| geneid | 1997 |
|---|---|
| ensemblid | ENSG00000120690.16 |
| hgncid | 3316 |
| symbol | ELF1 |
| name | E74 like ETS transcription factor 1 |
| refseq_nuc | NM_172373.4 |
| refseq_prot | NP_758961.1 |
| ensembl_nuc | ENST00000239882.7 |
| ensembl_prot | ENSP00000239882.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 40931924 |
| end | 41019316 |
| strand | - |
| ver | v1.2 |
| region | chr13:40931924-41019316 |
| region5000 | chr13:40926924-41024316 |
| regionname0 | ELF1_chr13_40931924_41019316 |
| regionname5000 | ELF1_chr13_40926924_41024316 |
| 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 | 619 | 233 | 51 | 18 | 141 | 6 | 15 | 110 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0002 | 0/0 | 619 | 95 | 5 | 33 | 38 | 6 | 13 | 31 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0003 | 0/0 | 619 | 15 | 5 | 0 | 7 | 0 | 3 | 6 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0004 | 0/0 | 619 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0005 | 0/0 | 619 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0006 | 0/0 | 619 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0007 | 0/0 | 619 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0008 | 0/0 | 619 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0009 | 0/0 | 619 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0010 | 0/0 | 619 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0011 | 0/0 | 619 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0012 | 0/0 | 619 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| 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 | 1/0 | 1860 | 175 | 38 | 10 | 112 | 1 | 13 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0002 | 0/0 | 1860 | 95 | 5 | 33 | 38 | 6 | 13 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0003 | 0/1 | 1860 | 46 | 13 | 8 | 18 | 5 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0004 | 0/0 | 1860 | 13 | 5 | 0 | 6 | 0 | 2 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0005 | 0/0 | 1860 | 10 | 0 | 0 | 9 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0006 | 0/0 | 1860 | 8 | 6 | 2 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0007 | 0/0 | 1860 | 3 | 0 | 0 | 3 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0008 | 0/0 | 1860 | 2 | 2 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0009 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0010 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0011 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0012 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0013 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0014 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0015 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0016 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0017 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| c0018 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1819 | 227 | 46 | 18 | 141 | 6 | 14 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| t0002 | 0/0 | 1819 | 97 | 6 | 34 | 38 | 6 | 13 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| t0003 | 0/0 | 1819 | 11 | 0 | 0 | 9 | 0 | 2 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| t0004 | 0/0 | 1819 | 9 | 7 | 2 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| t0005 | 0/0 | 1819 | 4 | 4 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| t0006 | 0/0 | 1814 | 3 | 3 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| t0007 | 0/0 | 1819 | 2 | 0 | 0 | 0 | 0 | 2 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| t0008 | 0/0 | 1819 | 2 | 2 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| t0009 | 0/0 | 1819 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| t0010 | 0/0 | 1819 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| t0011 | 0/0 | 1819 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| t0012 | 0/0 | 1819 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| t0013 | 0/0 | 1819 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| t0014 | 0/0 | 1819 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| t0015 | 0/0 | 1819 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| 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 | 1/0 | 1860 | 175 | 38 | 10 | 112 | 1 | 13 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0003 | 0/1 | 1860 | 46 | 13 | 8 | 18 | 5 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0005 | 0/0 | 1860 | 10 | 0 | 0 | 9 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0013 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0014 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0002c0002 | 0/0 | 1860 | 95 | 5 | 33 | 38 | 6 | 13 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0003c0004 | 0/0 | 1860 | 13 | 5 | 0 | 6 | 0 | 2 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0003c0016 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0003c0018 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0004c0006 | 0/0 | 1860 | 8 | 6 | 2 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0005c0007 | 0/0 | 1860 | 3 | 0 | 0 | 3 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0006c0008 | 0/0 | 1860 | 2 | 2 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0007c0012 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0008c0011 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0009c0010 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0010c0009 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0011c0015 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0012c0017 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3678 | 160 | 28 | 10 | 110 | 1 | 10 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0001t0002 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0001t0005 | 0/0 | 3678 | 4 | 4 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0001t0007 | 0/0 | 3678 | 2 | 0 | 0 | 0 | 0 | 2 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0001t0008 | 0/0 | 3678 | 2 | 2 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0001t0009 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0001t0010 | 0/0 | 3678 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0001t0011 | 0/0 | 3678 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0001t0013 | 0/0 | 3678 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0001t0014 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0001t0015 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0003t0001 | 0/1 | 3678 | 45 | 12 | 8 | 18 | 5 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0003t0012 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0005t0003 | 0/0 | 3678 | 10 | 0 | 0 | 9 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0013t0001 | 0/0 | 3678 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0001c0014t0001 | 0/0 | 3678 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0002c0002t0002 | 0/0 | 3678 | 95 | 5 | 33 | 38 | 6 | 13 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0003c0004t0001 | 0/0 | 3678 | 13 | 5 | 0 | 6 | 0 | 2 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0003c0016t0001 | 0/0 | 3678 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0003c0018t0003 | 0/0 | 3678 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0004c0006t0004 | 0/0 | 3678 | 8 | 6 | 2 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0005c0007t0001 | 0/0 | 3678 | 3 | 0 | 0 | 3 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0006c0008t0006 | 0/0 | 3673 | 2 | 2 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0007c0012t0001 | 0/0 | 3678 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0008c0011t0001 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0009c0010t0001 | 0/0 | 3678 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0010c0009t0006 | 0/0 | 3673 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0011c0015t0002 | 0/0 | 3678 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| a0012c0017t0004 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | copy fasta | chr13 | 40926924 | 41024316 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0007g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0007g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0008g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0010g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0011g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0013g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0014g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0015g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0012g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0013t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0014t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0016t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0018t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0005c0007t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0005c0007t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0005c0007t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0006c0008t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0006c0008t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0007c0012t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0008c0011t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0009c0010t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0010c0009t0006g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0011c0015t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0012c0017t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0209 | EUR | GBR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0165 | EUR | GBR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0190 | EUR | GBR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0304 | EUR | GBR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0041 | EUR | FIN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0123 | EUR | FIN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00408 | hp1 | a0001 | c0001 | t0010 | g0096 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00423 | hp2 | a0003 | c0004 | t0001 | g0203 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00438 | hp1 | a0001 | c0014 | t0001 | g0241 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00597 | hp2 | a0001 | c0003 | t0001 | g0093 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0171 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0124 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0256 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00733 | hp1 | a0001 | c0003 | t0001 | g0265 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0029 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0040 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0315 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0305 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0039 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0129 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0058 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0056 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0253 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0310 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01168 | hp2 | a0001 | c0003 | t0001 | g0164 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0312 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0054 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01192 | hp2 | a0004 | c0006 | t0004 | g0334 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0206 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01258 | hp2 | a0011 | c0015 | t0002 | g0038 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0003 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0031 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0003 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0030 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0251 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01496 | hp2 | a0004 | c0006 | t0004 | g0007 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0105 | EUR | IBS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0027 | EUR | IBS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0049 | EUR | IBS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0104 | EUR | IBS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0307 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0207 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0050 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02015 | hp2 | a0005 | c0007 | t0001 | g0127 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0294 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0306 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0192 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0131 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0120 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02083 | hp2 | a0001 | c0001 | t0011 | g0324 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0322 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0099 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CDX | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CDX | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02280 | hp2 | a0012 | c0017 | t0004 | g0047 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0048 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0212 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0351 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0249 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0353 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02572 | hp2 | a0006 | c0008 | t0006 | g0188 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0323 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02630 | hp1 | a0004 | c0006 | t0004 | g0069 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0073 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0051 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02683 | hp2 | a0003 | c0018 | t0003 | g0023 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0022 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02717 | hp1 | a0004 | c0006 | t0004 | g0338 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0021 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02723 | hp2 | a0004 | c0006 | t0004 | g0008 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02738 | hp1 | a0009 | c0010 | t0001 | g0278 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0078 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0159 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0163 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02895 | hp2 | a0006 | c0008 | t0006 | g0189 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0162 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02922 | hp1 | a0003 | c0004 | t0001 | g0214 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02922 | hp2 | a0004 | c0006 | t0004 | g0332 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02965 | hp1 | a0003 | c0004 | t0001 | g0215 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0319 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0280 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0089 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03098 | hp2 | a0010 | c0009 | t0006 | g0273 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0094 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03195 | hp2 | a0004 | c0006 | t0004 | g0333 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03225 | hp1 | a0004 | c0006 | t0004 | g0337 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0118 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03453 | hp2 | a0008 | c0011 | t0001 | g0270 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0095 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03491 | hp1 | a0001 | c0001 | t0007 | g0349 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03491 | hp2 | a0003 | c0004 | t0001 | g0250 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0035 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03492 | hp2 | a0003 | c0004 | t0001 | g0252 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0298 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0254 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0025 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0210 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03834 | hp2 | a0001 | c0005 | t0003 | g0346 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0299 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03942 | hp2 | a0001 | c0001 | t0013 | g0136 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0255 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0178 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0170 | SAS | STU | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | STU | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0033 | SAS | STU | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18522 | hp2 | a0003 | c0004 | t0001 | g0216 | AFR | YRI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18612 | hp1 | a0001 | c0005 | t0003 | g0348 | EAS | CHB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0260 | EAS | CHB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18906 | hp1 | a0003 | c0004 | t0001 | g0217 | AFR | YRI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0062 | AFR | YRI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0316 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0186 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18946 | hp1 | a0001 | c0003 | t0001 | g0261 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0309 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18950 | hp1 | a0001 | c0005 | t0003 | g0343 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0092 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18953 | hp1 | a0005 | c0007 | t0001 | g0090 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18960 | hp1 | a0001 | c0005 | t0003 | g0344 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18960 | hp2 | a0003 | c0016 | t0001 | g0052 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0259 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18963 | hp1 | a0007 | c0012 | t0001 | g0137 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18963 | hp2 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18964 | hp2 | a0003 | c0004 | t0001 | g0202 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18966 | hp1 | a0001 | c0005 | t0003 | g0132 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18970 | hp1 | a0001 | c0005 | t0003 | g0341 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0286 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18972 | hp2 | a0001 | c0013 | t0001 | g0181 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0292 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18983 | hp1 | a0003 | c0004 | t0001 | g0199 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18986 | hp2 | a0001 | c0005 | t0003 | g0342 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18988 | hp2 | a0003 | c0004 | t0001 | g0302 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0320 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0356 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0311 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0244 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19001 | hp2 | a0001 | c0005 | t0003 | g0347 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19004 | hp1 | a0001 | c0005 | t0003 | g0345 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19006 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0285 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0066 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19012 | hp2 | a0001 | c0003 | t0001 | g0262 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0046 | AFR | LWK | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0321 | AFR | LWK | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19054 | hp1 | a0001 | c0003 | t0001 | g0240 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19062 | hp1 | a0001 | c0003 | t0001 | g0187 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19064 | hp1 | a0003 | c0004 | t0001 | g0303 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0191 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0239 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19075 | hp2 | a0003 | c0004 | t0001 | g0198 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19082 | hp2 | a0001 | c0005 | t0003 | g0166 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0318 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19087 | hp1 | a0005 | c0007 | t0001 | g0079 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0220 | AFR | YRI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0098 | AFR | YRI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ASW | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA20129 | hp2 | a0001 | c0003 | t0012 | g0119 | AFR | ASW | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0020 | EUR | TSI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | TSI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0279 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0059 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02109 | hp2 | a0003 | c0004 | t0001 | g0219 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02559 | hp1 | a0001 | c0001 | t0015 | g0006 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0122 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | USA | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | USA | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0045 | AFR | USA | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA20300 | hp2 | a0001 | c0001 | t0014 | g0248 | AFR | USA | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0193 | AFR | LWK | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0140 | REF | REF | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0173 | REF | REF | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:40933830
|
C | T | 1 | a0008 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.1455G>A | p.Met485Ile | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 1772/3678 | 1455/1860 | 485/619 | chr13 | 40933830 | ||
| chr13:40933871
|
G | T | 1 | a0009 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.1414C>A | p.Pro472Thr | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 1731/3678 | 1414/1860 | 472/619 | chr13 | 40933871 | ||
| chr13:40933913
|
A | G | 1 | a0005 | 3 | HG02015.hp2 NA18953.hp1 NA19087.hp1 |
missense_variant | MODERATE | c.1372T>C | p.Ser458Pro | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 1689/3678 | 1372/1860 | 458/619 | chr13 | 40933913 | ||
| chr13:40940969
|
G | A | 2 | a0004a0012 | 9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
missense_variant | MODERATE | c.1208C>T | p.Thr403Ile | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1525/3678 | 1208/1860 | 403/619 | chr13 | 40940969 | ||
| chr13:40941088
|
T | G | 1 | a0007 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.1089A>C | p.Gln363His | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1406/3678 | 1089/1860 | 363/619 | chr13 | 40941088 | ||
| chr13:40941129
|
A | C | 1 | a0011 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.1048T>G | p.Ser350Ala | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1365/3678 | 1048/1860 | 350/619 | chr13 | 40941129 | ||
| chr13:40941150
|
T | A | 4 | a0002a0006a0010others(1): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
missense_variant | MODERATE | c.1027A>T | p.Thr343Ser | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1344/3678 | 1027/1860 | 343/619 | chr13 | 40941150 | ||
| chr13:40958907
|
A | G | 1 | a0010 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.182T>C | p.Ile61Thr | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/9 | 499/3678 | 182/1860 | 61/619 | chr13 | 40958907 | ||
| chr13:40958916
|
T | C | 4 | a0002a0003a0011others(1): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
missense_variant | MODERATE | c.173A>G | p.Asn58Ser | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/9 | 490/3678 | 173/1860 | 58/619 | chr13 | 40958916 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:40941046
|
T | C | 2 | a0001c0005a0003c0018 | 11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
synonymous_variant | LOW | c.1131A>G | p.Pro377Pro | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1448/3678 | 1131/1860 | 377/619 | chr13 | 40941046 | ||
| chr13:40941223
|
T | A | 1 | a0001c0013 | 1 | NA18972.hp2 | synonymous_variant | LOW | c.954A>T | p.Ser318Ser | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1271/3678 | 954/1860 | 318/619 | chr13 | 40941223 | ||
| chr13:40941232
|
T | C | 2 | a0001c0005a0003c0018 | 11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
synonymous_variant | LOW | c.945A>G | p.Leu315Leu | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1262/3678 | 945/1860 | 315/619 | chr13 | 40941232 | ||
| chr13:40941235
|
C | T | 3 | a0001c0003a0003c0016a0005c0007 | 50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
synonymous_variant | LOW | c.942G>A | p.Ser314Ser | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1259/3678 | 942/1860 | 314/619 | chr13 | 40941235 | ||
| chr13:40941325
|
G | A | 1 | a0001c0014 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.852C>T | p.Arg284Arg | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1169/3678 | 852/1860 | 284/619 | chr13 | 40941325 | ||
| chr13:40943849
|
A | G | 4 | a0002c0002a0006c0008a0010c0009others(1): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
synonymous_variant | LOW | c.606T>C | p.Asp202Asp | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 6/9 | 923/3678 | 606/1860 | 202/619 | chr13 | 40943849 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:40932094
|
C | T | 2 | a0001c0005t0003a0003c0018t0003 | 11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1331G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 1331 | chr13 | 40932094 | |||||
| chr13:40932330
|
C | G | 1 | a0001c0003t0012 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1095G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 1095 | chr13 | 40932330 | |||||
| chr13:40932330
|
C | T | 1 | a0001c0001t0011 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1095G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 1095 | chr13 | 40932330 | |||||
| chr13:40932339
|
G | T | 1 | a0001c0001t0008 | 2 | HG02145.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1086C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 1086 | chr13 | 40932339 | |||||
| chr13:40932446
|
A | T | 1 | a0001c0001t0007 | 2 | HG03017.hp2 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*979T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 979 | chr13 | 40932446 | |||||
| chr13:40932585
|
C | T | 8 | a0001c0001t0002a0001c0001t0008a0001c0005t0003others(5): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*840G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 840 | chr13 | 40932585 | |||||
| chr13:40932587
|
G | A | 1 | a0001c0001t0013 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*838C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 838 | chr13 | 40932587 | |||||
| chr13:40932714
|
G | T | 2 | a0004c0006t0004a0012c0017t0004 | 9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*711C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 711 | chr13 | 40932714 | |||||
| chr13:40932748
|
A | G | 7 | a0001c0001t0002a0001c0005t0003a0002c0002t0002others(4): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*677T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 677 | chr13 | 40932748 | |||||
| chr13:40932783
|
A | C | 1 | a0001c0001t0010 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*642T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 642 | chr13 | 40932783 | |||||
| chr13:40932820
|
G | T | 1 | a0001c0001t0009 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*605C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 605 | chr13 | 40932820 | |||||
| chr13:40932849
|
T | C | 1 | a0001c0001t0005 | 4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*576A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 576 | chr13 | 40932849 | |||||
| chr13:40933122
|
C | A | 1 | a0001c0001t0014 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*303G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 303 | chr13 | 40933122 | |||||
| chr13:40933133
|
TAGAAA | T | 2 | a0006c0008t0006a0010c0009t0006 | 3 | HG02572.hp2 HG02895.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*287_*291delTTTCT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 287 | chr13 | 40933133 | |||||
| chr13:40933225
|
C | A | 1 | a0001c0001t0008 | 2 | HG02145.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*200G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 200 | chr13 | 40933225 | |||||
| chr13:40982189
|
T | C | 1 | a0001c0001t0015 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-135A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/9 | 135 | chr13 | 40982189 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:40934171
|
T | C | 1 | a0001c0005t0003g0346 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1257-143A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934171 | ||||||
| chr13:40934258
|
G | A | 11 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(8): Show | 11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1257-230C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934258 | ||||||
| chr13:40934415
|
G | C | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1257-387C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934415 | ||||||
| chr13:40934416
|
C | CT | 9 | a0001c0001t0001g0126a0001c0001t0015g0006a0001c0003t0001g0099others(6): Show | 9 | HG00423.hp2 HG01169.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1257-389dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934416 | ||||||
| chr13:40934416
|
C | CTT | 97 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(94): Show | 98 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.1257-390_1257-389d others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934416 | ||||||
| chr13:40934416
|
C | CTTT | 10 | a0001c0001t0014g0248a0002c0002t0002g0037a0002c0002t0002g0041others(7): Show | 10 | HG00280.hp1 HG00738.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.1257-391_1257-389d others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934416 | ||||||
| chr13:40934416
|
CT | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(71): Show | 78 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1257-389delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934416 | ||||||
| chr13:40934416
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0061 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1257-399_1257-389d others(13): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934416 | ||||||
| chr13:40934416
|
CTTTTTTT others(5): Show |
C | 91 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(88): Show | 91 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1257-400_1257-389d others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934416 | ||||||
| chr13:40934503
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1257-475C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934503 | ||||||
| chr13:40934577
|
C | T | 2 | a0002c0002t0002g0310a0002c0002t0002g0312 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1257-549G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934577 | ||||||
| chr13:40934578
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1257-550C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934578 | ||||||
| chr13:40934672
|
G | A | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1257-644C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934672 | ||||||
| chr13:40934675
|
C | A | 1 | a0001c0001t0001g0087 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1257-647G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934675 | ||||||
| chr13:40934708
|
C | G | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1257-680G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934708 | ||||||
| chr13:40934715
|
C | T | 49 | a0001c0003t0001g0003a0001c0003t0001g0011a0001c0003t0001g0012others(46): Show | 50 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1257-687G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934715 | ||||||
| chr13:40934818
|
G | A | 1 | a0007c0012t0001g0137 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1257-790C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934818 | ||||||
| chr13:40935081
|
T | A | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1257-1053A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935081 | ||||||
| chr13:40935174
|
A | G | 1 | a0001c0003t0001g0353 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1257-1146T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935174 | ||||||
| chr13:40935177
|
G | C | 5 | a0004c0006t0004g0332a0004c0006t0004g0333a0004c0006t0004g0334others(2): Show | 5 | HG01192.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257-1149C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935177 | ||||||
| chr13:40935205
|
G | T | 1 | a0001c0001t0001g0074 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1257-1177C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935205 | ||||||
| chr13:40935436
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1257-1408A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935436 | ||||||
| chr13:40935509
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1257-1481T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935509 | ||||||
| chr13:40935626
|
G | C | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1257-1598C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935626 | ||||||
| chr13:40935675
|
A | AT | 12 | a0001c0001t0001g0114a0001c0001t0001g0126a0001c0001t0001g0128others(9): Show | 12 | HG02145.hp1 HG02630.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.1257-1648dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935675 | ||||||
| chr13:40935675
|
A | ATTT | 11 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(8): Show | 11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1257-1650_1257-164 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935675 | ||||||
| chr13:40935675
|
AT | A | 97 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(94): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1257-1648delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935675 | ||||||
| chr13:40935736
|
T | C | 110 | a0001c0001t0002g0172a0001c0005t0003g0132a0001c0005t0003g0166others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1257-1708A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935736 | ||||||
| chr13:40935797
|
C | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0075a0001c0001t0001g0116 | 3 | NA18991.hp2 NA19060.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1257-1769G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935797 | ||||||
| chr13:40935819
|
C | A | 11 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(8): Show | 11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1257-1791G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935819 | ||||||
| chr13:40935910
|
T | C | 1 | a0002c0002t0002g0018 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1257-1882A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935910 | ||||||
| chr13:40936117
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1257-2089G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936117 | ||||||
| chr13:40936188
|
T | C | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1257-2160A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936188 | ||||||
| chr13:40936194
|
T | C | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1257-2166A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936194 | ||||||
| chr13:40936203
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 82 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1257-2175C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936203 | ||||||
| chr13:40936219
|
A | G | 1 | a0002c0002t0002g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1257-2191T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936219 | ||||||
| chr13:40936440
|
C | G | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1257-2412G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936440 | ||||||
| chr13:40936476
|
G | A | 1 | a0002c0002t0002g0034 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1257-2448C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936476 | ||||||
| chr13:40936536
|
A | G | 113 | a0001c0001t0002g0172a0001c0001t0008g0073a0001c0001t0008g0322others(110): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1257-2508T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936536 | ||||||
| chr13:40936677
|
C | T | 109 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(106): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1257-2649G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936677 | ||||||
| chr13:40936693
|
G | A | 11 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(8): Show | 11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1257-2665C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936693 | ||||||
| chr13:40936715
|
C | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0185 | 2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1257-2687G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936715 | ||||||
| chr13:40936760
|
C | CA | 116 | a0001c0001t0001g0114a0001c0001t0001g0125a0001c0001t0001g0147others(113): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1257-2733dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936760 | ||||||
| chr13:40936760
|
C | CAA | 10 | a0001c0005t0003g0347a0002c0002t0002g0025a0002c0002t0002g0040others(7): Show | 10 | HG00621.hp2 HG00735.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1257-2734_1257-273 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936760 | ||||||
| chr13:40936773
|
A | G | 2 | a0001c0001t0002g0172a0001c0001t0015g0006 | 2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1257-2745T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936773 | ||||||
| chr13:40936778
|
G | A | 1 | a0002c0002t0002g0049 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1257-2750C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936778 | ||||||
| chr13:40936779
|
A | G | 1 | a0002c0002t0002g0049 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1257-2751T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936779 | ||||||
| chr13:40936818
|
G | A | 1 | a0002c0002t0002g0279 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1257-2790C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936818 | ||||||
| chr13:40936916
|
T | C | 4 | a0001c0005t0003g0342a0001c0005t0003g0343a0001c0005t0003g0345others(1): Show | 4 | NA18950.hp1 NA18986.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257-2888A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936916 | ||||||
| chr13:40936953
|
CA | C | 5 | a0003c0004t0001g0198a0003c0004t0001g0202a0003c0004t0001g0203others(2): Show | 5 | HG00423.hp2 NA18964.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257-2926delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936953 | ||||||
| chr13:40936963
|
G | T | 5 | a0003c0004t0001g0198a0003c0004t0001g0202a0003c0004t0001g0203others(2): Show | 5 | HG00423.hp2 NA18964.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257-2935C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936963 | ||||||
| chr13:40937668
|
A | G | 1 | a0001c0001t0001g0143 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1256+3253T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40937668 | ||||||
| chr13:40937720
|
C | T | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+3201G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40937720 | ||||||
| chr13:40937762
|
C | T | 9 | a0004c0006t0004g0007a0004c0006t0004g0008a0004c0006t0004g0069others(6): Show | 9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1256+3159G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40937762 | ||||||
| chr13:40937773
|
T | C | 2 | a0001c0001t0015g0006a0008c0011t0001g0270 | 2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1256+3148A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40937773 | ||||||
| chr13:40937976
|
C | T | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+2945G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40937976 | ||||||
| chr13:40938018
|
T | C | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+2903A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40938018 | ||||||
| chr13:40938044
|
C | T | 1 | a0002c0002t0002g0256 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1256+2877G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40938044 | ||||||
| chr13:40938464
|
T | C | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1256+2457A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40938464 | ||||||
| chr13:40938631
|
G | A | 1 | a0002c0002t0002g0016 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1256+2290C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40938631 | ||||||
| chr13:40938698
|
CTTG | C | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291 | 3 | HG03239.hp1 NA18957.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1256+2220_1256+222 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40938698 | ||||||
| chr13:40938821
|
A | C | 1 | a0002c0002t0002g0207 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1256+2100T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40938821 | ||||||
| chr13:40939112
|
T | C | 113 | a0001c0001t0002g0172a0001c0001t0008g0073a0001c0001t0008g0322others(110): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1256+1809A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939112 | ||||||
| chr13:40939246
|
T | G | 4 | a0001c0001t0005g0089a0001c0001t0005g0122a0001c0001t0005g0162others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1256+1675A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939246 | ||||||
| chr13:40939316
|
CA | C | 11 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(8): Show | 11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1256+1604delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939316 | ||||||
| chr13:40939383
|
G | A | 1 | a0008c0011t0001g0270 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1256+1538C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939383 | ||||||
| chr13:40939456
|
A | C | 5 | a0003c0004t0001g0214a0003c0004t0001g0215a0003c0004t0001g0216others(2): Show | 5 | HG02109.hp2 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1256+1465T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939456 | ||||||
| chr13:40939489
|
C | T | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+1432G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939489 | ||||||
| chr13:40939546
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1256+1375G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939546 | ||||||
| chr13:40939561
|
T | A | 1 | a0001c0001t0001g0269 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1256+1360A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939561 | ||||||
| chr13:40939733
|
G | C | 1 | a0001c0003t0001g0123 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1256+1188C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939733 | ||||||
| chr13:40939733
|
G | T | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(351): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1256+1188C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939733 | ||||||
| chr13:40939787
|
G | A | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+1134C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939787 | ||||||
| chr13:40939980
|
T | C | 5 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0150others(2): Show | 5 | NA18949.hp2 NA18983.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1256+941A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939980 | ||||||
| chr13:40940009
|
C | A | 1 | a0002c0002t0002g0288 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1256+912G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940009 | ||||||
| chr13:40940176
|
A | G | 39 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(36): Show | 40 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1256+745T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940176 | ||||||
| chr13:40940282
|
C | G | 1 | a0002c0002t0002g0032 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1256+639G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940282 | ||||||
| chr13:40940299
|
C | CAGA | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+619_1256+621d others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940299 | ||||||
| chr13:40940309
|
T | A | 1 | a0001c0013t0001g0181 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1256+612A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940309 | ||||||
| chr13:40940324
|
C | T | 97 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(94): Show | 97 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1256+597G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940324 | ||||||
| chr13:40940386
|
G | GA | 47 | a0001c0001t0001g0043a0001c0001t0001g0060a0001c0001t0001g0071others(44): Show | 47 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1256+534dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | ||||||
| chr13:40940386
|
G | GAA | 13 | a0001c0001t0001g0061a0001c0001t0001g0080a0001c0001t0001g0081others(10): Show | 13 | HG00423.hp2 HG01891.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.1256+533_1256+534d others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | ||||||
| chr13:40940386
|
G | GAAA | 6 | a0001c0001t0001g0072a0001c0001t0001g0101a0001c0001t0001g0223others(3): Show | 6 | HG00609.hp1 HG02165.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.1256+532_1256+534d others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | ||||||
| chr13:40940386
|
G | GAAAAAA | 7 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0150others(4): Show | 7 | HG03195.hp1 NA18949.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.1256+529_1256+534d others(8): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | ||||||
| chr13:40940386
|
GA | G | 47 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0001g0143others(44): Show | 47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.1256+534delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | ||||||
| chr13:40940386
|
GAA | G | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0057others(50): Show | 55 | HG00597.hp1 HG00673.hp1 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.1256+533_1256+534d others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | ||||||
| chr13:40940386
|
GAAA | G | 17 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0064others(14): Show | 17 | HG00408.hp2 HG00544.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1256+532_1256+534d others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | ||||||
| chr13:40940386
|
GAAAA | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0352a0001c0001t0001g0354others(1): Show | 6 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1256+531_1256+534d others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | ||||||
| chr13:40940386
|
GAAAAAAA others(4): Show |
G | 3 | a0001c0001t0001g0152a0001c0001t0008g0073a0001c0001t0008g0322 | 3 | HG02145.hp1 HG02630.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1256+524_1256+534d others(13): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | ||||||
| chr13:40940386
|
GAAAAAAA others(5): Show |
G | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+523_1256+534d others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | ||||||
| chr13:40940386
|
GAAAAAAA others(10): Show |
G | 9 | a0004c0006t0004g0007a0004c0006t0004g0008a0004c0006t0004g0069others(6): Show | 9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1256+518_1256+534d others(19): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | ||||||
| chr13:40940398
|
A | C | 1 | a0001c0001t0001g0053 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1256+523T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940398 | ||||||
| chr13:40940408
|
A | C | 15 | a0001c0001t0002g0172a0001c0001t0014g0248a0001c0001t0015g0006others(12): Show | 15 | HG02109.hp1 HG02559.hp1 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.1256+513T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940408 | ||||||
| chr13:40940409
|
A | C | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+512T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940409 | ||||||
| chr13:40940415
|
A | C | 4 | a0001c0003t0001g0098a0001c0003t0001g0099a0001c0003t0001g0159others(1): Show | 4 | HG02145.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1256+506T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940415 | ||||||
| chr13:40940418
|
A | C | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+503T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940418 | ||||||
| chr13:40940419
|
C | A | 3 | a0001c0001t0013g0136a0001c0003t0001g0120a0003c0004t0001g0203 | 3 | HG00423.hp2 HG02056.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1256+502G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940419 | ||||||
| chr13:40940456
|
G | T | 1 | a0001c0001t0001g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1256+465C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940456 | ||||||
| chr13:40940497
|
A | T | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+424T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940497 | ||||||
| chr13:40940560
|
A | G | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+361T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940560 | ||||||
| chr13:40940688
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1256+233C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940688 | ||||||
| chr13:40940889
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1256+32T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940889 | ||||||
| chr13:40941453
|
A | C | 1 | a0002c0002t0002g0048 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.807-83T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40941453 | ||||||
| chr13:40941482
|
G | A | 1 | a0002c0002t0002g0027 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.807-112C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40941482 | ||||||
| chr13:40941862
|
T | C | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.807-492A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40941862 | ||||||
| chr13:40941898
|
A | G | 12 | a0001c0001t0002g0172a0001c0005t0003g0132a0001c0005t0003g0166others(9): Show | 12 | HG02109.hp1 HG02683.hp2 HG03834.hp2 others(9): Show |
intron_variant | MODIFIER | c.807-528T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40941898 | ||||||
| chr13:40941916
|
C | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0229 | 2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.807-546G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40941916 | ||||||
| chr13:40941935
|
A | G | 54 | a0001c0003t0001g0003a0001c0003t0001g0011a0001c0003t0001g0012others(51): Show | 55 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.807-565T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40941935 | ||||||
| chr13:40942104
|
A | C | 1 | a0008c0011t0001g0270 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.807-734T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40942104 | ||||||
| chr13:40942303
|
T | C | 9 | a0004c0006t0004g0007a0004c0006t0004g0008a0004c0006t0004g0069others(6): Show | 9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.806+649A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40942303 | ||||||
| chr13:40942362
|
T | C | 1 | a0004c0006t0004g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.806+590A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40942362 | ||||||
| chr13:40942386
|
G | A | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0340 | 3 | HG02622.hp1 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.806+566C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40942386 | ||||||
| chr13:40942423
|
T | C | 1 | a0001c0001t0001g0009 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.806+529A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40942423 | ||||||
| chr13:40942663
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.806+289C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40942663 | ||||||
| chr13:40942732
|
G | A | 1 | a0001c0001t0014g0248 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.806+220C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40942732 | ||||||
| chr13:40943159
|
A | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0230 | 2 | HG01109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.614-15T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 6/8 | chr13 | 40943159 | ||||||
| chr13:40943372
|
C | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 149 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.614-228G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 6/8 | chr13 | 40943372 | ||||||
| chr13:40943382
|
A | G | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.614-238T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 6/8 | chr13 | 40943382 | ||||||
| chr13:40943405
|
G | C | 1 | a0003c0016t0001g0052 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.614-261C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 6/8 | chr13 | 40943405 | ||||||
| chr13:40943661
|
C | T | 14 | a0001c0001t0002g0172a0001c0001t0014g0248a0001c0005t0003g0132others(11): Show | 14 | HG00609.hp2 HG02109.hp1 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.613+181G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 6/8 | chr13 | 40943661 | ||||||
| chr13:40943683
|
T | C | 3 | a0005c0007t0001g0079a0005c0007t0001g0090a0005c0007t0001g0127 | 3 | HG02015.hp2 NA18953.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.613+159A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 6/8 | chr13 | 40943683 | ||||||
| chr13:40944038
|
T | G | 1 | a0001c0001t0001g0223 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.530-113A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944038 | ||||||
| chr13:40944223
|
C | G | 54 | a0001c0003t0001g0003a0001c0003t0001g0011a0001c0003t0001g0012others(51): Show | 55 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.530-298G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944223 | ||||||
| chr13:40944467
|
C | G | 1 | a0001c0001t0001g0231 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.530-542G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944467 | ||||||
| chr13:40944553
|
C | A | 1 | a0002c0002t0002g0307 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.530-628G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944553 | ||||||
| chr13:40944601
|
G | A | 3 | a0002c0002t0002g0213a0002c0002t0002g0306a0002c0002t0002g0307 | 3 | HG01934.hp1 HG02040.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.530-676C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944601 | ||||||
| chr13:40944602
|
T | C | 11 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(8): Show | 11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.530-677A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944602 | ||||||
| chr13:40944655
|
T | C | 1 | a0001c0001t0001g0336 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.530-730A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944655 | ||||||
| chr13:40944696
|
G | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(168): Show | 175 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.530-771C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944696 | ||||||
| chr13:40944732
|
A | G | 4 | a0001c0003t0001g0092a0001c0003t0001g0093a0001c0003t0001g0130others(1): Show | 4 | HG00597.hp2 NA18948.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-807T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944732 | ||||||
| chr13:40944783
|
T | C | 39 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(36): Show | 40 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.530-858A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944783 | ||||||
| chr13:40944812
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.530-887C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944812 | ||||||
| chr13:40945006
|
A | C | 11 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(8): Show | 11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.530-1081T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40945006 | ||||||
| chr13:40945191
|
T | C | 9 | a0004c0006t0004g0007a0004c0006t0004g0008a0004c0006t0004g0069others(6): Show | 9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.530-1266A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40945191 | ||||||
| chr13:40945524
|
T | C | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.530-1599A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40945524 | ||||||
| chr13:40945950
|
T | G | 1 | a0001c0003t0001g0165 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.530-2025A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40945950 | ||||||
| chr13:40946036
|
T | C | 93 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(90): Show | 93 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.530-2111A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946036 | ||||||
| chr13:40946059
|
G | A | 1 | a0001c0003t0001g0178 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.530-2134C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946059 | ||||||
| chr13:40946086
|
G | A | 3 | a0001c0001t0001g0266a0001c0001t0001g0300a0001c0001t0001g0301 | 3 | HG02040.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.530-2161C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946086 | ||||||
| chr13:40946158
|
T | C | 3 | a0001c0001t0001g0070a0001c0001t0001g0075a0001c0001t0001g0116 | 3 | NA18991.hp2 NA19060.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.530-2233A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946158 | ||||||
| chr13:40946374
|
T | C | 9 | a0004c0006t0004g0007a0004c0006t0004g0008a0004c0006t0004g0069others(6): Show | 9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.530-2449A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946374 | ||||||
| chr13:40946381
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.530-2456A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946381 | ||||||
| chr13:40946648
|
G | A | 2 | a0002c0002t0002g0019a0002c0002t0002g0020 | 2 | HG01169.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.530-2723C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946648 | ||||||
| chr13:40946783
|
T | C | 7 | a0001c0003t0001g0259a0001c0003t0001g0260a0001c0003t0001g0261others(4): Show | 7 | NA18612.hp2 NA18946.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.530-2858A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946783 | ||||||
| chr13:40947124
|
C | CA | 85 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 89 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.529+2681dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40947124 | ||||||
| chr13:40947142
|
T | C | 9 | a0004c0006t0004g0007a0004c0006t0004g0008a0004c0006t0004g0069others(6): Show | 9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+2664A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40947142 | ||||||
| chr13:40947393
|
T | C | 66 | a0001c0001t0001g0128a0001c0001t0001g0155a0001c0001t0014g0248others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.529+2413A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40947393 | ||||||
| chr13:40947681
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.529+2125T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40947681 | ||||||
| chr13:40948104
|
T | C | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.529+1702A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948104 | ||||||
| chr13:40948136
|
T | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 82 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.529+1670A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948136 | ||||||
| chr13:40948202
|
A | C | 13 | a0002c0002t0002g0016a0002c0002t0002g0017a0002c0002t0002g0037others(10): Show | 13 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.529+1604T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948202 | ||||||
| chr13:40948356
|
C | CT | 11 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(8): Show | 11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+1449dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948356 | ||||||
| chr13:40948366
|
C | T | 1 | a0001c0003t0001g0178 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.529+1440G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948366 | ||||||
| chr13:40948402
|
T | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0228 | 2 | NA18951.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.529+1404A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948402 | ||||||
| chr13:40948585
|
G | A | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(1): Show | 4 | HG03239.hp1 NA18957.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+1221C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948585 | ||||||
| chr13:40948704
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.529+1102A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948704 | ||||||
| chr13:40948726
|
C | CT | 5 | a0001c0001t0001g0167a0003c0004t0001g0198a0003c0004t0001g0202others(2): Show | 5 | HG00423.hp2 NA18964.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+1079_529+1080i others(3): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948726 | ||||||
| chr13:40948856
|
G | T | 1 | a0001c0001t0001g0142 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.529+950C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948856 | ||||||
| chr13:40948889
|
A | G | 1 | a0002c0002t0002g0170 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.529+917T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948889 | ||||||
| chr13:40949036
|
A | AGTTCAAT others(5): Show |
1 | a0001c0001t0001g0087 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.529+758_529+769dup others(12): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949036 | ||||||
| chr13:40949069
|
T | G | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.529+737A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949069 | ||||||
| chr13:40949074
|
T | C | 2 | a0001c0003t0001g0003a0001c0003t0001g0066 | 3 | HG01346.hp1 HG01358.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.529+732A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949074 | ||||||
| chr13:40949118
|
T | G | 1 | a0002c0002t0002g0254 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.529+688A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949118 | ||||||
| chr13:40949326
|
G | T | 2 | a0001c0003t0001g0011a0001c0003t0001g0012 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.529+480C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949326 | ||||||
| chr13:40949495
|
T | A | 1 | a0001c0001t0001g0233 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.529+311A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949495 | ||||||
| chr13:40949587
|
TCAAA | T | 11 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(8): Show | 11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+215_529+218del others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949587 | ||||||
| chr13:40949615
|
A | G | 60 | a0001c0001t0001g0128a0001c0001t0001g0155a0001c0001t0001g0297others(57): Show | 61 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.529+191T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949615 | ||||||
| chr13:40949631
|
A | T | 1 | a0002c0002t0002g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.529+175T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949631 | ||||||
| chr13:40949676
|
ATT | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0352a0001c0001t0001g0354others(1): Show | 6 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+128_529+129del others(2): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949676 | ||||||
| chr13:40949740
|
T | C | 40 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(37): Show | 41 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.529+66A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949740 | ||||||
| chr13:40950029
|
C | T | 11 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(8): Show | 11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-56G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950029 | ||||||
| chr13:40950030
|
G | A | 2 | a0002c0002t0002g0019a0002c0002t0002g0020 | 2 | HG01169.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.362-57C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950030 | ||||||
| chr13:40950087
|
T | C | 98 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.362-114A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950087 | ||||||
| chr13:40950393
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.362-420T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950393 | ||||||
| chr13:40950461
|
C | T | 1 | a0002c0002t0002g0027 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.362-488G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950461 | ||||||
| chr13:40950492
|
A | AT | 57 | a0001c0001t0001g0128a0001c0001t0001g0155a0001c0001t0014g0248others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.362-520dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950492 | ||||||
| chr13:40950492
|
AT | A | 6 | a0001c0001t0001g0087a0002c0002t0002g0131a0002c0002t0002g0171others(3): Show | 6 | HG00609.hp2 HG01123.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-520delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950492 | ||||||
| chr13:40950537
|
C | A | 1 | a0002c0002t0002g0209 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.362-564G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950537 | ||||||
| chr13:40950598
|
C | A | 66 | a0001c0001t0001g0057a0001c0001t0001g0128a0001c0001t0001g0155others(63): Show | 67 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.362-625G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950598 | ||||||
| chr13:40950928
|
A | G | 6 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0154others(3): Show | 6 | HG00673.hp1 HG02135.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+401T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950928 | ||||||
| chr13:40951450
|
A | G | 99 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(96): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.254-14T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951450 | ||||||
| chr13:40951598
|
G | A | 1 | a0002c0002t0002g0171 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.254-162C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951598 | ||||||
| chr13:40951633
|
A | G | 99 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(96): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.254-197T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951633 | ||||||
| chr13:40951732
|
T | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0352a0001c0001t0001g0354others(1): Show | 6 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.254-296A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951732 | ||||||
| chr13:40951782
|
G | A | 39 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(36): Show | 40 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.254-346C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951782 | ||||||
| chr13:40951783
|
T | C | 99 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(96): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.254-347A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951783 | ||||||
| chr13:40951798
|
T | C | 1 | a0001c0003t0001g0120 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.254-362A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951798 | ||||||
| chr13:40951904
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.254-468T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951904 | ||||||
| chr13:40952214
|
C | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(73): Show | 80 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.254-778G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952214 | ||||||
| chr13:40952233
|
A | G | 57 | a0001c0001t0001g0128a0001c0001t0001g0155a0001c0001t0014g0248others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.254-797T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952233 | ||||||
| chr13:40952286
|
A | C | 1 | a0012c0017t0004g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.254-850T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952286 | ||||||
| chr13:40952368
|
C | CT | 100 | a0001c0001t0001g0142a0002c0002t0002g0002a0002c0002t0002g0013others(97): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.254-933dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952368 | ||||||
| chr13:40952368
|
CT | C | 6 | a0001c0003t0001g0141a0001c0003t0001g0186a0001c0003t0001g0187others(3): Show | 6 | NA18940.hp2 NA18963.hp2 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.254-933delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952368 | ||||||
| chr13:40952395
|
C | T | 3 | a0001c0001t0002g0172a0001c0001t0008g0073a0001c0001t0008g0322 | 3 | HG02109.hp1 HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.254-959G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952395 | ||||||
| chr13:40952427
|
T | C | 3 | a0001c0001t0001g0070a0001c0001t0001g0075a0001c0001t0001g0116 | 3 | NA18991.hp2 NA19060.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.254-991A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952427 | ||||||
| chr13:40952472
|
C | T | 36 | a0001c0001t0001g0128a0001c0001t0001g0155a0001c0003t0001g0003others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.254-1036G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952472 | ||||||
| chr13:40952485
|
C | T | 3 | a0001c0001t0002g0172a0001c0001t0008g0073a0001c0001t0008g0322 | 3 | HG02109.hp1 HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.254-1049G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952485 | ||||||
| chr13:40952511
|
G | A | 99 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(96): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.254-1075C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952511 | ||||||
| chr13:40952513
|
C | T | 99 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(96): Show | 100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.254-1077G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952513 | ||||||
| chr13:40952751
|
T | C | 1 | a0001c0003t0001g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.254-1315A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952751 | ||||||
| chr13:40952847
|
TTACCCTC others(2): Show |
T | 57 | a0001c0001t0001g0128a0001c0001t0001g0155a0001c0001t0014g0248others(54): Show | 58 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.254-1420_254-1412d others(11): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952847 | ||||||
| chr13:40952978
|
C | CT | 326 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(323): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.254-1543dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952978 | ||||||
| chr13:40952978
|
C | CTT | 8 | a0001c0001t0001g0070a0001c0001t0001g0231a0001c0003t0001g0186others(5): Show | 8 | HG00642.hp1 HG02738.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.254-1544_254-1543d others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952978 | ||||||
| chr13:40953069
|
C | T | 95 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(92): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.254-1633G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953069 | ||||||
| chr13:40953218
|
T | C | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.254-1782A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953218 | ||||||
| chr13:40953228
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.254-1792C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953228 | ||||||
| chr13:40953272
|
G | A | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | NA18999.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.254-1836C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953272 | ||||||
| chr13:40953273
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.254-1837C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953273 | ||||||
| chr13:40953284
|
T | G | 1 | a0001c0001t0001g0116 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.254-1848A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953284 | ||||||
| chr13:40953296
|
A | G | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.254-1860T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953296 | ||||||
| chr13:40953323
|
C | G | 1 | a0001c0001t0001g0116 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.254-1887G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953323 | ||||||
| chr13:40953503
|
T | A | 1 | a0002c0002t0002g0279 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.254-2067A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953503 | ||||||
| chr13:40953522
|
G | T | 1 | a0002c0002t0002g0279 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.254-2086C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953522 | ||||||
| chr13:40953579
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.254-2143C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953579 | ||||||
| chr13:40953665
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.254-2229C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953665 | ||||||
| chr13:40953757
|
T | G | 13 | a0001c0001t0001g0175a0001c0001t0001g0317a0001c0005t0003g0132others(10): Show | 13 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(10): Show |
intron_variant | MODIFIER | c.254-2321A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953757 | ||||||
| chr13:40953882
|
A | T | 1 | a0001c0001t0001g0226 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.254-2446T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953882 | ||||||
| chr13:40953914
|
T | A | 1 | a0002c0002t0002g0194 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.254-2478A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953914 | ||||||
| chr13:40953976
|
CAAAGACT others(23): Show |
C | 1 | a0001c0001t0001g0116 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.254-2570_254-2541d others(32): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953976 | ||||||
| chr13:40954109
|
T | C | 2 | a0001c0005t0003g0341a0001c0005t0003g0348 | 2 | NA18612.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.254-2673A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954109 | ||||||
| chr13:40954252
|
A | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0227 | 2 | HG02165.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.254-2816T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954252 | ||||||
| chr13:40954268
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.254-2832A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954268 | ||||||
| chr13:40954420
|
G | GCTCTCCC others(14): Show |
111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.254-2985_254-2984i others(23): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954420 | ||||||
| chr13:40954421
|
CTCTCCCT others(10): Show |
C | 5 | a0001c0001t0001g0108a0001c0001t0001g0297a0006c0008t0006g0188others(2): Show | 5 | HG02572.hp2 HG02895.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.254-3002_254-2986d others(19): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954421 | ||||||
| chr13:40954490
|
G | A | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.254-3054C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954490 | ||||||
| chr13:40954580
|
T | C | 6 | a0001c0003t0001g0259a0001c0003t0001g0260a0001c0003t0001g0261others(3): Show | 6 | NA18612.hp2 NA18946.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.254-3144A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954580 | ||||||
| chr13:40954620
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254-3184C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954620 | ||||||
| chr13:40954753
|
A | G | 1 | a0001c0005t0003g0344 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.254-3317T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954753 | ||||||
| chr13:40954754
|
A | T | 230 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(227): Show | 235 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.254-3318T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954754 | ||||||
| chr13:40954777
|
T | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0101 | 2 | HG00609.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.254-3341A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954777 | ||||||
| chr13:40954868
|
A | AC | 4 | a0001c0001t0001g0116a0001c0003t0001g0192a0002c0002t0002g0033others(1): Show | 4 | HG02055.hp1 HG04228.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.254-3433dupG | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954868 | ||||||
| chr13:40954890
|
C | T | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.254-3454G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954890 | ||||||
| chr13:40954893
|
C | T | 1 | a0001c0005t0003g0347 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.254-3457G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954893 | ||||||
| chr13:40954904
|
G | C | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(351): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.254-3468C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954904 | ||||||
| chr13:40955007
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.254-3571C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955007 | ||||||
| chr13:40955060
|
G | A | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.254-3624C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955060 | ||||||
| chr13:40955064
|
T | C | 343 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.254-3628A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955064 | ||||||
| chr13:40955065
|
G | A | 74 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.254-3629C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955065 | ||||||
| chr13:40955077
|
A | C | 1 | a0001c0001t0001g0146 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.254-3641T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955077 | ||||||
| chr13:40955082
|
C | T | 6 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0080others(3): Show | 6 | HG00609.hp1 NA18952.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.254-3646G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955082 | ||||||
| chr13:40955093
|
G | A | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.254-3657C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955093 | ||||||
| chr13:40955096
|
T | C | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.254-3660A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955096 | ||||||
| chr13:40955102
|
G | A | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.254-3666C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955102 | ||||||
| chr13:40955136
|
C | T | 83 | a0001c0001t0001g0057a0001c0001t0001g0063a0001c0001t0001g0065others(80): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.253+3700G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955136 | ||||||
| chr13:40955140
|
G | A | 1 | a0002c0002t0002g0279 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.253+3696C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955140 | ||||||
| chr13:40955205
|
C | T | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+3631G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955205 | ||||||
| chr13:40955206
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.253+3630C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955206 | ||||||
| chr13:40955240
|
A | G | 353 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(350): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.253+3596T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955240 | ||||||
| chr13:40955263
|
T | C | 2 | a0001c0003t0001g0141a0001c0003t0001g0239 | 2 | NA18963.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.253+3573A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955263 | ||||||
| chr13:40955276
|
T | TG | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+3559dupC | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955276 | ||||||
| chr13:40955312
|
CGGAA | C | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3520_253+3523d others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955312 | ||||||
| chr13:40955325
|
G | A | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3511C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955325 | ||||||
| chr13:40955329
|
GGTTAGCC others(1): Show |
G | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3499_253+3506d others(10): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955329 | ||||||
| chr13:40955339
|
C | G | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3497G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955339 | ||||||
| chr13:40955341
|
A | C | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3495T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955341 | ||||||
| chr13:40955342
|
C | T | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3494G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955342 | ||||||
| chr13:40955344
|
C | T | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3492G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955344 | ||||||
| chr13:40955346
|
G | C | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3490C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955346 | ||||||
| chr13:40955349
|
A | G | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3487T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955349 | ||||||
| chr13:40955352
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.253+3484G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955352 | ||||||
| chr13:40955353
|
G | A | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.253+3483C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955353 | ||||||
| chr13:40955358
|
A | T | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3478T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955358 | ||||||
| chr13:40955359
|
T | A | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3477A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955359 | ||||||
| chr13:40955361
|
C | T | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3475G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955361 | ||||||
| chr13:40955366
|
G | A | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3470C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955366 | ||||||
| chr13:40955367
|
GGAGA | G | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3465_253+3468d others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955367 | ||||||
| chr13:40955371
|
A | G | 333 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(330): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.253+3465T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955371 | ||||||
| chr13:40955374
|
G | A | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3462C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955374 | ||||||
| chr13:40955377
|
G | A | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3459C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955377 | ||||||
| chr13:40955378
|
GGTCA | G | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3454_253+3457d others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955378 | ||||||
| chr13:40955387
|
C | T | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3449G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955387 | ||||||
| chr13:40955393
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(217): Show | 225 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.253+3443G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955393 | ||||||
| chr13:40955394
|
G | A | 4 | a0002c0002t0002g0033a0002c0002t0002g0035a0002c0002t0002g0048others(1): Show | 4 | HG01071.hp2 HG02293.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.253+3442C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955394 | ||||||
| chr13:40955401
|
T | C | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3435A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955401 | ||||||
| chr13:40955402
|
G | GC | 11 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(8): Show | 11 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.253+3433dupG | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955402 | ||||||
| chr13:40955406
|
A | G | 121 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(118): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.253+3430T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955406 | ||||||
| chr13:40955416
|
G | T | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3420C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955416 | ||||||
| chr13:40955441
|
C | T | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+3395G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955441 | ||||||
| chr13:40955450
|
G | A | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+3386C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955450 | ||||||
| chr13:40955458
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.253+3378G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955458 | ||||||
| chr13:40955464
|
GT | G | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3371delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955464 | ||||||
| chr13:40955470
|
G | T | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3366C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955470 | ||||||
| chr13:40955471
|
GCGCCTCT others(17): Show |
G | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3341_253+3364d others(26): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955471 | ||||||
| chr13:40955499
|
A | G | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3337T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955499 | ||||||
| chr13:40955500
|
A | G | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3336T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955500 | ||||||
| chr13:40955503
|
G | C | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3333C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955503 | ||||||
| chr13:40955505
|
GGAGT | G | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3327_253+3330d others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955505 | ||||||
| chr13:40955513
|
T | C | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3323A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955513 | ||||||
| chr13:40955515
|
T | C | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3321A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955515 | ||||||
| chr13:40955515
|
T | TGCCCGGC others(90): Show |
1 | a0001c0005t0003g0346 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.253+3320_253+3321i others(99): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955515 | ||||||
| chr13:40955519
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0221a0001c0001t0009g0220 | 3 | HG02615.hp1 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.253+3317G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955519 | ||||||
| chr13:40955528
|
G | A | 2 | a0002c0002t0002g0027a0003c0018t0003g0023 | 2 | HG01516.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.253+3308C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955528 | ||||||
| chr13:40955533
|
G | A | 10 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3303C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955533 | ||||||
| chr13:40955539
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0352others(2): Show | 7 | HG01884.hp2 HG01981.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.253+3297C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955539 | ||||||
| chr13:40955541
|
A | G | 11 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(8): Show | 11 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.253+3295T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955541 | ||||||
| chr13:40955543
|
T | G | 11 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(8): Show | 11 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.253+3293A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(93): Show |
2 | a0002c0002t0002g0016a0002c0002t0002g0194 | 2 | HG01981.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.253+3292_253+3293i others(102): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(93): Show |
1 | a0002c0002t0002g0307 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.253+3292_253+3293i others(102): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(93): Show |
2 | a0002c0002t0002g0251a0004c0006t0004g0334 | 2 | HG01192.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.253+3292_253+3293i others(102): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(93): Show |
1 | a0002c0002t0002g0028 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.253+3292_253+3293i others(102): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(92): Show |
107 | a0001c0001t0001g0175a0002c0002t0002g0002a0002c0002t0002g0013others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.253+3292_253+3293i others(101): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(92): Show |
1 | a0001c0003t0001g0093 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.253+3292_253+3293i others(101): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(92): Show |
1 | a0001c0001t0001g0269 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.253+3292_253+3293i others(101): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(91): Show |
2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+3292_253+3293i others(100): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(92): Show |
1 | a0001c0001t0001g0142 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.253+3292_253+3293i others(101): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(91): Show |
1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.253+3292_253+3293i others(100): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(42): Show |
1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.253+3292_253+3293i others(51): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(92): Show |
1 | a0001c0001t0001g0116 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.253+3292_253+3293i others(101): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(91): Show |
3 | a0001c0003t0001g0164a0001c0003t0001g0165a0001c0003t0001g0265 | 3 | HG00099.hp2 HG00733.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.253+3292_253+3293i others(100): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(91): Show |
80 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(77): Show | 80 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.253+3292_253+3293i others(100): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(91): Show |
69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(66): Show | 73 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.253+3292_253+3293i others(100): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955543
|
T | TAGGTGGG others(91): Show |
66 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(63): Show | 67 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.253+3292_253+3293i others(100): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | ||||||
| chr13:40955547
|
T | TGGGGGGG others(94): Show |
1 | a0002c0002t0002g0054 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.253+3288_253+3289i others(103): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955547 | ||||||
| chr13:40955547
|
T | TGGGGGGG others(92): Show |
1 | a0001c0001t0001g0225 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.253+3288_253+3289i others(101): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955547 | ||||||
| chr13:40955547
|
T | TGGGGGGG others(92): Show |
1 | a0001c0001t0001g0177 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.253+3288_253+3289i others(101): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955547 | ||||||
| chr13:40955558
|
G | GCCCCCCG others(93): Show |
1 | a0001c0003t0001g0120 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.253+3277_253+3278i others(102): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955558 | ||||||
| chr13:40955565
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.253+3271T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955565 | ||||||
| chr13:40955586
|
G | A | 74 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.253+3250C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955586 | ||||||
| chr13:40955609
|
T | C | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+3227A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955609 | ||||||
| chr13:40955637
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(50): Show | 57 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.253+3199G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955637 | ||||||
| chr13:40955655
|
G | C | 1 | a0001c0001t0001g0116 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.253+3181C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955655 | ||||||
| chr13:40955660
|
G | A | 1 | a0002c0002t0002g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.253+3176C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955660 | ||||||
| chr13:40955669
|
G | T | 83 | a0001c0001t0001g0057a0001c0001t0001g0063a0001c0001t0001g0065others(80): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.253+3167C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955669 | ||||||
| chr13:40955710
|
T | G | 1 | a0001c0003t0001g0123 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.253+3126A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955710 | ||||||
| chr13:40955728
|
A | G | 3 | a0001c0001t0001g0266a0001c0001t0001g0300a0001c0001t0001g0301 | 3 | HG02040.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.253+3108T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955728 | ||||||
| chr13:40955731
|
T | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | NA18988.hp1 NA19054.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.253+3105A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955731 | ||||||
| chr13:40955745
|
G | A | 1 | a0001c0005t0003g0342 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.253+3091C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955745 | ||||||
| chr13:40955753
|
G | A | 185 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.253+3083C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955753 | ||||||
| chr13:40955770
|
G | T | 3 | a0001c0001t0001g0266a0001c0001t0001g0300a0001c0001t0001g0301 | 3 | HG02040.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.253+3066C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955770 | ||||||
| chr13:40955772
|
C | A | 3 | a0001c0001t0001g0266a0001c0001t0001g0300a0001c0001t0001g0301 | 3 | HG02040.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.253+3064G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955772 | ||||||
| chr13:40955777
|
G | C | 3 | a0001c0001t0001g0266a0001c0001t0001g0300a0001c0001t0001g0301 | 3 | HG02040.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.253+3059C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955777 | ||||||
| chr13:40955787
|
C | T | 3 | a0001c0001t0001g0266a0001c0001t0001g0300a0001c0001t0001g0301 | 3 | HG02040.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.253+3049G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955787 | ||||||
| chr13:40955789
|
C | CCGCCCGG others(35): Show |
1 | a0009c0010t0001g0278 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.253+3046_253+3047i others(44): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955789 | ||||||
| chr13:40955789
|
C | T | 3 | a0001c0001t0001g0266a0001c0001t0001g0300a0001c0001t0001g0301 | 3 | HG02040.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.253+3047G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955789 | ||||||
| chr13:40955799
|
G | C | 4 | a0001c0001t0001g0266a0001c0001t0001g0300a0001c0001t0001g0301others(1): Show | 4 | HG02040.hp2 HG02523.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.253+3037C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955799 | ||||||
| chr13:40955799
|
G | GCCGCCCC others(34): Show |
230 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(227): Show | 235 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.253+2996_253+3036d others(43): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955799 | ||||||
| chr13:40955807
|
G | GTCCGGGA others(34): Show |
3 | a0001c0001t0001g0082a0001c0001t0001g0221a0001c0001t0009g0220 | 3 | HG02615.hp1 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.253+3028_253+3029i others(43): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955807 | ||||||
| chr13:40955839
|
A | ACCCGCCC others(36): Show |
1 | a0001c0001t0001g0116 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.253+2996_253+2997i others(45): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955839 | ||||||
| chr13:40955840
|
C | CCCGCCCC others(33): Show |
1 | a0001c0001t0001g0142 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.253+2995_253+2996i others(42): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955840 | ||||||
| chr13:40955844
|
T | G | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2992A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955844 | ||||||
| chr13:40955845
|
A | T | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2991T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955845 | ||||||
| chr13:40955847
|
T | C | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2989A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955847 | ||||||
| chr13:40955852
|
A | G | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2984T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955852 | ||||||
| chr13:40955854
|
A | T | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2982T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955854 | ||||||
| chr13:40955859
|
A | G | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2977T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955859 | ||||||
| chr13:40955862
|
C | G | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2974G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955862 | ||||||
| chr13:40955867
|
C | T | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2969G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955867 | ||||||
| chr13:40955885
|
A | C | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2951T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955885 | ||||||
| chr13:40955887
|
C | A | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2949G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955887 | ||||||
| chr13:40955889
|
A | G | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+2947T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955889 | ||||||
| chr13:40955892
|
A | T | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2944T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955892 | ||||||
| chr13:40955897
|
G | A | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2939C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955897 | ||||||
| chr13:40955899
|
C | A | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2937G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955899 | ||||||
| chr13:40955901
|
G | A | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2935C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955901 | ||||||
| chr13:40955910
|
G | C | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2926C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955910 | ||||||
| chr13:40955914
|
C | T | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2922G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955914 | ||||||
| chr13:40955920
|
C | T | 229 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(226): Show | 234 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.253+2916G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955920 | ||||||
| chr13:40955929
|
G | A | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2907C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955929 | ||||||
| chr13:40955934
|
G | A | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2902C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955934 | ||||||
| chr13:40955938
|
G | A | 113 | a0001c0001t0008g0073a0001c0001t0008g0322a0002c0002t0002g0002others(110): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.253+2898C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955938 | ||||||
| chr13:40955938
|
G | C | 1 | a0001c0001t0001g0067 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.253+2898C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955938 | ||||||
| chr13:40955938
|
G | GGGAGGTG others(71): Show |
1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.253+2897_253+2898i others(80): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955938 | ||||||
| chr13:40955947
|
G | GT | 73 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.253+2888_253+2889i others(3): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955947 | ||||||
| chr13:40955948
|
C | G | 74 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.253+2888G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955948 | ||||||
| chr13:40955953
|
G | A | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2883C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955953 | ||||||
| chr13:40955959
|
G | GC | 73 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.253+2876dupG | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955959 | ||||||
| chr13:40956010
|
T | C | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+2826A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956010 | ||||||
| chr13:40956028
|
A | G | 8 | a0002c0002t0002g0078a0002c0002t0002g0206a0002c0002t0002g0207others(5): Show | 8 | HG01106.hp1 HG01258.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.253+2808T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956028 | ||||||
| chr13:40956047
|
C | CGGCCACC others(12): Show |
1 | a0001c0001t0001g0116 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.253+2788_253+2789i others(21): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956047 | ||||||
| chr13:40956065
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.253+2771C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956065 | ||||||
| chr13:40956073
|
A | G | 2 | a0001c0001t0001g0297a0001c0005t0003g0341 | 2 | HG06807.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.253+2763T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956073 | ||||||
| chr13:40956075
|
T | C | 2 | a0001c0001t0001g0297a0001c0005t0003g0341 | 2 | HG06807.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.253+2761A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956075 | ||||||
| chr13:40956078
|
A | G | 2 | a0001c0001t0001g0297a0001c0005t0003g0341 | 2 | HG06807.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.253+2758T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956078 | ||||||
| chr13:40956080
|
A | G | 2 | a0001c0001t0001g0297a0001c0005t0003g0341 | 2 | HG06807.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.253+2756T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956080 | ||||||
| chr13:40956108
|
A | G | 2 | a0001c0005t0003g0345a0001c0005t0003g0347 | 2 | NA19001.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.253+2728T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956108 | ||||||
| chr13:40956113
|
G | A | 1 | a0001c0003t0001g0353 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.253+2723C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956113 | ||||||
| chr13:40956153
|
C | T | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+2683G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956153 | ||||||
| chr13:40956300
|
T | C | 1 | a0001c0001t0001g0301 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.253+2536A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956300 | ||||||
| chr13:40956432
|
T | G | 1 | a0001c0001t0001g0313 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.253+2404A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956432 | ||||||
| chr13:40956469
|
A | G | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+2367T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956469 | ||||||
| chr13:40956516
|
C | T | 1 | a0002c0002t0002g0284 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.253+2320G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956516 | ||||||
| chr13:40956571
|
C | CA | 6 | a0002c0002t0002g0018a0002c0002t0002g0021a0002c0002t0002g0046others(3): Show | 6 | HG02055.hp2 HG02300.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.253+2264dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956571 | ||||||
| chr13:40956571
|
CA | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 67 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.253+2264delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956571 | ||||||
| chr13:40956571
|
CAA | C | 171 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0043others(168): Show | 172 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.253+2263_253+2264d others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956571 | ||||||
| chr13:40956571
|
CAAAAAAA | C | 9 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(6): Show | 9 | NA18612.hp1 NA18950.hp1 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.253+2258_253+2264d others(9): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956571 | ||||||
| chr13:40956644
|
C | G | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+2192G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956644 | ||||||
| chr13:40956834
|
C | T | 8 | a0001c0001t0001g0263a0001c0001t0001g0275a0001c0001t0001g0276others(5): Show | 8 | HG01884.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.253+2002G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956834 | ||||||
| chr13:40956987
|
C | T | 1 | a0002c0002t0002g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.253+1849G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956987 | ||||||
| chr13:40957055
|
G | GTCTAAAT others(11): Show |
111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+1780_253+1781i others(20): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957055 | ||||||
| chr13:40957088
|
T | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(143): Show | 150 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.253+1748A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957088 | ||||||
| chr13:40957167
|
C | T | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+1669G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957167 | ||||||
| chr13:40957508
|
TA | T | 8 | a0001c0001t0001g0142a0001c0001t0001g0156a0001c0001t0001g0175others(5): Show | 8 | HG01496.hp2 HG01516.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.253+1327delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957508 | ||||||
| chr13:40957651
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(50): Show | 57 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.253+1185G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957651 | ||||||
| chr13:40957822
|
C | A | 1 | a0002c0002t0002g0021 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.253+1014G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957822 | ||||||
| chr13:40957880
|
T | C | 3 | a0005c0007t0001g0079a0005c0007t0001g0090a0005c0007t0001g0127 | 3 | HG02015.hp2 NA18953.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.253+956A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957880 | ||||||
| chr13:40957990
|
T | C | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+846A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957990 | ||||||
| chr13:40958290
|
T | C | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+546A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40958290 | ||||||
| chr13:40958330
|
A | G | 1 | a0001c0003t0001g0240 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.253+506T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40958330 | ||||||
| chr13:40958381
|
C | T | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(351): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.253+455G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40958381 | ||||||
| chr13:40958431
|
T | A | 1 | a0012c0017t0004g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.253+405A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40958431 | ||||||
| chr13:40958638
|
T | C | 4 | a0001c0003t0001g0003a0001c0003t0001g0066a0001c0003t0001g0129others(1): Show | 5 | HG00140.hp1 HG00741.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.253+198A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40958638 | ||||||
| chr13:40959137
|
T | C | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.73-121A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959137 | ||||||
| chr13:40959262
|
C | G | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.73-246G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959262 | ||||||
| chr13:40959294
|
A | T | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-278T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959294 | ||||||
| chr13:40959322
|
C | A | 1 | a0002c0002t0002g0024 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.73-306G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959322 | ||||||
| chr13:40959359
|
G | A | 9 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0080others(6): Show | 9 | HG00609.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.73-343C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959359 | ||||||
| chr13:40959387
|
T | C | 1 | a0001c0003t0001g0118 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.73-371A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959387 | ||||||
| chr13:40959530
|
G | A | 11 | a0001c0001t0001g0097a0001c0001t0001g0225a0001c0001t0001g0293others(8): Show | 11 | HG00408.hp1 NA18959.hp1 NA18977.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-514C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959530 | ||||||
| chr13:40959531
|
C | A | 11 | a0001c0001t0001g0097a0001c0001t0001g0225a0001c0001t0001g0293others(8): Show | 11 | HG00408.hp1 NA18959.hp1 NA18977.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-515G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959531 | ||||||
| chr13:40959546
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.73-530G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959546 | ||||||
| chr13:40959587
|
T | C | 11 | a0001c0001t0015g0006a0001c0005t0003g0132a0001c0005t0003g0166others(8): Show | 11 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-571A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959587 | ||||||
| chr13:40959752
|
G | GTATAAAC | 74 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.73-743_73-737dupGT others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959752 | ||||||
| chr13:40959845
|
T | C | 83 | a0001c0001t0001g0057a0001c0001t0001g0063a0001c0001t0001g0065others(80): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.73-829A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959845 | ||||||
| chr13:40960460
|
A | G | 1 | a0001c0003t0001g0259 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.73-1444T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40960460 | ||||||
| chr13:40960583
|
G | A | 1 | a0001c0003t0001g0262 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.73-1567C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40960583 | ||||||
| chr13:40960808
|
G | A | 1 | a0001c0003t0001g0261 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.73-1792C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40960808 | ||||||
| chr13:40960810
|
G | C | 9 | a0001c0001t0001g0057a0004c0006t0004g0007a0004c0006t0004g0008others(6): Show | 9 | HG01192.hp2 HG01496.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.73-1794C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40960810 | ||||||
| chr13:40960902
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(226): Show | 234 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.73-1886C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40960902 | ||||||
| chr13:40961065
|
A | G | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-2049T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40961065 | ||||||
| chr13:40961152
|
TTC | T | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.73-2138_73-2137del others(2): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40961152 | ||||||
| chr13:40961273
|
T | A | 60 | a0002c0002t0002g0016a0002c0002t0002g0017a0002c0002t0002g0018others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.73-2257A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40961273 | ||||||
| chr13:40961558
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-2542C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40961558 | ||||||
| chr13:40961618
|
C | T | 3 | a0002c0002t0002g0195a0002c0002t0002g0318a0002c0002t0002g0320 | 3 | NA18991.hp1 NA19079.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.73-2602G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40961618 | ||||||
| chr13:40961802
|
C | G | 1 | a0001c0001t0001g0236 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.73-2786G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40961802 | ||||||
| chr13:40961981
|
C | T | 5 | a0001c0001t0001g0148a0001c0001t0001g0153a0001c0001t0001g0222others(2): Show | 5 | NA18962.hp2 NA18972.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-2965G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40961981 | ||||||
| chr13:40962073
|
G | A | 8 | a0004c0006t0004g0007a0004c0006t0004g0008a0004c0006t0004g0069others(5): Show | 8 | HG01192.hp2 HG01496.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.73-3057C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40962073 | ||||||
| chr13:40962396
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 236 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.73-3380T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40962396 | ||||||
| chr13:40962463
|
A | G | 74 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.73-3447T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40962463 | ||||||
| chr13:40962520
|
T | C | 1 | a0001c0001t0013g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.73-3504A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40962520 | ||||||
| chr13:40962679
|
C | CA | 12 | a0001c0001t0001g0057a0001c0001t0001g0088a0001c0003t0001g0321others(9): Show | 12 | HG01192.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.73-3664dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40962679 | ||||||
| chr13:40962694
|
A | G | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-3678T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40962694 | ||||||
| chr13:40962995
|
C | T | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-3979G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40962995 | ||||||
| chr13:40963178
|
T | C | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-4162A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963178 | ||||||
| chr13:40963312
|
T | C | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-4296A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963312 | ||||||
| chr13:40963421
|
C | T | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-4405G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963421 | ||||||
| chr13:40963549
|
C | A | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(351): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.73-4533G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963549 | ||||||
| chr13:40963556
|
C | G | 2 | a0003c0004t0001g0217a0003c0004t0001g0219 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.73-4540G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963556 | ||||||
| chr13:40963633
|
G | C | 2 | a0003c0004t0001g0217a0003c0004t0001g0219 | 2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.73-4617C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963633 | ||||||
| chr13:40963686
|
A | G | 1 | a0002c0002t0002g0033 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.73-4670T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963686 | ||||||
| chr13:40963715
|
T | C | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.73-4699A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963715 | ||||||
| chr13:40963735
|
T | G | 1 | a0002c0002t0002g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.73-4719A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963735 | ||||||
| chr13:40963820
|
T | C | 9 | a0001c0001t0001g0057a0004c0006t0004g0007a0004c0006t0004g0008others(6): Show | 9 | HG01192.hp2 HG01496.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.73-4804A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963820 | ||||||
| chr13:40963837
|
C | T | 5 | a0003c0004t0001g0214a0003c0004t0001g0215a0003c0004t0001g0216others(2): Show | 5 | HG02109.hp2 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-4821G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963837 | ||||||
| chr13:40963911
|
G | GA | 7 | a0001c0001t0001g0242a0002c0002t0002g0022a0002c0002t0002g0029others(4): Show | 7 | HG00733.hp2 HG00738.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-4896dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963911 | ||||||
| chr13:40964053
|
C | T | 1 | a0002c0002t0002g0171 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.73-5037G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964053 | ||||||
| chr13:40964111
|
C | T | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(351): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.73-5095G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964111 | ||||||
| chr13:40964123
|
A | G | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.73-5107T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964123 | ||||||
| chr13:40964280
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.73-5264A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964280 | ||||||
| chr13:40964298
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.73-5282C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964298 | ||||||
| chr13:40964516
|
C | CT | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(351): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.73-5501dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964516 | ||||||
| chr13:40964598
|
A | G | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.73-5582T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964598 | ||||||
| chr13:40964817
|
G | A | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-5801C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964817 | ||||||
| chr13:40965031
|
A | G | 1 | a0001c0003t0001g0094 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.73-6015T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965031 | ||||||
| chr13:40965290
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.73-6274G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965290 | ||||||
| chr13:40965344
|
G | A | 8 | a0004c0006t0004g0007a0004c0006t0004g0008a0004c0006t0004g0069others(5): Show | 8 | HG01192.hp2 HG01496.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.73-6328C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965344 | ||||||
| chr13:40965592
|
A | G | 11 | a0001c0001t0015g0006a0001c0005t0003g0132a0001c0005t0003g0166others(8): Show | 11 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-6576T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965592 | ||||||
| chr13:40965635
|
A | AT | 13 | a0001c0001t0001g0068a0001c0001t0001g0114a0001c0001t0001g0115others(10): Show | 13 | HG02071.hp1 HG02132.hp1 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.73-6620_73-6619ins others(1): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965635 | ||||||
| chr13:40965637
|
A | G | 92 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(89): Show | 92 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.73-6621T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965637 | ||||||
| chr13:40965681
|
A | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 58 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.73-6665T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965681 | ||||||
| chr13:40965792
|
G | C | 1 | a0002c0002t0002g0037 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.73-6776C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965792 | ||||||
| chr13:40965836
|
C | T | 1 | a0001c0003t0001g0118 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.73-6820G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965836 | ||||||
| chr13:40965901
|
A | G | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-6885T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965901 | ||||||
| chr13:40965981
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0177a0001c0001t0001g0246 | 3 | HG02056.hp1 NA18999.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.73-6965G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965981 | ||||||
| chr13:40966228
|
A | C | 1 | a0001c0001t0001g0148 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.73-7212T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966228 | ||||||
| chr13:40966366
|
A | T | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.73-7350T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966366 | ||||||
| chr13:40966429
|
G | GA | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-7414dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966429 | ||||||
| chr13:40966493
|
G | A | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-7477C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966493 | ||||||
| chr13:40966532
|
C | T | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-7516G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966532 | ||||||
| chr13:40966642
|
C | T | 1 | a0001c0005t0003g0342 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.73-7626G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966642 | ||||||
| chr13:40966733
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.73-7717G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966733 | ||||||
| chr13:40966902
|
T | C | 11 | a0001c0001t0015g0006a0001c0005t0003g0132a0001c0005t0003g0166others(8): Show | 11 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-7886A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966902 | ||||||
| chr13:40966931
|
A | G | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-7915T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966931 | ||||||
| chr13:40967194
|
A | G | 7 | a0001c0001t0001g0061a0001c0001t0001g0071a0001c0001t0001g0072others(4): Show | 7 | HG00609.hp1 HG01934.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-8178T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967194 | ||||||
| chr13:40967215
|
T | C | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-8199A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967215 | ||||||
| chr13:40967244
|
C | T | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(351): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.73-8228G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967244 | ||||||
| chr13:40967383
|
T | A | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-8367A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967383 | ||||||
| chr13:40967522
|
A | G | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-8506T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967522 | ||||||
| chr13:40967524
|
T | C | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-8508A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967524 | ||||||
| chr13:40967695
|
A | T | 1 | a0002c0002t0002g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.73-8679T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967695 | ||||||
| chr13:40967712
|
C | T | 1 | a0012c0017t0004g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.73-8696G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967712 | ||||||
| chr13:40967737
|
G | A | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-8721C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967737 | ||||||
| chr13:40967758
|
AT | A | 11 | a0001c0001t0015g0006a0001c0005t0003g0132a0001c0005t0003g0166others(8): Show | 11 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-8743delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967758 | ||||||
| chr13:40967828
|
C | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | NA18954.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.73-8812G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967828 | ||||||
| chr13:40967845
|
G | A | 5 | a0001c0001t0014g0248a0001c0003t0001g0098a0001c0003t0001g0099others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-8829C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967845 | ||||||
| chr13:40967878
|
C | T | 74 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(71): Show | 75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.73-8862G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967878 | ||||||
| chr13:40968084
|
T | C | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-9068A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968084 | ||||||
| chr13:40968144
|
A | G | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-9128T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968144 | ||||||
| chr13:40968286
|
G | A | 1 | a0001c0003t0001g0118 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.73-9270C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968286 | ||||||
| chr13:40968335
|
G | A | 1 | a0001c0001t0001g0009 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.73-9319C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968335 | ||||||
| chr13:40968496
|
T | C | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-9480A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968496 | ||||||
| chr13:40968533
|
T | G | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | NA18999.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.73-9517A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968533 | ||||||
| chr13:40968545
|
G | A | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-9529C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968545 | ||||||
| chr13:40968572
|
A | G | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-9556T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968572 | ||||||
| chr13:40968654
|
T | C | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.73-9638A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968654 | ||||||
| chr13:40968702
|
T | C | 1 | a0008c0011t0001g0270 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.73-9686A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968702 | ||||||
| chr13:40968721
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-9717_73-9706dup others(12): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968721 | ||||||
| chr13:40968721
|
CT | C | 7 | a0001c0001t0001g0057a0001c0001t0001g0080a0001c0001t0001g0101others(4): Show | 7 | HG00609.hp1 NA18942.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-9706delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968721 | ||||||
| chr13:40968740
|
G | A | 6 | a0001c0001t0001g0148a0001c0001t0001g0153a0001c0001t0001g0222others(3): Show | 6 | NA18939.hp1 NA18962.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-9724C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968740 | ||||||
| chr13:40968911
|
G | A | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.73-9895C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968911 | ||||||
| chr13:40969020
|
A | T | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-10004T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969020 | ||||||
| chr13:40969152
|
G | A | 3 | a0001c0001t0001g0154a0001c0001t0001g0234a0001c0001t0001g0245 | 3 | NA18941.hp1 NA19065.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.73-10136C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969152 | ||||||
| chr13:40969228
|
T | C | 2 | a0001c0001t0001g0234a0001c0001t0001g0245 | 2 | NA18941.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.73-10212A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969228 | ||||||
| chr13:40969358
|
T | C | 111 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.73-10342A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969358 | ||||||
| chr13:40969567
|
T | C | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-10551A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969567 | ||||||
| chr13:40969693
|
A | G | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-10677T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969693 | ||||||
| chr13:40969766
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.73-10750G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969766 | ||||||
| chr13:40969878
|
A | AT | 353 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(350): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.73-10863dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969878 | ||||||
| chr13:40969962
|
A | T | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-10946T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969962 | ||||||
| chr13:40969967
|
T | A | 1 | a0002c0002t0002g0032 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.73-10951A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969967 | ||||||
| chr13:40970197
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0108a0001c0001t0001g0144others(4): Show | 8 | NA18942.hp2 NA18952.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.73-11181C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970197 | ||||||
| chr13:40970248
|
C | G | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-11232G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970248 | ||||||
| chr13:40970298
|
T | C | 1 | a0001c0003t0001g0095 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.73-11282A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970298 | ||||||
| chr13:40970365
|
TA | T | 8 | a0002c0002t0002g0022a0002c0002t0002g0029a0002c0002t0002g0030others(5): Show | 8 | HG00733.hp2 HG00738.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.73-11350delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970365 | ||||||
| chr13:40970424
|
C | T | 88 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(85): Show | 88 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.73-11408G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970424 | ||||||
| chr13:40970430
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0015g0006 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.73-11414T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970430 | ||||||
| chr13:40970516
|
T | C | 2 | a0001c0001t0001g0057a0001c0001t0015g0006 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.72+11467A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970516 | ||||||
| chr13:40970587
|
G | C | 12 | a0001c0001t0001g0057a0001c0001t0015g0006a0001c0005t0003g0132others(9): Show | 12 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+11396C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970587 | ||||||
| chr13:40970616
|
C | T | 3 | a0006c0008t0006g0188a0006c0008t0006g0189a0010c0009t0006g0273 | 3 | HG02572.hp2 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.72+11367G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970616 | ||||||
| chr13:40970698
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0015g0006 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.72+11285C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970698 | ||||||
| chr13:40970929
|
G | A | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.72+11054C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970929 | ||||||
| chr13:40970936
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0015g0006 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.72+11047G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970936 | ||||||
| chr13:40971109
|
TATAG | T | 8 | a0002c0002t0002g0022a0002c0002t0002g0029a0002c0002t0002g0030others(5): Show | 8 | HG00733.hp2 HG00738.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+10870_72+10873d others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971109 | ||||||
| chr13:40971152
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0015g0006 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.72+10831C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971152 | ||||||
| chr13:40971172
|
T | G | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+10811A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971172 | ||||||
| chr13:40971343
|
C | G | 3 | a0006c0008t0006g0188a0006c0008t0006g0189a0010c0009t0006g0273 | 3 | HG02572.hp2 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.72+10640G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971343 | ||||||
| chr13:40971352
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+10631C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971352 | ||||||
| chr13:40971371
|
A | C | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(351): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.72+10612T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971371 | ||||||
| chr13:40971433
|
T | G | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+10550A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971433 | ||||||
| chr13:40971651
|
A | C | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+10332T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971651 | ||||||
| chr13:40971949
|
T | TG | 12 | a0001c0001t0001g0083a0001c0001t0001g0097a0001c0001t0001g0225others(9): Show | 12 | HG00408.hp1 HG03654.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.72+10033_72+10034i others(3): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971949 | ||||||
| chr13:40971950
|
T | G | 89 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(86): Show | 89 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.72+10033A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971950 | ||||||
| chr13:40971950
|
TG | T | 119 | a0001c0001t0001g0208a0001c0001t0001g0293a0002c0002t0002g0002others(116): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.72+10032delC | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971950 | ||||||
| chr13:40971951
|
G | T | 1 | a0001c0001t0005g0122 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.72+10032C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971951 | ||||||
| chr13:40971959
|
G | T | 1 | a0001c0005t0003g0347 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.72+10024C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971959 | ||||||
| chr13:40972135
|
T | C | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+9848A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972135 | ||||||
| chr13:40972252
|
T | C | 4 | a0001c0003t0001g0186a0001c0003t0001g0187a0001c0003t0001g0191others(1): Show | 4 | NA18940.hp2 NA19054.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+9731A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972252 | ||||||
| chr13:40972301
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0223 | 2 | HG01981.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.72+9682G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972301 | ||||||
| chr13:40972320
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.72+9663C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972320 | ||||||
| chr13:40972434
|
T | C | 2 | a0002c0002t0002g0021a0002c0002t0002g0046 | 2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.72+9549A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972434 | ||||||
| chr13:40972502
|
G | A | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0340 | 3 | HG02622.hp1 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.72+9481C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972502 | ||||||
| chr13:40972577
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0229 | 2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.72+9406A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972577 | ||||||
| chr13:40972578
|
A | G | 75 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(72): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.72+9405T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972578 | ||||||
| chr13:40972831
|
T | G | 1 | a0001c0003t0001g0094 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72+9152A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972831 | ||||||
| chr13:40972905
|
T | G | 6 | a0001c0001t0001g0148a0001c0001t0001g0153a0001c0001t0001g0222others(3): Show | 6 | NA18939.hp1 NA18962.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+9078A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972905 | ||||||
| chr13:40973007
|
T | C | 46 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0074others(43): Show | 48 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.72+8976A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973007 | ||||||
| chr13:40973014
|
C | G | 1 | a0001c0003t0001g0118 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.72+8969G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973014 | ||||||
| chr13:40973016
|
G | C | 1 | a0002c0002t0002g0013 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.72+8967C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973016 | ||||||
| chr13:40973147
|
G | C | 2 | a0001c0001t0001g0057a0001c0001t0015g0006 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.72+8836C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973147 | ||||||
| chr13:40973221
|
C | T | 4 | a0001c0001t0005g0089a0001c0001t0005g0122a0001c0001t0005g0162others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+8762G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973221 | ||||||
| chr13:40973520
|
T | C | 2 | a0001c0001t0001g0057a0001c0001t0015g0006 | 2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.72+8463A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973520 | ||||||
| chr13:40973572
|
C | T | 1 | a0001c0003t0001g0066 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.72+8411G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973572 | ||||||
| chr13:40973642
|
C | CT | 10 | a0001c0001t0001g0060a0001c0001t0001g0233a0001c0001t0014g0248others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+8340dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973642 | ||||||
| chr13:40973642
|
CT | C | 12 | a0001c0001t0001g0087a0001c0001t0015g0006a0001c0005t0003g0132others(9): Show | 12 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+8340delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973642 | ||||||
| chr13:40974022
|
G | C | 1 | a0001c0005t0003g0343 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.72+7961C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40974022 | ||||||
| chr13:40974195
|
GT | G | 110 | a0001c0001t0001g0208a0002c0002t0002g0002a0002c0002t0002g0013others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.72+7787delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40974195 | ||||||
| chr13:40974204
|
A | T | 8 | a0001c0001t0001g0263a0001c0001t0001g0275a0001c0001t0001g0276others(5): Show | 8 | HG01884.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+7779T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40974204 | ||||||
| chr13:40974256
|
T | TACTA | 12 | a0001c0001t0001g0057a0001c0001t0015g0006a0001c0005t0003g0132others(9): Show | 12 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+7723_72+7726dup others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40974256 | ||||||
| chr13:40974368
|
T | C | 12 | a0001c0001t0001g0057a0001c0001t0015g0006a0001c0005t0003g0132others(9): Show | 12 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+7615A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40974368 | ||||||
| chr13:40975137
|
C | T | 354 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(351): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.72+6846G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40975137 | ||||||
| chr13:40975187
|
G | A | 1 | a0001c0001t0005g0089 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.72+6796C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40975187 | ||||||
| chr13:40975226
|
T | C | 1 | a0002c0002t0002g0283 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.72+6757A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40975226 | ||||||
| chr13:40975380
|
G | T | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+6603C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40975380 | ||||||
| chr13:40975423
|
G | C | 8 | a0004c0006t0004g0007a0004c0006t0004g0008a0004c0006t0004g0069others(5): Show | 8 | HG01192.hp2 HG01496.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+6560C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40975423 | ||||||
| chr13:40975481
|
C | A | 2 | a0003c0004t0001g0198a0003c0004t0001g0203 | 2 | HG00423.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.72+6502G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40975481 | ||||||
| chr13:40975804
|
GGTAA | G | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+6175_72+6178del others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40975804 | ||||||
| chr13:40976173
|
G | T | 3 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0113 | 3 | NA18993.hp1 NA18994.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.72+5810C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976173 | ||||||
| chr13:40976306
|
A | G | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.72+5677T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976306 | ||||||
| chr13:40976333
|
A | G | 1 | a0001c0001t0001g0354 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.72+5650T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976333 | ||||||
| chr13:40976379
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.72+5604G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976379 | ||||||
| chr13:40976519
|
G | C | 4 | a0001c0001t0005g0089a0001c0001t0005g0122a0001c0001t0005g0162others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+5464C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976519 | ||||||
| chr13:40976778
|
GAT | G | 12 | a0001c0001t0001g0057a0001c0001t0015g0006a0001c0005t0003g0132others(9): Show | 12 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+5203_72+5204del others(2): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976778 | ||||||
| chr13:40976789
|
C | T | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+5194G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976789 | ||||||
| chr13:40976791
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.72+5192G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976791 | ||||||
| chr13:40976792
|
G | A | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+5191C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976792 | ||||||
| chr13:40976832
|
A | G | 2 | a0001c0001t0008g0073a0001c0001t0008g0322 | 2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.72+5151T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976832 | ||||||
| chr13:40976859
|
C | A | 1 | a0001c0003t0001g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.72+5124G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976859 | ||||||
| chr13:40976998
|
CT | C | 12 | a0001c0001t0001g0057a0001c0001t0015g0006a0001c0005t0003g0132others(9): Show | 12 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+4984delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976998 | ||||||
| chr13:40977024
|
C | G | 1 | a0001c0001t0001g0128 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.72+4959G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40977024 | ||||||
| chr13:40977132
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.72+4851C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40977132 | ||||||
| chr13:40977203
|
C | A | 1 | a0001c0001t0001g0271 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.72+4780G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40977203 | ||||||
| chr13:40977219
|
G | A | 4 | a0001c0005t0003g0342a0001c0005t0003g0343a0001c0005t0003g0345others(1): Show | 4 | NA18950.hp1 NA18986.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+4764C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40977219 | ||||||
| chr13:40977468
|
T | C | 76 | a0001c0001t0001g0057a0001c0001t0001g0063a0001c0001t0001g0065others(73): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.72+4515A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40977468 | ||||||
| chr13:40977890
|
A | C | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+4093T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40977890 | ||||||
| chr13:40977893
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.72+4090G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40977893 | ||||||
| chr13:40978070
|
CAT | C | 8 | a0001c0001t0001g0225a0001c0001t0001g0325a0001c0001t0001g0326others(5): Show | 8 | NA18959.hp1 NA18977.hp2 NA18997.hp2 others(5): Show |
intron_variant | MODIFIER | c.72+3911_72+3912del others(2): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978070 | ||||||
| chr13:40978101
|
C | T | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+3882G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978101 | ||||||
| chr13:40978377
|
C | CA | 77 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0061others(74): Show | 77 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.72+3605dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978377 | ||||||
| chr13:40978387
|
A | AC | 12 | a0001c0001t0001g0009a0001c0001t0001g0067a0001c0001t0001g0097others(9): Show | 12 | HG00408.hp1 NA18942.hp1 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+3595dupG | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978387 | ||||||
| chr13:40978401
|
A | G | 4 | a0001c0001t0005g0089a0001c0001t0005g0122a0001c0001t0005g0162others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+3582T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978401 | ||||||
| chr13:40978404
|
A | C | 8 | a0001c0001t0001g0263a0001c0001t0001g0275a0001c0001t0001g0276others(5): Show | 8 | HG01884.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+3579T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978404 | ||||||
| chr13:40978560
|
G | C | 1 | a0001c0005t0003g0344 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.72+3423C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978560 | ||||||
| chr13:40978593
|
G | A | 113 | a0001c0001t0001g0183a0001c0001t0001g0208a0001c0001t0001g0269others(110): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.72+3390C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978593 | ||||||
| chr13:40978602
|
G | A | 297 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.72+3381C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978602 | ||||||
| chr13:40978652
|
C | T | 7 | a0001c0001t0001g0057a0001c0001t0014g0248a0001c0001t0015g0006others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+3331G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978652 | ||||||
| chr13:40978781
|
T | G | 4 | a0001c0001t0005g0089a0001c0001t0005g0122a0001c0001t0005g0162others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+3202A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978781 | ||||||
| chr13:40978903
|
G | C | 89 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(86): Show | 89 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.72+3080C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978903 | ||||||
| chr13:40979011
|
ATAGT | A | 70 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(67): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.72+2968_72+2971del others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979011 | ||||||
| chr13:40979012
|
T | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0080others(3): Show | 6 | HG00609.hp1 NA18952.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+2971A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979012 | ||||||
| chr13:40979088
|
A | C | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.72+2895T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979088 | ||||||
| chr13:40979165
|
TTC | T | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+2816_72+2817del others(2): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979165 | ||||||
| chr13:40979218
|
T | TAC | 22 | a0001c0001t0001g0057a0001c0001t0001g0109a0001c0001t0001g0110others(19): Show | 22 | HG00673.hp1 HG02135.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.72+2763_72+2764dup others(2): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979218 | ||||||
| chr13:40979218
|
T | TACAC | 220 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(217): Show | 225 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.72+2761_72+2764dup others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979218 | ||||||
| chr13:40979218
|
T | TACACAC | 110 | a0001c0001t0001g0208a0002c0002t0002g0002a0002c0002t0002g0013others(107): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.72+2759_72+2764dup others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979218 | ||||||
| chr13:40979234
|
T | C | 12 | a0001c0001t0001g0057a0001c0001t0001g0109a0001c0001t0001g0110others(9): Show | 12 | HG00673.hp1 HG02135.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.72+2749A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979234 | ||||||
| chr13:40979271
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.72+2712A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979271 | ||||||
| chr13:40979424
|
A | G | 1 | a0002c0002t0002g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.72+2559T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979424 | ||||||
| chr13:40979435
|
C | T | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+2548G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979435 | ||||||
| chr13:40979678
|
G | C | 1 | a0001c0001t0001g0009 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.72+2305C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979678 | ||||||
| chr13:40979768
|
G | A | 38 | a0001c0001t0001g0009a0001c0001t0001g0053a0001c0001t0001g0067others(35): Show | 38 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.72+2215C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979768 | ||||||
| chr13:40980145
|
C | T | 1 | a0002c0002t0002g0319 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.72+1838G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40980145 | ||||||
| chr13:40980495
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0002g0172 | 2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.72+1488T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40980495 | ||||||
| chr13:40980557
|
T | C | 111 | a0001c0001t0001g0208a0002c0002t0002g0002a0002c0002t0002g0013others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.72+1426A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40980557 | ||||||
| chr13:40980839
|
A | G | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.72+1144T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40980839 | ||||||
| chr13:40981110
|
TTA | T | 108 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(105): Show | 108 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+871_72+872delTA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40981110 | ||||||
| chr13:40981216
|
C | A | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.72+767G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40981216 | ||||||
| chr13:40981265
|
T | C | 6 | a0001c0001t0014g0248a0001c0001t0015g0006a0001c0003t0001g0098others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+718A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40981265 | ||||||
| chr13:40981588
|
G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.72+395C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40981588 | ||||||
| chr13:40981609
|
TGAA | T | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+371_72+373delTT others(1): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40981609 | ||||||
| chr13:40981665
|
A | C | 1 | a0002c0002t0002g0206 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.72+318T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40981665 | ||||||
| chr13:40981862
|
T | C | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+121A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40981862 | ||||||
| chr13:40982457
|
C | G | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-228-175G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40982457 | ||||||
| chr13:40982550
|
TA | T | 88 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0068others(85): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.-228-269delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40982550 | ||||||
| chr13:40982681
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-228-399T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40982681 | ||||||
| chr13:40982763
|
G | C | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-228-481C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40982763 | ||||||
| chr13:40982921
|
T | C | 353 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(350): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-228-639A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40982921 | ||||||
| chr13:40982954
|
CT | C | 14 | a0002c0002t0002g0016a0002c0002t0002g0017a0002c0002t0002g0078others(11): Show | 14 | HG00099.hp1 HG00140.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.-228-673delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40982954 | ||||||
| chr13:40982982
|
T | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0074others(42): Show | 47 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.-228-700A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40982982 | ||||||
| chr13:40983088
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-228-806C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983088 | ||||||
| chr13:40983187
|
C | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0257a0001c0001t0001g0287 | 3 | HG00639.hp1 HG03239.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-228-905G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983187 | ||||||
| chr13:40983640
|
T | G | 4 | a0001c0003t0001g0260a0001c0003t0001g0261a0001c0003t0001g0292others(1): Show | 4 | NA18612.hp2 NA18946.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-228-1358A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983640 | ||||||
| chr13:40983689
|
G | GA | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-1408dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983689 | ||||||
| chr13:40983817
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0121 | 2 | HG01109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-228-1535T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983817 | ||||||
| chr13:40983841
|
G | A | 353 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(350): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-228-1559C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983841 | ||||||
| chr13:40983861
|
TTC | T | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-1581_-228-158 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983861 | ||||||
| chr13:40983914
|
A | G | 3 | a0001c0003t0001g0003a0001c0003t0001g0066a0001c0003t0001g0129 | 4 | HG00741.hp2 HG01346.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-228-1632T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983914 | ||||||
| chr13:40983974
|
A | G | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-228-1692T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983974 | ||||||
| chr13:40984095
|
T | A | 8 | a0004c0006t0004g0007a0004c0006t0004g0008a0004c0006t0004g0069others(5): Show | 8 | HG01192.hp2 HG01496.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-228-1813A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984095 | ||||||
| chr13:40984163
|
C | A | 1 | a0001c0003t0001g0353 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-228-1881G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984163 | ||||||
| chr13:40984223
|
C | T | 4 | a0002c0002t0002g0033a0002c0002t0002g0035a0002c0002t0002g0048others(1): Show | 4 | HG01071.hp2 HG02293.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-228-1941G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984223 | ||||||
| chr13:40984226
|
C | T | 3 | a0002c0002t0002g0213a0002c0002t0002g0306a0002c0002t0002g0307 | 3 | HG01934.hp1 HG02040.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-228-1944G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984226 | ||||||
| chr13:40984278
|
A | C | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-1996T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984278 | ||||||
| chr13:40984360
|
T | C | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-2078A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984360 | ||||||
| chr13:40984492
|
C | T | 2 | a0002c0002t0002g0281a0003c0004t0001g0199 | 2 | NA18957.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-228-2210G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984492 | ||||||
| chr13:40984513
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-228-2231T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984513 | ||||||
| chr13:40984637
|
A | G | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-228-2355T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984637 | ||||||
| chr13:40984939
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-228-2657A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984939 | ||||||
| chr13:40984952
|
C | T | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-228-2670G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984952 | ||||||
| chr13:40985840
|
T | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0350 | 2 | HG00544.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-228-3558A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40985840 | ||||||
| chr13:40986018
|
TA | T | 353 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(350): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-228-3737delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986018 | ||||||
| chr13:40986103
|
C | T | 4 | a0001c0001t0005g0089a0001c0001t0005g0122a0001c0001t0005g0162others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-228-3821G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986103 | ||||||
| chr13:40986176
|
A | G | 108 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(105): Show | 108 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-228-3894T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986176 | ||||||
| chr13:40986294
|
T | A | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-4012A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986294 | ||||||
| chr13:40986466
|
C | T | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-4184G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986466 | ||||||
| chr13:40986567
|
T | C | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-4285A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986567 | ||||||
| chr13:40986642
|
C | T | 1 | a0001c0001t0011g0324 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-228-4360G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986642 | ||||||
| chr13:40986653
|
C | CTCTG | 353 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(350): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-228-4375_-228-437 others(8): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986653 | ||||||
| chr13:40986718
|
T | C | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-4436A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986718 | ||||||
| chr13:40986726
|
A | G | 6 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0080others(3): Show | 6 | HG00609.hp1 NA18952.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.-228-4444T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986726 | ||||||
| chr13:40986766
|
CA | C | 7 | a0001c0001t0001g0057a0001c0001t0014g0248a0001c0001t0015g0006others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-228-4485delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986766 | ||||||
| chr13:40986786
|
T | A | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-228-4504A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986786 | ||||||
| chr13:40986937
|
C | CTCT | 9 | a0001c0001t0001g0057a0001c0001t0014g0248a0001c0001t0015g0006others(6): Show | 9 | HG01168.hp1 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-228-4656_-228-465 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986937 | ||||||
| chr13:40986937
|
C | CTCTT | 112 | a0001c0001t0001g0208a0001c0001t0001g0242a0002c0002t0002g0002others(109): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-228-4656_-228-465 others(8): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986937 | ||||||
| chr13:40986937
|
C | CTCTTT | 96 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(93): Show | 96 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-228-4656_-228-465 others(9): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986937 | ||||||
| chr13:40986937
|
C | CTCTTTT | 62 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(59): Show | 66 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.-228-4656_-228-465 others(10): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986937 | ||||||
| chr13:40986937
|
C | CTTT | 69 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(66): Show | 70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-228-4658_-228-465 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986937 | ||||||
| chr13:40987004
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-228-4722G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987004 | ||||||
| chr13:40987081
|
G | A | 1 | a0002c0002t0002g0034 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-228-4799C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987081 | ||||||
| chr13:40987093
|
G | T | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-4811C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987093 | ||||||
| chr13:40987096
|
C | T | 2 | a0002c0002t0002g0035a0004c0006t0004g0008 | 2 | HG02723.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-228-4814G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987096 | ||||||
| chr13:40987102
|
A | T | 1 | a0002c0002t0002g0035 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-228-4820T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987102 | ||||||
| chr13:40987299
|
T | C | 1 | a0004c0006t0004g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-228-5017A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987299 | ||||||
| chr13:40987402
|
G | A | 4 | a0001c0005t0003g0342a0001c0005t0003g0343a0001c0005t0003g0345others(1): Show | 4 | NA18950.hp1 NA18986.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.-228-5120C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987402 | ||||||
| chr13:40987428
|
A | C | 19 | a0001c0001t0001g0125a0001c0001t0001g0147a0001c0001t0001g0167others(16): Show | 19 | HG00423.hp1 HG01192.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.-228-5146T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987428 | ||||||
| chr13:40987428
|
A | G | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-228-5146T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987428 | ||||||
| chr13:40987537
|
G | T | 6 | a0001c0001t0014g0248a0001c0001t0015g0006a0001c0003t0001g0098others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-228-5255C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987537 | ||||||
| chr13:40987584
|
C | CA | 150 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(147): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.-228-5303dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987584 | ||||||
| chr13:40987584
|
C | CAA | 25 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(22): Show | 25 | HG00408.hp2 HG00544.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-228-5304_-228-530 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987584 | ||||||
| chr13:40987584
|
CA | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 51 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.-228-5303delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987584 | ||||||
| chr13:40987600
|
A | AAG | 7 | a0002c0002t0002g0021a0002c0002t0002g0042a0002c0002t0002g0046others(4): Show | 7 | HG00673.hp2 HG02717.hp2 NA18998.hp2 others(4): Show |
intron_variant | MODIFIER | c.-228-5319_-228-531 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987600 | ||||||
| chr13:40987600
|
A | AG | 101 | a0001c0001t0001g0208a0002c0002t0002g0002a0002c0002t0002g0013others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-228-5319_-228-531 others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987600 | ||||||
| chr13:40987600
|
A | G | 3 | a0002c0002t0002g0283a0003c0004t0001g0215a0003c0016t0001g0052 | 3 | HG02965.hp1 NA18953.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-228-5318T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987600 | ||||||
| chr13:40987757
|
T | C | 1 | a0001c0001t0001g0326 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-228-5475A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987757 | ||||||
| chr13:40987827
|
TAA | T | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-5547_-228-554 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987827 | ||||||
| chr13:40987832
|
G | A | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-5550C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987832 | ||||||
| chr13:40987833
|
A | G | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-5551T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987833 | ||||||
| chr13:40987922
|
G | A | 1 | a0004c0006t0004g0334 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-228-5640C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987922 | ||||||
| chr13:40988121
|
A | G | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-5839T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988121 | ||||||
| chr13:40988191
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-228-5909G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988191 | ||||||
| chr13:40988297
|
G | C | 4 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0313others(1): Show | 4 | NA18954.hp2 NA18986.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-228-6015C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988297 | ||||||
| chr13:40988393
|
C | T | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-228-6111G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988393 | ||||||
| chr13:40988650
|
A | G | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-6368T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988650 | ||||||
| chr13:40988724
|
C | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-228-6442G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988724 | ||||||
| chr13:40988846
|
G | C | 1 | a0002c0002t0002g0059 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-228-6564C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988846 | ||||||
| chr13:40988883
|
C | T | 111 | a0001c0001t0001g0208a0002c0002t0002g0002a0002c0002t0002g0013others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-6601G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988883 | ||||||
| chr13:40988890
|
T | C | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-228-6608A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988890 | ||||||
| chr13:40989015
|
C | T | 108 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(105): Show | 108 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-228-6733G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989015 | ||||||
| chr13:40989150
|
C | T | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-6868G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989150 | ||||||
| chr13:40989237
|
A | G | 1 | a0001c0001t0013g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-228-6955T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989237 | ||||||
| chr13:40989248
|
G | A | 1 | a0002c0002t0002g0028 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-228-6966C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989248 | ||||||
| chr13:40989284
|
A | G | 1 | a0002c0002t0002g0014 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-228-7002T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989284 | ||||||
| chr13:40989452
|
T | C | 111 | a0001c0001t0001g0208a0002c0002t0002g0002a0002c0002t0002g0013others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-7170A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989452 | ||||||
| chr13:40989626
|
CT | C | 111 | a0001c0001t0001g0208a0002c0002t0002g0002a0002c0002t0002g0013others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-7345delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989626 | ||||||
| chr13:40989634
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-228-7352G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989634 | ||||||
| chr13:40989766
|
T | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-228-7484A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989766 | ||||||
| chr13:40989767
|
G | C | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-228-7485C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989767 | ||||||
| chr13:40989994
|
A | C | 1 | a0001c0003t0001g0321 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-228-7712T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989994 | ||||||
| chr13:40990003
|
C | T | 111 | a0001c0001t0001g0208a0002c0002t0002g0002a0002c0002t0002g0013others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-7721G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990003 | ||||||
| chr13:40990017
|
A | AAT | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-7737_-228-773 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990017 | ||||||
| chr13:40990039
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-228-7757T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990039 | ||||||
| chr13:40990151
|
A | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-228-7869T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990151 | ||||||
| chr13:40990286
|
G | A | 70 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(67): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.-228-8004C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990286 | ||||||
| chr13:40990387
|
A | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0155 | 2 | HG02698.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-228-8105T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990387 | ||||||
| chr13:40990448
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0081 | 2 | NA18985.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-228-8166A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990448 | ||||||
| chr13:40990545
|
A | G | 1 | a0004c0006t0004g0069 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-228-8263T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990545 | ||||||
| chr13:40990837
|
C | T | 111 | a0001c0001t0001g0208a0002c0002t0002g0002a0002c0002t0002g0013others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-8555G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990837 | ||||||
| chr13:40990850
|
C | CA | 141 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(138): Show | 142 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-228-8569dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990850 | ||||||
| chr13:40990850
|
C | CAA | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-228-8570_-228-856 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990850 | ||||||
| chr13:40990850
|
C | CAAA | 6 | a0001c0001t0001g0269a0001c0003t0001g0249a0001c0003t0001g0262others(3): Show | 6 | HG02135.hp2 HG02293.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-228-8571_-228-856 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990850 | ||||||
| chr13:40990850
|
CA | C | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-8569delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990850 | ||||||
| chr13:40990885
|
T | G | 1 | a0001c0001t0001g0074 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-228-8603A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990885 | ||||||
| chr13:40990904
|
C | T | 1 | a0001c0001t0001g0326 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-228-8622G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990904 | ||||||
| chr13:40991204
|
T | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0121 | 2 | HG01109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-228-8922A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991204 | ||||||
| chr13:40991204
|
T | C | 111 | a0001c0001t0001g0208a0002c0002t0002g0002a0002c0002t0002g0013others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-8922A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991204 | ||||||
| chr13:40991252
|
C | G | 1 | a0002c0002t0002g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-228-8970G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991252 | ||||||
| chr13:40991567
|
A | G | 1 | a0001c0001t0001g0222 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-228-9285T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991567 | ||||||
| chr13:40991577
|
C | T | 8 | a0001c0001t0001g0263a0001c0001t0001g0275a0001c0001t0001g0276others(5): Show | 8 | HG01884.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-228-9295G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991577 | ||||||
| chr13:40991582
|
C | T | 93 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(90): Show | 93 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-228-9300G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991582 | ||||||
| chr13:40991678
|
T | C | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-9396A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991678 | ||||||
| chr13:40991967
|
G | T | 1 | a0001c0001t0001g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-228-9685C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991967 | ||||||
| chr13:40992013
|
GA | G | 4 | a0001c0003t0001g0092a0001c0003t0001g0093a0001c0003t0001g0130others(1): Show | 4 | HG00597.hp2 NA18948.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.-228-9732delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992013 | ||||||
| chr13:40992021
|
T | C | 5 | a0001c0001t0014g0248a0001c0003t0001g0098a0001c0003t0001g0099others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-228-9739A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992021 | ||||||
| chr13:40992380
|
G | C | 1 | a0002c0002t0002g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-228-10098C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992380 | ||||||
| chr13:40992401
|
T | C | 1 | a0002c0002t0002g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-228-10119A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992401 | ||||||
| chr13:40992431
|
T | C | 1 | a0001c0003t0001g0249 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-228-10149A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992431 | ||||||
| chr13:40992629
|
T | TA | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-10348_-228-10 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992629 | ||||||
| chr13:40992641
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-228-10359G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992641 | ||||||
| chr13:40992645
|
G | A | 113 | a0001c0001t0001g0072a0001c0001t0001g0208a0001c0001t0001g0238others(110): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-228-10363C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992645 | ||||||
| chr13:40993112
|
C | G | 107 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(104): Show | 107 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-228-10830G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40993112 | ||||||
| chr13:40993394
|
G | T | 15 | a0001c0001t0001g0057a0001c0001t0014g0248a0001c0001t0015g0006others(12): Show | 15 | HG01192.hp2 HG01496.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-228-11112C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40993394 | ||||||
| chr13:40993428
|
C | A | 112 | a0001c0001t0001g0072a0001c0001t0001g0208a0002c0002t0002g0002others(109): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-228-11146G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40993428 | ||||||
| chr13:40993473
|
C | T | 1 | a0001c0005t0003g0343 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-228-11191G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40993473 | ||||||
| chr13:40993517
|
G | A | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-11235C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40993517 | ||||||
| chr13:40993521
|
C | T | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-11239G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40993521 | ||||||
| chr13:40993899
|
A | AT | 88 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(85): Show | 88 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-228-11618dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40993899 | ||||||
| chr13:40994009
|
T | TA | 9 | a0002c0002t0002g0022a0002c0002t0002g0029a0002c0002t0002g0030others(6): Show | 9 | HG00733.hp2 HG00738.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.-228-11728dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40994009 | ||||||
| chr13:40994009
|
T | TG | 11 | a0001c0001t0001g0112a0001c0005t0003g0132a0001c0005t0003g0166others(8): Show | 11 | HG02027.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.-228-11728_-228-11 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40994009 | ||||||
| chr13:40994010
|
A | G | 71 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(68): Show | 72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-11728T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40994010 | ||||||
| chr13:40994179
|
T | C | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-11897A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40994179 | ||||||
| chr13:40994505
|
T | G | 107 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(104): Show | 107 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-228-12223A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40994505 | ||||||
| chr13:40994656
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-228-12374A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40994656 | ||||||
| chr13:40994736
|
G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-228-12454C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40994736 | ||||||
| chr13:40995072
|
G | A | 2 | a0002c0002t0002g0019a0002c0002t0002g0020 | 2 | HG01169.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-228-12790C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40995072 | ||||||
| chr13:40995662
|
T | TA | 9 | a0001c0001t0001g0326a0004c0006t0004g0007a0004c0006t0004g0008others(6): Show | 9 | HG01192.hp2 HG01496.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-228-13381dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40995662 | ||||||
| chr13:40995662
|
TA | T | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-228-13381delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40995662 | ||||||
| chr13:40995998
|
T | C | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-13716A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40995998 | ||||||
| chr13:40996121
|
T | C | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-228-13839A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40996121 | ||||||
| chr13:40996195
|
T | TAGGAATT others(333): Show |
1 | a0001c0001t0001g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-228-13914_-228-13 others(346): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40996195 | ||||||
| chr13:40996372
|
G | A | 1 | a0001c0003t0001g0178 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-228-14090C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40996372 | ||||||
| chr13:40996442
|
A | G | 2 | a0001c0001t0001g0175a0001c0001t0001g0317 | 2 | NA18951.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-228-14160T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40996442 | ||||||
| chr13:40996621
|
G | A | 1 | a0001c0005t0003g0346 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-228-14339C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40996621 | ||||||
| chr13:40996668
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-228-14386C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40996668 | ||||||
| chr13:40996780
|
CT | C | 21 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(18): Show | 21 | HG00408.hp2 HG00544.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.-228-14499delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40996780 | ||||||
| chr13:40997089
|
C | A | 1 | a0001c0001t0001g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-228-14807G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40997089 | ||||||
| chr13:40997257
|
T | G | 1 | a0004c0006t0004g0332 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-228-14975A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40997257 | ||||||
| chr13:40997407
|
G | A | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-15125C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40997407 | ||||||
| chr13:40997789
|
T | G | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-15507A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40997789 | ||||||
| chr13:40997824
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-228-15542A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40997824 | ||||||
| chr13:40997891
|
A | G | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-15609T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40997891 | ||||||
| chr13:40997997
|
A | T | 111 | a0001c0001t0001g0208a0002c0002t0002g0002a0002c0002t0002g0013others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-15715T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40997997 | ||||||
| chr13:40998038
|
C | T | 353 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(350): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-228-15756G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40998038 | ||||||
| chr13:40998053
|
G | A | 2 | a0001c0001t0001g0146a0005c0007t0001g0127 | 2 | HG02015.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-228-15771C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40998053 | ||||||
| chr13:40998197
|
T | C | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-15915A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40998197 | ||||||
| chr13:40998731
|
C | A | 1 | a0002c0002t0002g0319 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-228-16449G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40998731 | ||||||
| chr13:40998967
|
C | T | 1 | a0002c0002t0002g0279 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-228-16685G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40998967 | ||||||
| chr13:40999064
|
C | T | 111 | a0001c0001t0001g0208a0002c0002t0002g0002a0002c0002t0002g0013others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-16782G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999064 | ||||||
| chr13:40999341
|
G | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(105): Show | 108 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-228-17059C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999341 | ||||||
| chr13:40999368
|
TA | T | 353 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(350): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-228-17087delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999368 | ||||||
| chr13:40999411
|
G | A | 7 | a0001c0001t0001g0057a0001c0001t0014g0248a0001c0001t0015g0006others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-228-17129C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999411 | ||||||
| chr13:40999513
|
T | A | 4 | a0002c0002t0002g0204a0002c0002t0002g0282a0002c0002t0002g0285others(1): Show | 4 | NA18970.hp2 NA18978.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-228-17231A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999513 | ||||||
| chr13:40999520
|
T | G | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-17238A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999520 | ||||||
| chr13:40999565
|
A | C | 15 | a0001c0001t0001g0057a0001c0001t0014g0248a0001c0001t0015g0006others(12): Show | 15 | HG01192.hp2 HG01496.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-228-17283T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999565 | ||||||
| chr13:40999600
|
T | G | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-17318A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999600 | ||||||
| chr13:40999672
|
A | C | 353 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(350): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-228-17390T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999672 | ||||||
| chr13:40999709
|
C | T | 2 | a0002c0002t0002g0039a0002c0002t0002g0040 | 2 | HG00735.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.-228-17427G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999709 | ||||||
| chr13:41000001
|
T | C | 1 | a0002c0002t0002g0319 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-228-17719A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000001 | ||||||
| chr13:41000160
|
T | C | 7 | a0001c0001t0001g0057a0001c0001t0014g0248a0001c0001t0015g0006others(4): Show | 7 | HG02145.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-228-17878A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000160 | ||||||
| chr13:41000237
|
CT | C | 40 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0061others(37): Show | 40 | HG00544.hp1 HG00621.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.-228-17956delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | ||||||
| chr13:41000237
|
CTT | C | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0057others(96): Show | 100 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.-228-17957_-228-17 others(8): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | ||||||
| chr13:41000237
|
CTTT | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 99 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.-228-17958_-228-17 others(9): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | ||||||
| chr13:41000237
|
CTTTT | C | 10 | a0002c0002t0002g0016a0002c0002t0002g0017a0002c0002t0002g0048others(7): Show | 10 | HG01106.hp1 HG01109.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-17959_-228-17 others(10): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | ||||||
| chr13:41000237
|
CTTTTTT | C | 10 | a0001c0001t0001g0068a0001c0001t0001g0115a0001c0001t0001g0150others(7): Show | 10 | HG02132.hp1 HG02165.hp1 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.-228-17961_-228-17 others(12): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | ||||||
| chr13:41000237
|
CTTTTTTT others(1): Show |
C | 68 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(65): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.-228-17963_-228-17 others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | ||||||
| chr13:41000237
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0275a0001c0001t0001g0276 | 2 | HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-228-17966_-228-17 others(17): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | ||||||
| chr13:41000237
|
CTTTTTTT others(7): Show |
C | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-17969_-228-17 others(20): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | ||||||
| chr13:41000382
|
G | A | 1 | a0002c0002t0002g0025 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-228-18100C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000382 | ||||||
| chr13:41000464
|
C | T | 89 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(86): Show | 89 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.-228-18182G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000464 | ||||||
| chr13:41000469
|
G | GC | 353 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(350): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-228-18188dupG | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000469 | ||||||
| chr13:41000500
|
C | T | 1 | a0001c0003t0001g0321 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-228-18218G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000500 | ||||||
| chr13:41000505
|
G | T | 1 | a0001c0003t0001g0186 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18223C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000505 | ||||||
| chr13:41000506
|
C | A | 1 | a0001c0003t0001g0186 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18224G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000506 | ||||||
| chr13:41000509
|
C | T | 1 | a0001c0003t0001g0186 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18227G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000509 | ||||||
| chr13:41000510
|
C | A | 1 | a0001c0003t0001g0186 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18228G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000510 | ||||||
| chr13:41000511
|
A | G | 1 | a0001c0003t0001g0186 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18229T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000511 | ||||||
| chr13:41000512
|
C | T | 1 | a0001c0003t0001g0186 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18230G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000512 | ||||||
| chr13:41000513
|
A | G | 1 | a0001c0003t0001g0186 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18231T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000513 | ||||||
| chr13:41000514
|
C | A | 1 | a0001c0003t0001g0186 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18232G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000514 | ||||||
| chr13:41000517
|
G | T | 1 | a0001c0003t0001g0186 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18235C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000517 | ||||||
| chr13:41000518
|
G | T | 1 | a0001c0003t0001g0186 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18236C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000518 | ||||||
| chr13:41000554
|
T | G | 1 | a0002c0002t0002g0014 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-228-18272A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000554 | ||||||
| chr13:41000566
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-228-18284A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000566 | ||||||
| chr13:41000615
|
G | A | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-18333C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000615 | ||||||
| chr13:41000627
|
G | C | 1 | a0001c0003t0001g0118 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-228-18345C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000627 | ||||||
| chr13:41000686
|
G | A | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-228-18404C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000686 | ||||||
| chr13:41000861
|
A | AAG | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-229+18365_-229+18 others(8): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000861 | ||||||
| chr13:41000875
|
A | C | 1 | a0001c0001t0001g0229 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-229+18353T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000875 | ||||||
| chr13:41000978
|
C | CT | 106 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(103): Show | 106 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-229+18249dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000978 | ||||||
| chr13:41000993
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-229+18235G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000993 | ||||||
| chr13:41001139
|
T | G | 83 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(80): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.-229+18089A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001139 | ||||||
| chr13:41001255
|
G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-229+17973C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001255 | ||||||
| chr13:41001287
|
T | A | 94 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(91): Show | 94 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-229+17941A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001287 | ||||||
| chr13:41001409
|
A | T | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-229+17819T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001409 | ||||||
| chr13:41001416
|
C | T | 1 | a0001c0003t0001g0120 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-229+17812G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001416 | ||||||
| chr13:41001431
|
T | A | 1 | a0001c0001t0001g0291 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-229+17797A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001431 | ||||||
| chr13:41001579
|
A | C | 1 | a0001c0003t0001g0066 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-229+17649T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001579 | ||||||
| chr13:41001584
|
G | A | 6 | a0002c0002t0002g0024a0002c0002t0002g0026a0002c0002t0002g0028others(3): Show | 6 | NA18947.hp1 NA18948.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.-229+17644C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001584 | ||||||
| chr13:41001588
|
G | C | 1 | a0002c0002t0002g0171 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-229+17640C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001588 | ||||||
| chr13:41001651
|
T | C | 1 | a0002c0002t0002g0356 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-229+17577A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001651 | ||||||
| chr13:41001668
|
T | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-229+17560A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001668 | ||||||
| chr13:41001866
|
C | T | 353 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(350): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-229+17362G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001866 | ||||||
| chr13:41002071
|
C | T | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-229+17157G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002071 | ||||||
| chr13:41002111
|
G | C | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-229+17117C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002111 | ||||||
| chr13:41002145
|
G | A | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-229+17083C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002145 | ||||||
| chr13:41002186
|
C | G | 72 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(69): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-229+17042G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002186 | ||||||
| chr13:41002246
|
G | C | 1 | a0001c0001t0001g0277 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-229+16982C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002246 | ||||||
| chr13:41002262
|
C | T | 3 | a0002c0002t0002g0213a0002c0002t0002g0306a0002c0002t0002g0307 | 3 | HG01934.hp1 HG02040.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-229+16966G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002262 | ||||||
| chr13:41002285
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0121 | 2 | HG01109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-229+16943C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002285 | ||||||
| chr13:41002327
|
T | A | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-229+16901A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002327 | ||||||
| chr13:41002333
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-229+16895T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002333 | ||||||
| chr13:41002410
|
G | A | 353 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(350): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-229+16818C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002410 | ||||||
| chr13:41002441
|
G | C | 108 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(105): Show | 108 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-229+16787C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002441 | ||||||
| chr13:41002555
|
CT | C | 355 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(352): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-229+16672delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002555 | ||||||
| chr13:41002584
|
TA | T | 15 | a0001c0001t0001g0103a0001c0001t0001g0144a0001c0001t0001g0179others(12): Show | 15 | HG01168.hp1 HG01192.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-229+16643delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002584 | ||||||
| chr13:41002759
|
G | A | 88 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(85): Show | 88 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-229+16469C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002759 | ||||||
| chr13:41003003
|
C | G | 2 | a0001c0001t0001g0354a0001c0001t0001g0355 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-229+16225G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003003 | ||||||
| chr13:41003028
|
CT | C | 10 | a0001c0005t0003g0132a0001c0005t0003g0166a0001c0005t0003g0341others(7): Show | 10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-229+16199delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003028 | ||||||
| chr13:41003035
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-229+16193A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003035 | ||||||
| chr13:41003054
|
G | C | 3 | a0001c0001t0001g0148a0001c0001t0001g0153a0001c0001t0001g0224 | 3 | NA18972.hp1 NA19011.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-229+16174C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003054 | ||||||
| chr13:41003070
|
T | C | 88 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(85): Show | 88 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-229+16158A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003070 | ||||||
| chr13:41003171
|
G | A | 1 | a0001c0001t0007g0280 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-229+16057C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003171 | ||||||
| chr13:41003395
|
AAATTAAA others(131): Show |
A | 52 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(49): Show | 56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-229+15695_-229+15 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003395 | ||||||
| chr13:41003539
|
C | T | 1 | a0012c0017t0004g0047 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-229+15689G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003539 | ||||||
| chr13:41003768
|
G | A | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-229+15460C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003768 | ||||||
| chr13:41003973
|
C | T | 82 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(79): Show | 83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-229+15255G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003973 | ||||||
| chr13:41004063
|
C | A | 10 | a0001c0001t0001g0225a0001c0001t0001g0325a0001c0001t0001g0326others(7): Show | 10 | HG02717.hp2 NA18959.hp1 NA18977.hp2 others(7): Show |
intron_variant | MODIFIER | c.-229+15165G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41004063 | ||||||
| chr13:41004359
|
G | A | 1 | a0002c0002t0002g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-229+14869C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41004359 | ||||||
| chr13:41004596
|
T | C | 1 | a0001c0005t0003g0346 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-229+14632A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41004596 | ||||||
| chr13:41004964
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-229+14264G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41004964 | ||||||
| chr13:41004977
|
A | G | 44 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(41): Show | 45 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-229+14251T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41004977 | ||||||
| chr13:41005342
|
G | A | 1 | a0001c0001t0008g0322 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-229+13886C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005342 | ||||||
| chr13:41005450
|
C | CA | 130 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 134 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-229+13777dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005450 | ||||||
| chr13:41005450
|
C | CAA | 14 | a0001c0001t0001g0182a0001c0001t0001g0272a0001c0005t0003g0341others(11): Show | 14 | HG01106.hp2 HG01934.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.-229+13776_-229+13 others(8): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005450 | ||||||
| chr13:41005466
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-229+13762T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005466 | ||||||
| chr13:41005673
|
A | C | 91 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(88): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-229+13555T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005673 | ||||||
| chr13:41005732
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(52): Show | 59 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.-229+13496A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005732 | ||||||
| chr13:41005802
|
G | A | 44 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(41): Show | 45 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-229+13426C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005802 | ||||||
| chr13:41005861
|
T | C | 7 | a0004c0006t0004g0008a0004c0006t0004g0069a0004c0006t0004g0332others(4): Show | 7 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+13367A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005861 | ||||||
| chr13:41005873
|
A | ATCATAAA others(273): Show |
4 | a0002c0002t0002g0131a0002c0002t0002g0279a0002c0002t0002g0310others(1): Show | 4 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-229+13075_-229+13 others(286): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005873 | ||||||
| chr13:41006044
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0352a0001c0001t0001g0354others(1): Show | 6 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-229+13184A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006044 | ||||||
| chr13:41006076
|
G | A | 1 | a0002c0002t0002g0356 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-229+13152C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006076 | ||||||
| chr13:41006123
|
C | G | 44 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(41): Show | 45 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-229+13105G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006123 | ||||||
| chr13:41006219
|
G | C | 1 | a0001c0001t0007g0349 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-229+13009C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006219 | ||||||
| chr13:41006324
|
G | GT | 71 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(68): Show | 72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-229+12903dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006324 | ||||||
| chr13:41006402
|
C | T | 5 | a0001c0001t0001g0139a0001c0001t0001g0235a0001c0001t0001g0267others(2): Show | 5 | NA18940.hp1 NA18963.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.-229+12826G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006402 | ||||||
| chr13:41006407
|
C | T | 1 | a0001c0003t0001g0118 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-229+12821G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006407 | ||||||
| chr13:41006442
|
T | TG | 9 | a0001c0001t0007g0349a0001c0005t0003g0341a0001c0005t0003g0342others(6): Show | 9 | HG03491.hp1 HG03834.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.-229+12785dupC | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006442 | ||||||
| chr13:41006465
|
T | C | 8 | a0001c0005t0003g0341a0001c0005t0003g0342a0001c0005t0003g0343others(5): Show | 8 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.-229+12763A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006465 | ||||||
| chr13:41006769
|
G | C | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | NA18999.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-229+12459C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006769 | ||||||
| chr13:41006803
|
G | A | 7 | a0004c0006t0004g0008a0004c0006t0004g0069a0004c0006t0004g0332others(4): Show | 7 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+12425C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006803 | ||||||
| chr13:41006867
|
C | T | 44 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(41): Show | 45 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-229+12361G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006867 | ||||||
| chr13:41006905
|
A | G | 4 | a0001c0001t0005g0089a0001c0001t0005g0122a0001c0001t0005g0162others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-229+12323T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006905 | ||||||
| chr13:41007001
|
T | C | 7 | a0004c0006t0004g0008a0004c0006t0004g0069a0004c0006t0004g0332others(4): Show | 7 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+12227A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41007001 | ||||||
| chr13:41007448
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-229+11780A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41007448 | ||||||
| chr13:41007530
|
C | A | 91 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(88): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-229+11698G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41007530 | ||||||
| chr13:41007794
|
C | T | 91 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(88): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-229+11434G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41007794 | ||||||
| chr13:41007847
|
G | A | 5 | a0001c0001t0014g0248a0001c0003t0001g0098a0001c0003t0001g0099others(2): Show | 5 | HG02145.hp2 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-229+11381C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41007847 | ||||||
| chr13:41008002
|
C | G | 61 | a0001c0001t0001g0208a0001c0001t0001g0218a0001c0001t0001g0257others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-229+11226G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41008002 | ||||||
| chr13:41008139
|
G | C | 88 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(85): Show | 88 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-229+11089C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41008139 | ||||||
| chr13:41008221
|
C | T | 13 | a0001c0001t0001g0068a0001c0001t0001g0114a0001c0001t0001g0115others(10): Show | 13 | HG02071.hp1 HG02132.hp1 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.-229+11007G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41008221 | ||||||
| chr13:41008617
|
G | T | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(1): Show | 4 | HG03239.hp1 NA18957.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.-229+10611C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41008617 | ||||||
| chr13:41008969
|
A | T | 281 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(278): Show | 286 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.-229+10259T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41008969 | ||||||
| chr13:41009181
|
T | C | 1 | a0002c0002t0002g0050 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-229+10047A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41009181 | ||||||
| chr13:41009231
|
T | C | 2 | a0002c0002t0002g0021a0002c0002t0002g0046 | 2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-229+9997A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41009231 | ||||||
| chr13:41009481
|
T | C | 1 | a0001c0001t0013g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-229+9747A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41009481 | ||||||
| chr13:41009698
|
G | A | 1 | a0001c0001t0001g0329 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-229+9530C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41009698 | ||||||
| chr13:41009805
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(52): Show | 59 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.-229+9423G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41009805 | ||||||
| chr13:41010051
|
GA | G | 70 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(67): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.-229+9176delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010051 | ||||||
| chr13:41010254
|
T | C | 1 | a0001c0003t0001g0353 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-229+8974A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010254 | ||||||
| chr13:41010279
|
GA | G | 88 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0065others(85): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.-229+8948delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010279 | ||||||
| chr13:41010313
|
C | T | 9 | a0001c0001t0001g0060a0001c0001t0007g0349a0004c0006t0004g0008others(6): Show | 9 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-229+8915G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010313 | ||||||
| chr13:41010338
|
T | C | 98 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(95): Show | 98 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-229+8890A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010338 | ||||||
| chr13:41010361
|
G | A | 1 | a0001c0003t0001g0124 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-229+8867C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010361 | ||||||
| chr13:41010454
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-229+8774G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010454 | ||||||
| chr13:41010493
|
A | ATG | 47 | a0001c0001t0001g0060a0001c0001t0001g0226a0001c0001t0001g0271others(44): Show | 47 | HG00423.hp2 HG00673.hp2 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.-229+8733_-229+873 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010493 | ||||||
| chr13:41010512
|
C | T | 7 | a0002c0002t0002g0031a0002c0002t0002g0034a0002c0002t0002g0039others(4): Show | 7 | HG00280.hp1 HG00735.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+8716G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010512 | ||||||
| chr13:41010513
|
A | G | 7 | a0002c0002t0002g0031a0002c0002t0002g0034a0002c0002t0002g0039others(4): Show | 7 | HG00280.hp1 HG00735.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+8715T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010513 | ||||||
| chr13:41010554
|
T | C | 182 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0053others(179): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-229+8674A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010554 | ||||||
| chr13:41010595
|
T | C | 7 | a0004c0006t0004g0008a0004c0006t0004g0069a0004c0006t0004g0332others(4): Show | 7 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+8633A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010595 | ||||||
| chr13:41010679
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-229+8549G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010679 | ||||||
| chr13:41010807
|
T | C | 1 | a0001c0001t0001g0233 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-229+8421A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010807 | ||||||
| chr13:41010898
|
G | C | 1 | a0002c0002t0002g0086 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-229+8330C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010898 | ||||||
| chr13:41010919
|
T | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0074others(15): Show | 20 | HG00438.hp2 HG00597.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.-229+8309A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010919 | ||||||
| chr13:41011287
|
T | C | 2 | a0002c0002t0002g0306a0002c0002t0002g0307 | 2 | HG01934.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.-229+7941A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011287 | ||||||
| chr13:41011362
|
A | T | 39 | a0001c0001t0001g0009a0001c0001t0001g0067a0001c0001t0001g0088others(36): Show | 39 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.-229+7866T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011362 | ||||||
| chr13:41011507
|
G | A | 1 | a0002c0002t0002g0024 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-229+7721C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011507 | ||||||
| chr13:41011590
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-229+7638G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011590 | ||||||
| chr13:41011644
|
G | A | 75 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0070others(72): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-229+7584C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011644 | ||||||
| chr13:41011778
|
G | T | 1 | a0001c0001t0001g0091 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-229+7450C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011778 | ||||||
| chr13:41011887
|
CT | C | 6 | a0004c0006t0004g0008a0004c0006t0004g0332a0004c0006t0004g0333others(3): Show | 6 | HG01192.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-229+7340delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011887 | ||||||
| chr13:41011918
|
C | A | 65 | a0001c0001t0001g0208a0001c0001t0001g0218a0001c0001t0001g0257others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-229+7310G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011918 | ||||||
| chr13:41012047
|
C | T | 1 | a0001c0001t0007g0349 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-229+7181G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012047 | ||||||
| chr13:41012262
|
G | A | 1 | a0002c0002t0002g0022 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-229+6966C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012262 | ||||||
| chr13:41012274
|
C | T | 16 | a0001c0001t0001g0060a0001c0001t0007g0349a0001c0005t0003g0341others(13): Show | 16 | HG01192.hp2 HG02717.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.-229+6954G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012274 | ||||||
| chr13:41012312
|
C | CA | 19 | a0001c0001t0001g0154a0001c0001t0001g0245a0001c0001t0002g0172others(16): Show | 19 | HG01192.hp2 HG01981.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-229+6915dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012312 | ||||||
| chr13:41012312
|
CA | C | 213 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(210): Show | 215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-229+6915delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012312 | ||||||
| chr13:41012312
|
CAA | C | 73 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0065others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.-229+6914_-229+691 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012312 | ||||||
| chr13:41012312
|
CAAAAAA | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0352a0001c0001t0001g0354others(1): Show | 6 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-229+6910_-229+691 others(10): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012312 | ||||||
| chr13:41012312
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0121 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-229+6904_-229+691 others(16): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012312 | ||||||
| chr13:41012545
|
CT | C | 53 | a0001c0001t0001g0087a0001c0001t0001g0106a0001c0001t0001g0128others(50): Show | 54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.-229+6682delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012545 | ||||||
| chr13:41012668
|
C | T | 86 | a0001c0001t0001g0009a0001c0001t0001g0061a0001c0001t0001g0064others(83): Show | 86 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-229+6560G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012668 | ||||||
| chr13:41012688
|
A | C | 1 | a0001c0001t0013g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-229+6540T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012688 | ||||||
| chr13:41012689
|
GTGTGACA others(12): Show |
G | 1 | a0001c0001t0001g0113 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-229+6520_-229+653 others(23): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012689 | ||||||
| chr13:41012736
|
C | T | 1 | a0002c0002t0002g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-229+6492G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012736 | ||||||
| chr13:41012778
|
G | C | 1 | a0001c0001t0001g0065 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-229+6450C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012778 | ||||||
| chr13:41012824
|
C | T | 70 | a0001c0001t0001g0208a0001c0001t0001g0218a0001c0001t0001g0257others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-229+6404G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012824 | ||||||
| chr13:41012919
|
T | C | 333 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(330): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.-229+6309A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012919 | ||||||
| chr13:41013239
|
T | C | 7 | a0002c0002t0002g0022a0002c0002t0002g0029a0002c0002t0002g0030others(4): Show | 7 | HG00733.hp2 HG00738.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+5989A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41013239 | ||||||
| chr13:41013260
|
C | A | 4 | a0001c0001t0014g0248a0001c0003t0001g0159a0001c0003t0001g0249others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-229+5968G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41013260 | ||||||
| chr13:41013326
|
G | A | 2 | a0002c0002t0002g0021a0002c0002t0002g0046 | 2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-229+5902C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41013326 | ||||||
| chr13:41013336
|
T | C | 1 | a0002c0002t0002g0316 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-229+5892A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41013336 | ||||||
| chr13:41013712
|
A | G | 46 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0057others(43): Show | 47 | HG00280.hp1 HG00621.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.-229+5516T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41013712 | ||||||
| chr13:41013918
|
A | C | 3 | a0001c0001t0001g0154a0001c0001t0001g0234a0001c0001t0001g0245 | 3 | NA18941.hp1 NA19065.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-229+5310T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41013918 | ||||||
| chr13:41013960
|
A | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0221a0001c0001t0009g0220 | 3 | HG02615.hp1 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-229+5268T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41013960 | ||||||
| chr13:41014200
|
C | A | 355 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(352): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-229+5028G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41014200 | ||||||
| chr13:41014294
|
C | T | 1 | a0002c0002t0002g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-229+4934G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41014294 | ||||||
| chr13:41014301
|
C | A | 1 | a0001c0001t0013g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-229+4927G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41014301 | ||||||
| chr13:41014301
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-229+4927G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41014301 | ||||||
| chr13:41014326
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(123): Show | 130 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-229+4902A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41014326 | ||||||
| chr13:41014696
|
G | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(53): Show | 60 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.-229+4532C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41014696 | ||||||
| chr13:41015155
|
G | A | 9 | a0001c0001t0007g0349a0001c0005t0003g0341a0001c0005t0003g0342others(6): Show | 9 | HG03491.hp1 HG03834.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.-229+4073C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015155 | ||||||
| chr13:41015261
|
G | A | 2 | a0002c0002t0002g0258a0002c0002t0002g0288 | 2 | NA18943.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-229+3967C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015261 | ||||||
| chr13:41015335
|
C | CA | 7 | a0001c0001t0001g0296a0002c0002t0002g0013a0002c0002t0002g0033others(4): Show | 7 | HG01071.hp2 HG01517.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+3892dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015335 | ||||||
| chr13:41015362
|
T | A | 6 | a0004c0006t0004g0008a0004c0006t0004g0332a0004c0006t0004g0333others(3): Show | 6 | HG01192.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-229+3866A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015362 | ||||||
| chr13:41015403
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-229+3825T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015403 | ||||||
| chr13:41015491
|
G | T | 10 | a0001c0001t0001g0060a0001c0001t0007g0349a0001c0005t0003g0341others(7): Show | 10 | HG02723.hp1 HG03491.hp1 HG03834.hp2 others(7): Show |
intron_variant | MODIFIER | c.-229+3737C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015491 | ||||||
| chr13:41015918
|
G | C | 3 | a0001c0001t0007g0280a0002c0002t0002g0298a0002c0002t0002g0299 | 3 | HG03017.hp2 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-229+3310C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015918 | ||||||
| chr13:41015930
|
GAAT | G | 86 | a0001c0001t0001g0009a0001c0001t0001g0061a0001c0001t0001g0064others(83): Show | 86 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-229+3295_-229+329 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015930 | ||||||
| chr13:41015960
|
A | G | 1 | a0002c0002t0002g0319 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-229+3268T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015960 | ||||||
| chr13:41016147
|
C | T | 1 | a0003c0018t0003g0023 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-229+3081G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016147 | ||||||
| chr13:41016196
|
T | C | 6 | a0004c0006t0004g0008a0004c0006t0004g0332a0004c0006t0004g0333others(3): Show | 6 | HG01192.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-229+3032A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016196 | ||||||
| chr13:41016252
|
C | T | 10 | a0001c0001t0001g0060a0001c0001t0007g0349a0001c0005t0003g0341others(7): Show | 10 | HG02723.hp1 HG03491.hp1 HG03834.hp2 others(7): Show |
intron_variant | MODIFIER | c.-229+2976G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016252 | ||||||
| chr13:41016271
|
G | A | 1 | a0011c0015t0002g0038 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-229+2957C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016271 | ||||||
| chr13:41016417
|
C | A | 4 | a0001c0001t0014g0248a0001c0003t0001g0159a0001c0003t0001g0249others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-229+2811G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016417 | ||||||
| chr13:41016542
|
G | T | 10 | a0001c0001t0001g0060a0001c0001t0007g0349a0001c0005t0003g0341others(7): Show | 10 | HG02723.hp1 HG03491.hp1 HG03834.hp2 others(7): Show |
intron_variant | MODIFIER | c.-229+2686C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016542 | ||||||
| chr13:41016572
|
T | C | 353 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(350): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-229+2656A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016572 | ||||||
| chr13:41016689
|
C | A | 2 | a0001c0001t0001g0102a0001c0001t0008g0073 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-229+2539G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016689 | ||||||
| chr13:41016756
|
A | T | 5 | a0001c0001t0007g0280a0002c0002t0002g0170a0002c0002t0002g0171others(2): Show | 5 | HG00609.hp2 HG03017.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-229+2472T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016756 | ||||||
| chr13:41016821
|
G | A | 1 | a0001c0003t0001g0244 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-229+2407C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016821 | ||||||
| chr13:41016867
|
T | C | 1 | a0002c0002t0002g0309 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-229+2361A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016867 | ||||||
| chr13:41016914
|
C | CA | 23 | a0001c0001t0001g0005a0001c0001t0001g0053a0001c0001t0001g0234others(20): Show | 24 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.-229+2313dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | ||||||
| chr13:41016914
|
C | CAA | 8 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(5): Show | 8 | HG00438.hp2 HG01071.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.-229+2312_-229+231 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | ||||||
| chr13:41016914
|
CA | C | 17 | a0001c0001t0001g0125a0001c0001t0001g0167a0001c0001t0001g0168others(14): Show | 17 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(14): Show |
intron_variant | MODIFIER | c.-229+2313delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | ||||||
| chr13:41016914
|
CAA | C | 11 | a0001c0001t0001g0121a0001c0001t0001g0160a0001c0001t0001g0161others(8): Show | 11 | HG01109.hp2 HG02056.hp2 NA18971.hp2 others(8): Show |
intron_variant | MODIFIER | c.-229+2312_-229+231 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | ||||||
| chr13:41016914
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0063a0001c0001t0001g0065 | 2 | NA18747.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-229+2304_-229+231 others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | ||||||
| chr13:41016914
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0003t0001g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-229+2302_-229+231 others(16): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | ||||||
| chr13:41016914
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0060a0001c0001t0001g0088 | 2 | HG02723.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.-229+2301_-229+231 others(17): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | ||||||
| chr13:41016914
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0001g0070a0005c0007t0001g0079 | 2 | NA19083.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-229+2300_-229+231 others(18): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | ||||||
| chr13:41016914
|
CAAAAAAA others(8): Show |
C | 1 | a0002c0002t0002g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-229+2299_-229+231 others(19): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | ||||||
| chr13:41016914
|
CAAAAAAA others(9): Show |
C | 9 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(6): Show | 9 | HG02071.hp2 HG03225.hp2 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.-229+2298_-229+231 others(20): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | ||||||
| chr13:41016914
|
CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0001g0116 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-229+2296_-229+231 others(22): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | ||||||
| chr13:41016935
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0335 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-229+2279_-229+229 others(18): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016935 | ||||||
| chr13:41016935
|
AAAAAAAA others(25): Show |
A | 1 | a0001c0003t0001g0323 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-229+2261_-229+229 others(36): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016935 | ||||||
| chr13:41016936
|
AAAAAAAA others(8): Show |
A | 1 | a0002c0002t0002g0279 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-229+2277_-229+229 others(19): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016936 | ||||||
| chr13:41016937
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-229+2291T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016937 | ||||||
| chr13:41016937
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0014g0248 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-229+2279_-229+229 others(16): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016937 | ||||||
| chr13:41016938
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0003t0001g0249 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-229+2279_-229+228 others(15): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016938 | ||||||
| chr13:41016939
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0061 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-229+2288_-229+228 others(16): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016939 | ||||||
| chr13:41016939
|
A | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0065 | 2 | NA18747.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-229+2289T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016939 | ||||||
| chr13:41016939
|
AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0015g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-229+2269_-229+228 others(24): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016939 | ||||||
| chr13:41016940
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0005t0003g0341 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-229+2277_-229+228 others(15): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016940 | ||||||
| chr13:41016940
|
AAAAAAAA others(14): Show |
A | 1 | a0004c0006t0004g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-229+2267_-229+228 others(25): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016940 | ||||||
| chr13:41016941
|
A | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0063others(2): Show | 5 | HG02723.hp1 NA18747.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.-229+2287T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016941 | ||||||
| chr13:41016941
|
AAAAAAAA others(1): Show |
A | 7 | a0001c0001t0001g0057a0002c0002t0002g0251a0002c0002t0002g0253others(4): Show | 7 | HG01106.hp1 HG01433.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.-229+2279_-229+228 others(12): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016941 | ||||||
| chr13:41016941
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0007g0280 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-229+2277_-229+228 others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016941 | ||||||
| chr13:41016941
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0005t0003g0342 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-229+2275_-229+228 others(16): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016941 | ||||||
| chr13:41016942
|
AAAAAAAT others(4): Show |
A | 6 | a0001c0005t0003g0343a0001c0005t0003g0344a0001c0005t0003g0345others(3): Show | 6 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.-229+2275_-229+228 others(15): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016942 | ||||||
| chr13:41016942
|
AAAAAAAT others(14): Show |
A | 1 | a0001c0001t0008g0322 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-229+2265_-229+228 others(25): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016942 | ||||||
| chr13:41016943
|
A | ATAT | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0008g0073 | 3 | HG01934.hp2 HG02630.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.-229+2284_-229+228 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016943 | ||||||
| chr13:41016943
|
A | ATATAT | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0003t0001g0066 | 3 | NA18945.hp1 NA19007.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-229+2284_-229+228 others(9): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016943 | ||||||
| chr13:41016943
|
A | T | 12 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0065others(9): Show | 12 | HG02717.hp2 HG02738.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.-229+2285T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016943 | ||||||
| chr13:41016943
|
AAAAAATA others(3): Show |
A | 3 | a0001c0001t0007g0349a0002c0002t0002g0298a0002c0002t0002g0299 | 3 | HG03491.hp1 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-229+2275_-229+228 others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016943 | ||||||
| chr13:41016943
|
AAAAAATA others(7): Show |
A | 1 | a0002c0002t0002g0319 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-229+2271_-229+228 others(18): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016943 | ||||||
| chr13:41016944
|
AAAAAT | A | 7 | a0001c0001t0001g0257a0001c0001t0001g0336a0002c0002t0002g0256others(4): Show | 7 | HG00673.hp2 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+2279_-229+228 others(9): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016944 | ||||||
| chr13:41016944
|
AAAAATAT others(4): Show |
A | 1 | a0001c0001t0001g0340 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-229+2273_-229+228 others(15): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016944 | ||||||
| chr13:41016945
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-229+2282_-229+228 others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016945 | ||||||
| chr13:41016945
|
A | AATATATA others(5): Show |
1 | a0001c0003t0001g0062 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-229+2282_-229+228 others(16): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016945 | ||||||
| chr13:41016945
|
A | AT | 6 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 7 | HG01346.hp1 HG01358.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+2282_-229+228 others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016945 | ||||||
| chr13:41016945
|
A | T | 43 | a0001c0001t0001g0009a0001c0001t0001g0060a0001c0001t0001g0061others(40): Show | 43 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.-229+2283T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016945 | ||||||
| chr13:41016945
|
AAAATAT | A | 8 | a0001c0001t0001g0287a0002c0002t0002g0281a0002c0002t0002g0282others(5): Show | 8 | HG03239.hp2 NA18953.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.-229+2277_-229+228 others(10): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016945 | ||||||
| chr13:41016945
|
AAAATATA others(1): Show |
A | 11 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0308others(8): Show | 11 | HG00140.hp2 HG00738.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.-229+2275_-229+228 others(12): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016945 | ||||||
| chr13:41016945
|
AAAATATA others(3): Show |
A | 1 | a0002c0002t0002g0316 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-229+2273_-229+228 others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016945 | ||||||
| chr13:41016947
|
A | AAAAAATA others(5): Show |
1 | a0001c0001t0001g0074 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-229+2280_-229+228 others(16): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | ||||||
| chr13:41016947
|
A | AAAT | 11 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0154others(8): Show | 14 | HG01358.hp2 HG01884.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-229+2280_-229+228 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | ||||||
| chr13:41016947
|
A | AAATATAT others(4): Show |
2 | a0002c0002t0002g0020a0004c0006t0004g0069 | 2 | HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-229+2280_-229+228 others(15): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | ||||||
| chr13:41016947
|
A | AAT | 16 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(13): Show | 16 | HG01109.hp1 HG01346.hp2 HG04228.hp2 others(13): Show |
intron_variant | MODIFIER | c.-229+2279_-229+228 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | ||||||
| chr13:41016947
|
A | AATATATA others(3): Show |
1 | a0002c0002t0002g0019 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-229+2271_-229+228 others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | ||||||
| chr13:41016947
|
A | AT | 11 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0003t0001g0140others(8): Show | 12 | HG00642.hp2 HG01433.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.-229+2280_-229+228 others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | ||||||
| chr13:41016947
|
A | ATAT | 11 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(8): Show | 11 | HG00673.hp1 HG02027.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.-229+2280_-229+228 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | ||||||
| chr13:41016947
|
A | ATATAT | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0002c0002t0002g0022 | 3 | HG02615.hp1 HG02698.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-229+2280_-229+228 others(9): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | ||||||
| chr13:41016947
|
A | T | 81 | a0001c0001t0001g0009a0001c0001t0001g0061a0001c0001t0001g0063others(78): Show | 82 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.-229+2281T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | ||||||
| chr13:41016947
|
AAT | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0263a0001c0001t0001g0290others(8): Show | 11 | HG01169.hp2 HG01884.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.-229+2279_-229+228 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | ||||||
| chr13:41016948
|
AT | A | 9 | a0001c0001t0001g0264a0001c0001t0001g0266a0001c0001t0001g0293others(6): Show | 9 | HG00733.hp1 HG01070.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.-229+2279delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016948 | ||||||
| chr13:41016948
|
ATAT | A | 4 | a0001c0001t0001g0289a0001c0003t0001g0011a0001c0003t0001g0012others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.-229+2277_-229+227 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016948 | ||||||
| chr13:41016948
|
ATATATAT | A | 4 | a0001c0001t0001g0317a0001c0003t0001g0321a0002c0002t0002g0318others(1): Show | 4 | NA18961.hp2 NA18991.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-229+2273_-229+227 others(11): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016948 | ||||||
| chr13:41016949
|
T | A | 14 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0001g0269others(11): Show | 14 | HG00544.hp1 HG02132.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.-229+2279A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016949 | ||||||
| chr13:41016951
|
T | A | 11 | a0001c0001t0001g0060a0001c0001t0001g0290a0001c0001t0001g0291others(8): Show | 11 | HG01169.hp2 HG02027.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.-229+2277A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016951 | ||||||
| chr13:41016953
|
T | A | 4 | a0001c0003t0001g0311a0002c0002t0002g0310a0002c0002t0002g0312others(1): Show | 4 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-229+2275A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016953 | ||||||
| chr13:41016955
|
T | A | 4 | a0001c0001t0001g0060a0001c0001t0001g0313a0001c0001t0001g0314others(1): Show | 4 | HG00735.hp2 HG02723.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-229+2273A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016955 | ||||||
| chr13:41016957
|
T | A | 2 | a0001c0003t0001g0321a0002c0002t0002g0320 | 2 | NA18991.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-229+2271A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016957 | ||||||
| chr13:41016959
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-229+2269A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016959 | ||||||
| chr13:41016963
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-229+2265A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016963 | ||||||
| chr13:41016977
|
T | C | 1 | a0001c0001t0011g0324 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-229+2251A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016977 | ||||||
| chr13:41016982
|
G | A | 7 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0327others(4): Show | 7 | NA18959.hp1 NA18997.hp2 NA19003.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+2246C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016982 | ||||||
| chr13:41017099
|
A | C | 10 | a0001c0001t0001g0060a0001c0001t0007g0349a0001c0005t0003g0341others(7): Show | 10 | HG02723.hp1 HG03491.hp1 HG03834.hp2 others(7): Show |
intron_variant | MODIFIER | c.-229+2129T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41017099 | ||||||
| chr13:41017140
|
T | C | 10 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0339others(7): Show | 10 | HG01192.hp2 HG02615.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-229+2088A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41017140 | ||||||
| chr13:41017278
|
C | T | 7 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(4): Show | 8 | HG00642.hp2 HG01109.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-229+1950G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41017278 | ||||||
| chr13:41017587
|
C | G | 48 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0057others(45): Show | 49 | HG00280.hp1 HG00621.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.-229+1641G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41017587 | ||||||
| chr13:41017630
|
C | T | 2 | a0001c0003t0001g0011a0001c0003t0001g0012 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-229+1598G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41017630 | ||||||
| chr13:41017741
|
G | A | 9 | a0001c0001t0007g0349a0001c0005t0003g0341a0001c0005t0003g0342others(6): Show | 9 | HG03491.hp1 HG03834.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.-229+1487C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41017741 | ||||||
| chr13:41017777
|
T | C | 1 | a0001c0001t0001g0350 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-229+1451A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41017777 | ||||||
| chr13:41018146
|
T | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0352others(4): Show | 9 | HG01884.hp2 HG01981.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-229+1082A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41018146 | ||||||
| chr13:41018179
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-229+1049G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41018179 | ||||||
| chr13:41018211
|
C | CAGAAATA others(33): Show |
1 | a0001c0001t0001g0009 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-229+977_-229+1016 others(43): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41018211 | ||||||
| chr13:41018494
|
G | C | 1 | a0002c0002t0002g0356 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-229+734C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41018494 | ||||||
| chr13:41019002
|
A | G | 3 | a0001c0001t0015g0006a0004c0006t0004g0007a0004c0006t0004g0008 | 3 | HG01496.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-229+226T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41019002 |