| geneid | 55140 |
|---|---|
| ensemblid | ENSG00000134014.18 |
| hgncid | 20696 |
| symbol | ELP3 |
| name | elongator acetyltransferase complex subunit 3 |
| refseq_nuc | NM_018091.6 |
| refseq_prot | NP_060561.3 |
| ensembl_nuc | ENST00000256398.13 |
| ensembl_prot | ENSP00000256398.8 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 28093139 |
| end | 28191153 |
| strand | + |
| ver | v1.2 |
| region | chr8:28093139-28191153 |
| region5000 | chr8:28088139-28196153 |
| regionname0 | ELP3_chr8_28093139_28191153 |
| regionname5000 | ELP3_chr8_28088139_28196153 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 547 | 397 | 94 | 76 | 172 | 17 | 36 | 136 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0002 | 0/0 | 547 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1644 | 382 | 86 | 75 | 166 | 17 | 36 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| c0002 | 0/0 | 1644 | 8 | 7 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| c0003 | 0/0 | 1644 | 6 | 0 | 0 | 6 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| c0004 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| c0005 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1505 | 113 | 42 | 5 | 54 | 2 | 9 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0002 | 0/0 | 1505 | 104 | 11 | 26 | 46 | 8 | 13 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0003 | 0/1 | 1506 | 75 | 18 | 28 | 9 | 7 | 12 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0004 | 0/0 | 1507 | 59 | 3 | 11 | 44 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0005 | 0/0 | 1511 | 9 | 0 | 5 | 4 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0006 | 0/0 | 1507 | 7 | 7 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0007 | 0/0 | 1507 | 6 | 6 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0008 | 0/0 | 1507 | 6 | 0 | 0 | 6 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0009 | 0/0 | 1505 | 5 | 4 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0010 | 0/0 | 1506 | 3 | 0 | 0 | 3 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0011 | 0/0 | 1505 | 2 | 2 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0012 | 0/0 | 1506 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0013 | 0/0 | 1506 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0014 | 0/0 | 1505 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0015 | 0/0 | 1506 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0016 | 0/0 | 1506 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0017 | 0/0 | 1506 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0018 | 0/0 | 1506 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0019 | 0/0 | 1507 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| t0020 | 0/0 | 1506 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| 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 | 4 | 0 | 0 | 4 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0004 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0326 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0350 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1644 | 382 | 86 | 75 | 166 | 17 | 36 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0002 | 0/0 | 1644 | 8 | 7 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0003 | 0/0 | 1644 | 6 | 0 | 0 | 6 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0004 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0002c0005 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3148 | 111 | 40 | 5 | 54 | 2 | 9 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0002 | 0/0 | 3148 | 103 | 11 | 26 | 46 | 7 | 13 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0003 | 0/1 | 3149 | 75 | 18 | 28 | 9 | 7 | 12 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0004 | 0/0 | 3150 | 59 | 3 | 11 | 44 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0005 | 0/0 | 3154 | 9 | 0 | 5 | 4 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0006 | 0/0 | 3150 | 7 | 7 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0007 | 0/0 | 3150 | 6 | 6 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0010 | 0/0 | 3149 | 3 | 0 | 0 | 3 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0012 | 0/0 | 3149 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0013 | 0/0 | 3149 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0014 | 0/0 | 3148 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0015 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0016 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0017 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0018 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0019 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0001t0020 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0002t0001 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0002t0009 | 0/0 | 3148 | 5 | 4 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0002t0011 | 0/0 | 3148 | 2 | 2 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0003t0008 | 0/0 | 3150 | 6 | 0 | 0 | 6 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0001c0004t0001 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| a0002c0005t0002 | 0/0 | 3148 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | copy fasta | chr8 | 28088139 | 28196153 |
| 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 | 4 | 0 | 0 | 4 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0350 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0326 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0006g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0010g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0010g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0010g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0012g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0013g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0014g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0015g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0016g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0017g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0018g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0019g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0020g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0002t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0002t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0002t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0002t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0002t0009g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0002t0011g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0002t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0003t0008g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0003t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0003t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0003t0008g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0003t0008g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0003t0008g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0002c0005t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0340 | EUR | GBR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | GBR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0095 | EUR | GBR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0320 | EUR | GBR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0053 | EUR | FIN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0355 | EUR | FIN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0354 | EUR | FIN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00323 | hp2 | a0002 | c0005 | t0002 | g0127 | EUR | FIN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0319 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0289 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0304 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00597 | hp1 | a0001 | c0003 | t0008 | g0106 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0283 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0366 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0323 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0351 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0360 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0344 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0327 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0328 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0349 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0359 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0293 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0346 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0318 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0348 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0280 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0262 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0329 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0294 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0331 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0367 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01243 | hp1 | a0001 | c0002 | t0009 | g0147 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0330 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0339 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0269 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0285 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0365 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0296 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0347 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0023 | EUR | IBS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0044 | EUR | IBS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0023 | EUR | IBS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0151 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0315 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0276 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0314 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0301 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0281 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0277 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0258 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0275 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02015 | hp2 | a0001 | c0001 | t0020 | g0138 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0257 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0325 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0334 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0253 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02155 | hp2 | a0001 | c0001 | t0010 | g0363 | EAS | CDX | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | CDX | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CDX | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02257 | hp1 | a0001 | c0002 | t0011 | g0144 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0343 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0239 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0353 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0345 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0150 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0254 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0364 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0154 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0332 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0153 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0352 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0155 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0307 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0145 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02895 | hp1 | a0001 | c0002 | t0009 | g0146 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0148 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0256 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02965 | hp2 | a0001 | c0002 | t0009 | g0141 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0322 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0152 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0255 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0273 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0321 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0324 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0316 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0342 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03669 | hp2 | a0001 | c0001 | t0013 | g0361 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | STU | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | STU | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0341 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0368 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0317 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0356 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0271 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0333 | SAS | STU | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | STU | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0357 | SAS | STU | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18522 | hp2 | a0001 | c0002 | t0009 | g0143 | AFR | YRI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | CHB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18612 | hp2 | a0001 | c0001 | t0010 | g0362 | EAS | CHB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | YRI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | YRI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18948 | hp2 | a0001 | c0001 | t0018 | g0244 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18952 | hp1 | a0001 | c0001 | t0010 | g0169 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18965 | hp1 | a0001 | c0003 | t0008 | g0107 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18966 | hp1 | a0001 | c0001 | t0014 | g0209 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0279 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18968 | hp1 | a0001 | c0003 | t0008 | g0104 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0303 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0286 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18974 | hp2 | a0001 | c0001 | t0016 | g0002 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18977 | hp1 | a0001 | c0001 | t0015 | g0338 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18987 | hp2 | a0001 | c0003 | t0008 | g0109 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18993 | hp2 | a0001 | c0001 | t0019 | g0291 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19000 | hp2 | a0001 | c0003 | t0008 | g0108 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | LWK | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19030 | hp2 | a0001 | c0002 | t0011 | g0149 | AFR | LWK | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | LWK | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19067 | hp2 | a0001 | c0001 | t0005 | g0287 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0290 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19076 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0337 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0299 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0305 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19240 | hp1 | a0001 | c0001 | t0017 | g0027 | AFR | YRI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0240 | AFR | YRI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ASW | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0369 | AFR | ASW | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20752 | hp1 | a0001 | c0001 | t0012 | g0358 | EUR | TSI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0123 | EUR | TSI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0048 | EUR | TSI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | TSI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | USA | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | USA | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18955 | hp1 | a0001 | c0003 | t0008 | g0105 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | USA | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20300 | hp2 | a0001 | c0002 | t0009 | g0142 | AFR | USA | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | LWK | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | LWK | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0326 | REF | REF | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0350 | REF | REF | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28106776
|
A | T | 1 | a0002 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.322A>T | p.Ile108Leu | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/15 | 398/3148 | 322/1644 | 108/547 | chr8 | 28106776 | ||
| chr8:28191151
|
A | C | 1 | a0001 | 79 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
splice_region_variant | LOW | c.*1426A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | chr8 | 28191151 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28097289
|
C | T | 1 | a0001c0003 | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
synonymous_variant | LOW | c.90C>T | p.His30His | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/15 | 166/3148 | 90/1644 | 30/547 | chr8 | 28097289 | ||
| chr8:28099858
|
C | A | 2 | a0001c0002a0001c0004 | 9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
synonymous_variant | LOW | c.150C>A | p.Gly50Gly | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/15 | 226/3148 | 150/1644 | 50/547 | chr8 | 28099858 | ||
| chr8:28160288
|
C | T | 1 | a0001c0002 | 8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
synonymous_variant | LOW | c.1317C>T | p.Tyr439Tyr | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/15 | 1393/3148 | 1317/1644 | 439/547 | chr8 | 28160288 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28093153
|
C | T | 3 | a0001c0001t0002a0001c0001t0020a0002c0005t0002 | 105 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(102): Show |
5_prime_UTR_variant | MODIFIER | c.-62C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/15 | 62 | chr8 | 28093153 | |||||
| chr8:28189774
|
G | A | 1 | a0001c0001t0007 | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*49G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 49 | chr8 | 28189774 | |||||
| chr8:28189905
|
C | G | 7 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(4): Show | 79 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*180C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 180 | chr8 | 28189905 | |||||
| chr8:28189912
|
C | T | 1 | a0001c0001t0019 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*187C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 187 | chr8 | 28189912 | |||||
| chr8:28189930
|
C | T | 1 | a0001c0001t0015 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*205C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 205 | chr8 | 28189930 | |||||
| chr8:28190024
|
G | A | 1 | a0001c0001t0012 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*299G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 299 | chr8 | 28190024 | |||||
| chr8:28190087
|
C | G | 1 | a0001c0001t0014 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*362C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 362 | chr8 | 28190087 | |||||
| chr8:28190096
|
A | AACTT | 1 | a0001c0001t0005 | 9 | HG01257.hp1 HG01358.hp2 HG01943.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*373_*376dupCTTA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 377 | INFO_REALIGN_3_PRIME | chr8 | 28190096 | ||||
| chr8:28190519
|
T | C | 1 | a0001c0002t0011 | 2 | HG02257.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*794T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 794 | chr8 | 28190519 | |||||
| chr8:28190573
|
A | AT | 9 | a0001c0001t0003a0001c0001t0010a0001c0001t0012others(6): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*862dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 863 | INFO_REALIGN_3_PRIME | chr8 | 28190573 | ||||
| chr8:28190573
|
A | ATT | 6 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(3): Show | 88 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*861_*862dupTT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 863 | INFO_REALIGN_3_PRIME | chr8 | 28190573 | ||||
| chr8:28190650
|
C | T | 5 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(2): Show | 77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*925C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 925 | chr8 | 28190650 | |||||
| chr8:28190651
|
G | C | 1 | a0001c0001t0016 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*926G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 926 | chr8 | 28190651 | |||||
| chr8:28190839
|
A | G | 1 | a0001c0001t0013 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1114A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 1114 | chr8 | 28190839 | |||||
| chr8:28190849
|
G | A | 2 | a0001c0002t0009a0001c0002t0011 | 7 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1124G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 1124 | chr8 | 28190849 | |||||
| chr8:28191016
|
T | C | 1 | a0001c0001t0006 | 7 | HG02055.hp1 HG02145.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1291T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 1291 | chr8 | 28191016 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28093508
|
G | A | 124 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(121): Show | 133 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.19+275G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28093508 | ||||||
| chr8:28093541
|
C | G | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.19+308C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28093541 | ||||||
| chr8:28093568
|
G | C | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0003g0024others(4): Show | 7 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+335G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28093568 | ||||||
| chr8:28093644
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(92): Show | 101 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.19+411T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28093644 | ||||||
| chr8:28093692
|
T | C | 3 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0003g0232 | 3 | HG02055.hp2 HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.19+459T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28093692 | ||||||
| chr8:28093914
|
A | C | 1 | a0001c0001t0001g0229 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.19+681A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28093914 | ||||||
| chr8:28094039
|
C | A | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.19+806C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094039 | ||||||
| chr8:28094184
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(92): Show | 101 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.19+951C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094184 | ||||||
| chr8:28094199
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.19+966T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094199 | ||||||
| chr8:28094249
|
A | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(75): Show | 84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.19+1016A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094249 | ||||||
| chr8:28094303
|
C | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+1070C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094303 | ||||||
| chr8:28094350
|
T | C | 1 | a0001c0001t0020g0138 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.19+1117T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094350 | ||||||
| chr8:28094618
|
G | GGAGGCT | 78 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(75): Show | 84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.19+1403_19+1408dup others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 28094618 | |||||
| chr8:28094641
|
C | T | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.19+1408C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094641 | ||||||
| chr8:28094681
|
G | A | 1 | a0001c0001t0003g0238 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.19+1448G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094681 | ||||||
| chr8:28094741
|
C | CA | 3 | a0001c0001t0001g0233a0001c0001t0002g0031a0001c0001t0002g0032 | 3 | NA18978.hp2 NA19057.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.19+1513dupA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 28094741 | |||||
| chr8:28094747
|
G | A | 300 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(297): Show | 321 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.19+1514G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094747 | ||||||
| chr8:28094931
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.19+1698A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094931 | ||||||
| chr8:28094976
|
A | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.19+1743A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094976 | ||||||
| chr8:28095062
|
C | G | 1 | a0001c0001t0002g0136 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.19+1829C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095062 | ||||||
| chr8:28095073
|
CCTGTTAG others(4): Show |
C | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.19+1844_19+1854del others(11): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 28095073 | |||||
| chr8:28095358
|
A | G | 26 | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0112others(23): Show | 28 | HG00323.hp2 HG01358.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.20-1861A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095358 | ||||||
| chr8:28095392
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.20-1827G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095392 | ||||||
| chr8:28095504
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 11 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-1715G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095504 | ||||||
| chr8:28095540
|
G | T | 2 | a0001c0001t0002g0110a0001c0001t0002g0111 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.20-1679G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095540 | ||||||
| chr8:28095579
|
T | C | 1 | a0001c0001t0002g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.20-1640T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095579 | ||||||
| chr8:28095758
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.20-1461G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095758 | ||||||
| chr8:28095762
|
A | G | 1 | a0001c0001t0003g0368 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.20-1457A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095762 | ||||||
| chr8:28095777
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 11 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-1442C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095777 | ||||||
| chr8:28095797
|
A | C | 1 | a0001c0001t0003g0367 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.20-1422A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095797 | ||||||
| chr8:28096039
|
C | T | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-1180C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28096039 | ||||||
| chr8:28096359
|
G | A | 117 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(114): Show | 126 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.20-860G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28096359 | ||||||
| chr8:28096452
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.20-767C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28096452 | ||||||
| chr8:28096589
|
G | A | 1 | a0001c0001t0005g0239 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.20-630G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28096589 | ||||||
| chr8:28096948
|
C | T | 117 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(114): Show | 126 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.20-271C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28096948 | ||||||
| chr8:28097108
|
A | G | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-111A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28097108 | ||||||
| chr8:28097134
|
C | T | 9 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(6): Show | 9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-85C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28097134 | ||||||
| chr8:28097398
|
T | G | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.119+80T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097398 | ||||||
| chr8:28097405
|
C | G | 1 | a0001c0001t0002g0102 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.119+87C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097405 | ||||||
| chr8:28097449
|
G | A | 1 | a0001c0001t0006g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.119+131G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097449 | ||||||
| chr8:28097460
|
C | CT | 5 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0103others(2): Show | 6 | HG02109.hp1 HG02970.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.119+155dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 28097460 | |||||
| chr8:28097460
|
CT | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(98): Show | 107 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.119+155delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 28097460 | |||||
| chr8:28097492
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.119+174G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097492 | ||||||
| chr8:28097495
|
A | C | 1 | a0001c0001t0001g0228 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.119+177A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097495 | ||||||
| chr8:28097587
|
G | A | 6 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237others(3): Show | 6 | HG03139.hp2 HG03195.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.119+269G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097587 | ||||||
| chr8:28097611
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.119+293C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097611 | ||||||
| chr8:28097685
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(75): Show | 84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.119+367C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097685 | ||||||
| chr8:28097811
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.119+493C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097811 | ||||||
| chr8:28097887
|
G | T | 1 | a0001c0001t0001g0227 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.119+569G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097887 | ||||||
| chr8:28097978
|
T | G | 5 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0003g0311others(2): Show | 5 | HG02056.hp2 NA18954.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.119+660T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097978 | ||||||
| chr8:28097990
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.119+672G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097990 | ||||||
| chr8:28098060
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(75): Show | 84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.119+742C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098060 | ||||||
| chr8:28098091
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.119+773C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098091 | ||||||
| chr8:28098203
|
AT | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.119+895delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 28098203 | |||||
| chr8:28098284
|
G | A | 2 | a0001c0001t0004g0245a0001c0001t0018g0244 | 2 | NA18948.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.119+966G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098284 | ||||||
| chr8:28098367
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.119+1049T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098367 | ||||||
| chr8:28098458
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.119+1140C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098458 | ||||||
| chr8:28098588
|
T | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0157others(9): Show | 16 | HG00558.hp1 HG02015.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.120-1240T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098588 | ||||||
| chr8:28098760
|
T | C | 1 | a0001c0001t0002g0042 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.120-1068T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098760 | ||||||
| chr8:28098929
|
ATG | A | 5 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(2): Show | 5 | HG02451.hp1 HG02976.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.120-889_120-888del others(2): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 28098929 | |||||
| chr8:28098934
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.120-894T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098934 | ||||||
| chr8:28099084
|
C | A | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.120-744C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099084 | ||||||
| chr8:28099302
|
C | G | 17 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0007g0150others(14): Show | 17 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.120-526C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099302 | ||||||
| chr8:28099422
|
A | G | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.120-406A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099422 | ||||||
| chr8:28099515
|
G | A | 1 | a0001c0001t0002g0112 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.120-313G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099515 | ||||||
| chr8:28099570
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.120-258T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099570 | ||||||
| chr8:28099593
|
C | T | 1 | a0001c0001t0004g0306 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.120-235C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099593 | ||||||
| chr8:28099655
|
G | A | 1 | a0001c0001t0002g0012 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.120-173G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099655 | ||||||
| chr8:28099747
|
G | T | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.120-81G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099747 | ||||||
| chr8:28099796
|
A | G | 106 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(103): Show | 112 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.120-32A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099796 | ||||||
| chr8:28100003
|
G | C | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+37G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100003 | ||||||
| chr8:28100012
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(75): Show | 84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.258+46C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100012 | ||||||
| chr8:28100039
|
G | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.258+73G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100039 | ||||||
| chr8:28100040
|
C | G | 3 | a0001c0001t0003g0311a0001c0001t0003g0312a0001c0001t0003g0313 | 3 | HG02056.hp2 NA18954.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.258+74C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100040 | ||||||
| chr8:28100404
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.258+438A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100404 | ||||||
| chr8:28100442
|
A | C | 1 | a0001c0001t0003g0366 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.258+476A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100442 | ||||||
| chr8:28100536
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.258+570C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100536 | ||||||
| chr8:28100543
|
G | C | 1 | a0001c0001t0003g0314 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.258+577G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100543 | ||||||
| chr8:28100832
|
A | G | 1 | a0001c0001t0004g0305 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.258+866A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100832 | ||||||
| chr8:28101010
|
C | T | 2 | a0001c0001t0002g0011a0001c0001t0002g0098 | 3 | HG01257.hp2 HG01258.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.258+1044C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101010 | ||||||
| chr8:28101026
|
A | C | 1 | a0001c0002t0011g0149 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+1060A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101026 | ||||||
| chr8:28101101
|
TTTTG | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.258+1145_258+1148d others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28101101 | |||||
| chr8:28101132
|
T | C | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.258+1166T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101132 | ||||||
| chr8:28101166
|
C | G | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+1200C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101166 | ||||||
| chr8:28101183
|
C | T | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+1217C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101183 | ||||||
| chr8:28101207
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.258+1241G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101207 | ||||||
| chr8:28101219
|
C | G | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.258+1253C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101219 | ||||||
| chr8:28101231
|
G | A | 5 | a0001c0001t0004g0017a0001c0001t0004g0246a0001c0001t0004g0247others(2): Show | 6 | HG02523.hp1 NA18941.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+1265G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101231 | ||||||
| chr8:28101314
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.258+1348A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101314 | ||||||
| chr8:28101345
|
G | C | 2 | a0001c0001t0003g0315a0001c0001t0003g0316 | 2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.258+1379G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101345 | ||||||
| chr8:28101549
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.258+1583A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101549 | ||||||
| chr8:28101590
|
C | CT | 268 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(265): Show | 286 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.258+1639dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28101590 | |||||
| chr8:28101590
|
C | CTT | 10 | a0001c0001t0001g0103a0001c0001t0001g0166a0001c0001t0001g0225others(7): Show | 10 | HG01243.hp1 HG01952.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.258+1638_258+1639d others(4): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28101590 | |||||
| chr8:28101608
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.258+1642C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101608 | ||||||
| chr8:28101643
|
A | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.258+1677A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101643 | ||||||
| chr8:28101823
|
G | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.258+1857G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101823 | ||||||
| chr8:28101869
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.258+1903C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101869 | ||||||
| chr8:28101933
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258+1967A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101933 | ||||||
| chr8:28102096
|
G | A | 32 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0320others(29): Show | 33 | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.258+2130G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102096 | ||||||
| chr8:28102150
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.258+2184G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102150 | ||||||
| chr8:28102302
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.258+2336C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102302 | ||||||
| chr8:28102324
|
C | T | 1 | a0001c0001t0002g0042 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.258+2358C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102324 | ||||||
| chr8:28102333
|
A | C | 1 | a0001c0001t0001g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.258+2367A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102333 | ||||||
| chr8:28102472
|
A | G | 1 | a0001c0001t0002g0097 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.258+2506A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102472 | ||||||
| chr8:28102647
|
A | G | 1 | a0001c0001t0004g0304 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.258+2681A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102647 | ||||||
| chr8:28102768
|
C | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.258+2802C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102768 | ||||||
| chr8:28102972
|
C | G | 3 | a0001c0003t0008g0107a0001c0003t0008g0108a0001c0003t0008g0109 | 3 | NA18965.hp1 NA18987.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.258+3006C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102972 | ||||||
| chr8:28103023
|
A | T | 2 | a0001c0001t0002g0110a0001c0001t0002g0111 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.258+3057A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103023 | ||||||
| chr8:28103043
|
G | A | 1 | a0001c0001t0002g0043 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.258+3077G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103043 | ||||||
| chr8:28103118
|
C | T | 1 | a0001c0001t0004g0303 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.258+3152C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103118 | ||||||
| chr8:28103167
|
C | G | 1 | a0001c0001t0004g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.258+3201C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103167 | ||||||
| chr8:28103169
|
CAAAA | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(75): Show | 84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.258+3207_258+3210d others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28103169 | |||||
| chr8:28103173
|
AAAAC | A | 6 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0241others(3): Show | 7 | HG02055.hp2 HG02572.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+3231_258+3234d others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28103173 | |||||
| chr8:28103309
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.258+3343C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103309 | ||||||
| chr8:28103363
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.259-3350A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103363 | ||||||
| chr8:28103427
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.259-3286G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103427 | ||||||
| chr8:28103437
|
C | T | 1 | a0001c0001t0005g0301 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.259-3276C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103437 | ||||||
| chr8:28103633
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.259-3080A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103633 | ||||||
| chr8:28103649
|
G | C | 2 | a0001c0001t0003g0339a0001c0001t0003g0340 | 2 | HG00099.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.259-3064G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103649 | ||||||
| chr8:28103713
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259-3000C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103713 | ||||||
| chr8:28103935
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.259-2778C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103935 | ||||||
| chr8:28104059
|
T | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(272): Show | 293 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.259-2654T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104059 | ||||||
| chr8:28104160
|
G | A | 15 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(12): Show | 15 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.259-2553G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104160 | ||||||
| chr8:28104362
|
C | T | 299 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(296): Show | 320 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.259-2351C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104362 | ||||||
| chr8:28104600
|
A | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.259-2113A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104600 | ||||||
| chr8:28104670
|
G | A | 1 | a0001c0001t0002g0008 | 2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.259-2043G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104670 | ||||||
| chr8:28104696
|
A | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(296): Show | 320 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.259-2017A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104696 | ||||||
| chr8:28104743
|
G | T | 1 | a0001c0001t0002g0134 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.259-1970G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104743 | ||||||
| chr8:28104990
|
G | A | 72 | a0001c0001t0001g0297a0001c0001t0004g0002a0001c0001t0004g0017others(69): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.259-1723G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104990 | ||||||
| chr8:28105052
|
T | G | 9 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(6): Show | 9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.259-1661T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105052 | ||||||
| chr8:28105219
|
T | TA | 6 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0001t0001g0139others(3): Show | 6 | HG02109.hp2 HG03098.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-1482dupA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28105219 | |||||
| chr8:28105227
|
A | AG | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.259-1486_259-1485i others(3): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105227 | ||||||
| chr8:28105314
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.259-1399C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105314 | ||||||
| chr8:28105347
|
G | A | 1 | a0001c0001t0004g0252 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.259-1366G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105347 | ||||||
| chr8:28105370
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.259-1343A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105370 | ||||||
| chr8:28105384
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.259-1329C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105384 | ||||||
| chr8:28105411
|
T | A | 1 | a0001c0001t0003g0341 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.259-1302T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105411 | ||||||
| chr8:28105438
|
T | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.259-1275T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105438 | ||||||
| chr8:28105638
|
C | T | 4 | a0001c0001t0001g0297a0001c0001t0004g0298a0001c0001t0004g0299others(1): Show | 4 | NA18949.hp1 NA18953.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-1075C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105638 | ||||||
| chr8:28105687
|
A | C | 1 | a0001c0001t0001g0235 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.259-1026A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105687 | ||||||
| chr8:28105695
|
C | T | 98 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(95): Show | 104 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.259-1018C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105695 | ||||||
| chr8:28105710
|
C | T | 1 | a0001c0002t0001g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.259-1003C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105710 | ||||||
| chr8:28105726
|
T | C | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.259-987T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105726 | ||||||
| chr8:28105825
|
T | A | 1 | a0001c0001t0010g0169 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.259-888T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105825 | ||||||
| chr8:28106040
|
A | G | 1 | a0001c0001t0005g0296 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.259-673A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106040 | ||||||
| chr8:28106283
|
G | A | 1 | a0001c0001t0007g0150 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.259-430G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106283 | ||||||
| chr8:28106307
|
G | A | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-406G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106307 | ||||||
| chr8:28106356
|
C | T | 1 | a0001c0001t0004g0295 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.259-357C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106356 | ||||||
| chr8:28106368
|
G | A | 1 | a0001c0001t0003g0342 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.259-345G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106368 | ||||||
| chr8:28106397
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.259-316G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106397 | ||||||
| chr8:28106409
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.259-304G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106409 | ||||||
| chr8:28106465
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.259-248G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106465 | ||||||
| chr8:28106472
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.259-241G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106472 | ||||||
| chr8:28106517
|
G | A | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.259-196G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106517 | ||||||
| chr8:28106539
|
C | CA | 22 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0003g0003others(19): Show | 25 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.259-146dupA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28106539 | |||||
| chr8:28106539
|
CAAAAAA | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0233a0001c0001t0001g0236others(3): Show | 6 | HG02723.hp1 HG02818.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-151_259-146del others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28106539 | |||||
| chr8:28106539
|
CAAAAAAA | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(8): Show | 14 | HG00733.hp1 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.259-152_259-146del others(7): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28106539 | |||||
| chr8:28106539
|
CAAAAAAA others(1): Show |
C | 9 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0234others(6): Show | 9 | HG02451.hp1 HG02572.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.259-153_259-146del others(8): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28106539 | |||||
| chr8:28106539
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0002t0011g0144 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.259-159_259-146del others(14): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28106539 | |||||
| chr8:28106539
|
CAAAAAAA others(8): Show |
C | 266 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(263): Show | 284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.259-160_259-146del others(15): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28106539 | |||||
| chr8:28106539
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0004g0294 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.259-161_259-146del others(16): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28106539 | |||||
| chr8:28106628
|
C | G | 1 | a0001c0001t0004g0293 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.259-85C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106628 | ||||||
| chr8:28107163
|
G | A | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.329+380G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107163 | ||||||
| chr8:28107197
|
G | A | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.329+414G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107197 | ||||||
| chr8:28107321
|
A | G | 1 | a0001c0001t0015g0338 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.329+538A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107321 | ||||||
| chr8:28107339
|
G | C | 269 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(266): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.329+556G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107339 | ||||||
| chr8:28107470
|
A | G | 1 | a0001c0001t0003g0238 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.330-443A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107470 | ||||||
| chr8:28107483
|
G | C | 9 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0234others(6): Show | 9 | HG02451.hp1 HG02572.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.330-430G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107483 | ||||||
| chr8:28107583
|
G | A | 6 | a0001c0001t0006g0240a0001c0001t0006g0253a0001c0001t0006g0254others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.330-330G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107583 | ||||||
| chr8:28107607
|
G | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.330-306G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107607 | ||||||
| chr8:28107822
|
T | C | 3 | a0001c0002t0009g0141a0001c0002t0009g0142a0001c0002t0009g0143 | 3 | HG02965.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.330-91T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107822 | ||||||
| chr8:28108194
|
A | C | 80 | a0001c0001t0002g0008a0001c0001t0002g0012a0001c0001t0002g0013others(77): Show | 83 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.393+218A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108194 | ||||||
| chr8:28108332
|
A | T | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.393+356A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108332 | ||||||
| chr8:28108457
|
C | CT | 276 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(273): Show | 294 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.393+499dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr8 | 28108457 | |||||
| chr8:28108457
|
C | CTT | 9 | a0001c0001t0001g0030a0001c0001t0001g0140a0001c0001t0002g0056others(6): Show | 9 | HG01981.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+498_393+499dup others(2): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr8 | 28108457 | |||||
| chr8:28108457
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0115 | 3 | HG02080.hp2 NA18963.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.393+489_393+499del others(11): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr8 | 28108457 | |||||
| chr8:28108464
|
T | C | 1 | a0001c0001t0003g0321 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.393+488T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108464 | ||||||
| chr8:28108508
|
A | G | 1 | a0001c0001t0001g0370 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.393+532A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108508 | ||||||
| chr8:28108528
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.393+552T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108528 | ||||||
| chr8:28108552
|
G | A | 1 | a0001c0001t0003g0341 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.393+576G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108552 | ||||||
| chr8:28108584
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.393+608G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108584 | ||||||
| chr8:28108614
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.393+638G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108614 | ||||||
| chr8:28108700
|
G | A | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+724G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108700 | ||||||
| chr8:28108723
|
T | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.393+747T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108723 | ||||||
| chr8:28108774
|
T | A | 74 | a0001c0001t0001g0297a0001c0001t0001g0369a0001c0001t0001g0370others(71): Show | 80 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.393+798T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108774 | ||||||
| chr8:28108874
|
G | A | 9 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237others(6): Show | 9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+898G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108874 | ||||||
| chr8:28109118
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.393+1142G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109118 | ||||||
| chr8:28109257
|
G | A | 1 | a0001c0001t0004g0293 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.394-1113G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109257 | ||||||
| chr8:28109392
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0001t0001g0308others(1): Show | 4 | HG02109.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-978C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109392 | ||||||
| chr8:28109440
|
T | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.394-930T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109440 | ||||||
| chr8:28109506
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.394-864A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109506 | ||||||
| chr8:28109518
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.394-852G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109518 | ||||||
| chr8:28109526
|
A | G | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-844A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109526 | ||||||
| chr8:28109722
|
C | T | 3 | a0001c0001t0004g0289a0001c0001t0004g0290a0001c0001t0004g0303 | 3 | HG00438.hp2 NA18970.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.394-648C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109722 | ||||||
| chr8:28109724
|
T | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0025 | 2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.394-646T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109724 | ||||||
| chr8:28109848
|
G | A | 299 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(296): Show | 320 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.394-522G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109848 | ||||||
| chr8:28110178
|
G | A | 4 | a0001c0001t0001g0173a0001c0001t0001g0233a0001c0001t0001g0236others(1): Show | 4 | NA18947.hp1 NA18978.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-192G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28110178 | ||||||
| chr8:28110339
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(272): Show | 293 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.394-31A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28110339 | ||||||
| chr8:28110628
|
T | C | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.462+190T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28110628 | ||||||
| chr8:28110718
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.462+280A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28110718 | ||||||
| chr8:28110742
|
A | G | 1 | a0001c0001t0003g0364 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.462+304A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28110742 | ||||||
| chr8:28110746
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.462+308G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28110746 | ||||||
| chr8:28111037
|
C | G | 2 | a0001c0001t0002g0131a0001c0001t0002g0135 | 2 | HG01952.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.462+599C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28111037 | ||||||
| chr8:28111481
|
G | A | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.462+1043G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28111481 | ||||||
| chr8:28111556
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0234a0001c0001t0001g0235 | 3 | HG02572.hp1 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.462+1118C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28111556 | ||||||
| chr8:28111824
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.463-1195G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28111824 | ||||||
| chr8:28111891
|
A | C | 8 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0003t0008g0104others(5): Show | 8 | HG00597.hp1 HG03098.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.463-1128A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28111891 | ||||||
| chr8:28111903
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.463-1116A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28111903 | ||||||
| chr8:28112037
|
T | C | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0003g0024others(4): Show | 7 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.463-982T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112037 | ||||||
| chr8:28112149
|
A | T | 1 | a0001c0001t0004g0288 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.463-870A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112149 | ||||||
| chr8:28112152
|
T | A | 141 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(138): Show | 150 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.463-867T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112152 | ||||||
| chr8:28112155
|
T | A | 11 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0002g0058others(8): Show | 11 | HG00438.hp1 HG00597.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.463-864T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112155 | ||||||
| chr8:28112226
|
C | A | 3 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0003g0232 | 3 | HG02055.hp2 HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.463-793C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112226 | ||||||
| chr8:28112231
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.463-788G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112231 | ||||||
| chr8:28112246
|
C | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.463-773C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112246 | ||||||
| chr8:28112288
|
A | G | 105 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0002g0008others(102): Show | 111 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.463-731A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112288 | ||||||
| chr8:28112421
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.463-598C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112421 | ||||||
| chr8:28112694
|
G | C | 1 | a0001c0001t0003g0003 | 3 | HG01069.hp2 HG01071.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.463-325G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112694 | ||||||
| chr8:28112878
|
A | G | 1 | a0001c0001t0002g0092 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.463-141A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112878 | ||||||
| chr8:28113274
|
A | T | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.617+101A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113274 | ||||||
| chr8:28113333
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.617+160C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113333 | ||||||
| chr8:28113416
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.617+243T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113416 | ||||||
| chr8:28113443
|
G | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(75): Show | 84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.617+270G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113443 | ||||||
| chr8:28113465
|
C | CTTTTCAG others(47): Show |
301 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 322 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.617+301_617+302ins others(54): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28113465 | |||||
| chr8:28113471
|
A | AGCCTTAG others(47): Show |
1 | a0001c0003t0008g0106 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.617+301_617+302ins others(54): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28113471 | |||||
| chr8:28113529
|
G | T | 1 | a0001c0001t0001g0222 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.617+356G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113529 | ||||||
| chr8:28113753
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.617+580G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113753 | ||||||
| chr8:28113771
|
C | G | 9 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237others(6): Show | 9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+598C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113771 | ||||||
| chr8:28113929
|
A | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.617+756A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113929 | ||||||
| chr8:28114091
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.617+918C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114091 | ||||||
| chr8:28114199
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 11 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.617+1026G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114199 | ||||||
| chr8:28114266
|
C | G | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG02559.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.617+1093C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114266 | ||||||
| chr8:28114271
|
G | A | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+1098G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114271 | ||||||
| chr8:28114493
|
A | C | 72 | a0001c0001t0001g0297a0001c0001t0004g0002a0001c0001t0004g0017others(69): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.617+1320A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114493 | ||||||
| chr8:28114495
|
A | G | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.617+1322A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114495 | ||||||
| chr8:28114498
|
A | T | 9 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(6): Show | 9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.617+1325A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114498 | ||||||
| chr8:28114522
|
CTT | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.617+1352_617+1353d others(4): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28114522 | |||||
| chr8:28114542
|
C | G | 3 | a0001c0001t0003g0343a0001c0001t0010g0362a0001c0001t0010g0363 | 3 | HG02155.hp2 HG02280.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.617+1369C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114542 | ||||||
| chr8:28114587
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.617+1414G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114587 | ||||||
| chr8:28114755
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.617+1582G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114755 | ||||||
| chr8:28114828
|
A | T | 2 | a0001c0001t0002g0090a0001c0001t0002g0091 | 2 | NA19056.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.617+1655A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114828 | ||||||
| chr8:28114845
|
A | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.617+1672A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114845 | ||||||
| chr8:28114865
|
G | T | 1 | a0001c0001t0001g0174 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.617+1692G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114865 | ||||||
| chr8:28114875
|
C | A | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.617+1702C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114875 | ||||||
| chr8:28115046
|
T | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.617+1873T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115046 | ||||||
| chr8:28115103
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.617+1930T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115103 | ||||||
| chr8:28115221
|
A | G | 2 | a0001c0001t0002g0089a0001c0001t0002g0101 | 2 | NA18995.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.617+2048A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115221 | ||||||
| chr8:28115243
|
C | G | 5 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(2): Show | 5 | HG02818.hp2 HG03139.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+2070C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115243 | ||||||
| chr8:28115243
|
C | T | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.617+2070C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115243 | ||||||
| chr8:28115287
|
T | C | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.617+2114T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115287 | ||||||
| chr8:28115545
|
G | C | 1 | a0001c0001t0001g0320 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.617+2372G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115545 | ||||||
| chr8:28115631
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.617+2458G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115631 | ||||||
| chr8:28115632
|
G | A | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.617+2459G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115632 | ||||||
| chr8:28115698
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.617+2525A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115698 | ||||||
| chr8:28115841
|
C | G | 1 | a0001c0001t0001g0218 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.617+2668C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115841 | ||||||
| chr8:28115918
|
T | C | 1 | a0001c0001t0006g0253 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.617+2745T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115918 | ||||||
| chr8:28115940
|
C | T | 1 | a0001c0001t0002g0100 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.617+2767C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115940 | ||||||
| chr8:28115957
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.617+2784T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115957 | ||||||
| chr8:28115973
|
G | A | 1 | a0001c0001t0004g0288 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.617+2800G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115973 | ||||||
| chr8:28116006
|
T | C | 1 | a0001c0001t0005g0258 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.617+2833T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116006 | ||||||
| chr8:28116016
|
G | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(272): Show | 293 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.617+2843G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116016 | ||||||
| chr8:28116164
|
C | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(272): Show | 293 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.617+2991C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116164 | ||||||
| chr8:28116261
|
C | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.617+3088C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116261 | ||||||
| chr8:28116281
|
G | A | 1 | a0001c0001t0003g0322 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.617+3108G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116281 | ||||||
| chr8:28116369
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(173): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.617+3196T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116369 | ||||||
| chr8:28116403
|
A | C | 72 | a0001c0001t0001g0297a0001c0001t0004g0002a0001c0001t0004g0017others(69): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.617+3230A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116403 | ||||||
| chr8:28116417
|
T | C | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+3244T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116417 | ||||||
| chr8:28116440
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.617+3267G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116440 | ||||||
| chr8:28116519
|
A | T | 1 | a0001c0001t0001g0040 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.617+3346A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116519 | ||||||
| chr8:28116763
|
A | C | 1 | a0001c0001t0013g0361 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.617+3590A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116763 | ||||||
| chr8:28116926
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.617+3753G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116926 | ||||||
| chr8:28116932
|
G | T | 1 | a0001c0001t0003g0316 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.617+3759G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116932 | ||||||
| chr8:28117074
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.617+3901A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28117074 | ||||||
| chr8:28117189
|
A | G | 1 | a0001c0001t0002g0008 | 2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.617+4016A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28117189 | ||||||
| chr8:28117208
|
A | G | 1 | a0001c0001t0003g0238 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.617+4035A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28117208 | ||||||
| chr8:28117726
|
C | A | 27 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(24): Show | 30 | HG00597.hp1 HG00733.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.617+4553C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28117726 | ||||||
| chr8:28117907
|
A | G | 1 | a0001c0001t0007g0155 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.617+4734A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28117907 | ||||||
| chr8:28117954
|
T | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.617+4781T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28117954 | ||||||
| chr8:28118203
|
T | A | 1 | a0001c0001t0001g0157 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.617+5030T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118203 | ||||||
| chr8:28118508
|
A | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(174): Show | 189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.617+5335A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118508 | ||||||
| chr8:28118550
|
T | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0001t0001g0308others(1): Show | 4 | HG02109.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+5377T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118550 | ||||||
| chr8:28118596
|
G | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0025 | 2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.617+5423G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118596 | ||||||
| chr8:28118636
|
G | C | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+5463G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118636 | ||||||
| chr8:28118716
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0037 | 3 | HG02109.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.617+5543T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118716 | ||||||
| chr8:28118775
|
T | C | 1 | a0001c0001t0003g0349 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.617+5602T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118775 | ||||||
| chr8:28118892
|
C | T | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+5719C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118892 | ||||||
| chr8:28118900
|
T | G | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.617+5727T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118900 | ||||||
| chr8:28119324
|
C | G | 1 | a0001c0001t0007g0154 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.617+6151C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119324 | ||||||
| chr8:28119373
|
G | A | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.617+6200G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119373 | ||||||
| chr8:28119380
|
C | T | 5 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(2): Show | 5 | HG02451.hp1 HG02976.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.617+6207C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119380 | ||||||
| chr8:28119416
|
G | A | 1 | a0001c0001t0002g0059 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.617+6243G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119416 | ||||||
| chr8:28119418
|
G | A | 1 | a0001c0001t0006g0253 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.617+6245G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119418 | ||||||
| chr8:28119425
|
T | G | 1 | a0001c0001t0002g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.617+6252T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119425 | ||||||
| chr8:28119548
|
C | A | 1 | a0001c0001t0002g0060 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.617+6375C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119548 | ||||||
| chr8:28119549
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.617+6376A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119549 | ||||||
| chr8:28119569
|
GTTTTATA others(4): Show |
G | 1 | a0001c0001t0002g0098 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.617+6398_617+6408d others(13): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119569 | |||||
| chr8:28119572
|
TTA | T | 6 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0002g0012others(3): Show | 7 | HG01515.hp2 HG01517.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+6455_617+6456d others(4): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATA | T | 19 | a0001c0001t0001g0033a0001c0001t0001g0158a0001c0001t0001g0159others(16): Show | 19 | HG00597.hp2 HG00642.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.617+6453_617+6456d others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATA | T | 39 | a0001c0001t0001g0015a0001c0001t0001g0157a0001c0001t0001g0160others(36): Show | 40 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.617+6451_617+6456d others(8): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(1): Show |
T | 39 | a0001c0001t0001g0001a0001c0001t0001g0139a0001c0001t0001g0156others(36): Show | 42 | HG00323.hp1 HG00408.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.617+6449_617+6456d others(10): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(3): Show |
T | 45 | a0001c0001t0001g0007a0001c0001t0001g0165a0001c0001t0001g0174others(42): Show | 47 | HG00280.hp2 HG00544.hp2 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.617+6447_617+6456d others(12): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(5): Show |
T | 42 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(39): Show | 47 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.617+6445_617+6456d others(14): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(7): Show |
T | 43 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0208others(40): Show | 46 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.617+6443_617+6456d others(16): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(9): Show |
T | 24 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0035others(21): Show | 28 | HG00733.hp1 HG01074.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.617+6441_617+6456d others(18): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(11): Show |
T | 7 | a0001c0001t0001g0036a0001c0001t0001g0039a0001c0001t0001g0168others(4): Show | 7 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.617+6439_617+6456d others(20): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(13): Show |
T | 4 | a0001c0001t0001g0233a0001c0001t0002g0055a0001c0001t0002g0086others(1): Show | 4 | HG01069.hp1 HG01081.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+6437_617+6456d others(22): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(15): Show |
T | 7 | a0001c0001t0001g0167a0001c0001t0002g0087a0001c0001t0003g0022others(4): Show | 8 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.617+6435_617+6456d others(24): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(17): Show |
T | 1 | a0001c0001t0004g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.617+6433_617+6456d others(26): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(19): Show |
T | 4 | a0001c0001t0003g0315a0001c0001t0003g0316a0001c0001t0004g0246others(1): Show | 4 | HG01891.hp2 HG03540.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+6431_617+6456d others(28): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(21): Show |
T | 6 | a0001c0001t0003g0028a0001c0001t0004g0262a0001c0001t0004g0263others(3): Show | 6 | HG01167.hp1 HG02155.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+6429_617+6456d others(30): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(23): Show |
T | 66 | a0001c0001t0001g0297a0001c0001t0004g0002a0001c0001t0004g0017others(63): Show | 72 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.617+6427_617+6456d others(32): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(27): Show |
T | 3 | a0001c0001t0001g0040a0001c0001t0001g0234a0001c0001t0001g0235 | 3 | HG02572.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.617+6423_617+6456d others(36): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(29): Show |
T | 1 | a0001c0001t0002g0088 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.617+6421_617+6456d others(38): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(31): Show |
T | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.617+6419_617+6456d others(40): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119572
|
TTATATAT others(35): Show |
T | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.617+6415_617+6456d others(44): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | |||||
| chr8:28119674
|
C | T | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+6501C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119674 | ||||||
| chr8:28119680
|
C | G | 1 | a0001c0001t0003g0216 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.617+6507C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119680 | ||||||
| chr8:28119722
|
A | G | 1 | a0001c0001t0003g0360 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.617+6549A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119722 | ||||||
| chr8:28119818
|
G | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.617+6645G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119818 | ||||||
| chr8:28119821
|
T | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(265): Show | 286 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.617+6648T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119821 | ||||||
| chr8:28120066
|
G | A | 300 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(297): Show | 321 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.617+6893G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120066 | ||||||
| chr8:28120112
|
A | C | 10 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237others(7): Show | 10 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+6939A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120112 | ||||||
| chr8:28120465
|
A | G | 71 | a0001c0001t0001g0297a0001c0001t0004g0002a0001c0001t0004g0017others(68): Show | 77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.617+7292A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120465 | ||||||
| chr8:28120524
|
C | T | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0003g0024others(4): Show | 7 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.617+7351C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120524 | ||||||
| chr8:28120548
|
G | T | 1 | a0001c0001t0001g0163 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.617+7375G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120548 | ||||||
| chr8:28120622
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(75): Show | 84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.617+7449C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120622 | ||||||
| chr8:28120828
|
C | G | 1 | a0001c0001t0003g0026 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.617+7655C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120828 | ||||||
| chr8:28120870
|
C | A | 1 | a0001c0001t0002g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.617+7697C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120870 | ||||||
| chr8:28120945
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.617+7772G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120945 | ||||||
| chr8:28120951
|
T | C | 1 | a0001c0001t0003g0334 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.617+7778T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120951 | ||||||
| chr8:28120986
|
T | A | 9 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(6): Show | 9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.617+7813T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120986 | ||||||
| chr8:28121054
|
G | A | 2 | a0001c0001t0003g0315a0001c0001t0003g0316 | 2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.617+7881G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121054 | ||||||
| chr8:28121187
|
A | C | 1 | a0001c0001t0001g0176 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.617+8014A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121187 | ||||||
| chr8:28121301
|
T | A | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0010g0362 | 3 | HG02572.hp1 HG02922.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.617+8128T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121301 | ||||||
| chr8:28121318
|
A | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0202 | 3 | NA18940.hp1 NA18991.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.617+8145A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121318 | ||||||
| chr8:28121321
|
A | AT | 3 | a0001c0001t0001g0103a0001c0001t0001g0308a0001c0001t0006g0307 | 3 | HG02818.hp2 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.617+8150dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28121321 | |||||
| chr8:28121321
|
A | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(79): Show | 89 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.617+8148A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121321 | ||||||
| chr8:28121324
|
A | T | 317 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(314): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.617+8151A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121324 | ||||||
| chr8:28121327
|
T | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0139others(1): Show | 4 | HG01106.hp1 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+8154T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121327 | ||||||
| chr8:28121380
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.618-8122C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121380 | ||||||
| chr8:28121381
|
G | T | 1 | a0001c0001t0002g0088 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.618-8121G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121381 | ||||||
| chr8:28121413
|
G | C | 3 | a0001c0001t0004g0250a0001c0001t0004g0251a0001c0001t0004g0267 | 3 | NA18943.hp2 NA18977.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.618-8089G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121413 | ||||||
| chr8:28121439
|
C | T | 88 | a0001c0001t0001g0297a0001c0001t0001g0369a0001c0001t0001g0370others(85): Show | 94 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.618-8063C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121439 | ||||||
| chr8:28121528
|
C | T | 1 | a0001c0001t0003g0023 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.618-7974C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121528 | ||||||
| chr8:28121562
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.618-7940C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121562 | ||||||
| chr8:28121571
|
C | T | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-7931C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121571 | ||||||
| chr8:28121599
|
T | C | 300 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(297): Show | 321 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.618-7903T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121599 | ||||||
| chr8:28121720
|
T | G | 4 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237others(1): Show | 4 | NA18978.hp2 NA18979.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-7782T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121720 | ||||||
| chr8:28121926
|
G | T | 1 | a0001c0001t0004g0280 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.618-7576G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121926 | ||||||
| chr8:28121928
|
A | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.618-7574A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121928 | ||||||
| chr8:28122098
|
T | A | 1 | a0001c0001t0003g0321 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.618-7404T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122098 | ||||||
| chr8:28122153
|
A | G | 10 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0039others(7): Show | 10 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-7349A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122153 | ||||||
| chr8:28122281
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.618-7221G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122281 | ||||||
| chr8:28122339
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.618-7163C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122339 | ||||||
| chr8:28122434
|
T | C | 1 | a0001c0001t0002g0008 | 2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.618-7068T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122434 | ||||||
| chr8:28122474
|
A | C | 1 | a0001c0001t0002g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.618-7028A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122474 | ||||||
| chr8:28122688
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.618-6814G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122688 | ||||||
| chr8:28122799
|
A | G | 1 | a0001c0001t0002g0081 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.618-6703A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122799 | ||||||
| chr8:28122899
|
G | A | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-6603G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122899 | ||||||
| chr8:28122966
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.618-6536A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122966 | ||||||
| chr8:28123136
|
A | G | 71 | a0001c0001t0001g0297a0001c0001t0004g0002a0001c0001t0004g0017others(68): Show | 77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.618-6366A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123136 | ||||||
| chr8:28123202
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.618-6300T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123202 | ||||||
| chr8:28123209
|
G | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.618-6293G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123209 | ||||||
| chr8:28123243
|
T | C | 300 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(297): Show | 321 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.618-6259T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123243 | ||||||
| chr8:28123260
|
A | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(272): Show | 293 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.618-6242A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123260 | ||||||
| chr8:28123344
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.618-6158T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123344 | ||||||
| chr8:28123598
|
T | G | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.618-5904T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123598 | ||||||
| chr8:28123669
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.618-5833G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123669 | ||||||
| chr8:28123671
|
A | T | 1 | a0001c0001t0005g0279 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.618-5831A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123671 | ||||||
| chr8:28123787
|
C | T | 1 | a0001c0001t0003g0322 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.618-5715C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123787 | ||||||
| chr8:28123828
|
G | GTCACAGC others(1): Show |
297 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(294): Show | 318 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.618-5671_618-5670i others(10): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28123828 | |||||
| chr8:28123910
|
A | G | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-5592A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123910 | ||||||
| chr8:28123943
|
CT | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(12): Show | 18 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.618-5548delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28123943 | |||||
| chr8:28124021
|
G | A | 2 | a0001c0001t0004g0268a0001c0001t0019g0291 | 2 | NA18993.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.618-5481G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124021 | ||||||
| chr8:28124206
|
A | T | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.618-5296A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124206 | ||||||
| chr8:28124288
|
G | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.618-5214G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124288 | ||||||
| chr8:28124300
|
A | G | 2 | a0001c0001t0004g0268a0001c0001t0019g0291 | 2 | NA18993.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.618-5202A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124300 | ||||||
| chr8:28124355
|
C | T | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-5147C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124355 | ||||||
| chr8:28124635
|
A | G | 104 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0002g0008others(101): Show | 110 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.618-4867A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124635 | ||||||
| chr8:28124651
|
G | C | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-4851G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124651 | ||||||
| chr8:28124677
|
C | T | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-4825C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124677 | ||||||
| chr8:28124750
|
C | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.618-4752C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124750 | ||||||
| chr8:28124799
|
C | T | 268 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(265): Show | 286 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.618-4703C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124799 | ||||||
| chr8:28124876
|
T | C | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.618-4626T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124876 | ||||||
| chr8:28124903
|
G | A | 1 | a0001c0001t0003g0356 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.618-4599G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124903 | ||||||
| chr8:28125095
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.618-4407G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125095 | ||||||
| chr8:28125148
|
C | A | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.618-4354C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125148 | ||||||
| chr8:28125327
|
G | A | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0003g0024others(4): Show | 7 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-4175G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125327 | ||||||
| chr8:28125353
|
G | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(294): Show | 318 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.618-4149G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125353 | ||||||
| chr8:28125437
|
A | G | 107 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0241others(104): Show | 113 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.618-4065A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125437 | ||||||
| chr8:28125469
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.618-4033G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125469 | ||||||
| chr8:28125594
|
G | T | 1 | a0001c0001t0002g0070 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.618-3908G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125594 | ||||||
| chr8:28125672
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.618-3830C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125672 | ||||||
| chr8:28125750
|
G | A | 2 | a0001c0001t0003g0325a0001c0001t0020g0138 | 2 | HG02015.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.618-3752G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125750 | ||||||
| chr8:28125759
|
C | CT | 7 | a0001c0001t0001g0215a0001c0001t0003g0317a0001c0001t0003g0343others(4): Show | 7 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-3720dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28125759 | |||||
| chr8:28125759
|
CT | C | 34 | a0001c0001t0001g0103a0001c0001t0001g0201a0001c0001t0001g0214others(31): Show | 34 | HG00597.hp1 HG01168.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.618-3720delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28125759 | |||||
| chr8:28125759
|
CTT | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(173): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.618-3721_618-3720d others(4): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28125759 | |||||
| chr8:28125759
|
CTTT | C | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 100 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.618-3722_618-3720d others(5): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28125759 | |||||
| chr8:28126027
|
A | AT | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-3475_618-3474i others(3): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126027 | ||||||
| chr8:28126028
|
C | G | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-3474C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126028 | ||||||
| chr8:28126152
|
G | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.618-3350G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126152 | ||||||
| chr8:28126437
|
C | T | 1 | a0001c0001t0004g0261 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.618-3065C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126437 | ||||||
| chr8:28126542
|
G | A | 2 | a0001c0001t0002g0090a0001c0001t0002g0091 | 2 | NA19056.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.618-2960G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126542 | ||||||
| chr8:28126792
|
A | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.618-2710A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126792 | ||||||
| chr8:28126798
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.618-2704A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126798 | ||||||
| chr8:28126816
|
T | C | 7 | a0001c0001t0001g0156a0001c0001t0001g0183a0001c0001t0001g0184others(4): Show | 7 | HG01884.hp2 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-2686T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126816 | ||||||
| chr8:28126842
|
T | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.618-2660T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126842 | ||||||
| chr8:28126960
|
C | A | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.618-2542C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126960 | ||||||
| chr8:28127016
|
A | G | 2 | a0001c0001t0003g0354a0001c0001t0003g0355 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.618-2486A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127016 | ||||||
| chr8:28127086
|
G | A | 1 | a0001c0001t0003g0356 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.618-2416G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127086 | ||||||
| chr8:28127157
|
A | G | 1 | a0001c0001t0003g0342 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.618-2345A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127157 | ||||||
| chr8:28127213
|
T | C | 1 | a0001c0002t0009g0146 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.618-2289T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127213 | ||||||
| chr8:28127412
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(76): Show | 85 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.618-2090A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127412 | ||||||
| chr8:28127477
|
G | A | 15 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(12): Show | 15 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.618-2025G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127477 | ||||||
| chr8:28127636
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.618-1866G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127636 | ||||||
| chr8:28127648
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.618-1854C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127648 | ||||||
| chr8:28127661
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(272): Show | 293 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.618-1841A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127661 | ||||||
| chr8:28127741
|
CTG | C | 79 | a0001c0001t0002g0008a0001c0001t0002g0012a0001c0001t0002g0013others(76): Show | 82 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.618-1760_618-1759d others(4): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127741 | ||||||
| chr8:28127981
|
T | C | 97 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(94): Show | 103 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.618-1521T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127981 | ||||||
| chr8:28128124
|
C | T | 1 | a0001c0001t0002g0059 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.618-1378C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128124 | ||||||
| chr8:28128200
|
G | A | 1 | a0001c0001t0002g0071 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.618-1302G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128200 | ||||||
| chr8:28128239
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(284): Show | 308 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.618-1263C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128239 | ||||||
| chr8:28128272
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.618-1230G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128272 | ||||||
| chr8:28128347
|
G | A | 18 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(15): Show | 21 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.618-1155G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128347 | ||||||
| chr8:28128349
|
A | G | 300 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(297): Show | 321 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.618-1153A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128349 | ||||||
| chr8:28128518
|
G | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.618-984G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128518 | ||||||
| chr8:28128776
|
G | A | 1 | a0001c0001t0002g0062 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.618-726G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128776 | ||||||
| chr8:28128873
|
A | C | 4 | a0001c0001t0001g0175a0001c0001t0001g0181a0001c0001t0001g0200others(1): Show | 4 | HG01261.hp1 HG01928.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-629A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128873 | ||||||
| chr8:28129047
|
TTTTTC | T | 9 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(6): Show | 9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.618-451_618-447del others(5): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28129047 | |||||
| chr8:28129268
|
A | G | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-234A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28129268 | ||||||
| chr8:28129348
|
G | A | 1 | a0001c0001t0002g0072 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.618-154G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28129348 | ||||||
| chr8:28129475
|
G | A | 1 | a0001c0001t0003g0356 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.618-27G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28129475 | ||||||
| chr8:28129489
|
A | T | 3 | a0001c0001t0003g0004a0001c0001t0003g0351a0001c0001t0003g0357 | 5 | HG00642.hp2 HG01975.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-13A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28129489 | ||||||
| chr8:28129876
|
C | T | 1 | a0001c0001t0010g0363 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.779+213C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28129876 | ||||||
| chr8:28130201
|
C | T | 4 | a0001c0001t0005g0278a0001c0001t0005g0279a0001c0001t0005g0286others(1): Show | 4 | NA18951.hp1 NA18967.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.779+538C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130201 | ||||||
| chr8:28130299
|
G | T | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.779+636G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130299 | ||||||
| chr8:28130356
|
C | T | 74 | a0001c0001t0001g0297a0001c0001t0001g0369a0001c0001t0001g0370others(71): Show | 80 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.779+693C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130356 | ||||||
| chr8:28130437
|
C | T | 1 | a0001c0001t0001g0006 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.779+774C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130437 | ||||||
| chr8:28130686
|
G | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.779+1023G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130686 | ||||||
| chr8:28130778
|
G | C | 1 | a0001c0001t0003g0177 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.779+1115G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130778 | ||||||
| chr8:28130795
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.779+1132A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130795 | ||||||
| chr8:28130969
|
C | T | 1 | a0001c0001t0002g0120 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.779+1306C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130969 | ||||||
| chr8:28131019
|
A | G | 1 | a0001c0001t0004g0305 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.780-1259A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28131019 | ||||||
| chr8:28131021
|
C | T | 9 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(6): Show | 9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.780-1257C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28131021 | ||||||
| chr8:28131124
|
A | G | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.780-1154A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28131124 | ||||||
| chr8:28131387
|
C | T | 5 | a0001c0001t0004g0275a0001c0001t0004g0276a0001c0001t0004g0277others(2): Show | 5 | HG01106.hp2 HG01168.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.780-891C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28131387 | ||||||
| chr8:28131572
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.780-706G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28131572 | ||||||
| chr8:28131773
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.780-505A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28131773 | ||||||
| chr8:28132044
|
C | T | 1 | a0001c0001t0003g0348 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.780-234C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28132044 | ||||||
| chr8:28132129
|
A | G | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.780-149A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28132129 | ||||||
| chr8:28132223
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.780-55C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28132223 | ||||||
| chr8:28132540
|
A | T | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.906+136A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28132540 | ||||||
| chr8:28132615
|
T | A | 1 | a0001c0001t0002g0135 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.906+211T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28132615 | ||||||
| chr8:28132664
|
A | G | 1 | a0001c0001t0002g0085 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.906+260A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28132664 | ||||||
| chr8:28132825
|
C | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(11): Show | 17 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.906+421C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28132825 | ||||||
| chr8:28132870
|
A | T | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.906+466A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28132870 | ||||||
| chr8:28132883
|
G | A | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.906+479G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28132883 | ||||||
| chr8:28132999
|
T | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.906+595T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28132999 | ||||||
| chr8:28133030
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.906+626A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133030 | ||||||
| chr8:28133114
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(72): Show | 81 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.906+710C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133114 | ||||||
| chr8:28133161
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(11): Show | 17 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.906+757C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133161 | ||||||
| chr8:28133272
|
A | C | 1 | a0001c0001t0004g0290 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.906+868A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133272 | ||||||
| chr8:28133273
|
T | G | 74 | a0001c0001t0001g0297a0001c0001t0001g0369a0001c0001t0001g0370others(71): Show | 80 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.906+869T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133273 | ||||||
| chr8:28133378
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.906+974C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133378 | ||||||
| chr8:28133426
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.906+1022T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133426 | ||||||
| chr8:28133428
|
C | CT | 281 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(278): Show | 299 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.906+1038dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 28133428 | |||||
| chr8:28133428
|
C | CTT | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 21 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.906+1037_906+1038d others(4): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 28133428 | |||||
| chr8:28133428
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.906+1024C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133428 | ||||||
| chr8:28133453
|
C | T | 275 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(272): Show | 293 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.906+1049C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133453 | ||||||
| chr8:28133564
|
A | G | 1 | a0001c0001t0004g0274 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.906+1160A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133564 | ||||||
| chr8:28133829
|
C | T | 9 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(6): Show | 9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.906+1425C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133829 | ||||||
| chr8:28133830
|
G | A | 5 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0103others(2): Show | 5 | HG02109.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.906+1426G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133830 | ||||||
| chr8:28133840
|
C | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.906+1436C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133840 | ||||||
| chr8:28133879
|
C | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(74): Show | 83 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.906+1475C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133879 | ||||||
| chr8:28133886
|
T | TA | 186 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(183): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.906+1484dupA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 28133886 | |||||
| chr8:28133905
|
C | T | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.906+1501C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133905 | ||||||
| chr8:28133952
|
G | GATT | 5 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0001t0001g0234others(2): Show | 5 | HG00597.hp1 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.906+1566_906+1568d others(5): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 28133952 | |||||
| chr8:28134036
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.906+1632C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134036 | ||||||
| chr8:28134173
|
G | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.906+1769G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134173 | ||||||
| chr8:28134194
|
G | T | 72 | a0001c0001t0001g0297a0001c0001t0004g0002a0001c0001t0004g0017others(69): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.906+1790G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134194 | ||||||
| chr8:28134277
|
C | A | 72 | a0001c0001t0001g0297a0001c0001t0004g0002a0001c0001t0004g0017others(69): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.906+1873C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134277 | ||||||
| chr8:28134408
|
T | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.906+2004T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134408 | ||||||
| chr8:28134476
|
C | G | 2 | a0001c0001t0003g0003a0001c0001t0003g0023 | 5 | HG01069.hp2 HG01071.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.906+2072C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134476 | ||||||
| chr8:28134631
|
A | G | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.906+2227A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134631 | ||||||
| chr8:28134684
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.906+2280C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134684 | ||||||
| chr8:28134717
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.906+2313T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134717 | ||||||
| chr8:28134722
|
C | G | 89 | a0001c0001t0001g0297a0001c0001t0001g0369a0001c0001t0001g0370others(86): Show | 95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.906+2318C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134722 | ||||||
| chr8:28134746
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0205 | 2 | HG02165.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.906+2342T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134746 | ||||||
| chr8:28134915
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.906+2511C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134915 | ||||||
| chr8:28134929
|
C | CT | 12 | a0001c0001t0002g0008a0001c0001t0002g0057a0001c0001t0002g0058others(9): Show | 13 | HG00438.hp1 HG01346.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.906+2538dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 28134929 | |||||
| chr8:28134932
|
T | C | 2 | a0001c0001t0001g0308a0001c0001t0006g0307 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.906+2528T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134932 | ||||||
| chr8:28135010
|
C | T | 1 | a0001c0001t0002g0081 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.906+2606C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135010 | ||||||
| chr8:28135017
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.906+2613C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135017 | ||||||
| chr8:28135078
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.907-2620A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135078 | ||||||
| chr8:28135142
|
C | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(11): Show | 17 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.907-2556C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135142 | ||||||
| chr8:28135171
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.907-2527G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135171 | ||||||
| chr8:28135171
|
G | T | 1 | a0001c0001t0002g0083 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.907-2527G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135171 | ||||||
| chr8:28135219
|
C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(11): Show | 17 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.907-2479C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135219 | ||||||
| chr8:28135340
|
G | A | 2 | a0001c0001t0004g0262a0001c0001t0004g0269 | 2 | HG01167.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.907-2358G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135340 | ||||||
| chr8:28135360
|
C | T | 1 | a0001c0001t0003g0321 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.907-2338C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135360 | ||||||
| chr8:28135368
|
T | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.907-2330T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135368 | ||||||
| chr8:28135502
|
T | C | 2 | a0001c0001t0005g0286a0001c0001t0005g0287 | 2 | NA18973.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.907-2196T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135502 | ||||||
| chr8:28135513
|
A | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0001t0001g0139others(7): Show | 10 | HG00597.hp1 HG02109.hp2 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.907-2185A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135513 | ||||||
| chr8:28135751
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.907-1947G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135751 | ||||||
| chr8:28135852
|
G | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(75): Show | 84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.907-1846G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135852 | ||||||
| chr8:28135918
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.907-1780G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135918 | ||||||
| chr8:28135960
|
C | CT | 10 | a0001c0001t0001g0233a0001c0001t0001g0308a0001c0001t0002g0038others(7): Show | 10 | HG00597.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.907-1722dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 28135960 | |||||
| chr8:28135976
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.907-1722T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135976 | ||||||
| chr8:28136107
|
G | A | 1 | a0001c0001t0002g0008 | 2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.907-1591G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136107 | ||||||
| chr8:28136179
|
C | T | 2 | a0001c0001t0004g0273a0001c0001t0004g0302 | 2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.907-1519C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136179 | ||||||
| chr8:28136371
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.907-1327G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136371 | ||||||
| chr8:28136378
|
C | G | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.907-1320C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136378 | ||||||
| chr8:28136541
|
T | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(265): Show | 286 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.907-1157T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136541 | ||||||
| chr8:28136546
|
C | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.907-1152C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136546 | ||||||
| chr8:28136600
|
G | T | 1 | a0001c0001t0006g0253 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.907-1098G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136600 | ||||||
| chr8:28136637
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.907-1061A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136637 | ||||||
| chr8:28136647
|
G | A | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.907-1051G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136647 | ||||||
| chr8:28136657
|
A | G | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.907-1041A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136657 | ||||||
| chr8:28136724
|
T | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.907-974T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136724 | ||||||
| chr8:28136779
|
G | C | 1 | a0001c0001t0002g0084 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.907-919G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136779 | ||||||
| chr8:28136984
|
C | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.907-714C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136984 | ||||||
| chr8:28137585
|
G | A | 1 | a0001c0001t0002g0012 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.907-113G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28137585 | ||||||
| chr8:28137596
|
G | C | 1 | a0001c0001t0002g0086 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.907-102G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28137596 | ||||||
| chr8:28138030
|
A | T | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+139A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138030 | ||||||
| chr8:28138072
|
A | G | 1 | a0001c0001t0002g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1100+181A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138072 | ||||||
| chr8:28138077
|
G | A | 9 | a0001c0001t0004g0260a0001c0001t0004g0273a0001c0001t0004g0302others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1100+186G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138077 | ||||||
| chr8:28138129
|
G | A | 1 | a0001c0001t0003g0349 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1100+238G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138129 | ||||||
| chr8:28138153
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1100+262C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138153 | ||||||
| chr8:28138163
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1100+272A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138163 | ||||||
| chr8:28138205
|
T | G | 100 | a0001c0001t0001g0194a0001c0001t0001g0204a0001c0001t0002g0008others(97): Show | 106 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1100+314T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138205 | ||||||
| chr8:28138236
|
T | A | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1100+345T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138236 | ||||||
| chr8:28138267
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1100+376C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138267 | ||||||
| chr8:28138404
|
TCTCATTT others(21): Show |
T | 1 | a0001c0001t0001g0233 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1100+516_1100+543d others(30): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28138404 | |||||
| chr8:28138520
|
C | G | 1 | a0001c0001t0002g0072 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1100+629C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138520 | ||||||
| chr8:28138532
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(10): Show | 16 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1100+641C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138532 | ||||||
| chr8:28138609
|
A | G | 2 | a0001c0001t0002g0043a0001c0001t0002g0059 | 2 | NA18944.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1100+718A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138609 | ||||||
| chr8:28138617
|
A | G | 1 | a0001c0001t0003g0345 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1100+726A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138617 | ||||||
| chr8:28138714
|
C | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0233others(2): Show | 5 | HG03098.hp2 HG03471.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1100+823C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138714 | ||||||
| chr8:28138787
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0227 | 2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1100+896A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138787 | ||||||
| chr8:28138849
|
G | A | 303 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 324 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1100+958G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138849 | ||||||
| chr8:28138863
|
G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0188 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1100+972G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138863 | ||||||
| chr8:28138923
|
G | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 98 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1100+1032G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138923 | ||||||
| chr8:28138932
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1100+1041G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138932 | ||||||
| chr8:28138990
|
C | T | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+1099C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138990 | ||||||
| chr8:28139002
|
C | T | 33 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0320others(30): Show | 34 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.1100+1111C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139002 | ||||||
| chr8:28139003
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(77): Show | 89 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1100+1112G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139003 | ||||||
| chr8:28139051
|
A | G | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+1160A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139051 | ||||||
| chr8:28139144
|
C | G | 2 | a0001c0001t0001g0309a0001c0001t0001g0310 | 2 | NA18999.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1100+1253C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139144 | ||||||
| chr8:28139298
|
G | GT | 66 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0002g0010others(63): Show | 74 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1100+1415dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28139298 | |||||
| chr8:28139515
|
GA | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(143): Show | 158 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1100+1628delA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28139515 | |||||
| chr8:28139528
|
A | G | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1100+1637A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139528 | ||||||
| chr8:28139631
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1100+1740A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139631 | ||||||
| chr8:28139720
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1100+1829G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139720 | ||||||
| chr8:28139742
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1100+1851C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139742 | ||||||
| chr8:28139916
|
A | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(267): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.1100+2025A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139916 | ||||||
| chr8:28139996
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1100+2105G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139996 | ||||||
| chr8:28140035
|
T | C | 1 | a0001c0001t0003g0345 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1100+2144T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140035 | ||||||
| chr8:28140114
|
T | TTG | 52 | a0001c0001t0001g0040a0001c0001t0001g0160a0001c0001t0001g0308others(49): Show | 55 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1100+2263_1100+226 others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | |||||
| chr8:28140114
|
T | TTGTG | 6 | a0001c0001t0002g0009a0001c0001t0002g0054a0001c0001t0003g0023others(3): Show | 8 | HG00642.hp1 HG00738.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1100+2261_1100+226 others(8): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | |||||
| chr8:28140114
|
T | TTGTGTG | 3 | a0001c0001t0003g0004a0001c0001t0003g0352a0001c0001t0003g0357 | 5 | HG01975.hp2 HG02809.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1100+2259_1100+226 others(10): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | |||||
| chr8:28140114
|
T | TTGTGTGT others(5): Show |
3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1100+2253_1100+226 others(16): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | |||||
| chr8:28140114
|
TTG | T | 7 | a0001c0001t0001g0034a0001c0001t0001g0140a0001c0001t0001g0194others(4): Show | 7 | HG01943.hp1 HG03098.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.1100+2263_1100+226 others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | |||||
| chr8:28140114
|
TTGTG | T | 33 | a0001c0001t0001g0041a0001c0001t0001g0156a0001c0001t0001g0165others(30): Show | 35 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.1100+2261_1100+226 others(8): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | |||||
| chr8:28140114
|
TTGTGTG | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(195): Show | 211 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.1100+2259_1100+226 others(10): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | |||||
| chr8:28140114
|
TTGTGTGT others(1): Show |
T | 16 | a0001c0001t0001g0103a0001c0001t0001g0139a0001c0001t0001g0234others(13): Show | 16 | HG00597.hp1 HG01261.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1100+2257_1100+226 others(12): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | |||||
| chr8:28140114
|
TTGTGTGT others(3): Show |
T | 5 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0003g0311others(2): Show | 5 | HG02056.hp2 NA18954.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1100+2255_1100+226 others(14): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | |||||
| chr8:28140114
|
TTGTGTGT others(5): Show |
T | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+2253_1100+226 others(16): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | |||||
| chr8:28140150
|
G | C | 1 | a0001c0001t0003g0212 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1100+2259G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140150 | ||||||
| chr8:28140196
|
T | A | 1 | a0001c0001t0001g0030 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1100+2305T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140196 | ||||||
| chr8:28140205
|
G | A | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1100+2314G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140205 | ||||||
| chr8:28140270
|
T | C | 1 | a0001c0001t0002g0062 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1100+2379T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140270 | ||||||
| chr8:28140346
|
T | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.1100+2455T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140346 | ||||||
| chr8:28140513
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1100+2622C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140513 | ||||||
| chr8:28140581
|
T | A | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0003g0024others(4): Show | 7 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1100+2690T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140581 | ||||||
| chr8:28140645
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1100+2754C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140645 | ||||||
| chr8:28140728
|
G | A | 73 | a0001c0001t0001g0039a0001c0001t0001g0297a0001c0001t0004g0002others(70): Show | 79 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1100+2837G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140728 | ||||||
| chr8:28140758
|
T | C | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1100+2867T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140758 | ||||||
| chr8:28140857
|
C | T | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1100+2966C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140857 | ||||||
| chr8:28140858
|
A | G | 304 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(301): Show | 325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.1100+2967A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140858 | ||||||
| chr8:28140974
|
C | A | 1 | a0001c0001t0001g0233 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1100+3083C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140974 | ||||||
| chr8:28141019
|
T | C | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+3128T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141019 | ||||||
| chr8:28141024
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(7): Show | 13 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1100+3133A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141024 | ||||||
| chr8:28141046
|
G | A | 1 | a0001c0001t0003g0328 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1100+3155G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141046 | ||||||
| chr8:28141250
|
T | A | 1 | a0001c0001t0003g0321 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1100+3359T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141250 | ||||||
| chr8:28141331
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1100+3440G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141331 | ||||||
| chr8:28141555
|
C | A | 1 | a0001c0001t0003g0368 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1100+3664C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141555 | ||||||
| chr8:28141613
|
T | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0188 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1100+3722T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141613 | ||||||
| chr8:28141760
|
G | T | 1 | a0001c0001t0001g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1100+3869G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141760 | ||||||
| chr8:28141848
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0140 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1100+3957A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141848 | ||||||
| chr8:28141977
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1100+4086C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141977 | ||||||
| chr8:28141984
|
G | A | 4 | a0001c0001t0001g0162a0001c0001t0001g0233a0001c0001t0001g0236others(1): Show | 4 | NA18950.hp2 NA18978.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100+4093G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141984 | ||||||
| chr8:28142217
|
C | T | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1100+4326C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142217 | ||||||
| chr8:28142310
|
T | C | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1100+4419T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142310 | ||||||
| chr8:28142329
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1100+4438C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142329 | ||||||
| chr8:28142379
|
C | T | 3 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152 | 3 | HG01891.hp1 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1100+4488C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142379 | ||||||
| chr8:28142464
|
A | G | 2 | a0001c0001t0003g0348a0001c0001t0003g0359 | 2 | HG01074.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1100+4573A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142464 | ||||||
| chr8:28142492
|
A | T | 72 | a0001c0001t0001g0297a0001c0001t0004g0002a0001c0001t0004g0017others(69): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1100+4601A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142492 | ||||||
| chr8:28142536
|
G | C | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+4645G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142536 | ||||||
| chr8:28142578
|
C | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0241others(7): Show | 10 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1100+4687C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142578 | ||||||
| chr8:28142767
|
T | G | 1 | a0001c0001t0006g0307 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1100+4876T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142767 | ||||||
| chr8:28142815
|
G | A | 1 | a0001c0001t0006g0307 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1100+4924G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142815 | ||||||
| chr8:28142845
|
C | G | 1 | a0001c0001t0001g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1100+4954C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142845 | ||||||
| chr8:28142848
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1100+4957G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142848 | ||||||
| chr8:28142864
|
AT | A | 8 | a0001c0001t0003g0343a0001c0001t0005g0279a0001c0003t0008g0104others(5): Show | 8 | HG00597.hp1 HG02280.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.1100+4983delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28142864 | |||||
| chr8:28142868
|
T | C | 2 | a0001c0001t0003g0348a0001c0001t0003g0359 | 2 | HG01074.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1100+4977T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142868 | ||||||
| chr8:28142884
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1100+4993T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142884 | ||||||
| chr8:28143009
|
G | A | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1100+5118G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143009 | ||||||
| chr8:28143163
|
A | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.1100+5272A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143163 | ||||||
| chr8:28143244
|
TC | T | 27 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(24): Show | 30 | HG00597.hp1 HG00733.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1100+5356delC | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28143244 | |||||
| chr8:28143289
|
TC | T | 11 | a0001c0001t0001g0016a0001c0001t0001g0171a0001c0001t0001g0172others(8): Show | 12 | HG00408.hp1 HG02165.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1100+5405delC | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28143289 | |||||
| chr8:28143310
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(7): Show | 13 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1100+5419A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143310 | ||||||
| chr8:28143389
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1100+5498T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143389 | ||||||
| chr8:28143445
|
A | G | 1 | a0001c0001t0006g0307 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1100+5554A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143445 | ||||||
| chr8:28143491
|
G | A | 284 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(281): Show | 305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.1100+5600G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143491 | ||||||
| chr8:28143605
|
C | A | 11 | a0001c0001t0002g0012a0001c0001t0002g0116a0001c0001t0002g0117others(8): Show | 12 | HG00323.hp2 HG01358.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.1100+5714C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143605 | ||||||
| chr8:28143684
|
T | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1100+5793T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143684 | ||||||
| chr8:28143704
|
A | G | 86 | a0001c0001t0001g0139a0001c0001t0001g0194a0001c0001t0001g0204others(83): Show | 89 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1100+5813A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143704 | ||||||
| chr8:28144163
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(187): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1100+6272A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28144163 | ||||||
| chr8:28144191
|
C | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(7): Show | 13 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1100+6300C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28144191 | ||||||
| chr8:28144407
|
C | T | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+6516C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28144407 | ||||||
| chr8:28144435
|
C | A | 10 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0241others(7): Show | 10 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1100+6544C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28144435 | ||||||
| chr8:28144743
|
A | G | 1 | a0001c0001t0003g0359 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1100+6852A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28144743 | ||||||
| chr8:28144764
|
C | T | 96 | a0001c0001t0001g0103a0001c0001t0001g0139a0001c0001t0001g0194others(93): Show | 99 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1100+6873C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28144764 | ||||||
| chr8:28144996
|
C | T | 1 | a0001c0001t0005g0278 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1100+7105C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28144996 | ||||||
| chr8:28145265
|
A | T | 1 | a0001c0001t0002g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1100+7374A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145265 | ||||||
| chr8:28145330
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1100+7439C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145330 | ||||||
| chr8:28145432
|
A | G | 1 | a0001c0001t0002g0130 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1100+7541A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145432 | ||||||
| chr8:28145472
|
A | G | 1 | a0001c0001t0002g0124 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1100+7581A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145472 | ||||||
| chr8:28145505
|
T | G | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+7614T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145505 | ||||||
| chr8:28145627
|
T | TG | 190 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(187): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1100+7736_1100+773 others(5): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145627 | ||||||
| chr8:28145648
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1100+7757A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145648 | ||||||
| chr8:28145725
|
G | C | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1100+7834G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145725 | ||||||
| chr8:28145843
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0037 | 3 | HG02109.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1100+7952C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145843 | ||||||
| chr8:28145885
|
A | G | 8 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0241others(5): Show | 8 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1100+7994A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145885 | ||||||
| chr8:28145930
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 224 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1100+8039A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145930 | ||||||
| chr8:28146257
|
T | C | 297 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(294): Show | 318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.1100+8366T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146257 | ||||||
| chr8:28146300
|
T | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(72): Show | 81 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1100+8409T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146300 | ||||||
| chr8:28146345
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 224 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1100+8454A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146345 | ||||||
| chr8:28146389
|
C | CA | 8 | a0001c0001t0002g0013a0001c0001t0002g0112a0001c0001t0002g0118others(5): Show | 9 | HG02040.hp1 NA18942.hp1 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1100+8505dupA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28146389 | |||||
| chr8:28146554
|
A | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0188 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1100+8663A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146554 | ||||||
| chr8:28146565
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0140 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1100+8674A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146565 | ||||||
| chr8:28146587
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(7): Show | 13 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1100+8696A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146587 | ||||||
| chr8:28146925
|
C | G | 9 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237others(6): Show | 9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1101-9017C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146925 | ||||||
| chr8:28146933
|
A | G | 9 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1101-9009A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146933 | ||||||
| chr8:28147014
|
A | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(268): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.1101-8928A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147014 | ||||||
| chr8:28147039
|
C | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1101-8903C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147039 | ||||||
| chr8:28147059
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1101-8883T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147059 | ||||||
| chr8:28147202
|
T | G | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101-8740T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147202 | ||||||
| chr8:28147456
|
A | C | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101-8486A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147456 | ||||||
| chr8:28147635
|
C | G | 1 | a0001c0001t0003g0343 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1101-8307C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147635 | ||||||
| chr8:28147793
|
T | A | 266 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(263): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.1101-8149T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147793 | ||||||
| chr8:28147824
|
C | G | 1 | a0001c0001t0001g0174 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1101-8118C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147824 | ||||||
| chr8:28147849
|
T | A | 301 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.1101-8093T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147849 | ||||||
| chr8:28147942
|
A | C | 1 | a0001c0001t0019g0291 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1101-8000A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147942 | ||||||
| chr8:28148032
|
T | C | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0308 | 3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1101-7910T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148032 | ||||||
| chr8:28148064
|
T | C | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1101-7878T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148064 | ||||||
| chr8:28148066
|
A | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1101-7876A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148066 | ||||||
| chr8:28148355
|
T | C | 1 | a0001c0001t0004g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1101-7587T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148355 | ||||||
| chr8:28148364
|
T | G | 8 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1101-7578T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148364 | ||||||
| chr8:28148375
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1101-7567C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148375 | ||||||
| chr8:28148457
|
T | C | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1101-7485T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148457 | ||||||
| chr8:28148528
|
G | C | 1 | a0001c0001t0002g0119 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1101-7414G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148528 | ||||||
| chr8:28148564
|
C | T | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1101-7378C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148564 | ||||||
| chr8:28148842
|
T | C | 1 | a0001c0001t0003g0334 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1101-7100T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148842 | ||||||
| chr8:28148902
|
A | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(8): Show | 14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1101-7040A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148902 | ||||||
| chr8:28149068
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1101-6874C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149068 | ||||||
| chr8:28149284
|
C | T | 1 | a0001c0001t0003g0356 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1101-6658C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149284 | ||||||
| chr8:28149298
|
T | C | 2 | a0001c0001t0002g0100a0001c0001t0002g0125 | 2 | NA18947.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1101-6644T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149298 | ||||||
| chr8:28149443
|
G | C | 2 | a0001c0001t0004g0245a0001c0001t0018g0244 | 2 | NA18948.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1101-6499G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149443 | ||||||
| chr8:28149466
|
AGTT | A | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0308 | 3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1101-6472_1101-647 others(7): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28149466 | |||||
| chr8:28149514
|
G | A | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0308 | 3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1101-6428G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149514 | ||||||
| chr8:28149530
|
T | C | 1 | a0001c0002t0011g0149 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1101-6412T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149530 | ||||||
| chr8:28149547
|
A | G | 266 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(263): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.1101-6395A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149547 | ||||||
| chr8:28149649
|
C | T | 297 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(294): Show | 318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.1101-6293C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149649 | ||||||
| chr8:28149735
|
G | C | 8 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1101-6207G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149735 | ||||||
| chr8:28149971
|
G | A | 6 | a0001c0001t0004g0018a0001c0001t0004g0021a0001c0001t0004g0264others(3): Show | 8 | HG00423.hp2 HG00621.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1101-5971G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149971 | ||||||
| chr8:28149975
|
G | C | 1 | a0001c0001t0003g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1101-5967G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149975 | ||||||
| chr8:28150105
|
T | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(287): Show | 311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1101-5837T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150105 | ||||||
| chr8:28150305
|
T | C | 8 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0241others(5): Show | 8 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1101-5637T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150305 | ||||||
| chr8:28150378
|
C | A | 8 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1101-5564C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150378 | ||||||
| chr8:28150431
|
C | A | 3 | a0001c0001t0003g0326a0001c0001t0003g0330a0001c0001t0003g0367 | 3 | HG01192.hp1 HG01243.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1101-5511C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150431 | ||||||
| chr8:28150807
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1101-5135A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150807 | ||||||
| chr8:28150808
|
T | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0204 | 2 | NA18974.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1101-5134T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150808 | ||||||
| chr8:28150831
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1101-5111G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150831 | ||||||
| chr8:28150898
|
A | G | 290 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(287): Show | 311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1101-5044A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150898 | ||||||
| chr8:28151056
|
T | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(13): Show | 19 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1101-4886T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151056 | ||||||
| chr8:28151215
|
C | G | 1 | a0001c0001t0002g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1101-4727C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151215 | ||||||
| chr8:28151260
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1101-4682G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151260 | ||||||
| chr8:28151304
|
A | AT | 290 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(287): Show | 311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1101-4635dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28151304 | |||||
| chr8:28151330
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1101-4612C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151330 | ||||||
| chr8:28151556
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1101-4386T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151556 | ||||||
| chr8:28151662
|
G | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(13): Show | 19 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1101-4280G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151662 | ||||||
| chr8:28151663
|
G | A | 1 | a0001c0001t0003g0349 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1101-4279G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151663 | ||||||
| chr8:28151818
|
A | C | 1 | a0001c0001t0002g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1101-4124A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151818 | ||||||
| chr8:28151879
|
T | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1101-4063T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151879 | ||||||
| chr8:28151901
|
T | C | 1 | a0001c0001t0003g0353 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1101-4041T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151901 | ||||||
| chr8:28151940
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0140 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1101-4002C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151940 | ||||||
| chr8:28152050
|
C | T | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101-3892C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152050 | ||||||
| chr8:28152222
|
T | C | 297 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(294): Show | 318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.1101-3720T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152222 | ||||||
| chr8:28152378
|
G | T | 2 | a0001c0001t0003g0314a0001c0001t0003g0328 | 2 | HG00741.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1101-3564G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152378 | ||||||
| chr8:28152662
|
C | T | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101-3280C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152662 | ||||||
| chr8:28152666
|
T | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(178): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1101-3276T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152666 | ||||||
| chr8:28152737
|
C | T | 2 | a0001c0001t0002g0118a0001c0001t0004g0288 | 2 | NA18951.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1101-3205C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152737 | ||||||
| chr8:28152781
|
G | A | 12 | a0001c0001t0004g0289a0001c0001t0004g0290a0001c0001t0004g0303others(9): Show | 12 | HG00438.hp2 HG01257.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.1101-3161G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152781 | ||||||
| chr8:28152857
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(178): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1101-3085A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152857 | ||||||
| chr8:28153037
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1101-2905C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153037 | ||||||
| chr8:28153040
|
C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(69): Show | 78 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1101-2902C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153040 | ||||||
| chr8:28153402
|
A | C | 2 | a0001c0002t0011g0144a0001c0002t0011g0149 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1101-2540A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153402 | ||||||
| chr8:28153428
|
A | G | 1 | a0001c0001t0002g0043 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1101-2514A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153428 | ||||||
| chr8:28153565
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1101-2377A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153565 | ||||||
| chr8:28153831
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1101-2111G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153831 | ||||||
| chr8:28153855
|
C | T | 1 | a0001c0001t0010g0362 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1101-2087C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153855 | ||||||
| chr8:28153876
|
A | G | 4 | a0001c0001t0003g0314a0001c0001t0003g0328a0001c0001t0003g0332others(1): Show | 4 | HG00741.hp1 HG01934.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1101-2066A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153876 | ||||||
| chr8:28154050
|
A | G | 1 | a0001c0001t0003g0364 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1101-1892A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154050 | ||||||
| chr8:28154274
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1101-1668C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154274 | ||||||
| chr8:28154275
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(154): Show | 166 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1101-1667A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154275 | ||||||
| chr8:28154344
|
G | A | 2 | a0001c0001t0003g0329a0001c0001t0003g0331 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1101-1598G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154344 | ||||||
| chr8:28154362
|
A | C | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101-1580A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154362 | ||||||
| chr8:28154394
|
C | T | 1 | a0001c0001t0004g0284 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1101-1548C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154394 | ||||||
| chr8:28154401
|
A | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(153): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1101-1541A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154401 | ||||||
| chr8:28154479
|
T | C | 1 | a0001c0001t0003g0326 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1101-1463T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154479 | ||||||
| chr8:28154496
|
T | C | 8 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1101-1446T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154496 | ||||||
| chr8:28154639
|
A | T | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101-1303A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154639 | ||||||
| chr8:28154704
|
G | A | 2 | a0001c0001t0004g0245a0001c0001t0018g0244 | 2 | NA18948.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1101-1238G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154704 | ||||||
| chr8:28154858
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1101-1084C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154858 | ||||||
| chr8:28154936
|
A | G | 1 | a0001c0001t0003g0339 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1101-1006A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154936 | ||||||
| chr8:28154949
|
C | T | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1101-993C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154949 | ||||||
| chr8:28155547
|
A | C | 1 | a0001c0001t0003g0346 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1101-395A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28155547 | ||||||
| chr8:28155921
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1101-21A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28155921 | ||||||
| chr8:28156062
|
A | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(271): Show | 292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.1191+30A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28156062 | ||||||
| chr8:28156226
|
A | G | 1 | a0001c0001t0002g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1191+194A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28156226 | ||||||
| chr8:28156347
|
G | A | 4 | a0001c0001t0003g0022a0001c0001t0003g0334a0001c0001t0003g0335others(1): Show | 5 | HG01256.hp1 HG01258.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1191+315G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28156347 | ||||||
| chr8:28156421
|
A | G | 3 | a0001c0001t0003g0318a0001c0001t0003g0323a0001c0001t0003g0327 | 3 | HG00642.hp1 HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1191+389A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28156421 | ||||||
| chr8:28156742
|
A | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0243 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1191+710A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28156742 | ||||||
| chr8:28156859
|
G | T | 297 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(294): Show | 318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.1191+827G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28156859 | ||||||
| chr8:28156908
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1191+876T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28156908 | ||||||
| chr8:28157044
|
G | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(262): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.1191+1012G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28157044 | ||||||
| chr8:28157054
|
G | T | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1191+1022G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28157054 | ||||||
| chr8:28157289
|
C | CA | 177 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(174): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1192-1263dupA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28157289 | |||||
| chr8:28157289
|
C | CAA | 84 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0041others(81): Show | 91 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1192-1264_1192-126 others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28157289 | |||||
| chr8:28157289
|
C | CAAA | 6 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0004g0273others(3): Show | 6 | HG00544.hp1 HG03139.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1192-1265_1192-126 others(7): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28157289 | |||||
| chr8:28157289
|
CA | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0140a0001c0001t0001g0234others(3): Show | 6 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1192-1263delA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28157289 | |||||
| chr8:28157289
|
CAA | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(8): Show | 14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1192-1264_1192-126 others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28157289 | |||||
| chr8:28157302
|
A | AC | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1192-1266_1192-126 others(5): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28157302 | ||||||
| chr8:28157509
|
T | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0025 | 2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1192-1059T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28157509 | ||||||
| chr8:28157522
|
G | A | 1 | a0001c0001t0004g0281 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1192-1046G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28157522 | ||||||
| chr8:28157796
|
C | T | 1 | a0001c0001t0004g0266 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1192-772C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28157796 | ||||||
| chr8:28157893
|
A | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(8): Show | 14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1192-675A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28157893 | ||||||
| chr8:28158050
|
CA | C | 99 | a0001c0001t0001g0029a0001c0001t0001g0040a0001c0001t0001g0194others(96): Show | 102 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1192-498delA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28158050 | |||||
| chr8:28158050
|
CAA | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(39): Show | 46 | HG00597.hp1 HG00733.hp1 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.1192-499_1192-498d others(4): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28158050 | |||||
| chr8:28158050
|
CAAA | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(150): Show | 167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1192-500_1192-498d others(5): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28158050 | |||||
| chr8:28158307
|
C | T | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1192-261C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28158307 | ||||||
| chr8:28158348
|
A | G | 1 | a0001c0001t0002g0134 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1192-220A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28158348 | ||||||
| chr8:28158390
|
G | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(29): Show | 35 | HG00733.hp1 HG01243.hp1 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1192-178G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28158390 | ||||||
| chr8:28158417
|
T | G | 1 | a0001c0001t0003g0316 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1192-151T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28158417 | ||||||
| chr8:28158485
|
AAATAAAG | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(169): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1192-81_1192-75del others(7): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28158485 | |||||
| chr8:28158543
|
C | T | 1 | a0001c0002t0001g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1192-25C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28158543 | ||||||
| chr8:28158549
|
C | T | 1 | a0001c0001t0002g0057 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1192-19C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28158549 | ||||||
| chr8:28158553
|
A | AT | 10 | a0001c0001t0003g0024a0001c0001t0004g0019a0001c0001t0004g0020others(7): Show | 12 | HG00544.hp1 HG00558.hp2 HG03471.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.1192-6dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28158553 | |||||
| chr8:28158756
|
C | T | 3 | a0001c0003t0008g0107a0001c0003t0008g0108a0001c0003t0008g0109 | 3 | NA18965.hp1 NA18987.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1257+123C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28158756 | ||||||
| chr8:28158771
|
G | A | 9 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237others(6): Show | 9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1257+138G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28158771 | ||||||
| chr8:28158840
|
T | C | 2 | a0001c0001t0002g0011a0001c0001t0002g0098 | 3 | HG01257.hp2 HG01258.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1257+207T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28158840 | ||||||
| chr8:28159023
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(68): Show | 77 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1257+390G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159023 | ||||||
| chr8:28159169
|
A | G | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221 | 3 | HG02559.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1257+536A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159169 | ||||||
| chr8:28159409
|
A | G | 8 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1257+776A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159409 | ||||||
| chr8:28159578
|
A | G | 8 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1258-651A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159578 | ||||||
| chr8:28159646
|
C | G | 1 | a0001c0001t0002g0128 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1258-583C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159646 | ||||||
| chr8:28159747
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1258-482C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159747 | ||||||
| chr8:28159788
|
A | G | 18 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(15): Show | 21 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1258-441A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159788 | ||||||
| chr8:28159825
|
T | G | 1 | a0001c0001t0002g0087 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1258-404T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159825 | ||||||
| chr8:28159834
|
AACCATTG others(3): Show |
A | 9 | a0001c0001t0005g0239a0001c0001t0005g0258a0001c0001t0005g0278others(6): Show | 9 | HG01257.hp1 HG01358.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1258-391_1258-382d others(12): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 28159834 | |||||
| chr8:28159944
|
A | T | 1 | a0001c0003t0008g0107 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1258-285A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159944 | ||||||
| chr8:28159995
|
G | A | 2 | a0001c0001t0004g0275a0001c0001t0004g0276 | 2 | HG01934.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1258-234G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159995 | ||||||
| chr8:28160005
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1258-224T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28160005 | ||||||
| chr8:28160700
|
A | T | 86 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0001t0001g0233others(83): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1485+244A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28160700 | ||||||
| chr8:28160704
|
G | GT | 5 | a0001c0001t0001g0168a0001c0001t0001g0218a0001c0001t0003g0317others(2): Show | 5 | HG01934.hp1 HG03831.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+256dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 28160704 | |||||
| chr8:28160790
|
GTTCAAGT others(2): Show |
G | 214 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1485+338_1485+346d others(11): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 28160790 | |||||
| chr8:28160802
|
C | G | 1 | a0001c0001t0006g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1485+346C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28160802 | ||||||
| chr8:28160821
|
A | G | 13 | a0001c0001t0003g0003a0001c0001t0003g0023a0001c0001t0003g0238others(10): Show | 16 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1485+365A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28160821 | ||||||
| chr8:28161024
|
C | T | 8 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1485+568C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161024 | ||||||
| chr8:28161059
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1485+603T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161059 | ||||||
| chr8:28161217
|
G | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(21): Show | 27 | HG00733.hp1 HG01243.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1485+761G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161217 | ||||||
| chr8:28161220
|
T | C | 3 | a0001c0001t0003g0004a0001c0001t0003g0351a0001c0001t0003g0357 | 5 | HG00642.hp2 HG01975.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+764T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161220 | ||||||
| chr8:28161224
|
A | T | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1485+768A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161224 | ||||||
| chr8:28161393
|
G | A | 1 | a0001c0001t0002g0047 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1486-604G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161393 | ||||||
| chr8:28161435
|
G | A | 1 | a0001c0001t0003g0343 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1486-562G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161435 | ||||||
| chr8:28161495
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1486-502G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161495 | ||||||
| chr8:28161506
|
G | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(7): Show | 13 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1486-491G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161506 | ||||||
| chr8:28161545
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1486-452G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161545 | ||||||
| chr8:28161600
|
C | T | 75 | a0001c0001t0001g0297a0001c0001t0001g0369a0001c0001t0001g0370others(72): Show | 81 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1486-397C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161600 | ||||||
| chr8:28161601
|
G | A | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1486-396G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161601 | ||||||
| chr8:28161610
|
GA | G | 14 | a0001c0001t0003g0177a0001c0001t0003g0187a0001c0001t0003g0189others(11): Show | 14 | HG00738.hp2 HG01243.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1486-368delA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 28161610 | |||||
| chr8:28161651
|
T | TA | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1486-343dupA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 28161651 | |||||
| chr8:28161944
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1486-53T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161944 | ||||||
| chr8:28162094
|
C | T | 8 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1567+16C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162094 | ||||||
| chr8:28162265
|
G | A | 16 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(13): Show | 19 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1567+187G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162265 | ||||||
| chr8:28162484
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1567+406C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162484 | ||||||
| chr8:28162494
|
A | G | 2 | a0001c0001t0003g0332a0001c0001t0003g0333 | 2 | HG02738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1567+416A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162494 | ||||||
| chr8:28162524
|
T | A | 1 | a0001c0001t0002g0010 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1567+446T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162524 | ||||||
| chr8:28162539
|
A | G | 3 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0003g0232 | 3 | HG02055.hp2 HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1567+461A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162539 | ||||||
| chr8:28162546
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1567+468G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162546 | ||||||
| chr8:28162554
|
T | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(8): Show | 14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1567+476T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162554 | ||||||
| chr8:28162570
|
G | A | 4 | a0001c0001t0003g0177a0001c0001t0003g0187a0001c0001t0003g0189others(1): Show | 4 | HG00738.hp2 HG02258.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1567+492G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162570 | ||||||
| chr8:28162649
|
A | G | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1567+571A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162649 | ||||||
| chr8:28162935
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1567+857G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162935 | ||||||
| chr8:28163120
|
G | T | 8 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0003t0008g0104others(5): Show | 8 | HG00597.hp1 HG02109.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1567+1042G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163120 | ||||||
| chr8:28163187
|
C | G | 1 | a0001c0001t0003g0367 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1567+1109C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163187 | ||||||
| chr8:28163376
|
A | T | 18 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(15): Show | 21 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1567+1298A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163376 | ||||||
| chr8:28163503
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1567+1425T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163503 | ||||||
| chr8:28163524
|
CT | C | 23 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0103others(20): Show | 24 | HG00408.hp1 HG00597.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1567+1461delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28163524 | |||||
| chr8:28163524
|
CTT | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(271): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1567+1460_1567+146 others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28163524 | |||||
| chr8:28163588
|
G | T | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1567+1510G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163588 | ||||||
| chr8:28163708
|
G | A | 9 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237others(6): Show | 9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1567+1630G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163708 | ||||||
| chr8:28163744
|
T | C | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+1666T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163744 | ||||||
| chr8:28163794
|
G | A | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1567+1716G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163794 | ||||||
| chr8:28163827
|
C | T | 5 | a0001c0001t0001g0156a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG01884.hp2 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1567+1749C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163827 | ||||||
| chr8:28164043
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1567+1965A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164043 | ||||||
| chr8:28164169
|
T | G | 1 | a0001c0001t0001g0041 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1567+2091T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164169 | ||||||
| chr8:28164252
|
G | T | 18 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(15): Show | 21 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1567+2174G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164252 | ||||||
| chr8:28164272
|
G | A | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0308 | 3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1567+2194G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164272 | ||||||
| chr8:28164278
|
C | T | 1 | a0001c0001t0003g0216 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1567+2200C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164278 | ||||||
| chr8:28164548
|
G | A | 27 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(24): Show | 30 | HG00733.hp1 HG01243.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1567+2470G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164548 | ||||||
| chr8:28164611
|
C | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1567+2533C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164611 | ||||||
| chr8:28164657
|
A | G | 11 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0001t0001g0233others(8): Show | 11 | HG00597.hp1 HG02109.hp2 HG03195.hp2 others(8): Show |
intron_variant | MODIFIER | c.1567+2579A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164657 | ||||||
| chr8:28164721
|
A | T | 1 | a0001c0001t0002g0083 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1567+2643A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164721 | ||||||
| chr8:28164900
|
G | T | 1 | a0001c0001t0003g0333 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1567+2822G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164900 | ||||||
| chr8:28165155
|
G | A | 11 | a0001c0001t0001g0016a0001c0001t0001g0171a0001c0001t0001g0172others(8): Show | 12 | HG00408.hp1 HG02165.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1567+3077G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165155 | ||||||
| chr8:28165190
|
G | C | 1 | a0001c0002t0009g0143 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1567+3112G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165190 | ||||||
| chr8:28165267
|
G | A | 33 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 36 | HG00733.hp1 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1567+3189G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165267 | ||||||
| chr8:28165274
|
G | A | 10 | a0001c0001t0001g0039a0001c0001t0001g0140a0001c0002t0001g0148others(7): Show | 10 | HG01243.hp1 HG02257.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1567+3196G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165274 | ||||||
| chr8:28165409
|
C | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(153): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1567+3331C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165409 | ||||||
| chr8:28165439
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(255): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1567+3361T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165439 | ||||||
| chr8:28165539
|
G | A | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1567+3461G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165539 | ||||||
| chr8:28165633
|
T | C | 2 | a0001c0001t0002g0064a0001c0001t0002g0073 | 2 | NA18983.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1567+3555T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165633 | ||||||
| chr8:28165720
|
G | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(293): Show | 317 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.1567+3642G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165720 | ||||||
| chr8:28165864
|
A | G | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG00639.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1567+3786A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165864 | ||||||
| chr8:28165891
|
A | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(8): Show | 14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1567+3813A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165891 | ||||||
| chr8:28166142
|
G | T | 281 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(278): Show | 302 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1567+4064G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166142 | ||||||
| chr8:28166191
|
C | T | 293 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1567+4113C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166191 | ||||||
| chr8:28166207
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1567+4129T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166207 | ||||||
| chr8:28166297
|
A | G | 1 | a0001c0001t0005g0239 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1567+4219A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166297 | ||||||
| chr8:28166384
|
T | G | 1 | a0001c0001t0001g0208 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1567+4306T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166384 | ||||||
| chr8:28166581
|
C | G | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1567+4503C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166581 | ||||||
| chr8:28166803
|
C | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(68): Show | 77 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1567+4725C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166803 | ||||||
| chr8:28166826
|
C | A | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1567+4748C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166826 | ||||||
| chr8:28166910
|
C | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(153): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1567+4832C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166910 | ||||||
| chr8:28166935
|
T | C | 1 | a0001c0001t0002g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1567+4857T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166935 | ||||||
| chr8:28166951
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1567+4873A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166951 | ||||||
| chr8:28166995
|
G | T | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(7): Show | 13 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1567+4917G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166995 | ||||||
| chr8:28167029
|
G | A | 1 | a0001c0001t0003g0212 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1567+4951G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167029 | ||||||
| chr8:28167270
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1567+5192G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167270 | ||||||
| chr8:28167272
|
C | G | 1 | a0001c0001t0002g0100 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1567+5194C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167272 | ||||||
| chr8:28167326
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1567+5248G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167326 | ||||||
| chr8:28167327
|
A | C | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+5249A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167327 | ||||||
| chr8:28167332
|
C | A | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0308 | 3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1567+5254C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167332 | ||||||
| chr8:28167384
|
A | T | 1 | a0001c0001t0001g0227 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1567+5306A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167384 | ||||||
| chr8:28167418
|
G | A | 8 | a0001c0001t0001g0041a0001c0001t0001g0103a0001c0003t0008g0104others(5): Show | 8 | HG00597.hp1 HG02109.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1567+5340G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167418 | ||||||
| chr8:28167424
|
C | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(68): Show | 77 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1567+5346C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167424 | ||||||
| chr8:28167425
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(254): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.1567+5347A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167425 | ||||||
| chr8:28167622
|
C | A | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+5544C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167622 | ||||||
| chr8:28167642
|
T | A | 2 | a0001c0001t0003g0332a0001c0001t0003g0333 | 2 | HG02738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1567+5564T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167642 | ||||||
| chr8:28167682
|
A | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1567+5604A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167682 | ||||||
| chr8:28167804
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1567+5726A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167804 | ||||||
| chr8:28167806
|
T | C | 370 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(367): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.1567+5728T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167806 | ||||||
| chr8:28167893
|
A | T | 1 | a0001c0001t0001g0168 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1567+5815A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167893 | ||||||
| chr8:28167900
|
A | G | 1 | a0001c0001t0003g0342 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1567+5822A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167900 | ||||||
| chr8:28167960
|
G | T | 1 | a0001c0001t0004g0290 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1567+5882G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167960 | ||||||
| chr8:28168008
|
T | A | 222 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1567+5930T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168008 | ||||||
| chr8:28168333
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1567+6255T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168333 | ||||||
| chr8:28168410
|
G | A | 75 | a0001c0001t0001g0297a0001c0001t0001g0369a0001c0001t0001g0370others(72): Show | 81 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1567+6332G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168410 | ||||||
| chr8:28168414
|
T | C | 10 | a0001c0001t0001g0039a0001c0001t0001g0140a0001c0002t0001g0148others(7): Show | 10 | HG01243.hp1 HG02257.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1567+6336T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168414 | ||||||
| chr8:28168649
|
T | C | 1 | a0001c0001t0003g0312 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1567+6571T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168649 | ||||||
| chr8:28168669
|
T | G | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1567+6591T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168669 | ||||||
| chr8:28168683
|
C | A | 1 | a0001c0001t0003g0333 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1567+6605C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168683 | ||||||
| chr8:28168750
|
G | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1567+6672G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168750 | ||||||
| chr8:28168776
|
C | T | 1 | a0001c0001t0004g0246 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1567+6698C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168776 | ||||||
| chr8:28168824
|
T | C | 1 | a0001c0001t0004g0247 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1567+6746T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168824 | ||||||
| chr8:28168868
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(8): Show | 14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1567+6790G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168868 | ||||||
| chr8:28168928
|
A | G | 9 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237others(6): Show | 9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1567+6850A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168928 | ||||||
| chr8:28169226
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1567+7148G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169226 | ||||||
| chr8:28169325
|
C | T | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0308 | 3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1567+7247C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169325 | ||||||
| chr8:28169347
|
G | A | 1 | a0001c0001t0004g0261 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1567+7269G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169347 | ||||||
| chr8:28169386
|
C | A | 2 | a0001c0001t0001g0369a0001c0001t0001g0370 | 2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1567+7308C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169386 | ||||||
| chr8:28169441
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1567+7363T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169441 | ||||||
| chr8:28169476
|
A | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1567+7398A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169476 | ||||||
| chr8:28169489
|
A | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(255): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1567+7411A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169489 | ||||||
| chr8:28169634
|
T | A | 1 | a0001c0001t0001g0218 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1567+7556T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169634 | ||||||
| chr8:28169677
|
T | G | 1 | a0001c0001t0003g0319 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1567+7599T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169677 | ||||||
| chr8:28169755
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(8): Show | 14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1567+7677G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169755 | ||||||
| chr8:28169841
|
T | C | 18 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(15): Show | 21 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1567+7763T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169841 | ||||||
| chr8:28169892
|
C | G | 1 | a0001c0001t0003g0330 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1567+7814C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169892 | ||||||
| chr8:28169912
|
C | T | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+7834C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169912 | ||||||
| chr8:28169982
|
C | G | 1 | a0001c0001t0004g0259 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1567+7904C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169982 | ||||||
| chr8:28170001
|
A | G | 81 | a0001c0001t0001g0297a0001c0001t0001g0369a0001c0001t0001g0370others(78): Show | 87 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1567+7923A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170001 | ||||||
| chr8:28170232
|
C | G | 8 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1567+8154C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170232 | ||||||
| chr8:28170367
|
A | G | 8 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1567+8289A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170367 | ||||||
| chr8:28170493
|
G | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(152): Show | 164 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1567+8415G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170493 | ||||||
| chr8:28170611
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1567+8533A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170611 | ||||||
| chr8:28170632
|
G | T | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+8554G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170632 | ||||||
| chr8:28170637
|
T | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0140 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1567+8559T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170637 | ||||||
| chr8:28170674
|
C | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1567+8596C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170674 | ||||||
| chr8:28170703
|
A | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1567+8625A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170703 | ||||||
| chr8:28170907
|
A | AT | 1 | a0001c0001t0003g0003 | 3 | HG01069.hp2 HG01071.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1567+8833dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28170907 | |||||
| chr8:28171020
|
T | C | 1 | a0001c0001t0002g0100 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1567+8942T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171020 | ||||||
| chr8:28171113
|
C | G | 1 | a0001c0001t0002g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1567+9035C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171113 | ||||||
| chr8:28171165
|
G | C | 81 | a0001c0001t0001g0297a0001c0001t0001g0369a0001c0001t0001g0370others(78): Show | 87 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1567+9087G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171165 | ||||||
| chr8:28171268
|
C | T | 2 | a0001c0001t0001g0040a0001c0004t0001g0145 | 2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1567+9190C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171268 | ||||||
| chr8:28171279
|
C | CT | 5 | a0001c0001t0002g0038a0001c0001t0002g0061a0001c0001t0002g0068others(2): Show | 5 | HG01261.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1567+9202dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28171279 | |||||
| chr8:28171352
|
CT | C | 293 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1567+9287delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28171352 | |||||
| chr8:28171362
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(255): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1567+9284T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171362 | ||||||
| chr8:28171492
|
T | C | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1567+9414T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171492 | ||||||
| chr8:28171501
|
C | T | 292 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(289): Show | 313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.1567+9423C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171501 | ||||||
| chr8:28171667
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1567+9589G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171667 | ||||||
| chr8:28171810
|
G | A | 1 | a0001c0001t0004g0274 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1567+9732G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171810 | ||||||
| chr8:28171856
|
A | G | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+9778A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171856 | ||||||
| chr8:28171926
|
A | G | 1 | a0001c0001t0006g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1567+9848A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171926 | ||||||
| chr8:28172142
|
A | G | 4 | a0001c0001t0001g0190a0001c0001t0001g0219a0001c0001t0001g0220others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1567+10064A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28172142 | ||||||
| chr8:28172227
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1567+10149T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28172227 | ||||||
| chr8:28172243
|
A | G | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0308 | 3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1567+10165A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28172243 | ||||||
| chr8:28172280
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0103 | 2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1567+10202A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28172280 | ||||||
| chr8:28172384
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1567+10306C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28172384 | ||||||
| chr8:28172498
|
T | C | 3 | a0001c0001t0001g0201a0001c0001t0001g0215a0001c0001t0001g0227 | 3 | HG03688.hp1 HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1567+10420T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28172498 | ||||||
| chr8:28172864
|
T | C | 9 | a0001c0001t0005g0239a0001c0001t0005g0258a0001c0001t0005g0278others(6): Show | 9 | HG01257.hp1 HG01358.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1567+10786T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28172864 | ||||||
| chr8:28173470
|
G | A | 1 | a0001c0001t0004g0252 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1567+11392G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28173470 | ||||||
| chr8:28173553
|
A | AT | 179 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(176): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1567+11486dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28173553 | |||||
| chr8:28173684
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(262): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.1567+11606T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28173684 | ||||||
| chr8:28173767
|
G | A | 1 | a0001c0001t0003g0367 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1567+11689G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28173767 | ||||||
| chr8:28173872
|
T | TAAGAATG others(325): Show |
1 | a0001c0001t0003g0212 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1567+11810_1567+11 others(338): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28173872 | |||||
| chr8:28174028
|
G | A | 1 | a0001c0001t0003g0364 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1567+11950G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174028 | ||||||
| chr8:28174051
|
T | C | 2 | a0001c0001t0003g0024a0001c0001t0003g0025 | 2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1567+11973T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174051 | ||||||
| chr8:28174139
|
C | T | 1 | a0001c0001t0003g0366 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1567+12061C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174139 | ||||||
| chr8:28174257
|
T | A | 72 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(69): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1567+12179T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174257 | ||||||
| chr8:28174290
|
A | G | 1 | a0001c0001t0002g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1567+12212A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174290 | ||||||
| chr8:28174409
|
C | G | 1 | a0001c0001t0001g0175 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1567+12331C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174409 | ||||||
| chr8:28174547
|
G | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(154): Show | 166 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1567+12469G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174547 | ||||||
| chr8:28174708
|
T | C | 359 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(356): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.1567+12630T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174708 | ||||||
| chr8:28174805
|
G | A | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0308 | 3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1567+12727G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174805 | ||||||
| chr8:28174925
|
G | A | 85 | a0001c0001t0001g0194a0001c0001t0001g0204a0001c0001t0001g0320others(82): Show | 88 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1567+12847G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174925 | ||||||
| chr8:28175119
|
C | G | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+13041C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175119 | ||||||
| chr8:28175129
|
C | T | 257 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(254): Show | 275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.1567+13051C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175129 | ||||||
| chr8:28175187
|
A | C | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1567+13109A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175187 | ||||||
| chr8:28175287
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1567+13209A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175287 | ||||||
| chr8:28175320
|
T | G | 351 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(348): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1567+13242T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175320 | ||||||
| chr8:28175370
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1567+13292G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175370 | ||||||
| chr8:28175386
|
T | C | 1 | a0001c0001t0013g0361 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1567+13308T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175386 | ||||||
| chr8:28175500
|
C | A | 72 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(69): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1567+13422C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175500 | ||||||
| chr8:28175662
|
C | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(8): Show | 14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1567+13584C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175662 | ||||||
| chr8:28175810
|
C | CT | 305 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(302): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1567+13753dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28175810 | |||||
| chr8:28175810
|
C | CTT | 35 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0159others(32): Show | 35 | HG00621.hp1 HG00741.hp2 HG01168.hp2 others(32): Show |
intron_variant | MODIFIER | c.1567+13752_1567+13 others(8): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28175810 | |||||
| chr8:28175810
|
CT | C | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+13753delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28175810 | |||||
| chr8:28175810
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0004g0306 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1567+13744_1567+13 others(16): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28175810 | |||||
| chr8:28175831
|
T | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1567+13753T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175831 | ||||||
| chr8:28175883
|
C | T | 3 | a0001c0001t0003g0318a0001c0001t0003g0323a0001c0001t0003g0327 | 3 | HG00642.hp1 HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1568-13766C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175883 | ||||||
| chr8:28175885
|
G | T | 85 | a0001c0001t0001g0194a0001c0001t0001g0204a0001c0001t0001g0320others(82): Show | 88 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1568-13764G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175885 | ||||||
| chr8:28175906
|
G | C | 368 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(365): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1568-13743G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175906 | ||||||
| chr8:28175918
|
T | A | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1568-13731T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175918 | ||||||
| chr8:28176005
|
C | T | 1 | a0001c0001t0002g0129 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1568-13644C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176005 | ||||||
| chr8:28176027
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0140 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1568-13622A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176027 | ||||||
| chr8:28176055
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1568-13594G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176055 | ||||||
| chr8:28176167
|
T | G | 5 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0003g0311others(2): Show | 5 | HG02056.hp2 NA18954.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1568-13482T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176167 | ||||||
| chr8:28176206
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1568-13443T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176206 | ||||||
| chr8:28176302
|
C | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(153): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1568-13347C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176302 | ||||||
| chr8:28176303
|
G | A | 1 | a0001c0001t0006g0253 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1568-13346G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176303 | ||||||
| chr8:28176663
|
AT | A | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0308 | 3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1568-12985delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176663 | ||||||
| chr8:28176726
|
T | C | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-12923T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176726 | ||||||
| chr8:28176873
|
A | G | 3 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0115 | 3 | HG02080.hp2 NA18963.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1568-12776A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176873 | ||||||
| chr8:28176920
|
C | T | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1568-12729C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176920 | ||||||
| chr8:28176994
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(260): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.1568-12655A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176994 | ||||||
| chr8:28177215
|
C | T | 1 | a0001c0001t0012g0358 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1568-12434C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177215 | ||||||
| chr8:28177225
|
A | AT | 9 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237others(6): Show | 9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1568-12414dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28177225 | |||||
| chr8:28177225
|
AT | A | 6 | a0001c0001t0004g0018a0001c0001t0004g0021a0001c0001t0004g0264others(3): Show | 8 | HG00423.hp2 HG00621.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1568-12414delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28177225 | |||||
| chr8:28177329
|
G | C | 368 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(365): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1568-12320G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177329 | ||||||
| chr8:28177347
|
T | C | 146 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(143): Show | 158 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1568-12302T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177347 | ||||||
| chr8:28177373
|
C | T | 1 | a0001c0001t0003g0368 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1568-12276C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177373 | ||||||
| chr8:28177415
|
A | G | 1 | a0001c0001t0003g0335 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1568-12234A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177415 | ||||||
| chr8:28177520
|
T | A | 8 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1568-12129T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177520 | ||||||
| chr8:28177711
|
CAAGT | C | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-11934_1568-11 others(10): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28177711 | |||||
| chr8:28177873
|
T | C | 1 | a0001c0001t0003g0332 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1568-11776T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177873 | ||||||
| chr8:28177935
|
A | G | 369 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(366): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.1568-11714A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177935 | ||||||
| chr8:28178070
|
A | C | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0003g0024others(4): Show | 7 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1568-11579A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178070 | ||||||
| chr8:28178178
|
A | G | 7 | a0001c0002t0009g0141a0001c0002t0009g0142a0001c0002t0009g0143others(4): Show | 7 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1568-11471A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178178 | ||||||
| chr8:28178240
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1568-11409A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178240 | ||||||
| chr8:28178244
|
G | C | 73 | a0001c0001t0001g0297a0001c0001t0004g0002a0001c0001t0004g0017others(70): Show | 79 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1568-11405G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178244 | ||||||
| chr8:28178295
|
C | T | 1 | a0001c0001t0003g0356 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1568-11354C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178295 | ||||||
| chr8:28178317
|
T | C | 3 | a0001c0001t0003g0004a0001c0001t0003g0351a0001c0001t0003g0357 | 5 | HG00642.hp2 HG01975.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1568-11332T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178317 | ||||||
| chr8:28178377
|
C | CCTAA | 12 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237others(9): Show | 12 | HG00597.hp1 HG02615.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.1568-11269_1568-11 others(10): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28178377 | |||||
| chr8:28178400
|
C | T | 3 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0002t0001g0148 | 3 | HG02615.hp1 HG02896.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1568-11249C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178400 | ||||||
| chr8:28178401
|
G | A | 1 | a0001c0001t0003g0177 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1568-11248G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178401 | ||||||
| chr8:28178461
|
T | C | 70 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0003g0003others(67): Show | 76 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.1568-11188T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178461 | ||||||
| chr8:28178470
|
T | G | 1 | a0001c0001t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1568-11179T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178470 | ||||||
| chr8:28178651
|
C | A | 72 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(69): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1568-10998C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178651 | ||||||
| chr8:28178700
|
T | C | 1 | a0001c0002t0001g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1568-10949T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178700 | ||||||
| chr8:28178835
|
G | A | 1 | a0001c0001t0003g0359 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1568-10814G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178835 | ||||||
| chr8:28178883
|
C | G | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1568-10766C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178883 | ||||||
| chr8:28178925
|
G | A | 1 | a0001c0001t0004g0267 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1568-10724G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178925 | ||||||
| chr8:28179078
|
G | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(153): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1568-10571G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179078 | ||||||
| chr8:28179332
|
T | G | 1 | a0001c0001t0006g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1568-10317T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179332 | ||||||
| chr8:28179338
|
A | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1568-10311A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179338 | ||||||
| chr8:28179345
|
G | A | 1 | a0001c0002t0001g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1568-10304G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179345 | ||||||
| chr8:28179521
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(7): Show | 13 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1568-10128G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179521 | ||||||
| chr8:28179739
|
G | A | 4 | a0001c0001t0001g0156a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 4 | HG01884.hp2 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568-9910G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179739 | ||||||
| chr8:28179763
|
C | T | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0308 | 3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1568-9886C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179763 | ||||||
| chr8:28179768
|
G | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(280): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1568-9881G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179768 | ||||||
| chr8:28179821
|
A | C | 75 | a0001c0001t0001g0297a0001c0001t0001g0369a0001c0001t0001g0370others(72): Show | 81 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1568-9828A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179821 | ||||||
| chr8:28180047
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1568-9602A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180047 | ||||||
| chr8:28180129
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(68): Show | 77 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1568-9520G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180129 | ||||||
| chr8:28180136
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1568-9513C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180136 | ||||||
| chr8:28180157
|
A | G | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-9492A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180157 | ||||||
| chr8:28180167
|
T | C | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1568-9482T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180167 | ||||||
| chr8:28180202
|
A | AACACATG others(5): Show |
4 | a0001c0001t0002g0063a0001c0001t0002g0094a0001c0001t0002g0099others(1): Show | 4 | HG01081.hp1 HG01175.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568-9446_1568-943 others(16): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28180202 | |||||
| chr8:28180309
|
T | G | 8 | a0001c0001t0001g0173a0001c0001t0001g0182a0001c0001t0001g0186others(5): Show | 8 | HG00597.hp2 NA18947.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.1568-9340T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180309 | ||||||
| chr8:28180470
|
A | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(284): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1568-9179A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180470 | ||||||
| chr8:28180489
|
T | G | 75 | a0001c0001t0001g0297a0001c0001t0001g0369a0001c0001t0001g0370others(72): Show | 81 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1568-9160T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180489 | ||||||
| chr8:28180500
|
A | G | 3 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0308 | 3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1568-9149A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180500 | ||||||
| chr8:28180503
|
G | A | 2 | a0001c0001t0002g0121a0001c0001t0002g0122 | 2 | HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1568-9146G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180503 | ||||||
| chr8:28180539
|
C | A | 283 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(280): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1568-9110C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180539 | ||||||
| chr8:28180557
|
GTC | G | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-9088_1568-908 others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28180557 | |||||
| chr8:28180841
|
T | A | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1568-8808T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180841 | ||||||
| chr8:28180877
|
C | A | 1 | a0001c0001t0002g0094 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1568-8772C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180877 | ||||||
| chr8:28180910
|
C | T | 368 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(365): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1568-8739C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180910 | ||||||
| chr8:28181259
|
A | G | 362 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(359): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.1568-8390A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181259 | ||||||
| chr8:28181272
|
C | A | 10 | a0001c0001t0003g0004a0001c0001t0003g0341a0001c0001t0003g0347others(7): Show | 12 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1568-8377C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181272 | ||||||
| chr8:28181314
|
C | A | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-8335C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181314 | ||||||
| chr8:28181602
|
A | G | 72 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(69): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1568-8047A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181602 | ||||||
| chr8:28181608
|
A | G | 7 | a0001c0002t0009g0141a0001c0002t0009g0142a0001c0002t0009g0143others(4): Show | 7 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1568-8041A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181608 | ||||||
| chr8:28181657
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1568-7992G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181657 | ||||||
| chr8:28181713
|
C | T | 3 | a0001c0001t0003g0230a0001c0001t0003g0231a0001c0001t0003g0232 | 3 | HG02055.hp2 HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1568-7936C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181713 | ||||||
| chr8:28181959
|
CTTTG | C | 3 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0006g0253 | 3 | HG02145.hp2 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1568-7674_1568-767 others(8): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28181959 | |||||
| chr8:28181966
|
TG | T | 90 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(87): Show | 99 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1568-7682delG | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181966 | ||||||
| chr8:28182227
|
T | A | 3 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1568-7422T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182227 | ||||||
| chr8:28182283
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1568-7366G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182283 | ||||||
| chr8:28182475
|
C | T | 1 | a0001c0001t0002g0092 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1568-7174C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182475 | ||||||
| chr8:28182517
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1568-7132C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182517 | ||||||
| chr8:28182608
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1568-7041C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182608 | ||||||
| chr8:28182677
|
T | G | 1 | a0001c0001t0003g0343 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1568-6972T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182677 | ||||||
| chr8:28182725
|
G | A | 21 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(18): Show | 24 | HG00733.hp1 HG01243.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1568-6924G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182725 | ||||||
| chr8:28182843
|
C | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0140a0001c0001t0001g0171others(1): Show | 4 | HG02723.hp1 HG03098.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.1568-6806C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182843 | ||||||
| chr8:28182854
|
G | T | 1 | a0001c0001t0001g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1568-6795G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182854 | ||||||
| chr8:28182874
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1568-6775G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182874 | ||||||
| chr8:28182957
|
C | G | 5 | a0001c0001t0001g0156a0001c0001t0001g0184a0001c0001t0001g0185others(2): Show | 5 | HG01884.hp2 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1568-6692C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182957 | ||||||
| chr8:28182964
|
G | A | 9 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237others(6): Show | 9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1568-6685G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182964 | ||||||
| chr8:28183000
|
C | T | 1 | a0001c0001t0002g0088 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1568-6649C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183000 | ||||||
| chr8:28183076
|
C | T | 1 | a0001c0001t0003g0339 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1568-6573C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183076 | ||||||
| chr8:28183158
|
G | A | 1 | a0001c0001t0002g0045 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1568-6491G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183158 | ||||||
| chr8:28183165
|
T | TAAAC | 8 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0241others(5): Show | 8 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1568-6482_1568-647 others(8): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28183165 | |||||
| chr8:28183195
|
G | A | 47 | a0001c0001t0002g0008a0001c0001t0002g0031a0001c0001t0002g0032others(44): Show | 48 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1568-6454G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183195 | ||||||
| chr8:28183531
|
C | A | 3 | a0001c0001t0004g0262a0001c0001t0004g0269a0001c0001t0004g0293 | 3 | HG01074.hp2 HG01167.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1568-6118C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183531 | ||||||
| chr8:28183645
|
G | T | 72 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(69): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1568-6004G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183645 | ||||||
| chr8:28183651
|
C | T | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-5998C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183651 | ||||||
| chr8:28183732
|
C | T | 368 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(365): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1568-5917C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183732 | ||||||
| chr8:28183889
|
G | A | 1 | a0001c0002t0001g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1568-5760G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183889 | ||||||
| chr8:28183916
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1568-5733C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183916 | ||||||
| chr8:28183921
|
A | G | 75 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0004g0002others(72): Show | 81 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1568-5728A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183921 | ||||||
| chr8:28183936
|
T | C | 9 | a0001c0001t0001g0369a0001c0001t0001g0370a0001c0001t0007g0150others(6): Show | 9 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1568-5713T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183936 | ||||||
| chr8:28183964
|
G | A | 1 | a0001c0001t0012g0358 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1568-5685G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183964 | ||||||
| chr8:28184045
|
T | A | 7 | a0001c0001t0006g0240a0001c0001t0006g0253a0001c0001t0006g0254others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1568-5604T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184045 | ||||||
| chr8:28184128
|
A | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(14): Show | 20 | HG00733.hp1 HG01255.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1568-5521A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184128 | ||||||
| chr8:28184154
|
G | A | 1 | a0001c0001t0002g0093 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1568-5495G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184154 | ||||||
| chr8:28184392
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0214 | 2 | NA18967.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1568-5257G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184392 | ||||||
| chr8:28184418
|
G | T | 4 | a0001c0001t0002g0063a0001c0001t0002g0094a0001c0001t0002g0099others(1): Show | 4 | HG01081.hp1 HG01175.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568-5231G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184418 | ||||||
| chr8:28184472
|
A | G | 1 | a0001c0001t0002g0084 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1568-5177A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184472 | ||||||
| chr8:28184578
|
G | A | 15 | a0001c0001t0003g0022a0001c0001t0003g0318a0001c0001t0003g0319others(12): Show | 16 | HG00423.hp1 HG00639.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1568-5071G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184578 | ||||||
| chr8:28184587
|
T | C | 7 | a0001c0001t0002g0070a0001c0001t0002g0076a0001c0001t0002g0088others(4): Show | 7 | NA18966.hp2 NA18988.hp2 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.1568-5062T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184587 | ||||||
| chr8:28184593
|
T | C | 86 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0241others(83): Show | 92 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1568-5056T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184593 | ||||||
| chr8:28184605
|
G | A | 2 | a0001c0001t0001g0309a0001c0001t0001g0310 | 2 | NA18999.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1568-5044G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184605 | ||||||
| chr8:28184670
|
A | G | 161 | a0001c0001t0001g0233a0001c0001t0001g0236a0001c0001t0001g0237others(158): Show | 173 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.1568-4979A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184670 | ||||||
| chr8:28184806
|
T | TGA | 3 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243 | 3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1568-4841_1568-484 others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28184806 | |||||
| chr8:28184876
|
T | C | 1 | a0001c0001t0002g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1568-4773T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184876 | ||||||
| chr8:28184961
|
T | TC | 261 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(258): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1568-4686dupC | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28184961 | |||||
| chr8:28184968
|
CA | C | 15 | a0001c0001t0001g0217a0001c0001t0001g0241a0001c0001t0001g0242others(12): Show | 15 | HG00597.hp1 HG01168.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.1568-4667delA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28184968 | |||||
| chr8:28184999
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1568-4650G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184999 | ||||||
| chr8:28185395
|
A | G | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-4254A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28185395 | ||||||
| chr8:28185617
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0014others(162): Show | 175 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.1568-4032A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28185617 | ||||||
| chr8:28185772
|
A | G | 1 | a0001c0002t0009g0146 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1568-3877A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28185772 | ||||||
| chr8:28185857
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0035others(5): Show | 10 | HG00733.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1568-3792C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28185857 | ||||||
| chr8:28185898
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1568-3751T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28185898 | ||||||
| chr8:28185948
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1568-3701C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28185948 | ||||||
| chr8:28186006
|
A | G | 7 | a0001c0001t0001g0103a0001c0001t0007g0150a0001c0001t0007g0151others(4): Show | 7 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1568-3643A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28186006 | ||||||
| chr8:28186031
|
A | G | 72 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(69): Show | 78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1568-3618A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28186031 | ||||||
| chr8:28186154
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1568-3495A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28186154 | ||||||
| chr8:28186156
|
C | T | 331 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(328): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.1568-3493C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28186156 | ||||||
| chr8:28186618
|
C | T | 1 | a0001c0001t0004g0252 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1568-3031C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28186618 | ||||||
| chr8:28186766
|
A | T | 2 | a0001c0001t0004g0020a0001c0001t0004g0263 | 3 | NA18944.hp2 NA18955.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1568-2883A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28186766 | ||||||
| chr8:28187071
|
G | A | 7 | a0001c0002t0009g0141a0001c0002t0009g0142a0001c0002t0009g0143others(4): Show | 7 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1568-2578G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187071 | ||||||
| chr8:28187172
|
T | C | 1 | a0001c0001t0017g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1568-2477T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187172 | ||||||
| chr8:28187177
|
A | G | 369 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(366): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.1568-2472A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187177 | ||||||
| chr8:28187216
|
C | A | 81 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0035others(78): Show | 89 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1568-2433C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187216 | ||||||
| chr8:28187486
|
C | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0140 | 2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1568-2163C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187486 | ||||||
| chr8:28187568
|
G | A | 1 | a0001c0001t0002g0031 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1568-2081G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187568 | ||||||
| chr8:28187572
|
G | A | 1 | a0001c0001t0007g0153 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1568-2077G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187572 | ||||||
| chr8:28187697
|
G | T | 4 | a0001c0001t0002g0074a0001c0001t0002g0077a0001c0001t0002g0078others(1): Show | 4 | HG01069.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568-1952G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187697 | ||||||
| chr8:28187848
|
T | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(10): Show | 14 | HG02109.hp1 HG02572.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1568-1801T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187848 | ||||||
| chr8:28187851
|
G | A | 1 | a0001c0001t0003g0365 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1568-1798G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187851 | ||||||
| chr8:28188114
|
T | G | 1 | a0001c0001t0002g0084 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1568-1535T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188114 | ||||||
| chr8:28188159
|
C | T | 1 | a0001c0003t0008g0106 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1568-1490C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188159 | ||||||
| chr8:28188180
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1568-1469C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188180 | ||||||
| chr8:28188181
|
C | T | 1 | a0001c0001t0002g0008 | 2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1568-1468C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188181 | ||||||
| chr8:28188194
|
G | A | 8 | a0001c0002t0001g0148a0001c0002t0009g0141a0001c0002t0009g0142others(5): Show | 8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1568-1455G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188194 | ||||||
| chr8:28188342
|
G | C | 1 | a0001c0001t0003g0353 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1568-1307G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188342 | ||||||
| chr8:28188347
|
G | T | 81 | a0001c0001t0001g0320a0001c0001t0002g0008a0001c0001t0002g0012others(78): Show | 84 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.1568-1302G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188347 | ||||||
| chr8:28188356
|
CAAGGGGC others(12): Show |
C | 76 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0003g0003others(73): Show | 82 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1568-1290_1568-127 others(23): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28188356 | |||||
| chr8:28188378
|
T | C | 368 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(365): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1568-1271T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188378 | ||||||
| chr8:28188647
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1568-1002C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188647 | ||||||
| chr8:28188679
|
T | C | 368 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(365): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1568-970T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188679 | ||||||
| chr8:28188706
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1568-943T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188706 | ||||||
| chr8:28188718
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1568-931G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188718 | ||||||
| chr8:28188883
|
T | C | 73 | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(70): Show | 79 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1568-766T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188883 | ||||||
| chr8:28188930
|
C | T | 5 | a0001c0001t0003g0177a0001c0001t0003g0187a0001c0001t0003g0189others(2): Show | 5 | HG00738.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1568-719C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188930 | ||||||
| chr8:28188965
|
A | G | 368 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(365): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1568-684A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188965 | ||||||
| chr8:28188974
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1568-675C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188974 | ||||||
| chr8:28189137
|
A | G | 6 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(3): Show | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-512A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28189137 | ||||||
| chr8:28189174
|
T | G | 6 | a0001c0003t0008g0104a0001c0003t0008g0105a0001c0003t0008g0106others(3): Show | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-475T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28189174 | ||||||
| chr8:28189294
|
C | G | 208 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(205): Show | 226 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1568-355C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28189294 | ||||||
| chr8:28189348
|
A | C | 1 | a0001c0001t0002g0134 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1568-301A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28189348 | ||||||
| chr8:28189444
|
T | A | 368 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(365): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1568-205T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28189444 | ||||||
| chr8:28189593
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1568-56G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28189593 |