| geneid | 26610 |
|---|---|
| ensemblid | ENSG00000109911.19 |
| hgncid | 1171 |
| symbol | ELP4 |
| name | elongator acetyltransferase complex subunit 4 |
| refseq_nuc | NM_019040.5 |
| refseq_prot | NP_061913.3 |
| ensembl_nuc | ENST00000640961.2 |
| ensembl_prot | ENSP00000492152.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 31509767 |
| end | 31790324 |
| strand | + |
| ver | v1.2 |
| region | chr11:31509767-31790324 |
| region5000 | chr11:31504767-31795324 |
| regionname0 | ELP4_chr11_31509767_31790324 |
| regionname5000 | ELP4_chr11_31504767_31795324 |
| 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 | 424 | 261 | 69 | 54 | 99 | 6 | 31 | 79 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0002 | 0/0 | 424 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0003 | 0/0 | 424 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0004 | 0/0 | 424 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0005 | 0/0 | 424 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0006 | 0/0 | 424 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| 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 | 1275 | 253 | 62 | 54 | 98 | 6 | 31 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| c0002 | 0/0 | 1275 | 7 | 7 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| c0003 | 0/0 | 1275 | 5 | 5 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| c0004 | 0/0 | 1275 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| c0005 | 0/0 | 1275 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| c0006 | 0/0 | 1275 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| c0007 | 0/0 | 1275 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| c0008 | 0/0 | 1275 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 6827 | 54 | 6 | 12 | 28 | 1 | 7 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0002 | 1/0 | 6819 | 34 | 0 | 3 | 22 | 2 | 6 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0003 | 0/0 | 6828 | 18 | 1 | 13 | 1 | 1 | 2 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0004 | 0/0 | 6828 | 14 | 3 | 1 | 6 | 0 | 4 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0005 | 0/0 | 6826 | 13 | 6 | 4 | 2 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0006 | 0/0 | 6824 | 7 | 2 | 4 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0007 | 0/0 | 6828 | 7 | 2 | 0 | 4 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0008 | 0/0 | 6826 | 7 | 7 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0009 | 0/0 | 6829 | 6 | 3 | 1 | 1 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0010 | 0/0 | 6820 | 5 | 0 | 1 | 4 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0011 | 0/1 | 6821 | 4 | 1 | 0 | 0 | 0 | 2 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0012 | 0/0 | 6829 | 4 | 0 | 0 | 3 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0013 | 0/0 | 6818 | 3 | 0 | 2 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0014 | 0/0 | 6826 | 3 | 3 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0015 | 0/0 | 6824 | 3 | 0 | 0 | 3 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0016 | 0/0 | 6825 | 3 | 0 | 1 | 2 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0017 | 0/0 | 6826 | 3 | 3 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0018 | 0/0 | 6820 | 3 | 0 | 0 | 2 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0019 | 0/0 | 6829 | 3 | 3 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0020 | 0/0 | 6827 | 3 | 3 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0021 | 0/0 | 6827 | 2 | 0 | 0 | 1 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0022 | 0/0 | 6820 | 2 | 1 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0023 | 0/0 | 6818 | 2 | 0 | 1 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0024 | 0/0 | 6825 | 2 | 2 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0025 | 0/0 | 6823 | 2 | 0 | 0 | 2 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0026 | 0/0 | 6816 | 2 | 1 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0027 | 0/0 | 6825 | 2 | 1 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0028 | 0/0 | 6829 | 2 | 0 | 1 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0029 | 0/0 | 6828 | 2 | 0 | 0 | 2 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0030 | 0/0 | 6826 | 2 | 2 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0031 | 0/0 | 6819 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0032 | 0/0 | 6825 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0033 | 0/0 | 6816 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0034 | 0/0 | 6829 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0035 | 0/0 | 6819 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0036 | 0/0 | 6827 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0037 | 0/0 | 6827 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0038 | 0/0 | 6827 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0039 | 0/0 | 6828 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0040 | 0/0 | 6827 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0041 | 0/0 | 6822 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0042 | 0/0 | 6822 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0043 | 0/0 | 6821 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0044 | 0/0 | 6826 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0045 | 0/0 | 6825 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0046 | 0/0 | 6823 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0047 | 0/0 | 6826 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0048 | 0/0 | 6824 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0049 | 0/0 | 6826 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0050 | 0/0 | 6824 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0051 | 0/0 | 6829 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0052 | 0/0 | 6825 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0053 | 0/0 | 6826 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0054 | 0/0 | 6826 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0055 | 0/0 | 6828 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0056 | 0/0 | 6815 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0057 | 0/0 | 6823 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0058 | 0/0 | 6826 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0059 | 0/0 | 6827 | 1 | 0 | 0 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0060 | 0/0 | 6830 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0061 | 0/0 | 6830 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0062 | 0/0 | 6829 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0063 | 0/0 | 6827 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0064 | 0/0 | 6827 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0065 | 0/0 | 6826 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0066 | 0/0 | 6825 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0067 | 0/0 | 6829 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0068 | 0/0 | 6830 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0069 | 0/0 | 6826 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0070 | 0/0 | 6822 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0071 | 0/0 | 6827 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0072 | 0/0 | 6827 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0073 | 0/0 | 6826 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0074 | 0/0 | 6825 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0075 | 0/0 | 6827 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0076 | 0/0 | 6827 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0077 | 0/0 | 6825 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0078 | 0/0 | 6828 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0079 | 0/0 | 6819 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0080 | 0/0 | 6819 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0081 | 0/0 | 6817 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0082 | 0/0 | 6827 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| t0083 | 0/0 | 6826 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| 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 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0144 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| 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 | 1275 | 253 | 62 | 54 | 98 | 6 | 31 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0002 | 0/0 | 1275 | 7 | 7 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0008 | 0/0 | 1275 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0002c0003 | 0/0 | 1275 | 5 | 5 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0003c0007 | 0/0 | 1275 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0004c0005 | 0/0 | 1275 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0005c0006 | 0/0 | 1275 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0006c0004 | 0/0 | 1275 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8101 | 50 | 3 | 12 | 27 | 1 | 7 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0002 | 1/0 | 8093 | 33 | 0 | 3 | 21 | 2 | 6 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0003 | 0/0 | 8102 | 18 | 1 | 13 | 1 | 1 | 2 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0004 | 0/0 | 8102 | 13 | 2 | 1 | 6 | 0 | 4 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0005 | 0/0 | 8100 | 13 | 6 | 4 | 2 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0006 | 0/0 | 8098 | 7 | 2 | 4 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0007 | 0/0 | 8102 | 7 | 2 | 0 | 4 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0008 | 0/0 | 8100 | 7 | 7 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0009 | 0/0 | 8103 | 5 | 2 | 1 | 1 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0010 | 0/0 | 8094 | 5 | 0 | 1 | 4 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0011 | 0/1 | 8095 | 4 | 1 | 0 | 0 | 0 | 2 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0012 | 0/0 | 8103 | 4 | 0 | 0 | 3 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0013 | 0/0 | 8092 | 3 | 0 | 2 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0015 | 0/0 | 8098 | 3 | 0 | 0 | 3 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0016 | 0/0 | 8099 | 3 | 0 | 1 | 2 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0017 | 0/0 | 8100 | 3 | 3 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0018 | 0/0 | 8094 | 3 | 0 | 0 | 2 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0019 | 0/0 | 8103 | 3 | 3 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0020 | 0/0 | 8101 | 3 | 3 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0021 | 0/0 | 8101 | 2 | 0 | 0 | 1 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0022 | 0/0 | 8094 | 2 | 1 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0023 | 0/0 | 8092 | 2 | 0 | 1 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0025 | 0/0 | 8097 | 2 | 0 | 0 | 2 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0026 | 0/0 | 8090 | 2 | 1 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0027 | 0/0 | 8099 | 2 | 1 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0028 | 0/0 | 8103 | 2 | 0 | 1 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0029 | 0/0 | 8102 | 2 | 0 | 0 | 2 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0030 | 0/0 | 8100 | 2 | 2 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0031 | 0/0 | 8093 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0033 | 0/0 | 8090 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0034 | 0/0 | 8103 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0035 | 0/0 | 8093 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0036 | 0/0 | 8101 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0037 | 0/0 | 8101 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0038 | 0/0 | 8101 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0039 | 0/0 | 8102 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0040 | 0/0 | 8101 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0041 | 0/0 | 8096 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0042 | 0/0 | 8096 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0043 | 0/0 | 8095 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0046 | 0/0 | 8097 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0047 | 0/0 | 8100 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0048 | 0/0 | 8098 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0049 | 0/0 | 8100 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0050 | 0/0 | 8098 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0051 | 0/0 | 8103 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0052 | 0/0 | 8099 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0053 | 0/0 | 8100 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0054 | 0/0 | 8100 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0055 | 0/0 | 8102 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0056 | 0/0 | 8089 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0057 | 0/0 | 8097 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0058 | 0/0 | 8100 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0059 | 0/0 | 8101 | 1 | 0 | 0 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0060 | 0/0 | 8104 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0061 | 0/0 | 8104 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0062 | 0/0 | 8103 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0063 | 0/0 | 8101 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0064 | 0/0 | 8101 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0065 | 0/0 | 8100 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0066 | 0/0 | 8099 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0067 | 0/0 | 8103 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0068 | 0/0 | 8104 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0069 | 0/0 | 8100 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0070 | 0/0 | 8096 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0071 | 0/0 | 8101 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0072 | 0/0 | 8101 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0073 | 0/0 | 8100 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0074 | 0/0 | 8099 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0075 | 0/0 | 8101 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0077 | 0/0 | 8099 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0078 | 0/0 | 8102 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0079 | 0/0 | 8093 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0080 | 0/0 | 8093 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0081 | 0/0 | 8091 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0001t0083 | 0/0 | 8100 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0002t0014 | 0/0 | 8100 | 3 | 3 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0002t0024 | 0/0 | 8099 | 2 | 2 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0002t0044 | 0/0 | 8100 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0002t0045 | 0/0 | 8099 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0001c0008t0002 | 0/0 | 8093 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0002c0003t0001 | 0/0 | 8101 | 3 | 3 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0002c0003t0004 | 0/0 | 8102 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0002c0003t0082 | 0/0 | 8101 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0003c0007t0001 | 0/0 | 8101 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0004c0005t0009 | 0/0 | 8103 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0005c0006t0032 | 0/0 | 8099 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| a0006c0004t0076 | 0/0 | 8101 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | copy fasta | chr11 | 31504767 | 31795324 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0144 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0007g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0007g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0008g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0008g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0008g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0009g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0009g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0009g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0010g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0010g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0010g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0010g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0010g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0011g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0011g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0011g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0012g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0012g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0012g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0012g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0013g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0013g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0013g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0015g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0015g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0015g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0016g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0016g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0016g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0017g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0017g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0017g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0018g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0018g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0018g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0019g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0019g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0019g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0020g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0020g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0020g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0021g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0021g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0022g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0022g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0023g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0023g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0025g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0025g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0026g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0026g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0027g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0027g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0028g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0028g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0029g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0029g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0030g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0030g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0031g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0033g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0034g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0035g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0036g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0037g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0038g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0039g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0040g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0041g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0042g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0043g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0046g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0047g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0048g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0049g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0050g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0051g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0052g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0053g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0054g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0055g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0056g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0057g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0058g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0059g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0060g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0061g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0062g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0063g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0064g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0065g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0066g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0067g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0068g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0069g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0070g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0071g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0072g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0073g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0074g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0075g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0077g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0078g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0079g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0080g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0081g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0001t0083g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0002t0014g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0002t0014g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0002t0014g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0002t0024g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0002t0024g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0002t0044g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0002t0045g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0001c0008t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0002c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0002c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0002c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0002c0003t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0002c0003t0082g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0003c0007t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0004c0005t0009g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0005c0006t0032g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| a0006c0004t0076g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0152 | EUR | FIN | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG00280 | hp2 | a0001 | c0001 | t0059 | g0182 | EUR | FIN | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG00323 | hp1 | a0001 | c0001 | t0013 | g0156 | EUR | FIN | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | FIN | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | CHS | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG00597 | hp2 | a0001 | c0001 | t0037 | g0147 | EAS | CHS | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | CHS | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0193 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0234 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG00642 | hp1 | a0001 | c0001 | t0075 | g0217 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0142 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01069 | hp1 | a0001 | c0001 | t0013 | g0149 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01071 | hp1 | a0001 | c0001 | t0071 | g0024 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01074 | hp1 | a0001 | c0001 | t0054 | g0140 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01074 | hp2 | a0001 | c0001 | t0009 | g0180 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01099 | hp2 | a0001 | c0001 | t0039 | g0212 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01168 | hp2 | a0001 | c0001 | t0013 | g0154 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01169 | hp2 | a0001 | c0001 | t0066 | g0141 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01175 | hp2 | a0001 | c0001 | t0051 | g0134 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01243 | hp2 | a0001 | c0001 | t0026 | g0251 | AMR | PUR | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0029 | AMR | CLM | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | CLM | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0190 | AMR | CLM | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01361 | hp1 | a0001 | c0001 | t0041 | g0129 | AMR | CLM | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | CLM | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01433 | hp2 | a0001 | c0001 | t0010 | g0145 | AMR | CLM | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | CLM | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01496 | hp2 | a0001 | c0001 | t0027 | g0048 | AMR | CLM | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01884 | hp1 | a0002 | c0003 | t0001 | g0096 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01884 | hp2 | a0001 | c0001 | t0064 | g0239 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0093 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01891 | hp2 | a0001 | c0001 | t0081 | g0223 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01943 | hp1 | a0001 | c0001 | t0023 | g0160 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0220 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01981 | hp1 | a0001 | c0001 | t0006 | g0230 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01981 | hp2 | a0001 | c0001 | t0043 | g0153 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01993 | hp1 | a0001 | c0001 | t0028 | g0204 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0229 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02027 | hp1 | a0001 | c0001 | t0015 | g0119 | EAS | KHV | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02056 | hp1 | a0001 | c0001 | t0016 | g0168 | EAS | KHV | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02056 | hp2 | a0001 | c0001 | t0012 | g0035 | EAS | KHV | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | KHV | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02080 | hp2 | a0001 | c0001 | t0047 | g0176 | EAS | KHV | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02132 | hp1 | a0001 | c0001 | t0015 | g0162 | EAS | KHV | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0075 | EAS | KHV | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02145 | hp1 | a0001 | c0001 | t0083 | g0105 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0264 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02148 | hp2 | a0001 | c0001 | t0016 | g0236 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CDX | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02165 | hp2 | a0001 | c0001 | t0015 | g0146 | EAS | CDX | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02257 | hp1 | a0002 | c0003 | t0082 | g0207 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02257 | hp2 | a0001 | c0001 | t0019 | g0095 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02258 | hp2 | a0001 | c0001 | t0062 | g0265 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02273 | hp1 | a0001 | c0001 | t0006 | g0227 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0191 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02280 | hp1 | a0001 | c0001 | t0017 | g0007 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02280 | hp2 | a0001 | c0001 | t0020 | g0241 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0131 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02523 | hp1 | a0001 | c0001 | t0023 | g0121 | EAS | KHV | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02572 | hp1 | a0001 | c0001 | t0022 | g0259 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0218 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0269 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02630 | hp1 | a0001 | c0001 | t0019 | g0233 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02630 | hp2 | a0001 | c0001 | t0027 | g0050 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02647 | hp1 | a0001 | c0002 | t0024 | g0244 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0089 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02698 | hp2 | a0006 | c0004 | t0076 | g0063 | SAS | PJL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02717 | hp1 | a0001 | c0001 | t0030 | g0232 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0216 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02738 | hp1 | a0001 | c0001 | t0042 | g0157 | SAS | PJL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02738 | hp2 | a0001 | c0001 | t0012 | g0023 | SAS | PJL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02809 | hp1 | a0001 | c0001 | t0020 | g0228 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02809 | hp2 | a0001 | c0001 | t0061 | g0086 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02818 | hp1 | a0001 | c0001 | t0048 | g0215 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02818 | hp2 | a0001 | c0001 | t0074 | g0169 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02897 | hp1 | a0001 | c0001 | t0069 | g0080 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02897 | hp2 | a0001 | c0001 | t0052 | g0267 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02922 | hp1 | a0001 | c0001 | t0017 | g0268 | AFR | ESN | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02922 | hp2 | a0001 | c0001 | t0070 | g0219 | AFR | ESN | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03041 | hp1 | a0002 | c0003 | t0004 | g0022 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03041 | hp2 | a0001 | c0001 | t0017 | g0266 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03098 | hp1 | a0001 | c0002 | t0014 | g0097 | AFR | MSL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03098 | hp2 | a0001 | c0002 | t0014 | g0246 | AFR | MSL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03130 | hp1 | a0001 | c0001 | t0049 | g0262 | AFR | ESN | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03130 | hp2 | a0001 | c0002 | t0044 | g0226 | AFR | ESN | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03139 | hp1 | a0001 | c0001 | t0011 | g0011 | AFR | ESN | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03139 | hp2 | a0001 | c0001 | t0009 | g0187 | AFR | ESN | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0092 | AFR | ESN | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03195 | hp2 | a0001 | c0001 | t0079 | g0249 | AFR | ESN | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | MSL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03209 | hp2 | a0005 | c0006 | t0032 | g0253 | AFR | MSL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03225 | hp1 | a0001 | c0001 | t0058 | g0010 | AFR | MSL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03225 | hp2 | a0001 | c0001 | t0077 | g0008 | AFR | MSL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03239 | hp1 | a0001 | c0001 | t0046 | g0172 | SAS | PJL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03239 | hp2 | a0001 | c0001 | t0011 | g0189 | SAS | PJL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03453 | hp1 | a0001 | c0001 | t0019 | g0084 | AFR | MSL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03453 | hp2 | a0001 | c0001 | t0026 | g0252 | AFR | MSL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0184 | SAS | PJL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03516 | hp1 | a0001 | c0001 | t0060 | g0202 | AFR | ESN | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0257 | AFR | ESN | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03540 | hp1 | a0001 | c0002 | t0045 | g0245 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0170 | AFR | GWD | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0045 | SAS | BEB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03831 | hp2 | a0001 | c0001 | t0011 | g0104 | SAS | BEB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03834 | hp1 | a0001 | c0001 | t0009 | g0195 | SAS | BEB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0021 | SAS | BEB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | BEB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0196 | SAS | BEB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03942 | hp2 | a0001 | c0001 | t0072 | g0159 | SAS | BEB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0051 | SAS | STU | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG04184 | hp2 | a0001 | c0001 | t0022 | g0101 | SAS | BEB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0133 | SAS | STU | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0017 | SAS | STU | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG04204 | hp1 | a0001 | c0001 | t0021 | g0107 | SAS | STU | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG04204 | hp2 | a0001 | c0001 | t0018 | g0205 | SAS | STU | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0020 | SAS | STU | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | STU | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18522 | hp1 | a0001 | c0002 | t0024 | g0248 | AFR | YRI | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | YRI | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18747 | hp1 | a0001 | c0001 | t0056 | g0111 | EAS | CHB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18906 | hp1 | a0001 | c0001 | t0080 | g0250 | AFR | YRI | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0231 | AFR | YRI | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18941 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18942 | hp1 | a0001 | c0001 | t0035 | g0108 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18943 | hp1 | a0001 | c0001 | t0068 | g0039 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18943 | hp2 | a0001 | c0001 | t0010 | g0122 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18947 | hp1 | a0001 | c0001 | t0010 | g0132 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18951 | hp1 | a0001 | c0001 | t0067 | g0161 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18954 | hp1 | a0001 | c0001 | t0025 | g0155 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18954 | hp2 | a0001 | c0001 | t0018 | g0031 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18960 | hp1 | a0001 | c0001 | t0065 | g0030 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18967 | hp1 | a0001 | c0001 | t0078 | g0099 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18970 | hp1 | a0001 | c0001 | t0055 | g0083 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18971 | hp1 | a0003 | c0007 | t0001 | g0225 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18974 | hp2 | a0001 | c0001 | t0057 | g0087 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18978 | hp1 | a0001 | c0001 | t0012 | g0136 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0163 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18984 | hp2 | a0001 | c0001 | t0031 | g0125 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18987 | hp1 | a0001 | c0001 | t0007 | g0054 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18987 | hp2 | a0001 | c0001 | t0025 | g0224 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18989 | hp2 | a0001 | c0001 | t0028 | g0201 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18990 | hp1 | a0001 | c0001 | t0010 | g0009 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18991 | hp1 | a0001 | c0008 | t0002 | g0113 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18991 | hp2 | a0001 | c0001 | t0007 | g0072 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18994 | hp1 | a0001 | c0001 | t0016 | g0171 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18994 | hp2 | a0001 | c0001 | t0012 | g0038 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA18999 | hp2 | a0001 | c0001 | t0007 | g0081 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19004 | hp1 | a0001 | c0001 | t0007 | g0158 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0061 | AFR | LWK | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19030 | hp2 | a0001 | c0001 | t0050 | g0235 | AFR | LWK | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19043 | hp1 | a0001 | c0001 | t0034 | g0238 | AFR | LWK | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19043 | hp2 | a0001 | c0001 | t0063 | g0047 | AFR | LWK | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19060 | hp1 | a0001 | c0001 | t0029 | g0165 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19065 | hp2 | a0001 | c0001 | t0040 | g0059 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19066 | hp1 | a0001 | c0001 | t0021 | g0112 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19068 | hp2 | a0001 | c0001 | t0009 | g0198 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19070 | hp1 | a0001 | c0001 | t0029 | g0164 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19079 | hp1 | a0001 | c0001 | t0038 | g0053 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19082 | hp1 | a0001 | c0001 | t0018 | g0013 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19082 | hp2 | a0001 | c0001 | t0010 | g0110 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19083 | hp2 | a0001 | c0001 | t0036 | g0090 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19240 | hp1 | a0001 | c0001 | t0053 | g0049 | AFR | YRI | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0240 | AFR | YRI | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0094 | AFR | ASW | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0270 | AFR | ASW | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0137 | EUR | TSI | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0192 | EUR | TSI | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | GIH | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02486 | hp1 | a0001 | c0001 | t0030 | g0247 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG02486 | hp2 | a0004 | c0005 | t0009 | g0188 | AFR | ACB | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0071 | AFR | MSL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG03471 | hp2 | a0001 | c0002 | t0014 | g0256 | AFR | MSL | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG06807 | hp1 | a0001 | c0001 | t0073 | g0237 | AFR | USA | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0209 | AFR | USA | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0208 | AFR | USA | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | USA | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA21309 | hp1 | a0001 | c0001 | t0020 | g0242 | AFR | LWK | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| NA21309 | hp2 | a0001 | c0001 | t0033 | g0060 | AFR | LWK | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0011 | g0197 | REF | REF | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0144 | REF | REF | ELP4_chr11_31504767_31795324 | ELP4 | chr11 | 31504767 | 31795324 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:31539740
|
T | C | 1 | a0006 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.338T>C | p.Leu113Ser | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/10 | 356/8093 | 338/1275 | 113/424 | chr11 | 31539740 | ||
| chr11:31627132
|
A | G | 1 | a0003 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.676A>G | p.Lys226Glu | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/10 | 694/8093 | 676/1275 | 226/424 | chr11 | 31627132 | ||
| chr11:31632376
|
A | C | 1 | a0005 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.898A>C | p.Ile300Leu | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/10 | 916/8093 | 898/1275 | 300/424 | chr11 | 31632376 | ||
| chr11:31650129
|
C | G | 1 | a0004 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.1051C>G | p.Arg351Gly | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/10 | 1069/8093 | 1051/1275 | 351/424 | chr11 | 31650129 | ||
| chr11:31783469
|
G | T | 1 | a0002 | 5 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(2): Show |
missense_variant | MODERATE | c.1220G>T | p.Arg407Leu | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 1238/8093 | 1220/1275 | 407/424 | chr11 | 31783469 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:31509847
|
C | G | 1 | a0001c0008 | 1 | NA18991.hp1 | synonymous_variant | LOW | c.63C>G | p.Ala21Ala | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/10 | 81/8093 | 63/1275 | 21/424 | chr11 | 31509847 | ||
| chr11:31783497
|
C | T | 2 | a0001c0002a0005c0006 | 8 | HG02647.hp1 HG03098.hp1 HG03098.hp2 others(5): Show |
synonymous_variant | LOW | c.1248C>T | p.Ala416Ala | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 1266/8093 | 1248/1275 | 416/424 | chr11 | 31783497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:31509771
|
C | G | 3 | a0001c0001t0081a0001c0001t0083a0002c0003t0082 | 3 | HG01891.hp2 HG02145.hp1 HG02257.hp1 |
5_prime_UTR_variant | MODIFIER | c.-14C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/10 | 14 | chr11 | 31509771 | |||||
| chr11:31783567
|
T | C | 1 | a0001c0001t0031 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*43T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 43 | chr11 | 31783567 | |||||
| chr11:31783721
|
T | G | 1 | a0005c0006t0032 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*197T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 197 | chr11 | 31783721 | |||||
| chr11:31783754
|
T | C | 1 | a0001c0001t0033 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*230T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 230 | chr11 | 31783754 | |||||
| chr11:31783865
|
A | C | 2 | a0001c0001t0079a0001c0001t0080 | 2 | HG03195.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*341A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 341 | chr11 | 31783865 | |||||
| chr11:31784172
|
A | G | 1 | a0001c0001t0030 | 2 | HG02486.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*648A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 648 | chr11 | 31784172 | |||||
| chr11:31784427
|
G | A | 1 | a0001c0001t0034 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*903G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 903 | chr11 | 31784427 | |||||
| chr11:31784452
|
G | A | 1 | a0001c0001t0035 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*928G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 928 | chr11 | 31784452 | |||||
| chr11:31784474
|
A | G | 1 | a0001c0001t0078 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*950A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 950 | chr11 | 31784474 | |||||
| chr11:31784630
|
G | A | 1 | a0001c0001t0036 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1106G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 1106 | chr11 | 31784630 | |||||
| chr11:31784818
|
T | C | 1 | a0001c0001t0037 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1294T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 1294 | chr11 | 31784818 | |||||
| chr11:31785307
|
T | G | 1 | a0001c0001t0038 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1783T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 1783 | chr11 | 31785307 | |||||
| chr11:31785335
|
A | C | 1 | a0001c0001t0077 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1811A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 1811 | chr11 | 31785335 | |||||
| chr11:31785497
|
A | G | 1 | a0006c0004t0076 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1973A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 1973 | chr11 | 31785497 | |||||
| chr11:31785564
|
G | C | 1 | a0001c0001t0039 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2040G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 2040 | chr11 | 31785564 | |||||
| chr11:31785638
|
C | G | 9 | a0001c0001t0008a0001c0001t0020a0001c0001t0030others(6): Show | 18 | HG00642.hp1 HG02145.hp1 HG02280.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2114C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 2114 | chr11 | 31785638 | |||||
| chr11:31785976
|
C | T | 49 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(46): Show | 166 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*2452C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 2452 | chr11 | 31785976 | |||||
| chr11:31786049
|
C | A | 1 | a0001c0001t0051 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2525C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 2525 | chr11 | 31786049 | |||||
| chr11:31786196
|
CTG | C | 4 | a0001c0001t0017a0001c0001t0027a0001c0001t0052others(1): Show | 7 | HG01496.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2673_*2674delTG | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 2673 | chr11 | 31786196 | |||||
| chr11:31786264
|
G | A | 1 | a0001c0001t0054 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2740G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 2740 | chr11 | 31786264 | |||||
| chr11:31786616
|
T | C | 2 | a0001c0001t0055a0001c0001t0056 | 2 | NA18747.hp1 NA18970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3092T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3092 | chr11 | 31786616 | |||||
| chr11:31786687
|
T | TAAAA | 51 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(48): Show | 169 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*3164_*3165insAAAA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3165 | INFO_REALIGN_3_PRIME | chr11 | 31786687 | ||||
| chr11:31786732
|
C | T | 77 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(74): Show | 219 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*3208C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3208 | chr11 | 31786732 | |||||
| chr11:31786854
|
A | G | 1 | a0001c0001t0072 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3330A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3330 | chr11 | 31786854 | |||||
| chr11:31786949
|
C | T | 1 | a0001c0001t0071 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3425C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3425 | chr11 | 31786949 | |||||
| chr11:31787033
|
A | G | 2 | a0001c0001t0026a0001c0001t0081 | 3 | HG01243.hp2 HG01891.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3509A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3509 | chr11 | 31787033 | |||||
| chr11:31787035
|
C | A | 1 | a0001c0001t0057 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3511C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3511 | chr11 | 31787035 | |||||
| chr11:31787037
|
A | AAAAT | 75 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(72): Show | 217 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*3514_*3517dupAAAT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3518 | INFO_REALIGN_3_PRIME | chr11 | 31787037 | ||||
| chr11:31787037
|
A | T | 1 | a0001c0001t0057 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3513A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3513 | chr11 | 31787037 | |||||
| chr11:31787042
|
T | A | 1 | a0001c0001t0070 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3518T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3518 | chr11 | 31787042 | |||||
| chr11:31787044
|
T | A | 1 | a0001c0001t0070 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3520T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3520 | chr11 | 31787044 | |||||
| chr11:31787227
|
G | A | 11 | a0001c0001t0003a0001c0001t0009a0001c0001t0011others(8): Show | 36 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*3703G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3703 | chr11 | 31787227 | |||||
| chr11:31787375
|
C | T | 2 | a0001c0001t0049a0001c0001t0050 | 2 | HG03130.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3851C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3851 | chr11 | 31787375 | |||||
| chr11:31787441
|
G | A | 1 | a0001c0001t0079 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3917G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3917 | chr11 | 31787441 | |||||
| chr11:31787518
|
C | A | 2 | a0001c0001t0034a0001c0001t0061 | 2 | HG02809.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3994C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3994 | chr11 | 31787518 | |||||
| chr11:31787522
|
C | T | 20 | a0001c0001t0006a0001c0001t0008a0001c0001t0015others(17): Show | 41 | HG00639.hp2 HG00642.hp1 HG01243.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3998C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 3998 | chr11 | 31787522 | |||||
| chr11:31787629
|
C | T | 4 | a0001c0001t0017a0001c0001t0027a0001c0001t0052others(1): Show | 7 | HG01496.hp2 HG02280.hp1 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4105C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 4105 | chr11 | 31787629 | |||||
| chr11:31787696
|
A | C | 2 | a0001c0001t0027a0001c0001t0053 | 3 | HG01496.hp2 HG02630.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4172A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 4172 | chr11 | 31787696 | |||||
| chr11:31787774
|
C | T | 30 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(27): Show | 119 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*4250C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 4250 | chr11 | 31787774 | |||||
| chr11:31788498
|
C | T | 1 | a0001c0001t0048 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4974C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 4974 | chr11 | 31788498 | |||||
| chr11:31788750
|
T | A | 51 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(48): Show | 169 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*5226T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 5226 | chr11 | 31788750 | |||||
| chr11:31788871
|
T | C | 2 | a0001c0001t0015a0001c0001t0047 | 4 | HG02027.hp1 HG02080.hp2 HG02132.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5347T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 5347 | chr11 | 31788871 | |||||
| chr11:31789085
|
A | G | 1 | a0001c0002t0045 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5561A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 5561 | chr11 | 31789085 | |||||
| chr11:31789092
|
C | T | 3 | a0001c0001t0008a0001c0001t0074a0001c0001t0075 | 9 | HG00642.hp1 HG02572.hp2 HG02615.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5568C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 5568 | chr11 | 31789092 | |||||
| chr11:31789517
|
G | A | 1 | a0001c0001t0061 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5993G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 5993 | chr11 | 31789517 | |||||
| chr11:31789577
|
TA | T | 5 | a0001c0001t0023a0001c0001t0050a0001c0001t0069others(2): Show | 6 | HG01943.hp1 HG02523.hp1 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6067delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 6067 | INFO_REALIGN_3_PRIME | chr11 | 31789577 | ||||
| chr11:31789578
|
A | T | 1 | a0001c0001t0031 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6054A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 6054 | chr11 | 31789578 | |||||
| chr11:31789642
|
T | G | 1 | a0001c0001t0064 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6118T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 6118 | chr11 | 31789642 | |||||
| chr11:31789912
|
C | CT | 17 | a0001c0001t0007a0001c0001t0008a0001c0001t0012others(14): Show | 40 | HG00642.hp1 HG01981.hp2 HG02055.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*6411dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 6412 | INFO_REALIGN_3_PRIME | chr11 | 31789912 | ||||
| chr11:31789912
|
CT | C | 16 | a0001c0001t0003a0001c0001t0009a0001c0001t0011others(13): Show | 44 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*6411delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 6411 | INFO_REALIGN_3_PRIME | chr11 | 31789912 | ||||
| chr11:31790074
|
T | C | 1 | a0001c0001t0042 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6550T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 6550 | chr11 | 31790074 | |||||
| chr11:31790097
|
C | A | 1 | a0001c0001t0058 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6573C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 6573 | chr11 | 31790097 | |||||
| chr11:31790097
|
C | CA | 27 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(24): Show | 102 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*6596dupA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 6597 | INFO_REALIGN_3_PRIME | chr11 | 31790097 | ||||
| chr11:31790097
|
C | CAA | 20 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(17): Show | 65 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*6595_*6596dupAA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 6597 | INFO_REALIGN_3_PRIME | chr11 | 31790097 | ||||
| chr11:31790097
|
C | CAAA | 15 | a0001c0001t0009a0001c0001t0020a0001c0001t0041others(12): Show | 21 | HG00642.hp1 HG01074.hp2 HG01175.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*6594_*6596dupAAA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 6597 | INFO_REALIGN_3_PRIME | chr11 | 31790097 | ||||
| chr11:31790097
|
CAAAAA | C | 3 | a0001c0001t0011a0001c0001t0079a0001c0001t0080 | 6 | HG03139.hp1 HG03195.hp2 HG03239.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6592_*6596delAAAA others(1): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 6592 | INFO_REALIGN_3_PRIME | chr11 | 31790097 | ||||
| chr11:31790097
|
CAAAAAA | C | 4 | a0001c0001t0018a0001c0001t0026a0001c0001t0033others(1): Show | 7 | HG01243.hp2 HG01891.hp2 HG03453.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6591_*6596delAAAA others(2): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 6591 | INFO_REALIGN_3_PRIME | chr11 | 31790097 | ||||
| chr11:31790097
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0056 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6586_*6596delAAAA others(7): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 6586 | INFO_REALIGN_3_PRIME | chr11 | 31790097 | ||||
| chr11:31790260
|
GA | G | 30 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(27): Show | 116 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*6746delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 10/10 | 6746 | INFO_REALIGN_3_PRIME | chr11 | 31790260 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:31510019
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0004g0001 | 3 | NA18977.hp1 NA18989.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.223+12G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31510019 | ||||||
| chr11:31510080
|
T | G | 1 | a0001c0001t0001g0004 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.223+73T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31510080 | ||||||
| chr11:31510324
|
G | A | 4 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0017g0007others(1): Show | 4 | HG02280.hp1 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+317G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31510324 | ||||||
| chr11:31510376
|
C | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.223+369C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31510376 | ||||||
| chr11:31510618
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.223+611A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31510618 | ||||||
| chr11:31510677
|
A | T | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.223+670A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31510677 | ||||||
| chr11:31510680
|
C | T | 2 | a0001c0001t0008g0269a0001c0001t0008g0270 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.223+673C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31510680 | ||||||
| chr11:31510924
|
A | G | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | NA18946.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.223+917A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31510924 | ||||||
| chr11:31510960
|
T | A | 1 | a0001c0001t0010g0009 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.223+953T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31510960 | ||||||
| chr11:31511080
|
A | G | 4 | a0001c0001t0001g0258a0001c0001t0004g0257a0001c0001t0022g0259others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+1073A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31511080 | ||||||
| chr11:31511205
|
A | G | 1 | a0001c0001t0001g0255 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.223+1198A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31511205 | ||||||
| chr11:31511326
|
A | G | 1 | a0001c0001t0002g0254 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.223+1319A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31511326 | ||||||
| chr11:31511412
|
T | C | 3 | a0001c0001t0005g0012a0001c0001t0011g0011a0001c0001t0058g0010 | 3 | HG02615.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.223+1405T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31511412 | ||||||
| chr11:31511508
|
A | G | 36 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(33): Show | 36 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.223+1501A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31511508 | ||||||
| chr11:31511961
|
A | C | 1 | a0005c0006t0032g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.223+1954A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31511961 | ||||||
| chr11:31511987
|
A | G | 3 | a0001c0001t0017g0266a0001c0001t0017g0268a0001c0001t0052g0267 | 3 | HG02897.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.223+1980A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31511987 | ||||||
| chr11:31512150
|
G | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(90): Show | 93 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.223+2143G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31512150 | ||||||
| chr11:31512188
|
G | T | 2 | a0001c0001t0026g0251a0001c0001t0026g0252 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.223+2181G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31512188 | ||||||
| chr11:31512420
|
A | T | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.223+2413A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31512420 | ||||||
| chr11:31512523
|
G | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.223+2516G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31512523 | ||||||
| chr11:31512615
|
C | T | 1 | a0003c0007t0001g0225 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.223+2608C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31512615 | ||||||
| chr11:31512791
|
G | GC | 15 | a0001c0001t0001g0016a0001c0001t0002g0015a0001c0001t0002g0100others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.223+2791dupC | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 31512791 | |||||
| chr11:31512891
|
T | C | 1 | a0001c0001t0001g0018 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.223+2884T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31512891 | ||||||
| chr11:31513037
|
A | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.223+3030A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31513037 | ||||||
| chr11:31513306
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.223+3299T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31513306 | ||||||
| chr11:31513808
|
G | A | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.223+3801G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31513808 | ||||||
| chr11:31513814
|
C | T | 2 | a0001c0001t0079g0249a0001c0001t0080g0250 | 2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.223+3807C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31513814 | ||||||
| chr11:31514372
|
G | T | 130 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(127): Show | 130 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.223+4365G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31514372 | ||||||
| chr11:31514677
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.223+4670G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31514677 | ||||||
| chr11:31514758
|
A | G | 3 | a0001c0001t0002g0102a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG03927.hp1 HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.223+4751A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31514758 | ||||||
| chr11:31515001
|
A | ATG | 18 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0004g0017others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.224-5023_224-5022d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 31515001 | |||||
| chr11:31515001
|
A | ATGTG | 4 | a0001c0001t0005g0264a0001c0001t0008g0270a0001c0001t0062g0265others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+5024_224-5022d others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 31515001 | |||||
| chr11:31515001
|
ATG | A | 26 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0002g0106others(23): Show | 26 | HG02027.hp1 HG02135.hp1 HG02523.hp1 others(23): Show |
intron_variant | MODIFIER | c.224-5023_224-5022d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 31515001 | |||||
| chr11:31515031
|
GTGTA | G | 3 | a0001c0001t0002g0260a0001c0001t0002g0261a0002c0003t0004g0022 | 3 | HG03041.hp1 NA18946.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.224-5023_224-5020d others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 31515031 | |||||
| chr11:31515033
|
G | A | 16 | a0001c0001t0002g0102a0001c0001t0002g0106a0001c0001t0002g0109others(13): Show | 16 | HG01074.hp2 HG01109.hp1 HG03453.hp2 others(13): Show |
intron_variant | MODIFIER | c.224-5023G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31515033 | ||||||
| chr11:31515033
|
G | GTA | 78 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(75): Show | 78 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.224-5001_224-5000d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 31515033 | |||||
| chr11:31515033
|
G | GTATA | 21 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0032others(18): Show | 21 | HG00280.hp2 HG00621.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.224-5003_224-5000d others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 31515033 | |||||
| chr11:31515033
|
G | GTATATA | 3 | a0001c0001t0001g0019a0001c0001t0012g0023a0001c0001t0071g0024 | 3 | HG01071.hp1 HG02300.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.224-5005_224-5000d others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 31515033 | |||||
| chr11:31515033
|
G | GTGTA | 9 | a0001c0001t0001g0088a0001c0001t0001g0263a0001c0001t0003g0220others(6): Show | 9 | HG00323.hp1 HG01943.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.224-5022_224-5021i others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 31515033 | |||||
| chr11:31515033
|
GTA | G | 23 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0174others(20): Show | 23 | HG00642.hp1 HG01109.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.224-5001_224-5000d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 31515033 | |||||
| chr11:31515035
|
A | G | 27 | a0001c0001t0001g0179a0001c0001t0002g0166a0001c0001t0002g0167others(24): Show | 27 | HG00597.hp1 HG01891.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.224-5021A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31515035 | ||||||
| chr11:31515037
|
A | G | 8 | a0001c0001t0001g0174a0001c0001t0002g0173a0001c0001t0002g0175others(5): Show | 8 | HG01891.hp2 HG02027.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.224-5019A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31515037 | ||||||
| chr11:31515039
|
A | G | 7 | a0001c0001t0001g0174a0001c0001t0002g0126a0001c0001t0002g0173others(4): Show | 7 | HG01891.hp2 HG02027.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.224-5017A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31515039 | ||||||
| chr11:31515255
|
A | G | 1 | a0001c0001t0010g0009 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.224-4801A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31515255 | ||||||
| chr11:31515650
|
C | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.224-4406C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31515650 | ||||||
| chr11:31515721
|
C | T | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0017g0007 | 3 | HG02280.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.224-4335C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31515721 | ||||||
| chr11:31515839
|
A | G | 2 | a0001c0001t0013g0154a0001c0001t0022g0101 | 2 | HG01168.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.224-4217A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31515839 | ||||||
| chr11:31515892
|
C | T | 3 | a0001c0001t0005g0012a0001c0001t0011g0011a0001c0001t0058g0010 | 3 | HG02615.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.224-4164C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31515892 | ||||||
| chr11:31515974
|
A | G | 140 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(137): Show | 140 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.224-4082A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31515974 | ||||||
| chr11:31516136
|
T | C | 1 | a0001c0001t0052g0267 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.224-3920T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31516136 | ||||||
| chr11:31516511
|
T | G | 1 | a0001c0001t0009g0180 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.224-3545T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31516511 | ||||||
| chr11:31516524
|
C | A | 1 | a0001c0001t0008g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.224-3532C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31516524 | ||||||
| chr11:31516524
|
C | T | 94 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(91): Show | 94 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.224-3532C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31516524 | ||||||
| chr11:31516549
|
G | A | 1 | a0001c0001t0068g0039 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.224-3507G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31516549 | ||||||
| chr11:31516553
|
T | C | 1 | a0001c0001t0041g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.224-3503T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31516553 | ||||||
| chr11:31516592
|
C | T | 1 | a0001c0001t0034g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.224-3464C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31516592 | ||||||
| chr11:31516608
|
T | G | 185 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(182): Show | 185 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(182): Show |
intron_variant | MODIFIER | c.224-3448T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31516608 | ||||||
| chr11:31516670
|
T | G | 1 | a0001c0001t0042g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.224-3386T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31516670 | ||||||
| chr11:31516779
|
A | C | 2 | a0001c0001t0002g0221a0001c0001t0002g0222 | 2 | NA18971.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.224-3277A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31516779 | ||||||
| chr11:31516834
|
T | A | 1 | a0001c0001t0020g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.224-3222T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31516834 | ||||||
| chr11:31516848
|
T | A | 1 | a0001c0001t0020g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.224-3208T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31516848 | ||||||
| chr11:31517180
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.224-2876C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31517180 | ||||||
| chr11:31517229
|
G | A | 1 | a0001c0001t0064g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.224-2827G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31517229 | ||||||
| chr11:31517555
|
A | G | 139 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(136): Show | 139 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.224-2501A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31517555 | ||||||
| chr11:31517636
|
T | TTTTTTTT others(50): Show |
1 | a0001c0001t0028g0204 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.224-2420_224-2419i others(59): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31517636 | ||||||
| chr11:31517637
|
A | G | 1 | a0001c0001t0028g0204 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.224-2419A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31517637 | ||||||
| chr11:31517639
|
T | C | 1 | a0001c0001t0028g0204 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.224-2417T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31517639 | ||||||
| chr11:31517648
|
A | G | 1 | a0001c0001t0028g0204 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.224-2408A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31517648 | ||||||
| chr11:31517672
|
A | G | 1 | a0001c0001t0022g0259 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.224-2384A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31517672 | ||||||
| chr11:31518040
|
G | A | 37 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(34): Show | 37 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.224-2016G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31518040 | ||||||
| chr11:31518114
|
T | C | 94 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(91): Show | 94 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.224-1942T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31518114 | ||||||
| chr11:31518141
|
T | C | 1 | a0001c0001t0003g0206 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.224-1915T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31518141 | ||||||
| chr11:31518244
|
T | C | 1 | a0001c0001t0001g0018 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.224-1812T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31518244 | ||||||
| chr11:31518348
|
C | T | 44 | a0001c0001t0001g0185a0001c0001t0002g0221a0001c0001t0002g0222others(41): Show | 44 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.224-1708C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31518348 | ||||||
| chr11:31518494
|
A | AT | 39 | a0001c0001t0002g0177a0001c0001t0002g0221a0001c0001t0002g0222others(36): Show | 39 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.224-1543dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 31518494 | |||||
| chr11:31518494
|
AT | A | 7 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 7 | HG00323.hp1 HG03041.hp1 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.224-1543delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 31518494 | |||||
| chr11:31518688
|
A | G | 2 | a0001c0001t0083g0105a0002c0003t0082g0207 | 2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.224-1368A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31518688 | ||||||
| chr11:31518768
|
T | C | 139 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(136): Show | 139 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.224-1288T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31518768 | ||||||
| chr11:31518895
|
C | CA | 58 | a0001c0001t0001g0042a0001c0001t0001g0114a0001c0001t0001g0243others(55): Show | 58 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(55): Show |
intron_variant | MODIFIER | c.224-1140dupA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 31518895 | |||||
| chr11:31518895
|
CA | C | 10 | a0001c0001t0002g0100a0001c0001t0002g0150a0001c0001t0002g0151others(7): Show | 10 | HG00280.hp1 HG01069.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-1140delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 31518895 | |||||
| chr11:31518922
|
G | A | 2 | a0001c0001t0008g0208a0001c0001t0008g0209 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.224-1134G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31518922 | ||||||
| chr11:31518978
|
A | G | 1 | a0001c0001t0006g0234 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.224-1078A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31518978 | ||||||
| chr11:31519220
|
A | G | 94 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(91): Show | 94 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.224-836A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31519220 | ||||||
| chr11:31519236
|
T | G | 1 | a0001c0001t0013g0149 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.224-820T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31519236 | ||||||
| chr11:31519347
|
A | G | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.224-709A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31519347 | ||||||
| chr11:31519438
|
A | G | 1 | a0001c0001t0013g0156 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.224-618A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31519438 | ||||||
| chr11:31519440
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.224-616A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31519440 | ||||||
| chr11:31519513
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.224-543G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31519513 | ||||||
| chr11:31519622
|
C | T | 5 | a0001c0001t0001g0041a0001c0001t0001g0079a0001c0001t0001g0255others(2): Show | 5 | NA18942.hp2 NA18946.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-434C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31519622 | ||||||
| chr11:31519957
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.224-99A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 1/9 | chr11 | 31519957 | ||||||
| chr11:31520197
|
A | G | 1 | a0001c0001t0025g0155 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.259+106A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31520197 | ||||||
| chr11:31520427
|
G | A | 4 | a0001c0001t0001g0174a0001c0001t0002g0173a0001c0001t0002g0175others(1): Show | 4 | HG02027.hp2 HG02080.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+336G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31520427 | ||||||
| chr11:31520729
|
C | T | 1 | a0001c0001t0010g0009 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.259+638C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31520729 | ||||||
| chr11:31520849
|
C | T | 1 | a0001c0001t0019g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.259+758C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31520849 | ||||||
| chr11:31520921
|
G | A | 2 | a0001c0001t0083g0105a0002c0003t0082g0207 | 2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.259+830G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31520921 | ||||||
| chr11:31520927
|
A | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+836A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31520927 | ||||||
| chr11:31521110
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.259+1019G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31521110 | ||||||
| chr11:31521137
|
C | T | 1 | a0001c0001t0004g0257 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.259+1046C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31521137 | ||||||
| chr11:31521489
|
CAT | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+1399_259+1400d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31521489 | ||||||
| chr11:31521590
|
T | G | 1 | a0001c0001t0004g0078 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.259+1499T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31521590 | ||||||
| chr11:31521954
|
C | A | 1 | a0001c0001t0002g0130 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.259+1863C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31521954 | ||||||
| chr11:31522398
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+2307A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31522398 | ||||||
| chr11:31522634
|
G | A | 4 | a0001c0001t0009g0240a0001c0001t0020g0228a0001c0001t0020g0241others(1): Show | 4 | HG02280.hp2 HG02809.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+2543G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31522634 | ||||||
| chr11:31522859
|
CT | C | 8 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0258others(5): Show | 8 | HG01993.hp1 HG02300.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+2785delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31522859 | |||||
| chr11:31523039
|
A | AT | 45 | a0001c0001t0001g0077a0001c0001t0001g0185a0001c0001t0002g0221others(42): Show | 45 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.259+2961dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31523039 | |||||
| chr11:31523039
|
AT | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+2961delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31523039 | |||||
| chr11:31523182
|
A | G | 1 | a0001c0001t0003g0184 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.259+3091A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31523182 | ||||||
| chr11:31523257
|
A | G | 7 | a0001c0001t0008g0208a0001c0001t0008g0209a0001c0001t0008g0216others(4): Show | 7 | HG00642.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+3166A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31523257 | ||||||
| chr11:31523428
|
G | A | 1 | a0001c0001t0074g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.259+3337G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31523428 | ||||||
| chr11:31523748
|
A | T | 1 | a0001c0001t0070g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.259+3657A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31523748 | ||||||
| chr11:31523947
|
T | C | 7 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0152others(4): Show | 7 | HG00280.hp1 HG01069.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.259+3856T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31523947 | ||||||
| chr11:31523994
|
C | T | 2 | a0001c0001t0008g0208a0001c0001t0008g0209 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.259+3903C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31523994 | ||||||
| chr11:31524230
|
A | G | 139 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(136): Show | 139 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.259+4139A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31524230 | ||||||
| chr11:31524306
|
A | T | 1 | a0001c0001t0062g0265 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.259+4215A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31524306 | ||||||
| chr11:31524360
|
G | A | 1 | a0001c0001t0003g0190 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.259+4269G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31524360 | ||||||
| chr11:31524394
|
G | A | 1 | a0001c0001t0004g0078 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.259+4303G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31524394 | ||||||
| chr11:31524476
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+4385C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31524476 | ||||||
| chr11:31524719
|
T | C | 1 | a0001c0001t0050g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.259+4628T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31524719 | ||||||
| chr11:31524765
|
A | T | 1 | a0001c0001t0002g0222 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.259+4674A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31524765 | ||||||
| chr11:31524767
|
G | A | 3 | a0001c0001t0009g0240a0001c0001t0020g0241a0001c0001t0020g0242 | 3 | HG02280.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.259+4676G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31524767 | ||||||
| chr11:31524987
|
T | A | 139 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(136): Show | 139 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.259+4896T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31524987 | ||||||
| chr11:31525287
|
T | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+5196T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31525287 | ||||||
| chr11:31525446
|
C | T | 2 | a0001c0001t0008g0092a0001c0001t0060g0202 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.259+5355C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31525446 | ||||||
| chr11:31525680
|
G | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(180): Show | 183 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(180): Show |
intron_variant | MODIFIER | c.259+5589G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31525680 | ||||||
| chr11:31525986
|
A | G | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0017g0007 | 3 | HG02280.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.259+5895A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31525986 | ||||||
| chr11:31526159
|
T | C | 1 | a0001c0001t0005g0005 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.259+6068T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31526159 | ||||||
| chr11:31526385
|
T | A | 36 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(33): Show | 36 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.259+6294T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31526385 | ||||||
| chr11:31526540
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+6449G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31526540 | ||||||
| chr11:31526975
|
G | A | 139 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(136): Show | 139 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.259+6884G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31526975 | ||||||
| chr11:31527387
|
C | A | 3 | a0001c0001t0001g0118a0001c0001t0002g0117a0003c0007t0001g0225 | 3 | NA18968.hp2 NA18971.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.259+7296C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31527387 | ||||||
| chr11:31527481
|
T | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+7390T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31527481 | ||||||
| chr11:31527603
|
A | G | 1 | a0001c0001t0077g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.259+7512A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31527603 | ||||||
| chr11:31527735
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.259+7644G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31527735 | ||||||
| chr11:31527865
|
A | G | 1 | a0001c0001t0003g0214 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.259+7774A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31527865 | ||||||
| chr11:31527931
|
T | C | 2 | a0001c0001t0025g0155a0001c0001t0025g0224 | 2 | NA18954.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.259+7840T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31527931 | ||||||
| chr11:31527949
|
C | T | 1 | a0001c0001t0013g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.259+7858C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31527949 | ||||||
| chr11:31528047
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.259+7956T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31528047 | ||||||
| chr11:31528196
|
C | T | 1 | a0001c0001t0005g0021 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.259+8105C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31528196 | ||||||
| chr11:31528283
|
G | T | 1 | a0001c0001t0046g0172 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.259+8192G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31528283 | ||||||
| chr11:31529040
|
G | GTA | 44 | a0001c0001t0001g0258a0001c0001t0002g0120a0001c0001t0002g0173others(41): Show | 44 | HG00639.hp2 HG01243.hp2 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.259+8965_259+8966d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31529040 | |||||
| chr11:31529071
|
A | G | 3 | a0001c0001t0017g0266a0001c0001t0017g0268a0001c0001t0052g0267 | 3 | HG02897.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.259+8980A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31529071 | ||||||
| chr11:31529115
|
G | GA | 20 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0052others(17): Show | 20 | HG01123.hp2 HG01891.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.259+9039dupA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31529115 | |||||
| chr11:31529274
|
C | T | 5 | a0001c0001t0002g0100a0001c0001t0002g0148a0001c0001t0007g0158others(2): Show | 5 | HG00597.hp2 HG00621.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+9183C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31529274 | ||||||
| chr11:31529543
|
T | C | 2 | a0001c0001t0003g0181a0001c0001t0003g0184 | 2 | HG02055.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.259+9452T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31529543 | ||||||
| chr11:31529608
|
G | C | 1 | a0001c0001t0005g0131 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.259+9517G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31529608 | ||||||
| chr11:31529619
|
A | G | 1 | a0001c0001t0060g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.259+9528A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31529619 | ||||||
| chr11:31530343
|
G | T | 10 | a0001c0001t0001g0243a0001c0001t0005g0012a0001c0001t0011g0011others(7): Show | 10 | HG01109.hp2 HG01243.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.260-9319G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31530343 | ||||||
| chr11:31530384
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.260-9278G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31530384 | ||||||
| chr11:31530411
|
G | T | 1 | a0001c0001t0002g0151 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.260-9251G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31530411 | ||||||
| chr11:31530469
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-9193G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31530469 | ||||||
| chr11:31530615
|
A | G | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.260-9047A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31530615 | ||||||
| chr11:31530691
|
T | G | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.260-8971T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31530691 | ||||||
| chr11:31530700
|
G | A | 2 | a0001c0001t0001g0258a0001c0001t0005g0028 | 2 | HG00621.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.260-8962G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31530700 | ||||||
| chr11:31530877
|
G | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(93): Show | 96 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.260-8785G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31530877 | ||||||
| chr11:31531052
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0069g0080 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.260-8610A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31531052 | ||||||
| chr11:31531158
|
T | C | 4 | a0001c0001t0001g0258a0001c0001t0004g0257a0001c0001t0022g0259others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-8504T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31531158 | ||||||
| chr11:31531269
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-8393C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31531269 | ||||||
| chr11:31531324
|
T | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-8338T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31531324 | ||||||
| chr11:31531386
|
T | C | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.260-8276T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31531386 | ||||||
| chr11:31531747
|
T | C | 4 | a0001c0001t0001g0258a0001c0001t0004g0257a0001c0001t0022g0259others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-7915T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31531747 | ||||||
| chr11:31531856
|
A | G | 2 | a0001c0001t0001g0258a0001c0002t0014g0256 | 2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.260-7806A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31531856 | ||||||
| chr11:31532292
|
G | T | 1 | a0001c0001t0005g0131 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.260-7370G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31532292 | ||||||
| chr11:31532637
|
T | A | 4 | a0001c0001t0009g0240a0001c0001t0020g0228a0001c0001t0020g0241others(1): Show | 4 | HG02280.hp2 HG02809.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-7025T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31532637 | ||||||
| chr11:31532675
|
A | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-6987A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31532675 | ||||||
| chr11:31532767
|
T | A | 1 | a0001c0001t0040g0059 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.260-6895T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31532767 | ||||||
| chr11:31532770
|
G | GT | 5 | a0001c0001t0001g0179a0001c0001t0004g0075a0001c0001t0005g0264others(2): Show | 5 | HG02055.hp2 HG02135.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-6874dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31532770 | |||||
| chr11:31532770
|
GT | G | 6 | a0001c0001t0001g0174a0001c0001t0002g0175a0001c0001t0006g0229others(3): Show | 6 | HG01993.hp2 HG02080.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.260-6874delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31532770 | |||||
| chr11:31532807
|
C | T | 140 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(137): Show | 140 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.260-6855C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31532807 | ||||||
| chr11:31532881
|
C | G | 36 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(33): Show | 36 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.260-6781C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31532881 | ||||||
| chr11:31533028
|
G | T | 1 | a0001c0001t0015g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.260-6634G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31533028 | ||||||
| chr11:31533368
|
C | CT | 5 | a0001c0001t0002g0130a0001c0001t0004g0091a0001c0001t0016g0171others(2): Show | 5 | HG02145.hp1 HG02602.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-6267dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533368
|
C | CTTT | 5 | a0001c0001t0008g0270a0001c0001t0017g0266a0001c0001t0017g0268others(2): Show | 5 | HG02258.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.260-6269_260-6267d others(5): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533368
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0069g0080 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.260-6276_260-6267d others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533368
|
C | CTTTTTTT others(4): Show |
8 | a0001c0001t0001g0076a0001c0001t0001g0088a0001c0001t0007g0089others(5): Show | 8 | HG01891.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-6277_260-6267d others(13): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533368
|
C | CTTTTTTT others(5): Show |
23 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0046others(20): Show | 23 | HG01071.hp1 HG01081.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.260-6278_260-6267d others(14): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533368
|
C | CTTTTTTT others(6): Show |
16 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0032others(13): Show | 16 | HG00621.hp1 HG00738.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.260-6279_260-6267d others(15): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533368
|
C | CTTTTTTT others(7): Show |
12 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0055others(9): Show | 12 | HG01175.hp1 HG02132.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.260-6280_260-6267d others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533368
|
C | CTTTTTTT others(8): Show |
9 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0042others(6): Show | 9 | HG00323.hp2 HG01928.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.260-6281_260-6267d others(17): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533368
|
C | CTTTTTTT others(9): Show |
3 | a0001c0001t0001g0098a0001c0001t0004g0071a0001c0001t0007g0081 | 3 | HG03471.hp1 NA18983.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.260-6282_260-6267d others(18): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533368
|
C | CTTTTTTT others(10): Show |
9 | a0001c0001t0001g0073a0001c0001t0005g0005a0001c0001t0005g0006others(6): Show | 9 | HG01496.hp2 HG02523.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.260-6283_260-6267d others(19): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533368
|
C | CTTTTTTT others(11): Show |
4 | a0001c0001t0001g0058a0001c0001t0001g0074a0001c0001t0007g0045others(1): Show | 4 | HG01934.hp1 HG02280.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-6284_260-6267d others(20): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533368
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0001g0082 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.260-6286_260-6267d others(22): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533368
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0004g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.260-6287_260-6267d others(23): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533368
|
CT | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(93): Show | 96 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.260-6267delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533368
|
CTT | C | 10 | a0001c0001t0001g0243a0001c0001t0003g0186a0001c0001t0006g0231others(7): Show | 10 | HG01069.hp1 HG01069.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.260-6268_260-6267d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533368
|
CTTT | C | 30 | a0001c0001t0001g0258a0001c0001t0002g0222a0001c0001t0004g0257others(27): Show | 30 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(27): Show |
intron_variant | MODIFIER | c.260-6269_260-6267d others(5): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533368 | |||||
| chr11:31533417
|
G | T | 43 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(40): Show | 43 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.260-6245G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31533417 | ||||||
| chr11:31533506
|
T | C | 1 | a0001c0001t0058g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.260-6156T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31533506 | ||||||
| chr11:31533520
|
T | C | 1 | a0001c0001t0020g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.260-6142T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31533520 | ||||||
| chr11:31533702
|
T | G | 36 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(33): Show | 36 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.260-5960T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31533702 | ||||||
| chr11:31533817
|
T | C | 1 | a0001c0001t0051g0134 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.260-5845T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31533817 | ||||||
| chr11:31533825
|
TTTTTG | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-5813_260-5809d others(7): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31533825 | |||||
| chr11:31533855
|
A | C | 1 | a0001c0001t0077g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.260-5807A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31533855 | ||||||
| chr11:31534027
|
C | T | 5 | a0001c0001t0008g0216a0001c0001t0008g0218a0001c0001t0048g0215others(2): Show | 5 | HG00642.hp1 HG02257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-5635C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31534027 | ||||||
| chr11:31534266
|
G | GGT | 4 | a0001c0001t0001g0004a0001c0001t0003g0220a0001c0001t0022g0101others(1): Show | 4 | HG01943.hp2 HG04184.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-5371_260-5370d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31534266 | |||||
| chr11:31534266
|
G | GGTGT | 42 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0032others(39): Show | 42 | HG00738.hp1 HG01123.hp2 HG01258.hp1 others(39): Show |
intron_variant | MODIFIER | c.260-5373_260-5370d others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31534266 | |||||
| chr11:31534266
|
G | GGTGTGT | 56 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0025others(53): Show | 56 | HG00323.hp2 HG00621.hp1 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.260-5375_260-5370d others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31534266 | |||||
| chr11:31534266
|
G | GGTGTGTG others(1): Show |
27 | a0001c0001t0004g0075a0001c0001t0004g0078a0001c0001t0005g0264others(24): Show | 27 | HG00639.hp2 HG01891.hp2 HG01981.hp1 others(24): Show |
intron_variant | MODIFIER | c.260-5377_260-5370d others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31534266 | |||||
| chr11:31534266
|
G | GGTGTGTG others(3): Show |
9 | a0001c0001t0001g0258a0001c0001t0004g0257a0001c0001t0005g0012others(6): Show | 9 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.260-5379_260-5370d others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31534266 | |||||
| chr11:31534266
|
G | GGTGTGTG others(5): Show |
2 | a0001c0001t0049g0262a0001c0001t0064g0239 | 2 | HG01884.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.260-5381_260-5370d others(14): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31534266 | |||||
| chr11:31534266
|
G | GGTGTGTG others(7): Show |
1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.260-5383_260-5370d others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31534266 | |||||
| chr11:31534266
|
G | GGTGTGTG others(9): Show |
1 | a0001c0002t0044g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.260-5385_260-5370d others(18): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31534266 | |||||
| chr11:31534478
|
T | G | 1 | a0001c0001t0001g0114 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.260-5184T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31534478 | ||||||
| chr11:31534621
|
A | G | 1 | a0001c0001t0004g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.260-5041A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31534621 | ||||||
| chr11:31534758
|
A | G | 1 | a0001c0001t0039g0212 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.260-4904A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31534758 | ||||||
| chr11:31534791
|
G | T | 1 | a0001c0001t0003g0220 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.260-4871G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31534791 | ||||||
| chr11:31534918
|
A | G | 1 | a0001c0001t0033g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.260-4744A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31534918 | ||||||
| chr11:31535015
|
C | T | 1 | a0001c0001t0016g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.260-4647C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31535015 | ||||||
| chr11:31535028
|
T | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-4634T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31535028 | ||||||
| chr11:31535199
|
A | G | 1 | a0001c0001t0010g0122 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.260-4463A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31535199 | ||||||
| chr11:31535206
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-4456C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31535206 | ||||||
| chr11:31535327
|
C | T | 2 | a0001c0001t0006g0231a0001c0001t0073g0237 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.260-4335C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31535327 | ||||||
| chr11:31535573
|
C | T | 1 | a0001c0001t0005g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.260-4089C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31535573 | ||||||
| chr11:31535691
|
A | G | 1 | a0001c0001t0061g0086 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.260-3971A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31535691 | ||||||
| chr11:31535899
|
T | A | 1 | a0001c0001t0071g0024 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.260-3763T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31535899 | ||||||
| chr11:31536200
|
TA | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-3452delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31536200 | |||||
| chr11:31536413
|
G | A | 1 | a0001c0001t0077g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.260-3249G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31536413 | ||||||
| chr11:31536494
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.260-3168C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31536494 | ||||||
| chr11:31536561
|
A | G | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.260-3101A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31536561 | ||||||
| chr11:31536582
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-3080C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31536582 | ||||||
| chr11:31536628
|
A | C | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.260-3034A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31536628 | ||||||
| chr11:31536642
|
G | A | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.260-3020G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31536642 | ||||||
| chr11:31536802
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.260-2860C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31536802 | ||||||
| chr11:31536848
|
T | C | 1 | a0002c0003t0082g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.260-2814T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31536848 | ||||||
| chr11:31536975
|
T | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-2687T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31536975 | ||||||
| chr11:31537225
|
G | A | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.260-2437G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31537225 | ||||||
| chr11:31537356
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.260-2306A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31537356 | ||||||
| chr11:31537402
|
C | CT | 140 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(137): Show | 140 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.260-2258dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31537402 | |||||
| chr11:31537536
|
T | C | 4 | a0001c0001t0001g0174a0001c0001t0002g0173a0001c0001t0002g0175others(1): Show | 4 | HG02027.hp2 HG02080.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-2126T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31537536 | ||||||
| chr11:31537543
|
A | G | 1 | a0001c0001t0002g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.260-2119A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31537543 | ||||||
| chr11:31537753
|
C | A | 1 | a0001c0002t0044g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.260-1909C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31537753 | ||||||
| chr11:31538111
|
G | A | 132 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(129): Show | 132 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.260-1551G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31538111 | ||||||
| chr11:31538220
|
A | G | 7 | a0001c0001t0002g0102a0001c0001t0002g0130a0001c0001t0002g0177others(4): Show | 7 | HG01168.hp2 HG02602.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.260-1442A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31538220 | ||||||
| chr11:31538589
|
A | T | 3 | a0001c0001t0001g0118a0001c0001t0002g0117a0003c0007t0001g0225 | 3 | NA18968.hp2 NA18971.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.260-1073A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31538589 | ||||||
| chr11:31538965
|
A | G | 6 | a0001c0001t0001g0258a0001c0001t0004g0257a0001c0001t0022g0259others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.260-697A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31538965 | ||||||
| chr11:31539024
|
G | A | 1 | a0001c0001t0002g0221 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.260-638G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31539024 | ||||||
| chr11:31539273
|
G | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.260-389G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31539273 | ||||||
| chr11:31539294
|
G | C | 140 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(137): Show | 140 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.260-368G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | chr11 | 31539294 | ||||||
| chr11:31539563
|
GA | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-91delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 31539563 | |||||
| chr11:31539899
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+116C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31539899 | ||||||
| chr11:31540021
|
T | C | 1 | a0001c0001t0026g0251 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.381+238T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31540021 | ||||||
| chr11:31540203
|
A | T | 1 | a0001c0001t0002g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.381+420A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31540203 | ||||||
| chr11:31540223
|
T | C | 1 | a0001c0001t0015g0162 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.381+440T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31540223 | ||||||
| chr11:31540303
|
G | A | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.381+520G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31540303 | ||||||
| chr11:31540350
|
A | C | 1 | a0001c0001t0005g0142 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.381+567A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31540350 | ||||||
| chr11:31540503
|
A | T | 1 | a0001c0001t0013g0156 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.381+720A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31540503 | ||||||
| chr11:31540505
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+722G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31540505 | ||||||
| chr11:31540776
|
T | C | 36 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(33): Show | 36 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.381+993T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31540776 | ||||||
| chr11:31540853
|
T | C | 1 | a0001c0001t0003g0213 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.381+1070T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31540853 | ||||||
| chr11:31540867
|
G | A | 1 | a0001c0001t0070g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.381+1084G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31540867 | ||||||
| chr11:31540955
|
A | G | 1 | a0001c0001t0002g0167 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.381+1172A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31540955 | ||||||
| chr11:31541435
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+1652A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31541435 | ||||||
| chr11:31541471
|
A | G | 132 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(129): Show | 132 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.381+1688A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31541471 | ||||||
| chr11:31541552
|
A | G | 1 | a0001c0002t0014g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.381+1769A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31541552 | ||||||
| chr11:31541793
|
T | G | 1 | a0001c0001t0005g0131 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.381+2010T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31541793 | ||||||
| chr11:31541976
|
CTT | C | 4 | a0001c0002t0014g0246a0001c0002t0024g0244a0001c0002t0024g0248others(1): Show | 4 | HG02647.hp1 HG03098.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+2194_381+2195d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31541976 | ||||||
| chr11:31542122
|
C | T | 4 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0069others(1): Show | 4 | NA18947.hp2 NA18978.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+2339C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31542122 | ||||||
| chr11:31542420
|
C | T | 36 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(33): Show | 36 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.381+2637C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31542420 | ||||||
| chr11:31542892
|
T | G | 1 | a0001c0001t0001g0032 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.381+3109T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31542892 | ||||||
| chr11:31543302
|
G | T | 1 | a0001c0001t0042g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.381+3519G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31543302 | ||||||
| chr11:31543325
|
G | A | 1 | a0001c0001t0009g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.381+3542G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31543325 | ||||||
| chr11:31543385
|
T | A | 1 | a0001c0001t0040g0059 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.381+3602T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31543385 | ||||||
| chr11:31543412
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+3629C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31543412 | ||||||
| chr11:31543447
|
G | A | 1 | a0001c0001t0005g0191 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.381+3664G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31543447 | ||||||
| chr11:31543465
|
A | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.381+3682A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31543465 | ||||||
| chr11:31543624
|
A | G | 1 | a0001c0001t0070g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.381+3841A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31543624 | ||||||
| chr11:31543732
|
T | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG00738.hp1 HG01258.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+3949T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31543732 | ||||||
| chr11:31543899
|
CTT | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+4118_381+4119d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31543899 | |||||
| chr11:31543918
|
C | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+4135C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31543918 | ||||||
| chr11:31543940
|
G | C | 5 | a0001c0001t0001g0041a0001c0001t0001g0079a0001c0001t0001g0255others(2): Show | 5 | NA18942.hp2 NA18946.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+4157G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31543940 | ||||||
| chr11:31544047
|
G | A | 1 | a0001c0001t0048g0215 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.381+4264G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31544047 | ||||||
| chr11:31544069
|
C | T | 13 | a0001c0001t0005g0012a0001c0001t0008g0216a0001c0001t0008g0218others(10): Show | 13 | HG00642.hp1 HG01243.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.381+4286C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31544069 | ||||||
| chr11:31544081
|
C | T | 2 | a0001c0001t0017g0266a0001c0001t0017g0268 | 2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.381+4298C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31544081 | ||||||
| chr11:31544216
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.381+4433C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31544216 | ||||||
| chr11:31544306
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+4523A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31544306 | ||||||
| chr11:31544329
|
C | T | 1 | a0001c0001t0057g0087 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.381+4546C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31544329 | ||||||
| chr11:31544339
|
G | C | 1 | a0001c0001t0002g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.381+4556G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31544339 | ||||||
| chr11:31544363
|
C | T | 1 | a0001c0001t0041g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.381+4580C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31544363 | ||||||
| chr11:31544430
|
C | T | 1 | a0001c0001t0003g0214 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.381+4647C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31544430 | ||||||
| chr11:31544565
|
C | G | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.381+4782C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31544565 | ||||||
| chr11:31544876
|
A | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.381+5093A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31544876 | ||||||
| chr11:31544928
|
A | C | 267 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(264): Show | 267 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.381+5145A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31544928 | ||||||
| chr11:31545047
|
T | C | 1 | a0001c0001t0037g0147 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.381+5264T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545047 | ||||||
| chr11:31545175
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.381+5392G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545175 | ||||||
| chr11:31545194
|
G | C | 1 | a0001c0001t0001g0079 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.381+5411G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545194 | ||||||
| chr11:31545238
|
A | C | 2 | a0001c0001t0009g0187a0004c0005t0009g0188 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.381+5455A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545238 | ||||||
| chr11:31545354
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.381+5571C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545354 | ||||||
| chr11:31545384
|
G | A | 1 | a0001c0001t0004g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.381+5601G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545384 | ||||||
| chr11:31545414
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+5631C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545414 | ||||||
| chr11:31545453
|
A | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.381+5670A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545453 | ||||||
| chr11:31545515
|
AC | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+5734delC | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31545515 | |||||
| chr11:31545545
|
G | T | 4 | a0001c0001t0004g0091a0001c0001t0057g0087a0001c0001t0067g0161others(1): Show | 4 | NA18943.hp1 NA18951.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+5762G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545545 | ||||||
| chr11:31545586
|
C | A | 1 | a0001c0001t0006g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.381+5803C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545586 | ||||||
| chr11:31545586
|
C | G | 1 | a0001c0001t0008g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.381+5803C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545586 | ||||||
| chr11:31545653
|
G | A | 1 | a0001c0001t0004g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.381+5870G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545653 | ||||||
| chr11:31545686
|
A | C | 5 | a0001c0001t0003g0103a0001c0001t0003g0186a0001c0001t0003g0199others(2): Show | 5 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+5903A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545686 | ||||||
| chr11:31545690
|
A | T | 1 | a0001c0001t0019g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.381+5907A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545690 | ||||||
| chr11:31545759
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.381+5976A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545759 | ||||||
| chr11:31545771
|
G | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(180): Show | 183 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(180): Show |
intron_variant | MODIFIER | c.381+5988G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545771 | ||||||
| chr11:31545779
|
G | A | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.381+5996G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545779 | ||||||
| chr11:31545788
|
T | A | 38 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(35): Show | 38 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.381+6005T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545788 | ||||||
| chr11:31545789
|
G | A | 1 | a0001c0001t0041g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.381+6006G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31545789 | ||||||
| chr11:31546013
|
C | A | 94 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(91): Show | 94 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.381+6230C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546013 | ||||||
| chr11:31546014
|
C | T | 1 | a0001c0001t0002g0106 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.381+6231C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546014 | ||||||
| chr11:31546018
|
T | C | 2 | a0001c0001t0009g0240a0001c0001t0083g0105 | 2 | HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.381+6235T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546018 | ||||||
| chr11:31546019
|
G | A | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.381+6236G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546019 | ||||||
| chr11:31546040
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+6257G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546040 | ||||||
| chr11:31546052
|
G | A | 1 | a0001c0001t0009g0180 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.381+6269G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546052 | ||||||
| chr11:31546171
|
T | C | 1 | a0001c0001t0002g0130 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.381+6388T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546171 | ||||||
| chr11:31546301
|
A | C | 6 | a0001c0001t0004g0071a0001c0001t0007g0014a0001c0001t0027g0048others(3): Show | 6 | HG01496.hp2 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+6518A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546301 | ||||||
| chr11:31546351
|
C | T | 4 | a0001c0001t0004g0091a0001c0001t0057g0087a0001c0001t0067g0161others(1): Show | 4 | NA18943.hp1 NA18951.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+6568C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546351 | ||||||
| chr11:31546355
|
C | A | 1 | a0001c0001t0007g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.381+6572C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546355 | ||||||
| chr11:31546483
|
A | C | 1 | a0001c0001t0041g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.381+6700A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546483 | ||||||
| chr11:31546676
|
A | G | 3 | a0001c0001t0009g0240a0001c0001t0020g0241a0001c0001t0020g0242 | 3 | HG02280.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.381+6893A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546676 | ||||||
| chr11:31546851
|
G | A | 4 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0123others(1): Show | 4 | NA18951.hp2 NA18988.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+7068G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546851 | ||||||
| chr11:31546852
|
T | C | 4 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0123others(1): Show | 4 | NA18951.hp2 NA18988.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+7069T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546852 | ||||||
| chr11:31546944
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.381+7161A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546944 | ||||||
| chr11:31546955
|
G | A | 2 | a0001c0001t0079g0249a0001c0001t0080g0250 | 2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.381+7172G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31546955 | ||||||
| chr11:31547028
|
A | T | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.381+7245A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547028 | ||||||
| chr11:31547101
|
G | C | 9 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0056others(6): Show | 9 | HG01123.hp2 HG01928.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+7318G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547101 | ||||||
| chr11:31547173
|
T | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+7390T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547173 | ||||||
| chr11:31547284
|
T | G | 2 | a0001c0001t0008g0208a0001c0001t0008g0209 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.381+7501T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547284 | ||||||
| chr11:31547313
|
G | A | 1 | a0001c0002t0044g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.381+7530G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547313 | ||||||
| chr11:31547363
|
C | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+7580C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547363 | ||||||
| chr11:31547411
|
A | G | 1 | a0001c0001t0009g0180 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.381+7628A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547411 | ||||||
| chr11:31547454
|
A | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+7671A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547454 | ||||||
| chr11:31547591
|
G | A | 137 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(134): Show | 137 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.381+7808G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547591 | ||||||
| chr11:31547666
|
G | A | 201 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(198): Show | 201 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(198): Show |
intron_variant | MODIFIER | c.381+7883G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547666 | ||||||
| chr11:31547680
|
C | CCAAAAAA others(2214): Show |
1 | a0001c0001t0003g0220 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.381+7913_381+7914i others(2223): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31547680 | |||||
| chr11:31547744
|
A | C | 2 | a0001c0001t0008g0208a0001c0001t0008g0209 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.381+7961A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547744 | ||||||
| chr11:31547784
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.381+8001C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547784 | ||||||
| chr11:31547789
|
C | T | 3 | a0001c0001t0002g0150a0001c0001t0003g0190a0001c0001t0043g0153 | 3 | HG01261.hp2 HG01934.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.381+8006C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547789 | ||||||
| chr11:31547790
|
G | C | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.381+8007G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547790 | ||||||
| chr11:31547918
|
C | T | 2 | a0001c0002t0014g0097a0002c0003t0004g0022 | 2 | HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.381+8135C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547918 | ||||||
| chr11:31547944
|
T | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+8161T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31547944 | ||||||
| chr11:31548016
|
A | C | 1 | a0001c0001t0066g0141 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.381+8233A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548016 | ||||||
| chr11:31548102
|
C | T | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.381+8319C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548102 | ||||||
| chr11:31548172
|
A | G | 1 | a0001c0001t0003g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.381+8389A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548172 | ||||||
| chr11:31548258
|
T | A | 137 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(134): Show | 137 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.381+8475T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548258 | ||||||
| chr11:31548259
|
C | T | 137 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(134): Show | 137 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.381+8476C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548259 | ||||||
| chr11:31548335
|
C | A | 1 | a0001c0001t0001g0135 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.381+8552C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548335 | ||||||
| chr11:31548442
|
C | T | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.381+8659C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548442 | ||||||
| chr11:31548455
|
A | G | 51 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(48): Show | 51 | HG00323.hp2 HG00621.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.381+8672A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548455 | ||||||
| chr11:31548527
|
G | T | 1 | a0001c0001t0002g0166 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.381+8744G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548527 | ||||||
| chr11:31548541
|
G | A | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.381+8758G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548541 | ||||||
| chr11:31548573
|
T | C | 2 | a0001c0002t0024g0244a0001c0002t0045g0245 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.381+8790T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548573 | ||||||
| chr11:31548672
|
G | C | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.381+8889G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548672 | ||||||
| chr11:31548681
|
A | C | 4 | a0001c0001t0003g0186a0001c0001t0003g0199a0001c0001t0003g0200others(1): Show | 4 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+8898A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548681 | ||||||
| chr11:31548716
|
T | C | 1 | a0001c0001t0004g0001 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.381+8933T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548716 | ||||||
| chr11:31548793
|
G | C | 1 | a0001c0001t0062g0265 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.381+9010G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548793 | ||||||
| chr11:31548843
|
A | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(93): Show | 96 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.381+9060A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548843 | ||||||
| chr11:31548893
|
T | C | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.381+9110T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548893 | ||||||
| chr11:31548897
|
A | G | 1 | a0001c0001t0005g0006 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.381+9114A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31548897 | ||||||
| chr11:31549008
|
C | T | 2 | a0001c0001t0030g0232a0001c0001t0030g0247 | 2 | HG02486.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.381+9225C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549008 | ||||||
| chr11:31549015
|
C | A | 2 | a0001c0001t0003g0206a0001c0001t0005g0191 | 2 | HG01496.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.381+9232C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549015 | ||||||
| chr11:31549018
|
A | G | 2 | a0001c0001t0008g0269a0001c0001t0008g0270 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.381+9235A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549018 | ||||||
| chr11:31549044
|
C | T | 136 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(133): Show | 136 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(133): Show |
intron_variant | MODIFIER | c.381+9261C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549044 | ||||||
| chr11:31549045
|
G | C | 1 | a0001c0001t0077g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.381+9262G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549045 | ||||||
| chr11:31549083
|
C | G | 1 | a0006c0004t0076g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.381+9300C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549083 | ||||||
| chr11:31549090
|
T | A | 1 | a0001c0001t0060g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.381+9307T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549090 | ||||||
| chr11:31549141
|
C | G | 2 | a0001c0001t0009g0198a0001c0001t0028g0201 | 2 | NA18989.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.381+9358C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549141 | ||||||
| chr11:31549254
|
A | G | 2 | a0001c0001t0008g0208a0001c0001t0008g0209 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.381+9471A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549254 | ||||||
| chr11:31549268
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.381+9485A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549268 | ||||||
| chr11:31549314
|
T | A | 145 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(142): Show | 145 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(142): Show |
intron_variant | MODIFIER | c.381+9531T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549314 | ||||||
| chr11:31549444
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.381+9661C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549444 | ||||||
| chr11:31549465
|
A | G | 1 | a0001c0001t0042g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.381+9682A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549465 | ||||||
| chr11:31549506
|
T | C | 5 | a0001c0001t0003g0181a0001c0001t0003g0184a0001c0001t0003g0192others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+9723T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549506 | ||||||
| chr11:31549597
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.381+9814G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549597 | ||||||
| chr11:31549756
|
G | T | 1 | a0001c0001t0013g0149 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.381+9973G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549756 | ||||||
| chr11:31549833
|
T | C | 137 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(134): Show | 137 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.381+10050T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549833 | ||||||
| chr11:31549875
|
T | A | 15 | a0001c0001t0001g0243a0001c0001t0005g0012a0001c0001t0008g0216others(12): Show | 15 | HG00642.hp1 HG01109.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+10092T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549875 | ||||||
| chr11:31549910
|
A | C | 145 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(142): Show | 145 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(142): Show |
intron_variant | MODIFIER | c.381+10127A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549910 | ||||||
| chr11:31549999
|
G | T | 1 | a0001c0001t0007g0089 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.381+10216G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31549999 | ||||||
| chr11:31550044
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.381+10261G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31550044 | ||||||
| chr11:31550141
|
A | T | 1 | a0001c0001t0003g0220 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.381+10358A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31550141 | ||||||
| chr11:31550143
|
A | G | 1 | a0001c0001t0062g0265 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.381+10360A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31550143 | ||||||
| chr11:31550150
|
A | G | 10 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(7): Show | 10 | HG00621.hp1 HG02056.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.381+10367A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31550150 | ||||||
| chr11:31550218
|
A | T | 1 | a0001c0001t0054g0140 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.381+10435A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31550218 | ||||||
| chr11:31550388
|
A | G | 1 | a0001c0001t0064g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.381+10605A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31550388 | ||||||
| chr11:31550415
|
C | T | 2 | a0001c0001t0003g0206a0001c0001t0005g0191 | 2 | HG01496.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.381+10632C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31550415 | ||||||
| chr11:31550593
|
A | T | 2 | a0001c0001t0026g0251a0001c0001t0026g0252 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.381+10810A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31550593 | ||||||
| chr11:31551064
|
A | G | 4 | a0001c0001t0005g0264a0001c0001t0017g0266a0001c0001t0017g0268others(1): Show | 4 | HG02145.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+11281A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31551064 | ||||||
| chr11:31551090
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.381+11307T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31551090 | ||||||
| chr11:31551232
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0005g0142 | 2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.381+11449G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31551232 | ||||||
| chr11:31551346
|
G | T | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.381+11563G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31551346 | ||||||
| chr11:31551376
|
A | G | 1 | a0003c0007t0001g0225 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.381+11593A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31551376 | ||||||
| chr11:31551420
|
A | G | 1 | a0001c0001t0021g0112 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.381+11637A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31551420 | ||||||
| chr11:31551442
|
T | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(93): Show | 96 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.381+11659T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31551442 | ||||||
| chr11:31551565
|
G | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0088 | 2 | NA18988.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.381+11782G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31551565 | ||||||
| chr11:31551573
|
A | G | 2 | a0001c0001t0029g0164a0001c0001t0029g0165 | 2 | NA19060.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.381+11790A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31551573 | ||||||
| chr11:31551887
|
T | A | 4 | a0001c0001t0026g0251a0001c0001t0026g0252a0001c0001t0030g0232others(1): Show | 4 | HG01243.hp2 HG02486.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+12104T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31551887 | ||||||
| chr11:31552073
|
T | A | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.381+12290T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31552073 | ||||||
| chr11:31552099
|
T | C | 137 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(134): Show | 137 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.381+12316T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31552099 | ||||||
| chr11:31552123
|
T | C | 2 | a0001c0001t0003g0193a0001c0001t0003g0194 | 2 | HG00639.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.381+12340T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31552123 | ||||||
| chr11:31552177
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+12394C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31552177 | ||||||
| chr11:31552291
|
G | A | 95 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(92): Show | 95 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.381+12508G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31552291 | ||||||
| chr11:31552357
|
C | T | 1 | a0001c0001t0034g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.381+12574C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31552357 | ||||||
| chr11:31552401
|
T | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG00738.hp1 HG01258.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+12618T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31552401 | ||||||
| chr11:31552410
|
C | T | 2 | a0001c0001t0003g0206a0001c0001t0005g0191 | 2 | HG01496.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.381+12627C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31552410 | ||||||
| chr11:31552775
|
C | A | 1 | a0001c0001t0011g0189 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.381+12992C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31552775 | ||||||
| chr11:31552798
|
T | G | 33 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(30): Show | 33 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.381+13015T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31552798 | ||||||
| chr11:31552877
|
C | G | 1 | a0001c0001t0008g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.381+13094C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31552877 | ||||||
| chr11:31553091
|
C | T | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.381+13308C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31553091 | ||||||
| chr11:31553336
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+13553A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31553336 | ||||||
| chr11:31553438
|
C | T | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.381+13655C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31553438 | ||||||
| chr11:31553715
|
T | C | 2 | a0001c0001t0002g0150a0001c0001t0043g0153 | 2 | HG01934.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.381+13932T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31553715 | ||||||
| chr11:31553725
|
A | AAC | 40 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0037others(37): Show | 40 | HG00323.hp1 HG00621.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.381+13981_381+1398 others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31553725 | |||||
| chr11:31553725
|
A | AACAC | 14 | a0001c0001t0001g0034a0001c0001t0001g0062a0001c0001t0001g0088others(11): Show | 14 | HG02056.hp2 HG02647.hp2 HG02698.hp2 others(11): Show |
intron_variant | MODIFIER | c.381+13979_381+1398 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31553725 | |||||
| chr11:31553725
|
A | AACACAC | 47 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(44): Show | 47 | HG00323.hp2 HG00738.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.381+13977_381+1398 others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31553725 | |||||
| chr11:31553725
|
A | AACACACA others(1): Show |
13 | a0001c0001t0001g0055a0001c0001t0001g0058a0001c0001t0001g0064others(10): Show | 13 | HG01934.hp1 HG02630.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.381+13975_381+1398 others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31553725 | |||||
| chr11:31553725
|
A | AACACACA others(3): Show |
1 | a0001c0001t0004g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.381+13973_381+1398 others(14): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31553725 | |||||
| chr11:31553725
|
A | AACACACA others(5): Show |
8 | a0001c0001t0001g0004a0001c0001t0001g0263a0001c0001t0004g0071others(5): Show | 8 | HG01496.hp2 HG03453.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+13971_381+1398 others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31553725 | |||||
| chr11:31553725
|
A | AACACACA others(11): Show |
1 | a0001c0001t0007g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.381+13965_381+1398 others(22): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31553725 | |||||
| chr11:31553725
|
A | ACAC | 3 | a0001c0001t0002g0177a0001c0001t0005g0012a0001c0001t0080g0250 | 3 | HG02615.hp1 HG03927.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.381+13942_381+1394 others(7): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31553725 | ||||||
| chr11:31553725
|
AAC | A | 56 | a0001c0001t0002g0166a0001c0001t0002g0173a0001c0001t0002g0175others(53): Show | 56 | HG00280.hp2 HG00597.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.381+13981_381+1398 others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31553725 | |||||
| chr11:31553725
|
AACAC | A | 28 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0001g0135others(25): Show | 28 | HG00738.hp2 HG01099.hp1 HG01993.hp1 others(25): Show |
intron_variant | MODIFIER | c.381+13979_381+1398 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31553725 | |||||
| chr11:31553725
|
AACACAC | A | 7 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0258others(4): Show | 7 | HG02132.hp2 HG02523.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+13977_381+1398 others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31553725 | |||||
| chr11:31553725
|
AACACACA others(3): Show |
A | 1 | a0001c0002t0014g0256 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.381+13973_381+1398 others(14): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31553725 | |||||
| chr11:31553764
|
A | ACACC | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.381+13982_381+1398 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31553764 | |||||
| chr11:31553764
|
A | C | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.381+13981A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31553764 | ||||||
| chr11:31553766
|
C | A | 1 | a0001c0001t0005g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.381+13983C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31553766 | ||||||
| chr11:31554045
|
C | T | 3 | a0001c0001t0011g0104a0001c0001t0011g0189a0001c0001t0011g0197 | 3 | HG03239.hp2 HG03831.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.381+14262C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31554045 | ||||||
| chr11:31554053
|
G | A | 1 | a0001c0001t0057g0087 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.381+14270G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31554053 | ||||||
| chr11:31554091
|
CCATCACC others(26): Show |
C | 1 | a0001c0001t0015g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.381+14311_381+1434 others(37): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31554091 | |||||
| chr11:31554137
|
T | G | 1 | a0001c0001t0015g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.381+14354T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31554137 | ||||||
| chr11:31554150
|
T | A | 1 | a0001c0001t0015g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.381+14367T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31554150 | ||||||
| chr11:31554165
|
T | A | 1 | a0001c0001t0015g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.381+14382T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31554165 | ||||||
| chr11:31554169
|
T | A | 1 | a0001c0001t0015g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.381+14386T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31554169 | ||||||
| chr11:31554174
|
T | TAATGTAA others(20): Show |
1 | a0001c0001t0015g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.381+14391_381+1439 others(31): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31554174 | ||||||
| chr11:31554175
|
G | T | 1 | a0001c0001t0015g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.381+14392G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31554175 | ||||||
| chr11:31554184
|
T | A | 1 | a0001c0001t0015g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.381+14401T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31554184 | ||||||
| chr11:31554187
|
A | C | 1 | a0001c0001t0015g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.381+14404A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31554187 | ||||||
| chr11:31554209
|
A | T | 1 | a0001c0001t0015g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.381+14426A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31554209 | ||||||
| chr11:31554218
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.381+14435G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31554218 | ||||||
| chr11:31554219
|
TAATGCTC others(49): Show |
T | 1 | a0001c0001t0015g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.381+14439_381+1449 others(60): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31554219 | |||||
| chr11:31554346
|
G | A | 1 | a0001c0001t0020g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.381+14563G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31554346 | ||||||
| chr11:31554793
|
T | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+15010T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31554793 | ||||||
| chr11:31555195
|
T | G | 1 | a0001c0001t0005g0029 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.381+15412T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31555195 | ||||||
| chr11:31555221
|
T | C | 41 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(38): Show | 41 | HG00639.hp2 HG00642.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.381+15438T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31555221 | ||||||
| chr11:31555331
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.381+15548T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31555331 | ||||||
| chr11:31555461
|
T | C | 1 | a0001c0001t0012g0136 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.381+15678T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31555461 | ||||||
| chr11:31555587
|
A | G | 3 | a0001c0001t0009g0240a0001c0001t0020g0241a0001c0001t0020g0242 | 3 | HG02280.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.381+15804A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31555587 | ||||||
| chr11:31556467
|
GCA | G | 95 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(92): Show | 95 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.381+16691_381+1669 others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31556467 | |||||
| chr11:31556711
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.381+16928A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31556711 | ||||||
| chr11:31556717
|
A | C | 1 | a0001c0001t0004g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.381+16934A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31556717 | ||||||
| chr11:31556942
|
G | T | 2 | a0001c0001t0002g0150a0001c0001t0043g0153 | 2 | HG01934.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.381+17159G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31556942 | ||||||
| chr11:31557079
|
A | G | 2 | a0001c0001t0004g0091a0001c0001t0068g0039 | 2 | NA18943.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.381+17296A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31557079 | ||||||
| chr11:31557159
|
A | G | 2 | a0001c0001t0003g0193a0001c0001t0003g0194 | 2 | HG00639.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.381+17376A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31557159 | ||||||
| chr11:31557751
|
G | A | 1 | a0001c0001t0009g0180 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.381+17968G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31557751 | ||||||
| chr11:31557811
|
C | A | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.381+18028C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31557811 | ||||||
| chr11:31558061
|
C | T | 7 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0152others(4): Show | 7 | HG00280.hp1 HG01069.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+18278C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31558061 | ||||||
| chr11:31558129
|
C | T | 7 | a0001c0001t0008g0208a0001c0001t0008g0209a0001c0001t0008g0216others(4): Show | 7 | HG00642.hp1 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.381+18346C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31558129 | ||||||
| chr11:31558361
|
A | G | 1 | a0001c0001t0009g0187 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+18578A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31558361 | ||||||
| chr11:31558389
|
A | G | 1 | a0001c0001t0040g0059 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.381+18606A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31558389 | ||||||
| chr11:31558655
|
G | A | 3 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0004g0044 | 3 | HG01175.hp1 HG03492.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.381+18872G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31558655 | ||||||
| chr11:31559043
|
C | T | 1 | a0001c0001t0070g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.381+19260C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31559043 | ||||||
| chr11:31559188
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+19405A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31559188 | ||||||
| chr11:31559243
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0069g0080 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.381+19460G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31559243 | ||||||
| chr11:31559643
|
C | T | 1 | a0001c0001t0007g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.381+19860C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31559643 | ||||||
| chr11:31559764
|
A | G | 1 | a0001c0001t0016g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.381+19981A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31559764 | ||||||
| chr11:31559818
|
G | A | 1 | a0001c0001t0034g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.381+20035G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31559818 | ||||||
| chr11:31559905
|
T | TA | 170 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(167): Show | 170 | HG00280.hp2 HG00621.hp1 HG00639.hp1 others(167): Show |
intron_variant | MODIFIER | c.381+20138dupA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31559905 | |||||
| chr11:31559905
|
T | TAA | 12 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0055others(9): Show | 12 | HG00323.hp2 HG01081.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+20137_381+2013 others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31559905 | |||||
| chr11:31559986
|
TA | T | 131 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(128): Show | 131 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.381+20212delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31559986 | |||||
| chr11:31560446
|
A | C | 132 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(129): Show | 132 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.381+20663A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31560446 | ||||||
| chr11:31560536
|
C | T | 1 | a0001c0001t0064g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.381+20753C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31560536 | ||||||
| chr11:31560684
|
A | ATTGTTTT others(19): Show |
127 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(124): Show | 127 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(124): Show |
intron_variant | MODIFIER | c.381+20927_381+2095 others(30): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31560684 | |||||
| chr11:31560684
|
A | ATTGTTTT others(45): Show |
8 | a0001c0001t0002g0221a0001c0001t0003g0190a0001c0001t0003g0213others(5): Show | 8 | HG01261.hp2 HG01361.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+20952_381+2095 others(56): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31560684 | |||||
| chr11:31560684
|
A | ATTGTTTT others(71): Show |
1 | a0001c0001t0077g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.381+20952_381+2095 others(82): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31560684 | |||||
| chr11:31560684
|
ATTGTTTT others(19): Show |
A | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.381+20927_381+2095 others(30): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31560684 | |||||
| chr11:31560729
|
A | T | 2 | a0001c0001t0026g0251a0001c0001t0026g0252 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.381+20946A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31560729 | ||||||
| chr11:31560736
|
A | G | 8 | a0001c0001t0003g0213a0001c0001t0005g0264a0001c0001t0008g0269others(5): Show | 8 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+20953A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31560736 | ||||||
| chr11:31560743
|
T | G | 2 | a0001c0001t0026g0251a0001c0001t0026g0252 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.381+20960T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31560743 | ||||||
| chr11:31561436
|
ATTATTTT | A | 51 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(48): Show | 51 | HG00323.hp2 HG00621.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.381+21670_381+2167 others(11): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31561436 | |||||
| chr11:31561669
|
C | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0062others(2): Show | 5 | NA18747.hp2 NA18984.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+21886C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31561669 | ||||||
| chr11:31561927
|
G | A | 1 | a0001c0001t0055g0083 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.381+22144G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31561927 | ||||||
| chr11:31562083
|
C | T | 132 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(129): Show | 132 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.381+22300C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31562083 | ||||||
| chr11:31562130
|
A | G | 1 | a0001c0001t0004g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.381+22347A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31562130 | ||||||
| chr11:31562247
|
T | C | 1 | a0001c0001t0009g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.381+22464T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31562247 | ||||||
| chr11:31562714
|
G | A | 9 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0056others(6): Show | 9 | HG01123.hp2 HG01928.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+22931G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31562714 | ||||||
| chr11:31563371
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.381+23588G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31563371 | ||||||
| chr11:31563374
|
T | A | 2 | a0001c0001t0006g0230a0001c0001t0016g0236 | 2 | HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.381+23591T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31563374 | ||||||
| chr11:31563514
|
C | T | 3 | a0001c0001t0010g0145a0001c0001t0054g0140a0001c0001t0066g0141 | 3 | HG01074.hp1 HG01169.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.381+23731C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31563514 | ||||||
| chr11:31563725
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+23942A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31563725 | ||||||
| chr11:31564297
|
T | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0017g0007 | 3 | HG02280.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.381+24514T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31564297 | ||||||
| chr11:31564378
|
C | CT | 9 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.381+24608dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31564378 | |||||
| chr11:31564620
|
A | T | 132 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(129): Show | 132 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.381+24837A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31564620 | ||||||
| chr11:31564701
|
C | T | 1 | a0001c0001t0012g0136 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.381+24918C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31564701 | ||||||
| chr11:31564908
|
G | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0005g0067 | 3 | HG02132.hp2 HG02523.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.381+25125G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31564908 | ||||||
| chr11:31565099
|
G | A | 95 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(92): Show | 95 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.381+25316G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565099 | ||||||
| chr11:31565411
|
C | T | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.381+25628C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565411 | ||||||
| chr11:31565432
|
A | T | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.381+25649A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565432 | ||||||
| chr11:31565466
|
G | A | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.381+25683G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565466 | ||||||
| chr11:31565477
|
C | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.381+25694C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565477 | ||||||
| chr11:31565490
|
G | A | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.381+25707G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565490 | ||||||
| chr11:31565505
|
C | A | 1 | a0001c0001t0012g0136 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.381+25722C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565505 | ||||||
| chr11:31565506
|
G | A | 3 | a0001c0001t0001g0243a0001c0001t0002g0115a0001c0001t0034g0238 | 3 | HG01109.hp2 NA18988.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.381+25723G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565506 | ||||||
| chr11:31565554
|
G | T | 1 | a0001c0001t0019g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.381+25771G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565554 | ||||||
| chr11:31565593
|
G | T | 1 | a0001c0001t0001g0052 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.381+25810G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565593 | ||||||
| chr11:31565625
|
C | T | 140 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(137): Show | 140 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.381+25842C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565625 | ||||||
| chr11:31565628
|
A | G | 140 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(137): Show | 140 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.381+25845A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565628 | ||||||
| chr11:31565644
|
C | T | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.381+25861C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565644 | ||||||
| chr11:31565881
|
G | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0057others(3): Show | 6 | HG01123.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+26098G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565881 | ||||||
| chr11:31565917
|
C | T | 140 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(137): Show | 140 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.381+26134C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565917 | ||||||
| chr11:31565943
|
G | A | 1 | a0001c0001t0080g0250 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.381+26160G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31565943 | ||||||
| chr11:31566060
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.381+26277G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31566060 | ||||||
| chr11:31566156
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+26373G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31566156 | ||||||
| chr11:31566336
|
C | T | 1 | a0001c0001t0003g0206 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.381+26553C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31566336 | ||||||
| chr11:31566463
|
T | C | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.381+26680T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31566463 | ||||||
| chr11:31566547
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0004g0001others(1): Show | 4 | HG01099.hp2 NA18977.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+26764C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31566547 | ||||||
| chr11:31566593
|
G | A | 5 | a0001c0001t0008g0216a0001c0001t0008g0218a0001c0001t0048g0215others(2): Show | 5 | HG00642.hp1 HG02257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+26810G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31566593 | ||||||
| chr11:31567036
|
AT | A | 132 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(129): Show | 132 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.381+27263delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31567036 | |||||
| chr11:31567158
|
C | T | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.381+27375C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31567158 | ||||||
| chr11:31567377
|
A | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-27393A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31567377 | ||||||
| chr11:31567569
|
G | A | 17 | a0001c0001t0001g0174a0001c0001t0001g0179a0001c0001t0002g0166others(14): Show | 17 | HG00597.hp1 HG02027.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.382-27201G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31567569 | ||||||
| chr11:31567652
|
A | G | 42 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(39): Show | 42 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.382-27118A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31567652 | ||||||
| chr11:31567692
|
A | G | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.382-27078A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31567692 | ||||||
| chr11:31567821
|
A | C | 3 | a0001c0001t0017g0266a0001c0001t0017g0268a0001c0001t0052g0267 | 3 | HG02897.hp2 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.382-26949A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31567821 | ||||||
| chr11:31568007
|
A | G | 1 | a0001c0001t0013g0156 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.382-26763A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31568007 | ||||||
| chr11:31568071
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.382-26699G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31568071 | ||||||
| chr11:31568126
|
A | T | 1 | a0001c0001t0001g0258 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.382-26644A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31568126 | ||||||
| chr11:31568151
|
A | G | 132 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(129): Show | 132 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.382-26619A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31568151 | ||||||
| chr11:31568448
|
A | T | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.382-26322A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31568448 | ||||||
| chr11:31568517
|
G | A | 2 | a0001c0001t0029g0164a0001c0001t0029g0165 | 2 | NA19060.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.382-26253G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31568517 | ||||||
| chr11:31568665
|
G | A | 140 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(137): Show | 140 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.382-26105G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31568665 | ||||||
| chr11:31568845
|
GA | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-25924delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31568845 | ||||||
| chr11:31568944
|
G | C | 1 | a0001c0002t0014g0246 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.382-25826G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31568944 | ||||||
| chr11:31569090
|
A | T | 1 | a0001c0002t0044g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.382-25680A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31569090 | ||||||
| chr11:31569126
|
C | T | 18 | a0001c0001t0006g0227a0001c0001t0006g0229a0001c0001t0006g0230others(15): Show | 18 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.382-25644C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31569126 | ||||||
| chr11:31569525
|
T | G | 8 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0055others(5): Show | 8 | HG00323.hp2 HG01081.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-25245T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31569525 | ||||||
| chr11:31570053
|
G | A | 140 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(137): Show | 140 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.382-24717G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31570053 | ||||||
| chr11:31570090
|
G | A | 1 | a0001c0001t0012g0038 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.382-24680G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31570090 | ||||||
| chr11:31570111
|
A | G | 132 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(129): Show | 132 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.382-24659A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31570111 | ||||||
| chr11:31570128
|
G | T | 1 | a0001c0001t0020g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.382-24642G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31570128 | ||||||
| chr11:31570466
|
C | CT | 5 | a0001c0001t0002g0106a0001c0001t0003g0213a0001c0001t0012g0038others(2): Show | 5 | HG01361.hp2 HG02738.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-24285dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31570466 | |||||
| chr11:31570466
|
CT | C | 115 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(112): Show | 115 | HG00323.hp2 HG00639.hp2 HG00738.hp1 others(112): Show |
intron_variant | MODIFIER | c.382-24285delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31570466 | |||||
| chr11:31570466
|
CTT | C | 7 | a0001c0001t0004g0051a0001c0001t0019g0095a0001c0002t0014g0097others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.382-24286_382-2428 others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31570466 | |||||
| chr11:31570479
|
T | G | 1 | a0001c0001t0008g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.382-24291T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31570479 | ||||||
| chr11:31570790
|
C | CT | 74 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0027others(71): Show | 74 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.382-23955dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31570790 | |||||
| chr11:31570790
|
C | CTT | 5 | a0001c0001t0002g0148a0001c0001t0008g0269a0001c0001t0012g0023others(2): Show | 5 | HG00621.hp2 HG02148.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-23956_382-2395 others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31570790 | |||||
| chr11:31570790
|
CT | C | 6 | a0001c0001t0001g0033a0001c0001t0001g0179a0001c0001t0005g0029others(3): Show | 6 | HG00738.hp1 HG01258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-23955delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31570790 | |||||
| chr11:31570839
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0069g0080 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.382-23931G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31570839 | ||||||
| chr11:31570948
|
C | T | 43 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(40): Show | 43 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.382-23822C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31570948 | ||||||
| chr11:31572035
|
G | A | 1 | a0001c0001t0073g0237 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.382-22735G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31572035 | ||||||
| chr11:31572093
|
A | G | 1 | a0001c0001t0005g0029 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.382-22677A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31572093 | ||||||
| chr11:31572116
|
G | T | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.382-22654G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31572116 | ||||||
| chr11:31572241
|
G | C | 2 | a0001c0001t0008g0269a0001c0001t0008g0270 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.382-22529G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31572241 | ||||||
| chr11:31572325
|
A | C | 43 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(40): Show | 43 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.382-22445A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31572325 | ||||||
| chr11:31572762
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-22008G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31572762 | ||||||
| chr11:31573396
|
C | T | 1 | a0001c0001t0019g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.382-21374C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31573396 | ||||||
| chr11:31573839
|
A | G | 3 | a0001c0001t0003g0186a0001c0001t0003g0199a0001c0001t0003g0200 | 3 | HG00642.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.382-20931A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31573839 | ||||||
| chr11:31573890
|
A | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(180): Show | 183 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(180): Show |
intron_variant | MODIFIER | c.382-20880A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31573890 | ||||||
| chr11:31574022
|
G | A | 2 | a0001c0002t0024g0244a0001c0002t0045g0245 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.382-20748G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31574022 | ||||||
| chr11:31574201
|
C | T | 25 | a0001c0001t0001g0258a0001c0001t0004g0257a0001c0001t0006g0227others(22): Show | 25 | HG00639.hp2 HG01884.hp2 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.382-20569C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31574201 | ||||||
| chr11:31574215
|
C | T | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.382-20555C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31574215 | ||||||
| chr11:31574301
|
G | A | 1 | a0001c0001t0022g0259 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382-20469G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31574301 | ||||||
| chr11:31574509
|
G | A | 1 | a0001c0001t0004g0075 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.382-20261G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31574509 | ||||||
| chr11:31574604
|
A | G | 140 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(137): Show | 140 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.382-20166A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31574604 | ||||||
| chr11:31574619
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.382-20151G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31574619 | ||||||
| chr11:31574782
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-19988C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31574782 | ||||||
| chr11:31574819
|
C | A | 1 | a0001c0001t0008g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.382-19951C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31574819 | ||||||
| chr11:31575038
|
T | C | 1 | a0001c0001t0018g0031 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.382-19732T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31575038 | ||||||
| chr11:31575047
|
G | A | 1 | a0001c0001t0015g0162 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.382-19723G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31575047 | ||||||
| chr11:31575334
|
G | A | 1 | a0001c0001t0003g0190 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.382-19436G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31575334 | ||||||
| chr11:31575349
|
A | C | 1 | a0001c0001t0008g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.382-19421A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31575349 | ||||||
| chr11:31575577
|
C | G | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.382-19193C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31575577 | ||||||
| chr11:31575709
|
G | A | 9 | a0001c0001t0003g0103a0001c0001t0003g0186a0001c0001t0003g0190others(6): Show | 9 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.382-19061G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31575709 | ||||||
| chr11:31575719
|
C | A | 140 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(137): Show | 140 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.382-19051C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31575719 | ||||||
| chr11:31575751
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-19019G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31575751 | ||||||
| chr11:31575775
|
G | A | 2 | a0001c0002t0014g0246a0001c0002t0024g0248 | 2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.382-18995G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31575775 | ||||||
| chr11:31575955
|
G | A | 6 | a0001c0001t0019g0095a0001c0002t0014g0097a0002c0003t0001g0093others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-18815G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31575955 | ||||||
| chr11:31575995
|
A | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-18775A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31575995 | ||||||
| chr11:31575999
|
T | A | 1 | a0001c0001t0008g0269 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.382-18771T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31575999 | ||||||
| chr11:31576069
|
A | G | 1 | a0001c0001t0062g0265 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.382-18701A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31576069 | ||||||
| chr11:31576171
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.382-18599A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31576171 | ||||||
| chr11:31576176
|
G | C | 1 | a0001c0001t0003g0196 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.382-18594G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31576176 | ||||||
| chr11:31576209
|
G | A | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.382-18561G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31576209 | ||||||
| chr11:31576217
|
T | G | 140 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(137): Show | 140 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.382-18553T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31576217 | ||||||
| chr11:31576267
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-18503G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31576267 | ||||||
| chr11:31576357
|
T | C | 9 | a0001c0001t0001g0258a0001c0001t0005g0264a0001c0001t0008g0269others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.382-18413T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31576357 | ||||||
| chr11:31576358
|
G | C | 1 | a0001c0001t0001g0258 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.382-18412G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31576358 | ||||||
| chr11:31576434
|
G | A | 10 | a0001c0001t0001g0243a0001c0001t0005g0012a0001c0001t0011g0011others(7): Show | 10 | HG01109.hp2 HG01243.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-18336G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31576434 | ||||||
| chr11:31576501
|
C | T | 1 | a0001c0002t0044g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.382-18269C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31576501 | ||||||
| chr11:31576505
|
A | G | 1 | a0001c0001t0004g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.382-18265A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31576505 | ||||||
| chr11:31576762
|
T | G | 1 | a0001c0001t0003g0213 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.382-18008T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31576762 | ||||||
| chr11:31576856
|
A | G | 1 | a0001c0001t0055g0083 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.382-17914A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31576856 | ||||||
| chr11:31576947
|
A | G | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.382-17823A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31576947 | ||||||
| chr11:31577171
|
A | G | 5 | a0001c0001t0008g0216a0001c0001t0008g0218a0001c0001t0048g0215others(2): Show | 5 | HG00642.hp1 HG02257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-17599A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31577171 | ||||||
| chr11:31577246
|
A | G | 6 | a0001c0001t0019g0095a0001c0002t0014g0097a0002c0003t0001g0093others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-17524A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31577246 | ||||||
| chr11:31577327
|
T | C | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.382-17443T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31577327 | ||||||
| chr11:31577328
|
G | A | 1 | a0001c0001t0073g0237 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.382-17442G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31577328 | ||||||
| chr11:31577651
|
A | T | 1 | a0001c0001t0004g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.382-17119A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31577651 | ||||||
| chr11:31577652
|
A | G | 1 | a0001c0001t0031g0125 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.382-17118A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31577652 | ||||||
| chr11:31577789
|
G | A | 95 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(92): Show | 95 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.382-16981G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31577789 | ||||||
| chr11:31577909
|
A | G | 1 | a0001c0001t0022g0259 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382-16861A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31577909 | ||||||
| chr11:31577922
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.382-16848A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31577922 | ||||||
| chr11:31578086
|
C | G | 1 | a0001c0001t0001g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.382-16684C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31578086 | ||||||
| chr11:31578105
|
T | C | 132 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(129): Show | 132 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.382-16665T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31578105 | ||||||
| chr11:31578245
|
G | A | 1 | a0001c0001t0006g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.382-16525G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31578245 | ||||||
| chr11:31578363
|
C | T | 95 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(92): Show | 95 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.382-16407C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31578363 | ||||||
| chr11:31578364
|
C | G | 132 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(129): Show | 132 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.382-16406C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31578364 | ||||||
| chr11:31578384
|
A | G | 1 | a0001c0002t0014g0246 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.382-16386A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31578384 | ||||||
| chr11:31578510
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.382-16260C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31578510 | ||||||
| chr11:31578717
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.382-16053G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31578717 | ||||||
| chr11:31578809
|
A | C | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.382-15961A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31578809 | ||||||
| chr11:31578813
|
T | G | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.382-15957T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31578813 | ||||||
| chr11:31578912
|
T | C | 8 | a0001c0001t0005g0012a0001c0001t0011g0011a0001c0001t0019g0233others(5): Show | 8 | HG01243.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-15858T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31578912 | ||||||
| chr11:31579118
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-15652G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31579118 | ||||||
| chr11:31579202
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.382-15568C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31579202 | ||||||
| chr11:31579230
|
A | G | 1 | a0001c0001t0040g0059 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.382-15540A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31579230 | ||||||
| chr11:31579312
|
C | T | 36 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(33): Show | 36 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.382-15458C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31579312 | ||||||
| chr11:31579358
|
A | G | 1 | a0001c0001t0008g0270 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.382-15412A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31579358 | ||||||
| chr11:31579524
|
G | T | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.382-15246G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31579524 | ||||||
| chr11:31579579
|
T | G | 1 | a0001c0001t0077g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.382-15191T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31579579 | ||||||
| chr11:31579632
|
A | G | 3 | a0001c0001t0004g0091a0001c0001t0006g0170a0001c0001t0068g0039 | 3 | HG03540.hp2 NA18943.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.382-15138A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31579632 | ||||||
| chr11:31579705
|
G | T | 6 | a0001c0001t0004g0071a0001c0001t0007g0014a0001c0001t0027g0048others(3): Show | 6 | HG01496.hp2 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-15065G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31579705 | ||||||
| chr11:31579768
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-15002C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31579768 | ||||||
| chr11:31579900
|
A | G | 1 | a0001c0001t0058g0010 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.382-14870A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31579900 | ||||||
| chr11:31580042
|
G | T | 3 | a0001c0001t0001g0258a0001c0001t0004g0257a0001c0002t0014g0256 | 3 | HG02896.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.382-14728G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31580042 | ||||||
| chr11:31580196
|
C | A | 1 | a0001c0001t0001g0258 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.382-14574C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31580196 | ||||||
| chr11:31580318
|
G | C | 1 | a0001c0001t0027g0050 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.382-14452G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31580318 | ||||||
| chr11:31580600
|
C | T | 1 | a0001c0001t0004g0257 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.382-14170C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31580600 | ||||||
| chr11:31580622
|
C | T | 1 | a0001c0001t0071g0024 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.382-14148C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31580622 | ||||||
| chr11:31580641
|
C | T | 140 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(137): Show | 140 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.382-14129C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31580641 | ||||||
| chr11:31581049
|
A | G | 1 | a0001c0001t0056g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.382-13721A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31581049 | ||||||
| chr11:31581251
|
C | G | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.382-13519C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31581251 | ||||||
| chr11:31581473
|
T | TAAAAATA others(713): Show |
3 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0007g0045 | 3 | HG00323.hp2 HG03831.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.382-13284_382-1328 others(724): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31581473 | |||||
| chr11:31581473
|
T | TAAAAATA others(718): Show |
1 | a0001c0001t0001g0098 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.382-13284_382-1328 others(729): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31581473 | |||||
| chr11:31581752
|
CT | C | 131 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(128): Show | 131 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.382-13004delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31581752 | |||||
| chr11:31581960
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.382-12810C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31581960 | ||||||
| chr11:31581961
|
C | G | 3 | a0001c0001t0002g0166a0001c0001t0015g0162a0001c0001t0016g0168 | 3 | HG00597.hp1 HG02056.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.382-12809C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31581961 | ||||||
| chr11:31582942
|
A | G | 1 | a0001c0001t0028g0201 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.382-11828A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31582942 | ||||||
| chr11:31583241
|
A | C | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | NA18946.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.382-11529A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31583241 | ||||||
| chr11:31583327
|
A | T | 1 | a0001c0001t0033g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.382-11443A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31583327 | ||||||
| chr11:31583414
|
G | A | 10 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(7): Show | 10 | HG00621.hp1 HG02056.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-11356G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31583414 | ||||||
| chr11:31583861
|
T | C | 36 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(33): Show | 36 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.382-10909T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31583861 | ||||||
| chr11:31584209
|
T | C | 2 | a0001c0001t0006g0231a0001c0001t0073g0237 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.382-10561T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31584209 | ||||||
| chr11:31584215
|
T | C | 2 | a0001c0001t0006g0231a0001c0001t0073g0237 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.382-10555T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31584215 | ||||||
| chr11:31584349
|
A | T | 16 | a0001c0001t0001g0174a0001c0001t0002g0166a0001c0001t0002g0173others(13): Show | 16 | HG00597.hp1 HG02027.hp2 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.382-10421A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31584349 | ||||||
| chr11:31584600
|
G | C | 140 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(137): Show | 140 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.382-10170G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31584600 | ||||||
| chr11:31584721
|
C | T | 1 | a0001c0001t0020g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.382-10049C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31584721 | ||||||
| chr11:31584859
|
C | A | 1 | a0001c0001t0001g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.382-9911C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31584859 | ||||||
| chr11:31584977
|
C | A | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.382-9793C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31584977 | ||||||
| chr11:31585131
|
C | T | 2 | a0001c0001t0002g0015a0001c0001t0004g0017 | 2 | HG02602.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.382-9639C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31585131 | ||||||
| chr11:31585191
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.382-9579T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31585191 | ||||||
| chr11:31585422
|
G | A | 1 | a0001c0001t0003g0206 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.382-9348G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31585422 | ||||||
| chr11:31585435
|
TA | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0040a0001c0001t0007g0014others(4): Show | 7 | HG01071.hp1 HG02055.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-9321delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31585435 | |||||
| chr11:31585575
|
C | T | 2 | a0001c0001t0029g0164a0001c0001t0029g0165 | 2 | NA19060.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.382-9195C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31585575 | ||||||
| chr11:31585576
|
C | T | 1 | a0001c0001t0003g0220 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.382-9194C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31585576 | ||||||
| chr11:31585689
|
G | A | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.382-9081G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31585689 | ||||||
| chr11:31585808
|
G | T | 2 | a0001c0001t0079g0249a0001c0001t0080g0250 | 2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.382-8962G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31585808 | ||||||
| chr11:31586439
|
G | A | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.382-8331G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31586439 | ||||||
| chr11:31586644
|
G | GT | 9 | a0001c0001t0001g0088a0001c0001t0002g0100a0001c0001t0002g0148others(6): Show | 9 | HG00621.hp2 HG00639.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.382-8115dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31586644 | |||||
| chr11:31586780
|
C | A | 3 | a0001c0001t0003g0192a0001c0001t0003g0210a0001c0001t0003g0211 | 3 | HG01168.hp1 HG01169.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.382-7990C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31586780 | ||||||
| chr11:31587485
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0069g0080 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.382-7285G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31587485 | ||||||
| chr11:31587504
|
T | C | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.382-7266T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31587504 | ||||||
| chr11:31587561
|
C | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.382-7209C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31587561 | ||||||
| chr11:31587662
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0004g0001 | 2 | NA18977.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.382-7108T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31587662 | ||||||
| chr11:31587836
|
A | G | 2 | a0001c0001t0007g0089a0001c0001t0008g0092 | 2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.382-6934A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31587836 | ||||||
| chr11:31588046
|
CAT | C | 23 | a0001c0001t0001g0114a0001c0001t0002g0106a0001c0001t0002g0109others(20): Show | 23 | HG02027.hp1 HG02135.hp1 HG02523.hp1 others(20): Show |
intron_variant | MODIFIER | c.382-6719_382-6718d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31588046 | |||||
| chr11:31588192
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-6578A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31588192 | ||||||
| chr11:31588417
|
T | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(93): Show | 96 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.382-6353T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31588417 | ||||||
| chr11:31588453
|
C | T | 1 | a0001c0001t0034g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382-6317C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31588453 | ||||||
| chr11:31588457
|
G | A | 2 | a0001c0001t0079g0249a0001c0001t0080g0250 | 2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.382-6313G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31588457 | ||||||
| chr11:31588475
|
A | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.382-6295A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31588475 | ||||||
| chr11:31588490
|
G | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-6280G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31588490 | ||||||
| chr11:31588541
|
A | G | 1 | a0001c0001t0003g0196 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.382-6229A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31588541 | ||||||
| chr11:31588589
|
A | T | 1 | a0001c0001t0015g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.382-6181A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31588589 | ||||||
| chr11:31588622
|
C | T | 4 | a0001c0001t0001g0174a0001c0001t0002g0173a0001c0001t0002g0175others(1): Show | 4 | HG02027.hp2 HG02080.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-6148C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31588622 | ||||||
| chr11:31588753
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0088 | 2 | NA18988.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.382-6017C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31588753 | ||||||
| chr11:31588843
|
C | T | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.382-5927C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31588843 | ||||||
| chr11:31588872
|
G | C | 1 | a0001c0001t0002g0126 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.382-5898G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31588872 | ||||||
| chr11:31589127
|
A | G | 1 | a0001c0001t0034g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382-5643A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31589127 | ||||||
| chr11:31589536
|
A | G | 4 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0017g0007others(1): Show | 4 | HG02280.hp1 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-5234A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31589536 | ||||||
| chr11:31589564
|
C | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(93): Show | 96 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.382-5206C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31589564 | ||||||
| chr11:31589584
|
G | C | 4 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0069others(1): Show | 4 | NA18947.hp2 NA18978.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-5186G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31589584 | ||||||
| chr11:31590190
|
C | T | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.382-4580C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31590190 | ||||||
| chr11:31590548
|
A | G | 1 | a0001c0001t0007g0072 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.382-4222A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31590548 | ||||||
| chr11:31590958
|
T | C | 95 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(92): Show | 95 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.382-3812T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31590958 | ||||||
| chr11:31591392
|
C | T | 5 | a0001c0001t0003g0103a0001c0001t0003g0186a0001c0001t0003g0199others(2): Show | 5 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-3378C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31591392 | ||||||
| chr11:31591421
|
AAG | A | 14 | a0001c0001t0001g0019a0001c0001t0001g0074a0001c0001t0001g0258others(11): Show | 14 | HG01175.hp1 HG02055.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.382-3348_382-3347d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31591421 | ||||||
| chr11:31591421
|
AAGG | A | 83 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(80): Show | 83 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.382-3348_382-3346d others(5): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31591421 | ||||||
| chr11:31591421
|
AAGGG | A | 9 | a0001c0001t0001g0098a0001c0001t0003g0183a0001c0001t0003g0193others(6): Show | 9 | HG00639.hp1 HG01081.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.382-3348_382-3345d others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31591421 | ||||||
| chr11:31591422
|
AGG | A | 30 | a0001c0001t0002g0102a0001c0001t0002g0139a0001c0001t0002g0148others(27): Show | 30 | HG00621.hp2 HG00639.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.382-3336_382-3335d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31591422 | |||||
| chr11:31591422
|
AGGG | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(80): Show | 83 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.382-3337_382-3335d others(5): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31591422 | |||||
| chr11:31591422
|
AGGGG | A | 34 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(31): Show | 34 | HG00642.hp1 HG00642.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.382-3338_382-3335d others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31591422 | |||||
| chr11:31591425
|
G | A | 3 | a0001c0001t0002g0260a0001c0001t0012g0136a0001c0001t0042g0157 | 3 | HG02738.hp1 NA18978.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.382-3345G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31591425 | ||||||
| chr11:31591426
|
G | A | 1 | a0001c0001t0028g0201 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.382-3344G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31591426 | ||||||
| chr11:31591435
|
G | A | 2 | a0001c0001t0030g0232a0001c0001t0030g0247 | 2 | HG02486.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.382-3335G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31591435 | ||||||
| chr11:31591543
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0005g0067 | 2 | HG02523.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.382-3227G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31591543 | ||||||
| chr11:31591579
|
A | C | 1 | a0001c0001t0008g0218 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.382-3191A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31591579 | ||||||
| chr11:31591633
|
A | G | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.382-3137A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31591633 | ||||||
| chr11:31591790
|
C | T | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(93): Show | 96 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.382-2980C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31591790 | ||||||
| chr11:31591961
|
T | C | 4 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0017g0007others(1): Show | 4 | HG02280.hp1 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-2809T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31591961 | ||||||
| chr11:31592005
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-2765A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31592005 | ||||||
| chr11:31592006
|
C | T | 1 | a0002c0003t0004g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.382-2764C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31592006 | ||||||
| chr11:31592020
|
C | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.382-2750C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31592020 | ||||||
| chr11:31592038
|
C | G | 2 | a0001c0001t0001g0243a0001c0001t0034g0238 | 2 | HG01109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.382-2732C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31592038 | ||||||
| chr11:31592310
|
G | A | 2 | a0001c0001t0009g0187a0004c0005t0009g0188 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.382-2460G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31592310 | ||||||
| chr11:31592650
|
T | C | 4 | a0001c0001t0005g0264a0001c0001t0017g0266a0001c0001t0017g0268others(1): Show | 4 | HG02145.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-2120T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31592650 | ||||||
| chr11:31592776
|
A | T | 2 | a0001c0001t0008g0208a0001c0001t0008g0209 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.382-1994A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31592776 | ||||||
| chr11:31593227
|
C | CTGT | 19 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0025others(16): Show | 19 | HG01981.hp1 HG02280.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.382-1502_382-1500d others(5): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31593227 | |||||
| chr11:31593227
|
C | CTGTTGT | 28 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0062others(25): Show | 28 | HG00639.hp2 HG01071.hp1 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.382-1505_382-1500d others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31593227 | |||||
| chr11:31593227
|
C | CTGTTGTT others(2): Show |
51 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0032others(48): Show | 51 | HG00323.hp2 HG00738.hp1 HG01123.hp2 others(48): Show |
intron_variant | MODIFIER | c.382-1508_382-1500d others(11): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31593227 | |||||
| chr11:31593227
|
C | CTGTTGTT others(5): Show |
22 | a0001c0001t0001g0036a0001c0001t0001g0052a0001c0001t0001g0055others(19): Show | 22 | HG01175.hp1 HG01496.hp2 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.382-1511_382-1500d others(14): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31593227 | |||||
| chr11:31593227
|
C | CTGTTGTT others(8): Show |
4 | a0001c0001t0001g0041a0001c0001t0005g0028a0001c0001t0018g0031others(1): Show | 4 | HG00621.hp1 NA18942.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-1514_382-1500d others(17): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31593227 | |||||
| chr11:31593227
|
C | CTGTTGTT others(11): Show |
2 | a0001c0001t0001g0046a0001c0001t0001g0079 | 2 | HG01081.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.382-1517_382-1500d others(20): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31593227 | |||||
| chr11:31593227
|
CTGTTGTT others(8): Show |
C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.382-1514_382-1500d others(17): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr11 | 31593227 | |||||
| chr11:31593446
|
G | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-1324G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31593446 | ||||||
| chr11:31593481
|
T | C | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.382-1289T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31593481 | ||||||
| chr11:31593772
|
C | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-998C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31593772 | ||||||
| chr11:31593986
|
T | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.382-784T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31593986 | ||||||
| chr11:31593994
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.382-776G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31593994 | ||||||
| chr11:31594020
|
C | T | 2 | a0001c0001t0003g0193a0001c0001t0003g0194 | 2 | HG00639.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.382-750C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31594020 | ||||||
| chr11:31594167
|
T | C | 1 | a0006c0004t0076g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.382-603T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31594167 | ||||||
| chr11:31594256
|
C | T | 1 | a0001c0001t0015g0146 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.382-514C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31594256 | ||||||
| chr11:31594371
|
A | G | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 233 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.382-399A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 3/9 | chr11 | 31594371 | ||||||
| chr11:31594957
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+56A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31594957 | ||||||
| chr11:31595361
|
G | A | 1 | a0001c0001t0037g0147 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.513+460G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31595361 | ||||||
| chr11:31595667
|
C | A | 1 | a0001c0001t0003g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.513+766C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31595667 | ||||||
| chr11:31595709
|
G | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.513+808G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31595709 | ||||||
| chr11:31595790
|
T | C | 2 | a0001c0001t0002g0100a0001c0001t0010g0132 | 2 | NA18947.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.513+889T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31595790 | ||||||
| chr11:31595893
|
T | C | 6 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0057others(3): Show | 6 | HG01123.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+992T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31595893 | ||||||
| chr11:31596094
|
T | G | 1 | a0001c0001t0052g0267 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.513+1193T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31596094 | ||||||
| chr11:31596130
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.513+1229T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31596130 | ||||||
| chr11:31596195
|
G | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+1294G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31596195 | ||||||
| chr11:31596382
|
C | T | 2 | a0001c0001t0008g0092a0001c0001t0039g0212 | 2 | HG01099.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.513+1481C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31596382 | ||||||
| chr11:31596717
|
A | G | 1 | a0001c0001t0003g0190 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.513+1816A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31596717 | ||||||
| chr11:31596977
|
A | G | 2 | a0001c0001t0079g0249a0001c0001t0080g0250 | 2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.513+2076A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31596977 | ||||||
| chr11:31597020
|
A | G | 51 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(48): Show | 51 | HG00323.hp2 HG00621.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.513+2119A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31597020 | ||||||
| chr11:31597049
|
T | C | 1 | a0001c0001t0027g0048 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.513+2148T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31597049 | ||||||
| chr11:31597103
|
C | T | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.513+2202C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31597103 | ||||||
| chr11:31597303
|
T | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.513+2402T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31597303 | ||||||
| chr11:31597372
|
G | A | 2 | a0001c0001t0079g0249a0001c0001t0080g0250 | 2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.513+2471G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31597372 | ||||||
| chr11:31597412
|
C | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.513+2511C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31597412 | ||||||
| chr11:31597420
|
A | G | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.513+2519A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31597420 | ||||||
| chr11:31597596
|
AC | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.513+2697delC | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31597596 | |||||
| chr11:31597952
|
C | CT | 51 | a0001c0001t0001g0185a0001c0001t0002g0175a0001c0001t0003g0103others(48): Show | 51 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.513+3072dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31597952 | |||||
| chr11:31597952
|
C | CTT | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0118others(80): Show | 83 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.513+3071_513+3072d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31597952 | |||||
| chr11:31597952
|
C | CTTT | 5 | a0001c0001t0001g0114a0001c0001t0001g0138a0001c0001t0004g0133others(2): Show | 5 | HG01261.hp1 HG02523.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+3070_513+3072d others(5): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31597952 | |||||
| chr11:31597952
|
CT | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0002g0222others(2): Show | 5 | NA18954.hp2 NA18984.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+3072delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31597952 | |||||
| chr11:31597994
|
C | T | 1 | a0001c0001t0008g0270 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.513+3093C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31597994 | ||||||
| chr11:31598033
|
G | T | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.513+3132G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31598033 | ||||||
| chr11:31598061
|
T | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+3160T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31598061 | ||||||
| chr11:31598196
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+3295C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31598196 | ||||||
| chr11:31598206
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0002g0117a0003c0007t0001g0225 | 3 | NA18968.hp2 NA18971.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.513+3305G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31598206 | ||||||
| chr11:31598240
|
C | T | 1 | a0001c0001t0028g0201 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.513+3339C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31598240 | ||||||
| chr11:31598244
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.513+3343G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31598244 | ||||||
| chr11:31598416
|
C | T | 9 | a0001c0001t0003g0103a0001c0001t0003g0186a0001c0001t0003g0190others(6): Show | 9 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.513+3515C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31598416 | ||||||
| chr11:31598503
|
C | CT | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(171): Show | 174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.513+3624dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31598503 | |||||
| chr11:31598503
|
C | CTT | 42 | a0001c0001t0001g0064a0001c0001t0001g0185a0001c0001t0003g0103others(39): Show | 42 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.513+3623_513+3624d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31598503 | |||||
| chr11:31598682
|
A | G | 1 | a0001c0001t0001g0114 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.513+3781A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31598682 | ||||||
| chr11:31598685
|
T | G | 1 | a0001c0002t0014g0256 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.513+3784T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31598685 | ||||||
| chr11:31598697
|
G | T | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.513+3796G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31598697 | ||||||
| chr11:31598721
|
G | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.513+3820G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31598721 | ||||||
| chr11:31598813
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.513+3912G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31598813 | ||||||
| chr11:31599044
|
T | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.513+4143T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31599044 | ||||||
| chr11:31599171
|
A | G | 1 | a0002c0003t0082g0207 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.513+4270A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31599171 | ||||||
| chr11:31599482
|
T | TAC | 4 | a0001c0001t0049g0262a0001c0002t0024g0244a0001c0002t0024g0248others(1): Show | 4 | HG02647.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-4246_514-4245d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31599482 | |||||
| chr11:31599482
|
T | TACAC | 9 | a0001c0001t0006g0227a0001c0001t0006g0230a0001c0001t0016g0236others(6): Show | 9 | HG01981.hp1 HG02148.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.514-4248_514-4245d others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31599482 | |||||
| chr11:31599482
|
T | TACACACA others(5): Show |
1 | a0001c0001t0022g0259 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.514-4256_514-4245d others(14): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31599482 | |||||
| chr11:31599482
|
TAC | T | 3 | a0001c0001t0006g0231a0001c0001t0064g0239a0001c0001t0073g0237 | 3 | HG01884.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.514-4246_514-4245d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31599482 | |||||
| chr11:31599510
|
CACACACA others(13): Show |
C | 2 | a0001c0001t0001g0098a0001c0001t0008g0092 | 2 | HG03195.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.514-4256_514-4237d others(22): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31599510 | |||||
| chr11:31599512
|
CACACACA others(11): Show |
C | 83 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(80): Show | 83 | HG00323.hp2 HG00738.hp1 HG01071.hp1 others(80): Show |
intron_variant | MODIFIER | c.514-4254_514-4237d others(20): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31599512 | |||||
| chr11:31599514
|
CACACACA others(9): Show |
C | 10 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(7): Show | 10 | HG00621.hp1 HG02056.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.514-4252_514-4237d others(18): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31599514 | |||||
| chr11:31599516
|
CACACACA others(7): Show |
C | 1 | a0001c0001t0001g0016 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.514-4250_514-4237d others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31599516 | |||||
| chr11:31599518
|
CACACAAA others(5): Show |
C | 1 | a0001c0001t0011g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.514-4248_514-4237d others(14): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31599518 | |||||
| chr11:31599520
|
CACAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0174a0001c0001t0002g0127a0001c0001t0002g0175others(1): Show | 4 | HG02080.hp2 HG02165.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-4246_514-4237d others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31599520 | |||||
| chr11:31599522
|
C | A | 1 | a0001c0001t0026g0251 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.514-4246C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31599522 | ||||||
| chr11:31599522
|
C | CACACACA others(3): Show |
1 | a0001c0001t0001g0258 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.514-4245_514-4244i others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31599522 | |||||
| chr11:31599522
|
CAAAA | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0002g0106others(10): Show | 13 | HG01175.hp2 HG02273.hp2 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.514-4237_514-4234d others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31599522 | |||||
| chr11:31599522
|
CAAAAAA | C | 62 | a0001c0001t0001g0114a0001c0001t0001g0185a0001c0001t0002g0102others(59): Show | 62 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.514-4239_514-4234d others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31599522 | |||||
| chr11:31599522
|
CAAAAAAA others(1): Show |
C | 55 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0135others(52): Show | 55 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.514-4241_514-4234d others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31599522 | |||||
| chr11:31599524
|
A | C | 18 | a0001c0001t0006g0230a0001c0001t0006g0234a0001c0001t0009g0240others(15): Show | 18 | HG00639.hp2 HG01981.hp1 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.514-4244A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31599524 | ||||||
| chr11:31599526
|
A | C | 11 | a0001c0001t0009g0240a0001c0001t0039g0212a0001c0001t0050g0235others(8): Show | 11 | HG01099.hp2 HG02647.hp1 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.514-4242A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31599526 | ||||||
| chr11:31599528
|
A | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0002g0106others(13): Show | 16 | HG01099.hp2 HG01175.hp2 HG02273.hp2 others(13): Show |
intron_variant | MODIFIER | c.514-4240A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31599528 | ||||||
| chr11:31599529
|
A | C | 1 | a0001c0001t0002g0177 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.514-4239A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31599529 | ||||||
| chr11:31599530
|
A | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(72): Show | 75 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.514-4238A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31599530 | ||||||
| chr11:31599531
|
A | C | 1 | a0001c0001t0002g0177 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.514-4237A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31599531 | ||||||
| chr11:31599611
|
C | T | 1 | a0001c0001t0019g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.514-4157C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31599611 | ||||||
| chr11:31599914
|
C | A | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.514-3854C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31599914 | ||||||
| chr11:31600200
|
A | T | 5 | a0001c0002t0014g0246a0001c0002t0024g0244a0001c0002t0024g0248others(2): Show | 5 | HG02647.hp1 HG03098.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-3568A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31600200 | ||||||
| chr11:31600218
|
TCAC | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.514-3547_514-3545d others(5): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31600218 | |||||
| chr11:31600319
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.514-3449C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31600319 | ||||||
| chr11:31600424
|
T | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-3344T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31600424 | ||||||
| chr11:31600676
|
C | T | 1 | a0001c0001t0011g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.514-3092C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31600676 | ||||||
| chr11:31600869
|
C | T | 1 | a0001c0001t0004g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.514-2899C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31600869 | ||||||
| chr11:31600883
|
C | T | 1 | a0001c0001t0028g0204 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.514-2885C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31600883 | ||||||
| chr11:31600987
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(91): Show | 94 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.514-2781C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31600987 | ||||||
| chr11:31601180
|
TTTTTTAG others(28): Show |
T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-2585_514-2551d others(37): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31601180 | |||||
| chr11:31601217
|
T | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-2551T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31601217 | ||||||
| chr11:31601220
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-2548A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31601220 | ||||||
| chr11:31601221
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-2547G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31601221 | ||||||
| chr11:31601222
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-2546G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31601222 | ||||||
| chr11:31601223
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-2545C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31601223 | ||||||
| chr11:31601268
|
T | C | 1 | a0001c0002t0044g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.514-2500T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31601268 | ||||||
| chr11:31601659
|
G | A | 1 | a0001c0001t0005g0021 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.514-2109G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31601659 | ||||||
| chr11:31601713
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.514-2055A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31601713 | ||||||
| chr11:31602501
|
A | C | 1 | a0001c0001t0016g0171 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.514-1267A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31602501 | ||||||
| chr11:31602564
|
ACT | A | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0017g0007 | 3 | HG02280.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.514-1201_514-1200d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 31602564 | |||||
| chr11:31602733
|
G | A | 1 | a0001c0001t0077g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.514-1035G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31602733 | ||||||
| chr11:31602742
|
A | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(93): Show | 96 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.514-1026A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31602742 | ||||||
| chr11:31602915
|
G | A | 2 | a0001c0001t0006g0231a0001c0001t0073g0237 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.514-853G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31602915 | ||||||
| chr11:31602940
|
G | C | 1 | a0001c0001t0001g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.514-828G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31602940 | ||||||
| chr11:31603077
|
G | A | 5 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0004g0133others(2): Show | 5 | HG00738.hp2 HG01099.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-691G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31603077 | ||||||
| chr11:31603328
|
C | T | 1 | a0001c0001t0064g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.514-440C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31603328 | ||||||
| chr11:31603350
|
C | G | 1 | a0001c0001t0070g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.514-418C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31603350 | ||||||
| chr11:31603516
|
T | G | 8 | a0001c0001t0001g0076a0001c0001t0004g0071a0001c0001t0007g0014others(5): Show | 8 | HG01496.hp2 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-252T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31603516 | ||||||
| chr11:31603539
|
C | T | 1 | a0001c0001t0004g0075 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.514-229C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 4/9 | chr11 | 31603539 | ||||||
| chr11:31603922
|
C | G | 1 | a0001c0001t0009g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.653+15C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31603922 | ||||||
| chr11:31604216
|
T | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.653+309T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31604216 | ||||||
| chr11:31604316
|
G | A | 43 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(40): Show | 43 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.653+409G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31604316 | ||||||
| chr11:31604468
|
G | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.653+561G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31604468 | ||||||
| chr11:31604614
|
A | G | 4 | a0001c0001t0027g0048a0001c0001t0027g0050a0001c0001t0053g0049others(1): Show | 4 | HG01496.hp2 HG02630.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.653+707A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31604614 | ||||||
| chr11:31604654
|
G | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.653+747G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31604654 | ||||||
| chr11:31604727
|
A | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.653+820A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31604727 | ||||||
| chr11:31604821
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0069g0080 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.653+914A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31604821 | ||||||
| chr11:31604844
|
G | A | 1 | a0001c0001t0078g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.653+937G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31604844 | ||||||
| chr11:31604847
|
G | A | 1 | a0001c0001t0046g0172 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.653+940G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31604847 | ||||||
| chr11:31605260
|
A | G | 7 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0152others(4): Show | 7 | HG00280.hp1 HG01069.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.653+1353A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31605260 | ||||||
| chr11:31605396
|
A | G | 1 | a0001c0001t0004g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.653+1489A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31605396 | ||||||
| chr11:31605485
|
A | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(93): Show | 96 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.653+1578A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31605485 | ||||||
| chr11:31605579
|
A | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.653+1672A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31605579 | ||||||
| chr11:31605861
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.653+1954A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31605861 | ||||||
| chr11:31605908
|
C | G | 6 | a0001c0001t0019g0095a0001c0002t0014g0097a0002c0003t0001g0093others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.653+2001C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31605908 | ||||||
| chr11:31605951
|
C | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.653+2044C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31605951 | ||||||
| chr11:31606457
|
C | A | 268 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.653+2550C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31606457 | ||||||
| chr11:31606842
|
A | G | 1 | a0001c0001t0004g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.653+2935A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31606842 | ||||||
| chr11:31606851
|
T | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.653+2944T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31606851 | ||||||
| chr11:31606986
|
G | C | 1 | a0001c0001t0046g0172 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.653+3079G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31606986 | ||||||
| chr11:31607061
|
C | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.653+3154C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31607061 | ||||||
| chr11:31607108
|
G | A | 6 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0005g0028others(3): Show | 6 | HG00621.hp1 HG02056.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.653+3201G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31607108 | ||||||
| chr11:31607133
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.653+3226G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31607133 | ||||||
| chr11:31607518
|
A | G | 4 | a0001c0001t0026g0251a0001c0001t0026g0252a0001c0001t0030g0232others(1): Show | 4 | HG01243.hp2 HG02486.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+3611A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31607518 | ||||||
| chr11:31607845
|
C | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.653+3938C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31607845 | ||||||
| chr11:31607853
|
C | T | 8 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0055others(5): Show | 8 | HG00323.hp2 HG01081.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.653+3946C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31607853 | ||||||
| chr11:31608039
|
AT | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.653+4147delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31608039 | |||||
| chr11:31608250
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.653+4343A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31608250 | ||||||
| chr11:31608267
|
G | A | 1 | a0001c0001t0062g0265 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.653+4360G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31608267 | ||||||
| chr11:31608364
|
A | G | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 229 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.653+4457A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31608364 | ||||||
| chr11:31608696
|
G | A | 2 | a0001c0001t0005g0012a0001c0001t0005g0028 | 2 | HG00621.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.653+4789G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31608696 | ||||||
| chr11:31608819
|
T | C | 1 | a0001c0001t0004g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.653+4912T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31608819 | ||||||
| chr11:31608822
|
G | T | 2 | a0001c0002t0024g0244a0001c0002t0045g0245 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.653+4915G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31608822 | ||||||
| chr11:31608826
|
G | T | 2 | a0001c0002t0024g0244a0001c0002t0045g0245 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.653+4919G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31608826 | ||||||
| chr11:31609016
|
GC | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.653+5111delC | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31609016 | |||||
| chr11:31609264
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.653+5357C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31609264 | ||||||
| chr11:31609266
|
C | T | 2 | a0001c0001t0008g0208a0001c0001t0008g0209 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.653+5359C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31609266 | ||||||
| chr11:31609491
|
A | G | 97 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(94): Show | 97 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.653+5584A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31609491 | ||||||
| chr11:31609518
|
CTCTTTGA others(6): Show |
C | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.653+5620_653+5632d others(15): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31609518 | |||||
| chr11:31609585
|
G | A | 4 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0123others(1): Show | 4 | NA18951.hp2 NA18988.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.653+5678G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31609585 | ||||||
| chr11:31609620
|
G | A | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.653+5713G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31609620 | ||||||
| chr11:31609799
|
C | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 233 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.653+5892C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31609799 | ||||||
| chr11:31609819
|
T | A | 1 | a0001c0001t0001g0046 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.653+5912T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31609819 | ||||||
| chr11:31609820
|
G | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.653+5913G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31609820 | ||||||
| chr11:31610039
|
G | T | 2 | a0001c0001t0025g0155a0001c0001t0025g0224 | 2 | NA18954.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.653+6132G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31610039 | ||||||
| chr11:31610225
|
A | T | 1 | a0001c0001t0001g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.653+6318A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31610225 | ||||||
| chr11:31610240
|
C | A | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.653+6333C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31610240 | ||||||
| chr11:31610327
|
GTTTGT | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.653+6439_653+6443d others(7): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31610327 | |||||
| chr11:31610519
|
C | A | 1 | a0001c0001t0003g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.653+6612C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31610519 | ||||||
| chr11:31610613
|
T | C | 1 | a0001c0001t0020g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.653+6706T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31610613 | ||||||
| chr11:31610663
|
C | A | 2 | a0001c0001t0001g0258a0001c0002t0014g0256 | 2 | HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.653+6756C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31610663 | ||||||
| chr11:31610795
|
G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.653+6888G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31610795 | ||||||
| chr11:31610852
|
G | A | 1 | a0001c0001t0005g0203 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.653+6945G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31610852 | ||||||
| chr11:31610955
|
A | G | 1 | a0001c0001t0018g0013 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.653+7048A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31610955 | ||||||
| chr11:31611021
|
A | T | 33 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(30): Show | 33 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.653+7114A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31611021 | ||||||
| chr11:31611027
|
C | G | 1 | a0001c0001t0003g0220 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.653+7120C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31611027 | ||||||
| chr11:31611126
|
C | T | 1 | a0001c0001t0004g0075 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.653+7219C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31611126 | ||||||
| chr11:31611168
|
G | A | 3 | a0001c0001t0002g0102a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG03927.hp1 HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.653+7261G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31611168 | ||||||
| chr11:31611220
|
G | A | 1 | a0001c0001t0038g0053 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.653+7313G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31611220 | ||||||
| chr11:31611452
|
G | A | 4 | a0001c0001t0002g0106a0001c0001t0002g0109a0001c0001t0010g0110others(1): Show | 4 | NA18942.hp1 NA18960.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.653+7545G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31611452 | ||||||
| chr11:31611598
|
G | A | 1 | a0001c0001t0016g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.653+7691G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31611598 | ||||||
| chr11:31611661
|
G | A | 1 | a0001c0001t0008g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.653+7754G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31611661 | ||||||
| chr11:31611671
|
T | G | 3 | a0001c0001t0009g0240a0001c0001t0020g0241a0001c0001t0020g0242 | 3 | HG02280.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.653+7764T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31611671 | ||||||
| chr11:31611691
|
C | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 233 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.653+7784C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31611691 | ||||||
| chr11:31612352
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0005g0067 | 3 | HG02132.hp2 HG02523.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.653+8445C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31612352 | ||||||
| chr11:31612498
|
G | A | 1 | a0001c0001t0011g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.653+8591G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31612498 | ||||||
| chr11:31612712
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.653+8805A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31612712 | ||||||
| chr11:31612810
|
G | T | 6 | a0001c0002t0014g0246a0001c0002t0024g0244a0001c0002t0024g0248others(3): Show | 6 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.653+8903G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31612810 | ||||||
| chr11:31612828
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.653+8921G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31612828 | ||||||
| chr11:31613443
|
A | G | 1 | a0001c0001t0002g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.653+9536A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31613443 | ||||||
| chr11:31613540
|
T | C | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.653+9633T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31613540 | ||||||
| chr11:31613716
|
C | CT | 8 | a0001c0001t0004g0091a0001c0001t0005g0012a0001c0001t0006g0229others(5): Show | 8 | HG00280.hp2 HG01243.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.653+9826dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31613716 | |||||
| chr11:31613716
|
CT | C | 5 | a0001c0001t0001g0255a0001c0001t0034g0238a0001c0001t0035g0108others(2): Show | 5 | HG02922.hp2 HG03195.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.653+9826delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31613716 | |||||
| chr11:31613736
|
G | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.653+9829G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31613736 | ||||||
| chr11:31613886
|
T | C | 2 | a0001c0001t0019g0084a0002c0003t0082g0207 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.653+9979T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31613886 | ||||||
| chr11:31614127
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.653+10220G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31614127 | ||||||
| chr11:31614526
|
T | G | 1 | a0001c0001t0004g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.653+10619T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31614526 | ||||||
| chr11:31614696
|
G | A | 1 | a0001c0001t0050g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.653+10789G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31614696 | ||||||
| chr11:31614724
|
A | T | 1 | a0001c0001t0002g0148 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.653+10817A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31614724 | ||||||
| chr11:31614934
|
G | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(65): Show | 68 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.653+11027G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31614934 | ||||||
| chr11:31614982
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.653+11075A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31614982 | ||||||
| chr11:31615321
|
A | G | 1 | a0001c0001t0040g0059 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.653+11414A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31615321 | ||||||
| chr11:31615364
|
A | T | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.653+11457A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31615364 | ||||||
| chr11:31615489
|
T | C | 1 | a0001c0001t0002g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.653+11582T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31615489 | ||||||
| chr11:31615503
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.653+11596C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31615503 | ||||||
| chr11:31615504
|
G | A | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.653+11597G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31615504 | ||||||
| chr11:31615547
|
G | A | 9 | a0001c0001t0002g0175a0001c0001t0005g0264a0001c0001t0008g0269others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.654-11563G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31615547 | ||||||
| chr11:31615613
|
A | G | 1 | a0001c0001t0030g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.654-11497A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31615613 | ||||||
| chr11:31615633
|
A | G | 1 | a0006c0004t0076g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.654-11477A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31615633 | ||||||
| chr11:31615653
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.654-11457A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31615653 | ||||||
| chr11:31615921
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.654-11189C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31615921 | ||||||
| chr11:31616016
|
A | G | 1 | a0002c0003t0001g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.654-11094A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31616016 | ||||||
| chr11:31616048
|
A | G | 2 | a0001c0001t0011g0189a0001c0001t0011g0197 | 2 | HG03239.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.654-11062A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31616048 | ||||||
| chr11:31616227
|
C | T | 1 | a0001c0001t0002g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.654-10883C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31616227 | ||||||
| chr11:31616466
|
A | G | 1 | a0001c0001t0010g0009 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.654-10644A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31616466 | ||||||
| chr11:31616514
|
G | A | 1 | a0001c0001t0050g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.654-10596G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31616514 | ||||||
| chr11:31616576
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.654-10534G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31616576 | ||||||
| chr11:31617007
|
G | A | 2 | a0001c0001t0025g0155a0001c0001t0025g0224 | 2 | NA18954.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.654-10103G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31617007 | ||||||
| chr11:31617089
|
G | A | 1 | a0001c0001t0039g0212 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.654-10021G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31617089 | ||||||
| chr11:31617215
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG00738.hp1 HG01258.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.654-9895G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31617215 | ||||||
| chr11:31617254
|
A | G | 42 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(39): Show | 42 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.654-9856A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31617254 | ||||||
| chr11:31617526
|
G | A | 1 | a0001c0001t0009g0180 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.654-9584G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31617526 | ||||||
| chr11:31617729
|
TA | T | 236 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(233): Show | 236 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.654-9367delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31617729 | |||||
| chr11:31617811
|
C | G | 2 | a0001c0001t0026g0251a0001c0001t0026g0252 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.654-9299C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31617811 | ||||||
| chr11:31617941
|
G | A | 1 | a0001c0001t0062g0265 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.654-9169G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31617941 | ||||||
| chr11:31618095
|
A | T | 2 | a0001c0001t0026g0251a0001c0001t0026g0252 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.654-9015A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31618095 | ||||||
| chr11:31618234
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.654-8876T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31618234 | ||||||
| chr11:31618261
|
G | A | 1 | a0001c0001t0050g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.654-8849G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31618261 | ||||||
| chr11:31618365
|
G | A | 1 | a0001c0001t0003g0206 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.654-8745G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31618365 | ||||||
| chr11:31618864
|
G | A | 42 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(39): Show | 42 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.654-8246G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31618864 | ||||||
| chr11:31619258
|
A | G | 1 | a0001c0001t0026g0251 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.654-7852A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31619258 | ||||||
| chr11:31619521
|
T | C | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.654-7589T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31619521 | ||||||
| chr11:31619588
|
G | A | 1 | a0003c0007t0001g0225 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.654-7522G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31619588 | ||||||
| chr11:31619663
|
G | GT | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.654-7436dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31619663 | |||||
| chr11:31619914
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.654-7196A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31619914 | ||||||
| chr11:31619926
|
A | G | 2 | a0001c0001t0008g0208a0001c0001t0008g0209 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.654-7184A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31619926 | ||||||
| chr11:31620025
|
A | G | 1 | a0001c0001t0012g0023 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.654-7085A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31620025 | ||||||
| chr11:31620389
|
G | C | 1 | a0001c0001t0011g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.654-6721G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31620389 | ||||||
| chr11:31620508
|
G | A | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.654-6602G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31620508 | ||||||
| chr11:31621044
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.654-6066A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31621044 | ||||||
| chr11:31621316
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.654-5794G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31621316 | ||||||
| chr11:31621346
|
C | T | 2 | a0001c0001t0006g0231a0001c0001t0073g0237 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.654-5764C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31621346 | ||||||
| chr11:31621414
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.654-5696C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31621414 | ||||||
| chr11:31621476
|
C | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.654-5634C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31621476 | ||||||
| chr11:31621614
|
A | G | 1 | a0001c0001t0007g0072 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.654-5496A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31621614 | ||||||
| chr11:31621782
|
T | C | 1 | a0001c0001t0006g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.654-5328T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31621782 | ||||||
| chr11:31621847
|
T | C | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.654-5263T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31621847 | ||||||
| chr11:31622008
|
A | G | 2 | a0001c0001t0079g0249a0001c0001t0080g0250 | 2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.654-5102A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31622008 | ||||||
| chr11:31622040
|
C | G | 1 | a0001c0001t0007g0089 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.654-5070C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31622040 | ||||||
| chr11:31622216
|
G | A | 268 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.654-4894G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31622216 | ||||||
| chr11:31622322
|
A | G | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.654-4788A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31622322 | ||||||
| chr11:31623041
|
AGTT | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.654-4064_654-4062d others(5): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623041 | |||||
| chr11:31623169
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.654-3941A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31623169 | ||||||
| chr11:31623231
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.654-3879A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31623231 | ||||||
| chr11:31623252
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.654-3858A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31623252 | ||||||
| chr11:31623354
|
A | T | 1 | a0001c0001t0015g0119 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.654-3756A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31623354 | ||||||
| chr11:31623354
|
AAT | A | 4 | a0001c0001t0002g0150a0001c0001t0002g0175a0001c0001t0047g0176others(1): Show | 4 | HG01884.hp2 HG01934.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.654-3720_654-3719d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623354 | |||||
| chr11:31623354
|
AATAT | A | 3 | a0001c0001t0043g0153a0001c0001t0059g0182a0001c0001t0070g0219 | 3 | HG00280.hp2 HG01981.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.654-3722_654-3719d others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623354 | |||||
| chr11:31623354
|
AATATAT | A | 7 | a0001c0001t0003g0183a0001c0001t0003g0193a0001c0001t0003g0194others(4): Show | 7 | HG00639.hp1 HG01081.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.654-3724_654-3719d others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623354 | |||||
| chr11:31623354
|
AATATATA others(1): Show |
A | 32 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(29): Show | 32 | HG00642.hp1 HG00642.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.654-3726_654-3719d others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623354 | |||||
| chr11:31623354
|
AATATATA others(3): Show |
A | 4 | a0001c0001t0025g0155a0001c0001t0025g0224a0001c0001t0029g0164others(1): Show | 4 | NA18954.hp1 NA18987.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-3728_654-3719d others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623354 | |||||
| chr11:31623378
|
T | TATATATA others(1): Show |
14 | a0001c0001t0001g0019a0001c0001t0001g0046a0001c0001t0001g0052others(11): Show | 14 | HG01081.hp2 HG01175.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.654-3725_654-3724i others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623378 | |||||
| chr11:31623378
|
T | TATATATA others(3): Show |
2 | a0001c0001t0001g0068a0001c0001t0001g0077 | 2 | HG02132.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.654-3725_654-3724i others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623378 | |||||
| chr11:31623378
|
T | TATATATA others(3): Show |
55 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0025others(52): Show | 55 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-3723_654-3722i others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623378 | |||||
| chr11:31623378
|
T | TATATATA others(4): Show |
1 | a0001c0001t0001g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.654-3731_654-3721d others(13): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623378 | |||||
| chr11:31623378
|
T | TATATATA others(5): Show |
17 | a0001c0001t0001g0004a0001c0001t0001g0042a0001c0001t0001g0057others(14): Show | 17 | HG01123.hp2 HG01928.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.654-3721_654-3720i others(14): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623378 | |||||
| chr11:31623378
|
T | TATATATA others(7): Show |
1 | a0001c0001t0033g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.654-3721_654-3720i others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623378 | |||||
| chr11:31623390
|
T | A | 158 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(155): Show | 158 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(155): Show |
intron_variant | MODIFIER | c.654-3720T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31623390 | ||||||
| chr11:31623390
|
T | TAA | 7 | a0001c0001t0005g0012a0001c0001t0006g0234a0001c0001t0008g0269others(4): Show | 7 | HG00639.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.654-3717_654-3716d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623390 | |||||
| chr11:31623390
|
T | TAAATATA others(7): Show |
3 | a0001c0001t0018g0013a0001c0002t0024g0248a0001c0002t0045g0245 | 3 | HG03540.hp1 NA18522.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.654-3717_654-3716i others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623390 | |||||
| chr11:31623390
|
T | TATAA | 7 | a0001c0001t0001g0243a0001c0001t0005g0264a0001c0001t0008g0270others(4): Show | 7 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.654-3719_654-3718i others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623390 | |||||
| chr11:31623390
|
T | TATAAATA others(9): Show |
1 | a0001c0002t0044g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.654-3719_654-3718i others(18): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623390 | |||||
| chr11:31623390
|
T | TATATAAA others(11): Show |
4 | a0001c0001t0004g0071a0001c0001t0027g0050a0001c0002t0024g0244others(1): Show | 4 | HG02630.hp2 HG02647.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.654-3719_654-3718i others(20): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623390 | |||||
| chr11:31623390
|
T | TATATATA others(1): Show |
11 | a0001c0001t0002g0100a0001c0001t0002g0143a0001c0001t0002g0167others(8): Show | 11 | HG02300.hp1 HG02572.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.654-3719_654-3718i others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623390 | |||||
| chr11:31623390
|
T | TATATATA others(3): Show |
26 | a0001c0001t0001g0114a0001c0001t0001g0174a0001c0001t0001g0179others(23): Show | 26 | HG00280.hp1 HG00738.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.654-3719_654-3718i others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623390 | |||||
| chr11:31623390
|
T | TATATATA others(5): Show |
1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.654-3719_654-3718i others(14): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623390 | |||||
| chr11:31623390
|
T | TATATATA others(5): Show |
27 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0135others(24): Show | 27 | HG00323.hp1 HG01074.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.654-3719_654-3718i others(14): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623390 | |||||
| chr11:31623390
|
T | TATATATA others(17): Show |
2 | a0001c0001t0053g0049a0001c0001t0063g0047 | 2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.654-3719_654-3718i others(26): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623390 | |||||
| chr11:31623390
|
T | TATATATA others(7): Show |
7 | a0001c0001t0002g0117a0001c0001t0002g0166a0001c0001t0002g0177others(4): Show | 7 | HG00597.hp1 HG01175.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.654-3719_654-3718i others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623390 | |||||
| chr11:31623390
|
T | TATATATA others(19): Show |
1 | a0001c0001t0027g0048 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.654-3719_654-3718i others(28): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623390 | |||||
| chr11:31623390
|
T | TATATATA others(9): Show |
10 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0138others(7): Show | 10 | HG00597.hp2 HG00621.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.654-3719_654-3718i others(18): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623390 | |||||
| chr11:31623390
|
T | TATATATA others(13): Show |
1 | a0001c0001t0007g0158 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.654-3719_654-3718i others(22): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31623390 | |||||
| chr11:31623446
|
T | G | 1 | a0001c0001t0001g0003 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.654-3664T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31623446 | ||||||
| chr11:31623565
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.654-3545C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31623565 | ||||||
| chr11:31623643
|
T | G | 1 | a0001c0001t0001g0046 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.654-3467T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31623643 | ||||||
| chr11:31623875
|
AT | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.654-3234delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31623875 | ||||||
| chr11:31623882
|
A | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.654-3228A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31623882 | ||||||
| chr11:31624043
|
T | C | 1 | a0001c0001t0023g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.654-3067T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31624043 | ||||||
| chr11:31624046
|
A | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.654-3064A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31624046 | ||||||
| chr11:31624234
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.654-2876C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31624234 | ||||||
| chr11:31624249
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.654-2861A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31624249 | ||||||
| chr11:31624395
|
T | C | 1 | a0001c0001t0080g0250 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.654-2715T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31624395 | ||||||
| chr11:31624475
|
G | T | 4 | a0001c0001t0025g0155a0001c0001t0025g0224a0001c0001t0029g0164others(1): Show | 4 | NA18954.hp1 NA18987.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-2635G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31624475 | ||||||
| chr11:31624499
|
A | G | 1 | a0001c0001t0008g0218 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.654-2611A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31624499 | ||||||
| chr11:31624720
|
T | A | 10 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(7): Show | 10 | HG00621.hp1 HG02056.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.654-2390T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31624720 | ||||||
| chr11:31624957
|
T | C | 1 | a0001c0001t0022g0259 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.654-2153T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31624957 | ||||||
| chr11:31624989
|
G | A | 1 | a0001c0001t0078g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.654-2121G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31624989 | ||||||
| chr11:31625054
|
ACT | A | 4 | a0001c0001t0009g0240a0001c0001t0020g0228a0001c0001t0020g0241others(1): Show | 4 | HG02280.hp2 HG02809.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.654-2053_654-2052d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 31625054 | |||||
| chr11:31625123
|
T | C | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.654-1987T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31625123 | ||||||
| chr11:31625228
|
A | G | 1 | a0001c0001t0002g0167 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.654-1882A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31625228 | ||||||
| chr11:31625373
|
G | A | 2 | a0001c0001t0029g0164a0001c0001t0029g0165 | 2 | NA19060.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.654-1737G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31625373 | ||||||
| chr11:31625647
|
A | G | 1 | a0001c0001t0034g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.654-1463A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31625647 | ||||||
| chr11:31625702
|
G | A | 1 | a0001c0001t0041g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.654-1408G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31625702 | ||||||
| chr11:31625808
|
T | C | 1 | a0001c0001t0070g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.654-1302T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31625808 | ||||||
| chr11:31626047
|
A | T | 1 | a0006c0004t0076g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.654-1063A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31626047 | ||||||
| chr11:31626560
|
A | C | 1 | a0001c0001t0002g0127 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.654-550A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31626560 | ||||||
| chr11:31626982
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.654-128G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 5/9 | chr11 | 31626982 | ||||||
| chr11:31627254
|
T | TG | 39 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0052others(36): Show | 39 | HG00621.hp1 HG01109.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.738+71dupG | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31627254 | |||||
| chr11:31627254
|
TG | T | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(116): Show | 119 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.738+71delG | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31627254 | |||||
| chr11:31627259
|
G | A | 19 | a0001c0001t0001g0258a0001c0001t0004g0257a0001c0001t0006g0227others(16): Show | 19 | HG00639.hp2 HG01884.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.738+65G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31627259 | ||||||
| chr11:31627265
|
G | T | 1 | a0001c0001t0061g0086 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.738+71G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31627265 | ||||||
| chr11:31627266
|
C | T | 2 | a0001c0001t0019g0084a0002c0003t0082g0207 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.738+72C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31627266 | ||||||
| chr11:31627670
|
G | A | 1 | a0001c0001t0041g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.738+476G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31627670 | ||||||
| chr11:31627928
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.738+734C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31627928 | ||||||
| chr11:31628436
|
T | TAC | 7 | a0001c0001t0001g0114a0001c0001t0013g0149a0001c0001t0017g0266others(4): Show | 7 | HG01069.hp1 HG02258.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.738+1274_738+1275d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31628436 | |||||
| chr11:31628436
|
T | TACAC | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0128others(79): Show | 82 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.738+1272_738+1275d others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31628436 | |||||
| chr11:31628436
|
T | TACACAC | 39 | a0001c0001t0001g0118a0001c0001t0001g0179a0001c0001t0002g0106others(36): Show | 39 | HG02027.hp1 HG02027.hp2 HG02080.hp2 others(36): Show |
intron_variant | MODIFIER | c.738+1270_738+1275d others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31628436 | |||||
| chr11:31628436
|
T | TACACACA others(1): Show |
3 | a0001c0001t0010g0009a0001c0001t0029g0164a0001c0001t0048g0215 | 3 | HG02818.hp1 NA18990.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.738+1268_738+1275d others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31628436 | |||||
| chr11:31628436
|
T | TACACACA others(3): Show |
2 | a0001c0001t0081g0223a0001c0001t0083g0105 | 2 | HG01891.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.738+1266_738+1275d others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31628436 | |||||
| chr11:31628436
|
TAC | T | 30 | a0001c0001t0001g0041a0001c0001t0001g0066a0001c0001t0001g0079others(27): Show | 30 | HG00639.hp2 HG01884.hp2 HG01981.hp1 others(27): Show |
intron_variant | MODIFIER | c.738+1274_738+1275d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31628436 | |||||
| chr11:31628436
|
TACAC | T | 92 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(89): Show | 92 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(89): Show |
intron_variant | MODIFIER | c.738+1272_738+1275d others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31628436 | |||||
| chr11:31628761
|
T | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.738+1567T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31628761 | ||||||
| chr11:31628864
|
T | A | 1 | a0001c0001t0020g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.738+1670T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31628864 | ||||||
| chr11:31628958
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.738+1764A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31628958 | ||||||
| chr11:31629022
|
G | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.738+1828G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31629022 | ||||||
| chr11:31629093
|
G | A | 1 | a0001c0001t0023g0160 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.738+1899G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31629093 | ||||||
| chr11:31629259
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.738+2065G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31629259 | ||||||
| chr11:31629318
|
A | C | 2 | a0001c0001t0019g0084a0002c0003t0082g0207 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.738+2124A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31629318 | ||||||
| chr11:31629392
|
G | A | 1 | a0001c0001t0051g0134 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.738+2198G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31629392 | ||||||
| chr11:31629538
|
T | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.738+2344T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31629538 | ||||||
| chr11:31629583
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.738+2389C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31629583 | ||||||
| chr11:31629745
|
G | A | 1 | a0001c0001t0050g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.739-2472G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31629745 | ||||||
| chr11:31629764
|
A | AT | 9 | a0001c0001t0002g0117a0001c0001t0005g0061a0001c0001t0006g0227others(6): Show | 9 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.739-2437dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31629764 | |||||
| chr11:31629764
|
A | ATT | 6 | a0001c0002t0014g0246a0001c0002t0024g0244a0001c0002t0024g0248others(3): Show | 6 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.739-2438_739-2437d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31629764 | |||||
| chr11:31629764
|
AT | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0046others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.739-2437delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31629764 | |||||
| chr11:31629764
|
ATT | A | 6 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(3): Show | 6 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.739-2438_739-2437d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31629764 | |||||
| chr11:31630085
|
T | TAA | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.739-2131_739-2130d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31630085 | |||||
| chr11:31630130
|
A | G | 2 | a0001c0001t0005g0005a0001c0001t0005g0006 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.739-2087A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31630130 | ||||||
| chr11:31630227
|
C | CT | 127 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(124): Show | 127 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(124): Show |
intron_variant | MODIFIER | c.739-1972dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31630227 | |||||
| chr11:31630227
|
C | CTT | 8 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0033others(5): Show | 8 | HG00738.hp1 HG01258.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.739-1973_739-1972d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31630227 | |||||
| chr11:31630227
|
CT | C | 6 | a0001c0001t0006g0229a0001c0001t0010g0145a0001c0001t0019g0233others(3): Show | 6 | HG01169.hp2 HG01433.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.739-1972delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31630227 | |||||
| chr11:31630227
|
CTTTTTTT others(1): Show |
C | 5 | a0001c0001t0003g0181a0001c0001t0003g0184a0001c0001t0003g0192others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.739-1979_739-1972d others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 31630227 | |||||
| chr11:31630580
|
C | T | 1 | a0001c0001t0007g0089 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.739-1637C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31630580 | ||||||
| chr11:31630621
|
G | T | 1 | a0001c0001t0006g0229 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.739-1596G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31630621 | ||||||
| chr11:31630662
|
G | A | 3 | a0001c0001t0003g0186a0001c0001t0003g0199a0001c0001t0003g0200 | 3 | HG00642.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.739-1555G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31630662 | ||||||
| chr11:31630822
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.739-1395G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31630822 | ||||||
| chr11:31630903
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.739-1314C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31630903 | ||||||
| chr11:31630945
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.739-1272A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31630945 | ||||||
| chr11:31631053
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.739-1164T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31631053 | ||||||
| chr11:31631357
|
T | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0055others(6): Show | 9 | HG00323.hp2 HG01081.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.739-860T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31631357 | ||||||
| chr11:31631399
|
G | C | 1 | a0001c0002t0024g0244 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.739-818G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31631399 | ||||||
| chr11:31631665
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.739-552G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31631665 | ||||||
| chr11:31631690
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.739-527C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31631690 | ||||||
| chr11:31631875
|
G | A | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.739-342G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31631875 | ||||||
| chr11:31632021
|
A | G | 95 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(92): Show | 95 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.739-196A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 6/9 | chr11 | 31632021 | ||||||
| chr11:31632409
|
C | A | 261 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
splice_region_variant&intron_variant | LOW | c.927+4C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31632409 | ||||||
| chr11:31632501
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.927+96A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31632501 | ||||||
| chr11:31632567
|
T | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0088 | 2 | NA18988.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.927+162T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31632567 | ||||||
| chr11:31632755
|
C | T | 1 | a0001c0001t0005g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.927+350C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31632755 | ||||||
| chr11:31632788
|
T | C | 1 | a0001c0001t0078g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.927+383T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31632788 | ||||||
| chr11:31632859
|
C | T | 81 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(78): Show | 81 | HG00323.hp2 HG00621.hp1 HG01071.hp1 others(78): Show |
intron_variant | MODIFIER | c.927+454C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31632859 | ||||||
| chr11:31633057
|
G | A | 1 | a0001c0001t0039g0212 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.927+652G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31633057 | ||||||
| chr11:31633078
|
G | A | 4 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0017g0007others(1): Show | 4 | HG02280.hp1 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+673G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31633078 | ||||||
| chr11:31633262
|
T | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.927+857T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31633262 | ||||||
| chr11:31633509
|
C | T | 1 | a0001c0001t0022g0259 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.927+1104C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31633509 | ||||||
| chr11:31633561
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.927+1156T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31633561 | ||||||
| chr11:31634157
|
C | T | 1 | a0001c0001t0005g0006 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.927+1752C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31634157 | ||||||
| chr11:31634324
|
G | C | 1 | a0001c0001t0001g0041 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.927+1919G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31634324 | ||||||
| chr11:31634630
|
AGATAACT | A | 86 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(83): Show | 86 | HG00323.hp2 HG00621.hp1 HG01071.hp1 others(83): Show |
intron_variant | MODIFIER | c.927+2229_927+2235d others(9): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 31634630 | |||||
| chr11:31634690
|
A | G | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.927+2285A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31634690 | ||||||
| chr11:31634762
|
T | C | 1 | a0001c0001t0055g0083 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.927+2357T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31634762 | ||||||
| chr11:31634783
|
A | G | 3 | a0001c0001t0001g0258a0001c0001t0004g0257a0001c0002t0014g0256 | 3 | HG02896.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.927+2378A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31634783 | ||||||
| chr11:31634852
|
G | A | 1 | a0001c0001t0021g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.927+2447G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31634852 | ||||||
| chr11:31634898
|
T | A | 1 | a0001c0001t0011g0189 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.927+2493T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31634898 | ||||||
| chr11:31634955
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.927+2550G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31634955 | ||||||
| chr11:31635219
|
G | A | 1 | a0001c0001t0007g0072 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.927+2814G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31635219 | ||||||
| chr11:31635388
|
C | T | 6 | a0001c0001t0019g0095a0001c0002t0014g0097a0002c0003t0001g0093others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+2983C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31635388 | ||||||
| chr11:31635839
|
A | G | 1 | a0001c0001t0003g0206 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.927+3434A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31635839 | ||||||
| chr11:31636189
|
A | G | 1 | a0001c0001t0002g0117 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.927+3784A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31636189 | ||||||
| chr11:31636323
|
A | G | 1 | a0001c0001t0020g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.927+3918A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31636323 | ||||||
| chr11:31636818
|
A | G | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.927+4413A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31636818 | ||||||
| chr11:31636939
|
A | C | 1 | a0001c0001t0007g0089 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.927+4534A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31636939 | ||||||
| chr11:31637038
|
C | T | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.927+4633C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31637038 | ||||||
| chr11:31637626
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.927+5221G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31637626 | ||||||
| chr11:31637654
|
A | G | 2 | a0001c0001t0008g0092a0001c0001t0015g0162 | 2 | HG02132.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.927+5249A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31637654 | ||||||
| chr11:31637846
|
C | T | 2 | a0001c0001t0008g0208a0001c0001t0008g0209 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.927+5441C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31637846 | ||||||
| chr11:31637947
|
A | G | 1 | a0001c0001t0070g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.927+5542A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31637947 | ||||||
| chr11:31637975
|
T | G | 1 | a0001c0001t0002g0148 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.927+5570T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31637975 | ||||||
| chr11:31638510
|
A | G | 2 | a0001c0002t0024g0244a0001c0002t0045g0245 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.927+6105A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31638510 | ||||||
| chr11:31638545
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.927+6140C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31638545 | ||||||
| chr11:31638623
|
A | T | 1 | a0001c0001t0007g0089 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.927+6218A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31638623 | ||||||
| chr11:31639275
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.927+6870C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31639275 | ||||||
| chr11:31639486
|
A | T | 9 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0056others(6): Show | 9 | HG01123.hp2 HG01928.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+7081A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31639486 | ||||||
| chr11:31639567
|
A | T | 6 | a0001c0001t0008g0208a0001c0001t0008g0209a0001c0001t0008g0216others(3): Show | 6 | HG00642.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+7162A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31639567 | ||||||
| chr11:31639767
|
T | C | 42 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(39): Show | 42 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.927+7362T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31639767 | ||||||
| chr11:31639786
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.927+7381C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31639786 | ||||||
| chr11:31639943
|
T | C | 1 | a0001c0002t0045g0245 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.927+7538T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31639943 | ||||||
| chr11:31639984
|
C | T | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.927+7579C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31639984 | ||||||
| chr11:31640088
|
G | T | 1 | a0001c0001t0009g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.928-7653G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31640088 | ||||||
| chr11:31640342
|
A | G | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.928-7399A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31640342 | ||||||
| chr11:31640570
|
C | T | 9 | a0001c0001t0003g0103a0001c0001t0003g0186a0001c0001t0003g0190others(6): Show | 9 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.928-7171C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31640570 | ||||||
| chr11:31640674
|
C | T | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.928-7067C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31640674 | ||||||
| chr11:31640832
|
G | C | 2 | a0001c0001t0008g0208a0001c0001t0008g0209 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.928-6909G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31640832 | ||||||
| chr11:31641108
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.928-6633C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31641108 | ||||||
| chr11:31641278
|
T | C | 1 | a0001c0001t0070g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.928-6463T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31641278 | ||||||
| chr11:31641328
|
CTG | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-6411_928-6410d others(4): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 31641328 | |||||
| chr11:31641520
|
G | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-6221G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31641520 | ||||||
| chr11:31641558
|
G | T | 1 | a0001c0001t0004g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.928-6183G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31641558 | ||||||
| chr11:31641971
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.928-5770G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31641971 | ||||||
| chr11:31642063
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-5678G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31642063 | ||||||
| chr11:31642252
|
G | A | 1 | a0005c0006t0032g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.928-5489G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31642252 | ||||||
| chr11:31642260
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.928-5481T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31642260 | ||||||
| chr11:31642324
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-5417A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31642324 | ||||||
| chr11:31642334
|
A | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.928-5407A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31642334 | ||||||
| chr11:31642792
|
A | G | 51 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(48): Show | 51 | HG00323.hp2 HG00621.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.928-4949A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31642792 | ||||||
| chr11:31643332
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.928-4409G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31643332 | ||||||
| chr11:31643347
|
G | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.928-4394G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31643347 | ||||||
| chr11:31643984
|
A | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-3757A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31643984 | ||||||
| chr11:31644236
|
A | G | 1 | a0001c0001t0070g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.928-3505A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31644236 | ||||||
| chr11:31644429
|
A | G | 1 | a0001c0001t0050g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.928-3312A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31644429 | ||||||
| chr11:31644604
|
T | G | 17 | a0001c0001t0001g0179a0001c0001t0002g0166a0001c0001t0002g0173others(14): Show | 17 | HG00597.hp1 HG02027.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.928-3137T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31644604 | ||||||
| chr11:31644660
|
G | T | 42 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(39): Show | 42 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.928-3081G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31644660 | ||||||
| chr11:31644821
|
C | T | 1 | a0001c0002t0014g0246 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.928-2920C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31644821 | ||||||
| chr11:31644952
|
T | C | 1 | a0001c0001t0048g0215 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.928-2789T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31644952 | ||||||
| chr11:31645040
|
A | G | 1 | a0001c0001t0019g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.928-2701A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31645040 | ||||||
| chr11:31645051
|
A | G | 1 | a0001c0001t0005g0021 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.928-2690A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31645051 | ||||||
| chr11:31645120
|
C | T | 1 | a0001c0001t0064g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.928-2621C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31645120 | ||||||
| chr11:31645282
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.928-2459T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31645282 | ||||||
| chr11:31645395
|
A | G | 1 | a0001c0001t0004g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.928-2346A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31645395 | ||||||
| chr11:31645413
|
C | G | 1 | a0001c0001t0003g0220 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.928-2328C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31645413 | ||||||
| chr11:31646271
|
T | C | 1 | a0001c0001t0005g0203 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.928-1470T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31646271 | ||||||
| chr11:31646302
|
T | C | 2 | a0001c0001t0007g0089a0001c0001t0008g0092 | 2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.928-1439T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31646302 | ||||||
| chr11:31646455
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.928-1286A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31646455 | ||||||
| chr11:31646474
|
T | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG00738.hp1 HG01258.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-1267T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31646474 | ||||||
| chr11:31647371
|
A | C | 1 | a0001c0001t0005g0028 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.928-370A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31647371 | ||||||
| chr11:31647461
|
A | G | 1 | a0001c0001t0046g0172 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.928-280A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31647461 | ||||||
| chr11:31647691
|
T | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-50T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 7/9 | chr11 | 31647691 | ||||||
| chr11:31647964
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036+115C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 8/9 | chr11 | 31647964 | ||||||
| chr11:31648106
|
A | G | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1036+257A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 8/9 | chr11 | 31648106 | ||||||
| chr11:31648409
|
G | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1036+560G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 8/9 | chr11 | 31648409 | ||||||
| chr11:31648519
|
T | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1036+670T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 8/9 | chr11 | 31648519 | ||||||
| chr11:31648522
|
A | C | 1 | a0001c0001t0005g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1036+673A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 8/9 | chr11 | 31648522 | ||||||
| chr11:31648934
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1036+1085A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 8/9 | chr11 | 31648934 | ||||||
| chr11:31649296
|
C | A | 1 | a0001c0001t0074g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1037-819C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 8/9 | chr11 | 31649296 | ||||||
| chr11:31649862
|
C | T | 1 | a0001c0001t0004g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1037-253C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 8/9 | chr11 | 31649862 | ||||||
| chr11:31650340
|
G | A | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1143+119G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31650340 | ||||||
| chr11:31650650
|
T | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.1143+429T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31650650 | ||||||
| chr11:31650696
|
A | C | 1 | a0001c0001t0020g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1143+475A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31650696 | ||||||
| chr11:31650792
|
C | T | 1 | a0001c0001t0080g0250 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1143+571C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31650792 | ||||||
| chr11:31651061
|
T | C | 1 | a0001c0001t0046g0172 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1143+840T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31651061 | ||||||
| chr11:31651262
|
A | T | 1 | a0001c0001t0003g0196 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1143+1041A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31651262 | ||||||
| chr11:31651327
|
T | A | 1 | a0001c0001t0013g0156 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1143+1106T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31651327 | ||||||
| chr11:31651391
|
C | G | 1 | a0001c0001t0035g0108 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1143+1170C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31651391 | ||||||
| chr11:31651583
|
A | G | 1 | a0001c0001t0078g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1143+1362A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31651583 | ||||||
| chr11:31651672
|
TC | T | 6 | a0001c0001t0004g0071a0001c0001t0007g0014a0001c0001t0027g0048others(3): Show | 6 | HG01496.hp2 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+1452delC | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31651672 | ||||||
| chr11:31651675
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+1454T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31651675 | ||||||
| chr11:31651702
|
G | A | 1 | a0001c0001t0003g0213 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1143+1481G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31651702 | ||||||
| chr11:31651806
|
C | T | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1143+1585C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31651806 | ||||||
| chr11:31651849
|
A | G | 1 | a0001c0001t0070g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1143+1628A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31651849 | ||||||
| chr11:31652362
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+2141G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31652362 | ||||||
| chr11:31652612
|
T | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+2391T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31652612 | ||||||
| chr11:31652648
|
T | C | 1 | a0001c0001t0062g0265 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1143+2427T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31652648 | ||||||
| chr11:31652735
|
A | G | 1 | a0001c0001t0002g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1143+2514A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31652735 | ||||||
| chr11:31652792
|
C | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+2571C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31652792 | ||||||
| chr11:31653042
|
T | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+2821T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31653042 | ||||||
| chr11:31653548
|
A | C | 4 | a0001c0001t0009g0240a0001c0001t0020g0228a0001c0001t0020g0241others(1): Show | 4 | HG02280.hp2 HG02809.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+3327A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31653548 | ||||||
| chr11:31653911
|
A | C | 1 | a0001c0001t0006g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1143+3690A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31653911 | ||||||
| chr11:31653938
|
A | C | 2 | a0001c0001t0007g0089a0001c0001t0008g0092 | 2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1143+3717A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31653938 | ||||||
| chr11:31654029
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+3808C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31654029 | ||||||
| chr11:31654125
|
G | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+3904G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31654125 | ||||||
| chr11:31654184
|
G | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+3963G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31654184 | ||||||
| chr11:31654248
|
T | TA | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+4028dupA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31654248 | |||||
| chr11:31654283
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1143+4062T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31654283 | ||||||
| chr11:31654358
|
A | C | 3 | a0001c0001t0027g0048a0001c0001t0053g0049a0001c0001t0063g0047 | 3 | HG01496.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1143+4137A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31654358 | ||||||
| chr11:31654388
|
T | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1143+4167T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31654388 | ||||||
| chr11:31654434
|
T | C | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1143+4213T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31654434 | ||||||
| chr11:31654493
|
A | T | 1 | a0001c0001t0006g0230 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1143+4272A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31654493 | ||||||
| chr11:31654614
|
A | G | 1 | a0001c0001t0068g0039 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1143+4393A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31654614 | ||||||
| chr11:31654747
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+4526T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31654747 | ||||||
| chr11:31654924
|
G | A | 51 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(48): Show | 51 | HG00323.hp2 HG00621.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.1143+4703G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31654924 | ||||||
| chr11:31654933
|
C | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+4712C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31654933 | ||||||
| chr11:31654974
|
C | G | 1 | a0001c0001t0050g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1143+4753C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31654974 | ||||||
| chr11:31654992
|
TA | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+4773delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31654992 | |||||
| chr11:31655378
|
GA | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(142): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.1143+5168delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31655378 | |||||
| chr11:31655529
|
T | C | 5 | a0001c0001t0006g0227a0001c0001t0006g0229a0001c0001t0006g0230others(2): Show | 5 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143+5308T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31655529 | ||||||
| chr11:31655957
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1143+5736T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31655957 | ||||||
| chr11:31656024
|
A | G | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1143+5803A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31656024 | ||||||
| chr11:31656270
|
C | A | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | NA18946.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1143+6049C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31656270 | ||||||
| chr11:31656458
|
A | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+6237A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31656458 | ||||||
| chr11:31656506
|
T | A | 1 | a0001c0001t0048g0215 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1143+6285T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31656506 | ||||||
| chr11:31656532
|
A | G | 2 | a0001c0001t0006g0230a0001c0001t0016g0236 | 2 | HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1143+6311A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31656532 | ||||||
| chr11:31656571
|
T | A | 1 | a0001c0001t0001g0004 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1143+6350T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31656571 | ||||||
| chr11:31656674
|
C | A | 1 | a0001c0001t0012g0023 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1143+6453C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31656674 | ||||||
| chr11:31656751
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1143+6530T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31656751 | ||||||
| chr11:31656765
|
G | C | 1 | a0001c0001t0021g0112 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1143+6544G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31656765 | ||||||
| chr11:31656904
|
G | A | 1 | a0001c0001t0064g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1143+6683G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31656904 | ||||||
| chr11:31657369
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0018g0205 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1143+7148G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31657369 | ||||||
| chr11:31657400
|
C | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(65): Show | 68 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1143+7179C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31657400 | ||||||
| chr11:31657500
|
T | C | 86 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(83): Show | 86 | HG00323.hp2 HG00621.hp1 HG01071.hp1 others(83): Show |
intron_variant | MODIFIER | c.1143+7279T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31657500 | ||||||
| chr11:31657675
|
C | G | 1 | a0001c0001t0071g0024 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1143+7454C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31657675 | ||||||
| chr11:31658022
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+7801C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31658022 | ||||||
| chr11:31658125
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+7904C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31658125 | ||||||
| chr11:31658236
|
T | C | 2 | a0001c0001t0009g0180a0001c0001t0009g0195 | 2 | HG01074.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1143+8015T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31658236 | ||||||
| chr11:31658267
|
G | A | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1143+8046G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31658267 | ||||||
| chr11:31658273
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+8052C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31658273 | ||||||
| chr11:31658361
|
TTA | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+8154_1143+815 others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31658361 | |||||
| chr11:31658507
|
A | G | 1 | a0001c0001t0080g0250 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1143+8286A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31658507 | ||||||
| chr11:31658952
|
T | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(263): Show | 266 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.1143+8731T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31658952 | ||||||
| chr11:31658983
|
A | T | 1 | a0001c0001t0031g0125 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1143+8762A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31658983 | ||||||
| chr11:31659207
|
T | A | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1143+8986T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31659207 | ||||||
| chr11:31659347
|
T | C | 1 | a0001c0001t0071g0024 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1143+9126T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31659347 | ||||||
| chr11:31659525
|
T | C | 1 | a0001c0001t0018g0205 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1143+9304T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31659525 | ||||||
| chr11:31659551
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1143+9330A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31659551 | ||||||
| chr11:31659768
|
A | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+9547A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31659768 | ||||||
| chr11:31659785
|
C | T | 1 | a0001c0001t0007g0158 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1143+9564C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31659785 | ||||||
| chr11:31659930
|
T | A | 1 | a0001c0001t0006g0234 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1143+9709T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31659930 | ||||||
| chr11:31659964
|
C | T | 1 | a0001c0001t0005g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1143+9743C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31659964 | ||||||
| chr11:31660090
|
A | G | 6 | a0001c0001t0008g0208a0001c0001t0008g0209a0001c0001t0008g0216others(3): Show | 6 | HG00642.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+9869A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31660090 | ||||||
| chr11:31660125
|
A | G | 1 | a0001c0001t0036g0090 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1143+9904A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31660125 | ||||||
| chr11:31660201
|
A | G | 1 | a0001c0001t0020g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1143+9980A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31660201 | ||||||
| chr11:31660218
|
C | G | 1 | a0001c0001t0016g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1143+9997C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31660218 | ||||||
| chr11:31660246
|
A | C | 1 | a0001c0001t0019g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1143+10025A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31660246 | ||||||
| chr11:31660286
|
G | A | 19 | a0001c0001t0001g0258a0001c0001t0004g0257a0001c0001t0006g0227others(16): Show | 19 | HG00639.hp2 HG01884.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1143+10065G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31660286 | ||||||
| chr11:31660303
|
A | G | 6 | a0001c0002t0014g0246a0001c0002t0024g0244a0001c0002t0024g0248others(3): Show | 6 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+10082A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31660303 | ||||||
| chr11:31660534
|
A | G | 10 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0062others(7): Show | 10 | NA18747.hp2 NA18947.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.1143+10313A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31660534 | ||||||
| chr11:31660568
|
A | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+10347A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31660568 | ||||||
| chr11:31660650
|
G | GT | 8 | a0001c0001t0001g0076a0001c0001t0004g0071a0001c0001t0007g0014others(5): Show | 8 | HG01496.hp2 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+10438dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31660650 | |||||
| chr11:31660952
|
A | G | 1 | a0001c0001t0042g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1143+10731A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31660952 | ||||||
| chr11:31660975
|
C | T | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1143+10754C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31660975 | ||||||
| chr11:31661075
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+10854A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31661075 | ||||||
| chr11:31661371
|
T | A | 1 | a0001c0001t0007g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1143+11150T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31661371 | ||||||
| chr11:31661372
|
A | C | 1 | a0001c0001t0003g0196 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1143+11151A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31661372 | ||||||
| chr11:31661454
|
G | A | 4 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0017g0007others(1): Show | 4 | HG02280.hp1 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+11233G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31661454 | ||||||
| chr11:31661502
|
A | G | 1 | a0001c0001t0003g0213 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1143+11281A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31661502 | ||||||
| chr11:31661534
|
T | G | 1 | a0001c0001t0026g0252 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1143+11313T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31661534 | ||||||
| chr11:31661675
|
TA | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+11461delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31661675 | |||||
| chr11:31661769
|
A | G | 13 | a0001c0001t0006g0227a0001c0001t0006g0229a0001c0001t0006g0230others(10): Show | 13 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1143+11548A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31661769 | ||||||
| chr11:31661937
|
A | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+11716A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31661937 | ||||||
| chr11:31661940
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+11719C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31661940 | ||||||
| chr11:31661961
|
G | C | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1143+11740G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31661961 | ||||||
| chr11:31661983
|
C | T | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1143+11762C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31661983 | ||||||
| chr11:31662083
|
T | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+11862T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31662083 | ||||||
| chr11:31662284
|
C | G | 1 | a0001c0001t0007g0158 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1143+12063C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31662284 | ||||||
| chr11:31662545
|
C | T | 1 | a0001c0002t0014g0256 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1143+12324C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31662545 | ||||||
| chr11:31662851
|
A | G | 1 | a0001c0001t0004g0044 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1143+12630A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31662851 | ||||||
| chr11:31663128
|
A | T | 42 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(39): Show | 42 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1143+12907A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31663128 | ||||||
| chr11:31663639
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1143+13418A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31663639 | ||||||
| chr11:31663721
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.1143+13500A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31663721 | ||||||
| chr11:31663737
|
G | T | 2 | a0001c0001t0009g0187a0004c0005t0009g0188 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1143+13516G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31663737 | ||||||
| chr11:31664450
|
G | A | 2 | a0001c0001t0002g0221a0001c0001t0002g0222 | 2 | NA18971.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1143+14229G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31664450 | ||||||
| chr11:31664901
|
G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+14680G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31664901 | ||||||
| chr11:31664938
|
G | T | 1 | a0001c0001t0023g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1143+14717G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31664938 | ||||||
| chr11:31665047
|
A | C | 1 | a0001c0001t0001g0074 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1143+14826A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31665047 | ||||||
| chr11:31665304
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+15083A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31665304 | ||||||
| chr11:31665395
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+15174T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31665395 | ||||||
| chr11:31665559
|
A | G | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1143+15338A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31665559 | ||||||
| chr11:31665560
|
A | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+15339A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31665560 | ||||||
| chr11:31665593
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+15372G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31665593 | ||||||
| chr11:31665655
|
C | CT | 5 | a0001c0001t0004g0051a0001c0001t0012g0023a0001c0001t0025g0224others(2): Show | 5 | HG02738.hp2 HG04115.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143+15457dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31665655 | |||||
| chr11:31665655
|
CT | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0041a0001c0001t0001g0114others(108): Show | 111 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1143+15457delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31665655 | |||||
| chr11:31665655
|
CTT | C | 9 | a0001c0001t0001g0135a0001c0001t0005g0264a0001c0001t0008g0269others(6): Show | 9 | HG01099.hp1 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143+15456_1143+15 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31665655 | |||||
| chr11:31665892
|
C | T | 3 | a0001c0001t0010g0145a0001c0001t0054g0140a0001c0001t0066g0141 | 3 | HG01074.hp1 HG01169.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1143+15671C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31665892 | ||||||
| chr11:31666004
|
C | CT | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(109): Show | 112 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(109): Show |
intron_variant | MODIFIER | c.1143+15805dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31666004 | |||||
| chr11:31666004
|
C | CTT | 20 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0001t0001g0055others(17): Show | 20 | HG01258.hp1 HG01433.hp1 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.1143+15804_1143+15 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31666004 | |||||
| chr11:31666367
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+16146A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31666367 | ||||||
| chr11:31666380
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+16159C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31666380 | ||||||
| chr11:31666482
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1143+16261A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31666482 | ||||||
| chr11:31666494
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1143+16273C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31666494 | ||||||
| chr11:31666561
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+16340A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31666561 | ||||||
| chr11:31666645
|
T | C | 1 | a0001c0002t0014g0246 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1143+16424T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31666645 | ||||||
| chr11:31666691
|
CA | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(134): Show | 137 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1143+16488delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31666691 | |||||
| chr11:31666766
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+16545G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31666766 | ||||||
| chr11:31666792
|
AACTT | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+16579_1143+16 others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31666792 | |||||
| chr11:31667126
|
T | C | 1 | a0001c0001t0006g0231 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1143+16905T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31667126 | ||||||
| chr11:31667664
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+17443T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31667664 | ||||||
| chr11:31667671
|
T | G | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1143+17450T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31667671 | ||||||
| chr11:31667712
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1143+17491C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31667712 | ||||||
| chr11:31667834
|
T | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+17613T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31667834 | ||||||
| chr11:31667898
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1143+17677A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31667898 | ||||||
| chr11:31667905
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.1143+17684G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31667905 | ||||||
| chr11:31668375
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+18154C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668375 | ||||||
| chr11:31668445
|
A | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+18224A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668445 | ||||||
| chr11:31668674
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0078g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1143+18453_1143+18 others(18): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668674 | ||||||
| chr11:31668675
|
C | CAT | 8 | a0001c0001t0005g0191a0001c0001t0008g0270a0001c0001t0017g0266others(5): Show | 8 | HG01175.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+18454_1143+18 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668675 | ||||||
| chr11:31668675
|
C | CATGTGTG others(3): Show |
4 | a0001c0001t0001g0114a0001c0001t0002g0102a0001c0001t0037g0147others(1): Show | 4 | HG00597.hp2 HG01074.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+18454_1143+18 others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668675 | ||||||
| chr11:31668675
|
C | CATGTGTG others(5): Show |
5 | a0001c0001t0002g0167a0001c0001t0002g0177a0001c0001t0010g0132others(2): Show | 5 | HG01943.hp1 HG01981.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143+18454_1143+18 others(18): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668675 | ||||||
| chr11:31668675
|
C | CATGTGTG others(7): Show |
7 | a0001c0001t0002g0100a0001c0001t0002g0116a0001c0001t0005g0131others(4): Show | 7 | HG01069.hp1 HG01168.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143+18454_1143+18 others(20): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668675 | ||||||
| chr11:31668675
|
C | CATGTGTG others(9): Show |
21 | a0001c0001t0001g0002a0001c0001t0002g0115a0001c0001t0002g0123others(18): Show | 21 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.1143+18454_1143+18 others(22): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668675 | ||||||
| chr11:31668675
|
C | CATGTGTG others(11): Show |
16 | a0001c0001t0001g0003a0001c0001t0001g0118a0001c0001t0001g0128others(13): Show | 16 | HG01123.hp1 HG01169.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.1143+18454_1143+18 others(24): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668675 | ||||||
| chr11:31668675
|
C | CATGTGTG others(13): Show |
17 | a0001c0001t0001g0135a0001c0001t0002g0106a0001c0001t0002g0109others(14): Show | 17 | HG01099.hp1 HG02027.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.1143+18454_1143+18 others(26): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668675 | ||||||
| chr11:31668675
|
C | CATGTGTG others(15): Show |
5 | a0001c0001t0002g0139a0001c0001t0002g0166a0001c0001t0021g0107others(2): Show | 5 | HG00597.hp1 HG01258.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143+18454_1143+18 others(28): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668675 | ||||||
| chr11:31668675
|
C | CATGTGTG others(17): Show |
4 | a0001c0001t0001g0179a0001c0001t0002g0175a0001c0001t0008g0209others(1): Show | 4 | HG02056.hp1 HG03704.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+18454_1143+18 others(30): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668675 | ||||||
| chr11:31668675
|
C | CATGTGTG others(21): Show |
3 | a0001c0001t0008g0216a0001c0001t0025g0155a0001c0001t0025g0224 | 3 | HG02717.hp2 NA18954.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1143+18454_1143+18 others(34): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668675 | ||||||
| chr11:31668675
|
C | CATGTGTG others(25): Show |
1 | a0001c0001t0047g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1143+18454_1143+18 others(38): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668675 | ||||||
| chr11:31668675
|
C | CATGTGTG others(31): Show |
1 | a0001c0001t0074g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1143+18454_1143+18 others(44): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668675 | ||||||
| chr11:31668675
|
C | CGT | 13 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0243others(10): Show | 13 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1143+18499_1143+18 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31668675 | |||||
| chr11:31668675
|
C | CGTGT | 3 | a0001c0001t0022g0259a0001c0001t0050g0235a0001c0001t0064g0239 | 3 | HG01884.hp2 HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1143+18497_1143+18 others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31668675 | |||||
| chr11:31668675
|
C | CGTGTGT | 5 | a0001c0001t0004g0257a0001c0001t0034g0238a0001c0001t0049g0262others(2): Show | 5 | HG03130.hp1 HG03195.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143+18495_1143+18 others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31668675 | |||||
| chr11:31668675
|
C | CGTGTGTG others(3): Show |
2 | a0001c0001t0001g0174a0001c0001t0019g0233 | 2 | HG02165.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1143+18491_1143+18 others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31668675 | |||||
| chr11:31668675
|
C | CGTGTGTG others(7): Show |
1 | a0001c0001t0035g0108 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1143+18487_1143+18 others(20): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31668675 | |||||
| chr11:31668675
|
C | CGTGTGTG others(15): Show |
1 | a0001c0001t0075g0217 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1143+18479_1143+18 others(28): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31668675 | |||||
| chr11:31668675
|
C | T | 1 | a0001c0001t0078g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1143+18454C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668675 | ||||||
| chr11:31668675
|
CGT | C | 30 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(27): Show | 30 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1143+18499_1143+18 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31668675 | |||||
| chr11:31668675
|
CGTGT | C | 3 | a0001c0001t0009g0198a0001c0001t0026g0252a0001c0001t0028g0201 | 3 | HG03453.hp2 NA18989.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1143+18497_1143+18 others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31668675 | |||||
| chr11:31668675
|
CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0008g0218 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1143+18483_1143+18 others(24): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31668675 | |||||
| chr11:31668676
|
G | A | 4 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0003g0206others(1): Show | 4 | HG00639.hp1 HG01099.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143+18455G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668676 | ||||||
| chr11:31668678
|
G | A | 26 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(23): Show | 26 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.1143+18457G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668678 | ||||||
| chr11:31668691
|
T | A | 1 | a0001c0001t0001g0040 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1143+18470T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668691 | ||||||
| chr11:31668694
|
G | A | 1 | a0001c0001t0008g0218 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1143+18473G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668694 | ||||||
| chr11:31668704
|
GTGTGTGT others(11): Show |
G | 5 | a0001c0001t0001g0004a0001c0001t0001g0068a0001c0001t0001g0073others(2): Show | 5 | HG02132.hp2 HG02135.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143+18484_1143+18 others(24): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668704 | ||||||
| chr11:31668712
|
GTGTGTGT others(3): Show |
G | 5 | a0001c0002t0014g0246a0001c0002t0024g0244a0001c0002t0024g0248others(2): Show | 5 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143+18492_1143+18 others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668712 | ||||||
| chr11:31668714
|
GTGTGTGT others(1): Show |
G | 11 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0082others(8): Show | 11 | HG01123.hp2 HG01496.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1143+18494_1143+18 others(14): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668714 | ||||||
| chr11:31668716
|
GTGTGTA | G | 11 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0004g0078others(8): Show | 11 | HG01884.hp1 HG01928.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.1143+18496_1143+18 others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668716 | ||||||
| chr11:31668718
|
GTGTA | G | 49 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0036others(46): Show | 49 | HG00323.hp2 HG01071.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.1143+18498_1143+18 others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668718 | ||||||
| chr11:31668720
|
GTA | G | 10 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0040others(7): Show | 10 | HG00621.hp1 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.1143+18500_1143+18 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668720 | ||||||
| chr11:31668722
|
A | G | 12 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0033others(9): Show | 12 | HG00738.hp1 HG01258.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1143+18501A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668722 | ||||||
| chr11:31668731
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+18510G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668731 | ||||||
| chr11:31668858
|
A | C | 97 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(94): Show | 97 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.1143+18637A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668858 | ||||||
| chr11:31668902
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+18681A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668902 | ||||||
| chr11:31668977
|
C | G | 1 | a0001c0001t0004g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1143+18756C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31668977 | ||||||
| chr11:31669026
|
C | G | 1 | a0001c0001t0056g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1143+18805C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31669026 | ||||||
| chr11:31669076
|
ATTTATTT others(15): Show |
A | 6 | a0001c0002t0014g0246a0001c0002t0024g0244a0001c0002t0024g0248others(3): Show | 6 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+18875_1143+18 others(28): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31669076 | |||||
| chr11:31669099
|
T | G | 1 | a0003c0007t0001g0225 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1143+18878T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31669099 | ||||||
| chr11:31669108
|
A | AT | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+18891dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31669108 | |||||
| chr11:31669139
|
A | C | 6 | a0001c0001t0004g0071a0001c0001t0007g0014a0001c0001t0027g0048others(3): Show | 6 | HG01496.hp2 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+18918A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31669139 | ||||||
| chr11:31669223
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1143+19002C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31669223 | ||||||
| chr11:31669424
|
A | G | 8 | a0001c0001t0003g0206a0001c0001t0005g0191a0001c0002t0014g0246others(5): Show | 8 | HG01496.hp1 HG02273.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1143+19203A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31669424 | ||||||
| chr11:31669503
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+19282T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31669503 | ||||||
| chr11:31669559
|
C | T | 1 | a0001c0001t0050g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1143+19338C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31669559 | ||||||
| chr11:31669634
|
T | C | 1 | a0001c0001t0004g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1143+19413T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31669634 | ||||||
| chr11:31669721
|
A | G | 1 | a0001c0001t0003g0214 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1143+19500A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31669721 | ||||||
| chr11:31669813
|
G | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+19592G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31669813 | ||||||
| chr11:31669905
|
C | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+19684C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31669905 | ||||||
| chr11:31670055
|
C | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+19834C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31670055 | ||||||
| chr11:31670161
|
C | A | 1 | a0001c0001t0077g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1143+19940C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31670161 | ||||||
| chr11:31670305
|
C | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+20084C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31670305 | ||||||
| chr11:31670458
|
G | A | 97 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(94): Show | 97 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.1143+20237G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31670458 | ||||||
| chr11:31670460
|
C | A | 1 | a0001c0001t0003g0184 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1143+20239C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31670460 | ||||||
| chr11:31670728
|
T | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+20507T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31670728 | ||||||
| chr11:31671409
|
T | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+21188T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31671409 | ||||||
| chr11:31671476
|
A | G | 1 | a0001c0001t0004g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1143+21255A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31671476 | ||||||
| chr11:31671511
|
A | G | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0017g0007 | 3 | HG02280.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1143+21290A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31671511 | ||||||
| chr11:31671678
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.1143+21457G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31671678 | ||||||
| chr11:31672154
|
T | C | 2 | a0001c0001t0003g0210a0001c0001t0003g0211 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1143+21933T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31672154 | ||||||
| chr11:31672237
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1143+22016G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31672237 | ||||||
| chr11:31672647
|
C | T | 1 | a0001c0001t0021g0112 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1143+22426C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31672647 | ||||||
| chr11:31672656
|
G | C | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1143+22435G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31672656 | ||||||
| chr11:31672860
|
C | T | 1 | a0001c0001t0011g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1143+22639C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31672860 | ||||||
| chr11:31672966
|
A | G | 1 | a0001c0001t0011g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1143+22745A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31672966 | ||||||
| chr11:31672977
|
G | A | 1 | a0001c0001t0005g0203 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1143+22756G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31672977 | ||||||
| chr11:31673172
|
A | G | 2 | a0001c0001t0008g0269a0001c0001t0008g0270 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1143+22951A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31673172 | ||||||
| chr11:31673465
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG00738.hp1 HG01258.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143+23244A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31673465 | ||||||
| chr11:31673528
|
C | A | 1 | a0001c0001t0022g0101 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1143+23307C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31673528 | ||||||
| chr11:31674168
|
G | A | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1143+23947G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31674168 | ||||||
| chr11:31674469
|
G | C | 1 | a0001c0001t0071g0024 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1143+24248G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31674469 | ||||||
| chr11:31674550
|
A | G | 1 | a0006c0004t0076g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1143+24329A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31674550 | ||||||
| chr11:31674592
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1143+24371A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31674592 | ||||||
| chr11:31674638
|
T | C | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1143+24417T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31674638 | ||||||
| chr11:31674783
|
A | T | 1 | a0002c0003t0001g0094 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1143+24562A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31674783 | ||||||
| chr11:31674788
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+24567A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31674788 | ||||||
| chr11:31674858
|
A | G | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+24637A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31674858 | ||||||
| chr11:31674859
|
T | C | 1 | a0001c0001t0055g0083 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1143+24638T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31674859 | ||||||
| chr11:31674942
|
A | T | 1 | a0001c0001t0010g0145 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1143+24721A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31674942 | ||||||
| chr11:31674986
|
A | G | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1143+24765A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31674986 | ||||||
| chr11:31675247
|
A | G | 2 | a0001c0001t0002g0221a0001c0001t0002g0222 | 2 | NA18971.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1143+25026A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31675247 | ||||||
| chr11:31675268
|
CT | C | 34 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(31): Show | 34 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1143+25060delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31675268 | |||||
| chr11:31675274
|
T | C | 1 | a0001c0001t0015g0162 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1143+25053T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31675274 | ||||||
| chr11:31675343
|
C | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.1143+25122C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31675343 | ||||||
| chr11:31675350
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+25129C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31675350 | ||||||
| chr11:31675551
|
G | A | 1 | a0001c0001t0042g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1143+25330G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31675551 | ||||||
| chr11:31676167
|
A | T | 1 | a0001c0001t0018g0205 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1143+25946A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31676167 | ||||||
| chr11:31676377
|
A | G | 33 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(30): Show | 33 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1143+26156A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31676377 | ||||||
| chr11:31676639
|
A | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+26418A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31676639 | ||||||
| chr11:31677417
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+27196A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31677417 | ||||||
| chr11:31677693
|
T | C | 1 | a0001c0001t0020g0242 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1143+27472T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31677693 | ||||||
| chr11:31677803
|
T | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+27582T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31677803 | ||||||
| chr11:31677830
|
A | G | 1 | a0001c0001t0019g0095 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1143+27609A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31677830 | ||||||
| chr11:31678153
|
A | G | 1 | a0001c0001t0061g0086 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1143+27932A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678153 | ||||||
| chr11:31678160
|
T | C | 1 | a0001c0001t0003g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1143+27939T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678160 | ||||||
| chr11:31678390
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0007g0081 | 2 | NA18977.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1143+28169A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678390 | ||||||
| chr11:31678398
|
G | A | 5 | a0001c0001t0006g0227a0001c0001t0006g0229a0001c0001t0006g0230others(2): Show | 5 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143+28177G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678398 | ||||||
| chr11:31678491
|
ATGTATGT others(3): Show |
A | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1143+28274_1143+28 others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678491 | |||||
| chr11:31678495
|
A | ATG | 8 | a0001c0001t0005g0264a0001c0001t0006g0234a0001c0001t0016g0236others(5): Show | 8 | HG00639.hp2 HG02145.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+28320_1143+28 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678495 | |||||
| chr11:31678495
|
A | ATGTGTG | 3 | a0001c0001t0006g0231a0001c0001t0030g0247a0001c0001t0073g0237 | 3 | HG02486.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1143+28316_1143+28 others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678495 | |||||
| chr11:31678495
|
A | G | 1 | a0001c0001t0064g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1143+28274A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678495 | ||||||
| chr11:31678495
|
ATG | A | 4 | a0001c0001t0001g0243a0001c0001t0022g0259a0001c0001t0026g0251others(1): Show | 4 | HG01109.hp2 HG01243.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143+28320_1143+28 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678495 | |||||
| chr11:31678495
|
ATGTG | A | 4 | a0001c0001t0003g0190a0001c0001t0019g0233a0001c0001t0070g0219others(1): Show | 4 | HG01261.hp2 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143+28318_1143+28 others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678495 | |||||
| chr11:31678495
|
ATGTGTG | A | 14 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0185others(11): Show | 14 | HG00642.hp1 HG01099.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1143+28316_1143+28 others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678495 | |||||
| chr11:31678495
|
ATGTGTGT others(1): Show |
A | 89 | a0001c0001t0001g0003a0001c0001t0001g0064a0001c0001t0001g0066others(86): Show | 89 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.1143+28314_1143+28 others(14): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678495 | |||||
| chr11:31678495
|
ATGTGTGT others(3): Show |
A | 6 | a0001c0001t0002g0102a0001c0001t0002g0166a0001c0001t0002g0177others(3): Show | 6 | HG00597.hp1 HG01168.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1143+28312_1143+28 others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678495 | |||||
| chr11:31678495
|
ATGTGTGT others(5): Show |
A | 15 | a0001c0001t0001g0002a0001c0001t0002g0173a0001c0001t0002g0175others(12): Show | 15 | HG00597.hp2 HG02027.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.1143+28310_1143+28 others(18): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678495 | |||||
| chr11:31678495
|
ATGTGTGT others(15): Show |
A | 1 | a0001c0001t0015g0162 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1143+28300_1143+28 others(28): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678495 | |||||
| chr11:31678497
|
G | A | 4 | a0001c0001t0002g0152a0001c0001t0004g0133a0001c0001t0029g0164others(1): Show | 4 | HG00280.hp1 HG04199.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143+28276G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678497 | ||||||
| chr11:31678501
|
G | A | 3 | a0001c0001t0003g0190a0001c0001t0070g0219a0001c0001t0083g0105 | 3 | HG01261.hp2 HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1143+28280G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678501 | ||||||
| chr11:31678503
|
G | A | 14 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0185others(11): Show | 14 | HG00642.hp1 HG01099.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1143+28282G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678503 | ||||||
| chr11:31678505
|
G | A | 89 | a0001c0001t0001g0003a0001c0001t0001g0064a0001c0001t0001g0066others(86): Show | 89 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.1143+28284G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678505 | ||||||
| chr11:31678507
|
G | A | 6 | a0001c0001t0002g0102a0001c0001t0002g0166a0001c0001t0002g0177others(3): Show | 6 | HG00597.hp1 HG01168.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1143+28286G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678507 | ||||||
| chr11:31678509
|
G | A | 15 | a0001c0001t0001g0002a0001c0001t0002g0173a0001c0001t0002g0175others(12): Show | 15 | HG00597.hp2 HG02027.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.1143+28288G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678509 | ||||||
| chr11:31678519
|
G | A | 1 | a0001c0001t0015g0162 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1143+28298G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678519 | ||||||
| chr11:31678525
|
GTGTGTGT others(11): Show |
G | 3 | a0001c0001t0055g0083a0001c0002t0045g0245a0005c0006t0032g0253 | 3 | HG03209.hp2 HG03540.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1143+28306_1143+28 others(24): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678525 | |||||
| chr11:31678527
|
GTGTGTGT others(9): Show |
G | 12 | a0001c0001t0001g0025a0001c0001t0001g0074a0001c0001t0001g0076others(9): Show | 12 | HG02257.hp1 HG02615.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1143+28308_1143+28 others(22): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678527 | |||||
| chr11:31678529
|
GTGTGTGT others(7): Show |
G | 3 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0019g0084 | 3 | HG03453.hp1 NA18971.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1143+28310_1143+28 others(20): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678529 | |||||
| chr11:31678531
|
GTGTGTGT others(5): Show |
G | 68 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(65): Show | 68 | HG00323.hp2 HG00621.hp1 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.1143+28312_1143+28 others(18): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678531 | |||||
| chr11:31678531
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1143+28315_1143+28 others(20): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678531 | |||||
| chr11:31678533
|
GTGTGTGT others(3): Show |
G | 9 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0263others(6): Show | 9 | HG01175.hp1 HG01884.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143+28314_1143+28 others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678533 | |||||
| chr11:31678535
|
GTGTGTGT others(1): Show |
G | 3 | a0001c0001t0002g0152a0001c0001t0004g0133a0006c0004t0076g0063 | 3 | HG00280.hp1 HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1143+28316_1143+28 others(14): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678535 | |||||
| chr11:31678537
|
GTGTGTA | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0033g0060 | 3 | HG01433.hp1 HG02300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1143+28318_1143+28 others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678537 | |||||
| chr11:31678539
|
GTGTA | G | 4 | a0001c0001t0001g0033a0001c0001t0005g0029a0001c0001t0008g0270others(1): Show | 4 | HG00738.hp1 HG01258.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143+28320_1143+28 others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678539 | |||||
| chr11:31678541
|
GTA | G | 3 | a0001c0001t0001g0258a0001c0001t0004g0257a0001c0002t0014g0256 | 3 | HG02896.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1143+28324_1143+28 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31678541 | |||||
| chr11:31678543
|
A | G | 16 | a0001c0001t0005g0264a0001c0001t0006g0227a0001c0001t0006g0229others(13): Show | 16 | HG00639.hp2 HG01891.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.1143+28322A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678543 | ||||||
| chr11:31678708
|
A | G | 2 | a0001c0001t0008g0269a0001c0001t0008g0270 | 2 | HG02615.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1143+28487A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678708 | ||||||
| chr11:31678772
|
A | G | 1 | a0006c0004t0076g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1143+28551A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678772 | ||||||
| chr11:31678994
|
T | C | 2 | a0001c0001t0009g0180a0001c0001t0009g0195 | 2 | HG01074.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1143+28773T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31678994 | ||||||
| chr11:31679014
|
A | C | 1 | a0001c0001t0002g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1143+28793A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31679014 | ||||||
| chr11:31679080
|
A | G | 1 | a0001c0001t0006g0230 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1143+28859A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31679080 | ||||||
| chr11:31679173
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+28952A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31679173 | ||||||
| chr11:31679326
|
G | A | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1143+29105G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31679326 | ||||||
| chr11:31679585
|
C | A | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1143+29364C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31679585 | ||||||
| chr11:31680021
|
G | T | 4 | a0001c0001t0002g0106a0001c0001t0002g0109a0001c0001t0010g0110others(1): Show | 4 | NA18942.hp1 NA18960.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+29800G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31680021 | ||||||
| chr11:31680050
|
G | C | 17 | a0001c0001t0001g0179a0001c0001t0002g0173a0001c0001t0002g0175others(14): Show | 17 | HG00597.hp2 HG02027.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.1143+29829G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31680050 | ||||||
| chr11:31680178
|
G | C | 1 | a0001c0001t0062g0265 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1143+29957G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31680178 | ||||||
| chr11:31680333
|
A | G | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+30112A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31680333 | ||||||
| chr11:31680380
|
T | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+30159T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31680380 | ||||||
| chr11:31680873
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+30652C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31680873 | ||||||
| chr11:31680968
|
G | T | 33 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(30): Show | 33 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1143+30747G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31680968 | ||||||
| chr11:31680988
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1143+30767G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31680988 | ||||||
| chr11:31681267
|
G | A | 13 | a0001c0001t0006g0227a0001c0001t0006g0229a0001c0001t0006g0230others(10): Show | 13 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1143+31046G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31681267 | ||||||
| chr11:31681285
|
G | A | 1 | a0001c0001t0011g0189 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1143+31064G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31681285 | ||||||
| chr11:31681348
|
A | G | 1 | a0001c0001t0064g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1143+31127A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31681348 | ||||||
| chr11:31681425
|
G | A | 1 | a0001c0001t0002g0167 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1143+31204G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31681425 | ||||||
| chr11:31681455
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1143+31234C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31681455 | ||||||
| chr11:31681529
|
A | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+31308A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31681529 | ||||||
| chr11:31681609
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+31388C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31681609 | ||||||
| chr11:31681634
|
T | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+31413T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31681634 | ||||||
| chr11:31681663
|
A | G | 1 | a0001c0001t0016g0171 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1143+31442A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31681663 | ||||||
| chr11:31681741
|
C | CT | 69 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0027others(66): Show | 69 | HG00323.hp2 HG00597.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.1143+31537dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31681741 | |||||
| chr11:31681741
|
C | CTT | 42 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0034others(39): Show | 42 | HG00621.hp1 HG01071.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.1143+31536_1143+31 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31681741 | |||||
| chr11:31681741
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1143+31520C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31681741 | ||||||
| chr11:31681758
|
T | A | 2 | a0001c0001t0006g0231a0001c0001t0073g0237 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1143+31537T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31681758 | ||||||
| chr11:31681787
|
G | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+31566G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31681787 | ||||||
| chr11:31681804
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+31583C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31681804 | ||||||
| chr11:31682016
|
C | T | 1 | a0001c0001t0004g0043 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1143+31795C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31682016 | ||||||
| chr11:31682381
|
C | G | 1 | a0001c0001t0002g0127 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1143+32160C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31682381 | ||||||
| chr11:31682632
|
C | T | 1 | a0001c0001t0008g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1143+32411C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31682632 | ||||||
| chr11:31682790
|
G | C | 2 | a0001c0001t0001g0076a0001c0001t0069g0080 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1143+32569G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31682790 | ||||||
| chr11:31682910
|
C | T | 1 | a0001c0001t0004g0078 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1143+32689C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31682910 | ||||||
| chr11:31682919
|
C | T | 1 | a0001c0001t0007g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1143+32698C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31682919 | ||||||
| chr11:31682927
|
G | A | 10 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0062others(7): Show | 10 | NA18747.hp2 NA18947.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.1143+32706G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31682927 | ||||||
| chr11:31682982
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1143+32761T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31682982 | ||||||
| chr11:31683139
|
GT | G | 95 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(92): Show | 95 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.1143+32922delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31683139 | |||||
| chr11:31683150
|
A | G | 1 | a0001c0001t0080g0250 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1143+32929A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31683150 | ||||||
| chr11:31683161
|
A | T | 41 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0034others(38): Show | 41 | HG00323.hp2 HG00621.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1143+32940A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31683161 | ||||||
| chr11:31683483
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+33262C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31683483 | ||||||
| chr11:31683898
|
G | A | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+33677G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31683898 | ||||||
| chr11:31684054
|
A | G | 5 | a0001c0001t0002g0106a0001c0001t0002g0109a0001c0001t0010g0110others(2): Show | 5 | NA18942.hp1 NA18960.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143+33833A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31684054 | ||||||
| chr11:31684216
|
T | TA | 15 | a0001c0001t0002g0173a0001c0001t0002g0175a0001c0001t0006g0163others(12): Show | 15 | HG02027.hp2 HG02056.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.1143+34006dupA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31684216 | |||||
| chr11:31684219
|
A | G | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+33998A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31684219 | ||||||
| chr11:31684465
|
C | T | 1 | a0001c0001t0002g0109 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1143+34244C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31684465 | ||||||
| chr11:31684472
|
G | T | 1 | a0001c0001t0005g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1143+34251G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31684472 | ||||||
| chr11:31684600
|
G | A | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1143+34379G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31684600 | ||||||
| chr11:31684944
|
C | G | 1 | a0001c0001t0011g0011 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1143+34723C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31684944 | ||||||
| chr11:31685454
|
C | G | 1 | a0001c0001t0002g0117 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1143+35233C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31685454 | ||||||
| chr11:31685457
|
A | T | 1 | a0001c0001t0004g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1143+35236A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31685457 | ||||||
| chr11:31685460
|
ACATAGTT others(3888): Show |
A | 1 | a0001c0001t0004g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1143+35242_1143+39 others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31685460 | |||||
| chr11:31685703
|
G | A | 9 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143+35482G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31685703 | ||||||
| chr11:31685879
|
C | T | 1 | a0001c0001t0013g0156 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1143+35658C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31685879 | ||||||
| chr11:31685930
|
T | TA | 12 | a0001c0001t0001g0064a0001c0001t0003g0190a0001c0001t0006g0227others(9): Show | 12 | HG00639.hp2 HG01261.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1143+35726dupA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31685930 | |||||
| chr11:31685930
|
TA | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0114a0001c0001t0001g0118others(83): Show | 86 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1143+35726delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31685930 | |||||
| chr11:31686244
|
T | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+36023T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31686244 | ||||||
| chr11:31686328
|
G | GT | 15 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0064others(12): Show | 15 | HG01433.hp1 HG02027.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1143+36124dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31686328 | |||||
| chr11:31686334
|
T | TG | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+36113_1143+36 others(7): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31686334 | ||||||
| chr11:31686506
|
A | G | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+36285A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31686506 | ||||||
| chr11:31686585
|
G | C | 1 | a0001c0001t0019g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1143+36364G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31686585 | ||||||
| chr11:31686868
|
C | CA | 104 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(101): Show | 104 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(101): Show |
intron_variant | MODIFIER | c.1143+36660dupA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31686868 | |||||
| chr11:31687144
|
C | G | 1 | a0001c0001t0048g0215 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1143+36923C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31687144 | ||||||
| chr11:31687276
|
A | T | 2 | a0001c0001t0001g0076a0001c0001t0069g0080 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1143+37055A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31687276 | ||||||
| chr11:31687326
|
T | TTAGATTC others(5): Show |
1 | a0001c0001t0020g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1143+37106_1143+37 others(18): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31687326 | |||||
| chr11:31687352
|
A | G | 4 | a0001c0001t0002g0173a0001c0001t0002g0175a0001c0001t0015g0146others(1): Show | 4 | HG02027.hp2 HG02080.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+37131A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31687352 | ||||||
| chr11:31687510
|
T | C | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1143+37289T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31687510 | ||||||
| chr11:31687533
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1143+37312T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31687533 | ||||||
| chr11:31687841
|
T | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+37620T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31687841 | ||||||
| chr11:31688132
|
T | C | 5 | a0001c0002t0014g0246a0001c0002t0024g0244a0001c0002t0024g0248others(2): Show | 5 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143+37911T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31688132 | ||||||
| chr11:31688712
|
A | G | 1 | a0001c0001t0070g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1143+38491A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31688712 | ||||||
| chr11:31688873
|
G | T | 1 | a0001c0001t0004g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1143+38652G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31688873 | ||||||
| chr11:31689345
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1143+39124G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31689345 | ||||||
| chr11:31689357
|
A | T | 1 | a0001c0001t0004g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1143+39136A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31689357 | ||||||
| chr11:31689360
|
T | A | 1 | a0001c0001t0004g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1143+39139T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31689360 | ||||||
| chr11:31689361
|
G | T | 1 | a0001c0001t0004g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1143+39140G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31689361 | ||||||
| chr11:31689444
|
TA | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0037others(132): Show | 135 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.1143+39240delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31689444 | |||||
| chr11:31689444
|
TAA | T | 8 | a0001c0001t0003g0206a0001c0001t0003g0210a0001c0001t0005g0191others(5): Show | 8 | HG00280.hp2 HG01074.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1143+39239_1143+39 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31689444 | |||||
| chr11:31689604
|
A | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+39383A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31689604 | ||||||
| chr11:31689690
|
T | C | 1 | a0001c0001t0050g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1143+39469T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31689690 | ||||||
| chr11:31689756
|
T | C | 2 | a0001c0001t0003g0190a0001c0001t0060g0202 | 2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1143+39535T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31689756 | ||||||
| chr11:31689853
|
G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+39632G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31689853 | ||||||
| chr11:31690043
|
G | A | 1 | a0001c0001t0008g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1143+39822G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31690043 | ||||||
| chr11:31690143
|
G | C | 1 | a0001c0001t0022g0259 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1143+39922G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31690143 | ||||||
| chr11:31690145
|
G | A | 1 | a0001c0001t0062g0265 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1143+39924G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31690145 | ||||||
| chr11:31690310
|
C | T | 1 | a0001c0001t0060g0202 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1143+40089C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31690310 | ||||||
| chr11:31690365
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1143+40144C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31690365 | ||||||
| chr11:31690422
|
T | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+40201T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31690422 | ||||||
| chr11:31690431
|
AT | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0004g0001others(2): Show | 5 | HG01069.hp1 HG02647.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.1143+40211delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31690431 | ||||||
| chr11:31690432
|
T | A | 262 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(259): Show | 262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.1143+40211T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31690432 | ||||||
| chr11:31690528
|
T | C | 1 | a0001c0001t0078g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1143+40307T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31690528 | ||||||
| chr11:31690532
|
C | G | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1143+40311C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31690532 | ||||||
| chr11:31690766
|
G | T | 11 | a0001c0001t0003g0103a0001c0001t0003g0186a0001c0001t0003g0190others(8): Show | 11 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1143+40545G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31690766 | ||||||
| chr11:31690795
|
C | T | 1 | a0001c0001t0011g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1143+40574C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31690795 | ||||||
| chr11:31690796
|
C | CT | 54 | a0001c0001t0001g0135a0001c0001t0001g0185a0001c0001t0002g0175others(51): Show | 54 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1143+40594dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31690796 | |||||
| chr11:31690932
|
T | A | 3 | a0001c0001t0001g0258a0001c0001t0004g0257a0001c0002t0014g0256 | 3 | HG02896.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1143+40711T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31690932 | ||||||
| chr11:31691133
|
A | G | 1 | a0001c0001t0002g0167 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1143+40912A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31691133 | ||||||
| chr11:31691183
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+40962G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31691183 | ||||||
| chr11:31691262
|
T | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+41041T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31691262 | ||||||
| chr11:31691356
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+41135C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31691356 | ||||||
| chr11:31692027
|
A | G | 4 | a0001c0001t0027g0048a0001c0001t0027g0050a0001c0001t0053g0049others(1): Show | 4 | HG01496.hp2 HG02630.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+41806A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31692027 | ||||||
| chr11:31692100
|
A | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+41879A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31692100 | ||||||
| chr11:31692254
|
G | A | 1 | a0005c0006t0032g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1143+42033G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31692254 | ||||||
| chr11:31692325
|
A | G | 2 | a0001c0001t0007g0089a0001c0001t0008g0092 | 2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1143+42104A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31692325 | ||||||
| chr11:31692576
|
G | T | 2 | a0001c0001t0006g0231a0001c0001t0073g0237 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1143+42355G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31692576 | ||||||
| chr11:31692634
|
T | A | 1 | a0001c0001t0004g0017 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1143+42413T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31692634 | ||||||
| chr11:31692844
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1143+42623A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31692844 | ||||||
| chr11:31692893
|
C | T | 1 | a0001c0001t0005g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1143+42672C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31692893 | ||||||
| chr11:31692900
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1143+42679A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31692900 | ||||||
| chr11:31693094
|
A | G | 1 | a0001c0001t0003g0220 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1143+42873A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31693094 | ||||||
| chr11:31693151
|
C | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+42930C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31693151 | ||||||
| chr11:31693157
|
T | TTTA | 4 | a0001c0001t0027g0048a0001c0001t0027g0050a0001c0001t0053g0049others(1): Show | 4 | HG01496.hp2 HG02630.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+42953_1143+42 others(9): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31693157 | |||||
| chr11:31693194
|
A | G | 1 | a0001c0001t0004g0017 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1143+42973A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31693194 | ||||||
| chr11:31693265
|
C | T | 4 | a0001c0001t0004g0091a0001c0001t0057g0087a0001c0001t0067g0161others(1): Show | 4 | NA18943.hp1 NA18951.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+43044C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31693265 | ||||||
| chr11:31693857
|
A | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+43636A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31693857 | ||||||
| chr11:31693944
|
G | T | 2 | a0001c0001t0003g0206a0001c0001t0005g0191 | 2 | HG01496.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1143+43723G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31693944 | ||||||
| chr11:31694186
|
T | G | 11 | a0001c0001t0006g0227a0001c0001t0006g0229a0001c0001t0006g0230others(8): Show | 11 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.1143+43965T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31694186 | ||||||
| chr11:31694231
|
C | G | 1 | a0001c0001t0006g0163 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1143+44010C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31694231 | ||||||
| chr11:31694256
|
G | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1143+44035G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31694256 | ||||||
| chr11:31694295
|
G | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(83): Show | 86 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1143+44074G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31694295 | ||||||
| chr11:31694317
|
T | A | 97 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(94): Show | 97 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(94): Show |
intron_variant | MODIFIER | c.1143+44096T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31694317 | ||||||
| chr11:31694318
|
C | T | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1143+44097C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31694318 | ||||||
| chr11:31694357
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+44136G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31694357 | ||||||
| chr11:31694473
|
T | C | 2 | a0001c0001t0019g0084a0002c0003t0082g0207 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1143+44252T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31694473 | ||||||
| chr11:31694605
|
T | C | 6 | a0001c0002t0014g0246a0001c0002t0024g0244a0001c0002t0024g0248others(3): Show | 6 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+44384T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31694605 | ||||||
| chr11:31694643
|
C | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+44422C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31694643 | ||||||
| chr11:31694759
|
C | A | 1 | a0001c0001t0019g0095 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1143+44538C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31694759 | ||||||
| chr11:31694768
|
G | A | 5 | a0001c0001t0006g0227a0001c0001t0006g0229a0001c0001t0006g0230others(2): Show | 5 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143+44547G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31694768 | ||||||
| chr11:31694857
|
C | T | 2 | a0001c0001t0009g0180a0001c0001t0009g0195 | 2 | HG01074.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1143+44636C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31694857 | ||||||
| chr11:31695043
|
A | G | 1 | a0001c0001t0003g0196 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1143+44822A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695043 | ||||||
| chr11:31695447
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+45226C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695447 | ||||||
| chr11:31695448
|
G | A | 8 | a0001c0001t0002g0115a0001c0001t0002g0116a0001c0001t0002g0120others(5): Show | 8 | HG02027.hp1 HG02135.hp1 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1143+45227G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695448 | ||||||
| chr11:31695542
|
C | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+45321C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695542 | ||||||
| chr11:31695624
|
T | G | 6 | a0001c0002t0014g0246a0001c0002t0024g0244a0001c0002t0024g0248others(3): Show | 6 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+45403T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695624 | ||||||
| chr11:31695788
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+45567A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695788 | ||||||
| chr11:31695793
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+45572A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695793 | ||||||
| chr11:31695798
|
G | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+45577G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695798 | ||||||
| chr11:31695799
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+45578A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695799 | ||||||
| chr11:31695800
|
G | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+45579G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695800 | ||||||
| chr11:31695814
|
G | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+45593G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695814 | ||||||
| chr11:31695817
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+45596A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695817 | ||||||
| chr11:31695819
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+45598C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695819 | ||||||
| chr11:31695822
|
T | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+45601T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695822 | ||||||
| chr11:31695824
|
G | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+45603G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695824 | ||||||
| chr11:31695833
|
C | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+45612C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695833 | ||||||
| chr11:31695900
|
G | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+45679G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31695900 | ||||||
| chr11:31696080
|
A | G | 1 | a0001c0001t0004g0017 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1143+45859A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31696080 | ||||||
| chr11:31696265
|
G | A | 1 | a0001c0001t0007g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1143+46044G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31696265 | ||||||
| chr11:31696388
|
G | A | 4 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0007g0054others(1): Show | 4 | NA18971.hp2 NA18987.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+46167G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31696388 | ||||||
| chr11:31696812
|
A | C | 42 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(39): Show | 42 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1143+46591A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31696812 | ||||||
| chr11:31696922
|
C | T | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1143+46701C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31696922 | ||||||
| chr11:31696923
|
G | A | 41 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0034others(38): Show | 41 | HG00323.hp2 HG00621.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1143+46702G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31696923 | ||||||
| chr11:31697003
|
T | C | 2 | a0001c0001t0006g0230a0001c0001t0016g0236 | 2 | HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1143+46782T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31697003 | ||||||
| chr11:31697014
|
C | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+46793C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31697014 | ||||||
| chr11:31697066
|
G | T | 1 | a0001c0001t0013g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1143+46845G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31697066 | ||||||
| chr11:31697278
|
C | T | 1 | a0001c0001t0002g0254 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1143+47057C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31697278 | ||||||
| chr11:31697360
|
T | C | 2 | a0001c0001t0011g0189a0001c0001t0011g0197 | 2 | HG03239.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1143+47139T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31697360 | ||||||
| chr11:31697556
|
T | C | 2 | a0001c0001t0001g0243a0001c0001t0034g0238 | 2 | HG01109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1143+47335T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31697556 | ||||||
| chr11:31697674
|
G | C | 2 | a0001c0001t0001g0076a0001c0001t0069g0080 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1143+47453G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31697674 | ||||||
| chr11:31697956
|
C | CT | 8 | a0001c0001t0005g0264a0001c0001t0007g0072a0001c0001t0008g0269others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+47744dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31697956 | |||||
| chr11:31697956
|
CT | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+47744delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31697956 | |||||
| chr11:31698080
|
T | C | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1143+47859T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31698080 | ||||||
| chr11:31698460
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1143+48239T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31698460 | ||||||
| chr11:31698483
|
A | G | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0036others(127): Show | 130 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1143+48262A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31698483 | ||||||
| chr11:31699073
|
A | G | 42 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(39): Show | 42 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1143+48852A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31699073 | ||||||
| chr11:31699149
|
A | G | 1 | a0001c0001t0005g0012 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1143+48928A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31699149 | ||||||
| chr11:31699535
|
C | G | 1 | a0001c0001t0071g0024 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1143+49314C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31699535 | ||||||
| chr11:31699560
|
C | T | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1143+49339C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31699560 | ||||||
| chr11:31699677
|
A | G | 6 | a0001c0002t0014g0246a0001c0002t0024g0244a0001c0002t0024g0248others(3): Show | 6 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+49456A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31699677 | ||||||
| chr11:31699745
|
G | A | 11 | a0001c0001t0006g0227a0001c0001t0006g0229a0001c0001t0006g0230others(8): Show | 11 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.1143+49524G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31699745 | ||||||
| chr11:31699821
|
A | G | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1143+49600A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31699821 | ||||||
| chr11:31700155
|
T | C | 1 | a0001c0001t0077g0008 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1143+49934T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31700155 | ||||||
| chr11:31700195
|
G | A | 3 | a0001c0001t0003g0192a0001c0001t0003g0210a0001c0001t0003g0211 | 3 | HG01168.hp1 HG01169.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1143+49974G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31700195 | ||||||
| chr11:31700226
|
T | A | 1 | a0001c0001t0002g0106 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1143+50005T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31700226 | ||||||
| chr11:31700613
|
T | G | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+50392T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31700613 | ||||||
| chr11:31700751
|
G | T | 6 | a0001c0002t0014g0246a0001c0002t0024g0244a0001c0002t0024g0248others(3): Show | 6 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+50530G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31700751 | ||||||
| chr11:31700865
|
A | G | 1 | a0003c0007t0001g0225 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1143+50644A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31700865 | ||||||
| chr11:31700875
|
T | G | 4 | a0001c0001t0003g0186a0001c0001t0003g0199a0001c0001t0003g0200others(1): Show | 4 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+50654T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31700875 | ||||||
| chr11:31700936
|
C | T | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(65): Show | 68 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1143+50715C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31700936 | ||||||
| chr11:31701116
|
C | T | 6 | a0001c0001t0019g0095a0001c0002t0014g0097a0002c0003t0001g0093others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+50895C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31701116 | ||||||
| chr11:31701193
|
C | G | 1 | a0001c0001t0016g0171 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1143+50972C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31701193 | ||||||
| chr11:31701474
|
G | T | 1 | a0001c0001t0012g0023 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1143+51253G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31701474 | ||||||
| chr11:31701760
|
T | C | 1 | a0005c0006t0032g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1143+51539T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31701760 | ||||||
| chr11:31701967
|
G | T | 1 | a0001c0001t0055g0083 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1143+51746G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31701967 | ||||||
| chr11:31702165
|
G | A | 1 | a0001c0001t0012g0136 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1143+51944G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31702165 | ||||||
| chr11:31702184
|
A | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+51963A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31702184 | ||||||
| chr11:31702298
|
G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+52077G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31702298 | ||||||
| chr11:31702313
|
A | T | 1 | a0001c0001t0070g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1143+52092A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31702313 | ||||||
| chr11:31702327
|
CAATAAT | C | 261 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.1143+52121_1143+52 others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31702327 | |||||
| chr11:31702647
|
T | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1143+52426T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31702647 | ||||||
| chr11:31702922
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+52701A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31702922 | ||||||
| chr11:31703015
|
G | A | 1 | a0002c0003t0001g0094 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1143+52794G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31703015 | ||||||
| chr11:31703051
|
C | G | 1 | a0001c0001t0002g0167 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1143+52830C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31703051 | ||||||
| chr11:31703057
|
G | T | 2 | a0001c0001t0001g0243a0001c0001t0034g0238 | 2 | HG01109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1143+52836G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31703057 | ||||||
| chr11:31703134
|
A | G | 1 | a0001c0001t0064g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1143+52913A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31703134 | ||||||
| chr11:31703640
|
C | T | 1 | a0001c0001t0004g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1143+53419C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31703640 | ||||||
| chr11:31703702
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+53481A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31703702 | ||||||
| chr11:31703763
|
C | G | 2 | a0001c0001t0019g0084a0002c0003t0082g0207 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1143+53542C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31703763 | ||||||
| chr11:31703864
|
A | G | 1 | a0001c0001t0009g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1143+53643A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31703864 | ||||||
| chr11:31703955
|
C | T | 2 | a0001c0001t0029g0164a0001c0001t0029g0165 | 2 | NA19060.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1143+53734C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31703955 | ||||||
| chr11:31704227
|
TA | T | 6 | a0001c0001t0001g0037a0001c0001t0001g0258a0001c0001t0004g0026others(3): Show | 6 | HG02080.hp1 HG02896.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+54019delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31704227 | |||||
| chr11:31704307
|
A | G | 6 | a0001c0001t0001g0027a0001c0001t0001g0042a0001c0001t0001g0057others(3): Show | 6 | HG01123.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1143+54086A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31704307 | ||||||
| chr11:31704421
|
G | C | 1 | a0001c0001t0033g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1143+54200G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31704421 | ||||||
| chr11:31704776
|
C | T | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1143+54555C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31704776 | ||||||
| chr11:31704867
|
C | T | 1 | a0001c0001t0010g0122 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1143+54646C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31704867 | ||||||
| chr11:31704914
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+54693A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31704914 | ||||||
| chr11:31705024
|
AT | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0058a0001c0001t0001g0082others(1): Show | 4 | HG01123.hp2 HG01934.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1143+54805delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31705024 | |||||
| chr11:31705025
|
T | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(96): Show | 99 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(96): Show |
intron_variant | MODIFIER | c.1143+54804T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31705025 | ||||||
| chr11:31705295
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+55074T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31705295 | ||||||
| chr11:31705395
|
T | C | 3 | a0001c0001t0010g0145a0001c0001t0054g0140a0001c0001t0066g0141 | 3 | HG01074.hp1 HG01169.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1143+55174T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31705395 | ||||||
| chr11:31705457
|
A | C | 1 | a0001c0001t0003g0206 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1143+55236A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31705457 | ||||||
| chr11:31705752
|
C | A | 1 | a0001c0001t0001g0004 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1143+55531C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31705752 | ||||||
| chr11:31705850
|
TTTTG | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1143+55637_1143+55 others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31705850 | |||||
| chr11:31705984
|
C | G | 2 | a0001c0001t0019g0084a0002c0003t0082g0207 | 2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1143+55763C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31705984 | ||||||
| chr11:31706099
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1143+55878G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31706099 | ||||||
| chr11:31706269
|
A | C | 2 | a0001c0001t0070g0219a0001c0001t0081g0223 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1143+56048A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31706269 | ||||||
| chr11:31706286
|
A | G | 1 | a0001c0001t0012g0023 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1143+56065A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31706286 | ||||||
| chr11:31706445
|
ATATAGTG others(11): Show |
A | 4 | a0001c0001t0027g0048a0001c0001t0027g0050a0001c0001t0053g0049others(1): Show | 4 | HG01496.hp2 HG02630.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+56225_1143+56 others(24): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31706445 | ||||||
| chr11:31706518
|
T | G | 1 | a0001c0001t0070g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1143+56297T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31706518 | ||||||
| chr11:31706535
|
G | T | 41 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0034others(38): Show | 41 | HG00323.hp2 HG00621.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.1143+56314G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31706535 | ||||||
| chr11:31706645
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1143+56424A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31706645 | ||||||
| chr11:31706722
|
G | T | 1 | a0001c0002t0014g0246 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1143+56501G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31706722 | ||||||
| chr11:31706925
|
A | G | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1143+56704A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31706925 | ||||||
| chr11:31707369
|
T | C | 1 | a0001c0001t0003g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1143+57148T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31707369 | ||||||
| chr11:31707375
|
G | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+57154G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31707375 | ||||||
| chr11:31707588
|
G | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1143+57367G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31707588 | ||||||
| chr11:31707898
|
A | C | 1 | a0001c0001t0048g0215 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1143+57677A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31707898 | ||||||
| chr11:31708096
|
G | A | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1143+57875G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31708096 | ||||||
| chr11:31708244
|
A | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+58023A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31708244 | ||||||
| chr11:31708341
|
C | T | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1143+58120C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31708341 | ||||||
| chr11:31708377
|
C | G | 1 | a0001c0001t0005g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1143+58156C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31708377 | ||||||
| chr11:31708378
|
A | G | 2 | a0001c0002t0024g0244a0001c0002t0045g0245 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1143+58157A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31708378 | ||||||
| chr11:31708426
|
A | G | 1 | a0001c0001t0002g0137 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1143+58205A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31708426 | ||||||
| chr11:31708867
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1143+58646A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31708867 | ||||||
| chr11:31708998
|
A | G | 1 | a0001c0001t0007g0072 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1143+58777A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31708998 | ||||||
| chr11:31709042
|
T | G | 6 | a0001c0001t0005g0264a0001c0001t0017g0266a0001c0001t0017g0268others(3): Show | 6 | HG02145.hp2 HG02258.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1143+58821T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31709042 | ||||||
| chr11:31709207
|
G | A | 1 | a0001c0002t0014g0256 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1143+58986G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31709207 | ||||||
| chr11:31709419
|
G | A | 1 | a0001c0001t0013g0156 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1143+59198G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31709419 | ||||||
| chr11:31709498
|
G | A | 1 | a0001c0001t0075g0217 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1143+59277G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31709498 | ||||||
| chr11:31709562
|
A | G | 2 | a0001c0001t0006g0231a0001c0001t0073g0237 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1143+59341A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31709562 | ||||||
| chr11:31709623
|
G | T | 1 | a0001c0001t0054g0140 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1143+59402G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31709623 | ||||||
| chr11:31709716
|
A | G | 1 | a0001c0001t0007g0072 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1143+59495A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31709716 | ||||||
| chr11:31710069
|
G | C | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(235): Show | 238 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.1143+59848G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31710069 | ||||||
| chr11:31710073
|
G | A | 1 | a0001c0001t0009g0180 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1143+59852G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31710073 | ||||||
| chr11:31710074
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1143+59853G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31710074 | ||||||
| chr11:31710264
|
G | C | 1 | a0001c0001t0062g0265 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1143+60043G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31710264 | ||||||
| chr11:31710303
|
G | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+60082G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31710303 | ||||||
| chr11:31710385
|
G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(125): Show | 128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1143+60164G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31710385 | ||||||
| chr11:31710727
|
A | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+60506A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31710727 | ||||||
| chr11:31710772
|
G | A | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1143+60551G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31710772 | ||||||
| chr11:31711091
|
C | T | 1 | a0001c0001t0008g0218 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1143+60870C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31711091 | ||||||
| chr11:31711275
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1143+61054G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31711275 | ||||||
| chr11:31711566
|
G | A | 2 | a0001c0001t0006g0231a0001c0001t0073g0237 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1143+61345G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31711566 | ||||||
| chr11:31711879
|
A | G | 2 | a0001c0001t0003g0181a0001c0001t0003g0184 | 2 | HG02055.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1143+61658A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31711879 | ||||||
| chr11:31712109
|
A | G | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+61888A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31712109 | ||||||
| chr11:31712321
|
A | T | 1 | a0001c0001t0033g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1143+62100A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31712321 | ||||||
| chr11:31712868
|
T | C | 3 | a0001c0001t0005g0005a0001c0001t0005g0006a0001c0001t0017g0007 | 3 | HG02280.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1143+62647T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31712868 | ||||||
| chr11:31713139
|
A | G | 2 | a0001c0001t0002g0127a0001c0001t0002g0167 | 2 | NA18945.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1143+62918A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31713139 | ||||||
| chr11:31713193
|
T | C | 102 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(99): Show | 102 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(99): Show |
intron_variant | MODIFIER | c.1143+62972T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31713193 | ||||||
| chr11:31713446
|
A | G | 31 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(28): Show | 31 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1143+63225A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31713446 | ||||||
| chr11:31713767
|
T | C | 10 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0062others(7): Show | 10 | NA18747.hp2 NA18947.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.1143+63546T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31713767 | ||||||
| chr11:31713926
|
A | G | 7 | a0001c0001t0002g0102a0001c0001t0002g0130a0001c0001t0002g0177others(4): Show | 7 | HG01168.hp2 HG02602.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1143+63705A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31713926 | ||||||
| chr11:31714079
|
A | G | 2 | a0001c0001t0003g0196a0001c0001t0005g0203 | 2 | HG02258.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1143+63858A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31714079 | ||||||
| chr11:31714145
|
A | G | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1143+63924A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31714145 | ||||||
| chr11:31714410
|
T | A | 1 | a0001c0001t0001g0082 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1143+64189T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31714410 | ||||||
| chr11:31714661
|
A | G | 1 | a0001c0001t0059g0182 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1143+64440A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31714661 | ||||||
| chr11:31715049
|
A | G | 4 | a0001c0001t0002g0173a0001c0001t0002g0175a0001c0001t0015g0146others(1): Show | 4 | HG02027.hp2 HG02080.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+64828A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31715049 | ||||||
| chr11:31715171
|
G | A | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1143+64950G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31715171 | ||||||
| chr11:31715202
|
G | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1143+64981G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31715202 | ||||||
| chr11:31715559
|
A | C | 1 | a0001c0001t0020g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1143+65338A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31715559 | ||||||
| chr11:31715725
|
C | G | 1 | a0001c0001t0005g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1143+65504C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31715725 | ||||||
| chr11:31715986
|
A | AGAGATAT others(55): Show |
1 | a0001c0001t0022g0101 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1143+65766_1143+65 others(68): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31715986 | |||||
| chr11:31715993
|
T | C | 4 | a0001c0001t0027g0048a0001c0001t0027g0050a0001c0001t0053g0049others(1): Show | 4 | HG01496.hp2 HG02630.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1143+65772T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31715993 | ||||||
| chr11:31716196
|
A | T | 5 | a0001c0001t0002g0102a0001c0001t0002g0177a0001c0001t0002g0178others(2): Show | 5 | HG01168.hp2 HG03927.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1143+65975A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31716196 | ||||||
| chr11:31716366
|
C | T | 1 | a0001c0001t0006g0227 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1143+66145C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31716366 | ||||||
| chr11:31716557
|
A | G | 1 | a0001c0001t0004g0075 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1143+66336A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31716557 | ||||||
| chr11:31716969
|
A | G | 1 | a0001c0001t0004g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1144-66424A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31716969 | ||||||
| chr11:31717144
|
G | A | 1 | a0001c0001t0051g0134 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1144-66249G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31717144 | ||||||
| chr11:31717251
|
A | C | 6 | a0001c0002t0014g0246a0001c0002t0024g0244a0001c0002t0024g0248others(3): Show | 6 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144-66142A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31717251 | ||||||
| chr11:31717300
|
A | G | 1 | a0001c0001t0047g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1144-66093A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31717300 | ||||||
| chr11:31717647
|
G | A | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1144-65746G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31717647 | ||||||
| chr11:31717725
|
A | T | 30 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(27): Show | 30 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1144-65668A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31717725 | ||||||
| chr11:31717851
|
T | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-65542T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31717851 | ||||||
| chr11:31718329
|
C | A | 2 | a0001c0001t0011g0189a0001c0001t0011g0197 | 2 | HG03239.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1144-65064C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31718329 | ||||||
| chr11:31718443
|
A | T | 1 | a0001c0001t0013g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1144-64950A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31718443 | ||||||
| chr11:31718717
|
A | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(93): Show | 96 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.1144-64676A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31718717 | ||||||
| chr11:31719003
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1144-64390A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31719003 | ||||||
| chr11:31719096
|
G | A | 6 | a0001c0002t0014g0246a0001c0002t0024g0244a0001c0002t0024g0248others(3): Show | 6 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144-64297G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31719096 | ||||||
| chr11:31719118
|
G | C | 31 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(28): Show | 31 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1144-64275G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31719118 | ||||||
| chr11:31719183
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1144-64210G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31719183 | ||||||
| chr11:31719212
|
G | T | 1 | a0001c0001t0002g0015 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1144-64181G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31719212 | ||||||
| chr11:31719351
|
T | A | 2 | a0001c0001t0009g0187a0004c0005t0009g0188 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1144-64042T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31719351 | ||||||
| chr11:31719372
|
G | A | 1 | a0001c0001t0037g0147 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1144-64021G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31719372 | ||||||
| chr11:31719441
|
A | C | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.1144-63952A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31719441 | ||||||
| chr11:31719530
|
C | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-63863C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31719530 | ||||||
| chr11:31719704
|
T | A | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1144-63689T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31719704 | ||||||
| chr11:31719742
|
G | T | 30 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(27): Show | 30 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1144-63651G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31719742 | ||||||
| chr11:31719827
|
G | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-63566G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31719827 | ||||||
| chr11:31720019
|
C | A | 1 | a0001c0001t0022g0101 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1144-63374C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31720019 | ||||||
| chr11:31720150
|
G | A | 6 | a0001c0002t0014g0246a0001c0002t0024g0244a0001c0002t0024g0248others(3): Show | 6 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144-63243G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31720150 | ||||||
| chr11:31720373
|
G | T | 1 | a0001c0001t0004g0078 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1144-63020G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31720373 | ||||||
| chr11:31720464
|
G | A | 1 | a0001c0001t0057g0087 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1144-62929G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31720464 | ||||||
| chr11:31720499
|
C | A | 1 | a0001c0001t0001g0064 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1144-62894C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31720499 | ||||||
| chr11:31720500
|
A | T | 1 | a0001c0001t0001g0064 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1144-62893A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31720500 | ||||||
| chr11:31720504
|
A | T | 1 | a0001c0001t0041g0129 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1144-62889A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31720504 | ||||||
| chr11:31720530
|
C | A | 1 | a0001c0001t0080g0250 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1144-62863C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31720530 | ||||||
| chr11:31720538
|
G | GT | 269 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(266): Show | 269 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.1144-62854dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31720538 | |||||
| chr11:31720570
|
G | A | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(93): Show | 96 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.1144-62823G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31720570 | ||||||
| chr11:31720767
|
A | G | 1 | a0006c0004t0076g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1144-62626A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31720767 | ||||||
| chr11:31720807
|
T | C | 102 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(99): Show | 102 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(99): Show |
intron_variant | MODIFIER | c.1144-62586T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31720807 | ||||||
| chr11:31720808
|
A | G | 1 | a0001c0001t0007g0089 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1144-62585A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31720808 | ||||||
| chr11:31720981
|
G | A | 1 | a0001c0001t0004g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1144-62412G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31720981 | ||||||
| chr11:31721268
|
G | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1144-62125G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31721268 | ||||||
| chr11:31721793
|
A | G | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(93): Show | 96 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.1144-61600A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31721793 | ||||||
| chr11:31721813
|
C | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1144-61580C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31721813 | ||||||
| chr11:31721968
|
G | A | 1 | a0001c0001t0012g0023 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1144-61425G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31721968 | ||||||
| chr11:31721974
|
A | G | 2 | a0001c0001t0006g0231a0001c0001t0073g0237 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1144-61419A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31721974 | ||||||
| chr11:31722059
|
T | G | 1 | a0001c0001t0003g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1144-61334T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31722059 | ||||||
| chr11:31722310
|
C | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-61083C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31722310 | ||||||
| chr11:31722415
|
A | G | 1 | a0001c0001t0030g0232 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1144-60978A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31722415 | ||||||
| chr11:31722417
|
G | A | 1 | a0003c0007t0001g0225 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1144-60976G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31722417 | ||||||
| chr11:31722511
|
C | A | 1 | a0001c0001t0007g0072 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1144-60882C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31722511 | ||||||
| chr11:31722566
|
G | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-60827G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31722566 | ||||||
| chr11:31722665
|
T | TTC | 5 | a0001c0001t0002g0152a0001c0001t0006g0170a0001c0001t0012g0136others(2): Show | 5 | HG00280.hp1 HG02145.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-60698_1144-60 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31722665 | |||||
| chr11:31722665
|
TTC | T | 141 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(138): Show | 141 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(138): Show |
intron_variant | MODIFIER | c.1144-60698_1144-60 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31722665 | |||||
| chr11:31722665
|
TTCTC | T | 20 | a0001c0001t0001g0138a0001c0001t0001g0185a0001c0001t0002g0117others(17): Show | 20 | HG01074.hp1 HG01169.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1144-60700_1144-60 others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31722665 | |||||
| chr11:31722665
|
TTCTCTC | T | 12 | a0001c0001t0001g0004a0001c0001t0006g0227a0001c0001t0006g0229others(9): Show | 12 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.1144-60702_1144-60 others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31722665 | |||||
| chr11:31722695
|
C | G | 1 | a0001c0001t0004g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1144-60698C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31722695 | ||||||
| chr11:31722721
|
C | CTT | 182 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(179): Show | 182 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(179): Show |
intron_variant | MODIFIER | c.1144-60671_1144-60 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31722721 | |||||
| chr11:31722721
|
C | T | 2 | a0001c0001t0007g0089a0001c0001t0008g0092 | 2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1144-60672C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31722721 | ||||||
| chr11:31722908
|
C | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-60485C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31722908 | ||||||
| chr11:31723193
|
A | G | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-60200A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31723193 | ||||||
| chr11:31723309
|
G | C | 1 | a0001c0001t0001g0056 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1144-60084G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31723309 | ||||||
| chr11:31723415
|
A | G | 4 | a0001c0001t0026g0251a0001c0001t0026g0252a0001c0001t0030g0232others(1): Show | 4 | HG01243.hp2 HG02486.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144-59978A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31723415 | ||||||
| chr11:31723613
|
C | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1144-59780C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31723613 | ||||||
| chr11:31723707
|
G | A | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-59686G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31723707 | ||||||
| chr11:31723736
|
C | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-59657C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31723736 | ||||||
| chr11:31723810
|
T | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-59583T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31723810 | ||||||
| chr11:31723966
|
G | A | 2 | a0001c0001t0027g0048a0001c0001t0063g0047 | 2 | HG01496.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1144-59427G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31723966 | ||||||
| chr11:31724263
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1144-59130C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31724263 | ||||||
| chr11:31724617
|
C | T | 5 | a0001c0001t0006g0227a0001c0001t0006g0229a0001c0001t0006g0230others(2): Show | 5 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1144-58776C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31724617 | ||||||
| chr11:31724824
|
T | A | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1144-58569T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31724824 | ||||||
| chr11:31724999
|
G | A | 3 | a0001c0001t0010g0145a0001c0001t0054g0140a0001c0001t0066g0141 | 3 | HG01074.hp1 HG01169.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1144-58394G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31724999 | ||||||
| chr11:31725163
|
CT | C | 7 | a0001c0001t0019g0095a0001c0002t0014g0097a0002c0003t0001g0093others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144-58226delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31725163 | |||||
| chr11:31725278
|
G | A | 2 | a0001c0001t0020g0241a0001c0001t0020g0242 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1144-58115G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31725278 | ||||||
| chr11:31725287
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1144-58106G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31725287 | ||||||
| chr11:31725719
|
G | A | 8 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0055others(5): Show | 8 | HG00323.hp2 HG01081.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1144-57674G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31725719 | ||||||
| chr11:31725753
|
T | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-57640T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31725753 | ||||||
| chr11:31725830
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0255a0001c0001t0004g0078others(1): Show | 4 | NA18942.hp2 NA18946.hp1 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-57563A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31725830 | ||||||
| chr11:31725921
|
G | A | 1 | a0001c0001t0062g0265 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1144-57472G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31725921 | ||||||
| chr11:31726210
|
T | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1144-57183T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31726210 | ||||||
| chr11:31726522
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1144-56871G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31726522 | ||||||
| chr11:31726683
|
A | G | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1144-56710A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31726683 | ||||||
| chr11:31726746
|
C | T | 5 | a0001c0001t0002g0102a0001c0001t0002g0177a0001c0001t0002g0178others(2): Show | 5 | HG01168.hp2 HG03927.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1144-56647C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31726746 | ||||||
| chr11:31727177
|
G | A | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1144-56216G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31727177 | ||||||
| chr11:31727191
|
A | G | 2 | a0001c0001t0007g0054a0001c0001t0038g0053 | 2 | NA18987.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1144-56202A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31727191 | ||||||
| chr11:31727212
|
C | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-56181C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31727212 | ||||||
| chr11:31727244
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1144-56149T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31727244 | ||||||
| chr11:31727264
|
T | G | 30 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(27): Show | 30 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1144-56129T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31727264 | ||||||
| chr11:31727429
|
G | A | 2 | a0001c0001t0002g0127a0001c0001t0002g0167 | 2 | NA18945.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1144-55964G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31727429 | ||||||
| chr11:31727574
|
T | C | 1 | a0001c0001t0016g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1144-55819T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31727574 | ||||||
| chr11:31727705
|
A | T | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1144-55688A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31727705 | ||||||
| chr11:31727728
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0033others(1): Show | 4 | HG00738.hp1 HG01258.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144-55665G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31727728 | ||||||
| chr11:31728317
|
A | G | 1 | a0001c0001t0009g0180 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1144-55076A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31728317 | ||||||
| chr11:31728577
|
G | A | 5 | a0001c0001t0003g0103a0001c0001t0003g0186a0001c0001t0003g0199others(2): Show | 5 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1144-54816G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31728577 | ||||||
| chr11:31728635
|
G | A | 1 | a0001c0001t0005g0191 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1144-54758G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31728635 | ||||||
| chr11:31729029
|
G | C | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | NA18946.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1144-54364G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31729029 | ||||||
| chr11:31729034
|
G | A | 1 | a0001c0001t0030g0232 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1144-54359G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31729034 | ||||||
| chr11:31729346
|
T | C | 1 | a0001c0001t0080g0250 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1144-54047T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31729346 | ||||||
| chr11:31729613
|
A | G | 1 | a0001c0001t0042g0157 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1144-53780A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31729613 | ||||||
| chr11:31729805
|
T | C | 2 | a0001c0001t0001g0074a0001c0001t0007g0045 | 2 | HG03831.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1144-53588T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31729805 | ||||||
| chr11:31729834
|
A | G | 1 | a0001c0001t0005g0142 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1144-53559A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31729834 | ||||||
| chr11:31729950
|
T | A | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1144-53443T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31729950 | ||||||
| chr11:31729982
|
A | T | 1 | a0003c0007t0001g0225 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1144-53411A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31729982 | ||||||
| chr11:31730022
|
A | G | 1 | a0001c0001t0004g0026 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1144-53371A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31730022 | ||||||
| chr11:31730155
|
C | T | 1 | a0001c0001t0048g0215 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1144-53238C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31730155 | ||||||
| chr11:31730516
|
G | A | 3 | a0001c0001t0003g0192a0001c0001t0003g0210a0001c0001t0003g0211 | 3 | HG01168.hp1 HG01169.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1144-52877G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31730516 | ||||||
| chr11:31730829
|
C | T | 1 | a0001c0001t0071g0024 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1144-52564C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31730829 | ||||||
| chr11:31730879
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1144-52514A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31730879 | ||||||
| chr11:31731014
|
C | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1144-52379C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31731014 | ||||||
| chr11:31731265
|
G | C | 1 | a0001c0001t0033g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1144-52128G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31731265 | ||||||
| chr11:31731323
|
G | A | 93 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(90): Show | 93 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.1144-52070G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31731323 | ||||||
| chr11:31731500
|
C | T | 1 | a0001c0001t0066g0141 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1144-51893C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31731500 | ||||||
| chr11:31731567
|
G | GGCGTGTG others(5): Show |
2 | a0001c0001t0001g0027a0001c0001t0007g0081 | 2 | NA18977.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1144-51825_1144-51 others(18): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31731567 | |||||
| chr11:31731567
|
G | GGT | 85 | a0001c0001t0001g0114a0001c0001t0001g0118a0001c0001t0001g0128others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.1144-51793_1144-51 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31731567 | |||||
| chr11:31731567
|
G | GGTGT | 11 | a0001c0001t0001g0174a0001c0001t0003g0220a0001c0001t0015g0146others(8): Show | 11 | HG00280.hp2 HG01943.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1144-51795_1144-51 others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31731567 | |||||
| chr11:31731567
|
G | GGTGTGT | 35 | a0001c0001t0001g0016a0001c0001t0001g0185a0001c0001t0003g0103others(32): Show | 35 | HG00639.hp1 HG00642.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1144-51797_1144-51 others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31731567 | |||||
| chr11:31731567
|
G | GGTGTGTG others(1): Show |
22 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0003g0181others(19): Show | 22 | HG01168.hp1 HG01169.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1144-51799_1144-51 others(14): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31731567 | |||||
| chr11:31731567
|
G | GGTGTGTG others(3): Show |
46 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0032others(43): Show | 46 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.1144-51801_1144-51 others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31731567 | |||||
| chr11:31731567
|
G | GGTGTGTG others(5): Show |
33 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0042others(30): Show | 33 | HG01123.hp2 HG01496.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.1144-51803_1144-51 others(18): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31731567 | |||||
| chr11:31731567
|
G | GGTGTGTG others(7): Show |
14 | a0001c0001t0001g0046a0001c0001t0001g0263a0001c0001t0002g0015others(11): Show | 14 | HG00639.hp2 HG01081.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1144-51805_1144-51 others(20): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31731567 | |||||
| chr11:31731567
|
G | GGTGTGTG others(9): Show |
7 | a0001c0001t0001g0058a0001c0001t0005g0012a0001c0001t0009g0240others(4): Show | 7 | HG01243.hp2 HG01934.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144-51807_1144-51 others(22): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31731567 | |||||
| chr11:31731567
|
G | GGTGTGTG others(11): Show |
4 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0026g0252others(1): Show | 4 | HG03195.hp2 HG03453.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-51809_1144-51 others(24): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31731567 | |||||
| chr11:31731567
|
G | GGTGTGTG others(13): Show |
2 | a0001c0001t0049g0262a0001c0001t0080g0250 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1144-51811_1144-51 others(26): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31731567 | |||||
| chr11:31731567
|
G | GGTGTGTG others(15): Show |
1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1144-51813_1144-51 others(28): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31731567 | |||||
| chr11:31731567
|
G | GGTGTGTG others(17): Show |
1 | a0001c0001t0001g0258 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1144-51815_1144-51 others(30): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31731567 | |||||
| chr11:31731567
|
G | GGTGTGTG others(21): Show |
1 | a0001c0001t0004g0257 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1144-51819_1144-51 others(34): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31731567 | |||||
| chr11:31731829
|
A | G | 31 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(28): Show | 31 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1144-51564A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31731829 | ||||||
| chr11:31731902
|
T | C | 1 | a0001c0001t0080g0250 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1144-51491T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31731902 | ||||||
| chr11:31732102
|
A | G | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-51291A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31732102 | ||||||
| chr11:31732200
|
T | A | 1 | a0001c0001t0003g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1144-51193T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31732200 | ||||||
| chr11:31732398
|
C | T | 104 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(101): Show | 104 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(101): Show |
intron_variant | MODIFIER | c.1144-50995C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31732398 | ||||||
| chr11:31732422
|
C | T | 1 | a0001c0001t0003g0183 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1144-50971C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31732422 | ||||||
| chr11:31732433
|
A | T | 1 | a0001c0001t0005g0021 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1144-50960A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31732433 | ||||||
| chr11:31732469
|
T | TA | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0016others(168): Show | 171 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(168): Show |
intron_variant | MODIFIER | c.1144-50910dupA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31732469 | |||||
| chr11:31732480
|
A | AT | 3 | a0001c0001t0007g0089a0001c0001t0008g0092a0001c0001t0057g0087 | 3 | HG02647.hp2 HG03195.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1144-50913_1144-50 others(7): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31732480 | ||||||
| chr11:31732480
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1144-50913A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31732480 | ||||||
| chr11:31733033
|
G | A | 2 | a0001c0001t0009g0180a0001c0001t0009g0195 | 2 | HG01074.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1144-50360G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31733033 | ||||||
| chr11:31733166
|
A | G | 1 | a0001c0001t0031g0125 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1144-50227A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31733166 | ||||||
| chr11:31733230
|
ATTTGG | A | 3 | a0001c0001t0003g0192a0001c0001t0003g0210a0001c0001t0003g0211 | 3 | HG01168.hp1 HG01169.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1144-50162_1144-50 others(11): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31733230 | ||||||
| chr11:31733276
|
G | C | 1 | a0001c0001t0011g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1144-50117G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31733276 | ||||||
| chr11:31733346
|
G | A | 1 | a0001c0001t0057g0087 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1144-50047G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31733346 | ||||||
| chr11:31733434
|
G | A | 1 | a0001c0001t0009g0198 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1144-49959G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31733434 | ||||||
| chr11:31733476
|
C | CA | 107 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(104): Show | 107 | HG00323.hp2 HG00597.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.1144-49898dupA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31733476 | |||||
| chr11:31733476
|
CA | C | 37 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0002g0150others(34): Show | 37 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.1144-49898delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31733476 | |||||
| chr11:31733515
|
AGAG | A | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-49874_1144-49 others(9): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31733515 | |||||
| chr11:31733607
|
A | C | 6 | a0001c0001t0004g0071a0001c0001t0007g0014a0001c0001t0027g0048others(3): Show | 6 | HG01496.hp2 HG02055.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144-49786A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31733607 | ||||||
| chr11:31733895
|
A | G | 7 | a0001c0002t0014g0246a0001c0002t0014g0256a0001c0002t0024g0244others(4): Show | 7 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-49498A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31733895 | ||||||
| chr11:31733982
|
A | G | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1144-49411A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31733982 | ||||||
| chr11:31734269
|
A | G | 1 | a0001c0001t0003g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1144-49124A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31734269 | ||||||
| chr11:31734448
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0005g0029 | 2 | HG00738.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1144-48945A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31734448 | ||||||
| chr11:31734451
|
T | C | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1144-48942T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31734451 | ||||||
| chr11:31734457
|
A | G | 111 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(108): Show | 111 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(108): Show |
intron_variant | MODIFIER | c.1144-48936A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31734457 | ||||||
| chr11:31734747
|
A | G | 1 | a0006c0004t0076g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1144-48646A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31734747 | ||||||
| chr11:31734878
|
A | C | 141 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(138): Show | 141 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(138): Show |
intron_variant | MODIFIER | c.1144-48515A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31734878 | ||||||
| chr11:31735104
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1144-48289G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31735104 | ||||||
| chr11:31735111
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0005g0067 | 2 | HG02523.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.1144-48282C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31735111 | ||||||
| chr11:31735159
|
C | CA | 106 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(103): Show | 106 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(103): Show |
intron_variant | MODIFIER | c.1144-48220dupA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31735159 | |||||
| chr11:31735159
|
C | CAA | 6 | a0001c0001t0001g0036a0001c0001t0001g0068a0001c0001t0001g0073others(3): Show | 6 | HG02132.hp2 HG02523.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144-48221_1144-48 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31735159 | |||||
| chr11:31735177
|
G | T | 29 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(26): Show | 29 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1144-48216G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31735177 | ||||||
| chr11:31735272
|
A | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-48121A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31735272 | ||||||
| chr11:31735412
|
C | T | 1 | a0001c0001t0039g0212 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1144-47981C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31735412 | ||||||
| chr11:31735649
|
A | G | 1 | a0001c0001t0005g0021 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1144-47744A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31735649 | ||||||
| chr11:31735736
|
G | C | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1144-47657G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31735736 | ||||||
| chr11:31735801
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1144-47592A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31735801 | ||||||
| chr11:31735898
|
T | G | 1 | a0001c0001t0067g0161 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1144-47495T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31735898 | ||||||
| chr11:31735921
|
A | G | 3 | a0001c0001t0019g0084a0001c0001t0019g0095a0002c0003t0082g0207 | 3 | HG02257.hp1 HG02257.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1144-47472A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31735921 | ||||||
| chr11:31735975
|
T | C | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.1144-47418T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31735975 | ||||||
| chr11:31735998
|
A | G | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-47395A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31735998 | ||||||
| chr11:31736008
|
G | A | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1144-47385G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31736008 | ||||||
| chr11:31736049
|
G | T | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-47344G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31736049 | ||||||
| chr11:31736207
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1144-47186G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31736207 | ||||||
| chr11:31736330
|
C | A | 200 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(197): Show | 200 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(197): Show |
intron_variant | MODIFIER | c.1144-47063C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31736330 | ||||||
| chr11:31736363
|
C | G | 2 | a0001c0001t0003g0181a0001c0001t0003g0184 | 2 | HG02055.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1144-47030C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31736363 | ||||||
| chr11:31736564
|
T | C | 269 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(266): Show | 269 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.1144-46829T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31736564 | ||||||
| chr11:31736591
|
A | G | 1 | a0001c0001t0011g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1144-46802A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31736591 | ||||||
| chr11:31736764
|
A | G | 1 | a0006c0004t0076g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1144-46629A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31736764 | ||||||
| chr11:31736772
|
A | G | 1 | a0001c0001t0050g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1144-46621A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31736772 | ||||||
| chr11:31736989
|
A | G | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1144-46404A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31736989 | ||||||
| chr11:31737017
|
C | T | 1 | a0001c0001t0067g0161 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1144-46376C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31737017 | ||||||
| chr11:31737025
|
T | C | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1144-46368T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31737025 | ||||||
| chr11:31737036
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0255a0001c0001t0004g0078others(1): Show | 4 | NA18942.hp2 NA18946.hp1 NA19083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-46357T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31737036 | ||||||
| chr11:31737232
|
A | G | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1144-46161A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31737232 | ||||||
| chr11:31737234
|
T | C | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1144-46159T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31737234 | ||||||
| chr11:31737235
|
G | A | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1144-46158G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31737235 | ||||||
| chr11:31737239
|
G | A | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1144-46154G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31737239 | ||||||
| chr11:31737265
|
C | G | 1 | a0001c0001t0005g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1144-46128C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31737265 | ||||||
| chr11:31737561
|
A | T | 1 | a0001c0001t0012g0136 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1144-45832A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31737561 | ||||||
| chr11:31737635
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1144-45758C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31737635 | ||||||
| chr11:31737856
|
A | G | 15 | a0001c0001t0002g0173a0001c0001t0006g0163a0001c0001t0006g0170others(12): Show | 15 | HG00597.hp2 HG02027.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.1144-45537A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31737856 | ||||||
| chr11:31737961
|
C | A | 2 | a0001c0001t0006g0230a0001c0001t0016g0236 | 2 | HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1144-45432C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31737961 | ||||||
| chr11:31738018
|
G | A | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-45375G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31738018 | ||||||
| chr11:31738232
|
C | CA | 35 | a0001c0001t0001g0003a0001c0001t0001g0074a0001c0001t0001g0258others(32): Show | 35 | HG00639.hp2 HG01175.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1144-45136dupA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31738232 | |||||
| chr11:31738232
|
CA | C | 10 | a0001c0001t0002g0143a0001c0001t0003g0186a0001c0001t0003g0206others(7): Show | 10 | HG00621.hp1 HG01069.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1144-45136delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31738232 | |||||
| chr11:31738232
|
CAAAAAAA others(3): Show |
C | 1 | a0005c0006t0032g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1144-45145_1144-45 others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31738232 | |||||
| chr11:31738268
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0005g0067 | 3 | HG02132.hp2 HG02523.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.1144-45125G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31738268 | ||||||
| chr11:31738421
|
T | A | 4 | a0001c0001t0005g0264a0001c0001t0017g0266a0001c0001t0017g0268others(1): Show | 4 | HG02145.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144-44972T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31738421 | ||||||
| chr11:31738423
|
A | C | 1 | a0001c0001t0003g0196 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1144-44970A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31738423 | ||||||
| chr11:31738494
|
G | A | 2 | a0001c0001t0030g0232a0001c0001t0030g0247 | 2 | HG02486.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1144-44899G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31738494 | ||||||
| chr11:31738593
|
G | A | 4 | a0001c0001t0009g0240a0001c0001t0020g0228a0001c0001t0020g0241others(1): Show | 4 | HG02280.hp2 HG02809.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-44800G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31738593 | ||||||
| chr11:31738694
|
T | C | 2 | a0001c0001t0003g0210a0001c0001t0003g0211 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1144-44699T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31738694 | ||||||
| chr11:31739056
|
G | A | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1144-44337G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31739056 | ||||||
| chr11:31739186
|
AC | A | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-44206delC | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31739186 | ||||||
| chr11:31739247
|
A | G | 1 | a0001c0001t0031g0125 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1144-44146A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31739247 | ||||||
| chr11:31739841
|
C | T | 1 | a0001c0001t0007g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1144-43552C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31739841 | ||||||
| chr11:31739846
|
C | A | 5 | a0001c0001t0006g0227a0001c0001t0006g0229a0001c0001t0006g0230others(2): Show | 5 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1144-43547C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31739846 | ||||||
| chr11:31740024
|
G | A | 29 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(26): Show | 29 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1144-43369G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31740024 | ||||||
| chr11:31740089
|
T | C | 2 | a0001c0001t0002g0143a0001c0001t0007g0014 | 2 | HG02055.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1144-43304T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31740089 | ||||||
| chr11:31740254
|
C | G | 5 | a0001c0001t0003g0181a0001c0001t0003g0184a0001c0001t0003g0192others(2): Show | 5 | HG01168.hp1 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-43139C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31740254 | ||||||
| chr11:31740552
|
T | A | 1 | a0001c0001t0055g0083 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1144-42841T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31740552 | ||||||
| chr11:31740583
|
A | G | 1 | a0001c0001t0004g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1144-42810A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31740583 | ||||||
| chr11:31740775
|
G | A | 2 | a0001c0001t0005g0012a0002c0003t0001g0094 | 2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1144-42618G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31740775 | ||||||
| chr11:31740901
|
T | G | 1 | a0001c0001t0002g0139 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1144-42492T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31740901 | ||||||
| chr11:31740944
|
C | T | 4 | a0001c0001t0001g0037a0001c0001t0004g0026a0001c0001t0012g0038others(1): Show | 4 | HG02080.hp1 NA18960.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-42449C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31740944 | ||||||
| chr11:31741000
|
C | T | 5 | a0001c0001t0006g0227a0001c0001t0006g0229a0001c0001t0006g0230others(2): Show | 5 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1144-42393C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31741000 | ||||||
| chr11:31741120
|
G | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1144-42273G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31741120 | ||||||
| chr11:31741176
|
G | T | 9 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0062others(6): Show | 9 | NA18747.hp2 NA18947.hp2 NA18978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1144-42217G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31741176 | ||||||
| chr11:31741181
|
G | A | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1144-42212G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31741181 | ||||||
| chr11:31741334
|
A | G | 1 | a0001c0001t0002g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1144-42059A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31741334 | ||||||
| chr11:31741413
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG00738.hp1 HG01258.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-41980C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31741413 | ||||||
| chr11:31741604
|
G | A | 1 | a0001c0001t0009g0187 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1144-41789G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31741604 | ||||||
| chr11:31741613
|
G | A | 42 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(39): Show | 42 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1144-41780G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31741613 | ||||||
| chr11:31741671
|
C | T | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1144-41722C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31741671 | ||||||
| chr11:31741908
|
C | A | 2 | a0001c0001t0006g0170a0001c0001t0048g0215 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1144-41485C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31741908 | ||||||
| chr11:31742403
|
A | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1144-40990A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31742403 | ||||||
| chr11:31742542
|
G | A | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-40851G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31742542 | ||||||
| chr11:31742775
|
A | G | 110 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(107): Show | 110 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.1144-40618A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31742775 | ||||||
| chr11:31742924
|
C | A | 1 | a0001c0001t0043g0153 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1144-40469C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31742924 | ||||||
| chr11:31743104
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1144-40289C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31743104 | ||||||
| chr11:31743434
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1144-39959C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31743434 | ||||||
| chr11:31743484
|
C | T | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1144-39909C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31743484 | ||||||
| chr11:31743607
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1144-39786T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31743607 | ||||||
| chr11:31743803
|
C | T | 4 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0069others(1): Show | 4 | NA18947.hp2 NA18978.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144-39590C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31743803 | ||||||
| chr11:31744167
|
G | A | 4 | a0001c0002t0014g0246a0001c0002t0014g0256a0001c0002t0024g0248others(1): Show | 4 | HG03098.hp2 HG03130.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-39226G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31744167 | ||||||
| chr11:31744223
|
C | T | 1 | a0001c0001t0039g0212 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1144-39170C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31744223 | ||||||
| chr11:31744369
|
A | G | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1144-39024A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31744369 | ||||||
| chr11:31744552
|
G | A | 4 | a0001c0001t0002g0173a0001c0001t0015g0146a0001c0001t0016g0171others(1): Show | 4 | HG02027.hp2 HG02080.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-38841G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31744552 | ||||||
| chr11:31744734
|
G | A | 4 | a0001c0001t0027g0048a0001c0001t0027g0050a0001c0001t0053g0049others(1): Show | 4 | HG01496.hp2 HG02630.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-38659G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31744734 | ||||||
| chr11:31744757
|
T | G | 1 | a0001c0001t0003g0184 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1144-38636T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31744757 | ||||||
| chr11:31744995
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0002g0175 | 2 | NA18959.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1144-38398C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31744995 | ||||||
| chr11:31744996
|
G | A | 3 | a0001c0001t0001g0258a0001c0001t0004g0257a0001c0001t0022g0259 | 3 | HG02572.hp1 HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1144-38397G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31744996 | ||||||
| chr11:31745024
|
T | A | 1 | a0001c0001t0023g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1144-38369T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31745024 | ||||||
| chr11:31745180
|
C | T | 1 | a0001c0001t0028g0204 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1144-38213C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31745180 | ||||||
| chr11:31745262
|
C | T | 1 | a0001c0001t0004g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1144-38131C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31745262 | ||||||
| chr11:31745295
|
T | C | 1 | a0001c0001t0027g0050 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1144-38098T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31745295 | ||||||
| chr11:31745313
|
G | T | 11 | a0001c0001t0001g0243a0001c0001t0005g0012a0001c0001t0011g0011others(8): Show | 11 | HG01109.hp2 HG01243.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1144-38080G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31745313 | ||||||
| chr11:31745319
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0007g0045 | 2 | HG03831.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1144-38074G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31745319 | ||||||
| chr11:31745336
|
A | G | 1 | a0001c0001t0033g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1144-38057A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31745336 | ||||||
| chr11:31745352
|
G | A | 4 | a0001c0001t0027g0048a0001c0001t0027g0050a0001c0001t0053g0049others(1): Show | 4 | HG01496.hp2 HG02630.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-38041G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31745352 | ||||||
| chr11:31745412
|
A | T | 1 | a0001c0001t0033g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1144-37981A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31745412 | ||||||
| chr11:31745453
|
A | G | 1 | a0001c0001t0006g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1144-37940A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31745453 | ||||||
| chr11:31746003
|
G | A | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-37390G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31746003 | ||||||
| chr11:31746041
|
A | C | 1 | a0001c0001t0011g0011 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1144-37352A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31746041 | ||||||
| chr11:31746107
|
C | T | 2 | a0001c0001t0009g0180a0001c0001t0009g0195 | 2 | HG01074.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1144-37286C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31746107 | ||||||
| chr11:31746114
|
GCA | G | 30 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(27): Show | 30 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1144-37278_1144-37 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31746114 | ||||||
| chr11:31746228
|
TCAGGAAA others(3): Show |
T | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1144-37160_1144-37 others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31746228 | |||||
| chr11:31746245
|
T | C | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1144-37148T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31746245 | ||||||
| chr11:31746340
|
C | A | 1 | a0001c0001t0009g0187 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1144-37053C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31746340 | ||||||
| chr11:31746341
|
G | A | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-37052G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31746341 | ||||||
| chr11:31746566
|
T | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-36827T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31746566 | ||||||
| chr11:31746571
|
A | T | 3 | a0001c0001t0027g0048a0001c0001t0053g0049a0001c0001t0063g0047 | 3 | HG01496.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1144-36822A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31746571 | ||||||
| chr11:31746608
|
T | A | 110 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(107): Show | 110 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.1144-36785T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31746608 | ||||||
| chr11:31746631
|
C | G | 1 | a0001c0001t0001g0065 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1144-36762C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31746631 | ||||||
| chr11:31746684
|
A | T | 1 | a0001c0001t0004g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1144-36709A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31746684 | ||||||
| chr11:31746897
|
T | A | 1 | a0001c0001t0033g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1144-36496T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31746897 | ||||||
| chr11:31746907
|
A | T | 2 | a0001c0001t0004g0091a0001c0001t0068g0039 | 2 | NA18943.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1144-36486A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31746907 | ||||||
| chr11:31746925
|
AAAAT | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1144-36464_1144-36 others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31746925 | |||||
| chr11:31747033
|
CTG | C | 11 | a0001c0001t0001g0258a0001c0001t0003g0181a0001c0001t0011g0011others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1144-36340_1144-36 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31747033 | |||||
| chr11:31747033
|
CTGTG | C | 96 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(93): Show | 96 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(93): Show |
intron_variant | MODIFIER | c.1144-36342_1144-36 others(10): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31747033 | |||||
| chr11:31747033
|
CTGTGTG | C | 7 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(4): Show | 7 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-36344_1144-36 others(12): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31747033 | |||||
| chr11:31747282
|
G | C | 1 | a0001c0001t0001g0088 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1144-36111G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31747282 | ||||||
| chr11:31747336
|
A | C | 110 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(107): Show | 110 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.1144-36057A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31747336 | ||||||
| chr11:31747408
|
G | C | 1 | a0001c0001t0004g0026 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1144-35985G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31747408 | ||||||
| chr11:31747643
|
T | C | 30 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(27): Show | 30 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1144-35750T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31747643 | ||||||
| chr11:31747775
|
G | A | 1 | a0001c0002t0024g0248 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1144-35618G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31747775 | ||||||
| chr11:31747965
|
A | G | 1 | a0001c0001t0019g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1144-35428A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31747965 | ||||||
| chr11:31748149
|
C | T | 2 | a0001c0001t0006g0231a0001c0001t0073g0237 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1144-35244C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31748149 | ||||||
| chr11:31748243
|
C | CT | 14 | a0001c0001t0001g0002a0001c0001t0001g0085a0001c0001t0001g0258others(11): Show | 14 | HG00621.hp2 HG02027.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1144-35131dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31748243 | |||||
| chr11:31748243
|
CT | C | 9 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0041others(6): Show | 9 | HG00738.hp1 HG01261.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1144-35131delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31748243 | |||||
| chr11:31748331
|
G | A | 5 | a0001c0001t0004g0071a0001c0001t0007g0014a0001c0001t0027g0048others(2): Show | 5 | HG01496.hp2 HG02055.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1144-35062G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31748331 | ||||||
| chr11:31748393
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1144-35000C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31748393 | ||||||
| chr11:31748450
|
G | C | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1144-34943G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31748450 | ||||||
| chr11:31748460
|
G | A | 1 | a0001c0001t0002g0139 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1144-34933G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31748460 | ||||||
| chr11:31748495
|
C | T | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(236): Show |
intron_variant | MODIFIER | c.1144-34898C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31748495 | ||||||
| chr11:31748628
|
T | C | 1 | a0001c0001t0008g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1144-34765T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31748628 | ||||||
| chr11:31748830
|
C | A | 2 | a0001c0001t0026g0251a0001c0001t0026g0252 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1144-34563C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31748830 | ||||||
| chr11:31749009
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1144-34384A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31749009 | ||||||
| chr11:31749026
|
G | A | 1 | a0001c0001t0050g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1144-34367G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31749026 | ||||||
| chr11:31749335
|
A | G | 13 | a0001c0001t0006g0227a0001c0001t0006g0229a0001c0001t0006g0230others(10): Show | 13 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1144-34058A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31749335 | ||||||
| chr11:31749347
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1144-34046C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31749347 | ||||||
| chr11:31749756
|
AAAATAAA others(3): Show |
A | 2 | a0001c0001t0010g0122a0001c0001t0064g0239 | 2 | HG01884.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.1144-33621_1144-33 others(16): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31749756 | |||||
| chr11:31749856
|
A | AT | 20 | a0001c0001t0001g0076a0001c0001t0002g0151a0001c0001t0004g0091others(17): Show | 20 | HG00639.hp2 HG01891.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.1144-33520dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31749856 | |||||
| chr11:31749856
|
AT | A | 9 | a0001c0001t0001g0258a0001c0001t0002g0222a0001c0001t0004g0257others(6): Show | 9 | HG01943.hp1 HG02572.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1144-33520delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31749856 | |||||
| chr11:31749941
|
C | T | 2 | a0001c0001t0078g0099a0001c0001t0081g0223 | 2 | HG01891.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1144-33452C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31749941 | ||||||
| chr11:31750000
|
T | C | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1144-33393T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31750000 | ||||||
| chr11:31750022
|
A | AT | 10 | a0001c0001t0001g0074a0001c0001t0002g0222a0001c0001t0025g0155others(7): Show | 10 | HG02145.hp1 HG02738.hp1 HG03540.hp1 others(7): Show |
intron_variant | MODIFIER | c.1144-33357dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31750022 | |||||
| chr11:31750055
|
G | A | 1 | a0001c0001t0016g0171 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1144-33338G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31750055 | ||||||
| chr11:31750175
|
T | C | 1 | a0001c0001t0034g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1144-33218T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31750175 | ||||||
| chr11:31750428
|
T | C | 26 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0027others(23): Show | 26 | HG01123.hp2 HG01928.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.1144-32965T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31750428 | ||||||
| chr11:31751014
|
T | G | 1 | a0001c0001t0001g0034 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1144-32379T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31751014 | ||||||
| chr11:31751210
|
A | G | 1 | a0001c0001t0033g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1144-32183A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31751210 | ||||||
| chr11:31751231
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1144-32162C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31751231 | ||||||
| chr11:31751390
|
T | C | 29 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(26): Show | 29 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1144-32003T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31751390 | ||||||
| chr11:31751443
|
G | A | 4 | a0001c0001t0026g0251a0001c0001t0026g0252a0001c0001t0030g0232others(1): Show | 4 | HG01243.hp2 HG02486.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144-31950G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31751443 | ||||||
| chr11:31751739
|
G | A | 3 | a0001c0001t0003g0186a0001c0001t0003g0199a0001c0001t0003g0200 | 3 | HG00642.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1144-31654G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31751739 | ||||||
| chr11:31751999
|
A | G | 1 | a0001c0001t0064g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1144-31394A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31751999 | ||||||
| chr11:31752053
|
G | T | 13 | a0001c0001t0006g0227a0001c0001t0006g0229a0001c0001t0006g0230others(10): Show | 13 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1144-31340G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31752053 | ||||||
| chr11:31752286
|
A | AG | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1144-31107_1144-31 others(7): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31752286 | ||||||
| chr11:31752522
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1144-30871G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31752522 | ||||||
| chr11:31752827
|
C | T | 1 | a0001c0001t0006g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1144-30566C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31752827 | ||||||
| chr11:31752833
|
CA | C | 111 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(108): Show | 111 | HG00621.hp1 HG00738.hp1 HG01071.hp1 others(108): Show |
intron_variant | MODIFIER | c.1144-30541delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31752833 | |||||
| chr11:31752849
|
A | G | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1144-30544A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31752849 | ||||||
| chr11:31753182
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1144-30211G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31753182 | ||||||
| chr11:31753516
|
A | C | 2 | a0001c0001t0001g0258a0001c0001t0004g0257 | 2 | HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1144-29877A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31753516 | ||||||
| chr11:31753615
|
C | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-29778C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31753615 | ||||||
| chr11:31753630
|
G | C | 7 | a0001c0002t0014g0246a0001c0002t0014g0256a0001c0002t0024g0244others(4): Show | 7 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-29763G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31753630 | ||||||
| chr11:31753692
|
A | G | 1 | a0001c0001t0048g0215 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1144-29701A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31753692 | ||||||
| chr11:31753706
|
G | A | 1 | a0001c0001t0022g0259 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1144-29687G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31753706 | ||||||
| chr11:31753747
|
G | A | 102 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(99): Show | 102 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(99): Show |
intron_variant | MODIFIER | c.1144-29646G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31753747 | ||||||
| chr11:31753848
|
T | C | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.1144-29545T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31753848 | ||||||
| chr11:31753895
|
T | C | 1 | a0001c0001t0016g0171 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1144-29498T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31753895 | ||||||
| chr11:31753896
|
A | T | 1 | a0001c0001t0004g0257 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1144-29497A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31753896 | ||||||
| chr11:31754037
|
T | C | 7 | a0001c0001t0008g0208a0001c0001t0008g0209a0001c0001t0008g0216others(4): Show | 7 | HG00642.hp1 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-29356T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31754037 | ||||||
| chr11:31754067
|
A | G | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1144-29326A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31754067 | ||||||
| chr11:31754354
|
C | T | 3 | a0001c0001t0003g0186a0001c0001t0003g0199a0001c0001t0003g0200 | 3 | HG00642.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1144-29039C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31754354 | ||||||
| chr11:31754458
|
A | C | 111 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(108): Show | 111 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(108): Show |
intron_variant | MODIFIER | c.1144-28935A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31754458 | ||||||
| chr11:31754746
|
C | T | 1 | a0001c0001t0002g0167 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1144-28647C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31754746 | ||||||
| chr11:31754787
|
G | A | 2 | a0001c0001t0006g0231a0001c0001t0073g0237 | 2 | HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1144-28606G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31754787 | ||||||
| chr11:31754827
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-28566A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31754827 | ||||||
| chr11:31754850
|
T | C | 111 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(108): Show | 111 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(108): Show |
intron_variant | MODIFIER | c.1144-28543T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31754850 | ||||||
| chr11:31755370
|
G | T | 1 | a0001c0001t0003g0184 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1144-28023G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31755370 | ||||||
| chr11:31755557
|
T | C | 1 | a0001c0001t0009g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1144-27836T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31755557 | ||||||
| chr11:31755730
|
CA | C | 103 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1144-27645delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31755730 | |||||
| chr11:31755894
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1144-27499A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31755894 | ||||||
| chr11:31756232
|
G | A | 1 | a0001c0001t0031g0125 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1144-27161G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31756232 | ||||||
| chr11:31756397
|
T | A | 1 | a0001c0001t0078g0099 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1144-26996T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31756397 | ||||||
| chr11:31756431
|
T | C | 2 | a0001c0001t0062g0265a0001c0001t0063g0047 | 2 | HG02258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1144-26962T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31756431 | ||||||
| chr11:31757377
|
A | AT | 6 | a0001c0001t0001g0174a0001c0001t0003g0210a0001c0001t0003g0211others(3): Show | 6 | HG01168.hp1 HG01169.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144-26004dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31757377 | |||||
| chr11:31757753
|
C | G | 11 | a0001c0001t0006g0227a0001c0001t0006g0229a0001c0001t0006g0230others(8): Show | 11 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.1144-25640C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31757753 | ||||||
| chr11:31757832
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0069g0080 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1144-25561G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31757832 | ||||||
| chr11:31758241
|
G | C | 1 | a0001c0001t0004g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1144-25152G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31758241 | ||||||
| chr11:31758423
|
A | G | 1 | a0001c0002t0024g0248 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1144-24970A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31758423 | ||||||
| chr11:31758483
|
G | C | 3 | a0001c0001t0004g0091a0001c0001t0067g0161a0001c0001t0068g0039 | 3 | NA18943.hp1 NA18951.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1144-24910G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31758483 | ||||||
| chr11:31758670
|
C | CT | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0114others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.1144-24707dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31758670 | |||||
| chr11:31758821
|
C | A | 1 | a0001c0001t0004g0017 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1144-24572C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31758821 | ||||||
| chr11:31758952
|
G | A | 141 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(138): Show | 141 | HG00323.hp2 HG00621.hp1 HG00639.hp2 others(138): Show |
intron_variant | MODIFIER | c.1144-24441G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31758952 | ||||||
| chr11:31759442
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1144-23951T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31759442 | ||||||
| chr11:31759686
|
CTTTTCTT others(6): Show |
C | 1 | a0001c0001t0004g0044 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1144-23696_1144-23 others(19): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31759686 | |||||
| chr11:31759711
|
CT | C | 29 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(26): Show | 29 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1144-23669delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31759711 | |||||
| chr11:31759730
|
G | A | 1 | a0001c0001t0005g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1144-23663G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31759730 | ||||||
| chr11:31759770
|
G | A | 111 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(108): Show | 111 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(108): Show |
intron_variant | MODIFIER | c.1144-23623G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31759770 | ||||||
| chr11:31759793
|
G | A | 1 | a0001c0001t0070g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1144-23600G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31759793 | ||||||
| chr11:31760219
|
A | T | 1 | a0001c0001t0004g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1144-23174A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31760219 | ||||||
| chr11:31760281
|
G | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(100): Show | 103 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.1144-23112G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31760281 | ||||||
| chr11:31760363
|
A | G | 1 | a0001c0001t0006g0227 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1144-23030A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31760363 | ||||||
| chr11:31760889
|
C | A | 1 | a0001c0001t0023g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1144-22504C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31760889 | ||||||
| chr11:31761088
|
C | T | 2 | a0001c0002t0024g0244a0001c0002t0045g0245 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1144-22305C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31761088 | ||||||
| chr11:31761100
|
C | T | 3 | a0001c0001t0005g0012a0001c0001t0011g0011a0001c0001t0058g0010 | 3 | HG02615.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1144-22293C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31761100 | ||||||
| chr11:31761136
|
G | A | 2 | a0001c0001t0009g0187a0004c0005t0009g0188 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1144-22257G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31761136 | ||||||
| chr11:31761141
|
C | T | 1 | a0001c0001t0003g0214 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1144-22252C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31761141 | ||||||
| chr11:31761405
|
C | G | 2 | a0001c0001t0007g0054a0001c0001t0038g0053 | 2 | NA18987.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1144-21988C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31761405 | ||||||
| chr11:31762034
|
T | C | 2 | a0001c0001t0006g0170a0001c0001t0048g0215 | 2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1144-21359T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31762034 | ||||||
| chr11:31762596
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1144-20797C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31762596 | ||||||
| chr11:31762651
|
C | T | 1 | a0001c0001t0019g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1144-20742C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31762651 | ||||||
| chr11:31762903
|
T | C | 184 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(181): Show | 184 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(181): Show |
intron_variant | MODIFIER | c.1144-20490T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31762903 | ||||||
| chr11:31763093
|
C | CA | 94 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(91): Show | 94 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.1144-20289dupA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31763093 | |||||
| chr11:31763865
|
G | A | 1 | a0001c0001t0005g0203 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1144-19528G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31763865 | ||||||
| chr11:31764107
|
G | T | 1 | a0001c0001t0016g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1144-19286G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31764107 | ||||||
| chr11:31764635
|
C | T | 1 | a0001c0001t0004g0020 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1144-18758C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31764635 | ||||||
| chr11:31764919
|
C | A | 1 | a0001c0001t0001g0243 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1144-18474C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31764919 | ||||||
| chr11:31765067
|
G | A | 3 | a0001c0001t0002g0102a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | HG03927.hp1 HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1144-18326G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31765067 | ||||||
| chr11:31765326
|
T | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-18067T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31765326 | ||||||
| chr11:31765590
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1144-17803G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31765590 | ||||||
| chr11:31765892
|
C | A | 1 | a0001c0001t0001g0040 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1144-17501C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31765892 | ||||||
| chr11:31765953
|
T | C | 1 | a0001c0001t0033g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1144-17440T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31765953 | ||||||
| chr11:31765963
|
A | T | 1 | a0001c0001t0033g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1144-17430A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31765963 | ||||||
| chr11:31766128
|
A | G | 1 | a0001c0001t0002g0143 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1144-17265A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31766128 | ||||||
| chr11:31766503
|
A | T | 4 | a0001c0001t0002g0106a0001c0001t0002g0109a0001c0001t0010g0110others(1): Show | 4 | NA18942.hp1 NA18960.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-16890A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31766503 | ||||||
| chr11:31766516
|
C | T | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1144-16877C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31766516 | ||||||
| chr11:31766829
|
T | C | 1 | a0001c0002t0044g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1144-16564T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31766829 | ||||||
| chr11:31767033
|
A | G | 1 | a0001c0002t0045g0245 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1144-16360A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31767033 | ||||||
| chr11:31767387
|
T | TA | 80 | a0001c0001t0001g0040a0001c0001t0001g0185a0001c0001t0001g0243others(77): Show | 80 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.1144-15990dupA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31767387 | |||||
| chr11:31767387
|
T | TAA | 102 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(99): Show | 102 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(99): Show |
intron_variant | MODIFIER | c.1144-15991_1144-15 others(8): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31767387 | |||||
| chr11:31767439
|
C | T | 4 | a0001c0001t0001g0258a0001c0001t0004g0257a0001c0001t0022g0259others(1): Show | 4 | HG01884.hp2 HG02572.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144-15954C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31767439 | ||||||
| chr11:31767566
|
G | C | 42 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(39): Show | 42 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1144-15827G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31767566 | ||||||
| chr11:31767727
|
C | T | 30 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0004g0257others(27): Show | 30 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1144-15666C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31767727 | ||||||
| chr11:31767911
|
C | G | 1 | a0001c0001t0074g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1144-15482C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31767911 | ||||||
| chr11:31768398
|
T | A | 1 | a0002c0003t0004g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1144-14995T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31768398 | ||||||
| chr11:31769273
|
A | C | 1 | a0005c0006t0032g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1144-14120A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31769273 | ||||||
| chr11:31769328
|
T | G | 1 | a0006c0004t0076g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1144-14065T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31769328 | ||||||
| chr11:31769551
|
G | A | 180 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(177): Show | 180 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(177): Show |
intron_variant | MODIFIER | c.1144-13842G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31769551 | ||||||
| chr11:31769646
|
C | T | 1 | a0001c0001t0003g0190 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1144-13747C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31769646 | ||||||
| chr11:31769744
|
G | T | 1 | a0001c0001t0049g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1144-13649G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31769744 | ||||||
| chr11:31769789
|
T | A | 7 | a0001c0002t0014g0246a0001c0002t0014g0256a0001c0002t0024g0244others(4): Show | 7 | HG02647.hp1 HG03098.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-13604T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31769789 | ||||||
| chr11:31770564
|
CA | C | 71 | a0001c0001t0001g0076a0001c0001t0001g0185a0001c0001t0001g0258others(68): Show | 71 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1144-12813delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31770564 | |||||
| chr11:31770580
|
A | G | 10 | a0001c0001t0005g0012a0001c0001t0011g0011a0001c0001t0019g0233others(7): Show | 10 | HG01243.hp2 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1144-12813A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31770580 | ||||||
| chr11:31770644
|
A | G | 95 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(92): Show | 95 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.1144-12749A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31770644 | ||||||
| chr11:31770747
|
T | A | 35 | a0001c0001t0001g0185a0001c0001t0003g0103a0001c0001t0003g0181others(32): Show | 35 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1144-12646T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31770747 | ||||||
| chr11:31770836
|
GA | G | 16 | a0001c0001t0001g0258a0001c0001t0004g0257a0001c0001t0006g0231others(13): Show | 16 | HG01884.hp2 HG02280.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.1144-12544delA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31770836 | |||||
| chr11:31771062
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1144-12331T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31771062 | ||||||
| chr11:31771170
|
G | C | 1 | a0001c0001t0016g0168 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1144-12223G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31771170 | ||||||
| chr11:31771503
|
T | G | 95 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(92): Show | 95 | HG00323.hp2 HG00621.hp1 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.1144-11890T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31771503 | ||||||
| chr11:31771706
|
T | G | 1 | a0001c0001t0061g0086 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1144-11687T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31771706 | ||||||
| chr11:31771708
|
A | G | 1 | a0001c0001t0061g0086 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1144-11685A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31771708 | ||||||
| chr11:31771717
|
C | A | 189 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(186): Show | 189 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(186): Show |
intron_variant | MODIFIER | c.1144-11676C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31771717 | ||||||
| chr11:31771762
|
A | G | 1 | a0001c0001t0002g0130 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1144-11631A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31771762 | ||||||
| chr11:31771790
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1144-11603T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31771790 | ||||||
| chr11:31771796
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1144-11597A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31771796 | ||||||
| chr11:31771904
|
C | T | 1 | a0001c0001t0022g0101 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1144-11489C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31771904 | ||||||
| chr11:31771975
|
C | A | 32 | a0001c0001t0001g0185a0001c0001t0002g0137a0001c0001t0003g0103others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.1144-11418C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31771975 | ||||||
| chr11:31771977
|
G | A | 8 | a0001c0002t0014g0097a0001c0002t0014g0246a0001c0002t0014g0256others(5): Show | 8 | HG02647.hp1 HG03098.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-11416G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31771977 | ||||||
| chr11:31771994
|
T | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-11399T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31771994 | ||||||
| chr11:31772120
|
C | CT | 160 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(157): Show | 160 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(157): Show |
intron_variant | MODIFIER | c.1144-11255dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31772120 | |||||
| chr11:31772260
|
G | A | 46 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0185others(43): Show | 46 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1144-11133G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31772260 | ||||||
| chr11:31772370
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1144-11023G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31772370 | ||||||
| chr11:31772633
|
T | C | 10 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1144-10760T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31772633 | ||||||
| chr11:31772751
|
G | A | 1 | a0001c0001t0003g0190 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1144-10642G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31772751 | ||||||
| chr11:31772946
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-10447C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31772946 | ||||||
| chr11:31772985
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-10408C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31772985 | ||||||
| chr11:31773009
|
A | G | 1 | a0001c0001t0007g0054 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1144-10384A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31773009 | ||||||
| chr11:31773347
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1144-10046A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31773347 | ||||||
| chr11:31773368
|
G | A | 5 | a0002c0003t0001g0093a0002c0003t0001g0094a0002c0003t0001g0096others(2): Show | 5 | HG01884.hp1 HG01891.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-10025G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31773368 | ||||||
| chr11:31773478
|
A | G | 10 | a0001c0001t0006g0231a0001c0001t0009g0240a0001c0001t0020g0228others(7): Show | 10 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1144-9915A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31773478 | ||||||
| chr11:31773524
|
C | G | 1 | a0001c0001t0026g0252 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1144-9869C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31773524 | ||||||
| chr11:31773622
|
G | A | 8 | a0001c0002t0014g0097a0001c0002t0014g0246a0001c0002t0014g0256others(5): Show | 8 | HG02647.hp1 HG03098.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-9771G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31773622 | ||||||
| chr11:31773939
|
G | A | 6 | a0001c0001t0019g0233a0001c0001t0026g0251a0001c0001t0026g0252others(3): Show | 6 | HG01243.hp2 HG02486.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1144-9454G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31773939 | ||||||
| chr11:31773954
|
A | G | 47 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0185others(44): Show | 47 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1144-9439A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31773954 | ||||||
| chr11:31774139
|
C | T | 1 | a0001c0001t0002g0167 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1144-9254C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31774139 | ||||||
| chr11:31774232
|
C | T | 8 | a0001c0002t0014g0097a0001c0002t0014g0246a0001c0002t0014g0256others(5): Show | 8 | HG02647.hp1 HG03098.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-9161C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31774232 | ||||||
| chr11:31774286
|
G | A | 2 | a0001c0001t0034g0238a0001c0001t0050g0235 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1144-9107G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31774286 | ||||||
| chr11:31774288
|
C | T | 2 | a0001c0001t0008g0208a0001c0001t0008g0209 | 2 | HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1144-9105C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31774288 | ||||||
| chr11:31774434
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-8959A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31774434 | ||||||
| chr11:31774443
|
G | A | 8 | a0001c0001t0009g0240a0001c0001t0020g0228a0001c0001t0020g0241others(5): Show | 8 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1144-8950G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31774443 | ||||||
| chr11:31774521
|
A | G | 47 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0185others(44): Show | 47 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1144-8872A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31774521 | ||||||
| chr11:31774659
|
C | T | 1 | a0001c0001t0004g0017 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1144-8734C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31774659 | ||||||
| chr11:31774713
|
C | G | 3 | a0001c0001t0027g0048a0001c0001t0027g0050a0001c0001t0053g0049 | 3 | HG01496.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1144-8680C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31774713 | ||||||
| chr11:31774823
|
C | T | 2 | a0001c0001t0025g0155a0001c0001t0025g0224 | 2 | NA18954.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1144-8570C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31774823 | ||||||
| chr11:31774904
|
G | A | 1 | a0001c0001t0011g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1144-8489G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31774904 | ||||||
| chr11:31775012
|
A | G | 188 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(185): Show | 188 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(185): Show |
intron_variant | MODIFIER | c.1144-8381A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31775012 | ||||||
| chr11:31775092
|
G | T | 3 | a0001c0001t0001g0243a0001c0001t0007g0089a0001c0001t0008g0092 | 3 | HG01109.hp2 HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1144-8301G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31775092 | ||||||
| chr11:31775184
|
A | G | 1 | a0001c0001t0011g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1144-8209A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31775184 | ||||||
| chr11:31775368
|
C | T | 8 | a0001c0001t0009g0240a0001c0001t0020g0228a0001c0001t0020g0241others(5): Show | 8 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1144-8025C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31775368 | ||||||
| chr11:31775394
|
A | G | 46 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0003g0103others(43): Show | 46 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1144-7999A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31775394 | ||||||
| chr11:31775593
|
C | G | 51 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0003g0103others(48): Show | 51 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1144-7800C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31775593 | ||||||
| chr11:31775673
|
A | G | 4 | a0001c0001t0002g0106a0001c0001t0002g0109a0001c0001t0010g0110others(1): Show | 4 | NA18942.hp1 NA18960.hp2 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-7720A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31775673 | ||||||
| chr11:31775705
|
A | G | 1 | a0001c0001t0074g0169 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1144-7688A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31775705 | ||||||
| chr11:31775809
|
G | A | 51 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0003g0103others(48): Show | 51 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1144-7584G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31775809 | ||||||
| chr11:31775854
|
A | G | 39 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0003g0103others(36): Show | 39 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1144-7539A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31775854 | ||||||
| chr11:31775906
|
A | C | 1 | a0001c0001t0003g0184 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1144-7487A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31775906 | ||||||
| chr11:31775937
|
C | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-7456C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31775937 | ||||||
| chr11:31775987
|
A | T | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1144-7406A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31775987 | ||||||
| chr11:31776030
|
G | A | 1 | a0001c0001t0026g0252 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1144-7363G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31776030 | ||||||
| chr11:31776055
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 193 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(190): Show |
intron_variant | MODIFIER | c.1144-7338A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31776055 | ||||||
| chr11:31776090
|
G | T | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-7303G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31776090 | ||||||
| chr11:31776152
|
C | CA | 60 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0258others(57): Show | 60 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1144-7218dupA | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31776152 | |||||
| chr11:31776175
|
A | G | 8 | a0001c0002t0014g0097a0001c0002t0014g0246a0001c0002t0014g0256others(5): Show | 8 | HG02647.hp1 HG03098.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-7218A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31776175 | ||||||
| chr11:31776185
|
A | T | 1 | a0001c0001t0009g0180 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1144-7208A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31776185 | ||||||
| chr11:31776525
|
G | A | 1 | a0001c0001t0005g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1144-6868G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31776525 | ||||||
| chr11:31776585
|
C | G | 1 | a0001c0001t0081g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1144-6808C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31776585 | ||||||
| chr11:31776638
|
A | G | 1 | a0001c0001t0004g0257 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1144-6755A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31776638 | ||||||
| chr11:31776644
|
T | A | 1 | a0001c0001t0008g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1144-6749T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31776644 | ||||||
| chr11:31776692
|
A | G | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-6701A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31776692 | ||||||
| chr11:31776709
|
A | T | 1 | a0001c0001t0011g0189 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1144-6684A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31776709 | ||||||
| chr11:31776731
|
G | T | 2 | a0001c0001t0001g0003a0001c0001t0004g0001 | 2 | NA18977.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1144-6662G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31776731 | ||||||
| chr11:31776864
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1144-6529C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31776864 | ||||||
| chr11:31776881
|
A | C | 1 | a0001c0001t0030g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1144-6512A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31776881 | ||||||
| chr11:31777104
|
G | A | 4 | a0001c0001t0001g0068a0001c0001t0001g0073a0001c0001t0001g0174others(1): Show | 4 | HG02132.hp2 HG02165.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144-6289G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31777104 | ||||||
| chr11:31777174
|
ATT | A | 5 | a0001c0001t0019g0233a0001c0001t0026g0251a0001c0001t0026g0252others(2): Show | 5 | HG01243.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-6210_1144-620 others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31777174 | |||||
| chr11:31777276
|
C | T | 8 | a0001c0002t0014g0097a0001c0002t0014g0246a0001c0002t0014g0256others(5): Show | 8 | HG02647.hp1 HG03098.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-6117C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31777276 | ||||||
| chr11:31777382
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1144-6011T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31777382 | ||||||
| chr11:31777628
|
G | C | 51 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0003g0103others(48): Show | 51 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1144-5765G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31777628 | ||||||
| chr11:31777684
|
G | T | 16 | a0001c0001t0006g0231a0001c0001t0008g0208a0001c0001t0008g0209others(13): Show | 16 | HG00642.hp1 HG02280.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1144-5709G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31777684 | ||||||
| chr11:31777806
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1144-5587G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31777806 | ||||||
| chr11:31777962
|
A | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 109 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.1144-5431A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31777962 | ||||||
| chr11:31778325
|
G | C | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 187 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(184): Show |
intron_variant | MODIFIER | c.1144-5068G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31778325 | ||||||
| chr11:31778356
|
G | C | 1 | a0001c0001t0005g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1144-5037G>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31778356 | ||||||
| chr11:31778582
|
G | A | 1 | a0001c0001t0007g0072 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1144-4811G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31778582 | ||||||
| chr11:31778874
|
T | C | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-4519T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31778874 | ||||||
| chr11:31779187
|
A | G | 3 | a0001c0001t0011g0104a0001c0001t0011g0189a0001c0001t0011g0197 | 3 | HG03239.hp2 HG03831.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1144-4206A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31779187 | ||||||
| chr11:31779326
|
G | T | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 189 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(186): Show |
intron_variant | MODIFIER | c.1144-4067G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31779326 | ||||||
| chr11:31779359
|
C | G | 17 | a0001c0001t0006g0163a0001c0001t0006g0170a0001c0001t0006g0227others(14): Show | 17 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.1144-4034C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31779359 | ||||||
| chr11:31779360
|
T | A | 8 | a0001c0001t0005g0264a0001c0001t0008g0269a0001c0001t0008g0270others(5): Show | 8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-4033T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31779360 | ||||||
| chr11:31779433
|
C | G | 1 | a0001c0001t0004g0044 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1144-3960C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31779433 | ||||||
| chr11:31779531
|
A | G | 1 | a0001c0001t0016g0171 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1144-3862A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31779531 | ||||||
| chr11:31779545
|
C | G | 1 | a0001c0001t0005g0131 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1144-3848C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31779545 | ||||||
| chr11:31779606
|
GCCTTATT others(6): Show |
G | 1 | a0001c0001t0005g0131 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1144-3785_1144-377 others(17): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31779606 | |||||
| chr11:31779996
|
A | T | 39 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0003g0103others(36): Show | 39 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1144-3397A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31779996 | ||||||
| chr11:31780477
|
A | T | 1 | a0001c0001t0004g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1144-2916A>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31780477 | ||||||
| chr11:31780611
|
C | G | 1 | a0001c0001t0007g0089 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1144-2782C>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31780611 | ||||||
| chr11:31780787
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1144-2606A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31780787 | ||||||
| chr11:31780809
|
G | A | 41 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0003g0103others(38): Show | 41 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.1144-2584G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31780809 | ||||||
| chr11:31780990
|
G | A | 1 | a0001c0001t0083g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1144-2403G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31780990 | ||||||
| chr11:31781275
|
T | A | 1 | a0001c0001t0050g0235 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1144-2118T>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31781275 | ||||||
| chr11:31781300
|
A | G | 1 | a0001c0001t0066g0141 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1144-2093A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31781300 | ||||||
| chr11:31781312
|
C | A | 2 | a0001c0001t0005g0005a0001c0001t0005g0006 | 2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1144-2081C>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31781312 | ||||||
| chr11:31781335
|
A | G | 5 | a0001c0001t0006g0227a0001c0001t0006g0229a0001c0001t0006g0230others(2): Show | 5 | HG00639.hp2 HG01981.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1144-2058A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31781335 | ||||||
| chr11:31781488
|
C | CT | 17 | a0001c0001t0002g0015a0001c0001t0002g0115a0001c0001t0002g0120others(14): Show | 17 | HG01175.hp2 HG01433.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1144-1875dupT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31781488 | |||||
| chr11:31781488
|
CT | C | 58 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0042others(55): Show | 58 | HG00642.hp1 HG01175.hp1 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.1144-1875delT | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31781488 | |||||
| chr11:31781488
|
CTT | C | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 124 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.1144-1876_1144-187 others(6): Show |
ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 31781488 | |||||
| chr11:31781536
|
A | G | 1 | a0001c0001t0040g0059 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1144-1857A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31781536 | ||||||
| chr11:31781584
|
C | T | 1 | a0001c0001t0008g0270 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1144-1809C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31781584 | ||||||
| chr11:31781700
|
T | G | 1 | a0001c0001t0064g0239 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1144-1693T>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31781700 | ||||||
| chr11:31781893
|
C | T | 1 | a0001c0001t0006g0227 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1144-1500C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31781893 | ||||||
| chr11:31781931
|
A | G | 3 | a0001c0001t0019g0084a0001c0001t0019g0095a0001c0001t0019g0233 | 3 | HG02257.hp2 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1144-1462A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31781931 | ||||||
| chr11:31782231
|
T | C | 8 | a0001c0002t0014g0097a0001c0002t0014g0246a0001c0002t0014g0256others(5): Show | 8 | HG02647.hp1 HG03098.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144-1162T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31782231 | ||||||
| chr11:31782243
|
A | G | 1 | a0001c0001t0004g0257 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1144-1150A>G | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31782243 | ||||||
| chr11:31782370
|
T | C | 1 | a0001c0001t0002g0261 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1144-1023T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31782370 | ||||||
| chr11:31782414
|
T | C | 3 | a0001c0001t0005g0264a0001c0001t0017g0266a0001c0001t0052g0267 | 3 | HG02145.hp2 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1144-979T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31782414 | ||||||
| chr11:31782517
|
G | T | 1 | a0001c0001t0022g0259 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1144-876G>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31782517 | ||||||
| chr11:31782625
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1144-768T>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31782625 | ||||||
| chr11:31782687
|
G | A | 1 | a0001c0001t0003g0206 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1144-706G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31782687 | ||||||
| chr11:31782979
|
C | T | 1 | a0001c0001t0033g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1144-414C>T | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31782979 | ||||||
| chr11:31783034
|
A | C | 4 | a0001c0001t0001g0064a0001c0001t0001g0066a0001c0001t0001g0069others(1): Show | 4 | NA18947.hp2 NA18978.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144-359A>C | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31783034 | ||||||
| chr11:31783045
|
G | A | 5 | a0001c0001t0002g0106a0001c0001t0002g0109a0001c0001t0010g0110others(2): Show | 5 | NA18942.hp1 NA18960.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144-348G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31783045 | ||||||
| chr11:31783068
|
G | A | 2 | a0001c0001t0017g0266a0001c0001t0017g0268 | 2 | HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1144-325G>A | ELP4 | ENSG00000109911.19 | transcript | ENST00000640961.2 | protein_coding | 9/9 | chr11 | 31783068 |