Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7091 |
|---|---|
| ensemblid | ENSG00000106829.21 |
| hgncid | 11840 |
| symbol | TLE4 |
| name | TLE family member 4, transcriptional corepressor |
| refseq_nuc | NM_007005.6 |
| refseq_prot | NP_008936.2 |
| ensembl_nuc | ENST00000376552.8 |
| ensembl_prot | ENSP00000365735.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 79571965 |
| end | 79726882 |
| strand | + |
| ver | v1.2 |
| region | chr9:79571965-79726882 |
| region5000 | chr9:79566965-79731882 |
| regionname0 | TLE4_chr9_79571965_79726882 |
| regionname5000 | TLE4_chr9_79566965_79731882 |
| 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 | 773 | 255 | 78 | 50 | 93 | 10 | 22 | 71 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0002 | 0/0 | 773 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0003 | 0/0 | 773 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0004 | 0/0 | 773 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2322 | 244 | 74 | 46 | 93 | 9 | 21 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| c0002 | 1/0 | 2322 | 2 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| c0003 | 0/0 | 2322 | 2 | 0 | 1 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| c0004 | 0/0 | 2322 | 2 | 2 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| c0005 | 0/0 | 2322 | 2 | 0 | 2 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| c0006 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| c0007 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| c0008 | 0/0 | 2322 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| c0009 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| c0010 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| c0011 | 0/0 | 2322 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2560 | 87 | 11 | 21 | 40 | 4 | 10 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0002 | 0/0 | 2565 | 82 | 22 | 17 | 32 | 4 | 7 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0003 | 0/0 | 2560 | 59 | 34 | 6 | 13 | 2 | 4 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0004 | 0/0 | 2557 | 9 | 7 | 2 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0005 | 0/0 | 2565 | 3 | 0 | 0 | 3 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0006 | 0/0 | 2565 | 2 | 0 | 2 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0007 | 1/0 | 2565 | 2 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0008 | 0/0 | 2560 | 2 | 1 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0009 | 0/0 | 2560 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0010 | 0/0 | 2560 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0011 | 0/0 | 2560 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0012 | 0/0 | 2560 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0013 | 0/0 | 2565 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0014 | 0/0 | 2561 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0015 | 0/0 | 2560 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0016 | 0/0 | 2560 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0017 | 0/0 | 2560 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0018 | 0/0 | 2560 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0019 | 0/0 | 2560 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| t0020 | 0/0 | 2560 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| 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 | 2 | 2 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2322 | 244 | 74 | 46 | 93 | 9 | 21 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0002 | 1/0 | 2322 | 2 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0003 | 0/0 | 2322 | 2 | 0 | 1 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0004 | 0/0 | 2322 | 2 | 2 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0005 | 0/0 | 2322 | 2 | 0 | 2 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0007 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0008 | 0/0 | 2322 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0010 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0002c0009 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0003c0006 | 0/0 | 2322 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0004c0011 | 0/0 | 2322 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4881 | 86 | 11 | 21 | 39 | 4 | 10 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0002 | 0/0 | 4886 | 80 | 21 | 16 | 32 | 4 | 7 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0003 | 0/0 | 4881 | 52 | 32 | 3 | 13 | 1 | 3 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0004 | 0/0 | 4878 | 7 | 5 | 2 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0005 | 0/0 | 4886 | 3 | 0 | 0 | 3 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0006 | 0/0 | 4886 | 2 | 0 | 2 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0007 | 0/0 | 4886 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0008 | 0/0 | 4881 | 2 | 1 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0009 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0010 | 0/0 | 4881 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0011 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0012 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0014 | 0/0 | 4882 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0015 | 0/0 | 4881 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0016 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0017 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0018 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0019 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0001t0020 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0002t0003 | 0/0 | 4881 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0002t0007 | 1/0 | 4886 | 1 | 0 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0003t0003 | 0/0 | 4881 | 2 | 0 | 1 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0004t0004 | 0/0 | 4878 | 2 | 2 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0005t0003 | 0/0 | 4881 | 2 | 0 | 2 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0007t0002 | 0/0 | 4886 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0008t0002 | 0/0 | 4886 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0001c0010t0013 | 0/0 | 4886 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0002c0009t0003 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0003c0006t0003 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| a0004c0011t0001 | 0/0 | 4881 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | copy fasta | chr9 | 79566965 | 79731882 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0006g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0008g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0009g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0010g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0011g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0012g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0014g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0015g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0016g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0017g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0018g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0019g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0001t0020g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0002t0007g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0003t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0003t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0004t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0004t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0005t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0005t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0007t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0008t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0001c0010t0013g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0002c0009t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0003c0006t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| a0004c0011t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0247 | EUR | GBR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0252 | EUR | GBR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0152 | EUR | GBR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | FIN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0181 | EUR | FIN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00423 | hp1 | a0001 | c0001 | t0009 | g0109 | EAS | CHS | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | CHS | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | CHS | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00673 | hp1 | a0001 | c0001 | t0017 | g0084 | EAS | CHS | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00741 | hp1 | a0001 | c0001 | t0015 | g0072 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01074 | hp2 | a0001 | c0008 | t0002 | g0024 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0160 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01106 | hp1 | a0001 | c0003 | t0003 | g0026 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0216 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0070 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0226 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0215 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01516 | hp1 | a0001 | c0003 | t0003 | g0025 | EUR | IBS | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01943 | hp1 | a0001 | c0005 | t0003 | g0253 | AMR | PEL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG01975 | hp2 | a0001 | c0005 | t0003 | g0254 | AMR | PEL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | KHV | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0166 | EAS | KHV | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | ACB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | KHV | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | KHV | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | KHV | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | ACB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | ACB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | ACB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02615 | hp1 | a0003 | c0006 | t0003 | g0027 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02615 | hp2 | a0001 | c0001 | t0020 | g0052 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02809 | hp1 | a0001 | c0001 | t0012 | g0043 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | ESN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02922 | hp2 | a0001 | c0001 | t0014 | g0251 | AFR | ESN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0239 | AFR | ESN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ESN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ESN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | ESN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0255 | AFR | MSL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0069 | AFR | MSL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03130 | hp1 | a0001 | c0004 | t0004 | g0250 | AFR | ESN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0229 | AFR | ESN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0227 | AFR | ESN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ESN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | ESN | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | MSL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | MSL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | MSL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03453 | hp1 | a0001 | c0001 | t0019 | g0023 | AFR | MSL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | MSL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | MSL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03486 | hp2 | a0001 | c0010 | t0013 | g0207 | AFR | MSL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | MSL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0041 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | STU | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | STU | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | YRI | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | YRI | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | CHB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | YRI | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | YRI | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18946 | hp2 | a0001 | c0001 | t0011 | g0013 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0029 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18959 | hp1 | a0001 | c0001 | t0016 | g0062 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0172 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18989 | hp2 | a0004 | c0011 | t0001 | g0014 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19005 | hp1 | a0001 | c0001 | t0018 | g0115 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | LWK | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | YRI | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | YRI | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ASW | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | ASW | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | TSI | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0241 | EUR | TSI | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA20905 | hp1 | a0001 | c0002 | t0003 | g0078 | SAS | GIH | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA20905 | hp2 | a0001 | c0001 | t0010 | g0210 | SAS | GIH | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | ACB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02486 | hp1 | a0001 | c0004 | t0004 | g0004 | AFR | ACB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG02486 | hp2 | a0001 | c0007 | t0002 | g0240 | AFR | ACB | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03471 | hp1 | a0002 | c0009 | t0003 | g0245 | AFR | MSL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | USA | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | USA | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | USA | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | USA | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0140 | REF | REF | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0007 | g0246 | REF | REF | TLE4_chr9_79566965_79731882 | TLE4 | chr9 | 79566965 | 79731882 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:79574890
|
A | T | 1 | a0004 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.161A>T | p.Glu54Val | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/20 | 987/4886 | 161/2322 | 54/773 | chr9 | 79574890 | ||
| chr9:79574925
|
C | A | 1 | a0004 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.196C>A | p.His66Asn | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/20 | 1022/4886 | 196/2322 | 66/773 | chr9 | 79574925 | ||
| chr9:79574935
|
T | A | 1 | a0004 | 1 | NA18989.hp2 | missense_variant&splice_region_variant | MODERATE | c.206T>A | p.Met69Lys | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/20 | 1032/4886 | 206/2322 | 69/773 | chr9 | 79574935 | ||
| chr9:79708703
|
G | C | 1 | a0003 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.1180G>C | p.Ala394Pro | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 13/20 | 2006/4886 | 1180/2322 | 394/773 | chr9 | 79708703 | ||
| chr9:79718940
|
A | G | 1 | a0002 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1559A>G | p.Asn520Ser | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 15/20 | 2385/4886 | 1559/2322 | 520/773 | chr9 | 79718940 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:79572835
|
A | G | 10 | a0001c0001a0001c0003a0001c0004others(7): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
splice_region_variant&synonymous_variant | LOW | c.45A>G | p.Pro15Pro | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/20 | 871/4886 | 45/2322 | 15/773 | chr9 | 79572835 | ||
| chr9:79708750
|
C | T | 1 | a0001c0005 | 2 | HG01943.hp1 HG01975.hp2 |
synonymous_variant | LOW | c.1227C>T | p.Ala409Ala | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 13/20 | 2053/4886 | 1227/2322 | 409/773 | chr9 | 79708750 | ||
| chr9:79718839
|
C | T | 1 | a0001c0010 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1458C>T | p.His486His | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 15/20 | 2284/4886 | 1458/2322 | 486/773 | chr9 | 79718839 | ||
| chr9:79720138
|
C | T | 1 | a0001c0008 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.1683C>T | p.Asp561Asp | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/20 | 2509/4886 | 1683/2322 | 561/773 | chr9 | 79720138 | ||
| chr9:79720246
|
C | T | 1 | a0001c0004 | 2 | HG02486.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.1791C>T | p.Ser597Ser | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/20 | 2617/4886 | 1791/2322 | 597/773 | chr9 | 79720246 | ||
| chr9:79721849
|
C | T | 1 | a0001c0003 | 2 | HG01106.hp1 HG01516.hp1 |
synonymous_variant | LOW | c.1947C>T | p.Arg649Arg | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 17/20 | 2773/4886 | 1947/2322 | 649/773 | chr9 | 79721849 | ||
| chr9:79721873
|
C | T | 1 | a0001c0007 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1971C>T | p.His657His | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 17/20 | 2797/4886 | 1971/2322 | 657/773 | chr9 | 79721873 | ||
| chr9:79722492
|
A | C | 1 | a0001c0010 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.2028A>C | p.Ala676Ala | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 18/20 | 2854/4886 | 2028/2322 | 676/773 | chr9 | 79722492 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:79571990
|
A | G | 1 | a0001c0001t0020 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-801A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/20 | 801 | chr9 | 79571990 | |||||
| chr9:79572013
|
G | A | 1 | a0001c0001t0009 | 1 | HG00423.hp1 | 5_prime_UTR_variant | MODIFIER | c.-778G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/20 | 778 | chr9 | 79572013 | |||||
| chr9:79572113
|
A | G | 1 | a0001c0001t0019 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-678A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/20 | 678 | chr9 | 79572113 | |||||
| chr9:79572180
|
G | A | 20 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(17): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
5_prime_UTR_variant | MODIFIER | c.-611G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/20 | 611 | chr9 | 79572180 | |||||
| chr9:79572267
|
A | C | 1 | a0001c0001t0018 | 1 | NA19005.hp1 | 5_prime_UTR_variant | MODIFIER | c.-524A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/20 | 524 | chr9 | 79572267 | |||||
| chr9:79572377
|
A | T | 1 | a0001c0001t0008 | 2 | HG01167.hp1 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-414A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/20 | 414 | chr9 | 79572377 | |||||
| chr9:79572456
|
G | A | 1 | a0001c0001t0010 | 1 | NA20905.hp2 | 5_prime_UTR_variant | MODIFIER | c.-335G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/20 | 335 | chr9 | 79572456 | |||||
| chr9:79572603
|
C | G | 1 | a0001c0001t0005 | 3 | HG00558.hp1 HG02040.hp1 NA18989.hp1 |
5_prime_UTR_variant | MODIFIER | c.-188C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/20 | 188 | chr9 | 79572603 | |||||
| chr9:79572653
|
C | T | 1 | a0001c0001t0017 | 1 | HG00673.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-138C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/20 | chr9 | 79572653 | ||||||
| chr9:79725380
|
A | G | 1 | a0001c0001t0016 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*236A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 20/20 | 236 | chr9 | 79725380 | |||||
| chr9:79725670
|
GT | G | 21 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(18): Show | 167 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*534delT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 20/20 | 534 | INFO_REALIGN_3_PRIME | chr9 | 79725670 | ||||
| chr9:79725711
|
G | A | 1 | a0001c0010t0013 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*567G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 20/20 | 567 | chr9 | 79725711 | |||||
| chr9:79725813
|
G | A | 1 | a0001c0001t0011 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*669G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 20/20 | 669 | chr9 | 79725813 | |||||
| chr9:79725850
|
G | A | 2 | a0001c0001t0006a0001c0001t0015 | 3 | HG00741.hp1 HG01109.hp1 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*706G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 20/20 | 706 | chr9 | 79725850 | |||||
| chr9:79725946
|
C | T | 1 | a0001c0001t0012 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*802C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 20/20 | 802 | chr9 | 79725946 | |||||
| chr9:79726289
|
ATGT | A | 2 | a0001c0001t0004a0001c0004t0004 | 9 | HG01081.hp2 HG01255.hp2 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1157_*1159delTTG | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 20/20 | 1157 | INFO_REALIGN_3_PRIME | chr9 | 79726289 | ||||
| chr9:79726542
|
GAAAA | G | 22 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(19): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1406_*1409delAAAA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 20/20 | 1406 | INFO_REALIGN_3_PRIME | chr9 | 79726542 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:79572878
|
G | A | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.45+43G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/19 | chr9 | 79572878 | ||||||
| chr9:79572893
|
C | T | 1 | a0001c0001t0003g0255 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.45+58C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/19 | chr9 | 79572893 | ||||||
| chr9:79572894
|
C | T | 2 | a0001c0005t0003g0253a0001c0005t0003g0254 | 2 | HG01943.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.45+59C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/19 | chr9 | 79572894 | ||||||
| chr9:79573125
|
G | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 8 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+290G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/19 | chr9 | 79573125 | ||||||
| chr9:79573293
|
C | T | 1 | a0001c0001t0003g0252 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.46-396C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/19 | chr9 | 79573293 | ||||||
| chr9:79573308
|
C | A | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.46-381C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/19 | chr9 | 79573308 | ||||||
| chr9:79573318
|
C | T | 1 | a0001c0001t0014g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.46-371C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/19 | chr9 | 79573318 | ||||||
| chr9:79573596
|
T | C | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.46-93T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/19 | chr9 | 79573596 | ||||||
| chr9:79573618
|
A | G | 2 | a0001c0004t0004g0004a0001c0004t0004g0250 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.46-71A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 1/19 | chr9 | 79573618 | ||||||
| chr9:79574054
|
T | G | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.143+268T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574054 | ||||||
| chr9:79574055
|
G | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.143+269G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574055 | ||||||
| chr9:79574056
|
A | T | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.143+270A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574056 | ||||||
| chr9:79574180
|
A | C | 1 | a0001c0001t0002g0249 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.143+394A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574180 | ||||||
| chr9:79574195
|
G | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.143+409G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574195 | ||||||
| chr9:79574273
|
G | T | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.143+487G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574273 | ||||||
| chr9:79574291
|
T | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.143+505T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574291 | ||||||
| chr9:79574297
|
T | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.143+511T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574297 | ||||||
| chr9:79574299
|
G | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.143+513G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574299 | ||||||
| chr9:79574301
|
T | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.143+515T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574301 | ||||||
| chr9:79574305
|
T | TCCCCCCC others(10): Show |
1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.143+519_143+520ins others(17): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574305 | ||||||
| chr9:79574306
|
A | T | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.143+520A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574306 | ||||||
| chr9:79574307
|
A | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.143+521A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574307 | ||||||
| chr9:79574447
|
G | T | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-426G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574447 | ||||||
| chr9:79574459
|
T | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-414T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574459 | ||||||
| chr9:79574464
|
A | T | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-409A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574464 | ||||||
| chr9:79574471
|
T | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-402T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574471 | ||||||
| chr9:79574484
|
T | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-389T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574484 | ||||||
| chr9:79574497
|
C | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-376C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574497 | ||||||
| chr9:79574501
|
T | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-372T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574501 | ||||||
| chr9:79574501
|
T | C | 6 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(3): Show | 6 | HG02717.hp1 HG02976.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.144-372T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574501 | ||||||
| chr9:79574508
|
T | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-365T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574508 | ||||||
| chr9:79574577
|
T | G | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-296T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574577 | ||||||
| chr9:79574578
|
G | T | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-295G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574578 | ||||||
| chr9:79574579
|
A | T | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-294A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574579 | ||||||
| chr9:79574583
|
T | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-290T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574583 | ||||||
| chr9:79574596
|
G | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-277G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574596 | ||||||
| chr9:79574597
|
A | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-276A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574597 | ||||||
| chr9:79574598
|
A | G | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-275A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574598 | ||||||
| chr9:79574599
|
G | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-274G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574599 | ||||||
| chr9:79574602
|
C | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-271C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574602 | ||||||
| chr9:79574607
|
ATTAAACT others(14): Show |
A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-263_144-243del others(21): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 79574607 | |||||
| chr9:79574632
|
C | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-241C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574632 | ||||||
| chr9:79574634
|
T | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-239T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574634 | ||||||
| chr9:79574658
|
C | T | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-215C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574658 | ||||||
| chr9:79574674
|
C | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-199C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574674 | ||||||
| chr9:79574676
|
C | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-197C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574676 | ||||||
| chr9:79574676
|
C | T | 2 | a0001c0001t0002g0003a0001c0001t0002g0247 | 3 | HG00099.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.144-197C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574676 | ||||||
| chr9:79574728
|
T | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-145T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574728 | ||||||
| chr9:79574785
|
T | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-88T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574785 | ||||||
| chr9:79574788
|
G | T | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-85G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574788 | ||||||
| chr9:79574791
|
GGTGAGAT others(7): Show |
G | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-81_144-68delGT others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574791 | ||||||
| chr9:79574802
|
G | C | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.144-71G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574802 | ||||||
| chr9:79574806
|
A | T | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.144-67A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 2/19 | chr9 | 79574806 | ||||||
| chr9:79574937
|
G | T | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | splice_donor_variant&intron_variant | HIGH | c.207+1G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574937 | ||||||
| chr9:79574938
|
T | G | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | splice_donor_variant&intron_variant | HIGH | c.207+2T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574938 | ||||||
| chr9:79574939
|
A | T | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | splice_region_variant&intron_variant | LOW | c.207+3A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574939 | ||||||
| chr9:79574951
|
T | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+15T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574951 | ||||||
| chr9:79574954
|
C | G | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+18C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574954 | ||||||
| chr9:79574959
|
T | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+23T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574959 | ||||||
| chr9:79574960
|
C | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+24C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574960 | ||||||
| chr9:79574961
|
A | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+25A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574961 | ||||||
| chr9:79574962
|
A | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+26A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574962 | ||||||
| chr9:79574964
|
G | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+28G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574964 | ||||||
| chr9:79574969
|
T | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+33T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574969 | ||||||
| chr9:79574971
|
T | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+35T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574971 | ||||||
| chr9:79574972
|
T | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+36T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574972 | ||||||
| chr9:79574975
|
T | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+39T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574975 | ||||||
| chr9:79574976
|
T | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+40T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574976 | ||||||
| chr9:79574978
|
G | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+42G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574978 | ||||||
| chr9:79574979
|
G | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+43G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574979 | ||||||
| chr9:79574982
|
T | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+46T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574982 | ||||||
| chr9:79574993
|
A | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+57A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574993 | ||||||
| chr9:79574999
|
T | C | 254 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(251): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.207+63T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79574999 | ||||||
| chr9:79575015
|
G | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+79G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79575015 | ||||||
| chr9:79575018
|
T | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+82T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79575018 | ||||||
| chr9:79575021
|
A | AAGAATCA others(15): Show |
1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+88_207+89insAT others(20): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr9 | 79575021 | |||||
| chr9:79575047
|
T | G | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+111T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79575047 | ||||||
| chr9:79575077
|
A | G | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+141A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79575077 | ||||||
| chr9:79575090
|
T | A | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+154T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79575090 | ||||||
| chr9:79575095
|
G | C | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+159G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79575095 | ||||||
| chr9:79575127
|
G | T | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.207+191G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79575127 | ||||||
| chr9:79575191
|
C | T | 1 | a0002c0009t0003g0245 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.207+255C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79575191 | ||||||
| chr9:79575201
|
T | G | 1 | a0001c0001t0002g0022 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.207+265T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79575201 | ||||||
| chr9:79575202
|
A | G | 1 | a0001c0001t0003g0244 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.207+266A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 3/19 | chr9 | 79575202 | ||||||
| chr9:79576246
|
G | A | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.252+69G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79576246 | ||||||
| chr9:79576388
|
A | G | 1 | a0001c0001t0002g0243 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.252+211A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79576388 | ||||||
| chr9:79576563
|
G | A | 1 | a0001c0001t0019g0023 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.252+386G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79576563 | ||||||
| chr9:79576822
|
T | A | 8 | a0001c0001t0002g0021a0001c0001t0003g0028a0001c0003t0003g0025others(5): Show | 8 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+645T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79576822 | ||||||
| chr9:79576937
|
C | G | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.252+760C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79576937 | ||||||
| chr9:79577370
|
G | A | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.252+1193G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79577370 | ||||||
| chr9:79577443
|
C | T | 99 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0022others(96): Show | 101 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.252+1266C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79577443 | ||||||
| chr9:79577809
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.252+1632A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79577809 | ||||||
| chr9:79578054
|
A | G | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.252+1877A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79578054 | ||||||
| chr9:79578169
|
C | G | 1 | a0001c0001t0001g0012 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.252+1992C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79578169 | ||||||
| chr9:79578324
|
C | T | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.252+2147C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79578324 | ||||||
| chr9:79578437
|
T | A | 1 | a0001c0001t0007g0029 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.252+2260T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79578437 | ||||||
| chr9:79578509
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.252+2332C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79578509 | ||||||
| chr9:79578510
|
T | G | 1 | a0001c0001t0001g0149 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.252+2333T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79578510 | ||||||
| chr9:79578556
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.252+2379C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79578556 | ||||||
| chr9:79578568
|
T | G | 40 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(37): Show | 41 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.252+2391T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79578568 | ||||||
| chr9:79578580
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.252+2403T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79578580 | ||||||
| chr9:79578582
|
TGTGGTGC others(3): Show |
T | 1 | a0001c0001t0001g0149 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.252+2406_252+2415d others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79578582 | ||||||
| chr9:79578675
|
A | G | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.252+2498A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79578675 | ||||||
| chr9:79578831
|
A | AT | 148 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0021others(145): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.252+2668dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79578831 | |||||
| chr9:79578937
|
T | C | 40 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(37): Show | 41 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.252+2760T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79578937 | ||||||
| chr9:79578942
|
C | CA | 11 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(8): Show | 11 | HG01069.hp2 HG01074.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.252+2779dupA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79578942 | |||||
| chr9:79578942
|
CA | C | 39 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(36): Show | 40 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.252+2779delA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79578942 | |||||
| chr9:79578977
|
T | C | 1 | a0001c0001t0002g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.252+2800T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79578977 | ||||||
| chr9:79579048
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.252+2871T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79579048 | ||||||
| chr9:79579195
|
T | C | 1 | a0001c0001t0007g0029 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.252+3018T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79579195 | ||||||
| chr9:79579347
|
A | G | 1 | a0001c0001t0002g0241 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.252+3170A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79579347 | ||||||
| chr9:79579680
|
G | A | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.252+3503G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79579680 | ||||||
| chr9:79579682
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0141a0001c0001t0003g0239others(1): Show | 4 | HG02486.hp2 HG02965.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+3505A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79579682 | ||||||
| chr9:79580000
|
G | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 7 | HG00639.hp2 HG00642.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+3823G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79580000 | ||||||
| chr9:79580096
|
G | C | 1 | a0001c0001t0001g0061 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.252+3919G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79580096 | ||||||
| chr9:79580214
|
C | T | 1 | a0001c0001t0001g0140 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.252+4037C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79580214 | ||||||
| chr9:79580237
|
G | A | 1 | a0001c0001t0002g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.252+4060G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79580237 | ||||||
| chr9:79580264
|
G | T | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.252+4087G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79580264 | ||||||
| chr9:79580269
|
G | A | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.252+4092G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79580269 | ||||||
| chr9:79580405
|
C | G | 1 | a0001c0001t0001g0138 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.252+4228C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79580405 | ||||||
| chr9:79580651
|
A | G | 7 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.252+4474A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79580651 | ||||||
| chr9:79580684
|
C | T | 7 | a0001c0001t0003g0028a0001c0003t0003g0025a0001c0003t0003g0026others(4): Show | 7 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.252+4507C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79580684 | ||||||
| chr9:79580698
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.252+4521A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79580698 | ||||||
| chr9:79580715
|
CT | C | 8 | a0001c0001t0003g0028a0001c0001t0004g0160a0001c0003t0003g0025others(5): Show | 8 | HG01074.hp2 HG01081.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+4549delT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79580715 | |||||
| chr9:79580754
|
A | C | 1 | a0001c0001t0002g0152 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.252+4577A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79580754 | ||||||
| chr9:79581042
|
A | G | 4 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0237others(1): Show | 4 | HG02055.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+4865A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79581042 | ||||||
| chr9:79581059
|
A | G | 6 | a0001c0001t0002g0003a0001c0001t0002g0152a0001c0001t0002g0233others(3): Show | 7 | HG00099.hp2 HG00140.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.252+4882A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79581059 | ||||||
| chr9:79581191
|
G | T | 1 | a0001c0001t0001g0137 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.252+5014G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79581191 | ||||||
| chr9:79581323
|
C | T | 7 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.252+5146C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79581323 | ||||||
| chr9:79581682
|
A | T | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.252+5505A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79581682 | ||||||
| chr9:79581742
|
A | G | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.252+5565A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79581742 | ||||||
| chr9:79581821
|
G | A | 1 | a0001c0001t0002g0161 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.252+5644G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79581821 | ||||||
| chr9:79582464
|
A | G | 2 | a0001c0001t0002g0231a0001c0001t0019g0023 | 2 | HG03453.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.252+6287A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79582464 | ||||||
| chr9:79582548
|
C | G | 3 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0020 | 3 | HG02717.hp1 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.252+6371C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79582548 | ||||||
| chr9:79582639
|
C | CT | 52 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(49): Show | 53 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.252+6479dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79582639 | |||||
| chr9:79582639
|
CT | C | 60 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(57): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.252+6479delT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79582639 | |||||
| chr9:79582820
|
G | A | 112 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0021others(109): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.252+6643G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79582820 | ||||||
| chr9:79582884
|
A | T | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.252+6707A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79582884 | ||||||
| chr9:79582905
|
A | G | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | HG01346.hp1 NA18954.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+6728A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79582905 | ||||||
| chr9:79583046
|
G | A | 2 | a0001c0001t0002g0152a0001c0001t0003g0232 | 2 | HG00140.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.252+6869G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79583046 | ||||||
| chr9:79583438
|
C | T | 40 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(37): Show | 41 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.252+7261C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79583438 | ||||||
| chr9:79583473
|
T | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | NA19000.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.252+7296T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79583473 | ||||||
| chr9:79583476
|
G | A | 9 | a0001c0001t0002g0021a0001c0001t0003g0028a0001c0001t0011g0013others(6): Show | 9 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.252+7299G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79583476 | ||||||
| chr9:79583657
|
T | G | 6 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(3): Show | 6 | HG02572.hp1 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+7480T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79583657 | ||||||
| chr9:79584017
|
A | G | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.252+7840A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79584017 | ||||||
| chr9:79584072
|
G | A | 2 | a0001c0001t0008g0069a0001c0001t0008g0070 | 2 | HG01167.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.252+7895G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79584072 | ||||||
| chr9:79584274
|
T | G | 2 | a0001c0001t0008g0069a0001c0001t0008g0070 | 2 | HG01167.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.252+8097T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79584274 | ||||||
| chr9:79584483
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.252+8306C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79584483 | ||||||
| chr9:79584834
|
A | G | 11 | a0001c0001t0002g0126a0001c0001t0002g0145a0001c0001t0002g0146others(8): Show | 11 | HG00673.hp2 NA18943.hp1 NA18957.hp2 others(8): Show |
intron_variant | MODIFIER | c.252+8657A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79584834 | ||||||
| chr9:79585096
|
G | C | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.252+8919G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79585096 | ||||||
| chr9:79585173
|
A | T | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.252+8996A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79585173 | ||||||
| chr9:79585202
|
A | C | 158 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0021others(155): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.252+9025A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79585202 | ||||||
| chr9:79585338
|
T | C | 158 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0021others(155): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.252+9161T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79585338 | ||||||
| chr9:79585509
|
T | G | 1 | a0001c0001t0003g0030 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.252+9332T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79585509 | ||||||
| chr9:79585593
|
T | G | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.252+9416T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79585593 | ||||||
| chr9:79585662
|
A | AT | 157 | a0001c0001t0001g0125a0001c0001t0002g0002a0001c0001t0002g0003others(154): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.252+9496dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79585662 | |||||
| chr9:79585703
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.252+9526T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79585703 | ||||||
| chr9:79585757
|
A | G | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.252+9580A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79585757 | ||||||
| chr9:79585790
|
A | G | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.252+9613A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79585790 | ||||||
| chr9:79585938
|
T | G | 2 | a0001c0001t0003g0239a0001c0007t0002g0240 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.252+9761T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79585938 | ||||||
| chr9:79585997
|
T | C | 8 | a0001c0001t0002g0021a0001c0001t0003g0028a0001c0003t0003g0025others(5): Show | 8 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+9820T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79585997 | ||||||
| chr9:79586101
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.252+9924C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79586101 | ||||||
| chr9:79586186
|
T | C | 158 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0021others(155): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.252+10009T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79586186 | ||||||
| chr9:79586196
|
C | T | 55 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0022others(52): Show | 57 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.252+10019C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79586196 | ||||||
| chr9:79586843
|
G | T | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.252+10666G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79586843 | ||||||
| chr9:79587086
|
A | C | 1 | a0001c0001t0001g0123 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.252+10909A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79587086 | ||||||
| chr9:79587089
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.252+10912A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79587089 | ||||||
| chr9:79587216
|
A | C | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.252+11039A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79587216 | ||||||
| chr9:79587267
|
G | A | 1 | a0001c0001t0002g0249 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.252+11090G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79587267 | ||||||
| chr9:79587301
|
C | A | 11 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(8): Show | 11 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.252+11124C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79587301 | ||||||
| chr9:79587308
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.252+11131A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79587308 | ||||||
| chr9:79587423
|
T | C | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.252+11246T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79587423 | ||||||
| chr9:79587432
|
T | C | 4 | a0001c0001t0004g0224a0001c0001t0004g0225a0001c0001t0004g0226others(1): Show | 4 | HG01255.hp2 HG02622.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+11255T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79587432 | ||||||
| chr9:79587501
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.252+11324C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79587501 | ||||||
| chr9:79587545
|
T | G | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.252+11368T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79587545 | ||||||
| chr9:79588135
|
C | CGT | 6 | a0001c0001t0001g0012a0001c0001t0001g0060a0001c0001t0001g0073others(3): Show | 6 | HG00280.hp1 HG00741.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.252+11985_252+1198 others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79588135 | |||||
| chr9:79588135
|
C | CGTGTGT | 59 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0142others(56): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.252+11981_252+1198 others(10): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79588135 | |||||
| chr9:79588135
|
C | CGTGTGTG others(1): Show |
40 | a0001c0001t0002g0022a0001c0001t0002g0126a0001c0001t0002g0159others(37): Show | 40 | HG00558.hp1 HG00733.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.252+11979_252+1198 others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79588135 | |||||
| chr9:79588135
|
C | CGTGTGTG others(3): Show |
15 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197others(12): Show | 16 | HG01106.hp1 HG01192.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.252+11977_252+1198 others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79588135 | |||||
| chr9:79588135
|
C | CGTGTGTG others(5): Show |
3 | a0001c0001t0003g0054a0001c0003t0003g0025a0001c0008t0002g0024 | 3 | HG01074.hp2 HG01516.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.252+11975_252+1198 others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79588135 | |||||
| chr9:79588135
|
C | CGTGTGTG others(7): Show |
2 | a0001c0001t0002g0021a0001c0001t0003g0248 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.252+11973_252+1198 others(18): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79588135 | |||||
| chr9:79588135
|
C | CGTGTGTG others(9): Show |
2 | a0001c0005t0003g0253a0001c0005t0003g0254 | 2 | HG01943.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.252+11971_252+1198 others(20): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79588135 | |||||
| chr9:79588135
|
C | CGTGTGTG others(11): Show |
7 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(4): Show | 7 | HG02074.hp2 HG02717.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+11969_252+1198 others(22): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79588135 | |||||
| chr9:79588135
|
C | CGTGTGTG others(13): Show |
17 | a0001c0001t0003g0018a0001c0001t0003g0030a0001c0001t0003g0031others(14): Show | 17 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.252+11967_252+1198 others(24): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79588135 | |||||
| chr9:79588135
|
C | CGTGTGTG others(15): Show |
9 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(6): Show | 9 | HG01346.hp2 HG02083.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.252+11965_252+1198 others(26): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79588135 | |||||
| chr9:79588135
|
C | CGTGTGTG others(17): Show |
2 | a0001c0001t0003g0032a0002c0009t0003g0245 | 2 | HG03471.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.252+11963_252+1198 others(28): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79588135 | |||||
| chr9:79588209
|
G | A | 8 | a0001c0001t0002g0021a0001c0001t0003g0028a0001c0003t0003g0025others(5): Show | 8 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+12032G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79588209 | ||||||
| chr9:79588427
|
G | A | 6 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0002g0200others(3): Show | 6 | HG01192.hp2 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.252+12250G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79588427 | ||||||
| chr9:79589019
|
T | G | 12 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(9): Show | 12 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.252+12842T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79589019 | ||||||
| chr9:79589032
|
G | C | 117 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0021others(114): Show | 119 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.252+12855G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79589032 | ||||||
| chr9:79589319
|
T | G | 1 | a0001c0001t0003g0018 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.252+13142T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79589319 | ||||||
| chr9:79589369
|
A | C | 1 | a0001c0001t0002g0190 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.252+13192A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79589369 | ||||||
| chr9:79589403
|
A | G | 19 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(16): Show | 19 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.252+13226A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79589403 | ||||||
| chr9:79589429
|
C | T | 1 | a0001c0001t0004g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.252+13252C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79589429 | ||||||
| chr9:79589430
|
G | A | 2 | a0001c0001t0003g0028a0003c0006t0003g0027 | 2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.252+13253G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79589430 | ||||||
| chr9:79589494
|
C | T | 3 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0008t0002g0024 | 3 | HG01074.hp2 HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.252+13317C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79589494 | ||||||
| chr9:79589519
|
A | G | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.252+13342A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79589519 | ||||||
| chr9:79589793
|
A | G | 1 | a0001c0001t0014g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.252+13616A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79589793 | ||||||
| chr9:79589899
|
G | T | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.252+13722G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79589899 | ||||||
| chr9:79589998
|
T | A | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.252+13821T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79589998 | ||||||
| chr9:79590006
|
C | T | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG00621.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.252+13829C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79590006 | ||||||
| chr9:79590045
|
C | G | 1 | a0001c0001t0002g0189 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.252+13868C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79590045 | ||||||
| chr9:79590112
|
G | A | 7 | a0001c0001t0001g0075a0001c0001t0001g0130a0001c0001t0001g0131others(4): Show | 7 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.252+13935G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79590112 | ||||||
| chr9:79590139
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.252+13962T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79590139 | ||||||
| chr9:79590318
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.252+14141A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79590318 | ||||||
| chr9:79590632
|
T | C | 11 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(8): Show | 11 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.252+14455T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79590632 | ||||||
| chr9:79590809
|
G | A | 3 | a0001c0001t0002g0191a0001c0001t0002g0192a0001c0001t0002g0193 | 3 | NA18943.hp1 NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.252+14632G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79590809 | ||||||
| chr9:79591024
|
A | C | 8 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG02572.hp1 HG02647.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+14847A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79591024 | ||||||
| chr9:79591249
|
C | T | 1 | a0001c0001t0004g0226 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.252+15072C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79591249 | ||||||
| chr9:79591715
|
G | A | 113 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0021others(110): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.252+15538G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79591715 | ||||||
| chr9:79591799
|
T | C | 1 | a0001c0001t0003g0015 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.252+15622T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79591799 | ||||||
| chr9:79591969
|
C | T | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.252+15792C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79591969 | ||||||
| chr9:79592004
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.252+15827C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592004 | ||||||
| chr9:79592092
|
T | TTTCTTC | 5 | a0001c0001t0003g0028a0001c0003t0003g0025a0001c0003t0003g0026others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+15930_252+1593 others(10): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592092 | |||||
| chr9:79592104
|
CTTCTTCT | C | 3 | a0001c0001t0003g0034a0001c0001t0003g0049a0001c0001t0003g0252 | 3 | HG00140.hp1 HG00639.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.252+15950_252+1595 others(11): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592104 | |||||
| chr9:79592118
|
TTTCTTCT others(3): Show |
T | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.252+15957_252+1596 others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592118 | |||||
| chr9:79592128
|
C | CTTCTTCT | 3 | a0001c0001t0002g0002a0001c0001t0002g0187a0001c0001t0003g0188 | 4 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+15974_252+1598 others(11): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592128 | |||||
| chr9:79592159
|
T | C | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.252+15982T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592159 | ||||||
| chr9:79592165
|
T | C | 2 | a0001c0001t0002g0170a0001c0001t0011g0013 | 2 | HG01257.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.252+15988T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592165 | ||||||
| chr9:79592176
|
C | A | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.252+15999C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592176 | ||||||
| chr9:79592177
|
C | T | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.252+16000C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592177 | ||||||
| chr9:79592183
|
C | CTCT | 3 | a0001c0001t0001g0110a0001c0001t0001g0122a0001c0001t0009g0109 | 3 | HG00423.hp1 NA18963.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.252+16036_252+1603 others(7): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592183 | |||||
| chr9:79592183
|
C | CTCTTCTT others(2): Show |
11 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(8): Show | 11 | HG00558.hp2 HG00642.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.252+16030_252+1603 others(13): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592183 | |||||
| chr9:79592183
|
C | CTCTTCTT others(5): Show |
2 | a0001c0001t0001g0148a0001c0001t0002g0147 | 2 | HG01106.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.252+16027_252+1603 others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592183 | |||||
| chr9:79592183
|
C | CTCTTCTT others(8): Show |
2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG01192.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.252+16024_252+1603 others(19): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592183 | |||||
| chr9:79592183
|
C | T | 3 | a0001c0001t0002g0151a0001c0001t0002g0170a0001c0001t0011g0013 | 3 | HG01257.hp1 HG02818.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.252+16006C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592183 | ||||||
| chr9:79592183
|
CTCT | C | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0124others(2): Show | 5 | HG01433.hp1 HG02683.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.252+16036_252+1603 others(7): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592183 | |||||
| chr9:79592183
|
CTCTTCT | C | 30 | a0001c0001t0001g0141a0001c0001t0003g0001a0001c0001t0003g0015others(27): Show | 31 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.252+16033_252+1603 others(10): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592183 | |||||
| chr9:79592183
|
CTCTTCTT others(2): Show |
C | 9 | a0001c0001t0003g0016a0001c0001t0003g0032a0001c0001t0003g0035others(6): Show | 9 | HG02074.hp2 HG03239.hp1 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.252+16030_252+1603 others(13): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592183 | |||||
| chr9:79592183
|
CTCTTCTT others(5): Show |
C | 1 | a0001c0001t0003g0255 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.252+16027_252+1603 others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592183 | |||||
| chr9:79592189
|
T | C | 5 | a0001c0001t0003g0028a0001c0001t0003g0042a0001c0001t0003g0248others(2): Show | 5 | HG02486.hp1 HG02615.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.252+16012T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592189 | ||||||
| chr9:79592201
|
T | C | 1 | a0001c0001t0002g0151 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.252+16024T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592201 | ||||||
| chr9:79592204
|
T | C | 1 | a0001c0001t0003g0232 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.252+16027T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592204 | ||||||
| chr9:79592207
|
T | C | 7 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0162others(4): Show | 7 | HG01257.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+16030T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592207 | ||||||
| chr9:79592210
|
T | C | 2 | a0001c0001t0002g0171a0001c0001t0003g0153 | 2 | HG03540.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.252+16033T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592210 | ||||||
| chr9:79592213
|
T | C | 89 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0022others(86): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.252+16036T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592213 | ||||||
| chr9:79592216
|
C | T | 100 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0021others(97): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.252+16039C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592216 | ||||||
| chr9:79592227
|
CTT | C | 7 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0162others(4): Show | 7 | HG01257.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+16051_252+1605 others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592227 | ||||||
| chr9:79592229
|
T | TC | 3 | a0001c0001t0002g0171a0001c0001t0003g0153a0001c0004t0004g0250 | 3 | HG03130.hp1 HG03540.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.252+16053dupC | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592229 | |||||
| chr9:79592229
|
T | TCTTC | 87 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0022others(84): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.252+16053_252+1605 others(8): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592229 | |||||
| chr9:79592229
|
T | TCTTCCTC others(3): Show |
2 | a0001c0003t0003g0026a0001c0008t0002g0024 | 2 | HG01074.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.252+16056_252+1605 others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592229 | |||||
| chr9:79592229
|
T | TCTTCTTC | 11 | a0001c0001t0002g0143a0001c0001t0002g0144a0001c0001t0002g0203others(8): Show | 11 | HG01081.hp2 HG01255.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.252+16058_252+1606 others(11): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592229 | |||||
| chr9:79592229
|
T | TCTTCTTC others(6): Show |
1 | a0001c0003t0003g0025 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.252+16061_252+1606 others(17): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592229 | |||||
| chr9:79592266
|
C | T | 30 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(27): Show | 30 | HG00733.hp2 HG01109.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.252+16089C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592266 | ||||||
| chr9:79592275
|
CT | C | 13 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0204others(10): Show | 13 | HG00733.hp2 HG02717.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.252+16115delT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79592275 | |||||
| chr9:79592436
|
C | T | 40 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(37): Show | 41 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.252+16259C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592436 | ||||||
| chr9:79592608
|
G | T | 1 | a0001c0001t0002g0163 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.252+16431G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592608 | ||||||
| chr9:79592729
|
T | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.252+16552T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592729 | ||||||
| chr9:79592765
|
T | C | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.252+16588T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592765 | ||||||
| chr9:79592879
|
C | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 7 | HG00639.hp2 HG00642.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+16702C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79592879 | ||||||
| chr9:79593033
|
A | G | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.252+16856A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79593033 | ||||||
| chr9:79593215
|
G | C | 1 | a0001c0001t0004g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.252+17038G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79593215 | ||||||
| chr9:79593274
|
A | C | 1 | a0001c0001t0003g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.252+17097A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79593274 | ||||||
| chr9:79593425
|
A | G | 5 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0004t0004g0004others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+17248A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79593425 | ||||||
| chr9:79593490
|
A | G | 3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197 | 3 | HG01891.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.252+17313A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79593490 | ||||||
| chr9:79593681
|
T | C | 4 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0221others(1): Show | 4 | HG02027.hp2 HG02074.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+17504T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79593681 | ||||||
| chr9:79593779
|
T | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.252+17602T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79593779 | ||||||
| chr9:79593831
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.252+17654A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79593831 | ||||||
| chr9:79593909
|
A | G | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.252+17732A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79593909 | ||||||
| chr9:79594303
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.252+18126A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79594303 | ||||||
| chr9:79594520
|
T | G | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.253-18136T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79594520 | ||||||
| chr9:79594684
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.253-17972C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79594684 | ||||||
| chr9:79594765
|
G | T | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.253-17891G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79594765 | ||||||
| chr9:79594820
|
C | T | 3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197 | 3 | HG01891.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.253-17836C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79594820 | ||||||
| chr9:79594921
|
G | A | 3 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0008t0002g0024 | 3 | HG01074.hp2 HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.253-17735G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79594921 | ||||||
| chr9:79595168
|
C | T | 30 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(27): Show | 30 | HG00733.hp2 HG01109.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.253-17488C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79595168 | ||||||
| chr9:79595555
|
T | A | 1 | a0001c0001t0002g0221 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.253-17101T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79595555 | ||||||
| chr9:79595637
|
G | T | 19 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(16): Show | 19 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.253-17019G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79595637 | ||||||
| chr9:79595682
|
A | G | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.253-16974A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79595682 | ||||||
| chr9:79595790
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.253-16866T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79595790 | ||||||
| chr9:79595849
|
C | CT | 8 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0108others(5): Show | 8 | HG00621.hp1 HG01346.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.253-16790dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79595849 | |||||
| chr9:79595849
|
CTTTTTT | C | 12 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(9): Show | 13 | HG02109.hp2 HG02647.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-16795_253-1679 others(10): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79595849 | |||||
| chr9:79595932
|
T | C | 1 | a0001c0001t0003g0048 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.253-16724T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79595932 | ||||||
| chr9:79595981
|
G | T | 55 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0022others(52): Show | 57 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.253-16675G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79595981 | ||||||
| chr9:79596036
|
C | T | 9 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(6): Show | 9 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-16620C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79596036 | ||||||
| chr9:79596036
|
CAG | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.253-16619_253-1661 others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79596036 | ||||||
| chr9:79596037
|
A | G | 17 | a0001c0001t0001g0075a0001c0001t0001g0130a0001c0001t0001g0131others(14): Show | 17 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.253-16619A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79596037 | ||||||
| chr9:79596081
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.253-16575C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79596081 | ||||||
| chr9:79596087
|
C | T | 1 | a0001c0001t0003g0255 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.253-16569C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79596087 | ||||||
| chr9:79596136
|
G | A | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.253-16520G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79596136 | ||||||
| chr9:79596413
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.253-16243G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79596413 | ||||||
| chr9:79596569
|
A | G | 4 | a0001c0001t0002g0184a0001c0001t0002g0185a0001c0001t0002g0186others(1): Show | 4 | HG01074.hp1 NA18953.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-16087A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79596569 | ||||||
| chr9:79596630
|
GAGAC | G | 40 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(37): Show | 41 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.253-16022_253-1601 others(8): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79596630 | |||||
| chr9:79596663
|
C | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0138 | 3 | HG00642.hp2 HG01192.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.253-15993C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79596663 | ||||||
| chr9:79596866
|
G | T | 2 | a0001c0001t0003g0019a0001c0001t0003g0020 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.253-15790G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79596866 | ||||||
| chr9:79596970
|
T | C | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.253-15686T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79596970 | ||||||
| chr9:79597081
|
A | G | 9 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(6): Show | 9 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.253-15575A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79597081 | ||||||
| chr9:79597134
|
C | T | 1 | a0001c0001t0003g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.253-15522C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79597134 | ||||||
| chr9:79597179
|
T | G | 148 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0022others(145): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.253-15477T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79597179 | ||||||
| chr9:79597329
|
T | C | 5 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0004t0004g0004others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-15327T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79597329 | ||||||
| chr9:79597425
|
C | T | 1 | a0001c0001t0002g0241 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.253-15231C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79597425 | ||||||
| chr9:79597747
|
T | C | 1 | a0001c0001t0003g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.253-14909T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79597747 | ||||||
| chr9:79597930
|
C | T | 1 | a0001c0007t0002g0240 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.253-14726C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79597930 | ||||||
| chr9:79598015
|
G | A | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.253-14641G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79598015 | ||||||
| chr9:79598020
|
C | T | 7 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(4): Show | 7 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-14636C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79598020 | ||||||
| chr9:79598075
|
G | GA | 23 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0058others(20): Show | 23 | HG00423.hp1 HG00621.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.253-14558dupA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79598075 | |||||
| chr9:79598075
|
GA | G | 30 | a0001c0001t0001g0106a0001c0001t0001g0118a0001c0001t0002g0198others(27): Show | 30 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.253-14558delA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79598075 | |||||
| chr9:79598078
|
A | G | 1 | a0003c0006t0003g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.253-14578A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79598078 | ||||||
| chr9:79598110
|
G | A | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.253-14546G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79598110 | ||||||
| chr9:79598126
|
G | A | 3 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0008t0002g0024 | 3 | HG01074.hp2 HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.253-14530G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79598126 | ||||||
| chr9:79598131
|
C | G | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.253-14525C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79598131 | ||||||
| chr9:79598248
|
C | CA | 5 | a0001c0001t0002g0021a0001c0001t0003g0235a0001c0001t0003g0236others(2): Show | 5 | HG02055.hp2 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-14394dupA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79598248 | |||||
| chr9:79598524
|
A | G | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.253-14132A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79598524 | ||||||
| chr9:79598644
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.253-14012A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79598644 | ||||||
| chr9:79598659
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.253-13997A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79598659 | ||||||
| chr9:79598702
|
T | A | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.253-13954T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79598702 | ||||||
| chr9:79598713
|
A | T | 1 | a0001c0001t0001g0148 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.253-13943A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79598713 | ||||||
| chr9:79598790
|
G | C | 2 | a0001c0004t0004g0004a0001c0004t0004g0250 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.253-13866G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79598790 | ||||||
| chr9:79598866
|
G | C | 5 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0004t0004g0004others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-13790G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79598866 | ||||||
| chr9:79598921
|
A | G | 2 | a0001c0001t0003g0239a0001c0007t0002g0240 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.253-13735A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79598921 | ||||||
| chr9:79599197
|
C | G | 5 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0004t0004g0004others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-13459C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79599197 | ||||||
| chr9:79599245
|
T | C | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.253-13411T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79599245 | ||||||
| chr9:79599398
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00639.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.253-13258T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79599398 | ||||||
| chr9:79599721
|
T | C | 1 | a0001c0001t0003g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.253-12935T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79599721 | ||||||
| chr9:79599952
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.253-12704T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79599952 | ||||||
| chr9:79600400
|
C | G | 3 | a0001c0001t0002g0022a0001c0001t0002g0171a0001c0001t0002g0183 | 3 | NA18961.hp2 NA18983.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.253-12256C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79600400 | ||||||
| chr9:79600405
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.253-12251A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79600405 | ||||||
| chr9:79600416
|
G | A | 5 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0004t0004g0004others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-12240G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79600416 | ||||||
| chr9:79600715
|
G | A | 5 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0004t0004g0004others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-11941G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79600715 | ||||||
| chr9:79600720
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.253-11936C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79600720 | ||||||
| chr9:79600744
|
C | T | 9 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(6): Show | 9 | HG01257.hp2 HG01258.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.253-11912C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79600744 | ||||||
| chr9:79600765
|
T | C | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.253-11891T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79600765 | ||||||
| chr9:79600997
|
C | T | 45 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0022others(42): Show | 47 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.253-11659C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79600997 | ||||||
| chr9:79601252
|
GTATCCTA others(12): Show |
G | 1 | a0001c0001t0001g0079 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.253-11403_253-1138 others(23): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79601252 | ||||||
| chr9:79601471
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.253-11185A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79601471 | ||||||
| chr9:79601654
|
T | C | 5 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0004t0004g0004others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-11002T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79601654 | ||||||
| chr9:79601856
|
C | T | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.253-10800C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79601856 | ||||||
| chr9:79602147
|
T | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.253-10509T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79602147 | ||||||
| chr9:79602456
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.253-10200C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79602456 | ||||||
| chr9:79602539
|
C | T | 103 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0022others(100): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.253-10117C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79602539 | ||||||
| chr9:79602595
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.253-10061G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79602595 | ||||||
| chr9:79602732
|
C | T | 40 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(37): Show | 41 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.253-9924C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79602732 | ||||||
| chr9:79602772
|
T | A | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.253-9884T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79602772 | ||||||
| chr9:79602830
|
C | CTGAGCAA others(7): Show |
1 | a0001c0001t0001g0110 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.253-9822_253-9809d others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79602830 | |||||
| chr9:79602955
|
C | G | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.253-9701C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79602955 | ||||||
| chr9:79603138
|
C | T | 9 | a0001c0001t0001g0075a0001c0001t0001g0101a0001c0001t0001g0102others(6): Show | 9 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.253-9518C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79603138 | ||||||
| chr9:79603412
|
G | A | 1 | a0003c0006t0003g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.253-9244G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79603412 | ||||||
| chr9:79603515
|
G | A | 1 | a0001c0001t0002g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.253-9141G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79603515 | ||||||
| chr9:79603693
|
C | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.253-8963C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79603693 | ||||||
| chr9:79603727
|
G | T | 3 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0008t0002g0024 | 3 | HG01074.hp2 HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.253-8929G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79603727 | ||||||
| chr9:79603780
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.253-8876A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79603780 | ||||||
| chr9:79604006
|
A | C | 2 | a0001c0001t0003g0054a0001c0001t0003g0056 | 2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.253-8650A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79604006 | ||||||
| chr9:79604073
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.253-8583G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79604073 | ||||||
| chr9:79604252
|
G | A | 1 | a0001c0001t0002g0249 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.253-8404G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79604252 | ||||||
| chr9:79604391
|
A | T | 1 | a0001c0004t0004g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.253-8265A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79604391 | ||||||
| chr9:79604591
|
G | T | 1 | a0001c0001t0003g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.253-8065G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79604591 | ||||||
| chr9:79604709
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.253-7947G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79604709 | ||||||
| chr9:79605006
|
G | A | 3 | a0001c0001t0002g0002a0001c0001t0002g0187a0001c0001t0003g0188 | 4 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-7650G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79605006 | ||||||
| chr9:79605230
|
G | C | 103 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0022others(100): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.253-7426G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79605230 | ||||||
| chr9:79605317
|
G | A | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.253-7339G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79605317 | ||||||
| chr9:79605850
|
T | C | 1 | a0001c0001t0002g0241 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.253-6806T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79605850 | ||||||
| chr9:79606170
|
A | G | 3 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0008t0002g0024 | 3 | HG01074.hp2 HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.253-6486A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79606170 | ||||||
| chr9:79606187
|
G | GT | 34 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0061others(31): Show | 35 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.253-6431dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
G | GTT | 30 | a0001c0001t0001g0058a0001c0001t0001g0068a0001c0001t0001g0092others(27): Show | 30 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.253-6432_253-6431d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
G | GTTT | 14 | a0001c0001t0001g0097a0001c0001t0001g0131a0001c0001t0001g0132others(11): Show | 14 | HG00741.hp1 HG01106.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.253-6433_253-6431d others(5): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
G | GTTTT | 12 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0075others(9): Show | 12 | HG00423.hp1 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.253-6434_253-6431d others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
G | GTTTTT | 11 | a0001c0001t0001g0011a0001c0001t0001g0099a0001c0001t0001g0139others(8): Show | 11 | HG00673.hp2 HG02451.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.253-6435_253-6431d others(7): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
G | GTTTTTTT | 6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0008others(3): Show | 6 | HG00639.hp2 HG00642.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-6437_253-6431d others(9): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
G | GTTTTTTT others(1): Show |
5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(2): Show | 5 | HG00741.hp2 HG01168.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-6438_253-6431d others(10): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
G | GTTTTTTT others(3): Show |
5 | a0001c0001t0001g0121a0001c0001t0002g0196a0001c0001t0002g0231others(2): Show | 5 | HG02155.hp2 HG03130.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.253-6440_253-6431d others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
G | GTTTTTTT others(4): Show |
4 | a0001c0001t0001g0120a0001c0001t0001g0138a0001c0001t0002g0164others(1): Show | 4 | HG00621.hp2 HG01192.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-6441_253-6431d others(13): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
G | GTTTTTTT others(5): Show |
7 | a0001c0001t0002g0022a0001c0001t0002g0162a0001c0001t0002g0163others(4): Show | 7 | HG00280.hp2 HG01255.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-6442_253-6431d others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
G | GTTTTTTT others(6): Show |
1 | a0001c0001t0001g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.253-6443_253-6431d others(15): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
G | GTTTTTTT others(7): Show |
3 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0002g0182 | 3 | HG01361.hp1 HG02723.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.253-6444_253-6431d others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
G | GTTTTTTT others(8): Show |
1 | a0001c0001t0001g0129 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.253-6445_253-6431d others(17): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
G | GTTTTTTT others(11): Show |
1 | a0001c0001t0003g0158 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.253-6448_253-6431d others(20): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
G | GTTTTTTT others(14): Show |
2 | a0001c0001t0001g0136a0001c0001t0002g0183 | 2 | NA18954.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.253-6451_253-6431d others(23): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
GT | G | 12 | a0001c0001t0001g0086a0001c0001t0002g0159a0001c0001t0002g0187others(9): Show | 12 | HG01069.hp1 HG01074.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.253-6431delT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
GTT | G | 12 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0002g0200others(9): Show | 12 | HG01192.hp2 HG01516.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.253-6432_253-6431d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
GTTTTTTT others(3): Show |
G | 9 | a0001c0001t0001g0060a0001c0001t0001g0110a0001c0001t0003g0018others(6): Show | 9 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.253-6440_253-6431d others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
GTTTTTTT others(4): Show |
G | 30 | a0001c0001t0001g0064a0001c0001t0001g0076a0001c0001t0003g0001others(27): Show | 31 | HG00423.hp2 HG01943.hp1 HG02074.hp2 others(28): Show |
intron_variant | MODIFIER | c.253-6441_253-6431d others(13): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
GTTTTTTT others(5): Show |
G | 4 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0004t0004g0250others(1): Show | 4 | HG01975.hp2 HG02083.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-6442_253-6431d others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
GTTTTTTT others(6): Show |
G | 8 | a0001c0001t0001g0079a0001c0001t0001g0083a0001c0001t0001g0085others(5): Show | 8 | HG00673.hp1 HG01256.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.253-6443_253-6431d others(15): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
GTTTTTTT others(7): Show |
G | 3 | a0001c0001t0002g0175a0001c0001t0003g0239a0001c0007t0002g0240 | 3 | HG02486.hp2 HG02965.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.253-6444_253-6431d others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
GTTTTTTT others(11): Show |
G | 1 | a0001c0001t0002g0212 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.253-6448_253-6431d others(20): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
GTTTTTTT others(12): Show |
G | 1 | a0001c0001t0002g0211 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.253-6449_253-6431d others(21): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
GTTTTTTT others(16): Show |
G | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.253-6453_253-6431d others(25): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606187
|
GTTTTTTT others(17): Show |
G | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0100 | 3 | NA18612.hp1 NA18939.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.253-6454_253-6431d others(26): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606187 | |||||
| chr9:79606201
|
T | G | 1 | a0001c0001t0001g0080 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.253-6455T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79606201 | ||||||
| chr9:79606237
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.253-6419G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79606237 | ||||||
| chr9:79606331
|
CT | C | 113 | a0001c0001t0001g0066a0001c0001t0001g0092a0001c0001t0002g0002others(110): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.253-6311delT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606331 | |||||
| chr9:79606373
|
G | GT | 16 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(13): Show | 16 | HG00558.hp2 HG00642.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.253-6267dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606373 | |||||
| chr9:79606373
|
GT | G | 141 | a0001c0001t0001g0075a0001c0001t0001g0086a0001c0001t0001g0110others(138): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.253-6267delT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606373 | |||||
| chr9:79606373
|
GTT | G | 13 | a0001c0001t0002g0168a0001c0001t0002g0217a0001c0001t0003g0028others(10): Show | 13 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-6268_253-6267d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79606373 | |||||
| chr9:79606375
|
T | G | 1 | a0002c0009t0003g0245 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.253-6281T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79606375 | ||||||
| chr9:79606376
|
T | G | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.253-6280T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79606376 | ||||||
| chr9:79606394
|
A | G | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.253-6262A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79606394 | ||||||
| chr9:79606404
|
T | G | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.253-6252T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79606404 | ||||||
| chr9:79606528
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.253-6128T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79606528 | ||||||
| chr9:79606694
|
A | G | 9 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(6): Show | 9 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-5962A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79606694 | ||||||
| chr9:79606707
|
C | A | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.253-5949C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79606707 | ||||||
| chr9:79606884
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.253-5772A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79606884 | ||||||
| chr9:79606971
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0016g0062 | 2 | NA18946.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.253-5685G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79606971 | ||||||
| chr9:79607144
|
A | T | 5 | a0001c0001t0003g0042a0001c0001t0003g0044a0001c0001t0003g0045others(2): Show | 5 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-5512A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79607144 | ||||||
| chr9:79607270
|
T | C | 1 | a0001c0001t0003g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.253-5386T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79607270 | ||||||
| chr9:79607355
|
G | A | 1 | a0001c0001t0002g0176 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.253-5301G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79607355 | ||||||
| chr9:79607722
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.253-4934T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79607722 | ||||||
| chr9:79607739
|
TCTGTTTT others(15): Show |
T | 36 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163others(33): Show | 36 | HG00733.hp2 HG01109.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.253-4884_253-4863d others(24): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79607739 | |||||
| chr9:79607869
|
C | G | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.253-4787C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79607869 | ||||||
| chr9:79608053
|
C | G | 1 | a0001c0001t0002g0214 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.253-4603C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79608053 | ||||||
| chr9:79608187
|
A | G | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.253-4469A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79608187 | ||||||
| chr9:79608323
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.253-4333T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79608323 | ||||||
| chr9:79608492
|
A | C | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.253-4164A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79608492 | ||||||
| chr9:79608495
|
T | G | 1 | a0001c0001t0004g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.253-4161T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79608495 | ||||||
| chr9:79608701
|
A | C | 1 | a0001c0001t0001g0075 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.253-3955A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79608701 | ||||||
| chr9:79608742
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.253-3914C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79608742 | ||||||
| chr9:79608835
|
T | G | 1 | a0001c0001t0002g0198 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.253-3821T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79608835 | ||||||
| chr9:79609473
|
A | T | 7 | a0001c0001t0001g0076a0001c0001t0001g0093a0001c0001t0001g0098others(4): Show | 7 | HG00621.hp2 HG02155.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.253-3183A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79609473 | ||||||
| chr9:79609678
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.253-2978A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79609678 | ||||||
| chr9:79609678
|
A | G | 1 | a0001c0001t0005g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.253-2978A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79609678 | ||||||
| chr9:79609918
|
A | G | 1 | a0001c0001t0004g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.253-2738A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79609918 | ||||||
| chr9:79610133
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.253-2523A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79610133 | ||||||
| chr9:79610138
|
G | A | 108 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0022others(105): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.253-2518G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79610138 | ||||||
| chr9:79610322
|
T | G | 59 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0022others(56): Show | 61 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.253-2334T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79610322 | ||||||
| chr9:79610373
|
G | A | 4 | a0001c0001t0003g0001a0001c0001t0003g0054a0001c0001t0003g0055others(1): Show | 5 | HG02109.hp2 HG02723.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.253-2283G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79610373 | ||||||
| chr9:79610663
|
C | T | 5 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0004t0004g0004others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-1993C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79610663 | ||||||
| chr9:79610835
|
C | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.253-1821C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79610835 | ||||||
| chr9:79610870
|
G | T | 1 | a0001c0001t0002g0178 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.253-1786G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79610870 | ||||||
| chr9:79610924
|
A | G | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.253-1732A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79610924 | ||||||
| chr9:79610951
|
C | T | 5 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0004t0004g0004others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-1705C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79610951 | ||||||
| chr9:79610963
|
T | C | 3 | a0001c0001t0003g0034a0001c0001t0003g0049a0001c0001t0003g0252 | 3 | HG00140.hp1 HG00639.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.253-1693T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79610963 | ||||||
| chr9:79611199
|
T | C | 1 | a0001c0001t0003g0035 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.253-1457T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79611199 | ||||||
| chr9:79611526
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.253-1130A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79611526 | ||||||
| chr9:79611770
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.253-886G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79611770 | ||||||
| chr9:79611786
|
A | G | 37 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163others(34): Show | 37 | HG00733.hp2 HG01109.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.253-870A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79611786 | ||||||
| chr9:79611837
|
T | TTACTGTA | 7 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(4): Show | 7 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.253-818_253-812dup others(7): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79611837 | |||||
| chr9:79611936
|
T | TA | 9 | a0001c0001t0001g0063a0001c0001t0001g0103a0001c0001t0001g0120others(6): Show | 9 | HG00621.hp2 HG02040.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.253-697dupA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79611936 | |||||
| chr9:79611936
|
TA | T | 51 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0002g0209others(48): Show | 51 | HG00140.hp1 HG00639.hp1 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.253-697delA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr9 | 79611936 | |||||
| chr9:79612065
|
T | C | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.253-591T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79612065 | ||||||
| chr9:79612169
|
G | A | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.253-487G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79612169 | ||||||
| chr9:79612298
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.253-358T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 4/19 | chr9 | 79612298 | ||||||
| chr9:79612752
|
G | A | 1 | a0001c0001t0003g0055 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.315+34G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79612752 | ||||||
| chr9:79612945
|
G | A | 1 | a0001c0001t0003g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.315+227G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79612945 | ||||||
| chr9:79612958
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.315+240G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79612958 | ||||||
| chr9:79613015
|
T | C | 1 | a0001c0001t0002g0214 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.315+297T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79613015 | ||||||
| chr9:79613068
|
G | A | 2 | a0001c0001t0006g0215a0001c0001t0006g0216 | 2 | HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.315+350G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79613068 | ||||||
| chr9:79613295
|
G | C | 1 | a0001c0004t0004g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.315+577G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79613295 | ||||||
| chr9:79613328
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.315+610C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79613328 | ||||||
| chr9:79613380
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.315+662A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79613380 | ||||||
| chr9:79613402
|
C | T | 11 | a0001c0001t0003g0001a0001c0001t0003g0017a0001c0001t0003g0018others(8): Show | 12 | HG02109.hp2 HG02647.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.315+684C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79613402 | ||||||
| chr9:79613553
|
C | T | 2 | a0001c0001t0003g0239a0001c0007t0002g0240 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.315+835C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79613553 | ||||||
| chr9:79613712
|
C | T | 2 | a0001c0001t0003g0036a0001c0001t0003g0039 | 2 | NA19009.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.315+994C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79613712 | ||||||
| chr9:79613743
|
T | G | 5 | a0001c0001t0003g0174a0001c0001t0003g0235a0001c0001t0003g0236others(2): Show | 5 | HG02055.hp2 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.315+1025T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79613743 | ||||||
| chr9:79613794
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.315+1076A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79613794 | ||||||
| chr9:79614097
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.315+1379C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79614097 | ||||||
| chr9:79614276
|
G | C | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.315+1558G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79614276 | ||||||
| chr9:79614429
|
A | G | 2 | a0001c0001t0002g0164a0001c0001t0002g0222 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.315+1711A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79614429 | ||||||
| chr9:79614782
|
G | T | 117 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0021others(114): Show | 119 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.315+2064G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79614782 | ||||||
| chr9:79614958
|
G | A | 4 | a0001c0001t0003g0042a0001c0001t0003g0044a0001c0001t0003g0045others(1): Show | 4 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.315+2240G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79614958 | ||||||
| chr9:79615010
|
T | C | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.315+2292T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79615010 | ||||||
| chr9:79615066
|
T | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 8 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.315+2348T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79615066 | ||||||
| chr9:79615210
|
G | A | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.315+2492G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79615210 | ||||||
| chr9:79615291
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.315+2573A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79615291 | ||||||
| chr9:79615642
|
TA | T | 38 | a0001c0001t0001g0086a0001c0001t0003g0001a0001c0001t0003g0017others(35): Show | 39 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.315+2931delA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 79615642 | |||||
| chr9:79615650
|
C | T | 9 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(6): Show | 9 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.315+2932C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79615650 | ||||||
| chr9:79615904
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.315+3186A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79615904 | ||||||
| chr9:79616099
|
C | T | 1 | a0001c0001t0003g0054 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.315+3381C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79616099 | ||||||
| chr9:79616149
|
T | C | 2 | a0001c0001t0003g0239a0001c0007t0002g0240 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.315+3431T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79616149 | ||||||
| chr9:79616232
|
A | G | 1 | a0001c0002t0003g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.315+3514A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79616232 | ||||||
| chr9:79617376
|
A | T | 17 | a0001c0001t0003g0028a0001c0001t0003g0153a0001c0001t0003g0154others(14): Show | 17 | HG01081.hp2 HG01255.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.315+4658A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79617376 | ||||||
| chr9:79617397
|
G | C | 1 | a0001c0001t0002g0241 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.315+4679G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79617397 | ||||||
| chr9:79617445
|
C | A | 2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | HG02027.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.315+4727C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79617445 | ||||||
| chr9:79617672
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.315+4954T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79617672 | ||||||
| chr9:79617774
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.315+5056G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79617774 | ||||||
| chr9:79617834
|
G | GA | 108 | a0001c0001t0001g0120a0001c0001t0001g0149a0001c0001t0002g0002others(105): Show | 110 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.315+5130dupA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 79617834 | |||||
| chr9:79617834
|
G | GAA | 10 | a0001c0001t0002g0145a0001c0001t0002g0230a0001c0001t0003g0154others(7): Show | 10 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.315+5129_315+5130d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 79617834 | |||||
| chr9:79617884
|
A | G | 1 | a0001c0001t0003g0055 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.315+5166A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79617884 | ||||||
| chr9:79617950
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.315+5232C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79617950 | ||||||
| chr9:79617972
|
G | C | 2 | a0001c0003t0003g0025a0001c0008t0002g0024 | 2 | HG01074.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.315+5254G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79617972 | ||||||
| chr9:79618591
|
T | G | 111 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0022others(108): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.315+5873T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79618591 | ||||||
| chr9:79618606
|
G | A | 1 | a0001c0001t0018g0115 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.315+5888G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79618606 | ||||||
| chr9:79618748
|
A | G | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.315+6030A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79618748 | ||||||
| chr9:79618784
|
A | G | 1 | a0001c0001t0018g0115 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.315+6066A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79618784 | ||||||
| chr9:79618927
|
T | G | 33 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(30): Show | 33 | HG00733.hp2 HG01106.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.315+6209T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79618927 | ||||||
| chr9:79619152
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.315+6434T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79619152 | ||||||
| chr9:79619153
|
A | G | 7 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(4): Show | 7 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.315+6435A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79619153 | ||||||
| chr9:79619466
|
A | G | 2 | a0001c0003t0003g0025a0001c0008t0002g0024 | 2 | HG01074.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.315+6748A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79619466 | ||||||
| chr9:79619480
|
G | T | 30 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(27): Show | 30 | HG00733.hp2 HG01109.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.315+6762G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79619480 | ||||||
| chr9:79619898
|
C | T | 10 | a0001c0001t0003g0153a0001c0001t0003g0154a0001c0001t0003g0155others(7): Show | 10 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.315+7180C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79619898 | ||||||
| chr9:79619899
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.315+7181G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79619899 | ||||||
| chr9:79619967
|
G | A | 119 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0021others(116): Show | 121 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.315+7249G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79619967 | ||||||
| chr9:79620016
|
T | C | 2 | a0001c0003t0003g0025a0001c0008t0002g0024 | 2 | HG01074.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.315+7298T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79620016 | ||||||
| chr9:79620129
|
A | T | 1 | a0001c0002t0003g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.316-7245A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79620129 | ||||||
| chr9:79620225
|
G | C | 7 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(4): Show | 7 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.316-7149G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79620225 | ||||||
| chr9:79620322
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.316-7052C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79620322 | ||||||
| chr9:79620619
|
C | G | 1 | a0001c0010t0013g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.316-6755C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79620619 | ||||||
| chr9:79620716
|
C | G | 1 | a0001c0001t0002g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.316-6658C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79620716 | ||||||
| chr9:79620737
|
G | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.316-6637G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79620737 | ||||||
| chr9:79621235
|
G | A | 1 | a0001c0001t0003g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.316-6139G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79621235 | ||||||
| chr9:79621279
|
A | T | 172 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.316-6095A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79621279 | ||||||
| chr9:79621516
|
T | C | 1 | a0001c0001t0004g0225 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.316-5858T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79621516 | ||||||
| chr9:79621664
|
C | T | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.316-5710C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79621664 | ||||||
| chr9:79621728
|
A | T | 1 | a0001c0001t0002g0179 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.316-5646A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79621728 | ||||||
| chr9:79621956
|
A | G | 1 | a0001c0001t0002g0249 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.316-5418A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79621956 | ||||||
| chr9:79622115
|
T | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.316-5259T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79622115 | ||||||
| chr9:79622242
|
T | C | 2 | a0001c0001t0002g0233a0001c0001t0002g0234 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.316-5132T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79622242 | ||||||
| chr9:79622343
|
C | G | 2 | a0001c0004t0004g0004a0001c0004t0004g0250 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.316-5031C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79622343 | ||||||
| chr9:79622381
|
G | A | 3 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0020 | 3 | HG02717.hp1 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.316-4993G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79622381 | ||||||
| chr9:79622449
|
T | G | 1 | a0001c0001t0010g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.316-4925T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79622449 | ||||||
| chr9:79622715
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.316-4659C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79622715 | ||||||
| chr9:79622746
|
T | C | 9 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(6): Show | 9 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.316-4628T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79622746 | ||||||
| chr9:79622995
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.316-4379C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79622995 | ||||||
| chr9:79623019
|
C | T | 138 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 139 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.316-4355C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79623019 | ||||||
| chr9:79623206
|
T | A | 2 | a0001c0001t0001g0012a0003c0006t0003g0027 | 2 | HG00741.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.316-4168T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79623206 | ||||||
| chr9:79623440
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.316-3934T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79623440 | ||||||
| chr9:79623617
|
T | A | 5 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0004t0004g0004others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.316-3757T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79623617 | ||||||
| chr9:79623629
|
G | A | 144 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(141): Show | 145 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.316-3745G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79623629 | ||||||
| chr9:79623699
|
G | GT | 123 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(120): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.316-3657dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 79623699 | |||||
| chr9:79623699
|
G | GTT | 8 | a0001c0001t0001g0068a0001c0001t0001g0096a0001c0001t0001g0097others(5): Show | 8 | HG00621.hp2 HG02647.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.316-3658_316-3657d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 79623699 | |||||
| chr9:79623888
|
T | G | 1 | a0001c0001t0004g0160 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.316-3486T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79623888 | ||||||
| chr9:79624051
|
T | C | 1 | a0001c0001t0003g0030 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.316-3323T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79624051 | ||||||
| chr9:79624177
|
G | GA | 8 | a0001c0001t0001g0087a0001c0001t0002g0170a0001c0001t0002g0171others(5): Show | 8 | HG00673.hp2 HG01257.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.316-3180dupA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 79624177 | |||||
| chr9:79624177
|
G | GAA | 6 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(3): Show | 6 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-3181_316-3180d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 79624177 | |||||
| chr9:79624177
|
GA | G | 176 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(173): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.316-3180delA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 79624177 | |||||
| chr9:79624179
|
A | G | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.316-3195A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79624179 | ||||||
| chr9:79624337
|
G | A | 1 | a0001c0001t0002g0147 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.316-3037G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79624337 | ||||||
| chr9:79624814
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.316-2560C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79624814 | ||||||
| chr9:79624896
|
T | G | 1 | a0001c0001t0004g0160 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.316-2478T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79624896 | ||||||
| chr9:79624940
|
T | A | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.316-2434T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79624940 | ||||||
| chr9:79625009
|
CTTTTCTT others(5): Show |
C | 3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197 | 3 | HG01891.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.316-2360_316-2349d others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 79625009 | |||||
| chr9:79625014
|
C | CT | 134 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(131): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.316-2337dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 79625014 | |||||
| chr9:79625014
|
C | CTT | 12 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0075others(9): Show | 12 | HG01106.hp2 HG01109.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.316-2338_316-2337d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 79625014 | |||||
| chr9:79625233
|
A | G | 1 | a0001c0001t0003g0045 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.316-2141A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79625233 | ||||||
| chr9:79625728
|
T | G | 1 | a0001c0001t0003g0018 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.316-1646T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79625728 | ||||||
| chr9:79625982
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.316-1392A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79625982 | ||||||
| chr9:79626053
|
A | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 8 | HG00639.hp2 HG00642.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.316-1321A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79626053 | ||||||
| chr9:79626077
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.316-1297A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79626077 | ||||||
| chr9:79626269
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.316-1105A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79626269 | ||||||
| chr9:79626357
|
A | C | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.316-1017A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79626357 | ||||||
| chr9:79626434
|
A | G | 10 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0088others(7): Show | 10 | NA18951.hp2 NA18960.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.316-940A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79626434 | ||||||
| chr9:79626500
|
T | G | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.316-874T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79626500 | ||||||
| chr9:79626588
|
T | G | 41 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(38): Show | 42 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.316-786T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79626588 | ||||||
| chr9:79626978
|
T | C | 1 | a0001c0007t0002g0240 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.316-396T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 5/19 | chr9 | 79626978 | ||||||
| chr9:79627545
|
C | G | 1 | a0001c0001t0001g0082 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.390+97C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79627545 | ||||||
| chr9:79627741
|
C | CA | 7 | a0001c0001t0001g0090a0001c0001t0001g0140a0001c0001t0002g0021others(4): Show | 7 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.390+304dupA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79627741 | |||||
| chr9:79627907
|
A | G | 5 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0004t0004g0004others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+459A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79627907 | ||||||
| chr9:79627951
|
C | G | 1 | a0001c0001t0003g0044 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.390+503C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79627951 | ||||||
| chr9:79628208
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.390+760A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79628208 | ||||||
| chr9:79628216
|
T | G | 1 | a0001c0001t0002g0161 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.390+768T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79628216 | ||||||
| chr9:79628230
|
C | A | 1 | a0001c0001t0003g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.390+782C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79628230 | ||||||
| chr9:79628290
|
G | A | 1 | a0001c0001t0002g0199 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.390+842G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79628290 | ||||||
| chr9:79628352
|
T | C | 3 | a0001c0001t0003g0033a0001c0005t0003g0253a0001c0005t0003g0254 | 3 | HG01943.hp1 HG01975.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.390+904T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79628352 | ||||||
| chr9:79628514
|
G | A | 3 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0008t0002g0024 | 3 | HG01074.hp2 HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.390+1066G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79628514 | ||||||
| chr9:79628580
|
C | CA | 6 | a0001c0001t0002g0177a0001c0001t0003g0174a0001c0001t0003g0235others(3): Show | 6 | HG02055.hp2 HG02976.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.390+1142dupA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79628580 | |||||
| chr9:79628607
|
A | C | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.390+1159A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79628607 | ||||||
| chr9:79628748
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.390+1300G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79628748 | ||||||
| chr9:79628786
|
T | C | 53 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(50): Show | 53 | HG00140.hp1 HG00733.hp2 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.390+1338T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79628786 | ||||||
| chr9:79628870
|
TTAAGTGT others(3): Show |
T | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.390+1424_390+1433d others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79628870 | |||||
| chr9:79628873
|
A | AGT | 14 | a0001c0001t0001g0089a0001c0001t0002g0143a0001c0001t0002g0184others(11): Show | 14 | HG00140.hp1 HG01255.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.390+1460_390+1461d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79628873 | |||||
| chr9:79628873
|
A | AGTGT | 22 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(19): Show | 22 | HG00733.hp2 HG01109.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.390+1458_390+1461d others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79628873 | |||||
| chr9:79628873
|
AGT | A | 83 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0057others(80): Show | 84 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.390+1460_390+1461d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79628873 | |||||
| chr9:79628873
|
AGTGT | A | 16 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(13): Show | 16 | HG00741.hp2 HG01071.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.390+1458_390+1461d others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79628873 | |||||
| chr9:79628873
|
AGTGTGT | A | 15 | a0001c0001t0001g0092a0001c0001t0001g0108a0001c0001t0001g0123others(12): Show | 15 | HG00621.hp1 HG00733.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.390+1456_390+1461d others(8): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79628873 | |||||
| chr9:79628873
|
AGTGTGTG others(7): Show |
A | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+1448_390+1461d others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79628873 | |||||
| chr9:79628908
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.390+1460G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79628908 | ||||||
| chr9:79628908
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0003g0015 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.390+1461_390+1462i others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79628908 | |||||
| chr9:79628910
|
A | G | 3 | a0001c0001t0003g0015a0001c0001t0003g0153a0001c0001t0019g0023 | 3 | HG03453.hp1 HG03540.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.390+1462A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79628910 | ||||||
| chr9:79628921
|
C | T | 1 | a0001c0001t0003g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.390+1473C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79628921 | ||||||
| chr9:79629106
|
G | C | 1 | a0001c0001t0003g0237 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.390+1658G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79629106 | ||||||
| chr9:79629151
|
C | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | NA19000.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.390+1703C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79629151 | ||||||
| chr9:79629208
|
A | T | 2 | a0001c0001t0002g0151a0001c0001t0011g0013 | 2 | HG02818.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.390+1760A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79629208 | ||||||
| chr9:79629216
|
T | C | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.390+1768T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79629216 | ||||||
| chr9:79629293
|
A | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00639.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.390+1845A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79629293 | ||||||
| chr9:79629336
|
C | A | 2 | a0001c0001t0008g0069a0001c0001t0008g0070 | 2 | HG01167.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.390+1888C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79629336 | ||||||
| chr9:79629684
|
T | A | 9 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(6): Show | 9 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.390+2236T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79629684 | ||||||
| chr9:79629694
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.390+2246T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79629694 | ||||||
| chr9:79629916
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.390+2468G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79629916 | ||||||
| chr9:79629965
|
C | G | 8 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0108others(5): Show | 8 | HG00621.hp1 HG01346.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.390+2517C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79629965 | ||||||
| chr9:79629996
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.390+2548G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79629996 | ||||||
| chr9:79630364
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.390+2916C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79630364 | ||||||
| chr9:79630628
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.390+3180C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79630628 | ||||||
| chr9:79630764
|
A | G | 1 | a0001c0001t0003g0239 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.390+3316A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79630764 | ||||||
| chr9:79630925
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0016g0062 | 2 | NA18946.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.390+3477G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79630925 | ||||||
| chr9:79630979
|
A | G | 1 | a0001c0004t0004g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.390+3531A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79630979 | ||||||
| chr9:79630997
|
T | A | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+3549T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79630997 | ||||||
| chr9:79631068
|
T | C | 1 | a0001c0001t0003g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.390+3620T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79631068 | ||||||
| chr9:79631113
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.390+3665G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79631113 | ||||||
| chr9:79631230
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.390+3782G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79631230 | ||||||
| chr9:79631240
|
T | G | 1 | a0001c0001t0002g0189 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.390+3792T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79631240 | ||||||
| chr9:79631436
|
A | T | 159 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.390+3988A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79631436 | ||||||
| chr9:79631605
|
T | G | 36 | a0001c0001t0003g0001a0001c0001t0003g0017a0001c0001t0003g0018others(33): Show | 37 | HG00423.hp2 HG00639.hp1 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.390+4157T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79631605 | ||||||
| chr9:79631616
|
A | ATG | 47 | a0001c0001t0001g0064a0001c0001t0001g0081a0001c0001t0001g0093others(44): Show | 47 | HG00558.hp1 HG00673.hp2 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.390+4214_390+4215d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79631616 | |||||
| chr9:79631616
|
A | ATGTG | 47 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(44): Show | 47 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.390+4212_390+4215d others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79631616 | |||||
| chr9:79631616
|
A | ATGTGTG | 23 | a0001c0001t0001g0008a0001c0001t0001g0060a0001c0001t0001g0061others(20): Show | 23 | HG00099.hp1 HG00280.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.390+4210_390+4215d others(8): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79631616 | |||||
| chr9:79631616
|
A | ATGTGTGT others(1): Show |
30 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0085others(27): Show | 30 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.390+4208_390+4215d others(10): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79631616 | |||||
| chr9:79631616
|
A | ATGTGTGT others(3): Show |
21 | a0001c0001t0001g0059a0001c0001t0001g0074a0001c0001t0001g0075others(18): Show | 21 | HG01069.hp2 HG01106.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.390+4206_390+4215d others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79631616 | |||||
| chr9:79631616
|
A | ATGTGTGT others(5): Show |
8 | a0001c0001t0001g0098a0001c0001t0001g0113a0001c0001t0001g0116others(5): Show | 8 | HG00558.hp2 HG01192.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.390+4204_390+4215d others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79631616 | |||||
| chr9:79631616
|
A | ATGTGTGT others(7): Show |
3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0002g0214 | 3 | HG02109.hp1 HG02132.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.390+4202_390+4215d others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79631616 | |||||
| chr9:79631616
|
ATG | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0090a0001c0001t0002g0147others(13): Show | 16 | HG00741.hp2 HG01081.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.390+4214_390+4215d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79631616 | |||||
| chr9:79631616
|
ATGTG | A | 5 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197others(2): Show | 6 | HG01243.hp2 HG01891.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+4212_390+4215d others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79631616 | |||||
| chr9:79631616
|
ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.390+4206_390+4215d others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79631616 | |||||
| chr9:79631616
|
ATGTGTGT others(5): Show |
A | 3 | a0001c0001t0003g0042a0001c0001t0003g0044a0001c0001t0012g0043 | 3 | HG02809.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.390+4204_390+4215d others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79631616 | |||||
| chr9:79631616
|
ATGTGTGT others(7): Show |
A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.390+4202_390+4215d others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79631616 | |||||
| chr9:79631678
|
A | G | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG01257.hp2 HG01258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.390+4230A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79631678 | ||||||
| chr9:79631772
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.390+4324G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79631772 | ||||||
| chr9:79631940
|
G | A | 7 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(4): Show | 7 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+4492G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79631940 | ||||||
| chr9:79631964
|
A | G | 3 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0252 | 3 | HG00140.hp1 HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.390+4516A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79631964 | ||||||
| chr9:79632020
|
T | C | 1 | a0001c0001t0003g0033 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.390+4572T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79632020 | ||||||
| chr9:79632349
|
A | G | 7 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(4): Show | 7 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.390+4901A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79632349 | ||||||
| chr9:79633155
|
G | A | 5 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0004t0004g0004others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+5707G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79633155 | ||||||
| chr9:79633340
|
A | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0111a0001c0001t0001g0123 | 3 | NA18943.hp2 NA18948.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.390+5892A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79633340 | ||||||
| chr9:79633470
|
G | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(14): Show | 17 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.390+6022G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79633470 | ||||||
| chr9:79633757
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.390+6309A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79633757 | ||||||
| chr9:79633843
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG01257.hp2 HG01258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.390+6395G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79633843 | ||||||
| chr9:79634126
|
C | T | 1 | a0001c0001t0003g0252 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.390+6678C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79634126 | ||||||
| chr9:79634200
|
A | G | 2 | a0001c0001t0002g0164a0001c0001t0002g0222 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.390+6752A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79634200 | ||||||
| chr9:79634379
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.390+6931A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79634379 | ||||||
| chr9:79634505
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.390+7057C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79634505 | ||||||
| chr9:79634548
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.390+7100T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79634548 | ||||||
| chr9:79634625
|
A | G | 1 | a0001c0001t0003g0255 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.390+7177A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79634625 | ||||||
| chr9:79634674
|
G | A | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.390+7226G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79634674 | ||||||
| chr9:79634726
|
A | G | 1 | a0001c0002t0003g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.390+7278A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79634726 | ||||||
| chr9:79634743
|
T | A | 1 | a0001c0001t0014g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.390+7295T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79634743 | ||||||
| chr9:79635084
|
T | C | 1 | a0001c0001t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.390+7636T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79635084 | ||||||
| chr9:79635548
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.390+8100G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79635548 | ||||||
| chr9:79635573
|
G | GT | 10 | a0001c0001t0002g0171a0001c0001t0002g0184a0001c0001t0002g0185others(7): Show | 10 | HG02055.hp2 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+8140dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79635573 | |||||
| chr9:79635791
|
C | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0140a0001c0001t0015g0072 | 3 | HG00741.hp1 HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.390+8343C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79635791 | ||||||
| chr9:79636191
|
G | A | 1 | a0001c0001t0016g0062 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.390+8743G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79636191 | ||||||
| chr9:79636433
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0111a0001c0001t0001g0123 | 3 | NA18943.hp2 NA18948.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.390+8985C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79636433 | ||||||
| chr9:79636444
|
T | C | 60 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(57): Show | 60 | HG00733.hp2 HG01074.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.390+8996T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79636444 | ||||||
| chr9:79636496
|
C | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0111a0001c0001t0001g0123 | 3 | NA18943.hp2 NA18948.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.390+9048C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79636496 | ||||||
| chr9:79636691
|
C | G | 1 | a0001c0001t0001g0082 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.390+9243C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79636691 | ||||||
| chr9:79636695
|
T | A | 2 | a0001c0004t0004g0004a0001c0004t0004g0250 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.390+9247T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79636695 | ||||||
| chr9:79636765
|
G | A | 1 | a0001c0003t0003g0025 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.390+9317G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79636765 | ||||||
| chr9:79636889
|
C | A | 1 | a0001c0001t0003g0239 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.390+9441C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79636889 | ||||||
| chr9:79636981
|
A | G | 60 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(57): Show | 60 | HG00733.hp2 HG01074.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.390+9533A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79636981 | ||||||
| chr9:79637091
|
G | GATAGCTA others(39): Show |
59 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(56): Show | 59 | HG00733.hp2 HG01074.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.390+9643_390+9644i others(48): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79637091 | ||||||
| chr9:79637094
|
C | G | 1 | a0001c0001t0001g0074 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.390+9646C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79637094 | ||||||
| chr9:79637097
|
T | C | 4 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(1): Show | 4 | HG02818.hp2 HG02970.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.390+9649T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79637097 | ||||||
| chr9:79637167
|
G | C | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.390+9719G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79637167 | ||||||
| chr9:79637190
|
A | G | 1 | a0001c0001t0003g0157 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.390+9742A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79637190 | ||||||
| chr9:79637262
|
T | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG00642.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.390+9814T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79637262 | ||||||
| chr9:79637309
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.390+9861A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79637309 | ||||||
| chr9:79637452
|
C | T | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.390+10004C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79637452 | ||||||
| chr9:79637706
|
C | A | 1 | a0001c0001t0003g0016 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.390+10258C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79637706 | ||||||
| chr9:79637741
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.390+10293G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79637741 | ||||||
| chr9:79637764
|
C | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.390+10316C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79637764 | ||||||
| chr9:79637836
|
C | CTG | 11 | a0001c0001t0001g0060a0001c0001t0001g0112a0001c0001t0001g0114others(8): Show | 11 | HG00280.hp1 HG01081.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.390+10406_390+1040 others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79637836 | |||||
| chr9:79637836
|
C | CTGTG | 6 | a0001c0001t0001g0094a0001c0001t0001g0111a0001c0001t0001g0123others(3): Show | 6 | HG02818.hp2 HG02970.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+10404_390+1040 others(8): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79637836 | |||||
| chr9:79637990
|
T | C | 1 | a0001c0001t0020g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.390+10542T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79637990 | ||||||
| chr9:79638002
|
T | C | 2 | a0001c0001t0003g0040a0001c0001t0003g0041 | 2 | HG02083.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.390+10554T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79638002 | ||||||
| chr9:79638072
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.390+10624G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79638072 | ||||||
| chr9:79638506
|
G | A | 2 | a0001c0001t0002g0164a0001c0001t0002g0222 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.390+11058G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79638506 | ||||||
| chr9:79638876
|
G | A | 1 | a0001c0001t0003g0054 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.390+11428G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79638876 | ||||||
| chr9:79638962
|
G | C | 9 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(6): Show | 9 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.390+11514G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79638962 | ||||||
| chr9:79639012
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.390+11564C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79639012 | ||||||
| chr9:79639341
|
A | G | 248 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 250 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.390+11893A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79639341 | ||||||
| chr9:79639593
|
T | C | 1 | a0001c0001t0004g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.390+12145T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79639593 | ||||||
| chr9:79639661
|
T | G | 10 | a0001c0001t0003g0028a0001c0001t0003g0153a0001c0001t0003g0154others(7): Show | 10 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.390+12213T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79639661 | ||||||
| chr9:79639735
|
T | C | 1 | a0001c0001t0003g0188 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.390+12287T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79639735 | ||||||
| chr9:79639884
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.390+12436A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79639884 | ||||||
| chr9:79640128
|
G | C | 1 | a0001c0001t0001g0092 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.391-12465G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79640128 | ||||||
| chr9:79640440
|
G | A | 3 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0008t0002g0024 | 3 | HG01074.hp2 HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.391-12153G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79640440 | ||||||
| chr9:79640484
|
A | G | 40 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(37): Show | 40 | HG00733.hp2 HG01081.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-12109A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79640484 | ||||||
| chr9:79640670
|
G | A | 195 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.391-11923G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79640670 | ||||||
| chr9:79640781
|
A | G | 23 | a0001c0001t0002g0161a0001c0001t0002g0204a0001c0001t0002g0205others(20): Show | 23 | HG00733.hp2 HG01109.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.391-11812A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79640781 | ||||||
| chr9:79640963
|
A | T | 13 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(10): Show | 13 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.391-11630A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79640963 | ||||||
| chr9:79641025
|
G | C | 10 | a0001c0001t0003g0028a0001c0001t0003g0153a0001c0001t0003g0154others(7): Show | 10 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-11568G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79641025 | ||||||
| chr9:79641034
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.391-11559G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79641034 | ||||||
| chr9:79641047
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.391-11546A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79641047 | ||||||
| chr9:79641119
|
T | TA | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(8): Show | 11 | HG01081.hp2 HG01255.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.391-11462dupA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79641119 | |||||
| chr9:79641119
|
TA | T | 6 | a0001c0001t0011g0013a0001c0003t0003g0025a0001c0003t0003g0026others(3): Show | 6 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-11462delA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79641119 | |||||
| chr9:79641412
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.391-11181G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79641412 | ||||||
| chr9:79641500
|
C | T | 15 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(12): Show | 15 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.391-11093C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79641500 | ||||||
| chr9:79641561
|
A | G | 3 | a0001c0001t0002g0022a0001c0001t0002g0171a0001c0001t0002g0183 | 3 | NA18961.hp2 NA18983.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.391-11032A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79641561 | ||||||
| chr9:79641667
|
G | A | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.391-10926G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79641667 | ||||||
| chr9:79641943
|
G | A | 32 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(29): Show | 32 | HG00733.hp2 HG01109.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.391-10650G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79641943 | ||||||
| chr9:79641967
|
A | T | 9 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(6): Show | 9 | HG02615.hp1 HG02818.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-10626A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79641967 | ||||||
| chr9:79641986
|
A | G | 1 | a0001c0001t0002g0176 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.391-10607A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79641986 | ||||||
| chr9:79642001
|
G | T | 2 | a0001c0001t0003g0239a0001c0007t0002g0240 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.391-10592G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79642001 | ||||||
| chr9:79642033
|
T | C | 1 | a0003c0006t0003g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.391-10560T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79642033 | ||||||
| chr9:79642034
|
G | C | 12 | a0001c0001t0002g0161a0001c0001t0002g0204a0001c0001t0002g0205others(9): Show | 12 | HG00733.hp2 HG01109.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.391-10559G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79642034 | ||||||
| chr9:79642045
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.391-10548C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79642045 | ||||||
| chr9:79642068
|
C | G | 6 | a0001c0001t0003g0028a0001c0001t0003g0153a0001c0001t0003g0158others(3): Show | 6 | HG02615.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-10525C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79642068 | ||||||
| chr9:79642159
|
G | A | 9 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(6): Show | 9 | HG02615.hp1 HG02818.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-10434G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79642159 | ||||||
| chr9:79642199
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-10394A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79642199 | ||||||
| chr9:79642311
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-10282A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79642311 | ||||||
| chr9:79642655
|
T | G | 10 | a0001c0001t0003g0028a0001c0001t0003g0153a0001c0001t0003g0154others(7): Show | 10 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.391-9938T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79642655 | ||||||
| chr9:79642865
|
G | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG00621.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.391-9728G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79642865 | ||||||
| chr9:79643025
|
C | T | 9 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(6): Show | 9 | HG02615.hp1 HG02818.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-9568C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643025 | ||||||
| chr9:79643067
|
T | G | 1 | a0001c0001t0003g0239 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.391-9526T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643067 | ||||||
| chr9:79643091
|
T | C | 2 | a0001c0001t0003g0239a0001c0007t0002g0240 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.391-9502T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643091 | ||||||
| chr9:79643138
|
A | G | 14 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(11): Show | 14 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.391-9455A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643138 | ||||||
| chr9:79643203
|
C | T | 1 | a0001c0001t0003g0157 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.391-9390C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643203 | ||||||
| chr9:79643294
|
A | G | 56 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(53): Show | 56 | HG00733.hp2 HG01074.hp2 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.391-9299A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643294 | ||||||
| chr9:79643349
|
T | A | 6 | a0001c0001t0003g0028a0001c0001t0003g0153a0001c0001t0003g0158others(3): Show | 6 | HG02615.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-9244T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643349 | ||||||
| chr9:79643351
|
T | C | 3 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0008t0002g0024 | 3 | HG01074.hp2 HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.391-9242T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643351 | ||||||
| chr9:79643363
|
C | G | 6 | a0001c0001t0003g0028a0001c0001t0003g0153a0001c0001t0003g0158others(3): Show | 6 | HG02615.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-9230C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643363 | ||||||
| chr9:79643386
|
A | G | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.391-9207A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643386 | ||||||
| chr9:79643446
|
C | T | 9 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(6): Show | 9 | HG02615.hp1 HG02818.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-9147C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643446 | ||||||
| chr9:79643529
|
G | A | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.391-9064G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643529 | ||||||
| chr9:79643542
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.391-9051T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643542 | ||||||
| chr9:79643646
|
C | T | 6 | a0001c0001t0003g0028a0001c0001t0003g0153a0001c0001t0003g0158others(3): Show | 6 | HG02615.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-8947C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643646 | ||||||
| chr9:79643647
|
G | A | 5 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0004t0004g0004others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.391-8946G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643647 | ||||||
| chr9:79643662
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-8931G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643662 | ||||||
| chr9:79643668
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.391-8925A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643668 | ||||||
| chr9:79643756
|
A | C | 41 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(38): Show | 41 | HG00733.hp2 HG01081.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.391-8837A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79643756 | ||||||
| chr9:79644068
|
A | G | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.391-8525A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79644068 | ||||||
| chr9:79644110
|
G | A | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.391-8483G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79644110 | ||||||
| chr9:79644161
|
C | G | 13 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(10): Show | 13 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.391-8432C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79644161 | ||||||
| chr9:79644174
|
A | G | 13 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(10): Show | 13 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.391-8419A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79644174 | ||||||
| chr9:79644275
|
A | G | 2 | a0001c0001t0002g0195a0001c0001t0002g0196 | 2 | NA18986.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.391-8318A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79644275 | ||||||
| chr9:79644348
|
T | C | 4 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0221others(1): Show | 4 | HG02027.hp2 HG02074.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.391-8245T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79644348 | ||||||
| chr9:79644390
|
G | A | 3 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0008t0002g0024 | 3 | HG01074.hp2 HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.391-8203G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79644390 | ||||||
| chr9:79644482
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-8111G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79644482 | ||||||
| chr9:79644546
|
A | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-8047A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79644546 | ||||||
| chr9:79644574
|
G | A | 13 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(10): Show | 13 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.391-8019G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79644574 | ||||||
| chr9:79644622
|
C | T | 39 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(36): Show | 40 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-7971C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79644622 | ||||||
| chr9:79644816
|
T | C | 2 | a0001c0001t0003g0239a0001c0007t0002g0240 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.391-7777T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79644816 | ||||||
| chr9:79644861
|
G | A | 6 | a0001c0001t0003g0028a0001c0001t0003g0153a0001c0001t0003g0158others(3): Show | 6 | HG02615.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-7732G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79644861 | ||||||
| chr9:79644975
|
C | G | 3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197 | 3 | HG01891.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.391-7618C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79644975 | ||||||
| chr9:79645107
|
T | C | 1 | a0001c0004t0004g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.391-7486T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79645107 | ||||||
| chr9:79645141
|
G | T | 1 | a0001c0001t0001g0088 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.391-7452G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79645141 | ||||||
| chr9:79645217
|
C | CA | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-7375dupA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79645217 | |||||
| chr9:79645340
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.391-7253C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79645340 | ||||||
| chr9:79645656
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0137a0001c0001t0018g0115 | 3 | HG00558.hp2 NA18983.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.391-6937A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79645656 | ||||||
| chr9:79645780
|
C | T | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.391-6813C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79645780 | ||||||
| chr9:79645928
|
G | A | 5 | a0001c0001t0003g0042a0001c0001t0003g0044a0001c0001t0003g0045others(2): Show | 5 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.391-6665G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79645928 | ||||||
| chr9:79645964
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.391-6629A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79645964 | ||||||
| chr9:79646084
|
TA | T | 7 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0011g0013others(4): Show | 7 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.391-6508delA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79646084 | ||||||
| chr9:79646085
|
A | T | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.391-6508A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79646085 | ||||||
| chr9:79646086
|
T | TA | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-6507_391-6506i others(3): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79646086 | ||||||
| chr9:79646087
|
T | A | 1 | a0001c0001t0003g0244 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.391-6506T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79646087 | ||||||
| chr9:79646088
|
T | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-6505T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79646088 | ||||||
| chr9:79646151
|
G | T | 2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | HG02027.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.391-6442G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79646151 | ||||||
| chr9:79646154
|
T | C | 2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | HG02027.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.391-6439T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79646154 | ||||||
| chr9:79646249
|
C | G | 1 | a0001c0001t0015g0072 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.391-6344C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79646249 | ||||||
| chr9:79646702
|
G | A | 7 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0156others(4): Show | 7 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.391-5891G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79646702 | ||||||
| chr9:79646974
|
G | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-5619G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79646974 | ||||||
| chr9:79647056
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-5537T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79647056 | ||||||
| chr9:79647478
|
A | G | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.391-5115A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79647478 | ||||||
| chr9:79647819
|
T | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-4774T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79647819 | ||||||
| chr9:79648145
|
C | G | 1 | a0001c0001t0004g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.391-4448C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79648145 | ||||||
| chr9:79648246
|
C | T | 2 | a0001c0001t0006g0215a0001c0001t0006g0216 | 2 | HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.391-4347C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79648246 | ||||||
| chr9:79648264
|
C | T | 3 | a0001c0001t0003g0033a0001c0005t0003g0253a0001c0005t0003g0254 | 3 | HG01943.hp1 HG01975.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.391-4329C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79648264 | ||||||
| chr9:79648265
|
T | G | 3 | a0001c0001t0003g0033a0001c0005t0003g0253a0001c0005t0003g0254 | 3 | HG01943.hp1 HG01975.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.391-4328T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79648265 | ||||||
| chr9:79648752
|
G | T | 11 | a0001c0001t0002g0161a0001c0001t0002g0204a0001c0001t0002g0205others(8): Show | 11 | HG00733.hp2 HG01109.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.391-3841G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79648752 | ||||||
| chr9:79648805
|
T | G | 3 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0008t0002g0024 | 3 | HG01074.hp2 HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.391-3788T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79648805 | ||||||
| chr9:79648815
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-3778G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79648815 | ||||||
| chr9:79648818
|
A | G | 1 | a0001c0001t0003g0156 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.391-3775A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79648818 | ||||||
| chr9:79649178
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-3415G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79649178 | ||||||
| chr9:79649244
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-3349G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79649244 | ||||||
| chr9:79649264
|
A | C | 1 | a0001c0001t0018g0115 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.391-3329A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79649264 | ||||||
| chr9:79649271
|
TAC | T | 120 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 120 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.391-3292_391-3291d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79649271 | |||||
| chr9:79649271
|
TACAC | T | 39 | a0001c0001t0001g0012a0001c0001t0002g0143a0001c0001t0002g0144others(36): Show | 40 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.391-3294_391-3291d others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79649271 | |||||
| chr9:79649271
|
TACACACA others(5): Show |
T | 2 | a0001c0005t0003g0253a0001c0005t0003g0254 | 2 | HG01943.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.391-3302_391-3291d others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79649271 | |||||
| chr9:79649275
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-3318C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79649275 | ||||||
| chr9:79649279
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-3314C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79649279 | ||||||
| chr9:79649315
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-3278T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79649315 | ||||||
| chr9:79649502
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.391-3091A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79649502 | ||||||
| chr9:79649923
|
G | GT | 21 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(18): Show | 21 | HG00280.hp1 HG00621.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.391-2660dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79649923 | |||||
| chr9:79650117
|
T | C | 1 | a0002c0009t0003g0245 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.391-2476T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79650117 | ||||||
| chr9:79650208
|
G | A | 5 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0004t0004g0004others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.391-2385G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79650208 | ||||||
| chr9:79650441
|
A | G | 2 | a0001c0001t0002g0003a0001c0001t0002g0247 | 3 | HG00099.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.391-2152A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79650441 | ||||||
| chr9:79650795
|
T | A | 2 | a0001c0001t0008g0069a0001c0001t0008g0070 | 2 | HG01167.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.391-1798T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79650795 | ||||||
| chr9:79650942
|
C | A | 1 | a0001c0001t0014g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.391-1651C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79650942 | ||||||
| chr9:79651031
|
A | ATC | 46 | a0001c0001t0001g0094a0001c0001t0001g0123a0001c0001t0002g0002others(43): Show | 48 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.391-1526_391-1525d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79651031 | |||||
| chr9:79651031
|
A | ATCTC | 12 | a0001c0001t0001g0111a0001c0001t0002g0143a0001c0001t0002g0161others(9): Show | 13 | HG01433.hp2 HG01975.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.391-1528_391-1525d others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79651031 | |||||
| chr9:79651031
|
A | ATCTCTC | 8 | a0001c0001t0003g0017a0001c0001t0003g0046a0001c0001t0003g0054others(5): Show | 8 | HG01081.hp2 HG02074.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-1530_391-1525d others(8): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79651031 | |||||
| chr9:79651031
|
A | ATCTCTCT others(1): Show |
6 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197others(3): Show | 6 | HG00733.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.391-1532_391-1525d others(10): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79651031 | |||||
| chr9:79651031
|
A | ATCTCTCT others(3): Show |
5 | a0001c0001t0002g0214a0001c0001t0002g0217a0001c0001t0002g0221others(2): Show | 5 | HG02083.hp2 HG02109.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.391-1534_391-1525d others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79651031 | |||||
| chr9:79651031
|
A | ATCTCTCT others(5): Show |
13 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0218others(10): Show | 13 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.391-1536_391-1525d others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79651031 | |||||
| chr9:79651031
|
A | ATCTCTCT others(7): Show |
3 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213 | 3 | HG01168.hp1 HG01169.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.391-1538_391-1525d others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79651031 | |||||
| chr9:79651031
|
A | ATCTCTCT others(9): Show |
1 | a0001c0001t0002g0208 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.391-1540_391-1525d others(18): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79651031 | |||||
| chr9:79651031
|
A | ATCTCTCT others(11): Show |
1 | a0001c0001t0002g0241 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.391-1542_391-1525d others(20): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79651031 | |||||
| chr9:79651031
|
ATC | A | 8 | a0001c0001t0003g0051a0001c0001t0003g0154a0001c0001t0003g0155others(5): Show | 8 | HG00423.hp2 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.391-1526_391-1525d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79651031 | |||||
| chr9:79651031
|
ATCTC | A | 3 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0003g0028 | 3 | HG02818.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.391-1528_391-1525d others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79651031 | |||||
| chr9:79651031
|
ATCTCTC | A | 9 | a0001c0001t0002g0021a0001c0001t0004g0224a0001c0001t0004g0225others(6): Show | 9 | HG01074.hp2 HG01106.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.391-1530_391-1525d others(8): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79651031 | |||||
| chr9:79651031
|
ATCTCTCT others(1): Show |
A | 3 | a0001c0001t0001g0076a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG00642.hp2 HG03471.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.391-1532_391-1525d others(10): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79651031 | |||||
| chr9:79651031
|
ATCTCTCT others(3): Show |
A | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 93 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.391-1534_391-1525d others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79651031 | |||||
| chr9:79651031
|
ATCTCTCT others(7): Show |
A | 1 | a0001c0001t0001g0119 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.391-1538_391-1525d others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 79651031 | |||||
| chr9:79651089
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-1504A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79651089 | ||||||
| chr9:79651146
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-1447C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79651146 | ||||||
| chr9:79651255
|
C | T | 1 | a0001c0001t0004g0160 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.391-1338C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79651255 | ||||||
| chr9:79651330
|
C | T | 1 | a0001c0001t0002g0152 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.391-1263C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79651330 | ||||||
| chr9:79651393
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.391-1200C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79651393 | ||||||
| chr9:79651458
|
A | C | 2 | a0001c0001t0002g0233a0001c0001t0002g0234 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.391-1135A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79651458 | ||||||
| chr9:79651600
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.391-993A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79651600 | ||||||
| chr9:79651835
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-758T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79651835 | ||||||
| chr9:79651876
|
C | G | 1 | a0001c0001t0002g0219 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.391-717C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79651876 | ||||||
| chr9:79651897
|
T | A | 1 | a0002c0009t0003g0245 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.391-696T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79651897 | ||||||
| chr9:79651903
|
C | T | 1 | a0001c0001t0003g0046 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.391-690C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79651903 | ||||||
| chr9:79652101
|
T | TCTTATA | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.391-492_391-491ins others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79652101 | ||||||
| chr9:79652102
|
A | C | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.391-491A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79652102 | ||||||
| chr9:79652194
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391-399C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79652194 | ||||||
| chr9:79652200
|
T | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(14): Show | 17 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.391-393T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79652200 | ||||||
| chr9:79652249
|
C | T | 1 | a0001c0001t0003g0015 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391-344C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79652249 | ||||||
| chr9:79652255
|
C | G | 30 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(27): Show | 30 | HG00733.hp2 HG01109.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.391-338C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79652255 | ||||||
| chr9:79652297
|
C | G | 1 | a0001c0001t0002g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.391-296C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79652297 | ||||||
| chr9:79652388
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0011g0013 | 2 | HG02280.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.391-205C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79652388 | ||||||
| chr9:79652390
|
T | C | 60 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(57): Show | 60 | HG00733.hp2 HG01074.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.391-203T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79652390 | ||||||
| chr9:79652429
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.391-164C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79652429 | ||||||
| chr9:79652477
|
G | A | 1 | a0001c0001t0020g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.391-116G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79652477 | ||||||
| chr9:79652478
|
T | C | 1 | a0001c0001t0020g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.391-115T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79652478 | ||||||
| chr9:79652544
|
G | A | 2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | HG02027.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.391-49G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 6/19 | chr9 | 79652544 | ||||||
| chr9:79652817
|
C | G | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.592+23C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 7/19 | chr9 | 79652817 | ||||||
| chr9:79653136
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.592+342T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 7/19 | chr9 | 79653136 | ||||||
| chr9:79653229
|
A | C | 1 | a0001c0001t0002g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.592+435A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 7/19 | chr9 | 79653229 | ||||||
| chr9:79653518
|
A | G | 1 | a0001c0001t0002g0142 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.593-541A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 7/19 | chr9 | 79653518 | ||||||
| chr9:79653617
|
T | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.593-442T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 7/19 | chr9 | 79653617 | ||||||
| chr9:79653660
|
G | A | 248 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 250 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.593-399G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 7/19 | chr9 | 79653660 | ||||||
| chr9:79654123
|
A | C | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.609+48A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79654123 | ||||||
| chr9:79654230
|
A | AT | 20 | a0001c0001t0001g0075a0001c0001t0001g0130a0001c0001t0001g0131others(17): Show | 20 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.609+173dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79654230 | |||||
| chr9:79654230
|
AT | A | 40 | a0001c0001t0001g0059a0001c0001t0001g0066a0001c0001t0001g0076others(37): Show | 40 | HG00423.hp2 HG00639.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.609+173delT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79654230 | |||||
| chr9:79654322
|
A | G | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.609+247A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79654322 | ||||||
| chr9:79654422
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+347A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79654422 | ||||||
| chr9:79654495
|
AT | A | 24 | a0001c0001t0001g0061a0001c0001t0002g0161a0001c0001t0002g0204others(21): Show | 24 | HG00733.hp2 HG01081.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.609+435delT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79654495 | |||||
| chr9:79654679
|
A | C | 2 | a0001c0001t0002g0164a0001c0001t0002g0222 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.609+604A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79654679 | ||||||
| chr9:79654876
|
G | T | 6 | a0001c0001t0003g0154a0001c0001t0003g0156a0001c0001t0003g0157others(3): Show | 6 | HG02572.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.609+801G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79654876 | ||||||
| chr9:79654945
|
C | A | 1 | a0001c0001t0003g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.609+870C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79654945 | ||||||
| chr9:79654971
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.609+896G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79654971 | ||||||
| chr9:79655144
|
A | AATAC | 6 | a0001c0001t0001g0079a0001c0001t0001g0085a0001c0001t0001g0096others(3): Show | 6 | HG01361.hp2 HG01943.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.609+1097_609+1100d others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79655144 | |||||
| chr9:79655144
|
A | AATACATA others(9): Show |
1 | a0001c0001t0001g0106 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.609+1085_609+1100d others(18): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79655144 | |||||
| chr9:79655144
|
AATACATA others(1): Show |
A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+1093_609+1100d others(10): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79655144 | |||||
| chr9:79655211
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+1136A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79655211 | ||||||
| chr9:79655511
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.609+1436G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79655511 | ||||||
| chr9:79655571
|
G | C | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.609+1496G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79655571 | ||||||
| chr9:79655742
|
C | T | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.609+1667C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79655742 | ||||||
| chr9:79655978
|
C | G | 1 | a0001c0001t0016g0062 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.609+1903C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79655978 | ||||||
| chr9:79656099
|
A | T | 1 | a0001c0001t0002g0178 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.609+2024A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79656099 | ||||||
| chr9:79656236
|
A | G | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.609+2161A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79656236 | ||||||
| chr9:79656337
|
C | T | 2 | a0001c0001t0002g0233a0001c0001t0002g0234 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.609+2262C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79656337 | ||||||
| chr9:79656490
|
AT | A | 5 | a0001c0003t0003g0025a0001c0003t0003g0026a0001c0004t0004g0004others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+2420delT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79656490 | |||||
| chr9:79656657
|
G | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+2582G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79656657 | ||||||
| chr9:79656933
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+2858T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79656933 | ||||||
| chr9:79657263
|
A | G | 1 | a0001c0001t0014g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.609+3188A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79657263 | ||||||
| chr9:79657359
|
T | C | 2 | a0001c0001t0002g0233a0001c0001t0002g0234 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.609+3284T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79657359 | ||||||
| chr9:79657368
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+3293A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79657368 | ||||||
| chr9:79657397
|
T | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+3322T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79657397 | ||||||
| chr9:79657511
|
G | A | 2 | a0001c0001t0008g0069a0001c0001t0008g0070 | 2 | HG01167.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.609+3436G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79657511 | ||||||
| chr9:79657717
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+3642C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79657717 | ||||||
| chr9:79657759
|
A | G | 17 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(14): Show | 18 | HG00140.hp1 HG01943.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.609+3684A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79657759 | ||||||
| chr9:79657780
|
G | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+3705G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79657780 | ||||||
| chr9:79657812
|
C | T | 1 | a0001c0001t0017g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.609+3737C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79657812 | ||||||
| chr9:79657847
|
C | T | 9 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(6): Show | 9 | NA18951.hp2 NA18960.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.609+3772C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79657847 | ||||||
| chr9:79658101
|
T | A | 1 | a0001c0001t0001g0119 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.609+4026T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79658101 | ||||||
| chr9:79658288
|
A | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+4213A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79658288 | ||||||
| chr9:79658555
|
G | A | 1 | a0001c0001t0017g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.609+4480G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79658555 | ||||||
| chr9:79658900
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+4825G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79658900 | ||||||
| chr9:79658949
|
G | C | 33 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(30): Show | 33 | HG00733.hp2 HG01109.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.609+4874G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79658949 | ||||||
| chr9:79659329
|
G | A | 1 | a0001c0001t0003g0031 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.609+5254G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79659329 | ||||||
| chr9:79659570
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+5495G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79659570 | ||||||
| chr9:79659577
|
A | T | 250 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(247): Show | 252 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.609+5502A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79659577 | ||||||
| chr9:79659740
|
G | A | 1 | a0001c0001t0003g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.609+5665G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79659740 | ||||||
| chr9:79660007
|
A | G | 1 | a0001c0001t0004g0225 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.609+5932A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79660007 | ||||||
| chr9:79660644
|
A | C | 77 | a0001c0001t0001g0094a0001c0001t0001g0111a0001c0001t0001g0123others(74): Show | 77 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.609+6569A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79660644 | ||||||
| chr9:79660676
|
T | G | 101 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(98): Show | 101 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.609+6601T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79660676 | ||||||
| chr9:79660918
|
C | T | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.609+6843C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79660918 | ||||||
| chr9:79661247
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+7172T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79661247 | ||||||
| chr9:79661269
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.609+7194A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79661269 | ||||||
| chr9:79661340
|
T | C | 1 | a0001c0001t0002g0171 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.609+7265T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79661340 | ||||||
| chr9:79661389
|
A | C | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.609+7314A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79661389 | ||||||
| chr9:79661444
|
G | A | 1 | a0001c0001t0002g0183 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.609+7369G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79661444 | ||||||
| chr9:79661445
|
G | T | 3 | a0001c0001t0004g0160a0001c0001t0004g0228a0001c0001t0004g0229 | 3 | HG01081.hp2 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.609+7370G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79661445 | ||||||
| chr9:79661544
|
A | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+7469A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79661544 | ||||||
| chr9:79661711
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.609+7636T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79661711 | ||||||
| chr9:79661792
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.609+7717A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79661792 | ||||||
| chr9:79661801
|
G | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+7726G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79661801 | ||||||
| chr9:79661846
|
T | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+7771T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79661846 | ||||||
| chr9:79661896
|
G | A | 1 | a0001c0001t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.609+7821G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79661896 | ||||||
| chr9:79662053
|
T | C | 1 | a0001c0001t0002g0204 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.609+7978T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79662053 | ||||||
| chr9:79662141
|
T | G | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.609+8066T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79662141 | ||||||
| chr9:79662188
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.609+8113T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79662188 | ||||||
| chr9:79662302
|
A | C | 107 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(104): Show | 107 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.609+8227A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79662302 | ||||||
| chr9:79662686
|
G | A | 2 | a0001c0001t0003g0040a0001c0001t0003g0041 | 2 | HG02083.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.609+8611G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79662686 | ||||||
| chr9:79662715
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.609+8640A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79662715 | ||||||
| chr9:79663045
|
TGGGTGGG others(5): Show |
T | 28 | a0001c0001t0001g0077a0001c0001t0002g0198a0001c0001t0002g0199others(25): Show | 28 | HG00733.hp2 HG01074.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.609+8989_609+9000d others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79663045 | |||||
| chr9:79663087
|
A | C | 1 | a0001c0001t0018g0115 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.609+9012A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79663087 | ||||||
| chr9:79663164
|
A | G | 1 | a0001c0004t0004g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.609+9089A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79663164 | ||||||
| chr9:79663399
|
T | C | 1 | a0001c0001t0003g0033 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.609+9324T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79663399 | ||||||
| chr9:79663403
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.609+9328G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79663403 | ||||||
| chr9:79663442
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.609+9367C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79663442 | ||||||
| chr9:79663559
|
C | A | 1 | a0001c0001t0004g0226 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.609+9484C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79663559 | ||||||
| chr9:79663560
|
C | G | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.609+9485C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79663560 | ||||||
| chr9:79663670
|
A | G | 1 | a0001c0001t0004g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.609+9595A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79663670 | ||||||
| chr9:79663681
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.609+9606T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79663681 | ||||||
| chr9:79663977
|
C | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0137a0001c0001t0018g0115 | 3 | HG00558.hp2 NA18983.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.609+9902C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79663977 | ||||||
| chr9:79664004
|
G | A | 2 | a0001c0001t0002g0221a0001c0001t0002g0230 | 2 | HG02083.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.609+9929G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79664004 | ||||||
| chr9:79664155
|
G | A | 2 | a0001c0004t0004g0004a0001c0004t0004g0250 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.609+10080G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79664155 | ||||||
| chr9:79664180
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.609+10105A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79664180 | ||||||
| chr9:79664433
|
G | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 7 | HG00639.hp2 HG00642.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+10358G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79664433 | ||||||
| chr9:79664501
|
G | A | 10 | a0001c0001t0002g0126a0001c0001t0002g0145a0001c0001t0002g0146others(7): Show | 10 | HG00673.hp2 NA18943.hp1 NA18975.hp1 others(7): Show |
intron_variant | MODIFIER | c.609+10426G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79664501 | ||||||
| chr9:79664534
|
T | G | 168 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(165): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.609+10459T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79664534 | ||||||
| chr9:79664627
|
C | T | 26 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(23): Show | 27 | HG00140.hp1 HG01943.hp1 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.609+10552C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79664627 | ||||||
| chr9:79664693
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+10618C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79664693 | ||||||
| chr9:79664852
|
C | T | 10 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 10 | HG00639.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.609+10777C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79664852 | ||||||
| chr9:79664997
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.609+10922G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79664997 | ||||||
| chr9:79665128
|
A | C | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.609+11053A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79665128 | ||||||
| chr9:79665329
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+11254T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79665329 | ||||||
| chr9:79665339
|
A | G | 2 | a0001c0001t0003g0158a0001c0001t0014g0251 | 2 | HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.609+11264A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79665339 | ||||||
| chr9:79665371
|
A | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0003g0035 | 3 | NA19000.hp1 NA19074.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.609+11296A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79665371 | ||||||
| chr9:79665383
|
G | A | 41 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(38): Show | 41 | HG00733.hp2 HG01074.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.609+11308G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79665383 | ||||||
| chr9:79665447
|
C | T | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 93 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.609+11372C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79665447 | ||||||
| chr9:79665629
|
G | A | 194 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(191): Show | 195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.609+11554G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79665629 | ||||||
| chr9:79665695
|
G | A | 194 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(191): Show | 195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.609+11620G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79665695 | ||||||
| chr9:79665737
|
A | AT | 23 | a0001c0001t0001g0094a0001c0001t0001g0123a0001c0001t0003g0030others(20): Show | 23 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.609+11668dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79665737 | |||||
| chr9:79665933
|
G | T | 1 | a0003c0006t0003g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.609+11858G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79665933 | ||||||
| chr9:79666054
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.609+11979G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666054 | ||||||
| chr9:79666077
|
C | G | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.609+12002C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666077 | ||||||
| chr9:79666163
|
C | CTG | 5 | a0001c0001t0002g0150a0001c0001t0002g0167a0001c0001t0002g0168others(2): Show | 5 | HG02809.hp2 HG02970.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.609+12121_609+1212 others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79666163 | |||||
| chr9:79666163
|
C | CTGTG | 13 | a0001c0001t0001g0089a0001c0001t0002g0173a0001c0001t0002g0175others(10): Show | 13 | HG00280.hp2 HG01255.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.609+12119_609+1212 others(8): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79666163 | |||||
| chr9:79666163
|
C | CTGTGTG | 2 | a0001c0001t0002g0002a0001c0001t0002g0187 | 3 | HG01069.hp1 HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.609+12117_609+1212 others(10): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79666163 | |||||
| chr9:79666163
|
CTG | C | 106 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0058others(103): Show | 107 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.609+12121_609+1212 others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79666163 | |||||
| chr9:79666163
|
CTGTG | C | 48 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0100others(45): Show | 48 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.609+12119_609+1212 others(8): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79666163 | |||||
| chr9:79666163
|
CTGTGTG | C | 3 | a0001c0001t0008g0069a0001c0001t0008g0070a0001c0001t0017g0084 | 3 | HG00673.hp1 HG01167.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.609+12117_609+1212 others(10): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79666163 | |||||
| chr9:79666163
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0001g0135 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.609+12111_609+1212 others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79666163 | |||||
| chr9:79666196
|
T | G | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.609+12121T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666196 | ||||||
| chr9:79666198
|
G | T | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.609+12123G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666198 | ||||||
| chr9:79666211
|
T | G | 29 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(26): Show | 29 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.609+12136T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666211 | ||||||
| chr9:79666212
|
T | G | 17 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0099others(14): Show | 17 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.609+12137T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666212 | ||||||
| chr9:79666213
|
T | G | 1 | a0001c0001t0001g0012 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.609+12138T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666213 | ||||||
| chr9:79666217
|
G | T | 1 | a0001c0001t0003g0044 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.609+12142G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666217 | ||||||
| chr9:79666217
|
GTTTTTTT others(3): Show |
G | 29 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(26): Show | 29 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.609+12155_609+1216 others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79666217 | |||||
| chr9:79666220
|
T | C | 1 | a0001c0001t0003g0155 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.609+12145T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666220 | ||||||
| chr9:79666220
|
T | TTG | 7 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(4): Show | 7 | HG00639.hp1 HG01167.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+12146_609+1214 others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79666220 | |||||
| chr9:79666221
|
T | G | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.609+12146T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666221 | ||||||
| chr9:79666221
|
T | TG | 120 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.609+12146_609+1214 others(5): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666221 | ||||||
| chr9:79666222
|
T | G | 94 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0022others(91): Show | 97 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.609+12147T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666222 | ||||||
| chr9:79666223
|
T | G | 2 | a0001c0001t0002g0164a0001c0001t0003g0018 | 2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.609+12148T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666223 | ||||||
| chr9:79666226
|
T | G | 97 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.609+12151T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666226 | ||||||
| chr9:79666227
|
T | G | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.609+12152T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666227 | ||||||
| chr9:79666330
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0003g0049 | 2 | HG00639.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.609+12255C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666330 | ||||||
| chr9:79666622
|
T | G | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.609+12547T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79666622 | ||||||
| chr9:79666846
|
TA | T | 41 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(38): Show | 41 | HG00733.hp2 HG01074.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.609+12773delA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79666846 | |||||
| chr9:79667084
|
C | G | 1 | a0001c0010t0013g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.609+13009C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79667084 | ||||||
| chr9:79667093
|
C | T | 17 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(14): Show | 17 | HG00423.hp2 HG00639.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.609+13018C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79667093 | ||||||
| chr9:79667230
|
C | A | 1 | a0001c0001t0002g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.609+13155C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79667230 | ||||||
| chr9:79667249
|
G | A | 1 | a0001c0001t0002g0179 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.609+13174G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79667249 | ||||||
| chr9:79667514
|
A | G | 1 | a0001c0001t0003g0255 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.609+13439A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79667514 | ||||||
| chr9:79667516
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.609+13441A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79667516 | ||||||
| chr9:79667530
|
C | T | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 93 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.609+13455C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79667530 | ||||||
| chr9:79667585
|
T | G | 1 | a0001c0007t0002g0240 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.609+13510T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79667585 | ||||||
| chr9:79667656
|
G | C | 2 | a0001c0004t0004g0004a0001c0004t0004g0250 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.609+13581G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79667656 | ||||||
| chr9:79667743
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.609+13668G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79667743 | ||||||
| chr9:79667782
|
T | C | 72 | a0001c0001t0001g0094a0001c0001t0001g0123a0001c0001t0002g0161others(69): Show | 72 | HG00423.hp2 HG00639.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.609+13707T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79667782 | ||||||
| chr9:79667859
|
A | G | 1 | a0001c0001t0002g0145 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.609+13784A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79667859 | ||||||
| chr9:79668093
|
C | G | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.609+14018C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79668093 | ||||||
| chr9:79668358
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18966.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.609+14283G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79668358 | ||||||
| chr9:79668360
|
G | A | 1 | a0001c0001t0003g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.609+14285G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79668360 | ||||||
| chr9:79668458
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.609+14383C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79668458 | ||||||
| chr9:79668501
|
C | T | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.609+14426C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79668501 | ||||||
| chr9:79668628
|
C | T | 2 | a0001c0004t0004g0004a0001c0004t0004g0250 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.609+14553C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79668628 | ||||||
| chr9:79668666
|
T | C | 2 | a0001c0001t0008g0069a0001c0001t0008g0070 | 2 | HG01167.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.609+14591T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79668666 | ||||||
| chr9:79668735
|
T | C | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.609+14660T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79668735 | ||||||
| chr9:79668747
|
C | CA | 201 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.609+14675dupA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79668747 | |||||
| chr9:79669010
|
G | A | 20 | a0001c0001t0003g0028a0001c0001t0003g0030a0001c0001t0003g0031others(17): Show | 20 | HG00423.hp2 HG00639.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+14935G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79669010 | ||||||
| chr9:79669139
|
C | T | 2 | a0001c0001t0003g0028a0001c0001t0014g0251 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.609+15064C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79669139 | ||||||
| chr9:79669550
|
G | A | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.609+15475G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79669550 | ||||||
| chr9:79669677
|
C | T | 1 | a0001c0001t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.609+15602C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79669677 | ||||||
| chr9:79669733
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+15658C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79669733 | ||||||
| chr9:79669744
|
ATCTAG | A | 18 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(15): Show | 18 | HG00423.hp2 HG00639.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.609+15670_609+1567 others(9): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79669744 | ||||||
| chr9:79669748
|
A | G | 5 | a0001c0001t0003g0028a0001c0001t0003g0153a0001c0001t0003g0248others(2): Show | 5 | HG02922.hp2 HG03195.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+15673A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79669748 | ||||||
| chr9:79669972
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+15897T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79669972 | ||||||
| chr9:79669973
|
G | C | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.609+15898G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79669973 | ||||||
| chr9:79670036
|
T | C | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.609+15961T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79670036 | ||||||
| chr9:79670173
|
A | T | 1 | a0001c0001t0001g0085 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.609+16098A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79670173 | ||||||
| chr9:79670201
|
A | G | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.609+16126A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79670201 | ||||||
| chr9:79670356
|
A | G | 34 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0163others(31): Show | 34 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.609+16281A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79670356 | ||||||
| chr9:79670623
|
G | C | 5 | a0001c0001t0003g0174a0001c0001t0003g0235a0001c0001t0003g0236others(2): Show | 5 | HG02055.hp2 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+16548G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79670623 | ||||||
| chr9:79670780
|
A | T | 3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197 | 3 | HG01891.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.609+16705A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79670780 | ||||||
| chr9:79670848
|
C | G | 1 | a0001c0001t0012g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.609+16773C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79670848 | ||||||
| chr9:79670877
|
T | G | 3 | a0001c0001t0003g0153a0001c0001t0014g0251a0001c0001t0019g0023 | 3 | HG02922.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.609+16802T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79670877 | ||||||
| chr9:79670893
|
A | T | 1 | a0001c0001t0014g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.609+16818A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79670893 | ||||||
| chr9:79671059
|
TA | T | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 93 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.609+16993delA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79671059 | |||||
| chr9:79671115
|
A | G | 2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | HG02027.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.609+17040A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79671115 | ||||||
| chr9:79671147
|
G | C | 2 | a0001c0003t0003g0025a0001c0003t0003g0026 | 2 | HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.609+17072G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79671147 | ||||||
| chr9:79671171
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.609+17096A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79671171 | ||||||
| chr9:79671248
|
C | G | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.609+17173C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79671248 | ||||||
| chr9:79671371
|
C | G | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 93 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.609+17296C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79671371 | ||||||
| chr9:79671437
|
G | A | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 93 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.609+17362G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79671437 | ||||||
| chr9:79671649
|
C | G | 1 | a0001c0001t0002g0179 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.609+17574C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79671649 | ||||||
| chr9:79671688
|
C | A | 1 | a0001c0001t0001g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.609+17613C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79671688 | ||||||
| chr9:79671848
|
C | T | 195 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.609+17773C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79671848 | ||||||
| chr9:79671925
|
TA | T | 49 | a0001c0001t0001g0094a0001c0001t0001g0111a0001c0001t0001g0123others(46): Show | 50 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.609+17864delA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79671925 | |||||
| chr9:79671995
|
C | CT | 16 | a0001c0001t0002g0145a0001c0001t0002g0147a0001c0001t0002g0162others(13): Show | 16 | HG00673.hp2 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.609+17949dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79671995 | |||||
| chr9:79671995
|
CT | C | 45 | a0001c0001t0001g0111a0001c0001t0001g0120a0001c0001t0001g0123others(42): Show | 46 | HG00140.hp1 HG00621.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.609+17949delT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79671995 | |||||
| chr9:79671995
|
CTT | C | 44 | a0001c0001t0001g0064a0001c0001t0001g0075a0001c0001t0001g0076others(41): Show | 44 | HG00423.hp1 HG00733.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.609+17948_609+1794 others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79671995 | |||||
| chr9:79671995
|
CTTT | C | 78 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(75): Show | 78 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.609+17947_609+1794 others(7): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79671995 | |||||
| chr9:79672263
|
A | C | 3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197 | 3 | HG01891.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.609+18188A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79672263 | ||||||
| chr9:79672390
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+18315A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79672390 | ||||||
| chr9:79672448
|
A | G | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 93 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.609+18373A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79672448 | ||||||
| chr9:79672556
|
G | A | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 93 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.609+18481G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79672556 | ||||||
| chr9:79672574
|
G | A | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.609+18499G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79672574 | ||||||
| chr9:79672614
|
G | A | 1 | a0001c0001t0003g0015 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.609+18539G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79672614 | ||||||
| chr9:79672692
|
G | A | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.609+18617G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79672692 | ||||||
| chr9:79672834
|
C | T | 1 | a0001c0001t0004g0226 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.609+18759C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79672834 | ||||||
| chr9:79672904
|
A | C | 142 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(139): Show | 142 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.609+18829A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79672904 | ||||||
| chr9:79673302
|
C | A | 1 | a0001c0001t0003g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.609+19227C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79673302 | ||||||
| chr9:79673355
|
A | G | 2 | a0001c0001t0002g0211a0001c0001t0002g0212 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.609+19280A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79673355 | ||||||
| chr9:79673996
|
C | T | 1 | a0001c0010t0013g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.609+19921C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79673996 | ||||||
| chr9:79674086
|
T | C | 204 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 205 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.609+20011T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79674086 | ||||||
| chr9:79674136
|
A | G | 1 | a0004c0011t0001g0014 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.609+20061A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79674136 | ||||||
| chr9:79674238
|
G | T | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.609+20163G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79674238 | ||||||
| chr9:79674319
|
AAGTGAGA others(3): Show |
A | 46 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(43): Show | 47 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.609+20253_609+2026 others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79674319 | |||||
| chr9:79674328
|
A | T | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.609+20253A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79674328 | ||||||
| chr9:79674610
|
T | G | 2 | a0001c0004t0004g0004a0001c0004t0004g0250 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.609+20535T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79674610 | ||||||
| chr9:79674698
|
G | A | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.609+20623G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79674698 | ||||||
| chr9:79674924
|
C | T | 3 | a0001c0001t0005g0165a0001c0001t0005g0166a0001c0001t0005g0172 | 3 | HG00558.hp1 HG02040.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.609+20849C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79674924 | ||||||
| chr9:79674971
|
A | C | 2 | a0001c0001t0004g0225a0001c0001t0004g0226 | 2 | HG01255.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.609+20896A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79674971 | ||||||
| chr9:79675065
|
A | G | 1 | a0001c0001t0003g0001 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.609+20990A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79675065 | ||||||
| chr9:79675080
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.609+21005A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79675080 | ||||||
| chr9:79675296
|
A | G | 1 | a0001c0001t0005g0172 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.609+21221A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79675296 | ||||||
| chr9:79675298
|
C | T | 16 | a0001c0001t0002g0002a0001c0001t0002g0167a0001c0001t0002g0168others(13): Show | 17 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.609+21223C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79675298 | ||||||
| chr9:79675564
|
C | G | 102 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.609+21489C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79675564 | ||||||
| chr9:79675851
|
G | T | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.609+21776G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79675851 | ||||||
| chr9:79675932
|
G | A | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.609+21857G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79675932 | ||||||
| chr9:79676044
|
A | C | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.609+21969A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79676044 | ||||||
| chr9:79676285
|
T | C | 1 | a0001c0001t0014g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.609+22210T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79676285 | ||||||
| chr9:79676441
|
A | G | 46 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(43): Show | 47 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.609+22366A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79676441 | ||||||
| chr9:79676697
|
T | C | 5 | a0001c0001t0003g0174a0001c0001t0003g0235a0001c0001t0003g0236others(2): Show | 5 | HG02055.hp2 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+22622T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79676697 | ||||||
| chr9:79676712
|
G | A | 195 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.609+22637G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79676712 | ||||||
| chr9:79676773
|
G | A | 1 | a0001c0010t0013g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.609+22698G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79676773 | ||||||
| chr9:79676807
|
G | A | 10 | a0001c0001t0003g0042a0001c0001t0003g0044a0001c0001t0003g0045others(7): Show | 10 | HG02572.hp1 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.609+22732G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79676807 | ||||||
| chr9:79677024
|
A | G | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.609+22949A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79677024 | ||||||
| chr9:79677152
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.609+23077T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79677152 | ||||||
| chr9:79677313
|
C | G | 2 | a0001c0004t0004g0004a0001c0004t0004g0250 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.609+23238C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79677313 | ||||||
| chr9:79677313
|
C | T | 53 | a0001c0001t0001g0094a0001c0001t0001g0123a0001c0001t0003g0001others(50): Show | 54 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.609+23238C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79677313 | ||||||
| chr9:79677355
|
A | G | 1 | a0001c0001t0003g0044 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.609+23280A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79677355 | ||||||
| chr9:79677463
|
C | T | 205 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 206 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.609+23388C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79677463 | ||||||
| chr9:79677608
|
A | AT | 32 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(29): Show | 32 | HG00423.hp2 HG00733.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.609+23549dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79677608 | |||||
| chr9:79677608
|
AT | A | 24 | a0001c0001t0002g0002a0001c0001t0002g0021a0001c0001t0002g0150others(21): Show | 25 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.609+23549delT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79677608 | |||||
| chr9:79677608
|
ATT | A | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(86): Show | 89 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.609+23548_609+2354 others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79677608 | |||||
| chr9:79677608
|
ATTT | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0074a0001c0001t0001g0103others(2): Show | 5 | HG03017.hp2 HG03710.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+23547_609+2354 others(7): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79677608 | |||||
| chr9:79677640
|
G | T | 1 | a0001c0010t0013g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.609+23565G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79677640 | ||||||
| chr9:79677659
|
C | T | 2 | a0001c0003t0003g0025a0001c0003t0003g0026 | 2 | HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.609+23584C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79677659 | ||||||
| chr9:79677671
|
C | T | 1 | a0001c0001t0003g0252 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.609+23596C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79677671 | ||||||
| chr9:79677815
|
G | A | 6 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0002g0200others(3): Show | 6 | HG01192.hp2 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.609+23740G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79677815 | ||||||
| chr9:79677934
|
G | A | 94 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.609+23859G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79677934 | ||||||
| chr9:79677946
|
C | T | 1 | a0002c0009t0003g0245 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.609+23871C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79677946 | ||||||
| chr9:79678008
|
C | A | 48 | a0001c0001t0001g0094a0001c0001t0001g0123a0001c0001t0003g0001others(45): Show | 49 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.609+23933C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79678008 | ||||||
| chr9:79678052
|
G | A | 94 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.609+23977G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79678052 | ||||||
| chr9:79678102
|
A | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.609+24027A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79678102 | ||||||
| chr9:79678119
|
A | G | 48 | a0001c0001t0001g0094a0001c0001t0001g0123a0001c0001t0003g0001others(45): Show | 49 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.609+24044A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79678119 | ||||||
| chr9:79678132
|
G | C | 5 | a0001c0001t0003g0174a0001c0001t0003g0235a0001c0001t0003g0236others(2): Show | 5 | HG02055.hp2 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+24057G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79678132 | ||||||
| chr9:79678248
|
C | A | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.609+24173C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79678248 | ||||||
| chr9:79678414
|
C | CT | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.609+24348dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79678414 | |||||
| chr9:79678514
|
G | A | 94 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.609+24439G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79678514 | ||||||
| chr9:79678556
|
C | T | 50 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(47): Show | 50 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.609+24481C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79678556 | ||||||
| chr9:79678562
|
G | A | 22 | a0001c0001t0002g0161a0001c0001t0002g0204a0001c0001t0002g0205others(19): Show | 22 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.609+24487G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79678562 | ||||||
| chr9:79678594
|
A | G | 2 | a0001c0005t0003g0253a0001c0005t0003g0254 | 2 | HG01943.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.609+24519A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79678594 | ||||||
| chr9:79678618
|
C | CT | 97 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.609+24553dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79678618 | |||||
| chr9:79678728
|
G | A | 12 | a0001c0001t0003g0042a0001c0001t0003g0044a0001c0001t0003g0045others(9): Show | 12 | HG01943.hp1 HG01975.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.609+24653G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79678728 | ||||||
| chr9:79678751
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.609+24676C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79678751 | ||||||
| chr9:79678795
|
C | T | 2 | a0001c0001t0008g0069a0001c0001t0008g0070 | 2 | HG01167.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.609+24720C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79678795 | ||||||
| chr9:79678842
|
A | G | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.609+24767A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79678842 | ||||||
| chr9:79679070
|
C | T | 94 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.609+24995C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79679070 | ||||||
| chr9:79679074
|
G | A | 94 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.609+24999G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79679074 | ||||||
| chr9:79679239
|
T | C | 1 | a0001c0001t0003g0239 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.609+25164T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79679239 | ||||||
| chr9:79679277
|
A | G | 200 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(197): Show | 201 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.609+25202A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79679277 | ||||||
| chr9:79679277
|
A | T | 1 | a0001c0001t0003g0156 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.609+25202A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79679277 | ||||||
| chr9:79679357
|
T | G | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.609+25282T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79679357 | ||||||
| chr9:79679389
|
C | A | 98 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.609+25314C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79679389 | ||||||
| chr9:79679409
|
A | G | 1 | a0001c0001t0002g0173 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.609+25334A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79679409 | ||||||
| chr9:79679449
|
C | T | 98 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.610-25334C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79679449 | ||||||
| chr9:79679486
|
C | G | 98 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 98 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.610-25297C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79679486 | ||||||
| chr9:79679784
|
A | G | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-24999A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79679784 | ||||||
| chr9:79679793
|
G | A | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-24990G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79679793 | ||||||
| chr9:79679882
|
C | G | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.610-24901C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79679882 | ||||||
| chr9:79679968
|
T | C | 30 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(27): Show | 30 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.610-24815T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79679968 | ||||||
| chr9:79680028
|
T | C | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.610-24755T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79680028 | ||||||
| chr9:79680060
|
G | A | 16 | a0001c0001t0002g0002a0001c0001t0002g0167a0001c0001t0002g0168others(13): Show | 17 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.610-24723G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79680060 | ||||||
| chr9:79680110
|
G | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.610-24673G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79680110 | ||||||
| chr9:79680153
|
G | C | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.610-24630G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79680153 | ||||||
| chr9:79680222
|
C | G | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-24561C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79680222 | ||||||
| chr9:79680224
|
T | C | 202 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 203 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.610-24559T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79680224 | ||||||
| chr9:79680399
|
G | C | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.610-24384G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79680399 | ||||||
| chr9:79680399
|
G | T | 2 | a0001c0001t0002g0164a0001c0001t0002g0222 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.610-24384G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79680399 | ||||||
| chr9:79680498
|
G | A | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.610-24285G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79680498 | ||||||
| chr9:79680514
|
A | C | 1 | a0001c0001t0003g0244 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.610-24269A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79680514 | ||||||
| chr9:79680640
|
A | C | 1 | a0001c0001t0003g0255 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.610-24143A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79680640 | ||||||
| chr9:79680839
|
G | A | 1 | a0001c0001t0002g0163 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.610-23944G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79680839 | ||||||
| chr9:79680869
|
C | T | 1 | a0001c0001t0003g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.610-23914C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79680869 | ||||||
| chr9:79680914
|
T | C | 1 | a0001c0007t0002g0240 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.610-23869T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79680914 | ||||||
| chr9:79680943
|
T | A | 202 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 203 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.610-23840T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79680943 | ||||||
| chr9:79681083
|
A | C | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.610-23700A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79681083 | ||||||
| chr9:79681209
|
A | G | 3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197 | 3 | HG01891.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.610-23574A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79681209 | ||||||
| chr9:79681310
|
A | G | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.610-23473A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79681310 | ||||||
| chr9:79681326
|
A | ACGTTACT others(327): Show |
1 | a0001c0001t0001g0064 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.610-23452_610-2345 others(338): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79681326 | |||||
| chr9:79681332
|
T | C | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.610-23451T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79681332 | ||||||
| chr9:79681650
|
A | G | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 93 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.610-23133A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79681650 | ||||||
| chr9:79681745
|
G | A | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.610-23038G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79681745 | ||||||
| chr9:79681825
|
T | A | 1 | a0001c0001t0020g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.610-22958T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79681825 | ||||||
| chr9:79681832
|
A | ATG | 89 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.610-22921_610-2292 others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79681832 | |||||
| chr9:79681832
|
A | ATGTG | 11 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0098others(8): Show | 11 | HG00642.hp1 HG00642.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.610-22923_610-2292 others(8): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79681832 | |||||
| chr9:79681832
|
ATG | A | 8 | a0001c0001t0002g0214a0001c0001t0002g0218a0001c0001t0002g0220others(5): Show | 8 | HG01167.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.610-22921_610-2292 others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79681832 | |||||
| chr9:79681832
|
ATGTG | A | 57 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(54): Show | 58 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.610-22923_610-2292 others(8): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79681832 | |||||
| chr9:79681832
|
ATGTGTG | A | 19 | a0001c0001t0002g0208a0001c0001t0002g0249a0001c0001t0003g0030others(16): Show | 19 | HG00639.hp1 HG01346.hp2 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.610-22925_610-2292 others(10): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79681832 | |||||
| chr9:79681832
|
ATGTGTGT others(3): Show |
A | 6 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(3): Show | 6 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.610-22929_610-2292 others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79681832 | |||||
| chr9:79681834
|
GTGTGTGT others(23): Show |
G | 3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197 | 3 | HG01891.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.610-22933_610-2290 others(34): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79681834 | |||||
| chr9:79681835
|
T | C | 1 | a0001c0001t0020g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.610-22948T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79681835 | ||||||
| chr9:79681836
|
G | A | 1 | a0001c0001t0020g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.610-22947G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79681836 | ||||||
| chr9:79681856
|
GTGTGTGT others(1): Show |
G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.610-22919_610-2291 others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79681856 | |||||
| chr9:79681910
|
T | A | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.610-22873T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79681910 | ||||||
| chr9:79681996
|
G | C | 1 | a0001c0001t0004g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.610-22787G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79681996 | ||||||
| chr9:79682390
|
C | A | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.610-22393C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79682390 | ||||||
| chr9:79682502
|
C | A | 1 | a0001c0001t0005g0166 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.610-22281C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79682502 | ||||||
| chr9:79682902
|
T | C | 4 | a0001c0001t0002g0208a0001c0001t0002g0218a0001c0001t0002g0219others(1): Show | 4 | HG01243.hp2 HG02257.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.610-21881T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79682902 | ||||||
| chr9:79682923
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.610-21860C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79682923 | ||||||
| chr9:79682975
|
A | C | 1 | a0001c0010t0013g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.610-21808A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79682975 | ||||||
| chr9:79683075
|
A | G | 100 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.610-21708A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79683075 | ||||||
| chr9:79683373
|
A | G | 57 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(54): Show | 58 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.610-21410A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79683373 | ||||||
| chr9:79683388
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.610-21395G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79683388 | ||||||
| chr9:79683409
|
A | G | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.610-21374A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79683409 | ||||||
| chr9:79683467
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.610-21316A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79683467 | ||||||
| chr9:79683584
|
T | C | 1 | a0001c0001t0002g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.610-21199T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79683584 | ||||||
| chr9:79683727
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.610-21056C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79683727 | ||||||
| chr9:79683906
|
G | A | 1 | a0001c0001t0003g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.610-20877G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79683906 | ||||||
| chr9:79683927
|
C | T | 4 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0237others(1): Show | 4 | HG02055.hp2 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.610-20856C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79683927 | ||||||
| chr9:79683975
|
C | G | 199 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(196): Show | 200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.610-20808C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79683975 | ||||||
| chr9:79683989
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.610-20794A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79683989 | ||||||
| chr9:79684132
|
A | G | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.610-20651A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79684132 | ||||||
| chr9:79684243
|
T | A | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.610-20540T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79684243 | ||||||
| chr9:79684391
|
C | T | 1 | a0001c0001t0002g0183 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.610-20392C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79684391 | ||||||
| chr9:79684408
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.610-20375C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79684408 | ||||||
| chr9:79684449
|
A | G | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.610-20334A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79684449 | ||||||
| chr9:79684452
|
CTCTATTG others(20): Show |
C | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.610-20299_610-2027 others(31): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79684452 | |||||
| chr9:79684483
|
A | G | 12 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0211others(9): Show | 13 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.610-20300A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79684483 | ||||||
| chr9:79684581
|
C | T | 6 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(3): Show | 6 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.610-20202C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79684581 | ||||||
| chr9:79684681
|
T | A | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.610-20102T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79684681 | ||||||
| chr9:79684704
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.610-20079C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79684704 | ||||||
| chr9:79684726
|
C | T | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-20057C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79684726 | ||||||
| chr9:79684971
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.610-19812C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79684971 | ||||||
| chr9:79685057
|
A | C | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.610-19726A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79685057 | ||||||
| chr9:79685072
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.610-19711G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79685072 | ||||||
| chr9:79685590
|
A | G | 1 | a0001c0001t0003g0037 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.610-19193A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79685590 | ||||||
| chr9:79685706
|
A | G | 2 | a0001c0003t0003g0025a0001c0003t0003g0026 | 2 | HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.610-19077A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79685706 | ||||||
| chr9:79685756
|
A | G | 1 | a0001c0010t0013g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.610-19027A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79685756 | ||||||
| chr9:79685811
|
C | T | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.610-18972C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79685811 | ||||||
| chr9:79685830
|
T | C | 1 | a0001c0004t0004g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.610-18953T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79685830 | ||||||
| chr9:79685836
|
G | A | 195 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.610-18947G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79685836 | ||||||
| chr9:79685850
|
G | A | 1 | a0001c0001t0014g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.610-18933G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79685850 | ||||||
| chr9:79686225
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18966.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.610-18558C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79686225 | ||||||
| chr9:79686313
|
T | G | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.610-18470T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79686313 | ||||||
| chr9:79686370
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.610-18413G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79686370 | ||||||
| chr9:79686381
|
G | A | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.610-18402G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79686381 | ||||||
| chr9:79686425
|
C | A | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.610-18358C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79686425 | ||||||
| chr9:79686427
|
G | A | 1 | a0001c0004t0004g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.610-18356G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79686427 | ||||||
| chr9:79686507
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.610-18276A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79686507 | ||||||
| chr9:79686852
|
G | A | 1 | a0001c0001t0003g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.610-17931G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79686852 | ||||||
| chr9:79686877
|
A | G | 1 | a0001c0001t0003g0252 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.610-17906A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79686877 | ||||||
| chr9:79686880
|
A | G | 97 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.610-17903A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79686880 | ||||||
| chr9:79686991
|
G | A | 195 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.610-17792G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79686991 | ||||||
| chr9:79687041
|
C | G | 1 | a0001c0001t0018g0115 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.610-17742C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79687041 | ||||||
| chr9:79687376
|
G | A | 195 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.610-17407G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79687376 | ||||||
| chr9:79687446
|
T | A | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.610-17337T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79687446 | ||||||
| chr9:79687497
|
G | A | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.610-17286G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79687497 | ||||||
| chr9:79687789
|
G | C | 1 | a0001c0001t0001g0141 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.610-16994G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79687789 | ||||||
| chr9:79687800
|
C | A | 10 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0211others(7): Show | 10 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.610-16983C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79687800 | ||||||
| chr9:79687939
|
A | G | 101 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(98): Show | 101 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.610-16844A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79687939 | ||||||
| chr9:79688022
|
C | T | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.610-16761C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79688022 | ||||||
| chr9:79688053
|
TC | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 7 | HG00639.hp2 HG00642.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.610-16728delC | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79688053 | |||||
| chr9:79688070
|
G | A | 46 | a0001c0001t0003g0001a0001c0001t0003g0015a0001c0001t0003g0016others(43): Show | 47 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.610-16713G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79688070 | ||||||
| chr9:79688333
|
C | A | 5 | a0001c0001t0001g0076a0001c0001t0001g0093a0001c0001t0001g0098others(2): Show | 5 | HG02738.hp1 HG03471.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-16450C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79688333 | ||||||
| chr9:79688411
|
G | A | 97 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(94): Show | 97 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.610-16372G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79688411 | ||||||
| chr9:79688421
|
A | G | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-16362A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79688421 | ||||||
| chr9:79688630
|
T | A | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.610-16153T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79688630 | ||||||
| chr9:79688651
|
T | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.610-16132T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79688651 | ||||||
| chr9:79688719
|
C | T | 1 | a0001c0001t0003g0037 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.610-16064C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79688719 | ||||||
| chr9:79688779
|
A | G | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.610-16004A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79688779 | ||||||
| chr9:79688881
|
C | T | 1 | a0001c0001t0002g0223 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.610-15902C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79688881 | ||||||
| chr9:79688907
|
A | G | 52 | a0001c0001t0001g0077a0001c0001t0003g0001a0001c0001t0003g0015others(49): Show | 53 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.610-15876A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79688907 | ||||||
| chr9:79689025
|
C | T | 12 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(9): Show | 12 | HG01081.hp2 HG01106.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.610-15758C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79689025 | ||||||
| chr9:79689048
|
TTATTAGC others(24): Show |
T | 2 | a0001c0001t0008g0069a0001c0001t0008g0070 | 2 | HG01167.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.610-15731_610-1570 others(35): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79689048 | |||||
| chr9:79689067
|
C | T | 1 | a0001c0001t0014g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.610-15716C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79689067 | ||||||
| chr9:79689327
|
GT | G | 5 | a0001c0001t0001g0108a0001c0001t0001g0120a0001c0001t0001g0121others(2): Show | 5 | HG00621.hp1 HG00621.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.610-15444delT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79689327 | |||||
| chr9:79689471
|
A | C | 1 | a0001c0010t0013g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.610-15312A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79689471 | ||||||
| chr9:79689499
|
T | TA | 3 | a0001c0001t0001g0108a0001c0001t0001g0120a0001c0001t0001g0121 | 3 | HG00621.hp1 HG00621.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.610-15282dupA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79689499 | |||||
| chr9:79689546
|
A | G | 4 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0100others(1): Show | 4 | NA18612.hp1 NA18939.hp1 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.610-15237A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79689546 | ||||||
| chr9:79689590
|
A | T | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.610-15193A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79689590 | ||||||
| chr9:79689609
|
C | T | 1 | a0001c0001t0002g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.610-15174C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79689609 | ||||||
| chr9:79689882
|
G | A | 3 | a0001c0001t0004g0224a0001c0001t0004g0225a0001c0001t0004g0226 | 3 | HG01255.hp2 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.610-14901G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79689882 | ||||||
| chr9:79690077
|
A | T | 48 | a0001c0001t0001g0094a0001c0001t0001g0123a0001c0001t0003g0001others(45): Show | 49 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.610-14706A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79690077 | ||||||
| chr9:79690085
|
TTTTAA | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 9 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.610-14697_610-1469 others(9): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79690085 | ||||||
| chr9:79690127
|
C | G | 1 | a0001c0003t0003g0025 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.610-14656C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79690127 | ||||||
| chr9:79690251
|
A | G | 14 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197others(11): Show | 14 | HG01081.hp2 HG01106.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.610-14532A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79690251 | ||||||
| chr9:79690576
|
T | C | 1 | a0001c0001t0014g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.610-14207T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79690576 | ||||||
| chr9:79690645
|
G | A | 194 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(191): Show | 195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.610-14138G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79690645 | ||||||
| chr9:79690779
|
C | CT | 25 | a0001c0001t0001g0112a0001c0001t0002g0179a0001c0001t0002g0182others(22): Show | 25 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.610-13976dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79690779 | |||||
| chr9:79690779
|
C | CTT | 5 | a0001c0001t0004g0160a0001c0001t0004g0225a0001c0001t0004g0226others(2): Show | 5 | HG01081.hp2 HG01255.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.610-13977_610-1397 others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79690779 | |||||
| chr9:79690779
|
CT | C | 67 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.610-13976delT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79690779 | |||||
| chr9:79690779
|
CTT | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0076a0001c0001t0001g0093others(4): Show | 7 | HG00741.hp2 HG02155.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-13977_610-1397 others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79690779 | |||||
| chr9:79690779
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0002g0177a0001c0001t0002g0201 | 2 | HG01192.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.610-13985_610-1397 others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79690779 | |||||
| chr9:79690779
|
CTTTTTTT others(4): Show |
C | 29 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(26): Show | 29 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.610-13986_610-1397 others(15): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79690779 | |||||
| chr9:79690779
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.610-13987_610-1397 others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79690779 | |||||
| chr9:79690780
|
T | G | 1 | a0001c0001t0003g0016 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.610-14003T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79690780 | ||||||
| chr9:79690781
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.610-14002T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79690781 | ||||||
| chr9:79691054
|
G | A | 2 | a0001c0001t0002g0164a0001c0001t0002g0222 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.610-13729G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79691054 | ||||||
| chr9:79691115
|
C | T | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.610-13668C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79691115 | ||||||
| chr9:79691545
|
G | A | 2 | a0001c0003t0003g0025a0001c0003t0003g0026 | 2 | HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.610-13238G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79691545 | ||||||
| chr9:79691660
|
C | T | 2 | a0001c0001t0008g0069a0001c0001t0008g0070 | 2 | HG01167.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.610-13123C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79691660 | ||||||
| chr9:79692380
|
C | T | 5 | a0001c0001t0003g0174a0001c0001t0003g0235a0001c0001t0003g0236others(2): Show | 5 | HG02055.hp2 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-12403C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79692380 | ||||||
| chr9:79692486
|
C | T | 191 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(188): Show | 192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.610-12297C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79692486 | ||||||
| chr9:79692526
|
T | A | 1 | a0001c0001t0002g0189 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.610-12257T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79692526 | ||||||
| chr9:79692576
|
G | A | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-12207G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79692576 | ||||||
| chr9:79692890
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.610-11893C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79692890 | ||||||
| chr9:79693069
|
C | G | 1 | a0001c0001t0002g0150 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.610-11714C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79693069 | ||||||
| chr9:79693155
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.610-11628A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79693155 | ||||||
| chr9:79693380
|
G | A | 1 | a0001c0001t0003g0239 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.610-11403G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79693380 | ||||||
| chr9:79693453
|
G | A | 3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197 | 3 | HG01891.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.610-11330G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79693453 | ||||||
| chr9:79693475
|
G | A | 102 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(99): Show | 102 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.610-11308G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79693475 | ||||||
| chr9:79693681
|
T | G | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.610-11102T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79693681 | ||||||
| chr9:79693755
|
A | G | 201 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.610-11028A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79693755 | ||||||
| chr9:79693811
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.610-10972A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79693811 | ||||||
| chr9:79694073
|
C | T | 29 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(26): Show | 29 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.610-10710C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79694073 | ||||||
| chr9:79694300
|
T | G | 2 | a0001c0001t0008g0069a0001c0001t0008g0070 | 2 | HG01167.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.610-10483T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79694300 | ||||||
| chr9:79694350
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.610-10433C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79694350 | ||||||
| chr9:79694362
|
G | C | 1 | a0001c0001t0002g0203 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.610-10421G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79694362 | ||||||
| chr9:79694367
|
G | A | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.610-10416G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79694367 | ||||||
| chr9:79694409
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.610-10374A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79694409 | ||||||
| chr9:79694472
|
G | C | 1 | a0001c0001t0002g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.610-10311G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79694472 | ||||||
| chr9:79694633
|
A | C | 48 | a0001c0001t0001g0094a0001c0001t0001g0123a0001c0001t0003g0001others(45): Show | 49 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.610-10150A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79694633 | ||||||
| chr9:79694641
|
G | A | 195 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.610-10142G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79694641 | ||||||
| chr9:79694776
|
G | GA | 59 | a0001c0001t0001g0061a0001c0001t0001g0090a0001c0001t0001g0094others(56): Show | 60 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.610-9995dupA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79694776 | |||||
| chr9:79695158
|
T | A | 194 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(191): Show | 195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.610-9625T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79695158 | ||||||
| chr9:79695348
|
ATC | A | 147 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(144): Show | 148 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.610-9432_610-9431d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79695348 | |||||
| chr9:79695349
|
T | TCA | 27 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(24): Show | 27 | HG00733.hp2 HG01074.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.610-9433_610-9432i others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79695349 | |||||
| chr9:79695349
|
TCTCA | T | 7 | a0001c0001t0001g0075a0001c0001t0001g0130a0001c0001t0001g0131others(4): Show | 7 | HG01891.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-9432_610-9429d others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79695349 | |||||
| chr9:79695351
|
T | A | 40 | a0001c0001t0001g0006a0001c0001t0001g0117a0001c0001t0002g0161others(37): Show | 40 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.610-9432T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79695351 | ||||||
| chr9:79695415
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0060a0001c0001t0001g0076others(4): Show | 7 | HG00280.hp1 HG00741.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-9368G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79695415 | ||||||
| chr9:79695605
|
G | A | 2 | a0001c0001t0003g0036a0001c0001t0003g0039 | 2 | NA19009.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.610-9178G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79695605 | ||||||
| chr9:79695792
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.610-8991A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79695792 | ||||||
| chr9:79695983
|
T | A | 248 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(245): Show | 250 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.610-8800T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79695983 | ||||||
| chr9:79696313
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.610-8470A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79696313 | ||||||
| chr9:79696353
|
A | G | 1 | a0001c0001t0014g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.610-8430A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79696353 | ||||||
| chr9:79696424
|
A | T | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.610-8359A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79696424 | ||||||
| chr9:79696529
|
C | T | 48 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0003g0001others(45): Show | 49 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.610-8254C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79696529 | ||||||
| chr9:79696537
|
A | T | 1 | a0001c0001t0004g0227 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.610-8246A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79696537 | ||||||
| chr9:79696547
|
G | A | 48 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0003g0001others(45): Show | 49 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.610-8236G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79696547 | ||||||
| chr9:79696653
|
GA | G | 10 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(7): Show | 10 | HG01891.hp2 HG02055.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.610-8120delA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79696653 | |||||
| chr9:79696917
|
A | G | 193 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(190): Show | 194 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.610-7866A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79696917 | ||||||
| chr9:79696971
|
T | C | 2 | a0001c0003t0003g0025a0001c0003t0003g0026 | 2 | HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.610-7812T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79696971 | ||||||
| chr9:79697131
|
G | A | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 91 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.610-7652G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79697131 | ||||||
| chr9:79697226
|
C | T | 2 | a0001c0001t0003g0019a0001c0001t0003g0020 | 2 | HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.610-7557C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79697226 | ||||||
| chr9:79697234
|
C | A | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.610-7549C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79697234 | ||||||
| chr9:79697514
|
A | G | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.610-7269A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79697514 | ||||||
| chr9:79697660
|
C | T | 1 | a0001c0001t0002g0218 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.610-7123C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79697660 | ||||||
| chr9:79697824
|
G | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.610-6959G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79697824 | ||||||
| chr9:79698004
|
A | T | 1 | a0001c0001t0001g0071 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.610-6779A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79698004 | ||||||
| chr9:79698031
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.610-6752G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79698031 | ||||||
| chr9:79698117
|
G | A | 6 | a0001c0001t0003g0001a0001c0001t0003g0054a0001c0001t0003g0055others(3): Show | 7 | HG02109.hp2 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.610-6666G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79698117 | ||||||
| chr9:79698351
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.610-6432G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79698351 | ||||||
| chr9:79698622
|
C | T | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-6161C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79698622 | ||||||
| chr9:79698678
|
A | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0091 | 2 | HG00099.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.610-6105A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79698678 | ||||||
| chr9:79698822
|
G | GT | 3 | a0001c0001t0003g0153a0001c0001t0003g0248a0001c0001t0019g0023 | 3 | HG03195.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.610-5957dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79698822 | |||||
| chr9:79698859
|
T | TTA | 3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197 | 3 | HG01891.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.610-5913_610-5912d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79698859 | |||||
| chr9:79698872
|
C | CAT | 10 | a0001c0001t0001g0061a0001c0001t0001g0095a0001c0001t0003g0174others(7): Show | 10 | HG01106.hp1 HG01516.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.610-5896_610-5895d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79698872 | |||||
| chr9:79698872
|
C | CATAT | 28 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(25): Show | 28 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.610-5898_610-5895d others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79698872 | |||||
| chr9:79698951
|
A | G | 13 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(10): Show | 13 | HG00423.hp2 HG02074.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.610-5832A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79698951 | ||||||
| chr9:79699081
|
A | T | 2 | a0001c0004t0004g0004a0001c0004t0004g0250 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.610-5702A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699081 | ||||||
| chr9:79699143
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0076a0001c0001t0001g0093others(3): Show | 6 | HG00741.hp2 HG02738.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.610-5640C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699143 | ||||||
| chr9:79699389
|
A | G | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.610-5394A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699389 | ||||||
| chr9:79699455
|
G | C | 1 | a0001c0001t0004g0160 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.610-5328G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699455 | ||||||
| chr9:79699494
|
A | G | 152 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(149): Show | 153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.610-5289A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699494 | ||||||
| chr9:79699640
|
G | A | 1 | a0001c0001t0002g0199 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.610-5143G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699640 | ||||||
| chr9:79699777
|
T | TTGCTTTC others(42): Show |
1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-5006_610-5005i others(51): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699777 | ||||||
| chr9:79699780
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-5003A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699780 | ||||||
| chr9:79699782
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-5001T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699782 | ||||||
| chr9:79699796
|
C | A | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4987C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699796 | ||||||
| chr9:79699805
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4978A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699805 | ||||||
| chr9:79699806
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4977G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699806 | ||||||
| chr9:79699820
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4963T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699820 | ||||||
| chr9:79699821
|
C | A | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4962C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699821 | ||||||
| chr9:79699823
|
T | G | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4960T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699823 | ||||||
| chr9:79699839
|
T | G | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4944T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699839 | ||||||
| chr9:79699840
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4943G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699840 | ||||||
| chr9:79699842
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4941A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699842 | ||||||
| chr9:79699852
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4931T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699852 | ||||||
| chr9:79699858
|
G | T | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4925G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699858 | ||||||
| chr9:79699861
|
T | G | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4922T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699861 | ||||||
| chr9:79699864
|
TGAAAGGA others(4): Show |
T | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4918_610-4908d others(13): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699864 | ||||||
| chr9:79699893
|
G | A | 3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197 | 3 | HG01891.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.610-4890G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699893 | ||||||
| chr9:79699907
|
T | G | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4876T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699907 | ||||||
| chr9:79699910
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4873A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699910 | ||||||
| chr9:79699928
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4855T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699928 | ||||||
| chr9:79699931
|
CTATGCTG others(3): Show |
C | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4851_610-4842d others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699931 | ||||||
| chr9:79699943
|
A | T | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4840A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699943 | ||||||
| chr9:79699945
|
G | T | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4838G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699945 | ||||||
| chr9:79699957
|
T | G | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4826T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699957 | ||||||
| chr9:79699961
|
T | A | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4822T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699961 | ||||||
| chr9:79699963
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4820G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699963 | ||||||
| chr9:79699966
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4817A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699966 | ||||||
| chr9:79699981
|
G | T | 1 | a0001c0001t0001g0100 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.610-4802G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79699981 | ||||||
| chr9:79700152
|
CAGCCCGT others(4): Show |
C | 4 | a0001c0001t0003g0028a0001c0001t0003g0153a0001c0001t0003g0248others(1): Show | 4 | HG03195.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.610-4630_610-4620d others(13): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79700152 | ||||||
| chr9:79700715
|
C | T | 1 | a0001c0001t0003g0030 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.610-4068C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79700715 | ||||||
| chr9:79700770
|
G | T | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-4013G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79700770 | ||||||
| chr9:79700955
|
T | A | 2 | a0001c0004t0004g0004a0001c0004t0004g0250 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.610-3828T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79700955 | ||||||
| chr9:79700974
|
A | G | 1 | a0001c0001t0015g0072 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.610-3809A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79700974 | ||||||
| chr9:79701019
|
TAATAA | T | 2 | a0001c0001t0002g0204a0001c0001t0002g0213 | 2 | HG00733.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.610-3756_610-3752d others(7): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79701019 | |||||
| chr9:79701060
|
C | T | 1 | a0001c0001t0003g0252 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.610-3723C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79701060 | ||||||
| chr9:79701285
|
A | T | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.610-3498A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79701285 | ||||||
| chr9:79701330
|
A | G | 1 | a0001c0001t0003g0236 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.610-3453A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79701330 | ||||||
| chr9:79701331
|
C | T | 29 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(26): Show | 29 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.610-3452C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79701331 | ||||||
| chr9:79701453
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.610-3330A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79701453 | ||||||
| chr9:79701655
|
T | A | 1 | a0001c0001t0003g0051 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.610-3128T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79701655 | ||||||
| chr9:79701656
|
A | T | 1 | a0001c0001t0003g0051 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.610-3127A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79701656 | ||||||
| chr9:79701765
|
G | A | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.610-3018G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79701765 | ||||||
| chr9:79701843
|
A | G | 2 | a0001c0001t0003g0031a0001c0001t0003g0054 | 2 | HG02723.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.610-2940A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79701843 | ||||||
| chr9:79701938
|
G | A | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.610-2845G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79701938 | ||||||
| chr9:79702155
|
G | C | 2 | a0001c0001t0008g0069a0001c0001t0008g0070 | 2 | HG01167.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.610-2628G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79702155 | ||||||
| chr9:79702573
|
C | T | 1 | a0001c0001t0010g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.610-2210C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79702573 | ||||||
| chr9:79702659
|
G | A | 1 | a0001c0001t0003g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.610-2124G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79702659 | ||||||
| chr9:79702669
|
T | G | 201 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(198): Show | 202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.610-2114T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79702669 | ||||||
| chr9:79702722
|
C | T | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.610-2061C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79702722 | ||||||
| chr9:79702900
|
A | C | 1 | a0001c0001t0003g0001 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.610-1883A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79702900 | ||||||
| chr9:79703014
|
A | T | 1 | a0001c0010t0013g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.610-1769A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79703014 | ||||||
| chr9:79703072
|
C | T | 2 | a0001c0005t0003g0253a0001c0005t0003g0254 | 2 | HG01943.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.610-1711C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79703072 | ||||||
| chr9:79703297
|
G | A | 2 | a0001c0001t0005g0165a0001c0001t0005g0166 | 2 | HG00558.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.610-1486G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79703297 | ||||||
| chr9:79703468
|
T | C | 2 | a0001c0001t0010g0210a0001c0002t0003g0078 | 2 | NA20905.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.610-1315T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79703468 | ||||||
| chr9:79703554
|
A | G | 30 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(27): Show | 30 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.610-1229A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79703554 | ||||||
| chr9:79703586
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.610-1197C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79703586 | ||||||
| chr9:79704049
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.610-734A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79704049 | ||||||
| chr9:79704114
|
ACTTT | A | 11 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0211others(8): Show | 11 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.610-660_610-657del others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr9 | 79704114 | |||||
| chr9:79704335
|
G | C | 53 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(50): Show | 54 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.610-448G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79704335 | ||||||
| chr9:79704422
|
A | C | 2 | a0001c0003t0003g0025a0001c0003t0003g0026 | 2 | HG01106.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.610-361A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79704422 | ||||||
| chr9:79704427
|
C | G | 1 | a0001c0001t0002g0142 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.610-356C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79704427 | ||||||
| chr9:79704484
|
T | A | 11 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(8): Show | 11 | HG01081.hp2 HG01106.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.610-299T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79704484 | ||||||
| chr9:79704523
|
C | T | 1 | a0001c0004t0004g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.610-260C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79704523 | ||||||
| chr9:79704746
|
A | T | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.610-37A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 8/19 | chr9 | 79704746 | ||||||
| chr9:79704947
|
T | C | 1 | a0001c0001t0001g0140 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.729+45T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 9/19 | chr9 | 79704947 | ||||||
| chr9:79705034
|
G | T | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.729+132G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 9/19 | chr9 | 79705034 | ||||||
| chr9:79705240
|
C | A | 2 | a0001c0001t0008g0069a0001c0001t0008g0070 | 2 | HG01167.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.729+338C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 9/19 | chr9 | 79705240 | ||||||
| chr9:79705347
|
T | C | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.729+445T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 9/19 | chr9 | 79705347 | ||||||
| chr9:79705462
|
A | G | 1 | a0001c0001t0002g0231 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.730-427A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 9/19 | chr9 | 79705462 | ||||||
| chr9:79705538
|
A | C | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.730-351A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 9/19 | chr9 | 79705538 | ||||||
| chr9:79705972
|
A | T | 190 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(187): Show | 191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.783+30A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 10/19 | chr9 | 79705972 | ||||||
| chr9:79706002
|
C | G | 1 | a0001c0001t0018g0115 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.783+60C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 10/19 | chr9 | 79706002 | ||||||
| chr9:79706017
|
C | A | 2 | a0001c0004t0004g0004a0001c0004t0004g0250 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.783+75C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 10/19 | chr9 | 79706017 | ||||||
| chr9:79706126
|
C | A | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.783+184C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 10/19 | chr9 | 79706126 | ||||||
| chr9:79706517
|
G | A | 3 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0157 | 3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.784-230G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 10/19 | chr9 | 79706517 | ||||||
| chr9:79706644
|
T | A | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.784-103T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 10/19 | chr9 | 79706644 | ||||||
| chr9:79706646
|
A | T | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.784-101A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 10/19 | chr9 | 79706646 | ||||||
| chr9:79706696
|
G | T | 1 | a0001c0001t0001g0123 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.784-51G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 10/19 | chr9 | 79706696 | ||||||
| chr9:79706731
|
C | T | 12 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(9): Show | 12 | HG01081.hp2 HG01106.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.784-16C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 10/19 | chr9 | 79706731 | ||||||
| chr9:79706996
|
G | A | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.936+97G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 11/19 | chr9 | 79706996 | ||||||
| chr9:79707397
|
A | C | 2 | a0001c0004t0004g0004a0001c0004t0004g0250 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.936+498A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 11/19 | chr9 | 79707397 | ||||||
| chr9:79707495
|
CA | C | 2 | a0001c0001t0002g0002a0001c0001t0002g0187 | 3 | HG01069.hp1 HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.936+597delA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 11/19 | chr9 | 79707495 | ||||||
| chr9:79707568
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.937-550A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 11/19 | chr9 | 79707568 | ||||||
| chr9:79707828
|
A | G | 1 | a0001c0001t0014g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.937-290A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 11/19 | chr9 | 79707828 | ||||||
| chr9:79708526
|
G | A | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1070-67G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 12/19 | chr9 | 79708526 | ||||||
| chr9:79709237
|
T | C | 112 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(109): Show | 112 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1264-386T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 13/19 | chr9 | 79709237 | ||||||
| chr9:79709471
|
A | G | 1 | a0001c0005t0003g0254 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1264-152A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 13/19 | chr9 | 79709471 | ||||||
| chr9:79709484
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1264-139T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 13/19 | chr9 | 79709484 | ||||||
| chr9:79709760
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0111 | 2 | NA18612.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1340+61G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79709760 | ||||||
| chr9:79710381
|
T | G | 14 | a0001c0001t0001g0101a0001c0001t0002g0198a0001c0001t0002g0201others(11): Show | 14 | HG01081.hp2 HG01192.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.1340+682T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79710381 | ||||||
| chr9:79710420
|
C | T | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1340+721C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79710420 | ||||||
| chr9:79710530
|
A | C | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1340+831A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79710530 | ||||||
| chr9:79710668
|
G | C | 1 | a0001c0001t0003g0051 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1340+969G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79710668 | ||||||
| chr9:79710760
|
C | G | 197 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(194): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1340+1061C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79710760 | ||||||
| chr9:79711117
|
T | G | 1 | a0001c0010t0013g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1340+1418T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79711117 | ||||||
| chr9:79711197
|
C | T | 198 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(195): Show | 199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1340+1498C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79711197 | ||||||
| chr9:79711294
|
A | G | 10 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0211others(7): Show | 10 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1340+1595A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79711294 | ||||||
| chr9:79711331
|
T | TTGAC | 202 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(199): Show | 203 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1340+1634_1340+163 others(8): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr9 | 79711331 | |||||
| chr9:79711453
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1340+1754C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79711453 | ||||||
| chr9:79711488
|
G | T | 1 | a0003c0006t0003g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1340+1789G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79711488 | ||||||
| chr9:79711650
|
A | G | 2 | a0001c0001t0004g0225a0001c0001t0004g0226 | 2 | HG01255.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1340+1951A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79711650 | ||||||
| chr9:79711699
|
G | A | 1 | a0001c0001t0002g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1340+2000G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79711699 | ||||||
| chr9:79711920
|
G | A | 1 | a0001c0001t0003g0019 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1340+2221G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79711920 | ||||||
| chr9:79711945
|
A | G | 12 | a0001c0001t0003g0042a0001c0001t0003g0044a0001c0001t0003g0045others(9): Show | 12 | HG01943.hp1 HG01975.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1340+2246A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79711945 | ||||||
| chr9:79712033
|
A | G | 1 | a0003c0006t0003g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1340+2334A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79712033 | ||||||
| chr9:79712487
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1340+2788A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79712487 | ||||||
| chr9:79712708
|
G | C | 1 | a0001c0001t0003g0244 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1340+3009G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79712708 | ||||||
| chr9:79712816
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1340+3117G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79712816 | ||||||
| chr9:79713059
|
A | C | 198 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(195): Show | 199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1340+3360A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79713059 | ||||||
| chr9:79713114
|
C | T | 1 | a0001c0010t0013g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1340+3415C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79713114 | ||||||
| chr9:79713323
|
C | A | 13 | a0001c0001t0001g0134a0001c0001t0004g0160a0001c0001t0004g0224others(10): Show | 13 | HG01081.hp2 HG01106.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.1340+3624C>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79713323 | ||||||
| chr9:79713493
|
T | C | 2 | a0001c0005t0003g0253a0001c0005t0003g0254 | 2 | HG01943.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1340+3794T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79713493 | ||||||
| chr9:79713521
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1340+3822C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79713521 | ||||||
| chr9:79713593
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1340+3894C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79713593 | ||||||
| chr9:79713851
|
TTTG | T | 146 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(143): Show | 146 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1340+4179_1340+418 others(7): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr9 | 79713851 | |||||
| chr9:79713896
|
G | T | 42 | a0001c0001t0001g0134a0001c0001t0002g0161a0001c0001t0002g0198others(39): Show | 42 | HG00733.hp2 HG01074.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.1340+4197G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79713896 | ||||||
| chr9:79714028
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1340+4329G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79714028 | ||||||
| chr9:79714237
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1341-4485A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79714237 | ||||||
| chr9:79714325
|
A | C | 148 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1341-4397A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79714325 | ||||||
| chr9:79714333
|
G | T | 3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197 | 3 | HG01891.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1341-4389G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79714333 | ||||||
| chr9:79714380
|
T | C | 129 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(126): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1341-4342T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79714380 | ||||||
| chr9:79714401
|
C | T | 13 | a0001c0001t0001g0134a0001c0001t0004g0160a0001c0001t0004g0224others(10): Show | 13 | HG01081.hp2 HG01106.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.1341-4321C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79714401 | ||||||
| chr9:79714405
|
T | C | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1341-4317T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79714405 | ||||||
| chr9:79714436
|
G | A | 1 | a0001c0004t0004g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1341-4286G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79714436 | ||||||
| chr9:79714669
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1341-4053T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79714669 | ||||||
| chr9:79714720
|
T | C | 1 | a0001c0001t0003g0050 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1341-4002T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79714720 | ||||||
| chr9:79714917
|
C | G | 1 | a0001c0001t0017g0084 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1341-3805C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79714917 | ||||||
| chr9:79715180
|
G | A | 34 | a0001c0001t0001g0012a0001c0001t0001g0076a0001c0001t0001g0093others(31): Show | 34 | HG00733.hp2 HG00741.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.1341-3542G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79715180 | ||||||
| chr9:79715197
|
T | A | 2 | a0001c0001t0002g0164a0001c0001t0002g0222 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1341-3525T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79715197 | ||||||
| chr9:79715198
|
A | T | 2 | a0001c0001t0002g0164a0001c0001t0002g0222 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1341-3524A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79715198 | ||||||
| chr9:79715438
|
G | A | 1 | a0001c0010t0013g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1341-3284G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79715438 | ||||||
| chr9:79715514
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0003g0035 | 3 | NA19000.hp1 NA19074.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1341-3208G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79715514 | ||||||
| chr9:79715526
|
A | G | 2 | a0001c0001t0002g0233a0001c0001t0002g0234 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1341-3196A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79715526 | ||||||
| chr9:79715614
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1341-3108C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79715614 | ||||||
| chr9:79715777
|
T | TG | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1341-2943dupG | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr9 | 79715777 | |||||
| chr9:79716001
|
T | C | 4 | a0001c0001t0001g0060a0001c0001t0001g0073a0001c0001t0001g0140others(1): Show | 4 | HG00280.hp1 HG01074.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.1341-2721T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79716001 | ||||||
| chr9:79716155
|
G | A | 29 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(26): Show | 29 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1341-2567G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79716155 | ||||||
| chr9:79716200
|
A | T | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1341-2522A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79716200 | ||||||
| chr9:79716286
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1341-2436G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79716286 | ||||||
| chr9:79716291
|
C | G | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1341-2431C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79716291 | ||||||
| chr9:79716502
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0076a0001c0001t0001g0093others(2): Show | 5 | HG00741.hp2 HG03471.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1341-2220C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79716502 | ||||||
| chr9:79716569
|
A | G | 1 | a0001c0001t0003g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1341-2153A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79716569 | ||||||
| chr9:79716682
|
C | G | 12 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(9): Show | 12 | HG01081.hp2 HG01106.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1341-2040C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79716682 | ||||||
| chr9:79716683
|
G | A | 29 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(26): Show | 29 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1341-2039G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79716683 | ||||||
| chr9:79716735
|
T | C | 1 | a0001c0001t0003g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1341-1987T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79716735 | ||||||
| chr9:79716758
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1341-1964T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79716758 | ||||||
| chr9:79716792
|
G | A | 5 | a0001c0001t0003g0053a0001c0001t0003g0154a0001c0001t0003g0155others(2): Show | 5 | HG02572.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1341-1930G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79716792 | ||||||
| chr9:79717047
|
T | C | 1 | a0001c0001t0003g0015 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1341-1675T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79717047 | ||||||
| chr9:79717119
|
G | A | 2 | a0001c0001t0002g0164a0001c0001t0002g0222 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1341-1603G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79717119 | ||||||
| chr9:79717178
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1341-1544G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79717178 | ||||||
| chr9:79717503
|
C | G | 4 | a0001c0001t0001g0099a0001c0001t0002g0191a0001c0001t0002g0192others(1): Show | 4 | NA18943.hp1 NA18960.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1341-1219C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79717503 | ||||||
| chr9:79717521
|
C | T | 11 | a0001c0001t0001g0012a0001c0001t0001g0076a0001c0001t0001g0093others(8): Show | 11 | HG00741.hp2 HG01167.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1341-1201C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79717521 | ||||||
| chr9:79717581
|
G | A | 1 | a0001c0001t0003g0040 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1341-1141G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79717581 | ||||||
| chr9:79717680
|
G | A | 2 | a0001c0001t0003g0015a0001c0001t0003g0016 | 2 | HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1341-1042G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79717680 | ||||||
| chr9:79717816
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1341-906G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79717816 | ||||||
| chr9:79717900
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1341-822C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79717900 | ||||||
| chr9:79717941
|
C | T | 7 | a0001c0001t0004g0160a0001c0001t0004g0224a0001c0001t0004g0225others(4): Show | 7 | HG01081.hp2 HG01255.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1341-781C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79717941 | ||||||
| chr9:79718085
|
G | A | 32 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(29): Show | 32 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1341-637G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79718085 | ||||||
| chr9:79718095
|
T | C | 32 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(29): Show | 32 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1341-627T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79718095 | ||||||
| chr9:79718147
|
A | C | 1 | a0001c0001t0003g0239 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1341-575A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79718147 | ||||||
| chr9:79718147
|
A | G | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1341-575A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79718147 | ||||||
| chr9:79718590
|
A | G | 9 | a0001c0001t0001g0077a0001c0001t0001g0139a0001c0001t0003g0015others(6): Show | 9 | HG00140.hp1 HG01433.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1341-132A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79718590 | ||||||
| chr9:79718659
|
C | G | 2 | a0001c0001t0002g0164a0001c0001t0002g0222 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1341-63C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 14/19 | chr9 | 79718659 | ||||||
| chr9:79719175
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0076a0001c0001t0001g0093others(2): Show | 5 | HG00741.hp2 HG03471.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1590+204C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 15/19 | chr9 | 79719175 | ||||||
| chr9:79719179
|
A | G | 2 | a0001c0001t0008g0069a0001c0001t0008g0070 | 2 | HG01167.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1590+208A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 15/19 | chr9 | 79719179 | ||||||
| chr9:79719206
|
A | T | 1 | a0001c0001t0002g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1590+235A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 15/19 | chr9 | 79719206 | ||||||
| chr9:79719266
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1590+295C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 15/19 | chr9 | 79719266 | ||||||
| chr9:79719290
|
A | G | 29 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(26): Show | 29 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1590+319A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 15/19 | chr9 | 79719290 | ||||||
| chr9:79719329
|
T | TG | 3 | a0001c0001t0003g0153a0001c0001t0003g0248a0001c0001t0019g0023 | 3 | HG03195.hp2 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1590+359dupG | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr9 | 79719329 | |||||
| chr9:79719490
|
A | G | 1 | a0001c0001t0003g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1590+519A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 15/19 | chr9 | 79719490 | ||||||
| chr9:79719528
|
T | C | 1 | a0001c0001t0003g0239 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1591-518T>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 15/19 | chr9 | 79719528 | ||||||
| chr9:79719620
|
C | T | 13 | a0001c0001t0001g0134a0001c0001t0004g0160a0001c0001t0004g0224others(10): Show | 13 | HG01081.hp2 HG01106.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.1591-426C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 15/19 | chr9 | 79719620 | ||||||
| chr9:79719774
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1591-272G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 15/19 | chr9 | 79719774 | ||||||
| chr9:79719925
|
A | G | 2 | a0001c0004t0004g0004a0001c0004t0004g0250 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1591-121A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 15/19 | chr9 | 79719925 | ||||||
| chr9:79719936
|
C | T | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1591-110C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 15/19 | chr9 | 79719936 | ||||||
| chr9:79720325
|
A | G | 29 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(26): Show | 29 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1838+32A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79720325 | ||||||
| chr9:79720375
|
T | TGG | 5 | a0001c0001t0001g0057a0001c0001t0003g0001a0001c0001t0003g0239others(2): Show | 6 | HG01261.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1838+84_1838+85dup others(2): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 79720375 | |||||
| chr9:79720377
|
GGT | G | 52 | a0001c0001t0001g0012a0001c0001t0001g0076a0001c0001t0001g0105others(49): Show | 52 | HG00099.hp2 HG00280.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1838+131_1838+132d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 79720377 | |||||
| chr9:79720377
|
GGTGT | G | 101 | a0001c0001t0001g0011a0001c0001t0001g0064a0001c0001t0001g0065others(98): Show | 103 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1838+129_1838+132d others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 79720377 | |||||
| chr9:79720377
|
GGTGTGT | G | 48 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(45): Show | 48 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.1838+127_1838+132d others(8): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 79720377 | |||||
| chr9:79720377
|
GGTGTGTG others(1): Show |
G | 12 | a0001c0001t0001g0060a0001c0001t0001g0099a0001c0001t0001g0124others(9): Show | 12 | HG00280.hp1 HG01074.hp1 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.1838+125_1838+132d others(10): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 79720377 | |||||
| chr9:79720377
|
GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0001g0071a0001c0001t0003g0028 | 2 | HG00099.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1838+123_1838+132d others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 79720377 | |||||
| chr9:79720377
|
GGTGTGTG others(11): Show |
G | 1 | a0001c0010t0013g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1838+115_1838+132d others(20): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 79720377 | |||||
| chr9:79720377
|
GGTGTGTG others(15): Show |
G | 1 | a0001c0001t0002g0144 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1838+111_1838+132d others(24): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 79720377 | |||||
| chr9:79720378
|
GTGT | G | 3 | a0001c0001t0001g0080a0001c0001t0010g0210a0001c0002t0003g0078 | 3 | NA19009.hp2 NA20905.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1838+86_1838+88del others(3): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79720378 | ||||||
| chr9:79720379
|
T | G | 13 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(10): Show | 13 | HG01069.hp2 HG01074.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1838+86T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79720379 | ||||||
| chr9:79720381
|
T | G | 30 | a0001c0001t0001g0012a0001c0001t0001g0058a0001c0001t0001g0059others(27): Show | 30 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1838+88T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79720381 | ||||||
| chr9:79720383
|
T | G | 86 | a0001c0001t0001g0011a0001c0001t0001g0064a0001c0001t0001g0065others(83): Show | 86 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1838+90T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79720383 | ||||||
| chr9:79720385
|
T | G | 69 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(66): Show | 69 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1838+92T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79720385 | ||||||
| chr9:79720387
|
T | G | 17 | a0001c0001t0001g0060a0001c0001t0001g0099a0001c0001t0001g0124others(14): Show | 17 | HG00280.hp1 HG01074.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1838+94T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79720387 | ||||||
| chr9:79720389
|
T | G | 5 | a0001c0001t0001g0071a0001c0001t0001g0128a0001c0001t0001g0129others(2): Show | 5 | HG00099.hp1 HG03453.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1838+96T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79720389 | ||||||
| chr9:79720414
|
GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0002g0021 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1838+122_1838+133d others(14): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79720414 | ||||||
| chr9:79720416
|
GTGTGTGT others(3): Show |
G | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1838+124_1838+133d others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79720416 | ||||||
| chr9:79720579
|
G | A | 32 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151others(29): Show | 32 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1838+286G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79720579 | ||||||
| chr9:79720654
|
C | T | 13 | a0001c0001t0001g0134a0001c0001t0004g0160a0001c0001t0004g0224others(10): Show | 13 | HG01081.hp2 HG01106.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.1838+361C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79720654 | ||||||
| chr9:79720810
|
C | G | 148 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1838+517C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79720810 | ||||||
| chr9:79720875
|
G | A | 1 | a0001c0010t0013g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1838+582G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79720875 | ||||||
| chr9:79720932
|
GA | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0076a0001c0001t0001g0093others(2): Show | 5 | HG00741.hp2 HG03471.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1838+643delA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 79720932 | |||||
| chr9:79721471
|
A | AT | 6 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1839-263dupT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 79721471 | |||||
| chr9:79721563
|
C | T | 7 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0091others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1839-178C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79721563 | ||||||
| chr9:79721704
|
C | T | 1 | a0001c0010t0013g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1839-37C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 16/19 | chr9 | 79721704 | ||||||
| chr9:79721921
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1986+33C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 17/19 | chr9 | 79721921 | ||||||
| chr9:79722057
|
T | A | 3 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0197 | 3 | HG01891.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1986+169T>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 17/19 | chr9 | 79722057 | ||||||
| chr9:79722058
|
A | G | 198 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(195): Show | 199 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1986+170A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 17/19 | chr9 | 79722058 | ||||||
| chr9:79722106
|
A | G | 3 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0020 | 3 | HG02717.hp1 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1986+218A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 17/19 | chr9 | 79722106 | ||||||
| chr9:79722678
|
C | T | 1 | a0001c0001t0003g0030 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2137+77C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 18/19 | chr9 | 79722678 | ||||||
| chr9:79722955
|
A | G | 1 | a0001c0007t0002g0240 | 1 | HG02486.hp2 | splice_region_variant&intron_variant | LOW | c.2138-4A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 18/19 | chr9 | 79722955 | ||||||
| chr9:79723041
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG03195.hp2 | splice_region_variant&intron_variant | LOW | c.2214+6A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79723041 | ||||||
| chr9:79723124
|
T | G | 1 | a0001c0001t0011g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2214+89T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79723124 | ||||||
| chr9:79723346
|
TTG | T | 29 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(26): Show | 29 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2214+313_2214+314d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79723346 | |||||
| chr9:79723348
|
G | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2214+313G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79723348 | ||||||
| chr9:79723491
|
T | G | 1 | a0001c0001t0003g0255 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2214+456T>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79723491 | ||||||
| chr9:79723513
|
A | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2214+478A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79723513 | ||||||
| chr9:79723870
|
G | C | 1 | a0001c0001t0003g0017 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2214+835G>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79723870 | ||||||
| chr9:79723889
|
A | G | 197 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(194): Show | 198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.2214+854A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79723889 | ||||||
| chr9:79723932
|
A | T | 1 | a0001c0001t0003g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2214+897A>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79723932 | ||||||
| chr9:79723991
|
A | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0150a0001c0001t0002g0151 | 3 | HG02818.hp2 HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2214+956A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79723991 | ||||||
| chr9:79724037
|
A | C | 11 | a0001c0001t0001g0012a0001c0001t0001g0060a0001c0001t0001g0073others(8): Show | 11 | HG00280.hp1 HG00621.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.2215-1000A>C | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79724037 | ||||||
| chr9:79724062
|
A | G | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2215-975A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79724062 | ||||||
| chr9:79724069
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2215-968A>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79724069 | ||||||
| chr9:79724099
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2215-938C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79724099 | ||||||
| chr9:79724169
|
CT | C | 8 | a0001c0001t0001g0101a0001c0001t0003g0235a0001c0001t0003g0236others(5): Show | 8 | HG02055.hp2 HG02486.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2215-855delT | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79724169 | |||||
| chr9:79724290
|
C | G | 29 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(26): Show | 29 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2215-747C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79724290 | ||||||
| chr9:79724642
|
G | A | 29 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0002g0199others(26): Show | 29 | HG00733.hp2 HG01074.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2215-395G>A | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79724642 | ||||||
| chr9:79724815
|
G | T | 1 | a0001c0001t0014g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2215-222G>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79724815 | ||||||
| chr9:79724816
|
C | T | 1 | a0001c0001t0014g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2215-221C>T | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79724816 | ||||||
| chr9:79724848
|
TTAAAAAA others(7): Show |
T | 1 | a0001c0001t0003g0045 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2215-188_2215-175d others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79724848 | ||||||
| chr9:79724848
|
TTAAAAAA others(8): Show |
T | 17 | a0001c0001t0003g0042a0001c0001t0003g0044a0001c0001t0003g0046others(14): Show | 17 | HG01943.hp1 HG01975.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2215-188_2215-174d others(17): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79724848 | ||||||
| chr9:79724849
|
T | TA | 18 | a0001c0001t0001g0134a0001c0001t0002g0159a0001c0001t0002g0162others(15): Show | 18 | HG01106.hp1 HG01255.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.2215-156dupA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79724849 | |||||
| chr9:79724849
|
T | TAA | 7 | a0001c0001t0002g0171a0001c0001t0002g0183a0001c0001t0002g0218others(4): Show | 7 | HG02257.hp1 HG02622.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2215-157_2215-156d others(4): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79724849 | |||||
| chr9:79724849
|
T | TAAA | 7 | a0001c0001t0001g0082a0001c0001t0001g0091a0001c0001t0002g0021others(4): Show | 7 | HG01081.hp2 HG02735.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2215-158_2215-156d others(5): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79724849 | |||||
| chr9:79724849
|
T | TAAAA | 38 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0065others(35): Show | 38 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.2215-159_2215-156d others(6): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79724849 | |||||
| chr9:79724849
|
T | TAAAAA | 44 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(41): Show | 45 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.2215-160_2215-156d others(7): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79724849 | |||||
| chr9:79724849
|
T | TAAAAAA | 20 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0077others(17): Show | 20 | HG00423.hp1 HG00423.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.2215-161_2215-156d others(8): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79724849 | |||||
| chr9:79724849
|
T | TAAAAAAA | 8 | a0001c0001t0001g0058a0001c0001t0001g0087a0001c0001t0001g0090others(5): Show | 8 | HG00140.hp1 HG01109.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.2215-162_2215-156d others(9): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79724849 | |||||
| chr9:79724849
|
T | TAAAAAAA others(3): Show |
4 | a0001c0001t0001g0102a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | HG02970.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2215-165_2215-156d others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79724849 | |||||
| chr9:79724849
|
T | TAAAAAAA others(4): Show |
1 | a0001c0001t0001g0130 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2215-166_2215-156d others(13): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79724849 | |||||
| chr9:79724849
|
T | TAAAAAAA others(7): Show |
1 | a0001c0001t0001g0135 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2215-169_2215-156d others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79724849 | |||||
| chr9:79724849
|
TA | T | 17 | a0001c0001t0001g0012a0001c0001t0001g0076a0001c0001t0001g0093others(14): Show | 17 | HG00558.hp1 HG00741.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.2215-156delA | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79724849 | |||||
| chr9:79724849
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0112 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2215-165_2215-156d others(12): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79724849 | |||||
| chr9:79724849
|
TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0001g0103a0001c0001t0001g0114 | 2 | HG04204.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2215-166_2215-156d others(13): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79724849 | |||||
| chr9:79724849
|
TAAAAAAA others(7): Show |
T | 1 | a0001c0001t0014g0251 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2215-169_2215-156d others(16): Show |
TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr9 | 79724849 | |||||
| chr9:79724922
|
C | G | 2 | a0001c0001t0003g0153a0001c0001t0019g0023 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2215-115C>G | TLE4 | ENSG00000106829.21 | transcript | ENST00000376552.8 | protein_coding | 19/19 | chr9 | 79724922 |