Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9524 |
|---|---|
| ensemblid | ENSG00000099797.15 |
| hgncid | 4551 |
| symbol | TECR |
| name | trans-2,3-enoyl-CoA reductase |
| refseq_nuc | NM_138501.6 |
| refseq_prot | NP_612510.1 |
| ensembl_nuc | ENST00000215567.10 |
| ensembl_prot | ENSP00000215567.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 14529594 |
| end | 14565980 |
| strand | + |
| ver | v1.2 |
| region | chr19:14529594-14565980 |
| region5000 | chr19:14524594-14570980 |
| regionname0 | TECR_chr19_14529594_14565980 |
| regionname5000 | TECR_chr19_14524594_14570980 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 927 | 271 | 49 | 78 | 94 | 14 | 34 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| c0002 | 0/0 | 927 | 30 | 22 | 1 | 2 | 1 | 4 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| c0003 | 0/0 | 927 | 15 | 15 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| c0004 | 0/0 | 928 | 6 | 0 | 2 | 3 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| c0005 | 0/0 | 927 | 6 | 6 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| c0006 | 0/0 | 928 | 3 | 0 | 1 | 0 | 1 | 1 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| c0007 | 0/0 | 927 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 213 | 325 | 92 | 82 | 98 | 16 | 35 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| t0002 | 0/0 | 213 | 5 | 0 | 0 | 0 | 0 | 5 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| t0003 | 0/0 | 213 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| t0004 | 0/0 | 213 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0314 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 927 | 271 | 49 | 78 | 94 | 14 | 34 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| a0001c0002 | 0/0 | 927 | 30 | 22 | 1 | 2 | 1 | 4 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| a0001c0003 | 0/0 | 927 | 15 | 15 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| a0001c0005 | 0/0 | 927 | 6 | 6 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| a0001c0007 | 0/0 | 927 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| a0002c0004 | 0/0 | 928 | 6 | 0 | 2 | 3 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| a0002c0006 | 0/0 | 928 | 3 | 0 | 1 | 0 | 1 | 1 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1139 | 264 | 49 | 78 | 92 | 14 | 29 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| a0001c0001t0002 | 0/0 | 1139 | 5 | 0 | 0 | 0 | 0 | 5 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| a0001c0001t0003 | 0/0 | 1139 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| a0001c0001t0004 | 0/0 | 1139 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| a0001c0002t0001 | 0/0 | 1139 | 30 | 22 | 1 | 2 | 1 | 4 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| a0001c0003t0001 | 0/0 | 1139 | 15 | 15 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| a0001c0005t0001 | 0/0 | 1139 | 6 | 6 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| a0001c0007t0001 | 0/0 | 1139 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| a0002c0004t0001 | 0/0 | 1140 | 6 | 0 | 2 | 3 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| a0002c0006t0001 | 0/0 | 1140 | 3 | 0 | 1 | 0 | 1 | 1 | TECR_chr19_14524594_14570980 | TECR | copy fasta | chr19 | 14524594 | 14570980 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0314 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0003t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0003t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0003t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0003t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0003t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0005t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0005t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0005t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0005t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0001c0007t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0002c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0002c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0002c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0002c0004t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0002c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0002c0004t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0002c0006t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0002c0006t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| a0002c0006t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | GBR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0307 | EUR | GBR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0283 | EUR | GBR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | GBR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | FIN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | FIN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0284 | EUR | FIN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0256 | EUR | FIN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00673 | hp2 | a0002 | c0004 | t0001 | g0081 | EAS | CHS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0097 | EUR | IBS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | IBS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0322 | EUR | IBS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01517 | hp2 | a0002 | c0006 | t0001 | g0128 | EUR | IBS | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01934 | hp2 | a0002 | c0006 | t0001 | g0316 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02132 | hp2 | a0002 | c0004 | t0001 | g0076 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02148 | hp1 | a0002 | c0004 | t0001 | g0161 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02148 | hp2 | a0002 | c0004 | t0001 | g0276 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CDX | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CDX | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0297 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0028 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0041 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0051 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02738 | hp2 | a0002 | c0006 | t0001 | g0209 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0024 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0017 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02897 | hp1 | a0001 | c0005 | t0001 | g0021 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0291 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0325 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0247 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03195 | hp1 | a0001 | c0005 | t0001 | g0034 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03209 | hp1 | a0001 | c0003 | t0001 | g0298 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0123 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0304 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0040 | AFR | GWD | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0320 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | MSL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0102 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0224 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03942 | hp1 | a0002 | c0004 | t0001 | g0129 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0216 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0230 | AFR | YRI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | YRI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | YRI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18944 | hp1 | a0001 | c0007 | t0001 | g0073 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18963 | hp1 | a0002 | c0004 | t0001 | g0199 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19240 | hp1 | a0001 | c0005 | t0001 | g0066 | AFR | YRI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | YRI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0303 | AFR | ASW | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | ASW | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | TSI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | TSI | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0134 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02486 | hp2 | a0001 | c0005 | t0001 | g0033 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0062 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | USA | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | USA | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0314 | REF | REF | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0177 | REF | REF | TECR_chr19_14524594_14570980 | TECR | chr19 | 14524594 | 14570980 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:14563670
|
A | AC | 1 | a0002 | 9 | HG00673.hp2 HG01517.hp2 HG01934.hp2 others(6): Show |
frameshift_variant | HIGH | c.135dupC | p.Ala46fs | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 4/13 | 239/1139 | 136/927 | 46/308 | INFO_REALIGN_3_PRIME | chr19 | 14563670 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:14564260
|
C | A | 1 | a0001c0003 | 15 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
synonymous_variant | LOW | c.462C>A | p.Gly154Gly | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 7/13 | 565/1139 | 462/927 | 154/308 | chr19 | 14564260 | ||
| chr19:14564791
|
C | T | 1 | a0001c0007 | 1 | NA18944.hp1 | synonymous_variant | LOW | c.495C>T | p.Cys165Cys | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 8/13 | 598/1139 | 495/927 | 165/308 | chr19 | 14564791 | ||
| chr19:14565077
|
C | T | 2 | a0001c0003a0001c0005 | 21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
synonymous_variant | LOW | c.618C>T | p.Leu206Leu | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 10/13 | 721/1139 | 618/927 | 206/308 | chr19 | 14565077 | ||
| chr19:14565766
|
C | T | 2 | a0001c0002a0002c0006 | 33 | HG01515.hp1 HG01517.hp2 HG01934.hp2 others(30): Show |
synonymous_variant | LOW | c.822C>T | p.Gly274Gly | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 13/13 | 925/1139 | 822/927 | 274/308 | chr19 | 14565766 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:14529601
|
C | T | 1 | a0001c0001t0004 | 1 | NA19066.hp2 | 5_prime_UTR_variant | MODIFIER | c.-96C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/13 | 96 | chr19 | 14529601 | |||||
| chr19:14529623
|
T | C | 1 | a0001c0001t0002 | 5 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-74T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/13 | 74 | chr19 | 14529623 | |||||
| chr19:14529672
|
G | A | 1 | a0001c0001t0003 | 1 | HG00558.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/13 | 25 | chr19 | 14529672 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:14529876
|
A | G | 1 | a0001c0001t0001g0331 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15+165A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14529876 | ||||||
| chr19:14529965
|
C | T | 1 | a0001c0001t0001g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.15+254C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14529965 | ||||||
| chr19:14529986
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0002g0003a0001c0001t0002g0004others(3): Show | 6 | HG02055.hp1 HG03710.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+275T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14529986 | ||||||
| chr19:14530225
|
A | G | 37 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(34): Show | 37 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.15+514A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14530225 | ||||||
| chr19:14530242
|
T | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(46): Show | 49 | HG00099.hp2 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.15+531T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14530242 | ||||||
| chr19:14530484
|
T | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+773T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14530484 | ||||||
| chr19:14530656
|
G | C | 1 | a0001c0001t0001g0331 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15+945G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14530656 | ||||||
| chr19:14530828
|
A | G | 5 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(2): Show | 5 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+1117A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14530828 | ||||||
| chr19:14530855
|
G | T | 1 | a0001c0001t0001g0292 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.15+1144G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14530855 | ||||||
| chr19:14531056
|
CAG | C | 3 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0329 | 3 | HG01070.hp2 HG01071.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.15+1348_15+1349del others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14531056 | |||||
| chr19:14531097
|
C | T | 1 | a0001c0002t0001g0291 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.15+1386C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531097 | ||||||
| chr19:14531240
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.15+1529T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531240 | ||||||
| chr19:14531284
|
T | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(13): Show | 16 | HG02145.hp2 HG02451.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+1573T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531284 | ||||||
| chr19:14531288
|
C | G | 1 | a0001c0001t0001g0290 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.15+1577C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531288 | ||||||
| chr19:14531326
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(185): Show | 189 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.15+1615T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531326 | ||||||
| chr19:14531327
|
G | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(3): Show | 6 | HG01123.hp1 HG02109.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+1616G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531327 | ||||||
| chr19:14531329
|
G | A | 1 | a0001c0002t0001g0027 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.15+1618G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531329 | ||||||
| chr19:14531332
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+1621C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531332 | ||||||
| chr19:14531350
|
G | C | 21 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(18): Show | 21 | HG02145.hp2 HG02451.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.15+1639G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531350 | ||||||
| chr19:14531382
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+1671C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531382 | ||||||
| chr19:14531399
|
A | G | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG02083.hp2 HG03831.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.15+1688A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531399 | ||||||
| chr19:14531453
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01934.hp1 HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.15+1742G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531453 | ||||||
| chr19:14531679
|
C | A | 6 | a0001c0001t0001g0296a0001c0001t0001g0299a0001c0001t0001g0300others(3): Show | 6 | HG01109.hp2 HG02257.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+1968C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531679 | ||||||
| chr19:14531869
|
C | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+2158C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14531869 | ||||||
| chr19:14532009
|
G | GA | 18 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0035others(15): Show | 18 | HG01123.hp1 HG01243.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.15+2320dupA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14532009 | |||||
| chr19:14532009
|
GA | G | 14 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0142others(11): Show | 14 | HG00140.hp2 HG01070.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.15+2320delA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14532009 | |||||
| chr19:14532009
|
GAAAA | G | 14 | a0001c0001t0001g0019a0001c0001t0001g0145a0001c0001t0001g0146others(11): Show | 14 | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.15+2317_15+2320del others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14532009 | |||||
| chr19:14532010
|
A | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.15+2299A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532010 | ||||||
| chr19:14532032
|
G | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+2321G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532032 | ||||||
| chr19:14532033
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(50): Show | 54 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.15+2322C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532033 | ||||||
| chr19:14532283
|
C | T | 14 | a0001c0001t0001g0019a0001c0001t0001g0145a0001c0001t0001g0146others(11): Show | 14 | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.15+2572C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532283 | ||||||
| chr19:14532344
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(224): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.15+2633A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532344 | ||||||
| chr19:14532420
|
C | T | 2 | a0001c0001t0001g0328a0001c0001t0001g0329 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.15+2709C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532420 | ||||||
| chr19:14532456
|
T | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(160): Show | 164 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.15+2745T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532456 | ||||||
| chr19:14532512
|
C | CA | 22 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0037others(19): Show | 22 | HG01074.hp2 HG01175.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.15+2824dupA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14532512 | |||||
| chr19:14532512
|
CA | C | 70 | a0001c0001t0001g0036a0001c0001t0001g0068a0001c0001t0001g0069others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.15+2824delA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14532512 | |||||
| chr19:14532512
|
CAA | C | 11 | a0001c0001t0001g0146a0001c0001t0001g0284a0001c0001t0001g0288others(8): Show | 11 | HG00323.hp1 HG01975.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.15+2823_15+2824del others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14532512 | |||||
| chr19:14532527
|
A | T | 1 | a0001c0001t0001g0244 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.15+2816A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532527 | ||||||
| chr19:14532542
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.15+2831C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532542 | ||||||
| chr19:14532613
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0005t0001g0021others(1): Show | 4 | HG01123.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+2902C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532613 | ||||||
| chr19:14532687
|
C | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(65): Show | 69 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.15+2976C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532687 | ||||||
| chr19:14532696
|
G | A | 18 | a0001c0001t0001g0019a0001c0001t0001g0145a0001c0001t0001g0146others(15): Show | 18 | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.15+2985G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532696 | ||||||
| chr19:14532799
|
G | A | 8 | a0001c0001t0001g0019a0001c0002t0001g0013a0001c0002t0001g0015others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+3088G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532799 | ||||||
| chr19:14532831
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.15+3120C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532831 | ||||||
| chr19:14532907
|
C | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+3196C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532907 | ||||||
| chr19:14532908
|
G | C | 2 | a0001c0002t0001g0303a0001c0002t0001g0304 | 2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.15+3197G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14532908 | ||||||
| chr19:14533044
|
C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(59): Show | 63 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.15+3333C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533044 | ||||||
| chr19:14533216
|
T | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+3505T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533216 | ||||||
| chr19:14533350
|
G | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+3639G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533350 | ||||||
| chr19:14533397
|
G | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+3686G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533397 | ||||||
| chr19:14533407
|
C | T | 82 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0036others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.15+3696C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533407 | ||||||
| chr19:14533548
|
A | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+3837A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533548 | ||||||
| chr19:14533595
|
C | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+3884C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533595 | ||||||
| chr19:14533595
|
C | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+3884C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533595 | ||||||
| chr19:14533680
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.15+3969T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533680 | ||||||
| chr19:14533797
|
C | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+4086C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533797 | ||||||
| chr19:14533849
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.15+4138A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533849 | ||||||
| chr19:14533992
|
T | A | 88 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.15+4281T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533992 | ||||||
| chr19:14533997
|
C | A | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.15+4286C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14533997 | ||||||
| chr19:14534003
|
A | G | 8 | a0001c0001t0001g0019a0001c0002t0001g0013a0001c0002t0001g0015others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+4292A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534003 | ||||||
| chr19:14534009
|
T | C | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+4298T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534009 | ||||||
| chr19:14534063
|
C | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+4352C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534063 | ||||||
| chr19:14534089
|
T | G | 1 | a0001c0001t0001g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.15+4378T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534089 | ||||||
| chr19:14534116
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.15+4405A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534116 | ||||||
| chr19:14534126
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.15+4415C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534126 | ||||||
| chr19:14534164
|
G | A | 84 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.15+4453G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534164 | ||||||
| chr19:14534193
|
T | C | 51 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(48): Show | 51 | HG00099.hp2 HG00558.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.15+4482T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534193 | ||||||
| chr19:14534239
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.15+4528C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534239 | ||||||
| chr19:14534273
|
T | C | 92 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.15+4562T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534273 | ||||||
| chr19:14534300
|
AT | A | 84 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.15+4594delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534300 | |||||
| chr19:14534306
|
A | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+4595A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534306 | ||||||
| chr19:14534366
|
C | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+4655C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534366 | ||||||
| chr19:14534371
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.15+4660G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534371 | ||||||
| chr19:14534408
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.15+4697G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534408 | ||||||
| chr19:14534423
|
C | CT | 83 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(80): Show | 83 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.15+4742dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | |||||
| chr19:14534423
|
C | CTT | 34 | a0001c0001t0001g0010a0001c0001t0001g0050a0001c0001t0001g0052others(31): Show | 34 | HG00735.hp2 HG01081.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.15+4741_15+4742dup others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | |||||
| chr19:14534423
|
C | CTTT | 16 | a0001c0001t0001g0148a0001c0001t0001g0296a0001c0001t0001g0299others(13): Show | 16 | HG01109.hp2 HG01192.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+4740_15+4742dup others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | |||||
| chr19:14534423
|
CT | C | 39 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0042others(36): Show | 39 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.15+4742delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | |||||
| chr19:14534423
|
CTT | C | 20 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0095others(17): Show | 21 | HG00558.hp2 HG01081.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.15+4741_15+4742del others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | |||||
| chr19:14534423
|
CTTTT | C | 29 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0084others(26): Show | 29 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.15+4739_15+4742del others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | |||||
| chr19:14534423
|
CTTTTT | C | 35 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0077others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(32): Show |
intron_variant | MODIFIER | c.15+4738_15+4742del others(5): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | |||||
| chr19:14534423
|
CTTTTTT | C | 7 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0145others(4): Show | 7 | HG02280.hp1 HG02572.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+4737_15+4742del others(6): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | |||||
| chr19:14534423
|
CTTTTTTT | C | 7 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(4): Show | 7 | HG02622.hp1 HG02630.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+4736_15+4742del others(7): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | |||||
| chr19:14534423
|
CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0146others(6): Show | 9 | HG02109.hp1 HG02451.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+4735_15+4742del others(8): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | |||||
| chr19:14534423
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0305 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.15+4732_15+4742del others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | |||||
| chr19:14534423
|
CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0001g0160a0001c0001t0001g0170a0001c0001t0001g0171others(12): Show | 15 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.15+4731_15+4742del others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | |||||
| chr19:14534423
|
CTTTTTTT others(6): Show |
C | 7 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0001g0165others(4): Show | 7 | HG01070.hp1 HG01358.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.15+4730_15+4742del others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14534423 | |||||
| chr19:14534479
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.15+4768A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534479 | ||||||
| chr19:14534491
|
A | C | 1 | a0001c0001t0001g0156 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.15+4780A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534491 | ||||||
| chr19:14534528
|
C | T | 2 | a0001c0001t0001g0270a0001c0001t0001g0282 | 2 | HG00738.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.15+4817C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534528 | ||||||
| chr19:14534549
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+4838C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534549 | ||||||
| chr19:14534648
|
G | C | 1 | a0001c0001t0001g0036 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.15+4937G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534648 | ||||||
| chr19:14534804
|
G | A | 3 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0329 | 3 | HG01070.hp2 HG01071.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.15+5093G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534804 | ||||||
| chr19:14534995
|
G | A | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+5284G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14534995 | ||||||
| chr19:14535198
|
C | A | 68 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(65): Show | 68 | HG00099.hp2 HG00558.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.15+5487C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535198 | ||||||
| chr19:14535245
|
T | C | 92 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.15+5534T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535245 | ||||||
| chr19:14535391
|
C | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+5680C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535391 | ||||||
| chr19:14535438
|
C | T | 2 | a0001c0002t0001g0236a0001c0002t0001g0243 | 2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.15+5727C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535438 | ||||||
| chr19:14535455
|
CGAGATCG others(242): Show |
C | 2 | a0001c0002t0001g0029a0001c0005t0001g0028 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.15+5753_15+6001del | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535455 | |||||
| chr19:14535456
|
G | A | 51 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(48): Show | 51 | HG00099.hp2 HG00558.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.15+5745G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535456 | ||||||
| chr19:14535475
|
C | G | 4 | a0001c0001t0001g0190a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG01261.hp2 HG01943.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+5764C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535475 | ||||||
| chr19:14535493
|
C | T | 1 | a0002c0006t0001g0316 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.15+5782C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535493 | ||||||
| chr19:14535494
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.15+5783G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535494 | ||||||
| chr19:14535506
|
CA | C | 11 | a0001c0001t0001g0031a0001c0001t0001g0044a0001c0001t0001g0055others(8): Show | 11 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+5833delA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535506 | |||||
| chr19:14535506
|
CAA | C | 8 | a0001c0001t0001g0156a0001c0001t0001g0187a0001c0001t0001g0188others(5): Show | 8 | HG01099.hp2 HG01169.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+5832_15+5833del others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535506 | |||||
| chr19:14535506
|
CAAA | C | 14 | a0001c0001t0001g0147a0001c0001t0001g0223a0001c0001t0001g0256others(11): Show | 14 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(11): Show |
intron_variant | MODIFIER | c.15+5831_15+5833del others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535506 | |||||
| chr19:14535506
|
CAAAA | C | 7 | a0001c0001t0001g0067a0001c0001t0001g0160a0001c0001t0001g0167others(4): Show | 7 | HG01109.hp2 HG01358.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.15+5830_15+5833del others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535506 | |||||
| chr19:14535506
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0318 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.15+5824_15+5833del others(10): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535506 | |||||
| chr19:14535506
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0003t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.15+5822_15+5833del others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535506 | |||||
| chr19:14535506
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0231 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.15+5821_15+5833del others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535506 | |||||
| chr19:14535517
|
AAAAAAAA others(21): Show |
A | 1 | a0001c0001t0001g0232 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.15+5808_15+5835del others(28): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535517 | |||||
| chr19:14535521
|
AAAAAAAA others(35): Show |
A | 2 | a0001c0001t0001g0143a0001c0003t0001g0141 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.15+5812_15+5853del others(42): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535521 | |||||
| chr19:14535523
|
AAAAAAAA others(35): Show |
A | 1 | a0001c0001t0001g0144 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.15+5814_15+5855del others(42): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535523 | |||||
| chr19:14535523
|
AAAAAAAA others(37): Show |
A | 1 | a0001c0001t0001g0142 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.15+5814_15+5857del others(44): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535523 | |||||
| chr19:14535525
|
AAAAAAAA others(19): Show |
A | 1 | a0001c0001t0001g0137 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.15+5816_15+5841del others(26): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535525 | |||||
| chr19:14535528
|
AAAAAAAA others(28): Show |
A | 3 | a0001c0001t0001g0023a0001c0005t0001g0021a0001c0005t0001g0024 | 3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.15+5819_15+5853del others(35): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535528 | |||||
| chr19:14535529
|
AAAAAAAA others(29): Show |
A | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.15+5820_15+5855del others(36): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535529 | |||||
| chr19:14535530
|
AAAAAAAA others(24): Show |
A | 1 | a0001c0003t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.15+5821_15+5851del others(31): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535530 | |||||
| chr19:14535530
|
AAAAAAAA others(28): Show |
A | 1 | a0001c0001t0001g0022 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.15+5821_15+5855del others(35): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535530 | |||||
| chr19:14535531
|
AAAAAAAA others(21): Show |
A | 1 | a0001c0001t0001g0322 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.15+5822_15+5849del others(28): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535531 | |||||
| chr19:14535531
|
AAAAAAAA others(23): Show |
A | 2 | a0001c0001t0001g0323a0001c0001t0001g0324 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.15+5822_15+5851del others(30): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535531 | |||||
| chr19:14535531
|
AAAAAAAA others(33): Show |
A | 1 | a0001c0005t0001g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.15+5822_15+5861del others(40): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535531 | |||||
| chr19:14535532
|
AAAAAAAA others(6): Show |
A | 2 | a0001c0001t0001g0319a0001c0005t0001g0034 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.15+5823_15+5835del others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535532 | |||||
| chr19:14535532
|
AAAAAAAA others(30): Show |
A | 1 | a0001c0001t0001g0251 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.15+5823_15+5859del others(37): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535532 | |||||
| chr19:14535533
|
AAAAAAAA others(19): Show |
A | 1 | a0001c0002t0001g0320 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.15+5824_15+5849del others(26): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535533 | |||||
| chr19:14535533
|
AAAAAAAA others(23): Show |
A | 6 | a0001c0001t0001g0135a0001c0001t0001g0305a0001c0001t0001g0321others(3): Show | 6 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+5824_15+5853del others(30): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535533 | |||||
| chr19:14535533
|
AAAAAAAA others(25): Show |
A | 1 | a0001c0001t0001g0092 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.15+5824_15+5855del others(32): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535533 | |||||
| chr19:14535533
|
AAAAAAAA others(29): Show |
A | 3 | a0001c0001t0001g0250a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG01891.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.15+5824_15+5859del others(36): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535533 | |||||
| chr19:14535533
|
AAAAAAAA others(31): Show |
A | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.15+5824_15+5861del others(38): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535533 | |||||
| chr19:14535534
|
AAAAAAAA others(18): Show |
A | 3 | a0001c0001t0001g0025a0001c0001t0002g0003a0001c0002t0001g0026 | 3 | HG02109.hp1 HG02723.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.15+5825_15+5849del others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535534 | |||||
| chr19:14535534
|
AAAAAAAA others(24): Show |
A | 1 | a0001c0001t0001g0002 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15+5825_15+5855del others(31): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535534 | |||||
| chr19:14535534
|
AAAAAAAA others(26): Show |
A | 2 | a0001c0001t0001g0133a0001c0001t0001g0331 | 2 | HG01257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.15+5825_15+5857del others(33): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535534 | |||||
| chr19:14535534
|
AAAAAAAA others(28): Show |
A | 1 | a0001c0001t0001g0269 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.15+5825_15+5859del others(35): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535534 | |||||
| chr19:14535534
|
AAAAAAAA others(30): Show |
A | 3 | a0001c0001t0001g0246a0001c0001t0001g0249a0001c0001t0001g0281 | 3 | HG01243.hp1 HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.15+5825_15+5861del others(37): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535534 | |||||
| chr19:14535534
|
AAAAAAAA others(32): Show |
A | 3 | a0001c0001t0001g0037a0001c0003t0001g0134a0001c0003t0001g0247 | 3 | HG02055.hp2 HG02109.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.15+5825_15+5863del others(39): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535534 | |||||
| chr19:14535535
|
AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0001g0229 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.15+5826_15+5845del others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535535 | |||||
| chr19:14535535
|
AAAAAAAA others(23): Show |
A | 2 | a0001c0001t0001g0112a0001c0001t0002g0007 | 2 | HG01081.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.15+5826_15+5855del others(30): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535535 | |||||
| chr19:14535535
|
AAAAAAAA others(25): Show |
A | 5 | a0001c0001t0001g0038a0001c0001t0001g0098a0001c0001t0001g0103others(2): Show | 5 | HG00280.hp2 HG01243.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+5826_15+5857del others(32): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535535 | |||||
| chr19:14535535
|
AAAAAAAA others(27): Show |
A | 2 | a0001c0001t0001g0091a0001c0001t0001g0295 | 2 | HG03834.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.15+5826_15+5859del others(34): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535535 | |||||
| chr19:14535535
|
AAAAAAAA others(29): Show |
A | 2 | a0001c0001t0001g0036a0001c0001t0001g0149 | 2 | HG03831.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.15+5826_15+5861del others(36): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535535 | |||||
| chr19:14535535
|
AAAAAAAA others(31): Show |
A | 4 | a0001c0001t0001g0136a0001c0001t0001g0248a0001c0001t0001g0280others(1): Show | 4 | HG00323.hp1 HG01433.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+5826_15+5863del others(38): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535535 | |||||
| chr19:14535536
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0002t0001g0243 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.15+5827_15+5837del others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | |||||
| chr19:14535536
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.15+5827_15+5839del others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | |||||
| chr19:14535536
|
AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0001g0315 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.15+5827_15+5845del others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | |||||
| chr19:14535536
|
AAAAAAAA others(14): Show |
A | 1 | a0001c0001t0001g0227 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.15+5827_15+5847del others(21): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | |||||
| chr19:14535536
|
AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0002g0006 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.15+5827_15+5849del others(23): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | |||||
| chr19:14535536
|
AAAAAAAA others(18): Show |
A | 3 | a0001c0001t0001g0058a0001c0001t0001g0071a0001c0001t0001g0095 | 3 | HG02735.hp2 HG03017.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.15+5827_15+5851del others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | |||||
| chr19:14535536
|
AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0001g0122 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.15+5827_15+5855del others(29): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | |||||
| chr19:14535536
|
AAAAAAAA others(24): Show |
A | 8 | a0001c0001t0001g0096a0001c0001t0001g0100a0001c0001t0001g0106others(5): Show | 8 | HG00735.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+5827_15+5857del others(31): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | |||||
| chr19:14535536
|
AAAAAAAA others(26): Show |
A | 11 | a0001c0001t0001g0101a0001c0001t0001g0107a0001c0001t0001g0108others(8): Show | 11 | HG00558.hp2 HG01074.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+5827_15+5859del others(33): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | |||||
| chr19:14535536
|
AAAAAAAA others(28): Show |
A | 4 | a0001c0001t0001g0083a0001c0001t0001g0131a0001c0001t0001g0228others(1): Show | 4 | HG00642.hp1 HG01515.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+5827_15+5861del others(35): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | |||||
| chr19:14535536
|
AAAAAAAA others(30): Show |
A | 5 | a0001c0001t0001g0158a0001c0001t0001g0252a0001c0001t0001g0268others(2): Show | 5 | HG01346.hp2 HG01928.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+5827_15+5863del others(37): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535536 | |||||
| chr19:14535537
|
A | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0169a0001c0001t0001g0174 | 3 | HG03486.hp1 NA18946.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.15+5826A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535537 | ||||||
| chr19:14535537
|
AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0317a0001c0002t0001g0048 | 2 | HG01192.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.15+5828_15+5837del others(10): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | |||||
| chr19:14535537
|
AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0001g0049a0001c0001t0001g0242 | 2 | HG02630.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.15+5828_15+5845del others(18): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | |||||
| chr19:14535537
|
AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0001g0070 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.15+5828_15+5847del others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | |||||
| chr19:14535537
|
AAAAAAAA others(23): Show |
A | 2 | a0001c0001t0001g0094a0001c0001t0001g0104 | 2 | HG02074.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.15+5828_15+5857del others(30): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | |||||
| chr19:14535537
|
AAAAAAAA others(25): Show |
A | 6 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(3): Show | 6 | HG01952.hp1 HG02683.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+5828_15+5859del others(32): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | |||||
| chr19:14535537
|
AAAAAAAA others(27): Show |
A | 4 | a0001c0001t0001g0080a0001c0001t0001g0105a0001c0001t0001g0226others(1): Show | 4 | HG00673.hp2 HG02602.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+5828_15+5861del others(34): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | |||||
| chr19:14535537
|
AAAAAAAA others(29): Show |
A | 11 | a0001c0001t0001g0078a0001c0001t0001g0090a0001c0001t0001g0093others(8): Show | 11 | HG00639.hp2 HG01069.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+5828_15+5863del others(36): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | |||||
| chr19:14535537
|
AAAAAAAA others(31): Show |
A | 1 | a0001c0001t0001g0042 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.15+5828_15+5865del others(38): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | |||||
| chr19:14535537
|
AAAAAAAA others(35): Show |
A | 1 | a0001c0001t0002g0004 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.15+5828_15+5869del others(42): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535537 | |||||
| chr19:14535538
|
AAAAAAAT others(20): Show |
A | 4 | a0001c0001t0001g0056a0001c0001t0001g0069a0001c0001t0001g0072others(1): Show | 4 | HG00558.hp1 HG01993.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+5829_15+5855del others(27): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535538 | |||||
| chr19:14535538
|
AAAAAAAT others(24): Show |
A | 2 | a0001c0001t0001g0099a0001c0001t0001g0118 | 2 | HG01175.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.15+5829_15+5859del others(31): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535538 | |||||
| chr19:14535538
|
AAAAAAAT others(26): Show |
A | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.15+5829_15+5861del others(33): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535538 | |||||
| chr19:14535538
|
AAAAAAAT others(28): Show |
A | 5 | a0001c0001t0001g0035a0001c0001t0001g0075a0001c0001t0001g0077others(2): Show | 5 | HG02074.hp1 HG02132.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+5829_15+5863del others(35): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535538 | |||||
| chr19:14535538
|
AAAAAAAT others(30): Show |
A | 2 | a0001c0001t0001g0277a0002c0004t0001g0276 | 2 | HG01074.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.15+5829_15+5865del others(37): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535538 | |||||
| chr19:14535539
|
A | T | 15 | a0001c0001t0001g0059a0001c0001t0001g0148a0001c0001t0001g0166others(12): Show | 15 | HG01070.hp1 HG01261.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.15+5828A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535539 | ||||||
| chr19:14535539
|
AAAAAATA others(3): Show |
A | 2 | a0001c0002t0001g0236a0001c0005t0001g0033 | 2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.15+5830_15+5839del others(10): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | |||||
| chr19:14535539
|
AAAAAATA others(5): Show |
A | 2 | a0001c0001t0001g0089a0001c0001t0001g0312 | 2 | HG01358.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.15+5830_15+5841del others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | |||||
| chr19:14535539
|
AAAAAATA others(15): Show |
A | 1 | a0001c0001t0002g0005 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.15+5830_15+5851del others(22): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | |||||
| chr19:14535539
|
AAAAAATA others(17): Show |
A | 1 | a0001c0001t0001g0139 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.15+5830_15+5853del others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | |||||
| chr19:14535539
|
AAAAAATA others(19): Show |
A | 1 | a0001c0001t0001g0068 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.15+5830_15+5855del others(26): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | |||||
| chr19:14535539
|
AAAAAATA others(25): Show |
A | 1 | a0001c0001t0001g0117 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.15+5830_15+5861del others(32): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | |||||
| chr19:14535539
|
AAAAAATA others(27): Show |
A | 5 | a0001c0001t0001g0074a0001c0001t0001g0087a0001c0001t0001g0088others(2): Show | 5 | HG02040.hp1 HG03654.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+5830_15+5863del others(34): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | |||||
| chr19:14535539
|
AAAAAATA others(29): Show |
A | 5 | a0001c0001t0001g0150a0001c0001t0001g0262a0001c0001t0001g0283others(2): Show | 5 | HG00140.hp1 HG00733.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+5830_15+5865del others(36): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535539 | |||||
| chr19:14535540
|
AAAAATAT others(4): Show |
A | 1 | a0001c0001t0001g0008 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.15+5831_15+5841del others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | |||||
| chr19:14535540
|
AAAAATAT others(8): Show |
A | 1 | a0001c0001t0001g0326 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.15+5831_15+5845del others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | |||||
| chr19:14535540
|
AAAAATAT others(10): Show |
A | 1 | a0001c0002t0001g0011 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.15+5831_15+5847del others(17): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | |||||
| chr19:14535540
|
AAAAATAT others(12): Show |
A | 1 | a0001c0001t0001g0182 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.15+5831_15+5849del others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | |||||
| chr19:14535540
|
AAAAATAT others(16): Show |
A | 1 | a0001c0001t0001g0046 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.15+5831_15+5853del others(23): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | |||||
| chr19:14535540
|
AAAAATAT others(18): Show |
A | 1 | a0001c0001t0001g0054 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.15+5831_15+5855del others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | |||||
| chr19:14535540
|
AAAAATAT others(20): Show |
A | 1 | a0001c0001t0001g0218 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.15+5831_15+5857del others(27): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | |||||
| chr19:14535540
|
AAAAATAT others(22): Show |
A | 1 | a0001c0001t0001g0219 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.15+5831_15+5859del others(29): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | |||||
| chr19:14535540
|
AAAAATAT others(24): Show |
A | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG01192.hp2 HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.15+5831_15+5861del others(31): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | |||||
| chr19:14535540
|
AAAAATAT others(26): Show |
A | 1 | a0001c0001t0001g0170 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.15+5831_15+5863del others(33): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | |||||
| chr19:14535540
|
AAAAATAT others(30): Show |
A | 1 | a0001c0001t0001g0183 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.15+5831_15+5867del others(37): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535540 | |||||
| chr19:14535541
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0155 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.15+5831_15+5832ins others(10): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535541 | |||||
| chr19:14535541
|
A | AATATATA others(15): Show |
1 | a0001c0001t0001g0239 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.15+5831_15+5832ins others(22): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535541 | |||||
| chr19:14535541
|
A | AT | 4 | a0001c0001t0001g0159a0001c0001t0001g0181a0001c0001t0001g0240others(1): Show | 4 | NA18940.hp2 NA18970.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+5830_15+5831ins others(1): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535541 | ||||||
| chr19:14535541
|
A | ATAT | 5 | a0001c0001t0001g0019a0001c0001t0001g0053a0001c0001t0001g0163others(2): Show | 5 | HG00408.hp1 HG00438.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+5830_15+5831ins others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535541 | ||||||
| chr19:14535541
|
A | T | 36 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0055others(33): Show | 36 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.15+5830A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535541 | ||||||
| chr19:14535541
|
AAAATATA others(5): Show |
A | 1 | a0001c0001t0001g0299 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.15+5832_15+5843del others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535541 | |||||
| chr19:14535541
|
AAAATATA others(9): Show |
A | 2 | a0001c0001t0001g0010a0001c0001t0001g0191 | 2 | HG03098.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.15+5832_15+5847del others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535541 | |||||
| chr19:14535541
|
AAAATATA others(11): Show |
A | 1 | a0001c0001t0001g0214 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.15+5832_15+5849del others(18): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535541 | |||||
| chr19:14535541
|
AAAATATA others(17): Show |
A | 1 | a0001c0002t0001g0045 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.15+5832_15+5855del others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535541 | |||||
| chr19:14535542
|
AAATATAT others(26): Show |
A | 1 | a0002c0004t0001g0161 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.15+5833_15+5865del others(33): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535542 | |||||
| chr19:14535543
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0192 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.15+5833_15+5834ins others(10): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535543 | |||||
| chr19:14535543
|
A | T | 82 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0031others(79): Show | 82 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.15+5832A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535543 | ||||||
| chr19:14535544
|
ATAT | A | 3 | a0001c0001t0001g0175a0001c0003t0001g0012a0001c0003t0001g0017 | 3 | HG02896.hp1 HG02897.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.15+5834_15+5836del others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535544 | ||||||
| chr19:14535544
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0193 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.15+5834_15+5846del others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535544 | ||||||
| chr19:14535544
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0001g0009 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.15+5834_15+5848del others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535544 | ||||||
| chr19:14535544
|
ATATATAT others(18): Show |
A | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | NA18962.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.15+5834_15+5858del others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535544 | ||||||
| chr19:14535547
|
T | A | 1 | a0001c0001t0001g0196 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.15+5836T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535547 | ||||||
| chr19:14535549
|
T | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0196a0001c0003t0001g0012others(1): Show | 4 | HG00738.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+5838T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535549 | ||||||
| chr19:14535551
|
T | A | 1 | a0001c0001t0001g0175 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.15+5840T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535551 | ||||||
| chr19:14535558
|
ATATATAT others(29): Show |
A | 5 | a0001c0001t0001g0084a0001c0001t0001g0255a0001c0001t0001g0271others(2): Show | 5 | HG00140.hp2 HG00738.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+5856_15+5891del others(36): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535558 | |||||
| chr19:14535559
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.15+5848T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535559 | ||||||
| chr19:14535560
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.15+5849A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535560 | ||||||
| chr19:14535560
|
ATATATAT others(27): Show |
A | 4 | a0001c0001t0001g0085a0001c0001t0001g0254a0001c0001t0001g0256others(1): Show | 4 | HG00323.hp2 HG01123.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+5858_15+5891del others(34): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535560 | |||||
| chr19:14535562
|
ATATATAT others(25): Show |
A | 8 | a0001c0001t0001g0086a0001c0001t0001g0257a0001c0001t0001g0258others(5): Show | 8 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+5860_15+5891del others(32): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535562 | |||||
| chr19:14535563
|
T | A | 2 | a0001c0001t0001g0025a0001c0002t0001g0026 | 2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.15+5852T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535563 | ||||||
| chr19:14535566
|
ATATATAT others(21): Show |
A | 1 | a0001c0001t0001g0274 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.15+5864_15+5891del others(28): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535566 | |||||
| chr19:14535571
|
T | A | 1 | a0001c0001t0001g0331 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15+5860T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535571 | ||||||
| chr19:14535575
|
T | A | 1 | a0001c0001t0001g0331 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15+5864T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535575 | ||||||
| chr19:14535584
|
A | ATATATG | 3 | a0001c0001t0001g0052a0001c0002t0001g0057a0001c0002t0001g0063 | 3 | HG02717.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.15+5877_15+5882dup others(6): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535584 | |||||
| chr19:14535584
|
A | ATATG | 3 | a0001c0001t0001g0308a0001c0002t0001g0064a0001c0003t0001g0062 | 3 | HG02280.hp2 HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.15+5876_15+5877ins others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535584 | |||||
| chr19:14535584
|
A | G | 21 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0053others(18): Show | 21 | HG00558.hp1 HG01168.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.15+5873A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535584 | ||||||
| chr19:14535586
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0207 | 2 | HG02027.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.15+5875A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535586 | ||||||
| chr19:14535590
|
G | A | 70 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.15+5879G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535590 | ||||||
| chr19:14535594
|
G | A | 45 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0074others(42): Show | 45 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.15+5883G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535594 | ||||||
| chr19:14535659
|
C | CAGGAGAA others(4): Show |
1 | a0001c0001t0001g0321 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.15+5949_15+5959dup others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535659 | |||||
| chr19:14535693
|
C | T | 88 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.15+5982C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535693 | ||||||
| chr19:14535700
|
G | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 68 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.15+5989G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535700 | ||||||
| chr19:14535756
|
C | CA | 69 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0037others(66): Show | 69 | HG00099.hp2 HG00558.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.15+6066dupA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535756 | |||||
| chr19:14535756
|
C | CAAAAA | 53 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0078others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.15+6062_15+6066dup others(5): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535756 | |||||
| chr19:14535756
|
C | CAAAAAA | 19 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0036others(16): Show | 19 | HG00642.hp2 HG00741.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.15+6061_15+6066dup others(6): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535756 | |||||
| chr19:14535756
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0130 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.15+6056_15+6066del others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14535756 | |||||
| chr19:14535778
|
G | A | 2 | a0001c0001t0001g0025a0001c0002t0001g0026 | 2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.15+6067G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535778 | ||||||
| chr19:14535779
|
G | A | 23 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0050others(20): Show | 23 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.15+6068G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535779 | ||||||
| chr19:14535948
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.15+6237A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535948 | ||||||
| chr19:14535990
|
C | T | 8 | a0001c0001t0001g0019a0001c0002t0001g0013a0001c0002t0001g0015others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+6279C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14535990 | ||||||
| chr19:14536022
|
C | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+6311C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536022 | ||||||
| chr19:14536023
|
A | G | 84 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.15+6312A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536023 | ||||||
| chr19:14536091
|
C | G | 88 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.15+6380C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536091 | ||||||
| chr19:14536106
|
G | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02280.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+6395G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536106 | ||||||
| chr19:14536161
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+6450G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536161 | ||||||
| chr19:14536219
|
C | T | 4 | a0001c0001t0001g0046a0001c0001t0001g0058a0001c0001t0001g0139others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+6508C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536219 | ||||||
| chr19:14536267
|
G | GT | 30 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0054others(27): Show | 30 | HG00408.hp1 HG00408.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.15+6573dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14536267 | |||||
| chr19:14536267
|
GT | G | 8 | a0001c0001t0001g0086a0001c0001t0001g0135a0001c0001t0001g0182others(5): Show | 8 | HG02040.hp2 HG02109.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+6573delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14536267 | |||||
| chr19:14536267
|
GTT | G | 79 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.15+6572_15+6573del others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14536267 | |||||
| chr19:14536414
|
C | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+6703C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536414 | ||||||
| chr19:14536470
|
A | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+6759A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536470 | ||||||
| chr19:14536547
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.15+6836G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536547 | ||||||
| chr19:14536641
|
G | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 4 | HG01934.hp1 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+6930G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536641 | ||||||
| chr19:14536690
|
C | A | 2 | a0001c0002t0001g0123a0001c0002t0001g0124 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.15+6979C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536690 | ||||||
| chr19:14536696
|
T | A | 86 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.15+6985T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536696 | ||||||
| chr19:14536820
|
C | A | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0005t0001g0021others(1): Show | 4 | HG01123.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+7109C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536820 | ||||||
| chr19:14536923
|
C | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(66): Show | 70 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.15+7212C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14536923 | ||||||
| chr19:14537033
|
G | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0139a0001c0002t0001g0045 | 3 | HG01168.hp2 HG01169.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.15+7322G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537033 | ||||||
| chr19:14537252
|
T | TGGGGGAG others(13): Show |
5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0005t0001g0021others(2): Show | 5 | HG01123.hp1 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+7577_15+7596dup others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537252 | |||||
| chr19:14537252
|
TGGGGGAG others(13): Show |
T | 1 | a0001c0001t0001g0043 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.15+7577_15+7596del others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537252 | |||||
| chr19:14537275
|
G | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+7564G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537275 | ||||||
| chr19:14537431
|
G | T | 8 | a0001c0001t0001g0019a0001c0002t0001g0013a0001c0002t0001g0015others(5): Show | 8 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+7720G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537431 | ||||||
| chr19:14537445
|
T | TGAG | 89 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.15+7735_15+7737dup others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537445 | |||||
| chr19:14537497
|
C | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(58): Show | 62 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.15+7786C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537497 | ||||||
| chr19:14537547
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15+7836A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537547 | ||||||
| chr19:14537732
|
T | G | 85 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.15+8021T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537732 | ||||||
| chr19:14537744
|
G | GT | 21 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0160others(18): Show | 21 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.15+8052dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537744 | |||||
| chr19:14537744
|
G | GTT | 60 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(57): Show | 61 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.15+8051_15+8052dup others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537744 | |||||
| chr19:14537744
|
G | GTTT | 6 | a0001c0001t0001g0042a0001c0001t0001g0103a0001c0001t0001g0117others(3): Show | 6 | HG01952.hp1 HG02027.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+8050_15+8052dup others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537744 | |||||
| chr19:14537744
|
GT | G | 7 | a0001c0001t0001g0067a0001c0001t0001g0088a0001c0001t0001g0158others(4): Show | 7 | HG00738.hp2 HG01346.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+8052delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537744 | |||||
| chr19:14537744
|
GTT | G | 84 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.15+8051_15+8052del others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14537744 | |||||
| chr19:14537834
|
C | T | 85 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.15+8123C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537834 | ||||||
| chr19:14537849
|
G | T | 1 | a0001c0001t0001g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.15+8138G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537849 | ||||||
| chr19:14537907
|
G | C | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+8196G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14537907 | ||||||
| chr19:14538172
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.15+8461C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538172 | ||||||
| chr19:14538229
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.15+8518G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538229 | ||||||
| chr19:14538388
|
G | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+8677G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538388 | ||||||
| chr19:14538398
|
C | T | 64 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0074others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.15+8687C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538398 | ||||||
| chr19:14538443
|
G | A | 5 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0132others(2): Show | 5 | HG00280.hp2 HG01074.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+8732G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538443 | ||||||
| chr19:14538452
|
G | A | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+8741G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538452 | ||||||
| chr19:14538536
|
CT | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.15+8840delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14538536 | |||||
| chr19:14538544
|
T | C | 1 | a0001c0002t0001g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.15+8833T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538544 | ||||||
| chr19:14538546
|
T | C | 1 | a0001c0002t0001g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.15+8835T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538546 | ||||||
| chr19:14538687
|
C | A | 64 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0074others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.15+8976C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538687 | ||||||
| chr19:14538721
|
C | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+9010C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538721 | ||||||
| chr19:14538744
|
G | A | 6 | a0001c0001t0001g0158a0001c0001t0001g0252a0001c0001t0001g0253others(3): Show | 6 | HG00323.hp1 HG00639.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+9033G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538744 | ||||||
| chr19:14538769
|
G | A | 85 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.15+9058G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538769 | ||||||
| chr19:14538778
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.15+9067G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538778 | ||||||
| chr19:14538779
|
C | A | 1 | a0001c0001t0001g0271 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.15+9068C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538779 | ||||||
| chr19:14538821
|
A | G | 89 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.15+9110A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538821 | ||||||
| chr19:14538851
|
A | G | 3 | a0001c0001t0001g0023a0001c0005t0001g0021a0001c0005t0001g0024 | 3 | HG02809.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.15+9140A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538851 | ||||||
| chr19:14538978
|
T | A | 1 | a0001c0001t0001g0331 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15+9267T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14538978 | ||||||
| chr19:14539004
|
C | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+9293C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539004 | ||||||
| chr19:14539105
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0005t0001g0021others(1): Show | 4 | HG01123.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+9394C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539105 | ||||||
| chr19:14539140
|
A | AT | 29 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0030others(26): Show | 29 | HG00738.hp1 HG01123.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.15+9456dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539140 | |||||
| chr19:14539140
|
AT | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0098others(8): Show | 11 | HG01516.hp1 HG01943.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+9456delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539140 | |||||
| chr19:14539140
|
ATT | A | 45 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0025others(42): Show | 45 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.15+9455_15+9456del others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539140 | |||||
| chr19:14539140
|
ATTT | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0035others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.15+9454_15+9456del others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539140 | |||||
| chr19:14539140
|
ATTTT | A | 10 | a0001c0001t0001g0070a0001c0001t0001g0083a0001c0001t0001g0101others(7): Show | 10 | HG01069.hp2 HG01074.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+9453_15+9456del others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539140 | |||||
| chr19:14539140
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001g0002 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15+9441_15+9456del others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539140 | |||||
| chr19:14539346
|
T | C | 13 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0146others(10): Show | 13 | HG02109.hp1 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.15+9635T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539346 | ||||||
| chr19:14539358
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.15+9647A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539358 | ||||||
| chr19:14539684
|
C | A | 1 | a0001c0002t0001g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.15+9973C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539684 | ||||||
| chr19:14539710
|
C | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(62): Show | 66 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.15+9999C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539710 | ||||||
| chr19:14539750
|
C | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0044others(49): Show | 52 | HG00099.hp2 HG00558.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.15+10039C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539750 | ||||||
| chr19:14539811
|
C | T | 85 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.15+10100C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539811 | ||||||
| chr19:14539880
|
CT | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(116): Show | 120 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.15+10184delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539880 | |||||
| chr19:14539880
|
CTTT | C | 88 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.15+10182_15+10184d others(5): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14539880 | |||||
| chr19:14539919
|
G | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+10208G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539919 | ||||||
| chr19:14539973
|
G | T | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.15+10262G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14539973 | ||||||
| chr19:14540014
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15+10303G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540014 | ||||||
| chr19:14540063
|
A | AT | 79 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(76): Show | 79 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.15+10366dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14540063 | |||||
| chr19:14540082
|
C | T | 1 | a0001c0003t0001g0141 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.15+10371C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540082 | ||||||
| chr19:14540090
|
C | T | 3 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0001g0290 | 3 | HG00642.hp1 HG01515.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.15+10379C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540090 | ||||||
| chr19:14540237
|
A | C | 6 | a0001c0001t0001g0042a0001c0001t0001g0246a0001c0001t0001g0248others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+10526A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540237 | ||||||
| chr19:14540244
|
A | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(58): Show | 62 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.15+10533A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540244 | ||||||
| chr19:14540330
|
A | C | 2 | a0001c0001t0001g0106a0001c0001t0002g0007 | 2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.15+10619A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540330 | ||||||
| chr19:14540422
|
G | C | 1 | a0001c0002t0001g0320 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.15+10711G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540422 | ||||||
| chr19:14540469
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.15+10758T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540469 | ||||||
| chr19:14540528
|
A | G | 64 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0074others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.15+10817A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540528 | ||||||
| chr19:14540592
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.15+10881G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540592 | ||||||
| chr19:14540709
|
A | G | 5 | a0001c0001t0001g0160a0001c0001t0001g0166a0001c0001t0001g0169others(2): Show | 5 | NA18946.hp2 NA18994.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+10998A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540709 | ||||||
| chr19:14540713
|
GA | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(66): Show | 70 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.15+11003delA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540713 | ||||||
| chr19:14540774
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(1): Show | 4 | HG02145.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+11063C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540774 | ||||||
| chr19:14540813
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0005t0001g0021others(1): Show | 4 | HG01123.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+11102A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540813 | ||||||
| chr19:14540861
|
G | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0094others(39): Show | 43 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.15+11150G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540861 | ||||||
| chr19:14540904
|
G | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+11193G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540904 | ||||||
| chr19:14540970
|
G | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02280.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+11259G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540970 | ||||||
| chr19:14540976
|
A | C | 51 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(48): Show | 51 | HG00099.hp2 HG00558.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.15+11265A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14540976 | ||||||
| chr19:14541033
|
C | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(58): Show | 62 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.15+11322C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541033 | ||||||
| chr19:14541045
|
C | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+11334C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541045 | ||||||
| chr19:14541074
|
A | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(155): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.15+11363A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541074 | ||||||
| chr19:14541166
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.15+11455C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541166 | ||||||
| chr19:14541306
|
A | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(58): Show | 62 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.15+11595A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541306 | ||||||
| chr19:14541307
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(51): Show | 55 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.15+11596C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541307 | ||||||
| chr19:14541466
|
A | G | 89 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.15+11755A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541466 | ||||||
| chr19:14541586
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.15+11875A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541586 | ||||||
| chr19:14541783
|
A | AT | 6 | a0001c0001t0001g0145a0001c0001t0001g0160a0001c0001t0001g0294others(3): Show | 6 | HG02280.hp1 HG03453.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+12088dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14541783 | |||||
| chr19:14541798
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.15+12087T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541798 | ||||||
| chr19:14541885
|
C | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0146a0001c0001t0001g0326others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+12174C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541885 | ||||||
| chr19:14541907
|
C | T | 2 | a0001c0003t0001g0012a0001c0003t0001g0017 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.15+12196C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14541907 | ||||||
| chr19:14542103
|
C | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+12392C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542103 | ||||||
| chr19:14542260
|
C | T | 64 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0074others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.15+12549C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542260 | ||||||
| chr19:14542282
|
C | T | 1 | a0001c0002t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.15+12571C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542282 | ||||||
| chr19:14542296
|
T | C | 69 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(66): Show | 70 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.15+12585T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542296 | ||||||
| chr19:14542347
|
G | GGGTTTTT others(3): Show |
2 | a0001c0002t0001g0013a0001c0003t0001g0016 | 2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.15+12636_15+12637i others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542347 | ||||||
| chr19:14542347
|
G | GGGTTTTT others(4): Show |
1 | a0001c0002t0001g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.15+12636_15+12637i others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542347 | ||||||
| chr19:14542347
|
G | GGTTTTTT others(2): Show |
3 | a0001c0001t0001g0019a0001c0003t0001g0012a0001c0003t0001g0017 | 3 | HG02896.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.15+12636_15+12637i others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542347 | ||||||
| chr19:14542347
|
G | GGTTTTTT others(4): Show |
1 | a0001c0003t0001g0020 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.15+12636_15+12637i others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542347 | ||||||
| chr19:14542347
|
G | GT | 28 | a0001c0001t0001g0025a0001c0001t0001g0153a0001c0001t0001g0160others(25): Show | 28 | HG00741.hp1 HG01070.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.15+12665dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | |||||
| chr19:14542347
|
G | GTT | 9 | a0001c0001t0001g0053a0001c0001t0001g0192a0001c0001t0001g0196others(6): Show | 9 | HG00738.hp1 HG01071.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+12664_15+12665d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | |||||
| chr19:14542347
|
G | GTTTTTTT others(2): Show |
25 | a0001c0001t0001g0035a0001c0001t0001g0074a0001c0001t0001g0080others(22): Show | 25 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.15+12657_15+12665d others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | |||||
| chr19:14542347
|
G | GTTTTTTT others(3): Show |
22 | a0001c0001t0001g0036a0001c0001t0001g0075a0001c0001t0001g0077others(19): Show | 22 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.15+12656_15+12665d others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | |||||
| chr19:14542347
|
G | GTTTTTTT others(4): Show |
3 | a0001c0001t0001g0090a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | HG02083.hp1 HG02083.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.15+12655_15+12665d others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | |||||
| chr19:14542347
|
G | GTTTTTTT others(5): Show |
4 | a0001c0001t0001g0149a0001c0001t0001g0252a0001c0001t0001g0277others(1): Show | 4 | HG00673.hp2 HG01074.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+12654_15+12665d others(14): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | |||||
| chr19:14542347
|
G | GTTTTTTT others(8): Show |
3 | a0001c0001t0001g0267a0001c0001t0001g0269a0001c0001t0001g0274 | 3 | HG01167.hp2 HG02300.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.15+12651_15+12665d others(17): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | |||||
| chr19:14542347
|
G | GTTTTTTT others(9): Show |
1 | a0001c0002t0001g0082 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.15+12650_15+12665d others(18): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | |||||
| chr19:14542347
|
G | GTTTTTTT others(10): Show |
1 | a0001c0002t0001g0079 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.15+12649_15+12665d others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | |||||
| chr19:14542347
|
GT | G | 40 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0052others(37): Show | 40 | HG00099.hp2 HG00558.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.15+12665delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | |||||
| chr19:14542347
|
GTT | G | 8 | a0001c0001t0001g0046a0001c0001t0001g0056a0001c0001t0001g0070others(5): Show | 8 | HG00323.hp1 HG00639.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+12664_15+12665d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | |||||
| chr19:14542347
|
GTTTTT | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(52): Show | 56 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.15+12661_15+12665d others(7): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | |||||
| chr19:14542347
|
GTTTTTTT others(3): Show |
G | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0005t0001g0021others(1): Show | 4 | HG01123.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+12656_15+12665d others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | |||||
| chr19:14542347
|
GTTTTTTT others(4): Show |
G | 4 | a0001c0001t0001g0145a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02280.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+12655_15+12665d others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542347 | |||||
| chr19:14542348
|
T | G | 1 | a0001c0001t0001g0002 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15+12637T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542348 | ||||||
| chr19:14542352
|
T | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+12641T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542352 | ||||||
| chr19:14542355
|
T | G | 1 | a0001c0003t0001g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.15+12644T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542355 | ||||||
| chr19:14542378
|
T | A | 1 | a0001c0001t0001g0228 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.15+12667T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542378 | ||||||
| chr19:14542380
|
AG | A | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+12670delG | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542380 | ||||||
| chr19:14542463
|
T | C | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+12752T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542463 | ||||||
| chr19:14542625
|
G | A | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+12914G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542625 | ||||||
| chr19:14542744
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.15+13033C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542744 | ||||||
| chr19:14542908
|
C | T | 85 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.15+13197C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14542908 | ||||||
| chr19:14542989
|
C | CT | 9 | a0001c0001t0001g0031a0001c0001t0001g0149a0001c0001t0001g0154others(6): Show | 9 | HG01175.hp1 HG01192.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+13294dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14542989 | |||||
| chr19:14543040
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.15+13329C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543040 | ||||||
| chr19:14543272
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0220 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.15+13561G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543272 | ||||||
| chr19:14543301
|
GGT | G | 89 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.15+13602_15+13603d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543301 | |||||
| chr19:14543319
|
T | C | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+13608T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543319 | ||||||
| chr19:14543388
|
A | AATATATA others(7): Show |
2 | a0001c0001t0001g0296a0001c0001t0001g0300 | 2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.15+13696_15+13709d others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543388 | |||||
| chr19:14543388
|
AAT | A | 5 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0168others(2): Show | 5 | HG01070.hp1 HG01255.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+13708_15+13709d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543388 | |||||
| chr19:14543388
|
AATATAT | A | 8 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0070others(5): Show | 8 | HG01081.hp1 HG01175.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+13704_15+13709d others(8): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543388 | |||||
| chr19:14543395
|
A | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+13684A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543395 | ||||||
| chr19:14543403
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0181 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.15+13694_15+13713d others(22): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543403 | |||||
| chr19:14543403
|
ATATATAT others(16): Show |
A | 10 | a0001c0001t0001g0052a0001c0001t0001g0147a0001c0001t0001g0148others(7): Show | 10 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.15+13694_15+13716d others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543403 | |||||
| chr19:14543403
|
ATATATAT others(19): Show |
A | 1 | a0001c0001t0001g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.15+13694_15+13719d others(28): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543403 | |||||
| chr19:14543405
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0069 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.15+13696_15+13715d others(22): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | |||||
| chr19:14543405
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0068 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.15+13696_15+13716d others(23): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | |||||
| chr19:14543405
|
ATATATAT others(15): Show |
A | 4 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0072others(1): Show | 4 | HG00558.hp1 HG01993.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+13696_15+13717d others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | |||||
| chr19:14543405
|
ATATATAT others(16): Show |
A | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(5): Show | 8 | HG00280.hp2 HG01358.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+13696_15+13718d others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | |||||
| chr19:14543405
|
ATATATAT others(17): Show |
A | 26 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0096others(23): Show | 27 | HG00558.hp2 HG00735.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.15+13696_15+13719d others(26): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | |||||
| chr19:14543405
|
ATATATAT others(18): Show |
A | 12 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0099others(9): Show | 12 | HG01175.hp2 HG01515.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.15+13696_15+13720d others(27): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | |||||
| chr19:14543405
|
ATATATAT others(19): Show |
A | 1 | a0001c0002t0001g0102 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.15+13696_15+13721d others(28): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | |||||
| chr19:14543405
|
ATATATAT others(20): Show |
A | 1 | a0001c0001t0001g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.15+13696_15+13722d others(29): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | |||||
| chr19:14543405
|
ATATATAT others(32): Show |
A | 3 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0278 | 3 | HG01069.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.15+13696_15+13734d others(41): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543405 | |||||
| chr19:14543406
|
TATATATA | T | 5 | a0001c0001t0001g0310a0001c0001t0001g0313a0001c0002t0001g0041others(2): Show | 5 | HG01167.hp1 HG01934.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+13696_15+13702d others(9): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543406 | ||||||
| chr19:14543407
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0067 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.15+13698_15+13715d others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543407 | |||||
| chr19:14543407
|
ATATATAT others(15): Show |
A | 4 | a0001c0001t0001g0046a0001c0001t0001g0058a0001c0001t0001g0139others(1): Show | 4 | HG01168.hp2 HG01169.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+13698_15+13719d others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543407 | |||||
| chr19:14543407
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0112 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.15+13698_15+13720d others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543407 | |||||
| chr19:14543407
|
ATATATAT others(17): Show |
A | 11 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0105others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.15+13698_15+13721d others(26): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543407 | |||||
| chr19:14543407
|
ATATATAT others(18): Show |
A | 3 | a0001c0001t0001g0103a0001c0001t0001g0119a0001c0001t0001g0127 | 3 | HG02738.hp1 NA19081.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.15+13698_15+13722d others(27): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543407 | |||||
| chr19:14543409
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.15+13700_15+13716d others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543409 | |||||
| chr19:14543409
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0240 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.15+13700_15+13717d others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543409 | |||||
| chr19:14543409
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0001g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.15+13700_15+13719d others(22): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543409 | |||||
| chr19:14543409
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0001g0131 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.15+13700_15+13721d others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543409 | |||||
| chr19:14543409
|
ATATATAT others(16): Show |
A | 1 | a0001c0005t0001g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.15+13700_15+13722d others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543409 | |||||
| chr19:14543409
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.15+13700_15+13723d others(26): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543409 | |||||
| chr19:14543411
|
A | T | 1 | a0001c0001t0001g0239 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.15+13700A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543411 | ||||||
| chr19:14543411
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0299 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.15+13702_15+13712d others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543411 | |||||
| chr19:14543411
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.15+13702_15+13724d others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543411 | |||||
| chr19:14543411
|
ATATATAT others(26): Show |
A | 1 | a0001c0001t0001g0086 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.15+13702_15+13734d others(35): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543411 | |||||
| chr19:14543413
|
A | T | 5 | a0001c0001t0001g0049a0001c0001t0001g0070a0001c0001t0001g0205others(2): Show | 5 | HG01081.hp1 HG01175.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+13702A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543413 | ||||||
| chr19:14543413
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0234 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.15+13704_15+13716d others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543413 | |||||
| chr19:14543413
|
ATATATAT others(7): Show |
A | 2 | a0001c0001t0001g0233a0001c0001t0001g0235 | 2 | HG01261.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.15+13704_15+13717d others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543413 | |||||
| chr19:14543413
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0178 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.15+13704_15+13720d others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543413 | |||||
| chr19:14543413
|
ATATATAT others(26): Show |
A | 1 | a0001c0002t0001g0291 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.15+13704_15+13736d others(35): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543413 | |||||
| chr19:14543415
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0228 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.15+13705_15+13706i others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543415 | |||||
| chr19:14543415
|
A | T | 17 | a0001c0001t0001g0049a0001c0001t0001g0070a0001c0001t0001g0205others(14): Show | 17 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.15+13704A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543415 | ||||||
| chr19:14543415
|
ATATATTT others(10): Show |
A | 3 | a0001c0001t0001g0025a0001c0001t0001g0231a0001c0002t0001g0026 | 3 | HG02109.hp1 HG02723.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.15+13706_15+13722d others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543415 | |||||
| chr19:14543415
|
ATATATTT others(11): Show |
A | 2 | a0001c0001t0001g0195a0001c0001t0001g0223 | 2 | HG02080.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.15+13706_15+13723d others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543415 | |||||
| chr19:14543415
|
ATATATTT others(13): Show |
A | 3 | a0001c0001t0001g0019a0001c0002t0001g0013a0001c0002t0001g0015 | 3 | HG02622.hp1 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.15+13706_15+13725d others(22): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543415 | |||||
| chr19:14543417
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0219 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.15+13707_15+13708i others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | |||||
| chr19:14543417
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0207 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.15+13707_15+13708i others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | |||||
| chr19:14543417
|
A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0238 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.15+13707_15+13708i others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | |||||
| chr19:14543417
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0159 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.15+13707_15+13708i others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | |||||
| chr19:14543417
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.15+13707_15+13708i others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | |||||
| chr19:14543417
|
A | ATTTTTTT others(12): Show |
1 | a0001c0001t0001g0032 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.15+13707_15+13708i others(21): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | |||||
| chr19:14543417
|
A | T | 23 | a0001c0001t0001g0049a0001c0001t0001g0070a0001c0001t0001g0205others(20): Show | 23 | HG00099.hp2 HG01081.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.15+13706A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543417 | ||||||
| chr19:14543417
|
ATATTTTT others(1): Show |
A | 7 | a0001c0001t0001g0155a0001c0001t0001g0182a0001c0001t0001g0192others(4): Show | 7 | HG02040.hp2 HG02080.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+13708_15+13715d others(10): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | |||||
| chr19:14543417
|
ATATTTTT others(4): Show |
A | 1 | a0001c0002t0001g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.15+13708_15+13718d others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | |||||
| chr19:14543417
|
ATATTTTT others(6): Show |
A | 1 | a0001c0001t0001g0157 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.15+13708_15+13720d others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | |||||
| chr19:14543417
|
ATATTTTT others(9): Show |
A | 1 | a0001c0001t0001g0194 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.15+13708_15+13723d others(18): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | |||||
| chr19:14543417
|
ATATTTTT others(12): Show |
A | 1 | a0001c0001t0001g0326 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.15+13708_15+13726d others(21): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | |||||
| chr19:14543417
|
ATATTTTT others(13): Show |
A | 5 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(2): Show | 5 | HG02451.hp2 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+13708_15+13727d others(22): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | |||||
| chr19:14543417
|
ATATTTTT others(15): Show |
A | 5 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0327others(2): Show | 5 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+13708_15+13729d others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | |||||
| chr19:14543417
|
ATATTTTT others(18): Show |
A | 4 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0005others(1): Show | 4 | HG03710.hp2 HG04115.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+13708_15+13732d others(27): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543417 | |||||
| chr19:14543419
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.15+13709_15+13710i others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0221 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.15+13709_15+13710i others(31): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
A | ATATATAT others(7): Show |
1 | a0001c0003t0001g0297 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.15+13709_15+13710i others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0189 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.15+13709_15+13710i others(31): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0002 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15+13709_15+13710i others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0185 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.15+13709_15+13710i others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
A | ATATATTT others(10): Show |
1 | a0001c0001t0001g0190 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.15+13709_15+13710i others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
A | ATATTTTT others(8): Show |
3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0330 | 3 | HG01934.hp1 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.15+13709_15+13710i others(17): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
A | ATATTTTT others(18): Show |
1 | a0001c0001t0001g0175 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.15+13709_15+13710i others(27): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0152 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.15+13735_15+13745d others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0214 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.15+13734_15+13745d others(14): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
A | ATTTTTTT others(6): Show |
3 | a0001c0001t0001g0184a0001c0001t0001g0191a0001c0001t0001g0220 | 3 | HG01069.hp1 HG01071.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.15+13733_15+13745d others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
A | ATTTTTTT others(7): Show |
1 | a0001c0003t0001g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15+13732_15+13745d others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
A | ATTTTTTT others(23): Show |
1 | a0001c0001t0001g0188 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.15+13716_15+13745d others(32): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
A | T | 36 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0049others(33): Show | 36 | HG00099.hp2 HG00438.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.15+13708A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543419 | ||||||
| chr19:14543419
|
ATT | A | 6 | a0001c0001t0001g0142a0001c0001t0001g0165a0001c0001t0001g0171others(3): Show | 6 | HG01928.hp1 HG02300.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+13744_15+13745d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
ATTTTTT | A | 6 | a0001c0001t0001g0193a0001c0001t0001g0196a0001c0001t0001g0227others(3): Show | 6 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+13740_15+13745d others(8): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
ATTTTTTT others(3): Show |
A | 8 | a0001c0001t0001g0039a0001c0001t0001g0162a0001c0001t0001g0176others(5): Show | 8 | HG00323.hp2 HG01361.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+13736_15+13745d others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
ATTTTTTT others(4): Show |
A | 13 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0001g0089others(10): Show | 13 | HG00741.hp2 HG01346.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.15+13735_15+13745d others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0270 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.15+13734_15+13745d others(14): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
ATTTTTTT others(6): Show |
A | 7 | a0001c0001t0001g0035a0001c0001t0001g0074a0001c0001t0001g0093others(4): Show | 7 | HG01243.hp1 HG02040.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+13733_15+13745d others(15): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0075 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.15+13732_15+13745d others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
ATTTTTTT others(8): Show |
A | 21 | a0001c0001t0001g0036a0001c0001t0001g0077a0001c0001t0001g0078others(18): Show | 21 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.15+13731_15+13745d others(17): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
ATTTTTTT others(9): Show |
A | 2 | a0001c0001t0001g0295a0001c0001t0001g0331 | 2 | HG03834.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.15+13730_15+13745d others(18): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
ATTTTTTT others(10): Show |
A | 8 | a0001c0001t0001g0183a0001c0001t0001g0254a0001c0001t0001g0258others(5): Show | 8 | HG00099.hp1 HG00733.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+13729_15+13745d others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
ATTTTTTT others(11): Show |
A | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.15+13728_15+13745d others(20): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
ATTTTTTT others(12): Show |
A | 1 | a0001c0001t0001g0092 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.15+13727_15+13745d others(21): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
ATTTTTTT others(15): Show |
A | 1 | a0001c0001t0001g0322 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.15+13724_15+13745d others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543419
|
ATTTTTTT others(16): Show |
A | 1 | a0001c0001t0001g0283 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.15+13723_15+13745d others(25): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14543419 | |||||
| chr19:14543420
|
T | TATA | 3 | a0001c0001t0001g0305a0001c0002t0001g0202a0001c0003t0001g0141 | 3 | HG02145.hp1 HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.15+13709_15+13710i others(5): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543420 | ||||||
| chr19:14543421
|
T | A | 4 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0211others(1): Show | 4 | HG00280.hp1 HG02738.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+13710T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543421 | ||||||
| chr19:14543422
|
T | A | 5 | a0001c0001t0001g0153a0001c0001t0001g0172a0001c0001t0001g0187others(2): Show | 5 | HG01099.hp2 HG01978.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+13711T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543422 | ||||||
| chr19:14543423
|
T | A | 5 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(2): Show | 5 | HG03130.hp2 HG03540.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+13712T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543423 | ||||||
| chr19:14543424
|
T | A | 2 | a0001c0001t0001g0169a0001c0003t0001g0141 | 2 | HG02572.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.15+13713T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543424 | ||||||
| chr19:14543425
|
T | A | 3 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG03130.hp2 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.15+13714T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543425 | ||||||
| chr19:14543426
|
T | A | 2 | a0001c0001t0001g0286a0001c0003t0001g0141 | 2 | HG00140.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.15+13715T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543426 | ||||||
| chr19:14543427
|
T | A | 5 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0277others(2): Show | 5 | HG00738.hp2 HG01074.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+13716T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543427 | ||||||
| chr19:14543428
|
T | A | 3 | a0001c0001t0001g0252a0001c0001t0001g0286a0001c0001t0001g0288 | 3 | HG00140.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.15+13717T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543428 | ||||||
| chr19:14543429
|
T | A | 5 | a0001c0001t0001g0277a0001c0001t0001g0282a0001c0001t0001g0293others(2): Show | 5 | HG00738.hp2 HG01074.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+13718T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543429 | ||||||
| chr19:14543430
|
T | A | 5 | a0001c0001t0001g0252a0001c0001t0001g0284a0001c0001t0001g0286others(2): Show | 5 | HG00140.hp2 HG00323.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+13719T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543430 | ||||||
| chr19:14543431
|
T | A | 12 | a0001c0001t0001g0039a0001c0001t0001g0162a0001c0001t0001g0176others(9): Show | 12 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.15+13720T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543431 | ||||||
| chr19:14543432
|
T | A | 16 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0001g0089others(13): Show | 16 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.15+13721T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543432 | ||||||
| chr19:14543433
|
T | A | 12 | a0001c0001t0001g0039a0001c0001t0001g0162a0001c0001t0001g0176others(9): Show | 12 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.15+13722T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543433 | ||||||
| chr19:14543434
|
T | A | 23 | a0001c0001t0001g0035a0001c0001t0001g0074a0001c0001t0001g0080others(20): Show | 23 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.15+13723T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543434 | ||||||
| chr19:14543435
|
T | A | 8 | a0001c0001t0001g0075a0001c0001t0001g0256a0001c0001t0001g0270others(5): Show | 8 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.15+13724T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543435 | ||||||
| chr19:14543436
|
T | A | 44 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0074others(41): Show | 44 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.15+13725T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543436 | ||||||
| chr19:14543437
|
T | A | 10 | a0001c0001t0001g0075a0001c0001t0001g0256a0001c0001t0001g0270others(7): Show | 10 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+13726T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543437 | ||||||
| chr19:14543438
|
T | A | 50 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0074others(47): Show | 50 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.15+13727T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543438 | ||||||
| chr19:14543439
|
T | A | 9 | a0001c0001t0001g0075a0001c0001t0001g0256a0001c0001t0001g0270others(6): Show | 9 | HG00323.hp2 HG00738.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+13728T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543439 | ||||||
| chr19:14543440
|
T | A | 51 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0074others(48): Show | 51 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.15+13729T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543440 | ||||||
| chr19:14543441
|
T | A | 5 | a0001c0001t0001g0075a0001c0001t0001g0256a0001c0001t0001g0270others(2): Show | 5 | HG00323.hp2 HG00738.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+13730T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543441 | ||||||
| chr19:14543442
|
T | A | 46 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0074others(43): Show | 46 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.15+13731T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543442 | ||||||
| chr19:14543443
|
T | A | 2 | a0001c0001t0001g0256a0001c0001t0001g0287 | 2 | HG00323.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.15+13732T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543443 | ||||||
| chr19:14543444
|
T | A | 29 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0087others(26): Show | 29 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.15+13733T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543444 | ||||||
| chr19:14543446
|
T | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0274 | 2 | HG04115.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.15+13735T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543446 | ||||||
| chr19:14543456
|
T | G | 1 | a0001c0001t0001g0223 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.15+13745T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543456 | ||||||
| chr19:14543590
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.15+13879T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543590 | ||||||
| chr19:14543629
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0245 | 2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.15+13918G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543629 | ||||||
| chr19:14543645
|
A | T | 2 | a0001c0001t0001g0106a0001c0001t0002g0007 | 2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.15+13934A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543645 | ||||||
| chr19:14543680
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.15+13969C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543680 | ||||||
| chr19:14543681
|
T | G | 89 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(86): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.15+13970T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543681 | ||||||
| chr19:14543697
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0239 | 2 | NA18992.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.15+13986C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543697 | ||||||
| chr19:14543727
|
C | T | 11 | a0001c0001t0001g0019a0001c0001t0001g0255a0001c0001t0001g0266others(8): Show | 11 | HG00642.hp2 HG01258.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+14016C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543727 | ||||||
| chr19:14543730
|
G | T | 1 | a0001c0001t0001g0327 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.15+14019G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543730 | ||||||
| chr19:14543874
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.15+14163T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14543874 | ||||||
| chr19:14544114
|
A | G | 85 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.15+14403A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544114 | ||||||
| chr19:14544136
|
C | G | 4 | a0001c0001t0001g0145a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02280.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+14425C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544136 | ||||||
| chr19:14544297
|
C | G | 4 | a0001c0001t0001g0145a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02280.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+14586C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544297 | ||||||
| chr19:14544388
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.15+14677T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544388 | ||||||
| chr19:14544568
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.15+14857A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544568 | ||||||
| chr19:14544576
|
AG | A | 85 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.15+14868delG | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14544576 | |||||
| chr19:14544635
|
CT | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(65): Show | 69 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.15+14940delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14544635 | |||||
| chr19:14544635
|
CTT | C | 90 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.15+14939_15+14940d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14544635 | |||||
| chr19:14544651
|
T | A | 4 | a0001c0001t0001g0145a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | HG02280.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+14940T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544651 | ||||||
| chr19:14544690
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(155): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.15+14979G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544690 | ||||||
| chr19:14544749
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.15+15038C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544749 | ||||||
| chr19:14544796
|
C | G | 52 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0046others(49): Show | 52 | HG00099.hp2 HG00558.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.15+15085C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544796 | ||||||
| chr19:14544797
|
T | A | 1 | a0001c0002t0001g0216 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.15+15086T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544797 | ||||||
| chr19:14544904
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.15+15193A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544904 | ||||||
| chr19:14544979
|
G | A | 2 | a0001c0001t0001g0025a0001c0002t0001g0026 | 2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.15+15268G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14544979 | ||||||
| chr19:14545000
|
T | C | 64 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0074others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.15+15289T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545000 | ||||||
| chr19:14545053
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(156): Show | 160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.15+15342T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545053 | ||||||
| chr19:14545318
|
C | T | 4 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02572.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+15607C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545318 | ||||||
| chr19:14545319
|
G | A | 83 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.15+15608G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545319 | ||||||
| chr19:14545377
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0001g0220 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.15+15666C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545377 | ||||||
| chr19:14545392
|
T | TGGCCCTC others(2): Show |
11 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(8): Show | 11 | HG02257.hp1 HG02615.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.15+15691_15+15699d others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14545392 | |||||
| chr19:14545410
|
G | GCACCGCT others(10): Show |
26 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0094others(23): Show | 27 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.15+15703_15+15719d others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14545410 | |||||
| chr19:14545414
|
C | CGCTGTCT others(10): Show |
11 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG01192.hp2 HG01257.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+15707_15+15723d others(19): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14545414 | |||||
| chr19:14545506
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0003t0001g0141 | 3 | HG02572.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.15+15795G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545506 | ||||||
| chr19:14545510
|
G | A | 3 | a0001c0001t0001g0309a0001c0002t0001g0303a0001c0002t0001g0304 | 3 | HG01891.hp2 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.15+15799G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545510 | ||||||
| chr19:14545515
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.15+15804G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545515 | ||||||
| chr19:14545563
|
A | C | 1 | a0001c0001t0001g0330 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.15+15852A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545563 | ||||||
| chr19:14545591
|
C | T | 1 | a0001c0003t0001g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.15+15880C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545591 | ||||||
| chr19:14545643
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.15+15932C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545643 | ||||||
| chr19:14545658
|
A | G | 3 | a0001c0001t0001g0309a0001c0002t0001g0303a0001c0002t0001g0304 | 3 | HG01891.hp2 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.15+15947A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545658 | ||||||
| chr19:14545682
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0326a0001c0002t0001g0026 | 3 | HG02109.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.15+15971C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545682 | ||||||
| chr19:14545741
|
A | G | 1 | a0001c0003t0001g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15+16030A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545741 | ||||||
| chr19:14545758
|
A | T | 1 | a0001c0003t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.15+16047A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545758 | ||||||
| chr19:14545835
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0019others(203): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.15+16124T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545835 | ||||||
| chr19:14545865
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.15+16154C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545865 | ||||||
| chr19:14545926
|
A | C | 1 | a0001c0001t0002g0004 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.15+16215A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14545926 | ||||||
| chr19:14546074
|
T | G | 20 | a0001c0001t0001g0046a0001c0001t0001g0052a0001c0001t0001g0054others(17): Show | 20 | HG00558.hp1 HG01168.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.15+16363T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546074 | ||||||
| chr19:14546090
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.15+16379G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546090 | ||||||
| chr19:14546159
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.16-16366A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546159 | ||||||
| chr19:14546193
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.16-16332A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546193 | ||||||
| chr19:14546208
|
T | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0326 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.16-16317T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546208 | ||||||
| chr19:14546233
|
T | G | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-16292T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546233 | ||||||
| chr19:14546240
|
C | T | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-16285C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546240 | ||||||
| chr19:14546258
|
T | A | 71 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0035others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.16-16267T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546258 | ||||||
| chr19:14546271
|
A | AT | 81 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0036others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.16-16243dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14546271 | |||||
| chr19:14546352
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0146 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.16-16173T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546352 | ||||||
| chr19:14546418
|
T | G | 1 | a0001c0003t0001g0325 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.16-16107T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546418 | ||||||
| chr19:14546458
|
G | A | 1 | a0001c0002t0001g0291 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.16-16067G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546458 | ||||||
| chr19:14546599
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-15926C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546599 | ||||||
| chr19:14546616
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0005t0001g0021others(1): Show | 4 | HG01123.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-15909C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546616 | ||||||
| chr19:14546741
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(52): Show | 56 | HG00280.hp2 HG00558.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.16-15784G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546741 | ||||||
| chr19:14546765
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.16-15760A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546765 | ||||||
| chr19:14546782
|
C | T | 1 | a0001c0007t0001g0073 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.16-15743C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546782 | ||||||
| chr19:14546846
|
C | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0206a0001c0001t0001g0331 | 3 | HG02738.hp1 NA18977.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.16-15679C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546846 | ||||||
| chr19:14546941
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-15584C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546941 | ||||||
| chr19:14546987
|
A | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0139a0001c0002t0001g0045 | 3 | HG01168.hp2 HG01169.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.16-15538A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14546987 | ||||||
| chr19:14547104
|
G | T | 13 | a0001c0001t0001g0042a0001c0001t0001g0146a0001c0001t0001g0248others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.16-15421G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547104 | ||||||
| chr19:14547115
|
AAG | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(73): Show | 76 | HG00558.hp1 HG00733.hp2 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.16-15405_16-15404d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547115 | |||||
| chr19:14547118
|
A | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(73): Show | 76 | HG00558.hp1 HG00733.hp2 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.16-15407A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547118 | ||||||
| chr19:14547143
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.16-15382A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547143 | ||||||
| chr19:14547192
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(207): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.16-15333G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547192 | ||||||
| chr19:14547262
|
G | A | 5 | a0001c0001t0001g0144a0001c0002t0001g0013a0001c0002t0001g0015others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-15263G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547262 | ||||||
| chr19:14547343
|
CTATTTTA others(3): Show |
C | 39 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(36): Show | 40 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.16-15163_16-15154d others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547343 | |||||
| chr19:14547603
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.16-14922C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547603 | ||||||
| chr19:14547636
|
A | G | 1 | a0001c0005t0001g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.16-14889A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547636 | ||||||
| chr19:14547661
|
A | AT | 124 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.16-14849dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547661 | |||||
| chr19:14547661
|
A | ATT | 6 | a0001c0001t0001g0095a0001c0001t0001g0103a0001c0001t0001g0145others(3): Show | 6 | HG00323.hp1 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-14850_16-14849d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547661 | |||||
| chr19:14547661
|
AT | A | 18 | a0001c0001t0001g0042a0001c0001t0001g0101a0001c0001t0001g0143others(15): Show | 18 | HG01074.hp2 HG01109.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.16-14849delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547661 | |||||
| chr19:14547714
|
A | G | 15 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0143others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.16-14811A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547714 | ||||||
| chr19:14547779
|
T | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(37): Show | 41 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.16-14746T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547779 | ||||||
| chr19:14547827
|
CT | C | 3 | a0001c0001t0001g0246a0001c0002t0001g0026a0001c0003t0001g0247 | 3 | HG02109.hp1 HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.16-14694delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547827 | |||||
| chr19:14547963
|
C | CT | 10 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0068others(7): Show | 10 | HG00558.hp1 HG01496.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-14544dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547963 | |||||
| chr19:14547963
|
CT | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(46): Show | 49 | HG00639.hp2 HG01074.hp2 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.16-14544delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14547963 | |||||
| chr19:14547985
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-14540A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547985 | ||||||
| chr19:14547986
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0005t0001g0021others(1): Show | 4 | HG01123.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-14539C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14547986 | ||||||
| chr19:14548072
|
T | C | 6 | a0001c0001t0001g0098a0001c0001t0001g0122a0001c0001t0002g0003others(3): Show | 6 | HG03490.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-14453T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548072 | ||||||
| chr19:14548088
|
AAGTAGCT others(7279): Show |
A | 6 | a0001c0001t0001g0098a0001c0001t0001g0122a0001c0001t0002g0003others(3): Show | 6 | HG03490.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-14425_16-7140de others(1): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14548088 | |||||
| chr19:14548144
|
T | A | 40 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(37): Show | 41 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.16-14381T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548144 | ||||||
| chr19:14548164
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0132 | 2 | HG00280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.16-14361G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548164 | ||||||
| chr19:14548181
|
G | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(37): Show | 41 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.16-14344G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548181 | ||||||
| chr19:14548241
|
G | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(36): Show | 40 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.16-14284G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548241 | ||||||
| chr19:14548250
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.16-14275T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548250 | ||||||
| chr19:14548268
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(36): Show | 40 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.16-14257G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548268 | ||||||
| chr19:14548291
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-14234A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548291 | ||||||
| chr19:14548500
|
G | A | 7 | a0001c0001t0001g0035a0001c0001t0001g0154a0001c0001t0001g0162others(4): Show | 7 | HG02056.hp2 HG02074.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-14025G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548500 | ||||||
| chr19:14548577
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0038others(36): Show | 40 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.16-13948G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548577 | ||||||
| chr19:14548600
|
C | T | 1 | a0001c0005t0001g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.16-13925C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548600 | ||||||
| chr19:14548648
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(211): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.16-13877A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548648 | ||||||
| chr19:14548735
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-13790G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548735 | ||||||
| chr19:14548888
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-13637C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14548888 | ||||||
| chr19:14549016
|
AT | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(89): Show | 92 | HG00323.hp1 HG00558.hp2 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.16-13499delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14549016 | |||||
| chr19:14549033
|
G | C | 4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(1): Show | 4 | HG01934.hp1 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-13492G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549033 | ||||||
| chr19:14549100
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0002t0001g0011 | 3 | HG02145.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.16-13425G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549100 | ||||||
| chr19:14549126
|
G | A | 7 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0103others(4): Show | 7 | HG01123.hp1 HG02486.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-13399G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549126 | ||||||
| chr19:14549211
|
C | CTTTT | 68 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0025others(65): Show | 68 | HG00558.hp2 HG00642.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.16-13297_16-13294d others(6): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14549211 | |||||
| chr19:14549211
|
C | CTTTTT | 13 | a0001c0001t0001g0002a0001c0001t0001g0139a0001c0001t0001g0296others(10): Show | 13 | HG01109.hp2 HG01169.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.16-13298_16-13294d others(7): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14549211 | |||||
| chr19:14549211
|
CT | C | 9 | a0001c0001t0001g0085a0001c0001t0001g0100a0001c0001t0001g0133others(6): Show | 9 | HG00639.hp2 HG01257.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-13294delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14549211 | |||||
| chr19:14549300
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0022 | 2 | HG01123.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.16-13225C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549300 | ||||||
| chr19:14549358
|
A | G | 32 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0031others(29): Show | 32 | HG01884.hp1 HG01934.hp1 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.16-13167A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549358 | ||||||
| chr19:14549390
|
T | G | 1 | a0001c0001t0001g0312 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.16-13135T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549390 | ||||||
| chr19:14549600
|
T | C | 3 | a0001c0002t0001g0202a0001c0002t0001g0236a0001c0002t0001g0243 | 3 | HG02145.hp1 HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.16-12925T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549600 | ||||||
| chr19:14549671
|
G | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0046a0001c0001t0001g0068others(37): Show | 41 | HG00438.hp2 HG00733.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.16-12854G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549671 | ||||||
| chr19:14549703
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.16-12822G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549703 | ||||||
| chr19:14549772
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.16-12753A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549772 | ||||||
| chr19:14549907
|
C | T | 2 | a0001c0005t0001g0021a0001c0005t0001g0024 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.16-12618C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14549907 | ||||||
| chr19:14549954
|
T | TA | 16 | a0001c0001t0001g0252a0001c0001t0001g0299a0001c0003t0001g0012others(13): Show | 16 | HG01928.hp2 HG02109.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.16-12563dupA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14549954 | |||||
| chr19:14550003
|
CCCTTT | C | 5 | a0001c0001t0001g0038a0001c0001t0001g0205a0001c0001t0001g0274others(2): Show | 5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-12515_16-12511d others(7): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14550003 | |||||
| chr19:14550031
|
C | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0205a0001c0001t0001g0274others(2): Show | 5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-12494C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550031 | ||||||
| chr19:14550049
|
A | G | 14 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(11): Show | 14 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.16-12476A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550049 | ||||||
| chr19:14550052
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-12473T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550052 | ||||||
| chr19:14550111
|
G | A | 3 | a0001c0001t0001g0172a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG03491.hp1 HG03492.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.16-12414G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550111 | ||||||
| chr19:14550214
|
A | T | 1 | a0001c0001t0001g0238 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.16-12311A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550214 | ||||||
| chr19:14550257
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.16-12268T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550257 | ||||||
| chr19:14550291
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.16-12234G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550291 | ||||||
| chr19:14550310
|
G | A | 2 | a0001c0001t0001g0321a0001c0003t0001g0247 | 2 | HG01981.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.16-12215G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550310 | ||||||
| chr19:14550464
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0259 | 2 | HG01099.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.16-12061C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550464 | ||||||
| chr19:14550496
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.16-12029G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550496 | ||||||
| chr19:14550587
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.16-11938A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550587 | ||||||
| chr19:14550812
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.16-11713C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550812 | ||||||
| chr19:14550873
|
T | C | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0100 | 3 | NA18960.hp2 NA18973.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.16-11652T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550873 | ||||||
| chr19:14550964
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-11561A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14550964 | ||||||
| chr19:14551061
|
G | A | 2 | a0001c0005t0001g0021a0001c0005t0001g0024 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.16-11464G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551061 | ||||||
| chr19:14551108
|
G | A | 4 | a0001c0005t0001g0028a0001c0005t0001g0033a0001c0005t0001g0034others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-11417G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551108 | ||||||
| chr19:14551311
|
G | A | 2 | a0001c0002t0001g0041a0001c0002t0001g0048 | 2 | HG02602.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.16-11214G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551311 | ||||||
| chr19:14551354
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-11171C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551354 | ||||||
| chr19:14551895
|
T | TTC | 3 | a0001c0001t0001g0145a0001c0005t0001g0021a0001c0005t0001g0024 | 3 | HG02280.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.16-10615_16-10614d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14551895 | |||||
| chr19:14551913
|
C | G | 15 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(12): Show | 15 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.16-10612C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551913 | ||||||
| chr19:14551913
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.16-10612C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551913 | ||||||
| chr19:14551931
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(101): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.16-10594C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551931 | ||||||
| chr19:14551946
|
C | CCT | 47 | a0001c0001t0001g0086a0001c0001t0001g0115a0001c0001t0001g0116others(44): Show | 47 | HG01070.hp2 HG01071.hp1 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.16-10554_16-10553d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14551946 | |||||
| chr19:14551946
|
C | CCTCT | 3 | a0001c0001t0001g0182a0001c0001t0001g0242a0001c0001t0001g0255 | 3 | HG01346.hp1 HG02040.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.16-10556_16-10553d others(6): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14551946 | |||||
| chr19:14551946
|
C | CCTCTCTC others(15): Show |
1 | a0001c0001t0001g0092 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.16-10568_16-10567i others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14551946 | |||||
| chr19:14551946
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.16-10579C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551946 | ||||||
| chr19:14551946
|
CCT | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.16-10554_16-10553d others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14551946 | |||||
| chr19:14551948
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.16-10577T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551948 | ||||||
| chr19:14551967
|
C | T | 23 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0087others(20): Show | 23 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-10558C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551967 | ||||||
| chr19:14551973
|
T | C | 24 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0087others(21): Show | 24 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.16-10552T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551973 | ||||||
| chr19:14551974
|
TCTCTC | T | 23 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0087others(20): Show | 23 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-10550_16-10546d others(7): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551974 | ||||||
| chr19:14551979
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.16-10546C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14551979 | ||||||
| chr19:14552014
|
G | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0205a0001c0001t0001g0274others(2): Show | 5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-10511G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552014 | ||||||
| chr19:14552044
|
T | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0204a0001c0001t0001g0212others(1): Show | 4 | NA18982.hp2 NA18999.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-10481T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552044 | ||||||
| chr19:14552131
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0144 | 2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.16-10394G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552131 | ||||||
| chr19:14552145
|
T | TTTTC | 23 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0087others(20): Show | 23 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-10360_16-10357d others(6): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14552145 | |||||
| chr19:14552145
|
TTTTC | T | 21 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.16-10360_16-10357d others(6): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14552145 | |||||
| chr19:14552157
|
CTTTCTTT others(4): Show |
C | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-10360_16-10350d others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14552157 | |||||
| chr19:14552172
|
C | CT | 6 | a0001c0001t0001g0049a0001c0001t0001g0132a0001c0001t0001g0135others(3): Show | 6 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-10338dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14552172 | |||||
| chr19:14552172
|
CT | C | 10 | a0001c0001t0001g0121a0001c0001t0001g0176a0001c0001t0001g0195others(7): Show | 10 | HG01169.hp2 HG01261.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-10338delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14552172 | |||||
| chr19:14552196
|
G | A | 3 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0304 | 3 | HG02486.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.16-10329G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552196 | ||||||
| chr19:14552313
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-10212C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552313 | ||||||
| chr19:14552429
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.16-10096A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552429 | ||||||
| chr19:14552511
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0242 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.16-10014G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552511 | ||||||
| chr19:14552517
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.16-10008A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552517 | ||||||
| chr19:14552526
|
T | C | 1 | a0001c0001t0001g0315 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.16-9999T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552526 | ||||||
| chr19:14552630
|
G | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0248a0001c0001t0001g0326 | 3 | HG02055.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.16-9895G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552630 | ||||||
| chr19:14552638
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.16-9887C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552638 | ||||||
| chr19:14552686
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0136a0001c0001t0001g0248others(5): Show | 8 | HG01109.hp2 HG02055.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-9839C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552686 | ||||||
| chr19:14552757
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.16-9768T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552757 | ||||||
| chr19:14552871
|
G | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0205a0001c0001t0001g0274others(2): Show | 5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-9654G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552871 | ||||||
| chr19:14552936
|
C | T | 1 | a0001c0002t0001g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.16-9589C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552936 | ||||||
| chr19:14552941
|
G | C | 322 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(319): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.16-9584G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14552941 | ||||||
| chr19:14553016
|
T | C | 34 | a0001c0001t0001g0053a0001c0001t0001g0309a0001c0002t0001g0011others(31): Show | 34 | HG01361.hp1 HG01515.hp1 HG01517.hp2 others(31): Show |
intron_variant | MODIFIER | c.16-9509T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553016 | ||||||
| chr19:14553041
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.16-9484C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553041 | ||||||
| chr19:14553190
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0242 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.16-9335C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553190 | ||||||
| chr19:14553190
|
CGCTCGGG others(5): Show |
C | 1 | a0002c0004t0001g0161 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.16-9331_16-9320del others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14553190 | |||||
| chr19:14553224
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.16-9301C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553224 | ||||||
| chr19:14553234
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0130 | 2 | HG02683.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.16-9291G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553234 | ||||||
| chr19:14553256
|
C | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0205a0001c0001t0001g0274others(2): Show | 5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-9269C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553256 | ||||||
| chr19:14553330
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.16-9195C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553330 | ||||||
| chr19:14553332
|
G | C | 17 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(14): Show | 17 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.16-9193G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553332 | ||||||
| chr19:14553402
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.16-9123C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553402 | ||||||
| chr19:14553507
|
T | G | 1 | a0001c0001t0001g0272 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.16-9018T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553507 | ||||||
| chr19:14553511
|
G | C | 1 | a0001c0001t0001g0178 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.16-9014G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553511 | ||||||
| chr19:14553736
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.16-8789G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553736 | ||||||
| chr19:14553835
|
G | A | 1 | a0001c0007t0001g0073 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.16-8690G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553835 | ||||||
| chr19:14553915
|
T | C | 17 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(14): Show | 17 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.16-8610T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14553915 | ||||||
| chr19:14554015
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.16-8510C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554015 | ||||||
| chr19:14554036
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.16-8489G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554036 | ||||||
| chr19:14554047
|
G | A | 22 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0087others(19): Show | 22 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.16-8478G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554047 | ||||||
| chr19:14554121
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(99): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.16-8404C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554121 | ||||||
| chr19:14554367
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.16-8158G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554367 | ||||||
| chr19:14554378
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.16-8147C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554378 | ||||||
| chr19:14554380
|
A | T | 23 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0087others(20): Show | 23 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-8145A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554380 | ||||||
| chr19:14554388
|
G | C | 321 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(318): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.16-8137G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554388 | ||||||
| chr19:14554598
|
C | T | 8 | a0001c0001t0001g0038a0001c0001t0001g0071a0001c0001t0001g0144others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-7927C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554598 | ||||||
| chr19:14554610
|
G | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0205a0001c0001t0001g0274others(2): Show | 5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-7915G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554610 | ||||||
| chr19:14554660
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(99): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.16-7865T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554660 | ||||||
| chr19:14554850
|
C | T | 3 | a0001c0001t0001g0267a0001c0001t0001g0269a0001c0001t0001g0312 | 3 | HG01167.hp2 HG01358.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.16-7675C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14554850 | ||||||
| chr19:14555137
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-7388T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555137 | ||||||
| chr19:14555143
|
A | G | 5 | a0001c0001t0001g0136a0001c0001t0001g0296a0001c0001t0001g0299others(2): Show | 5 | HG01109.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-7382A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555143 | ||||||
| chr19:14555188
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-7337T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555188 | ||||||
| chr19:14555193
|
C | T | 1 | a0001c0001t0001g0310 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.16-7332C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555193 | ||||||
| chr19:14555228
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.16-7297G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555228 | ||||||
| chr19:14555242
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-7283A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555242 | ||||||
| chr19:14555351
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.16-7174C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555351 | ||||||
| chr19:14555400
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-7125T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555400 | ||||||
| chr19:14555411
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0242 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.16-7114G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555411 | ||||||
| chr19:14555413
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-7112A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555413 | ||||||
| chr19:14555438
|
C | CT | 27 | a0001c0001t0001g0002a0001c0001t0001g0119a0001c0001t0001g0130others(24): Show | 27 | HG01071.hp1 HG01099.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.16-7061dupT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14555438 | |||||
| chr19:14555438
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-7072_16-7061dup others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14555438 | |||||
| chr19:14555438
|
CT | C | 59 | a0001c0001t0001g0019a0001c0001t0001g0054a0001c0001t0001g0056others(56): Show | 59 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.16-7061delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14555438 | |||||
| chr19:14555438
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0058 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.16-7071_16-7061del others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14555438 | |||||
| chr19:14555438
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0280 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.16-7073_16-7061del others(13): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14555438 | |||||
| chr19:14555601
|
A | G | 1 | a0001c0001t0001g0308 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.16-6924A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555601 | ||||||
| chr19:14555629
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-6896C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555629 | ||||||
| chr19:14555698
|
C | G | 12 | a0001c0002t0001g0027a0001c0002t0001g0041a0001c0002t0001g0048others(9): Show | 12 | HG01515.hp1 HG01517.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.16-6827C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555698 | ||||||
| chr19:14555741
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-6784A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14555741 | ||||||
| chr19:14556048
|
C | G | 6 | a0001c0001t0001g0098a0001c0001t0001g0122a0001c0001t0002g0003others(3): Show | 6 | HG03490.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-6477C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556048 | ||||||
| chr19:14556072
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.16-6453C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556072 | ||||||
| chr19:14556096
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-6429C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556096 | ||||||
| chr19:14556142
|
C | A | 5 | a0001c0001t0001g0039a0001c0001t0001g0204a0001c0001t0001g0212others(2): Show | 5 | NA18982.hp2 NA18983.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-6383C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556142 | ||||||
| chr19:14556391
|
C | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0205a0001c0001t0001g0274others(2): Show | 5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-6134C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556391 | ||||||
| chr19:14556408
|
C | CAAAACAA others(5): Show |
24 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0098others(21): Show | 24 | HG00408.hp2 HG00673.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.16-6113_16-6112ins others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14556408 | |||||
| chr19:14556413
|
A | AAAAAACA others(5): Show |
166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(163): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.16-6106_16-6095dup others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14556413 | |||||
| chr19:14556413
|
A | AAAAACAA others(4): Show |
1 | a0001c0001t0001g0322 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.16-6108_16-6107ins others(11): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14556413 | |||||
| chr19:14556413
|
A | C | 25 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0098others(22): Show | 25 | HG00408.hp2 HG00673.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.16-6112A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556413 | ||||||
| chr19:14556415
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-6107_16-6106ins others(10): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14556415 | |||||
| chr19:14556434
|
C | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(98): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.16-6091C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556434 | ||||||
| chr19:14556498
|
A | G | 2 | a0001c0001t0001g0146a0001c0001t0001g0242 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.16-6027A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556498 | ||||||
| chr19:14556504
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0059 | 2 | HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.16-6021A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556504 | ||||||
| chr19:14556605
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.16-5920A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556605 | ||||||
| chr19:14556776
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0131 | 2 | NA18964.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.16-5749G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556776 | ||||||
| chr19:14556855
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-5670C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556855 | ||||||
| chr19:14556919
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-5606C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556919 | ||||||
| chr19:14556926
|
G | C | 2 | a0001c0002t0001g0236a0001c0002t0001g0243 | 2 | HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.16-5599G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556926 | ||||||
| chr19:14556987
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.16-5538C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14556987 | ||||||
| chr19:14557027
|
C | T | 2 | a0001c0005t0001g0021a0001c0005t0001g0024 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.16-5498C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557027 | ||||||
| chr19:14557071
|
C | A | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-5454C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557071 | ||||||
| chr19:14557114
|
C | CGTATTAA others(5): Show |
1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-5411_16-5410ins others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557114 | ||||||
| chr19:14557114
|
C | CTTAT | 132 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0035others(129): Show | 132 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.16-5372_16-5369dup others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14557114 | |||||
| chr19:14557114
|
C | CTTATTTA others(1): Show |
85 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0023others(82): Show | 86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.16-5376_16-5369dup others(8): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14557114 | |||||
| chr19:14557114
|
C | CTTATTTA others(5): Show |
52 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0030others(49): Show | 52 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.16-5380_16-5369dup others(12): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14557114 | |||||
| chr19:14557114
|
C | CTTATTTA others(9): Show |
8 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0067others(5): Show | 8 | HG01361.hp2 HG01433.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.16-5384_16-5369dup others(16): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14557114 | |||||
| chr19:14557114
|
C | CTTATTTA others(17): Show |
1 | a0001c0001t0001g0252 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.16-5392_16-5369dup others(24): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14557114 | |||||
| chr19:14557114
|
CTTAT | C | 4 | a0001c0001t0001g0054a0001c0001t0001g0152a0001c0001t0001g0266others(1): Show | 4 | HG01258.hp1 HG02056.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-5372_16-5369del others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14557114 | |||||
| chr19:14557116
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-5409T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557116 | ||||||
| chr19:14557120
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-5405T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557120 | ||||||
| chr19:14557124
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-5401T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557124 | ||||||
| chr19:14557127
|
T | G | 1 | a0001c0002t0001g0102 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.16-5398T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557127 | ||||||
| chr19:14557127
|
T | TTATG | 32 | a0001c0001t0001g0309a0001c0002t0001g0011a0001c0002t0001g0013others(29): Show | 32 | HG01515.hp1 HG01517.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.16-5395_16-5394ins others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14557127 | |||||
| chr19:14557128
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-5397T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557128 | ||||||
| chr19:14557131
|
T | G | 33 | a0001c0001t0001g0309a0001c0002t0001g0011a0001c0002t0001g0013others(30): Show | 33 | HG01515.hp1 HG01517.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.16-5394T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557131 | ||||||
| chr19:14557132
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-5393T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557132 | ||||||
| chr19:14557135
|
T | G | 1 | a0001c0002t0001g0303 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.16-5390T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557135 | ||||||
| chr19:14557157
|
T | A | 1 | a0001c0001t0001g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.16-5368T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557157 | ||||||
| chr19:14557168
|
C | T | 6 | a0001c0001t0001g0098a0001c0001t0001g0122a0001c0001t0002g0003others(3): Show | 6 | HG03490.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-5357C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557168 | ||||||
| chr19:14557258
|
A | T | 1 | a0001c0001t0001g0049 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.16-5267A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557258 | ||||||
| chr19:14557825
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.16-4700G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557825 | ||||||
| chr19:14557830
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(99): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.16-4695A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557830 | ||||||
| chr19:14557857
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.16-4668G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557857 | ||||||
| chr19:14557916
|
C | T | 2 | a0001c0002t0001g0123a0001c0002t0001g0124 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.16-4609C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14557916 | ||||||
| chr19:14558001
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.16-4524C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558001 | ||||||
| chr19:14558007
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.16-4518G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558007 | ||||||
| chr19:14558155
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-4370A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558155 | ||||||
| chr19:14558225
|
T | G | 1 | a0001c0001t0001g0254 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.16-4300T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558225 | ||||||
| chr19:14558240
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG01123.hp1 HG01891.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.16-4285C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558240 | ||||||
| chr19:14558330
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-4195C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558330 | ||||||
| chr19:14558369
|
C | G | 4 | a0001c0001t0001g0075a0001c0001t0001g0163a0001c0001t0001g0218others(1): Show | 4 | HG00408.hp1 HG00438.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-4156C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558369 | ||||||
| chr19:14558399
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-4126C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558399 | ||||||
| chr19:14558440
|
G | A | 17 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(14): Show | 17 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.16-4085G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558440 | ||||||
| chr19:14558480
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-4045G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558480 | ||||||
| chr19:14558517
|
C | A | 1 | a0001c0001t0001g0053 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.16-4008C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558517 | ||||||
| chr19:14558597
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.16-3928C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558597 | ||||||
| chr19:14558607
|
T | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(168): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.16-3918T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558607 | ||||||
| chr19:14558624
|
G | A | 11 | a0001c0001t0001g0044a0001c0001t0001g0110a0001c0001t0001g0153others(8): Show | 11 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.16-3901G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558624 | ||||||
| chr19:14558660
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-3865A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14558660 | ||||||
| chr19:14558982
|
C | CGT | 6 | a0001c0001t0001g0098a0001c0001t0001g0122a0001c0001t0002g0003others(3): Show | 6 | HG03490.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-3531_16-3530dup others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14558982 | |||||
| chr19:14559154
|
C | T | 1 | a0001c0002t0001g0041 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.16-3371C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559154 | ||||||
| chr19:14559266
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.16-3259A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559266 | ||||||
| chr19:14559289
|
T | G | 2 | a0001c0002t0001g0123a0001c0002t0001g0124 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.16-3236T>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559289 | ||||||
| chr19:14559348
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-3177C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559348 | ||||||
| chr19:14559525
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.16-3000C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559525 | ||||||
| chr19:14559528
|
C | CTA | 17 | a0001c0001t0001g0038a0001c0001t0001g0071a0001c0001t0001g0144others(14): Show | 17 | HG01243.hp2 HG02280.hp2 HG02723.hp1 others(14): Show |
intron_variant | MODIFIER | c.16-2994_16-2993dup others(2): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14559528 | |||||
| chr19:14559742
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.16-2783G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559742 | ||||||
| chr19:14559777
|
A | G | 6 | a0001c0001t0001g0098a0001c0001t0001g0122a0001c0001t0002g0003others(3): Show | 6 | HG03490.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-2748A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559777 | ||||||
| chr19:14559786
|
CA | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(165): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.16-2724delA | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14559786 | |||||
| chr19:14559857
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-2668A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14559857 | ||||||
| chr19:14559981
|
AT | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.16-2541delT | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14559981 | |||||
| chr19:14560002
|
C | T | 4 | a0001c0005t0001g0028a0001c0005t0001g0033a0001c0005t0001g0034others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-2523C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560002 | ||||||
| chr19:14560006
|
G | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0205a0001c0001t0001g0274others(2): Show | 5 | HG01243.hp2 HG03579.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-2519G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560006 | ||||||
| chr19:14560025
|
G | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.16-2500G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560025 | ||||||
| chr19:14560121
|
A | AC | 33 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0035others(30): Show | 34 | HG00733.hp2 HG01175.hp2 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.16-2399dupC | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr19 | 14560121 | |||||
| chr19:14560141
|
G | A | 25 | a0001c0001t0001g0309a0001c0002t0001g0013a0001c0002t0001g0015others(22): Show | 25 | HG01515.hp1 HG01517.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.16-2384G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560141 | ||||||
| chr19:14560164
|
C | T | 1 | a0001c0001t0002g0006 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.16-2361C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560164 | ||||||
| chr19:14560180
|
G | A | 6 | a0001c0001t0001g0075a0001c0001t0001g0163a0001c0001t0001g0166others(3): Show | 6 | HG00408.hp1 HG00438.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-2345G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560180 | ||||||
| chr19:14560229
|
G | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.16-2296G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560229 | ||||||
| chr19:14560233
|
C | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.16-2292C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560233 | ||||||
| chr19:14560249
|
A | G | 22 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0087others(19): Show | 22 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.16-2276A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560249 | ||||||
| chr19:14560393
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-2132C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560393 | ||||||
| chr19:14560396
|
G | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.16-2129G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560396 | ||||||
| chr19:14560469
|
G | A | 1 | a0001c0002t0001g0045 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.16-2056G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560469 | ||||||
| chr19:14560488
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.16-2037T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560488 | ||||||
| chr19:14560576
|
G | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.16-1949G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560576 | ||||||
| chr19:14560577
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.16-1948C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560577 | ||||||
| chr19:14560763
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-1762A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560763 | ||||||
| chr19:14560911
|
A | C | 1 | a0001c0001t0001g0249 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.16-1614A>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560911 | ||||||
| chr19:14560931
|
G | A | 1 | a0001c0003t0001g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.16-1594G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14560931 | ||||||
| chr19:14561075
|
GCTGTCGT others(33): Show |
G | 1 | a0001c0001t0001g0198 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.16-1449_16-1410del others(40): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561075 | ||||||
| chr19:14561167
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-1358C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561167 | ||||||
| chr19:14561217
|
C | T | 21 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.16-1308C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561217 | ||||||
| chr19:14561353
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(195): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.16-1172T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561353 | ||||||
| chr19:14561354
|
G | A | 3 | a0001c0001t0001g0159a0001c0001t0001g0172a0001c0001t0001g0179 | 3 | NA18999.hp2 NA19074.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.16-1171G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561354 | ||||||
| chr19:14561459
|
G | A | 1 | a0001c0001t0001g0310 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.16-1066G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561459 | ||||||
| chr19:14561467
|
C | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0144 | 2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.16-1058C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561467 | ||||||
| chr19:14561524
|
G | T | 15 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(12): Show | 15 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.16-1001G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561524 | ||||||
| chr19:14561539
|
G | A | 4 | a0001c0005t0001g0028a0001c0005t0001g0033a0001c0005t0001g0034others(1): Show | 4 | HG02451.hp1 HG02486.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-986G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561539 | ||||||
| chr19:14561735
|
G | A | 8 | a0001c0001t0001g0038a0001c0001t0001g0071a0001c0001t0001g0144others(5): Show | 8 | HG01243.hp2 HG02280.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.16-790G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561735 | ||||||
| chr19:14561773
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.16-752A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561773 | ||||||
| chr19:14561885
|
C | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(97): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.16-640C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561885 | ||||||
| chr19:14561921
|
T | C | 94 | a0001c0001t0001g0038a0001c0001t0001g0071a0001c0001t0001g0077others(91): Show | 94 | HG00323.hp1 HG00408.hp2 HG00673.hp1 others(91): Show |
intron_variant | MODIFIER | c.16-604T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561921 | ||||||
| chr19:14561937
|
C | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.16-588C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561937 | ||||||
| chr19:14561958
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.16-567T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561958 | ||||||
| chr19:14561997
|
T | C | 328 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(325): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.16-528T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14561997 | ||||||
| chr19:14562109
|
C | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0242 | 2 | HG02630.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.16-416C>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562109 | ||||||
| chr19:14562140
|
G | A | 1 | a0001c0003t0001g0247 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.16-385G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562140 | ||||||
| chr19:14562147
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.16-378G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562147 | ||||||
| chr19:14562221
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.16-304C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562221 | ||||||
| chr19:14562236
|
C | T | 2 | a0001c0001t0001g0288a0001c0001t0001g0307 | 2 | HG00099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.16-289C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562236 | ||||||
| chr19:14562275
|
C | T | 1 | a0002c0004t0001g0081 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.16-250C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562275 | ||||||
| chr19:14562424
|
G | A | 12 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(9): Show | 12 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.16-101G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562424 | ||||||
| chr19:14562510
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.16-15G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 1/12 | chr19 | 14562510 | ||||||
| chr19:14562731
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.66+156C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 2/12 | chr19 | 14562731 | ||||||
| chr19:14562791
|
G | A | 8 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0052others(5): Show | 8 | HG01361.hp1 HG02258.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+216G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 2/12 | chr19 | 14562791 | ||||||
| chr19:14562961
|
C | T | 2 | a0001c0002t0001g0097a0002c0006t0001g0128 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.67-245C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 2/12 | chr19 | 14562961 | ||||||
| chr19:14562985
|
G | C | 20 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(17): Show | 20 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.67-221G>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 2/12 | chr19 | 14562985 | ||||||
| chr19:14563016
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(96): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.67-190C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 2/12 | chr19 | 14563016 | ||||||
| chr19:14563189
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0167 | 2 | HG01358.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.67-17G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 2/12 | chr19 | 14563189 | ||||||
| chr19:14563304
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.118+47G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563304 | ||||||
| chr19:14563312
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.118+55A>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563312 | ||||||
| chr19:14563336
|
A | AGAGGGG | 21 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.118+79_118+80insGA others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563336 | ||||||
| chr19:14563339
|
C | T | 21 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.118+82C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563339 | ||||||
| chr19:14563340
|
C | CAGAGA | 21 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.118+83_118+84insAG others(3): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563340 | ||||||
| chr19:14563342
|
C | G | 21 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.118+85C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563342 | ||||||
| chr19:14563343
|
T | C | 21 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.118+86T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563343 | ||||||
| chr19:14563348
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.118+91G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563348 | ||||||
| chr19:14563405
|
C | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0306 | 2 | HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.118+148C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563405 | ||||||
| chr19:14563414
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.118+157G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563414 | ||||||
| chr19:14563423
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.118+166C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563423 | ||||||
| chr19:14563445
|
T | C | 1 | a0001c0001t0002g0003 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.118+188T>C | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563445 | ||||||
| chr19:14563474
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.119-184C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563474 | ||||||
| chr19:14563603
|
G | A | 21 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(18): Show | 21 | HG02109.hp2 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.119-55G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 3/12 | chr19 | 14563603 | ||||||
| chr19:14564341
|
C | T | 6 | a0001c0001t0001g0098a0001c0001t0001g0122a0001c0001t0002g0003others(3): Show | 6 | HG03490.hp1 HG03654.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+54C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 7/12 | chr19 | 14564341 | ||||||
| chr19:14564395
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(98): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.489+108A>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 7/12 | chr19 | 14564395 | ||||||
| chr19:14564499
|
GGCCT | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(96): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.489+217_489+220del others(4): Show |
TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 14564499 | |||||
| chr19:14564560
|
G | T | 1 | a0001c0001t0001g0283 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.490-226G>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 7/12 | chr19 | 14564560 | ||||||
| chr19:14564917
|
C | T | 1 | a0001c0005t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.563-32C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 8/12 | chr19 | 14564917 | ||||||
| chr19:14565000
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG03654.hp1 | splice_region_variant&intron_variant | LOW | c.606+8G>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 9/12 | chr19 | 14565000 | ||||||
| chr19:14565360
|
T | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0009others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.753+70T>A | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 11/12 | chr19 | 14565360 | ||||||
| chr19:14565473
|
C | T | 17 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(14): Show | 17 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.754-145C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 11/12 | chr19 | 14565473 | ||||||
| chr19:14565589
|
C | T | 4 | a0001c0001t0001g0267a0001c0001t0001g0269a0001c0001t0001g0287others(1): Show | 4 | HG01167.hp2 HG01358.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-29C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 11/12 | chr19 | 14565589 | ||||||
| chr19:14565669
|
C | T | 20 | a0001c0003t0001g0012a0001c0003t0001g0014a0001c0003t0001g0016others(17): Show | 20 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(17): Show |
splice_region_variant&intron_variant | LOW | c.799+6C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 12/12 | chr19 | 14565669 | ||||||
| chr19:14565676
|
C | G | 1 | a0002c0004t0001g0129 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.799+13C>G | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 12/12 | chr19 | 14565676 | ||||||
| chr19:14565676
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.799+13C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 12/12 | chr19 | 14565676 | ||||||
| chr19:14565728
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.800-16C>T | TECR | ENSG00000099797.15 | transcript | ENST00000215567.10 | protein_coding | 12/12 | chr19 | 14565728 |