18:45906173
|
C | T | 6 | a0004c0004t0005g0023a0004c0004t0005g0024a0004c0004t0005g0025others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.4329+1785G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906173 | ||||||
| chr18:45906319
|
A | G | 1 | a0002c0009t0002g0279 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4329+1639T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906319 | ||||||
| chr18:45906394
|
C | T | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0137others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.4329+1564G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906394 | ||||||
| chr18:45906655
|
AT | A | 16 | a0001c0001t0001g0101a0001c0001t0001g0143a0001c0001t0001g0155others(13): Show | 16 | HG01884.hp1 HG01981.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.4329+1302delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906655 | ||||||
| chr18:45906670
|
T | A | 1 | a0002c0002t0002g0239 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.4329+1288A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906670 | ||||||
| chr18:45906679
|
G | GTC | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4329+1277_4329+127 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906679 | ||||||
| chr18:45906815
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.4329+1143G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906815 | ||||||
| chr18:45906888
|
T | G | 1 | a0008c0008t0002g0019 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4329+1070A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906888 | ||||||
| chr18:45906937
|
T | C | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4329+1021A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45906937 | ||||||
| chr18:45907281
|
A | G | 4 | a0019c0016t0010g0225a0019c0016t0010g0226a0020c0017t0010g0223others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4329+677T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907281 | ||||||
| chr18:45907350
|
A | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0080 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.4329+608T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907350 | ||||||
| chr18:45907406
|
G | T | 1 | a0005c0005t0016g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4329+552C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907406 | ||||||
| chr18:45907408
|
C | A | 1 | a0005c0005t0016g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4329+550G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907408 | ||||||
| chr18:45907453
|
G | A | 1 | a0005c0005t0033g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4329+505C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907453 | ||||||
| chr18:45907514
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4329+444G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907514 | ||||||
| chr18:45907548
|
C | G | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4329+410G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907548 | ||||||
| chr18:45907611
|
T | C | 75 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0002others(72): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.4329+347A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907611 | ||||||
| chr18:45907658
|
A | G | 9 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4329+300T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907658 | ||||||
| chr18:45907704
|
T | C | 9 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4329+254A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907704 | ||||||
| chr18:45907761
|
C | T | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4329+197G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907761 | ||||||
| chr18:45907920
|
TA | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(118): Show | 125 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.4329+37delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907920 | ||||||
| chr18:45907920
|
TAA | T | 6 | a0001c0001t0001g0068a0001c0001t0001g0131a0001c0001t0001g0134others(3): Show | 6 | HG00099.hp1 HG01081.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.4329+36_4329+37del others(2): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 24/43 | chr18 | 45907920 | ||||||
| chr18:45908107
|
G | A | 4 | a0001c0001t0011g0151a0001c0001t0011g0180a0001c0001t0011g0181others(1): Show | 4 | HG01109.hp2 HG01261.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.4206-26C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45908107 | ||||||
| chr18:45908874
|
G | A | 90 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(87): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.4206-793C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45908874 | ||||||
| chr18:45908948
|
C | CA | 12 | a0002c0002t0002g0284a0004c0004t0015g0014a0004c0048t0003g0015others(9): Show | 12 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.4206-868dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45908948 | ||||||
| chr18:45909138
|
T | C | 1 | a0002c0002t0031g0048 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4206-1057A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909138 | ||||||
| chr18:45909301
|
A | G | 103 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(100): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.4205+1220T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909301 | ||||||
| chr18:45909329
|
C | T | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4205+1192G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909329 | ||||||
| chr18:45909389
|
T | C | 1 | a0018c0042t0022g0043 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4205+1132A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909389 | ||||||
| chr18:45909445
|
G | C | 9 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.4205+1076C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909445 | ||||||
| chr18:45909451
|
G | A | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4205+1070C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909451 | ||||||
| chr18:45909682
|
T | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0166 | 2 | NA18992.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.4205+839A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909682 | ||||||
| chr18:45909692
|
A | C | 1 | a0001c0001t0040g0140 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4205+829T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909692 | ||||||
| chr18:45909742
|
G | A | 1 | a0002c0002t0025g0067 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4205+779C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909742 | ||||||
| chr18:45909752
|
T | C | 4 | a0002c0002t0014g0220a0006c0012t0006g0221a0006c0012t0006g0222others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4205+769A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909752 | ||||||
| chr18:45909922
|
T | C | 1 | a0015c0020t0004g0217 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4205+599A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45909922 | ||||||
| chr18:45910135
|
G | A | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0166others(2): Show | 5 | NA18948.hp2 NA18967.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.4205+386C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45910135 | ||||||
| chr18:45910189
|
A | G | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4205+332T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45910189 | ||||||
| chr18:45910447
|
T | C | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.4205+74A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 23/43 | chr18 | 45910447 | ||||||
| chr18:45910762
|
G | C | 1 | a0002c0002t0002g0266 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.3984-20C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45910762 | ||||||
| chr18:45910983
|
C | T | 1 | a0017c0023t0002g0258 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3984-241G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45910983 | ||||||
| chr18:45911073
|
ATC | A | 3 | a0003c0013t0001g0204a0003c0013t0001g0207a0004c0004t0015g0014 | 3 | HG02922.hp2 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3984-333_3984-332d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911073 | ||||||
| chr18:45911075
|
C | A | 1 | a0004c0048t0003g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3984-333G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911075 | ||||||
| chr18:45911076
|
T | C | 1 | a0004c0048t0003g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3984-334A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911076 | ||||||
| chr18:45911078
|
T | C | 4 | a0003c0013t0001g0204a0003c0013t0001g0207a0004c0004t0015g0014others(1): Show | 4 | HG02922.hp2 HG03130.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3984-336A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911078 | ||||||
| chr18:45911078
|
T | TACACACA others(3): Show |
2 | a0009c0007t0007g0011a0009c0007t0007g0013 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3984-346_3984-337d others(12): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911078 | ||||||
| chr18:45911078
|
T | TCTATAC | 20 | a0004c0004t0001g0028a0004c0004t0004g0012a0004c0004t0005g0023others(17): Show | 20 | HG01358.hp2 HG01361.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.3984-337_3984-336i others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911078 | ||||||
| chr18:45911078
|
TAC | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.3984-338_3984-337d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911078 | ||||||
| chr18:45911078
|
TACAC | T | 3 | a0001c0001t0001g0123a0001c0001t0005g0098a0002c0002t0002g0266 | 3 | HG00639.hp1 HG02055.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.3984-340_3984-337d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911078 | ||||||
| chr18:45911080
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3984-338G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911080 | ||||||
| chr18:45911104
|
C | T | 1 | a0004c0048t0003g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3984-362G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911104 | ||||||
| chr18:45911106
|
C | CAT | 5 | a0001c0001t0001g0085a0001c0001t0001g0111a0001c0001t0001g0112others(2): Show | 5 | HG01243.hp2 HG02071.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.3984-365_3984-364i others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911106 | ||||||
| chr18:45911106
|
C | T | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3984-364G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911106 | ||||||
| chr18:45911108
|
C | T | 38 | a0001c0001t0001g0085a0001c0001t0001g0111a0001c0001t0001g0112others(35): Show | 38 | HG01243.hp2 HG01358.hp2 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.3984-366G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911108 | ||||||
| chr18:45911110
|
C | CACACACA others(1): Show |
4 | a0002c0002t0017g0229a0006c0012t0006g0222a0006c0012t0006g0227others(1): Show | 4 | HG02647.hp2 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3984-369_3984-368i others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911110 | ||||||
| chr18:45911110
|
C | CACACATA others(1): Show |
4 | a0002c0002t0014g0220a0002c0002t0029g0228a0006c0012t0006g0221others(1): Show | 4 | HG01109.hp1 HG01891.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3984-369_3984-368i others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911110 | ||||||
| chr18:45911110
|
C | CAT | 33 | a0002c0038t0007g0008a0003c0003t0001g0202a0003c0003t0002g0287others(30): Show | 33 | HG00323.hp1 HG00733.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.3984-370_3984-369d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911110 | ||||||
| chr18:45911110
|
C | CATAT | 23 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295others(20): Show | 23 | HG01928.hp2 HG02622.hp1 HG02723.hp1 others(20): Show |
intron_variant | MODIFIER | c.3984-372_3984-369d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911110 | ||||||
| chr18:45911110
|
C | T | 113 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0060others(110): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.3984-368G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911110 | ||||||
| chr18:45911129
|
A | AT | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3984-388dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911129 | ||||||
| chr18:45911153
|
G | A | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3984-411C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911153 | ||||||
| chr18:45911289
|
G | GT | 27 | a0001c0001t0004g0058a0002c0002t0002g0231a0003c0003t0003g0186others(24): Show | 27 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.3984-548dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911289 | ||||||
| chr18:45911363
|
G | A | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.3984-621C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911363 | ||||||
| chr18:45911388
|
C | T | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3984-646G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911388 | ||||||
| chr18:45911462
|
A | AT | 9 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3984-721dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911462 | ||||||
| chr18:45911464
|
T | A | 1 | a0008c0008t0002g0020 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3984-722A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911464 | ||||||
| chr18:45911509
|
G | A | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3984-767C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911509 | ||||||
| chr18:45911544
|
G | A | 1 | a0005c0005t0033g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3983+746C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911544 | ||||||
| chr18:45911572
|
G | A | 1 | a0003c0003t0002g0287 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3983+718C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911572 | ||||||
| chr18:45911626
|
A | G | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3983+664T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911626 | ||||||
| chr18:45911924
|
G | A | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3983+366C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911924 | ||||||
| chr18:45911926
|
G | A | 1 | a0006c0012t0006g0272 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3983+364C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45911926 | ||||||
| chr18:45912099
|
C | T | 2 | a0002c0002t0002g0246a0002c0002t0002g0247 | 2 | HG01943.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3983+191G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45912099 | ||||||
| chr18:45912156
|
CAGAG | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.3983+130_3983+133d others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 22/43 | chr18 | 45912156 | ||||||
| chr18:45912520
|
T | C | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3817-64A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45912520 | ||||||
| chr18:45912673
|
A | C | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3817-217T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45912673 | ||||||
| chr18:45912787
|
A | G | 1 | a0002c0002t0008g0275 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3817-331T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45912787 | ||||||
| chr18:45912895
|
C | A | 2 | a0002c0002t0002g0257a0002c0002t0002g0264 | 2 | HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.3817-439G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45912895 | ||||||
| chr18:45913065
|
C | T | 103 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(100): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.3817-609G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45913065 | ||||||
| chr18:45913090
|
CA | C | 102 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(99): Show | 106 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.3816+615delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45913090 | ||||||
| chr18:45913194
|
C | T | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.3816+512G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45913194 | ||||||
| chr18:45913265
|
C | T | 1 | a0002c0002t0003g0237 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3816+441G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45913265 | ||||||
| chr18:45913363
|
G | A | 2 | a0001c0001t0004g0117a0001c0001t0004g0118 | 2 | HG01071.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.3816+343C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45913363 | ||||||
| chr18:45913622
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3816+84T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45913622 | ||||||
| chr18:45913624
|
A | G | 15 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(12): Show | 15 | HG01109.hp2 HG02165.hp1 NA18747.hp2 others(12): Show |
intron_variant | MODIFIER | c.3816+82T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 21/43 | chr18 | 45913624 | ||||||
| chr18:45913912
|
C | A | 1 | a0003c0003t0002g0287 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3694-84G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45913912 | ||||||
| chr18:45914138
|
C | T | 9 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3694-310G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914138 | ||||||
| chr18:45914149
|
A | G | 9 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3694-321T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914149 | ||||||
| chr18:45914220
|
G | A | 2 | a0001c0001t0001g0144a0010c0010t0001g0145 | 2 | NA18968.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.3694-392C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914220 | ||||||
| chr18:45914376
|
C | T | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.3694-548G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914376 | ||||||
| chr18:45914451
|
G | T | 78 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0002others(75): Show | 81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.3694-623C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914451 | ||||||
| chr18:45914513
|
C | A | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.3694-685G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914513 | ||||||
| chr18:45914765
|
C | T | 7 | a0002c0002t0002g0231a0002c0002t0002g0260a0002c0002t0002g0261others(4): Show | 7 | HG00733.hp1 NA18968.hp1 NA19006.hp2 others(4): Show |
intron_variant | MODIFIER | c.3693+746G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914765 | ||||||
| chr18:45914776
|
G | A | 2 | a0001c0001t0005g0098a0001c0001t0032g0113 | 2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3693+735C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914776 | ||||||
| chr18:45914875
|
G | C | 1 | a0001c0001t0001g0120 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3693+636C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914875 | ||||||
| chr18:45914876
|
G | A | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3693+635C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914876 | ||||||
| chr18:45914905
|
A | G | 1 | a0025c0036t0013g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3693+606T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914905 | ||||||
| chr18:45914970
|
TA | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.3693+540delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914970 | ||||||
| chr18:45914970
|
TAA | T | 13 | a0001c0001t0001g0101a0001c0001t0001g0141a0001c0001t0004g0070others(10): Show | 13 | HG00323.hp2 HG01891.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.3693+539_3693+540d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45914970 | ||||||
| chr18:45915004
|
C | T | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.3693+507G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915004 | ||||||
| chr18:45915045
|
G | A | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3693+466C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915045 | ||||||
| chr18:45915072
|
A | G | 90 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(87): Show | 94 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.3693+439T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915072 | ||||||
| chr18:45915096
|
T | C | 1 | a0001c0001t0011g0151 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3693+415A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915096 | ||||||
| chr18:45915111
|
T | C | 12 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(9): Show | 12 | HG01884.hp1 HG01884.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.3693+400A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915111 | ||||||
| chr18:45915147
|
G | A | 3 | a0002c0002t0017g0229a0002c0002t0029g0228a0006c0012t0006g0227 | 3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3693+364C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915147 | ||||||
| chr18:45915255
|
G | A | 1 | a0001c0001t0005g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3693+256C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915255 | ||||||
| chr18:45915299
|
T | A | 103 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(100): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.3693+212A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915299 | ||||||
| chr18:45915392
|
T | C | 1 | a0001c0001t0039g0097 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.3693+119A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915392 | ||||||
| chr18:45915425
|
T | G | 1 | a0015c0020t0004g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3693+86A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915425 | ||||||
| chr18:45915451
|
G | T | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.3693+60C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 20/43 | chr18 | 45915451 | ||||||
| chr18:45915802
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3583-181G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 19/43 | chr18 | 45915802 | ||||||
| chr18:45915997
|
C | G | 1 | a0003c0003t0003g0201 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3582+12G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 19/43 | chr18 | 45915997 | ||||||
| chr18:45916226
|
G | A | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3385-20C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 18/43 | chr18 | 45916226 | ||||||
| chr18:45916415
|
T | C | 1 | a0003c0003t0003g0201 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3384+23A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 18/43 | chr18 | 45916415 | ||||||
| chr18:45916728
|
A | T | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3240-146T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45916728 | ||||||
| chr18:45916798
|
G | A | 26 | a0001c0001t0001g0060a0001c0001t0001g0068a0001c0001t0001g0085others(23): Show | 26 | HG00099.hp1 HG01081.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.3240-216C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45916798 | ||||||
| chr18:45916865
|
C | T | 9 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3240-283G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45916865 | ||||||
| chr18:45917022
|
G | A | 15 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0052others(12): Show | 18 | HG00733.hp1 NA18951.hp2 NA18966.hp1 others(15): Show |
intron_variant | MODIFIER | c.3240-440C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917022 | ||||||
| chr18:45917102
|
G | A | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3240-520C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917102 | ||||||
| chr18:45917151
|
A | G | 1 | a0001c0001t0004g0079 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3239+528T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917151 | ||||||
| chr18:45917188
|
C | T | 1 | a0001c0001t0004g0108 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3239+491G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917188 | ||||||
| chr18:45917225
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3239+454A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917225 | ||||||
| chr18:45917272
|
T | C | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3239+407A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917272 | ||||||
| chr18:45917541
|
G | A | 3 | a0002c0002t0017g0229a0002c0002t0029g0228a0006c0012t0006g0227 | 3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3239+138C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917541 | ||||||
| chr18:45917643
|
T | C | 1 | a0004c0004t0001g0028 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3239+36A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 17/43 | chr18 | 45917643 | ||||||
| chr18:45917972
|
G | A | 1 | a0021c0028t0018g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3099-153C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45917972 | ||||||
| chr18:45918091
|
G | A | 5 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3099-272C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45918091 | ||||||
| chr18:45918130
|
C | T | 75 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0002others(72): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.3099-311G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45918130 | ||||||
| chr18:45918329
|
G | A | 1 | a0004c0004t0009g0036 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3099-510C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45918329 | ||||||
| chr18:45918403
|
C | T | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3099-584G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45918403 | ||||||
| chr18:45918561
|
C | T | 104 | a0001c0001t0001g0125a0002c0002t0001g0063a0002c0002t0001g0064others(101): Show | 108 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.3099-742G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45918561 | ||||||
| chr18:45918564
|
A | T | 4 | a0019c0016t0010g0225a0019c0016t0010g0226a0020c0017t0010g0223others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3099-745T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45918564 | ||||||
| chr18:45919042
|
C | T | 1 | a0002c0002t0004g0285 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3099-1223G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919042 | ||||||
| chr18:45919177
|
C | T | 24 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(21): Show | 24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.3099-1358G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919177 | ||||||
| chr18:45919336
|
A | C | 1 | a0009c0007t0007g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3099-1517T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919336 | ||||||
| chr18:45919431
|
G | A | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3099-1612C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919431 | ||||||
| chr18:45919439
|
A | G | 1 | a0002c0002t0008g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3099-1620T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919439 | ||||||
| chr18:45919459
|
T | C | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3099-1640A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919459 | ||||||
| chr18:45919514
|
G | GT | 38 | a0001c0001t0004g0081a0001c0001t0004g0117a0001c0021t0001g0135others(35): Show | 38 | HG00140.hp1 HG00621.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.3099-1696dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919514 | ||||||
| chr18:45919573
|
C | T | 3 | a0002c0002t0004g0053a0002c0002t0004g0230a0002c0002t0026g0235 | 3 | HG02615.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3099-1754G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919573 | ||||||
| chr18:45919576
|
A | C | 3 | a0002c0002t0004g0053a0002c0002t0004g0230a0002c0002t0026g0235 | 3 | HG02615.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3099-1757T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919576 | ||||||
| chr18:45919584
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3099-1765G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919584 | ||||||
| chr18:45919597
|
C | T | 70 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0002others(67): Show | 73 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.3099-1778G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919597 | ||||||
| chr18:45919653
|
C | T | 1 | a0025c0036t0013g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3099-1834G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919653 | ||||||
| chr18:45919705
|
G | T | 4 | a0002c0002t0014g0220a0006c0012t0006g0221a0006c0012t0006g0222others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3099-1886C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45919705 | ||||||
| chr18:45920081
|
G | A | 5 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3098+2260C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45920081 | ||||||
| chr18:45920089
|
G | A | 2 | a0015c0020t0004g0170a0015c0020t0004g0217 | 2 | HG00621.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.3098+2252C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45920089 | ||||||
| chr18:45920102
|
A | G | 3 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043 | 3 | HG01496.hp1 HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3098+2239T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45920102 | ||||||
| chr18:45920317
|
T | G | 2 | a0001c0001t0001g0162a0001c0001t0009g0161 | 2 | NA18980.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.3098+2024A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45920317 | ||||||
| chr18:45920442
|
G | A | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3098+1899C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45920442 | ||||||
| chr18:45920575
|
G | A | 1 | a0005c0014t0003g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3098+1766C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45920575 | ||||||
| chr18:45921333
|
A | T | 2 | a0011c0015t0014g0290a0011c0015t0019g0291 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3098+1008T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921333 | ||||||
| chr18:45921503
|
T | C | 2 | a0003c0003t0003g0208a0003c0003t0003g0209 | 2 | NA18957.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.3098+838A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921503 | ||||||
| chr18:45921779
|
A | C | 4 | a0019c0016t0010g0225a0019c0016t0010g0226a0020c0017t0010g0223others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3098+562T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921779 | ||||||
| chr18:45921801
|
A | G | 125 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(122): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.3098+540T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921801 | ||||||
| chr18:45921811
|
A | G | 103 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(100): Show | 107 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.3098+530T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921811 | ||||||
| chr18:45921939
|
T | C | 1 | a0001c0001t0001g0004 | 2 | HG02083.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.3098+402A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921939 | ||||||
| chr18:45921963
|
T | TGAA | 4 | a0019c0016t0010g0225a0019c0016t0010g0226a0020c0017t0010g0223others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3098+377_3098+378i others(5): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921963 | ||||||
| chr18:45921963
|
TA | T | 11 | a0001c0001t0001g0087a0001c0001t0001g0095a0001c0001t0001g0101others(8): Show | 11 | HG02735.hp2 HG03834.hp2 HG06807.hp1 others(8): Show |
intron_variant | MODIFIER | c.3098+377delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45921963 | ||||||
| chr18:45922071
|
C | T | 1 | a0003c0013t0001g0203 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3098+270G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45922071 | ||||||
| chr18:45922090
|
A | G | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3098+251T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45922090 | ||||||
| chr18:45922224
|
G | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 119 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.3098+117C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 16/43 | chr18 | 45922224 | ||||||
| chr18:45922697
|
A | G | 1 | a0005c0005t0033g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2839-97T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 15/43 | chr18 | 45922697 | ||||||
| chr18:45922762
|
T | C | 128 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(125): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.2839-162A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 15/43 | chr18 | 45922762 | ||||||
| chr18:45922901
|
T | C | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2839-301A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 15/43 | chr18 | 45922901 | ||||||
| chr18:45922978
|
T | G | 1 | a0002c0002t0027g0233 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2838+290A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 15/43 | chr18 | 45922978 | ||||||
| chr18:45923074
|
T | C | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2838+194A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 15/43 | chr18 | 45923074 | ||||||
| chr18:45923190
|
A | G | 1 | a0002c0002t0002g0245 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2838+78T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 15/43 | chr18 | 45923190 | ||||||
| chr18:45923697
|
G | A | 1 | a0002c0002t0001g0064 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2719-310C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45923697 | ||||||
| chr18:45923769
|
C | T | 3 | a0003c0003t0003g0193a0003c0003t0003g0195a0003c0003t0042g0194 | 3 | NA18966.hp2 NA19004.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.2719-382G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45923769 | ||||||
| chr18:45923771
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2719-384C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45923771 | ||||||
| chr18:45923891
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2719-504C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45923891 | ||||||
| chr18:45924026
|
CA | C | 12 | a0001c0001t0001g0112a0001c0001t0001g0156a0002c0009t0002g0277others(9): Show | 12 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.2719-640delT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924026 | ||||||
| chr18:45924041
|
A | G | 9 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(6): Show | 9 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2719-654T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924041 | ||||||
| chr18:45924108
|
T | A | 1 | a0001c0001t0001g0085 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2719-721A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924108 | ||||||
| chr18:45924173
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2719-786T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924173 | ||||||
| chr18:45924274
|
C | T | 5 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2719-887G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924274 | ||||||
| chr18:45924392
|
T | C | 1 | a0001c0001t0004g0079 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2719-1005A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924392 | ||||||
| chr18:45924393
|
A | T | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2719-1006T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924393 | ||||||
| chr18:45924456
|
T | A | 23 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0116others(20): Show | 24 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.2719-1069A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924456 | ||||||
| chr18:45924812
|
C | T | 70 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0002others(67): Show | 73 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.2718+926G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924812 | ||||||
| chr18:45924813
|
G | A | 1 | a0001c0001t0005g0098 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2718+925C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924813 | ||||||
| chr18:45924942
|
A | G | 1 | a0004c0004t0015g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2718+796T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45924942 | ||||||
| chr18:45925011
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2718+727A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45925011 | ||||||
| chr18:45925231
|
G | A | 70 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0002others(67): Show | 73 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.2718+507C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45925231 | ||||||
| chr18:45925293
|
A | G | 100 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0293others(97): Show | 104 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.2718+445T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45925293 | ||||||
| chr18:45925508
|
G | A | 1 | a0006c0011t0006g0041 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2718+230C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45925508 | ||||||
| chr18:45925592
|
C | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2718+146G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 14/43 | chr18 | 45925592 | ||||||
| chr18:45926141
|
A | G | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2554-239T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45926141 | ||||||
| chr18:45926331
|
G | C | 2 | a0006c0012t0006g0272a0018c0043t0023g0046 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2554-429C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45926331 | ||||||
| chr18:45926464
|
A | C | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2554-562T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45926464 | ||||||
| chr18:45926514
|
A | T | 5 | a0002c0002t0002g0054a0002c0002t0002g0239a0002c0002t0002g0269others(2): Show | 5 | NA18940.hp2 NA18942.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.2554-612T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45926514 | ||||||
| chr18:45926727
|
C | G | 4 | a0019c0016t0010g0225a0019c0016t0010g0226a0020c0017t0010g0223others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2554-825G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45926727 | ||||||
| chr18:45926816
|
G | GA | 291 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(288): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2554-915dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45926816 | ||||||
| chr18:45926962
|
G | A | 3 | a0002c0002t0017g0229a0002c0002t0029g0228a0006c0012t0006g0227 | 3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2554-1060C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45926962 | ||||||
| chr18:45927035
|
C | CT | 62 | a0001c0001t0001g0102a0001c0001t0040g0140a0001c0021t0001g0135others(59): Show | 65 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.2554-1134dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927035 | ||||||
| chr18:45927035
|
C | CTT | 6 | a0002c0002t0002g0284a0002c0009t0002g0276a0019c0016t0010g0225others(3): Show | 6 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2554-1135_2554-113 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927035 | ||||||
| chr18:45927094
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2554-1192C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927094 | ||||||
| chr18:45927146
|
C | T | 1 | a0025c0036t0013g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2554-1244G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927146 | ||||||
| chr18:45927193
|
C | T | 6 | a0002c0002t0002g0051a0002c0002t0002g0238a0002c0002t0002g0270others(3): Show | 6 | NA18747.hp1 NA18941.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2554-1291G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927193 | ||||||
| chr18:45927203
|
G | GT | 7 | a0001c0001t0001g0149a0001c0001t0004g0056a0001c0001t0004g0069others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.2554-1302dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927203 | ||||||
| chr18:45927214
|
C | T | 1 | a0001c0001t0004g0108 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2554-1312G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927214 | ||||||
| chr18:45927241
|
G | A | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2554-1339C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927241 | ||||||
| chr18:45927257
|
T | C | 1 | a0002c0002t0002g0266 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2554-1355A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927257 | ||||||
| chr18:45927291
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2554-1389C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927291 | ||||||
| chr18:45927299
|
G | A | 3 | a0002c0002t0017g0229a0002c0002t0029g0228a0006c0012t0006g0227 | 3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2554-1397C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927299 | ||||||
| chr18:45927405
|
T | C | 36 | a0003c0003t0001g0184a0003c0003t0001g0188a0003c0003t0001g0192others(33): Show | 36 | HG00323.hp1 HG01346.hp2 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.2553+1464A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927405 | ||||||
| chr18:45927507
|
C | T | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2553+1362G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927507 | ||||||
| chr18:45927513
|
C | T | 117 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0002others(114): Show | 121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.2553+1356G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927513 | ||||||
| chr18:45927591
|
T | TACAC | 3 | a0019c0016t0010g0225a0019c0016t0010g0226a0020c0017t0010g0223 | 3 | HG02818.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2553+1277_2553+127 others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927591 | ||||||
| chr18:45927591
|
TATAC | T | 9 | a0002c0002t0029g0228a0002c0038t0007g0008a0009c0007t0007g0006others(6): Show | 10 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2553+1274_2553+127 others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927591 | ||||||
| chr18:45927591
|
TATACAC | T | 4 | a0002c0002t0017g0229a0002c0002t0030g0049a0002c0009t0002g0277others(1): Show | 4 | HG02647.hp2 HG02897.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2553+1272_2553+127 others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927591 | ||||||
| chr18:45927591
|
TATACACA others(1): Show |
T | 57 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(54): Show | 60 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.2553+1270_2553+127 others(12): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927591 | ||||||
| chr18:45927591
|
TATACACA others(5): Show |
T | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2553+1266_2553+127 others(16): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927591 | ||||||
| chr18:45927592
|
A | G | 6 | a0002c0002t0014g0220a0006c0012t0006g0221a0006c0012t0006g0222others(3): Show | 6 | HG01891.hp1 HG01891.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2553+1277T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927592 | ||||||
| chr18:45927593
|
T | C | 10 | a0002c0002t0014g0220a0006c0012t0006g0221a0006c0012t0006g0222others(7): Show | 10 | HG01891.hp1 HG01891.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2553+1276A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | ||||||
| chr18:45927593
|
T | TAC | 41 | a0001c0001t0001g0037a0001c0001t0001g0087a0001c0001t0001g0095others(38): Show | 41 | HG00323.hp1 HG00323.hp2 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.2553+1274_2553+127 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | ||||||
| chr18:45927593
|
T | TACAC | 77 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0060others(74): Show | 80 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.2553+1272_2553+127 others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | ||||||
| chr18:45927593
|
T | TACACAC | 41 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0080others(38): Show | 42 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.2553+1270_2553+127 others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | ||||||
| chr18:45927593
|
T | TACACACA others(1): Show |
11 | a0001c0001t0001g0127a0001c0001t0001g0156a0001c0001t0001g0158others(8): Show | 11 | HG00609.hp1 HG01346.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.2553+1268_2553+127 others(12): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | ||||||
| chr18:45927593
|
T | TATAC | 20 | a0004c0004t0001g0028a0004c0004t0004g0012a0004c0004t0005g0023others(17): Show | 20 | HG01358.hp2 HG01361.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.2553+1275_2553+127 others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | ||||||
| chr18:45927593
|
T | TATACAC | 3 | a0004c0004t0003g0030a0004c0004t0015g0014a0008c0008t0002g0020 | 3 | HG00140.hp1 HG02071.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2553+1275_2553+127 others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | ||||||
| chr18:45927593
|
TACACACA others(5): Show |
T | 1 | a0024c0035t0001g0133 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2553+1264_2553+127 others(16): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927593 | ||||||
| chr18:45927594
|
A | G | 1 | a0009c0007t0007g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2553+1275T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927594 | ||||||
| chr18:45927596
|
A | G | 8 | a0002c0002t0029g0228a0009c0007t0007g0006a0009c0007t0007g0010others(5): Show | 9 | HG01109.hp1 HG01496.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2553+1273T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927596 | ||||||
| chr18:45927598
|
A | G | 4 | a0002c0002t0017g0229a0002c0002t0030g0049a0002c0009t0002g0277others(1): Show | 4 | HG02647.hp2 HG02897.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2553+1271T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927598 | ||||||
| chr18:45927600
|
A | G | 57 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(54): Show | 60 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.2553+1269T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927600 | ||||||
| chr18:45927604
|
A | G | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2553+1265T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927604 | ||||||
| chr18:45927613
|
C | CAT | 5 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2553+1255_2553+125 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927613 | ||||||
| chr18:45927871
|
T | G | 89 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0002others(86): Show | 93 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.2553+998A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927871 | ||||||
| chr18:45927935
|
T | C | 2 | a0001c0001t0001g0147a0032c0049t0001g0178 | 2 | HG01109.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.2553+934A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927935 | ||||||
| chr18:45927959
|
C | T | 1 | a0001c0001t0004g0071 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2553+910G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927959 | ||||||
| chr18:45927962
|
G | C | 1 | a0002c0002t0003g0237 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2553+907C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45927962 | ||||||
| chr18:45928053
|
G | T | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2553+816C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928053 | ||||||
| chr18:45928189
|
G | C | 5 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2553+680C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928189 | ||||||
| chr18:45928213
|
C | CA | 89 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0002others(86): Show | 93 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.2553+655dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928213 | ||||||
| chr18:45928312
|
A | G | 2 | a0004c0004t0005g0027a0004c0004t0005g0031 | 2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2553+557T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928312 | ||||||
| chr18:45928632
|
G | A | 5 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2553+237C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928632 | ||||||
| chr18:45928641
|
A | G | 81 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0002others(78): Show | 85 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.2553+228T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928641 | ||||||
| chr18:45928822
|
A | C | 5 | a0002c0002t0014g0220a0006c0012t0006g0221a0006c0012t0006g0222others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2553+47T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928822 | ||||||
| chr18:45928833
|
T | TA | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2553+35_2553+36ins others(1): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928833 | ||||||
| chr18:45928834
|
G | A | 90 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(87): Show | 94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.2553+35C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 13/43 | chr18 | 45928834 | ||||||
| chr18:45929079
|
A | G | 84 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0002others(81): Show | 88 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.2413-70T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45929079 | ||||||
| chr18:45929178
|
G | A | 1 | a0001c0034t0001g0088 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2413-169C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45929178 | ||||||
| chr18:45929273
|
C | T | 6 | a0001c0001t0001g0037a0006c0011t0006g0038a0006c0011t0006g0040others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2413-264G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45929273 | ||||||
| chr18:45929434
|
T | C | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2413-425A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45929434 | ||||||
| chr18:45929486
|
A | G | 1 | a0003c0003t0003g0283 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2413-477T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45929486 | ||||||
| chr18:45930008
|
A | C | 1 | a0023c0046t0003g0200 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2412+668T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45930008 | ||||||
| chr18:45930091
|
T | C | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2412+585A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45930091 | ||||||
| chr18:45930204
|
T | C | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2412+472A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45930204 | ||||||
| chr18:45930212
|
G | A | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2412+464C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45930212 | ||||||
| chr18:45930472
|
A | G | 1 | a0025c0036t0013g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2412+204T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45930472 | ||||||
| chr18:45930596
|
A | G | 2 | a0006c0012t0006g0272a0018c0043t0023g0046 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2412+80T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 12/43 | chr18 | 45930596 | ||||||
| chr18:45931477
|
A | G | 2 | a0003c0003t0003g0191a0003c0003t0003g0201 | 2 | HG04184.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2258-647T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45931477 | ||||||
| chr18:45931495
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2258-665G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45931495 | ||||||
| chr18:45931559
|
C | T | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2258-729G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45931559 | ||||||
| chr18:45931618
|
T | G | 77 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0002others(74): Show | 81 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.2258-788A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45931618 | ||||||
| chr18:45931698
|
G | C | 1 | a0001c0001t0001g0087 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2258-868C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45931698 | ||||||
| chr18:45931766
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2258-936G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45931766 | ||||||
| chr18:45931767
|
G | A | 4 | a0019c0016t0010g0225a0019c0016t0010g0226a0020c0017t0010g0223others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2258-937C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45931767 | ||||||
| chr18:45932110
|
C | G | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2258-1280G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932110 | ||||||
| chr18:45932115
|
G | A | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2258-1285C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932115 | ||||||
| chr18:45932226
|
A | C | 1 | a0005c0005t0033g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2258-1396T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932226 | ||||||
| chr18:45932638
|
T | C | 1 | a0004c0004t0005g0025 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2258-1808A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932638 | ||||||
| chr18:45932740
|
T | TA | 90 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(87): Show | 94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.2258-1911dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932740 | ||||||
| chr18:45932745
|
A | G | 1 | a0005c0025t0003g0016 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2258-1915T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932745 | ||||||
| chr18:45932795
|
C | T | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2258-1965G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932795 | ||||||
| chr18:45932968
|
CT | C | 36 | a0003c0003t0001g0184a0003c0003t0001g0188a0003c0003t0001g0192others(33): Show | 36 | HG00323.hp1 HG01346.hp2 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.2257+1840delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45932968 | ||||||
| chr18:45933167
|
C | T | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2257+1642G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933167 | ||||||
| chr18:45933296
|
G | A | 90 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(87): Show | 94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.2257+1513C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933296 | ||||||
| chr18:45933314
|
G | A | 1 | a0002c0002t0002g0266 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2257+1495C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933314 | ||||||
| chr18:45933405
|
A | G | 90 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(87): Show | 94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.2257+1404T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933405 | ||||||
| chr18:45933431
|
C | T | 1 | a0003c0003t0003g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2257+1378G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933431 | ||||||
| chr18:45933669
|
C | CA | 57 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0077others(54): Show | 58 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.2257+1139dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933669 | ||||||
| chr18:45933832
|
G | A | 3 | a0002c0002t0004g0053a0002c0002t0004g0230a0002c0002t0026g0235 | 3 | HG02615.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2257+977C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933832 | ||||||
| chr18:45933877
|
G | A | 155 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(152): Show | 159 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(156): Show |
intron_variant | MODIFIER | c.2257+932C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933877 | ||||||
| chr18:45933974
|
C | T | 10 | a0001c0001t0001g0037a0006c0011t0006g0038a0006c0011t0006g0040others(7): Show | 10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2257+835G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933974 | ||||||
| chr18:45933975
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2257+834C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45933975 | ||||||
| chr18:45934027
|
C | T | 79 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0002others(76): Show | 83 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.2257+782G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934027 | ||||||
| chr18:45934055
|
G | A | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2257+754C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934055 | ||||||
| chr18:45934142
|
A | G | 59 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(56): Show | 62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.2257+667T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934142 | ||||||
| chr18:45934157
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2257+652G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934157 | ||||||
| chr18:45934266
|
G | C | 1 | a0004c0004t0005g0031 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2257+543C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934266 | ||||||
| chr18:45934344
|
C | T | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2257+465G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934344 | ||||||
| chr18:45934765
|
A | G | 5 | a0002c0009t0002g0276a0002c0009t0002g0277a0002c0009t0002g0278others(2): Show | 5 | HG00621.hp1 HG02074.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.2257+44T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934765 | ||||||
| chr18:45934784
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2257+25G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 11/43 | chr18 | 45934784 | ||||||
| chr18:45935010
|
T | C | 1 | a0025c0036t0013g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2100-44A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935010 | ||||||
| chr18:45935086
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2100-120A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935086 | ||||||
| chr18:45935411
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0123a0001c0001t0001g0124others(2): Show | 6 | HG00140.hp2 HG00639.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.2100-445C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935411 | ||||||
| chr18:45935496
|
C | T | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2100-530G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935496 | ||||||
| chr18:45935550
|
A | G | 1 | a0002c0002t0002g0240 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2100-584T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935550 | ||||||
| chr18:45935592
|
CTACTAAG others(11): Show |
C | 90 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(87): Show | 94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.2100-644_2100-627d others(20): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935592 | ||||||
| chr18:45935610
|
G | GC | 65 | a0003c0003t0001g0184a0003c0003t0001g0188a0003c0003t0001g0192others(62): Show | 65 | HG00140.hp1 HG00323.hp1 HG01346.hp2 others(62): Show |
intron_variant | MODIFIER | c.2100-645_2100-644i others(3): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935610 | ||||||
| chr18:45935673
|
C | G | 10 | a0001c0001t0001g0037a0006c0011t0006g0038a0006c0011t0006g0040others(7): Show | 10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2100-707G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935673 | ||||||
| chr18:45935681
|
G | T | 1 | a0022c0029t0001g0059 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2100-715C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45935681 | ||||||
| chr18:45936142
|
T | C | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2100-1176A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936142 | ||||||
| chr18:45936341
|
C | T | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2100-1375G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936341 | ||||||
| chr18:45936353
|
T | A | 1 | a0025c0036t0013g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2100-1387A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936353 | ||||||
| chr18:45936399
|
T | C | 1 | a0018c0043t0023g0046 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2100-1433A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936399 | ||||||
| chr18:45936455
|
CG | C | 80 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0002others(77): Show | 84 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.2100-1490delC | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936455 | ||||||
| chr18:45936507
|
C | A | 80 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0002others(77): Show | 84 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.2100-1541G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936507 | ||||||
| chr18:45936568
|
A | G | 1 | a0001c0001t0004g0108 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2100-1602T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936568 | ||||||
| chr18:45936576
|
A | C | 1 | a0004c0048t0003g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2100-1610T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936576 | ||||||
| chr18:45936623
|
G | A | 10 | a0001c0001t0001g0037a0006c0011t0006g0038a0006c0011t0006g0040others(7): Show | 10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2100-1657C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936623 | ||||||
| chr18:45936683
|
T | C | 59 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(56): Show | 62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.2100-1717A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936683 | ||||||
| chr18:45936720
|
C | CA | 72 | a0001c0001t0001g0060a0002c0002t0001g0293a0002c0002t0001g0294others(69): Show | 75 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.2100-1755dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936720 | ||||||
| chr18:45936784
|
T | TA | 76 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0231others(73): Show | 77 | HG00140.hp1 HG00323.hp1 HG01109.hp1 others(74): Show |
intron_variant | MODIFIER | c.2100-1819dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936784 | ||||||
| chr18:45936784
|
T | TAA | 67 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(64): Show | 70 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.2100-1820_2100-181 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936784 | ||||||
| chr18:45936811
|
G | A | 1 | a0002c0002t0002g0238 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2100-1845C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936811 | ||||||
| chr18:45936915
|
G | C | 80 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0002others(77): Show | 84 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.2100-1949C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45936915 | ||||||
| chr18:45937007
|
T | C | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2100-2041A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937007 | ||||||
| chr18:45937065
|
G | A | 114 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(111): Show | 118 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.2100-2099C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937065 | ||||||
| chr18:45937110
|
C | T | 1 | a0002c0002t0002g0238 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2100-2144G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937110 | ||||||
| chr18:45937227
|
CAT | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0085others(5): Show | 11 | HG01169.hp2 HG01361.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2100-2263_2100-226 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937227 | ||||||
| chr18:45937233
|
TATACAC | T | 10 | a0001c0001t0001g0037a0001c0001t0001g0148a0006c0011t0006g0038others(7): Show | 10 | HG01884.hp1 HG02723.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2100-2273_2100-226 others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937233 | ||||||
| chr18:45937235
|
T | C | 3 | a0001c0001t0001g0162a0001c0001t0009g0161a0001c0024t0001g0163 | 3 | NA18980.hp2 NA18994.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2100-2269A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | ||||||
| chr18:45937235
|
T | TAC | 17 | a0001c0001t0001g0125a0001c0001t0004g0081a0004c0004t0001g0028others(14): Show | 17 | HG00140.hp1 HG01358.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.2100-2271_2100-227 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | ||||||
| chr18:45937235
|
T | TACAC | 3 | a0004c0004t0005g0033a0012c0026t0005g0021a0012c0026t0005g0022 | 3 | HG01516.hp2 HG01517.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2100-2273_2100-227 others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | ||||||
| chr18:45937235
|
TAC | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0060a0001c0001t0001g0068others(114): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.2100-2271_2100-227 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | ||||||
| chr18:45937235
|
TACAC | T | 22 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0003g0093others(19): Show | 22 | HG00323.hp1 HG01081.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2100-2273_2100-227 others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | ||||||
| chr18:45937235
|
TACACAC | T | 12 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(9): Show | 12 | HG02572.hp2 HG02886.hp2 HG03486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2100-2275_2100-227 others(10): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | ||||||
| chr18:45937235
|
TACACACA others(1): Show |
T | 6 | a0002c0002t0001g0063a0002c0002t0008g0062a0002c0033t0001g0061others(3): Show | 6 | HG00280.hp2 HG00323.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.2100-2277_2100-227 others(12): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | ||||||
| chr18:45937235
|
TACACACA others(7): Show |
T | 1 | a0002c0002t0002g0263 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2100-2283_2100-227 others(18): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | ||||||
| chr18:45937235
|
TACACACA others(9): Show |
T | 4 | a0002c0002t0030g0049a0002c0002t0031g0048a0016c0022t0020g0044others(1): Show | 4 | HG01496.hp1 HG02615.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2100-2285_2100-227 others(20): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | ||||||
| chr18:45937235
|
TACACACA others(11): Show |
T | 61 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(58): Show | 64 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2100-2287_2100-227 others(22): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | ||||||
| chr18:45937235
|
TACACACA others(13): Show |
T | 9 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295others(6): Show | 10 | HG02280.hp2 HG02622.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.2100-2289_2100-227 others(24): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | ||||||
| chr18:45937235
|
TACACACA others(15): Show |
T | 5 | a0002c0002t0014g0220a0006c0012t0006g0221a0006c0012t0006g0222others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2100-2291_2100-227 others(26): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | ||||||
| chr18:45937235
|
TACACACA others(19): Show |
T | 1 | a0002c0009t0002g0276 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2100-2295_2100-227 others(30): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937235 | ||||||
| chr18:45937237
|
C | T | 5 | a0003c0003t0003g0189a0003c0013t0001g0203a0003c0013t0001g0204others(2): Show | 5 | HG02145.hp2 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2100-2271G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937237 | ||||||
| chr18:45937239
|
C | T | 18 | a0003c0003t0001g0184a0003c0003t0001g0188a0003c0003t0001g0192others(15): Show | 18 | HG01346.hp2 HG01928.hp2 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.2100-2273G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937239 | ||||||
| chr18:45937241
|
C | T | 9 | a0003c0003t0001g0202a0003c0003t0003g0193a0003c0003t0003g0195others(6): Show | 9 | HG03239.hp2 HG03471.hp2 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.2100-2275G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937241 | ||||||
| chr18:45937243
|
C | T | 2 | a0021c0028t0018g0292a0025c0036t0013g0286 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2100-2277G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937243 | ||||||
| chr18:45937245
|
C | T | 4 | a0003c0003t0003g0185a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 4 | HG01884.hp2 HG02572.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2100-2279G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937245 | ||||||
| chr18:45937251
|
C | T | 1 | a0002c0002t0002g0263 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2100-2285G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937251 | ||||||
| chr18:45937253
|
C | T | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2100-2287G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937253 | ||||||
| chr18:45937255
|
C | T | 59 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(56): Show | 62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.2100-2289G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937255 | ||||||
| chr18:45937257
|
C | T | 9 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295others(6): Show | 10 | HG02280.hp2 HG02622.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.2100-2291G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937257 | ||||||
| chr18:45937259
|
C | T | 5 | a0002c0002t0014g0220a0006c0012t0006g0221a0006c0012t0006g0222others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2100-2293G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937259 | ||||||
| chr18:45937263
|
C | T | 1 | a0002c0009t0002g0276 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2100-2297G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937263 | ||||||
| chr18:45937279
|
T | C | 10 | a0001c0001t0001g0037a0006c0011t0006g0038a0006c0011t0006g0040others(7): Show | 10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2100-2313A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937279 | ||||||
| chr18:45937295
|
T | A | 80 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0002others(77): Show | 84 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.2099+2305A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937295 | ||||||
| chr18:45937320
|
T | TTA | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2099+2278_2099+227 others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937320 | ||||||
| chr18:45937327
|
T | TATATACA others(11): Show |
2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2099+2255_2099+227 others(22): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937327 | ||||||
| chr18:45937331
|
T | C | 1 | a0024c0035t0001g0133 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2099+2269A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937331 | ||||||
| chr18:45937349
|
T | TACACATA others(11): Show |
2 | a0001c0001t0001g0168a0001c0001t0036g0167 | 2 | HG02165.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2099+2233_2099+225 others(22): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937349 | ||||||
| chr18:45937371
|
C | T | 80 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0002others(77): Show | 84 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.2099+2229G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937371 | ||||||
| chr18:45937374
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2099+2226T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937374 | ||||||
| chr18:45937399
|
C | T | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2099+2201G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937399 | ||||||
| chr18:45937415
|
T | C | 10 | a0001c0001t0001g0037a0006c0011t0006g0038a0006c0011t0006g0040others(7): Show | 10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.2099+2185A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937415 | ||||||
| chr18:45937470
|
G | A | 66 | a0001c0001t0009g0218a0002c0002t0002g0002a0002c0002t0002g0005others(63): Show | 69 | HG00438.hp1 HG00609.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.2099+2130C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937470 | ||||||
| chr18:45937586
|
T | G | 2 | a0006c0012t0006g0272a0018c0043t0023g0046 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2099+2014A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937586 | ||||||
| chr18:45937670
|
G | C | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2099+1930C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937670 | ||||||
| chr18:45937800
|
C | T | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.2099+1800G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937800 | ||||||
| chr18:45937902
|
T | C | 5 | a0002c0002t0017g0229a0002c0002t0029g0228a0006c0012t0006g0227others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2099+1698A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45937902 | ||||||
| chr18:45938039
|
C | T | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2099+1561G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938039 | ||||||
| chr18:45938162
|
G | A | 2 | a0001c0001t0004g0117a0001c0001t0004g0118 | 2 | HG01071.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.2099+1438C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938162 | ||||||
| chr18:45938182
|
C | T | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2099+1418G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938182 | ||||||
| chr18:45938420
|
C | T | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2099+1180G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938420 | ||||||
| chr18:45938423
|
C | T | 1 | a0003c0003t0001g0184 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2099+1177G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938423 | ||||||
| chr18:45938461
|
C | CA | 79 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(76): Show | 83 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.2099+1138dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938461 | ||||||
| chr18:45938615
|
A | G | 1 | a0005c0005t0033g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2099+985T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938615 | ||||||
| chr18:45938627
|
C | G | 1 | a0004c0004t0015g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2099+973G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938627 | ||||||
| chr18:45938651
|
T | C | 5 | a0002c0002t0014g0220a0006c0012t0006g0221a0006c0012t0006g0222others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2099+949A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938651 | ||||||
| chr18:45938784
|
C | T | 59 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(56): Show | 62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.2099+816G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938784 | ||||||
| chr18:45938785
|
G | A | 6 | a0001c0001t0001g0037a0006c0011t0006g0038a0006c0011t0006g0040others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2099+815C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938785 | ||||||
| chr18:45938985
|
G | A | 2 | a0001c0001t0004g0117a0001c0001t0004g0118 | 2 | HG01071.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.2099+615C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45938985 | ||||||
| chr18:45939028
|
A | T | 1 | a0005c0014t0003g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2099+572T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45939028 | ||||||
| chr18:45939313
|
T | C | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2099+287A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45939313 | ||||||
| chr18:45939408
|
G | A | 1 | a0008c0008t0002g0020 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2099+192C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45939408 | ||||||
| chr18:45939475
|
A | G | 115 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(112): Show | 119 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.2099+125T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 10/43 | chr18 | 45939475 | ||||||
| chr18:45939807
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0171 | 2 | HG01243.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1944-52G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45939807 | ||||||
| chr18:45939859
|
C | T | 24 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(21): Show | 24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1944-104G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45939859 | ||||||
| chr18:45940012
|
G | A | 3 | a0002c0002t0017g0229a0002c0002t0029g0228a0006c0012t0006g0227 | 3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1944-257C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940012 | ||||||
| chr18:45940113
|
G | C | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1944-358C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940113 | ||||||
| chr18:45940203
|
C | T | 4 | a0002c0002t0014g0220a0006c0012t0006g0221a0006c0012t0006g0222others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1944-448G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940203 | ||||||
| chr18:45940248
|
G | A | 84 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(81): Show | 88 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1944-493C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940248 | ||||||
| chr18:45940299
|
C | T | 1 | a0001c0001t0004g0117 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1944-544G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940299 | ||||||
| chr18:45940313
|
C | T | 1 | a0009c0007t0007g0009 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1944-558G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940313 | ||||||
| chr18:45940334
|
C | T | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1944-579G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940334 | ||||||
| chr18:45940463
|
C | T | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1944-708G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940463 | ||||||
| chr18:45940493
|
AT | A | 6 | a0001c0001t0001g0037a0006c0011t0006g0038a0006c0011t0006g0040others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1944-739delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940493 | ||||||
| chr18:45940620
|
A | G | 6 | a0002c0002t0014g0220a0006c0012t0006g0221a0006c0012t0006g0222others(3): Show | 6 | HG01891.hp1 HG01891.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1944-865T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940620 | ||||||
| chr18:45940629
|
G | A | 24 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(21): Show | 24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1944-874C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940629 | ||||||
| chr18:45940902
|
G | C | 29 | a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0080others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.1944-1147C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45940902 | ||||||
| chr18:45941001
|
G | C | 24 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(21): Show | 24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1944-1246C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45941001 | ||||||
| chr18:45941285
|
G | A | 1 | a0004c0004t0015g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1944-1530C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45941285 | ||||||
| chr18:45941309
|
G | A | 38 | a0001c0001t0002g0190a0002c0002t0003g0183a0003c0003t0001g0184others(35): Show | 38 | HG00323.hp1 HG01346.hp2 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.1944-1554C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45941309 | ||||||
| chr18:45941639
|
T | C | 6 | a0007c0006t0003g0211a0007c0006t0003g0212a0007c0006t0003g0213others(3): Show | 6 | HG00323.hp1 HG01346.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1943+1522A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45941639 | ||||||
| chr18:45941946
|
G | A | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1943+1215C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45941946 | ||||||
| chr18:45941993
|
G | A | 24 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(21): Show | 24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1943+1168C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45941993 | ||||||
| chr18:45942019
|
T | C | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1943+1142A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942019 | ||||||
| chr18:45942094
|
A | G | 24 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(21): Show | 24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1943+1067T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942094 | ||||||
| chr18:45942118
|
G | A | 90 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(87): Show | 94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1943+1043C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942118 | ||||||
| chr18:45942258
|
C | T | 1 | a0005c0005t0033g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1943+903G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942258 | ||||||
| chr18:45942280
|
T | C | 1 | a0008c0008t0002g0020 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1943+881A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942280 | ||||||
| chr18:45942385
|
T | G | 1 | a0001c0001t0001g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1943+776A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942385 | ||||||
| chr18:45942393
|
A | G | 1 | a0002c0002t0038g0236 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1943+768T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942393 | ||||||
| chr18:45942465
|
T | C | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1943+696A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942465 | ||||||
| chr18:45942480
|
G | A | 1 | a0002c0002t0002g0270 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1943+681C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942480 | ||||||
| chr18:45942524
|
AC | A | 38 | a0001c0001t0002g0190a0002c0002t0003g0183a0003c0003t0001g0184others(35): Show | 38 | HG00323.hp1 HG01346.hp2 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.1943+636delG | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942524 | ||||||
| chr18:45942535
|
G | A | 24 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(21): Show | 24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1943+626C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942535 | ||||||
| chr18:45942557
|
C | T | 1 | a0002c0002t0002g0270 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1943+604G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942557 | ||||||
| chr18:45942558
|
G | A | 1 | a0005c0025t0003g0016 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1943+603C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942558 | ||||||
| chr18:45942766
|
A | G | 90 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(87): Show | 94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1943+395T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45942766 | ||||||
| chr18:45943107
|
T | C | 1 | a0006c0012t0006g0272 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1943+54A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45943107 | ||||||
| chr18:45943139
|
G | C | 1 | a0001c0001t0001g0134 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1943+22C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 9/43 | chr18 | 45943139 | ||||||
| chr18:45943346
|
G | A | 117 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(114): Show | 121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.1793-35C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943346 | ||||||
| chr18:45943475
|
G | T | 1 | a0018c0042t0022g0043 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1793-164C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943475 | ||||||
| chr18:45943499
|
A | G | 1 | a0001c0001t0040g0140 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1793-188T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943499 | ||||||
| chr18:45943520
|
T | G | 24 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(21): Show | 24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1793-209A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943520 | ||||||
| chr18:45943605
|
A | G | 59 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(56): Show | 62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.1793-294T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943605 | ||||||
| chr18:45943606
|
C | T | 1 | a0006c0011t0013g0042 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1793-295G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943606 | ||||||
| chr18:45943609
|
G | A | 2 | a0001c0021t0001g0135a0001c0021t0004g0136 | 2 | HG01346.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1793-298C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943609 | ||||||
| chr18:45943732
|
T | A | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1792+273A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943732 | ||||||
| chr18:45943794
|
G | A | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1792+211C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943794 | ||||||
| chr18:45943853
|
A | G | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1792+152T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 8/43 | chr18 | 45943853 | ||||||
| chr18:45944179
|
C | A | 27 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(24): Show | 27 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.1678-60G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944179 | ||||||
| chr18:45944273
|
G | T | 2 | a0002c0002t0017g0229a0006c0012t0006g0227 | 2 | HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1678-154C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944273 | ||||||
| chr18:45944332
|
A | G | 24 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(21): Show | 24 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1678-213T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944332 | ||||||
| chr18:45944426
|
T | C | 1 | a0025c0036t0013g0286 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1678-307A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944426 | ||||||
| chr18:45944483
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1678-364C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944483 | ||||||
| chr18:45944511
|
T | C | 2 | a0012c0026t0005g0021a0012c0026t0005g0022 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1678-392A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944511 | ||||||
| chr18:45944674
|
G | A | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1678-555C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944674 | ||||||
| chr18:45944687
|
G | A | 90 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(87): Show | 94 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1678-568C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944687 | ||||||
| chr18:45944727
|
G | C | 117 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(114): Show | 121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.1678-608C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944727 | ||||||
| chr18:45944741
|
C | T | 1 | a0004c0004t0015g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1678-622G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944741 | ||||||
| chr18:45944879
|
G | A | 1 | a0002c0002t0002g0264 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1678-760C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45944879 | ||||||
| chr18:45945479
|
G | T | 1 | a0018c0042t0022g0043 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1677+1184C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45945479 | ||||||
| chr18:45945608
|
C | T | 1 | a0027c0041t0007g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1677+1055G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45945608 | ||||||
| chr18:45945772
|
T | C | 117 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(114): Show | 121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.1677+891A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45945772 | ||||||
| chr18:45945845
|
G | A | 67 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(64): Show | 70 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.1677+818C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45945845 | ||||||
| chr18:45945852
|
G | A | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1677+811C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45945852 | ||||||
| chr18:45945854
|
G | A | 9 | a0003c0003t0003g0193a0003c0003t0003g0195a0003c0003t0003g0197others(6): Show | 9 | NA18944.hp2 NA18948.hp1 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.1677+809C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45945854 | ||||||
| chr18:45946081
|
C | A | 153 | a0001c0001t0001g0037a0001c0001t0002g0190a0002c0002t0001g0293others(150): Show | 157 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(154): Show |
intron_variant | MODIFIER | c.1677+582G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45946081 | ||||||
| chr18:45946097
|
T | C | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1677+566A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45946097 | ||||||
| chr18:45946321
|
A | C | 1 | a0021c0028t0018g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1677+342T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45946321 | ||||||
| chr18:45946333
|
C | T | 1 | a0004c0004t0005g0026 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1677+330G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45946333 | ||||||
| chr18:45946532
|
A | G | 2 | a0001c0001t0004g0117a0001c0001t0004g0118 | 2 | HG01071.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1677+131T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 7/43 | chr18 | 45946532 | ||||||
| chr18:45946806
|
T | C | 10 | a0001c0001t0001g0037a0006c0011t0006g0038a0006c0011t0006g0040others(7): Show | 10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1572-38A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45946806 | ||||||
| chr18:45947012
|
C | T | 3 | a0002c0002t0017g0229a0002c0002t0029g0228a0006c0012t0006g0227 | 3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1572-244G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947012 | ||||||
| chr18:45947131
|
G | C | 1 | a0002c0002t0024g0265 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1572-363C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947131 | ||||||
| chr18:45947285
|
T | C | 117 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(114): Show | 121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.1572-517A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947285 | ||||||
| chr18:45947393
|
A | G | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1572-625T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947393 | ||||||
| chr18:45947406
|
C | A | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1572-638G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947406 | ||||||
| chr18:45947435
|
G | A | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0137others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1572-667C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947435 | ||||||
| chr18:45947441
|
C | G | 2 | a0001c0001t0001g0116a0028c0045t0001g0115 | 2 | HG01192.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1572-673G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947441 | ||||||
| chr18:45947506
|
C | T | 3 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043 | 3 | HG01496.hp1 HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1572-738G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947506 | ||||||
| chr18:45947775
|
CT | C | 8 | a0001c0001t0001g0037a0001c0001t0001g0126a0001c0001t0001g0127others(5): Show | 8 | HG00140.hp2 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1571+727delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947775 | ||||||
| chr18:45947814
|
G | A | 1 | a0001c0001t0032g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1571+689C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947814 | ||||||
| chr18:45947835
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1571+668G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947835 | ||||||
| chr18:45947935
|
C | T | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1571+568G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45947935 | ||||||
| chr18:45948015
|
T | G | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1571+488A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45948015 | ||||||
| chr18:45948167
|
G | A | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1571+336C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45948167 | ||||||
| chr18:45948283
|
A | G | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1571+220T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45948283 | ||||||
| chr18:45948382
|
A | C | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1571+121T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45948382 | ||||||
| chr18:45948396
|
A | G | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1571+107T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 6/43 | chr18 | 45948396 | ||||||
| chr18:45948741
|
C | T | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1498-165G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 5/43 | chr18 | 45948741 | ||||||
| chr18:45949417
|
C | T | 4 | a0006c0011t0006g0038a0006c0011t0006g0040a0006c0011t0006g0041others(1): Show | 4 | HG01884.hp1 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1497+67G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 5/43 | chr18 | 45949417 | ||||||
| chr18:45949449
|
C | T | 3 | a0004c0004t0005g0023a0004c0004t0005g0024a0004c0004t0005g0025 | 3 | HG02257.hp1 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1497+35G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 5/43 | chr18 | 45949449 | ||||||
| chr18:45949869
|
C | T | 1 | a0003c0003t0003g0201 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1390-278G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45949869 | ||||||
| chr18:45949884
|
A | G | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1390-293T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45949884 | ||||||
| chr18:45949966
|
T | C | 1 | a0001c0001t0032g0113 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1390-375A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45949966 | ||||||
| chr18:45949977
|
A | T | 32 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(29): Show | 33 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.1390-386T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45949977 | ||||||
| chr18:45950016
|
T | C | 69 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(66): Show | 72 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1390-425A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950016 | ||||||
| chr18:45950124
|
C | T | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1390-533G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950124 | ||||||
| chr18:45950153
|
T | C | 1 | a0003c0003t0003g0201 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1390-562A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950153 | ||||||
| chr18:45950184
|
C | T | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1390-593G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950184 | ||||||
| chr18:45950239
|
T | C | 1 | a0014c0019t0006g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1390-648A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950239 | ||||||
| chr18:45950377
|
C | T | 7 | a0004c0004t0015g0014a0004c0048t0003g0015a0009c0007t0007g0006others(4): Show | 8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1389+725G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950377 | ||||||
| chr18:45950378
|
G | A | 6 | a0001c0001t0001g0037a0006c0011t0006g0038a0006c0011t0006g0040others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1389+724C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950378 | ||||||
| chr18:45950491
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1389+611C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950491 | ||||||
| chr18:45950504
|
C | T | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1389+598G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950504 | ||||||
| chr18:45950614
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1389+488G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950614 | ||||||
| chr18:45950759
|
A | G | 7 | a0004c0004t0015g0014a0004c0048t0003g0015a0009c0007t0007g0006others(4): Show | 8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1389+343T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950759 | ||||||
| chr18:45950935
|
G | C | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1389+167C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950935 | ||||||
| chr18:45950966
|
AAAG | A | 29 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(26): Show | 30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.1389+133_1389+135d others(5): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 4/43 | chr18 | 45950966 | ||||||
| chr18:45951275
|
T | C | 6 | a0001c0001t0001g0060a0001c0001t0001g0111a0001c0001t0001g0112others(3): Show | 6 | HG01169.hp1 HG01243.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1253-37A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951275 | ||||||
| chr18:45951283
|
T | C | 1 | a0002c0002t0002g0266 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1253-45A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951283 | ||||||
| chr18:45951344
|
G | A | 2 | a0002c0009t0002g0276a0002c0009t0002g0277 | 2 | NA18964.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1253-106C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951344 | ||||||
| chr18:45951385
|
T | G | 1 | a0003c0003t0003g0209 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1253-147A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951385 | ||||||
| chr18:45951398
|
C | T | 29 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(26): Show | 30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.1253-160G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951398 | ||||||
| chr18:45951399
|
A | C | 59 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(56): Show | 62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.1253-161T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951399 | ||||||
| chr18:45951436
|
T | C | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1253-198A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951436 | ||||||
| chr18:45951461
|
AT | A | 86 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(83): Show | 89 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.1253-224delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951461 | ||||||
| chr18:45951461
|
ATTT | A | 29 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(26): Show | 30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.1253-226_1253-224d others(5): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951461 | ||||||
| chr18:45951510
|
A | G | 30 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(27): Show | 31 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1253-272T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951510 | ||||||
| chr18:45951527
|
T | C | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | NA18957.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1253-289A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951527 | ||||||
| chr18:45951545
|
G | A | 69 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(66): Show | 72 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1253-307C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951545 | ||||||
| chr18:45951674
|
A | G | 117 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(114): Show | 121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.1253-436T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951674 | ||||||
| chr18:45951675
|
T | C | 1 | a0006c0011t0013g0042 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1253-437A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951675 | ||||||
| chr18:45951735
|
A | G | 1 | a0003c0044t0003g0182 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1253-497T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951735 | ||||||
| chr18:45951736
|
G | C | 1 | a0002c0040t0002g0267 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1253-498C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951736 | ||||||
| chr18:45951902
|
A | G | 60 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(57): Show | 63 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1252+498T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951902 | ||||||
| chr18:45951903
|
A | G | 60 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(57): Show | 63 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1252+497T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 3/43 | chr18 | 45951903 | ||||||
| chr18:45952769
|
G | A | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1009-126C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45952769 | ||||||
| chr18:45952940
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1009-297C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45952940 | ||||||
| chr18:45952956
|
G | A | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1009-313C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45952956 | ||||||
| chr18:45953027
|
G | T | 1 | a0005c0005t0033g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1009-384C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953027 | ||||||
| chr18:45953117
|
G | A | 1 | a0006c0012t0006g0272 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1009-474C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953117 | ||||||
| chr18:45953129
|
C | T | 1 | a0004c0004t0015g0014 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1009-486G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953129 | ||||||
| chr18:45953152
|
G | A | 7 | a0004c0004t0015g0014a0004c0048t0003g0015a0009c0007t0007g0006others(4): Show | 8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1009-509C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953152 | ||||||
| chr18:45953254
|
C | A | 85 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(82): Show | 88 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1009-611G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953254 | ||||||
| chr18:45953498
|
T | C | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1009-855A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953498 | ||||||
| chr18:45953904
|
ACT | A | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1008+488_1008+489d others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953904 | ||||||
| chr18:45953955
|
T | C | 71 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0002others(68): Show | 74 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1008+439A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45953955 | ||||||
| chr18:45954077
|
T | C | 29 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(26): Show | 30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.1008+317A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45954077 | ||||||
| chr18:45954327
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1008+67G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45954327 | ||||||
| chr18:45954346
|
A | G | 1 | a0020c0017t0010g0223 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1008+48T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 2/43 | chr18 | 45954346 | ||||||
| chr18:45955398
|
A | C | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.64-60T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955398 | ||||||
| chr18:45955537
|
G | A | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-199C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955537 | ||||||
| chr18:45955551
|
T | C | 29 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(26): Show | 30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-213A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955551 | ||||||
| chr18:45955617
|
A | G | 1 | a0028c0045t0001g0115 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.64-279T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955617 | ||||||
| chr18:45955661
|
G | A | 64 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(61): Show | 67 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.64-323C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955661 | ||||||
| chr18:45955673
|
A | G | 1 | a0021c0028t0018g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.64-335T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955673 | ||||||
| chr18:45955782
|
T | C | 7 | a0004c0004t0015g0014a0004c0048t0003g0015a0009c0007t0007g0006others(4): Show | 8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-444A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955782 | ||||||
| chr18:45955883
|
A | G | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-545T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45955883 | ||||||
| chr18:45956018
|
G | A | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-680C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956018 | ||||||
| chr18:45956019
|
G | A | 1 | a0018c0043t0023g0046 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-681C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956019 | ||||||
| chr18:45956074
|
C | T | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-736G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956074 | ||||||
| chr18:45956090
|
A | T | 29 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(26): Show | 30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-752T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956090 | ||||||
| chr18:45956294
|
C | T | 117 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(114): Show | 121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.64-956G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956294 | ||||||
| chr18:45956336
|
C | A | 1 | a0005c0005t0033g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-998G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956336 | ||||||
| chr18:45956368
|
A | T | 29 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(26): Show | 30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-1030T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956368 | ||||||
| chr18:45956461
|
A | AT | 7 | a0003c0003t0001g0202a0003c0013t0001g0203a0003c0013t0001g0204others(4): Show | 7 | HG02145.hp1 HG02145.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-1124dupA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956461 | ||||||
| chr18:45956461
|
A | ATTTAT | 29 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(26): Show | 30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-1124_64-1123ins others(5): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956461 | ||||||
| chr18:45956465
|
T | A | 81 | a0001c0001t0001g0078a0002c0002t0001g0293a0002c0002t0001g0294others(78): Show | 84 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.64-1127A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956465 | ||||||
| chr18:45956469
|
T | A | 3 | a0002c0002t0008g0050a0019c0016t0010g0225a0019c0016t0010g0226 | 3 | HG03209.hp2 HG03453.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.64-1131A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956469 | ||||||
| chr18:45956469
|
T | C | 29 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(26): Show | 30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-1131A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956469 | ||||||
| chr18:45956480
|
G | A | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-1142C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956480 | ||||||
| chr18:45956518
|
G | A | 1 | a0002c0002t0002g0269 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.64-1180C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956518 | ||||||
| chr18:45956545
|
C | T | 85 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(82): Show | 88 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.64-1207G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956545 | ||||||
| chr18:45956607
|
A | G | 117 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(114): Show | 121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.64-1269T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956607 | ||||||
| chr18:45956608
|
C | A | 7 | a0004c0004t0015g0014a0004c0048t0003g0015a0009c0007t0007g0006others(4): Show | 8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-1270G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956608 | ||||||
| chr18:45956726
|
G | A | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-1388C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956726 | ||||||
| chr18:45956775
|
C | T | 1 | a0001c0001t0003g0114 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.64-1437G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956775 | ||||||
| chr18:45956882
|
A | T | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.64-1544T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956882 | ||||||
| chr18:45956899
|
T | TA | 116 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(113): Show | 120 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.64-1562dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956899 | ||||||
| chr18:45956913
|
T | C | 1 | a0002c0002t0017g0229 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.64-1575A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45956913 | ||||||
| chr18:45957144
|
C | T | 5 | a0009c0007t0007g0006a0009c0007t0007g0009a0009c0007t0007g0010others(2): Show | 6 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-1806G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957144 | ||||||
| chr18:45957179
|
T | C | 10 | a0001c0001t0001g0037a0006c0011t0006g0038a0006c0011t0006g0040others(7): Show | 10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-1841A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957179 | ||||||
| chr18:45957203
|
A | C | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-1865T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957203 | ||||||
| chr18:45957287
|
T | C | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-1949A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957287 | ||||||
| chr18:45957309
|
T | C | 29 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(26): Show | 30 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.64-1971A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957309 | ||||||
| chr18:45957363
|
A | T | 5 | a0008c0008t0002g0018a0008c0008t0002g0019a0008c0008t0002g0020others(2): Show | 5 | HG01358.hp2 HG02071.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-2025T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957363 | ||||||
| chr18:45957419
|
A | G | 11 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0002g0065others(8): Show | 11 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-2081T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957419 | ||||||
| chr18:45957601
|
G | A | 4 | a0001c0001t0032g0113a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 4 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-2263C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957601 | ||||||
| chr18:45957821
|
T | C | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-2483A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957821 | ||||||
| chr18:45957825
|
A | G | 117 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(114): Show | 121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.64-2487T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45957825 | ||||||
| chr18:45958185
|
A | T | 59 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(56): Show | 62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.64-2847T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958185 | ||||||
| chr18:45958366
|
A | C | 32 | a0001c0001t0002g0190a0002c0002t0003g0183a0003c0003t0001g0184others(29): Show | 32 | HG00323.hp1 HG01346.hp2 HG01928.hp2 others(29): Show |
intron_variant | MODIFIER | c.64-3028T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958366 | ||||||
| chr18:45958369
|
C | A | 2 | a0001c0001t0001g0168a0001c0001t0036g0167 | 2 | HG02165.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.64-3031G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958369 | ||||||
| chr18:45958425
|
C | T | 1 | a0001c0034t0001g0088 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.64-3087G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958425 | ||||||
| chr18:45958439
|
A | G | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-3101T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958439 | ||||||
| chr18:45958444
|
T | C | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-3106A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958444 | ||||||
| chr18:45958469
|
G | GGACA | 117 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(114): Show | 121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.64-3135_64-3132dup others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958469 | ||||||
| chr18:45958575
|
G | A | 1 | a0008c0008t0002g0035 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.64-3237C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958575 | ||||||
| chr18:45958709
|
G | A | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-3371C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958709 | ||||||
| chr18:45958843
|
T | C | 6 | a0002c0002t0014g0220a0006c0012t0006g0221a0006c0012t0006g0222others(3): Show | 6 | HG01891.hp1 HG01891.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-3505A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958843 | ||||||
| chr18:45958870
|
T | C | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-3532A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45958870 | ||||||
| chr18:45959008
|
A | C | 1 | a0004c0048t0003g0015 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-3670T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959008 | ||||||
| chr18:45959008
|
A | T | 6 | a0004c0004t0015g0014a0009c0007t0007g0006a0009c0007t0007g0009others(3): Show | 7 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-3670T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959008 | ||||||
| chr18:45959009
|
A | T | 7 | a0004c0004t0015g0014a0004c0048t0003g0015a0009c0007t0007g0006others(4): Show | 8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3671T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959009 | ||||||
| chr18:45959010
|
G | GGGGGTT | 7 | a0004c0004t0015g0014a0004c0048t0003g0015a0009c0007t0007g0006others(4): Show | 8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3673_64-3672ins others(6): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959010 | ||||||
| chr18:45959040
|
C | G | 16 | a0001c0001t0001g0003a0001c0001t0001g0116a0001c0001t0001g0119others(13): Show | 17 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.64-3702G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959040 | ||||||
| chr18:45959057
|
A | G | 1 | a0004c0004t0004g0012 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.64-3719T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959057 | ||||||
| chr18:45959060
|
A | C | 1 | a0001c0001t0001g0087 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64-3722T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959060 | ||||||
| chr18:45959230
|
A | T | 1 | a0005c0005t0034g0086 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.64-3892T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959230 | ||||||
| chr18:45959275
|
A | C | 4 | a0019c0016t0010g0225a0019c0016t0010g0226a0020c0017t0010g0223others(1): Show | 4 | HG02723.hp1 HG02818.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-3937T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959275 | ||||||
| chr18:45959290
|
G | A | 2 | a0003c0003t0003g0208a0003c0003t0003g0209 | 2 | NA18957.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.64-3952C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959290 | ||||||
| chr18:45959324
|
G | A | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-3986C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959324 | ||||||
| chr18:45959339
|
T | C | 3 | a0002c0002t0017g0229a0002c0002t0029g0228a0006c0012t0006g0227 | 3 | HG01109.hp1 HG02647.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.64-4001A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959339 | ||||||
| chr18:45959363
|
GGGCCA | G | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-4030_64-4026del others(5): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959363 | ||||||
| chr18:45959368
|
A | G | 114 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(111): Show | 118 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(115): Show |
intron_variant | MODIFIER | c.64-4030T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959368 | ||||||
| chr18:45959386
|
C | A | 1 | a0001c0001t0004g0079 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.64-4048G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959386 | ||||||
| chr18:45959418
|
AG | A | 5 | a0002c0002t0014g0220a0006c0012t0006g0221a0006c0012t0006g0222others(2): Show | 5 | HG01891.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-4081delC | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959418 | ||||||
| chr18:45959532
|
G | C | 10 | a0001c0001t0001g0037a0006c0011t0006g0038a0006c0011t0006g0040others(7): Show | 10 | HG01884.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-4194C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959532 | ||||||
| chr18:45959658
|
C | CTAAA | 70 | a0001c0001t0001g0003a0001c0001t0001g0068a0001c0001t0001g0073others(67): Show | 71 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-4324_64-4321dup others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959658 | ||||||
| chr18:45959658
|
CTAAA | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0037others(115): Show | 124 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(121): Show |
intron_variant | MODIFIER | c.64-4324_64-4321del others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959658 | ||||||
| chr18:45959658
|
CTAAATAA others(1): Show |
C | 10 | a0002c0002t0002g0231a0002c0002t0002g0232a0002c0002t0002g0284others(7): Show | 11 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-4328_64-4321del others(8): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959658 | ||||||
| chr18:45959658
|
CTAAATAA others(5): Show |
C | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.64-4332_64-4321del others(12): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959658 | ||||||
| chr18:45959703
|
G | A | 85 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(82): Show | 88 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.64-4365C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959703 | ||||||
| chr18:45959705
|
T | C | 117 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(114): Show | 121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.64-4367A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959705 | ||||||
| chr18:45959836
|
G | A | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.64-4498C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959836 | ||||||
| chr18:45959948
|
T | C | 7 | a0004c0004t0015g0014a0004c0048t0003g0015a0009c0007t0007g0006others(4): Show | 8 | HG02280.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-4610A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45959948 | ||||||
| chr18:45960023
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.64-4685T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960023 | ||||||
| chr18:45960240
|
A | G | 1 | a0002c0002t0004g0230 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.64-4902T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960240 | ||||||
| chr18:45960425
|
C | A | 37 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0141others(34): Show | 40 | HG00609.hp1 HG01109.hp2 HG02074.hp2 others(37): Show |
intron_variant | MODIFIER | c.64-5087G>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960425 | ||||||
| chr18:45960526
|
T | TA | 32 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(29): Show | 33 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.64-5189dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960526 | ||||||
| chr18:45960533
|
C | T | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-5195G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960533 | ||||||
| chr18:45960583
|
A | G | 68 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(65): Show | 71 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-5245T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960583 | ||||||
| chr18:45960590
|
TGATA | T | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.64-5256_64-5253del others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960590 | ||||||
| chr18:45960715
|
T | C | 3 | a0011c0015t0014g0290a0011c0015t0019g0291a0021c0028t0018g0292 | 3 | HG01884.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.64-5377A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960715 | ||||||
| chr18:45960720
|
T | G | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.64-5382A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45960720 | ||||||
| chr18:45961289
|
C | T | 28 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(25): Show | 28 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.63+5888G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45961289 | ||||||
| chr18:45961290
|
C | T | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+5887G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45961290 | ||||||
| chr18:45961635
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.63+5542G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45961635 | ||||||
| chr18:45961858
|
C | CA | 47 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0171others(44): Show | 47 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.63+5318dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45961858 | ||||||
| chr18:45962031
|
T | A | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+5146A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962031 | ||||||
| chr18:45962067
|
GT | G | 65 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0002g0002others(62): Show | 68 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.63+5109delA | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962067 | ||||||
| chr18:45962108
|
G | A | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+5069C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962108 | ||||||
| chr18:45962142
|
A | C | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+5035T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962142 | ||||||
| chr18:45962209
|
A | C | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+4968T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962209 | ||||||
| chr18:45962322
|
T | C | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+4855A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962322 | ||||||
| chr18:45962348
|
T | C | 32 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(29): Show | 33 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.63+4829A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962348 | ||||||
| chr18:45962527
|
C | T | 117 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(114): Show | 121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.63+4650G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962527 | ||||||
| chr18:45962598
|
C | T | 117 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(114): Show | 121 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.63+4579G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962598 | ||||||
| chr18:45962821
|
T | C | 1 | a0002c0002t0002g0271 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.63+4356A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962821 | ||||||
| chr18:45962823
|
G | A | 59 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0051others(56): Show | 62 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.63+4354C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45962823 | ||||||
| chr18:45963018
|
T | A | 1 | a0002c0002t0002g0052 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.63+4159A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963018 | ||||||
| chr18:45963058
|
G | A | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+4119C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963058 | ||||||
| chr18:45963060
|
C | T | 2 | a0002c0009t0002g0276a0002c0009t0002g0277 | 2 | NA18964.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.63+4117G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963060 | ||||||
| chr18:45963067
|
T | G | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+4110A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963067 | ||||||
| chr18:45963254
|
C | T | 1 | a0005c0005t0003g0084 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.63+3923G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963254 | ||||||
| chr18:45963262
|
T | G | 1 | a0002c0002t0002g0052 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.63+3915A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963262 | ||||||
| chr18:45963273
|
C | T | 34 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0077others(31): Show | 34 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.63+3904G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963273 | ||||||
| chr18:45963334
|
A | G | 2 | a0001c0001t0001g0060a0022c0029t0001g0059 | 2 | HG01169.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.63+3843T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963334 | ||||||
| chr18:45963359
|
A | G | 1 | a0001c0001t0004g0058 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.63+3818T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963359 | ||||||
| chr18:45963372
|
G | C | 38 | a0001c0001t0002g0190a0002c0002t0003g0183a0003c0003t0001g0184others(35): Show | 38 | HG00323.hp1 HG01346.hp2 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.63+3805C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963372 | ||||||
| chr18:45963409
|
G | C | 22 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(19): Show | 22 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.63+3768C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963409 | ||||||
| chr18:45963442
|
G | A | 1 | a0004c0004t0009g0036 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.63+3735C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963442 | ||||||
| chr18:45963453
|
G | A | 3 | a0001c0001t0004g0179a0001c0001t0011g0180a0001c0001t0011g0181 | 3 | HG01261.hp1 HG02293.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.63+3724C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963453 | ||||||
| chr18:45963465
|
C | T | 6 | a0001c0001t0001g0037a0006c0011t0006g0038a0006c0011t0006g0040others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+3712G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963465 | ||||||
| chr18:45963613
|
T | G | 2 | a0016c0022t0020g0044a0016c0022t0021g0045 | 2 | HG01496.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.63+3564A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963613 | ||||||
| chr18:45963665
|
T | G | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+3512A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963665 | ||||||
| chr18:45963719
|
A | G | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+3458T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963719 | ||||||
| chr18:45963727
|
T | A | 85 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(82): Show | 88 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.63+3450A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963727 | ||||||
| chr18:45963794
|
A | G | 1 | a0001c0001t0043g0057 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.63+3383T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963794 | ||||||
| chr18:45963798
|
T | A | 1 | a0002c0002t0002g0052 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.63+3379A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963798 | ||||||
| chr18:45963872
|
G | C | 1 | a0004c0004t0009g0036 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.63+3305C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963872 | ||||||
| chr18:45963898
|
G | A | 156 | a0001c0001t0001g0037a0001c0001t0002g0190a0002c0002t0001g0293others(153): Show | 160 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(157): Show |
intron_variant | MODIFIER | c.63+3279C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45963898 | ||||||
| chr18:45964031
|
C | T | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+3146G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964031 | ||||||
| chr18:45964115
|
T | C | 4 | a0001c0001t0001g0215a0001c0001t0004g0216a0001c0001t0009g0218others(1): Show | 4 | HG00438.hp1 HG00621.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3062A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964115 | ||||||
| chr18:45964191
|
T | TTC | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2985_63+2986ins others(2): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964191 | ||||||
| chr18:45964209
|
A | C | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2968T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964209 | ||||||
| chr18:45964239
|
T | G | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2938A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964239 | ||||||
| chr18:45964270
|
G | A | 85 | a0001c0001t0001g0037a0002c0002t0001g0293a0002c0002t0001g0294others(82): Show | 88 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.63+2907C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964270 | ||||||
| chr18:45964302
|
T | A | 1 | a0002c0002t0002g0052 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.63+2875A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964302 | ||||||
| chr18:45964552
|
C | G | 1 | a0001c0001t0004g0056 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.63+2625G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964552 | ||||||
| chr18:45964555
|
T | C | 2 | a0006c0012t0006g0272a0018c0043t0023g0046 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.63+2622A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964555 | ||||||
| chr18:45964827
|
C | G | 1 | a0003c0003t0016g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.63+2350G>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964827 | ||||||
| chr18:45964874
|
A | C | 1 | a0002c0002t0002g0054 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.63+2303T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964874 | ||||||
| chr18:45964907
|
CG | C | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2269delC | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964907 | ||||||
| chr18:45964910
|
G | A | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2267C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45964910 | ||||||
| chr18:45965001
|
T | C | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2176A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965001 | ||||||
| chr18:45965051
|
A | G | 1 | a0002c0002t0004g0053 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.63+2126T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965051 | ||||||
| chr18:45965110
|
T | G | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+2067A>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965110 | ||||||
| chr18:45965140
|
TC | T | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2036delG | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965140 | ||||||
| chr18:45965145
|
T | A | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2032A>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965145 | ||||||
| chr18:45965223
|
CACTT | C | 28 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(25): Show | 28 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.63+1950_63+1953del others(4): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965223 | ||||||
| chr18:45965303
|
A | G | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+1874T>C | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965303 | ||||||
| chr18:45965308
|
G | T | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+1869C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965308 | ||||||
| chr18:45965320
|
G | T | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+1857C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965320 | ||||||
| chr18:45965346
|
C | T | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+1831G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965346 | ||||||
| chr18:45965458
|
G | A | 1 | a0003c0003t0002g0287 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.63+1719C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965458 | ||||||
| chr18:45965773
|
G | T | 1 | a0021c0028t0018g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.63+1404C>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965773 | ||||||
| chr18:45965940
|
T | C | 3 | a0002c0002t0002g0273a0002c0002t0002g0274a0002c0002t0008g0275 | 3 | HG01071.hp2 HG01192.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.63+1237A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45965940 | ||||||
| chr18:45966053
|
T | C | 2 | a0004c0004t0015g0014a0004c0048t0003g0015 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.63+1124A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966053 | ||||||
| chr18:45966094
|
T | C | 5 | a0002c0009t0002g0276a0002c0009t0002g0277a0002c0009t0002g0278others(2): Show | 5 | HG00621.hp1 HG02074.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+1083A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966094 | ||||||
| chr18:45966098
|
C | T | 1 | a0002c0002t0002g0052 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.63+1079G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966098 | ||||||
| chr18:45966139
|
G | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.63+1038C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966139 | ||||||
| chr18:45966150
|
A | C | 1 | a0002c0002t0002g0051 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.63+1027T>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966150 | ||||||
| chr18:45966244
|
C | T | 1 | a0002c0002t0008g0050 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.63+933G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966244 | ||||||
| chr18:45966265
|
G | C | 23 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(20): Show | 23 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.63+912C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966265 | ||||||
| chr18:45966324
|
C | T | 3 | a0002c0002t0030g0049a0002c0002t0031g0048a0005c0005t0033g0047 | 3 | HG02615.hp2 HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.63+853G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966324 | ||||||
| chr18:45966375
|
C | CA | 33 | a0001c0001t0001g0282a0002c0002t0002g0281a0002c0002t0002g0284others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.63+801dupT | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966375 | ||||||
| chr18:45966391
|
A | T | 4 | a0016c0022t0020g0044a0016c0022t0021g0045a0018c0042t0022g0043others(1): Show | 4 | HG01496.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+786T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966391 | ||||||
| chr18:45966421
|
T | C | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.63+756A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966421 | ||||||
| chr18:45966442
|
A | ATGTATAT others(21): Show |
6 | a0001c0001t0001g0037a0006c0011t0006g0038a0006c0011t0006g0040others(3): Show | 6 | HG01884.hp1 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+707_63+734dupCA others(26): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966442 | ||||||
| chr18:45966457
|
CATATGTA others(11): Show |
C | 2 | a0007c0006t0003g0288a0007c0006t0003g0289 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.63+702_63+719delAT others(16): Show |
EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966457 | ||||||
| chr18:45966543
|
T | C | 4 | a0009c0007t0007g0006a0011c0015t0014g0290a0011c0015t0019g0291others(1): Show | 5 | HG01884.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+634A>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966543 | ||||||
| chr18:45966569
|
C | T | 29 | a0004c0004t0001g0028a0004c0004t0003g0030a0004c0004t0004g0012others(26): Show | 29 | HG00140.hp1 HG01358.hp2 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.63+608G>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966569 | ||||||
| chr18:45966716
|
G | A | 1 | a0021c0028t0018g0292 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.63+461C>T | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966716 | ||||||
| chr18:45966727
|
A | T | 1 | a0002c0038t0007g0008 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+450T>A | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966727 | ||||||
| chr18:45966988
|
G | C | 3 | a0002c0002t0001g0293a0002c0002t0001g0294a0002c0002t0037g0295 | 3 | HG02622.hp1 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.63+189C>G | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45966988 | ||||||
| chr18:45967161
|
TG | T | 295 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.63+15delC | EPG5 | ENSG00000152223.16 | transcript | ENST00000282041.11 | protein_coding | 1/43 | chr18 | 45967161 |