| geneid | 79573 |
|---|---|
| ensemblid | ENSG00000143643.13 |
| hgncid | 26204 |
| symbol | TTC13 |
| name | tetratricopeptide repeat domain 13 |
| refseq_nuc | NM_024525.5 |
| refseq_prot | NP_078801.3 |
| ensembl_nuc | ENST00000366661.9 |
| ensembl_prot | ENSP00000355621.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 230906243 |
| end | 230978861 |
| strand | - |
| ver | v1.2 |
| region | chr1:230906243-230978861 |
| region5000 | chr1:230901243-230983861 |
| regionname0 | TTC13_chr1_230906243_230978861 |
| regionname5000 | TTC13_chr1_230901243_230983861 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 860 | 247 | 75 | 41 | 92 | 12 | 25 | 73 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0002 | 0/0 | 860 | 78 | 11 | 7 | 46 | 2 | 12 | 37 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0003 | 0/0 | 860 | 3 | 0 | 0 | 0 | 2 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0004 | 0/0 | 860 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0005 | 0/0 | 860 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0006 | 0/0 | 860 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0007 | 0/0 | 860 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0008 | 0/0 | 860 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0009 | 0/0 | 860 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0010 | 0/0 | 860 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2583 | 126 | 7 | 24 | 73 | 6 | 15 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0002 | 1/0 | 2583 | 83 | 39 | 13 | 15 | 5 | 10 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0003 | 0/0 | 2583 | 69 | 9 | 5 | 43 | 1 | 11 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0004 | 0/0 | 2583 | 15 | 12 | 2 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0005 | 0/0 | 2583 | 14 | 13 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0006 | 0/0 | 2583 | 3 | 0 | 0 | 0 | 2 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0007 | 0/0 | 2583 | 3 | 1 | 2 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0008 | 0/0 | 2583 | 3 | 0 | 0 | 3 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0009 | 0/0 | 2583 | 3 | 0 | 1 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0010 | 0/0 | 2583 | 2 | 0 | 0 | 0 | 1 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0011 | 0/0 | 2583 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0012 | 0/0 | 2583 | 2 | 0 | 1 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0013 | 0/0 | 2583 | 2 | 2 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0014 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0015 | 0/0 | 2583 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0016 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0017 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0018 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0019 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0020 | 0/0 | 2583 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0021 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| c0022 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 694 | 171 | 34 | 17 | 82 | 11 | 27 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| t0002 | 1/1 | 694 | 158 | 51 | 33 | 56 | 4 | 12 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| t0003 | 0/0 | 694 | 2 | 2 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| t0004 | 0/0 | 694 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| t0005 | 0/0 | 694 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| t0006 | 0/0 | 694 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| t0007 | 0/0 | 676 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| t0008 | 0/0 | 694 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0004 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0230 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2583 | 126 | 7 | 24 | 73 | 6 | 15 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0002 | 1/0 | 2583 | 83 | 39 | 13 | 15 | 5 | 10 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0004 | 0/0 | 2583 | 15 | 12 | 2 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0005 | 0/0 | 2583 | 14 | 13 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0009 | 0/0 | 2583 | 3 | 0 | 1 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0011 | 0/0 | 2583 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0013 | 0/0 | 2583 | 2 | 2 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0017 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0018 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0002c0003 | 0/0 | 2583 | 69 | 9 | 5 | 43 | 1 | 11 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0002c0007 | 0/0 | 2583 | 3 | 1 | 2 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0002c0008 | 0/0 | 2583 | 3 | 0 | 0 | 3 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0002c0010 | 0/0 | 2583 | 2 | 0 | 0 | 0 | 1 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0002c0014 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0003c0006 | 0/0 | 2583 | 3 | 0 | 0 | 0 | 2 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0004c0012 | 0/0 | 2583 | 2 | 0 | 1 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0005c0022 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0006c0020 | 0/0 | 2583 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0007c0019 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0008c0021 | 0/0 | 2583 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0009c0016 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0010c0015 | 0/0 | 2583 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3276 | 51 | 5 | 4 | 29 | 4 | 9 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0001t0002 | 0/1 | 3276 | 74 | 2 | 20 | 43 | 2 | 6 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0001t0005 | 0/0 | 3276 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0002t0001 | 0/0 | 3276 | 39 | 18 | 6 | 7 | 3 | 5 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0002t0002 | 1/0 | 3276 | 44 | 21 | 7 | 8 | 2 | 5 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0004t0002 | 0/0 | 3276 | 14 | 12 | 2 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0004t0008 | 0/0 | 3276 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0005t0002 | 0/0 | 3276 | 14 | 13 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0009t0002 | 0/0 | 3276 | 3 | 0 | 1 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0011t0002 | 0/0 | 3276 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0013t0003 | 0/0 | 3276 | 2 | 2 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0017t0007 | 0/0 | 3258 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0001c0018t0002 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0002c0003t0001 | 0/0 | 3276 | 68 | 9 | 5 | 43 | 1 | 10 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0002c0003t0006 | 0/0 | 3276 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0002c0007t0001 | 0/0 | 3276 | 3 | 1 | 2 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0002c0008t0001 | 0/0 | 3276 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0002c0008t0004 | 0/0 | 3276 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0002c0010t0001 | 0/0 | 3276 | 2 | 0 | 0 | 0 | 1 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0002c0014t0001 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0003c0006t0001 | 0/0 | 3276 | 3 | 0 | 0 | 0 | 2 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0004c0012t0002 | 0/0 | 3276 | 2 | 0 | 1 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0005c0022t0002 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0006c0020t0002 | 0/0 | 3276 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0007c0019t0002 | 0/0 | 3276 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0008c0021t0002 | 0/0 | 3276 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0009c0016t0001 | 0/0 | 3276 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| a0010c0015t0001 | 0/0 | 3276 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | copy fasta | chr1 | 230901243 | 230983861 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0230 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0004t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0004t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0004t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0004t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0004t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0004t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0004t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0004t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0004t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0004t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0004t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0004t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0004t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0004t0008g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0005t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0005t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0005t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0005t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0005t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0005t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0005t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0005t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0005t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0005t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0005t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0005t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0005t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0005t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0009t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0009t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0009t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0011t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0011t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0013t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0013t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0017t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0001c0018t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0001 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0003t0006g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0007t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0007t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0007t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0008t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0008t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0008t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0010t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0010t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0002c0014t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0003c0006t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0003c0006t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0003c0006t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0004c0012t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0004c0012t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0005c0022t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0006c0020t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0007c0019t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0008c0021t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0009c0016t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| a0010c0015t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0003 | t0001 | g0033 | EUR | GBR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | GBR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00280 | hp2 | a0003 | c0006 | t0001 | g0028 | EUR | FIN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00323 | hp1 | a0002 | c0010 | t0001 | g0042 | EUR | FIN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00323 | hp2 | a0003 | c0006 | t0001 | g0027 | EUR | FIN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00408 | hp1 | a0002 | c0003 | t0001 | g0069 | EAS | CHS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | CHS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | CHS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | CHS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00597 | hp1 | a0002 | c0003 | t0001 | g0062 | EAS | CHS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | CHS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00609 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | CHS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00621 | hp1 | a0009 | c0016 | t0001 | g0038 | EAS | CHS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0152 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00642 | hp1 | a0002 | c0003 | t0001 | g0008 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | CHS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00673 | hp2 | a0002 | c0003 | t0001 | g0051 | EAS | CHS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00733 | hp2 | a0002 | c0007 | t0001 | g0044 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00735 | hp2 | a0002 | c0003 | t0001 | g0031 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00738 | hp1 | a0002 | c0007 | t0001 | g0072 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00741 | hp1 | a0002 | c0003 | t0001 | g0008 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0022 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0036 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01109 | hp1 | a0001 | c0004 | t0002 | g0185 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01109 | hp2 | a0001 | c0005 | t0002 | g0170 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01167 | hp1 | a0004 | c0012 | t0002 | g0259 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0022 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0272 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0198 | AMR | PUR | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0239 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0086 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01261 | hp1 | a0001 | c0004 | t0002 | g0181 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01346 | hp1 | a0006 | c0020 | t0002 | g0248 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0093 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0256 | AMR | CLM | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0294 | EUR | IBS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0019 | EUR | IBS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | IBS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0019 | EUR | IBS | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0114 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0032 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01891 | hp2 | a0001 | c0004 | t0002 | g0188 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PEL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PEL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02015 | hp1 | a0001 | c0009 | t0002 | g0273 | EAS | KHV | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | KHV | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02055 | hp1 | a0001 | c0005 | t0002 | g0180 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0255 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02074 | hp1 | a0001 | c0009 | t0002 | g0274 | EAS | KHV | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | KHV | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02132 | hp2 | a0002 | c0003 | t0001 | g0058 | EAS | KHV | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0018 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | CDX | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02155 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | CDX | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02165 | hp2 | a0007 | c0019 | t0002 | g0244 | EAS | CDX | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02257 | hp1 | a0001 | c0018 | t0002 | g0165 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0265 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0119 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PEL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02273 | hp2 | a0001 | c0009 | t0002 | g0242 | AMR | PEL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02280 | hp1 | a0001 | c0004 | t0002 | g0182 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02280 | hp2 | a0001 | c0005 | t0002 | g0173 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02523 | hp1 | a0002 | c0003 | t0001 | g0056 | EAS | KHV | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0196 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02572 | hp2 | a0001 | c0005 | t0002 | g0278 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02602 | hp1 | a0004 | c0012 | t0002 | g0296 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0270 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02615 | hp2 | a0001 | c0005 | t0002 | g0276 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0225 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02622 | hp2 | a0008 | c0021 | t0002 | g0189 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02630 | hp2 | a0001 | c0004 | t0002 | g0167 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02683 | hp2 | a0002 | c0003 | t0001 | g0035 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02698 | hp2 | a0002 | c0003 | t0001 | g0055 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02717 | hp1 | a0002 | c0003 | t0001 | g0082 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02717 | hp2 | a0001 | c0013 | t0003 | g0091 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0037 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02723 | hp2 | a0001 | c0005 | t0002 | g0280 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02738 | hp1 | a0002 | c0003 | t0001 | g0034 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02809 | hp1 | a0001 | c0004 | t0002 | g0200 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0080 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0195 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02818 | hp2 | a0005 | c0022 | t0002 | g0183 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02895 | hp2 | a0001 | c0004 | t0002 | g0017 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0202 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02896 | hp2 | a0001 | c0005 | t0002 | g0275 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02897 | hp1 | a0001 | c0004 | t0002 | g0017 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02897 | hp2 | a0001 | c0005 | t0002 | g0277 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02922 | hp2 | a0001 | c0004 | t0002 | g0191 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02965 | hp2 | a0001 | c0005 | t0002 | g0172 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0061 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02976 | hp1 | a0001 | c0004 | t0002 | g0186 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0204 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0266 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0271 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03041 | hp2 | a0001 | c0004 | t0002 | g0192 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0267 | AFR | MSL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03098 | hp2 | a0002 | c0003 | t0001 | g0075 | AFR | MSL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0226 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0175 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03139 | hp2 | a0001 | c0005 | t0002 | g0169 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03195 | hp1 | a0001 | c0013 | t0003 | g0092 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | MSL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0211 | AFR | MSL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | MSL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03453 | hp2 | a0001 | c0005 | t0002 | g0281 | AFR | MSL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03486 | hp1 | a0002 | c0003 | t0001 | g0081 | AFR | MSL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | MSL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03491 | hp1 | a0010 | c0015 | t0001 | g0041 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03491 | hp2 | a0002 | c0003 | t0001 | g0009 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03492 | hp2 | a0002 | c0003 | t0001 | g0009 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0222 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03516 | hp2 | a0002 | c0014 | t0001 | g0045 | AFR | ESN | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0201 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0269 | AFR | GWD | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0302 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03669 | hp2 | a0002 | c0010 | t0001 | g0043 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03688 | hp1 | a0002 | c0003 | t0001 | g0029 | SAS | STU | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0251 | SAS | STU | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0049 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0133 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0176 | SAS | PJL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0084 | SAS | BEB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0110 | SAS | STU | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG04184 | hp2 | a0002 | c0003 | t0001 | g0001 | SAS | BEB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0109 | SAS | STU | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0001 | SAS | STU | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG04228 | hp1 | a0002 | c0003 | t0006 | g0085 | SAS | STU | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | YRI | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18522 | hp2 | a0002 | c0003 | t0001 | g0040 | AFR | YRI | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | CHB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18612 | hp2 | a0002 | c0003 | t0001 | g0050 | EAS | CHB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | CHB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | CHB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18906 | hp1 | a0001 | c0005 | t0002 | g0279 | AFR | YRI | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18906 | hp2 | a0001 | c0005 | t0002 | g0171 | AFR | YRI | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18941 | hp1 | a0002 | c0003 | t0001 | g0039 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18942 | hp2 | a0002 | c0003 | t0001 | g0059 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18945 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18946 | hp1 | a0002 | c0008 | t0001 | g0088 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18947 | hp2 | a0002 | c0003 | t0001 | g0066 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18956 | hp2 | a0002 | c0003 | t0001 | g0052 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18964 | hp1 | a0002 | c0003 | t0001 | g0064 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18968 | hp2 | a0002 | c0003 | t0001 | g0078 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18977 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18977 | hp2 | a0001 | c0011 | t0002 | g0257 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18978 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0300 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18982 | hp2 | a0002 | c0003 | t0001 | g0054 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18983 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18985 | hp1 | a0002 | c0008 | t0001 | g0089 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18986 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18989 | hp1 | a0002 | c0003 | t0001 | g0046 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18993 | hp1 | a0002 | c0003 | t0001 | g0068 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18997 | hp2 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18999 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19004 | hp2 | a0002 | c0003 | t0001 | g0063 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19006 | hp2 | a0002 | c0003 | t0001 | g0070 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19007 | hp1 | a0002 | c0003 | t0001 | g0065 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19011 | hp1 | a0002 | c0003 | t0001 | g0057 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0179 | AFR | LWK | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19030 | hp2 | a0002 | c0003 | t0001 | g0060 | AFR | LWK | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19043 | hp1 | a0001 | c0017 | t0007 | g0166 | AFR | LWK | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | LWK | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19055 | hp1 | a0002 | c0003 | t0001 | g0076 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19056 | hp1 | a0002 | c0003 | t0001 | g0048 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19062 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19063 | hp1 | a0002 | c0003 | t0001 | g0073 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19067 | hp1 | a0002 | c0003 | t0001 | g0079 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19072 | hp2 | a0002 | c0003 | t0001 | g0030 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19075 | hp1 | a0001 | c0011 | t0002 | g0205 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19075 | hp2 | a0002 | c0003 | t0001 | g0083 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19076 | hp1 | a0002 | c0003 | t0001 | g0053 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19077 | hp1 | a0002 | c0003 | t0001 | g0047 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19078 | hp1 | a0002 | c0003 | t0001 | g0074 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19080 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19085 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19087 | hp2 | a0002 | c0003 | t0001 | g0077 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19089 | hp1 | a0002 | c0003 | t0001 | g0067 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0264 | AFR | ASW | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | ASW | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | TSI | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0290 | EUR | TSI | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | TSI | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA20805 | hp2 | a0001 | c0004 | t0008 | g0184 | EUR | TSI | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | GIH | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA20905 | hp2 | a0003 | c0006 | t0001 | g0026 | SAS | GIH | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0116 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02486 | hp1 | a0001 | c0004 | t0002 | g0187 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0178 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02559 | hp1 | a0001 | c0004 | t0002 | g0194 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0177 | AFR | ACB | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03471 | hp1 | a0001 | c0004 | t0002 | g0190 | AFR | MSL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | MSL | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG06807 | hp1 | a0001 | c0005 | t0002 | g0193 | AFR | USA | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | USA | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18955 | hp1 | a0002 | c0008 | t0004 | g0087 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| NA21309 | hp2 | a0002 | c0007 | t0001 | g0071 | AFR | LWK | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0240 | REF | REF | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0230 | REF | REF | TTC13_chr1_230901243_230983861 | TTC13 | chr1 | 230901243 | 230983861 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:230906978
|
G | A | 1 | a0010 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.2510C>T | p.Thr837Met | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 23/23 | 2541/3276 | 2510/2583 | 837/860 | chr1 | 230906978 | ||
| chr1:230911525
|
T | C | 1 | a0007 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.2254A>G | p.Ile752Val | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/23 | 2285/3276 | 2254/2583 | 752/860 | chr1 | 230911525 | ||
| chr1:230912724
|
T | C | 1 | a0006 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.2128A>G | p.Thr710Ala | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/23 | 2159/3276 | 2128/2583 | 710/860 | chr1 | 230912724 | ||
| chr1:230931453
|
G | A | 1 | a0009 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1145C>T | p.Pro382Leu | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/23 | 1176/3276 | 1145/2583 | 382/860 | chr1 | 230931453 | ||
| chr1:230940481
|
G | A | 1 | a0004 | 2 | HG01167.hp1 HG02602.hp1 |
missense_variant | MODERATE | c.748C>T | p.Arg250Trp | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 7/23 | 779/3276 | 748/2583 | 250/860 | chr1 | 230940481 | ||
| chr1:230943834
|
C | A | 1 | a0005 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.644G>T | p.Arg215Leu | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/23 | 675/3276 | 644/2583 | 215/860 | chr1 | 230943834 | ||
| chr1:230954398
|
C | G | 1 | a0008 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.448G>C | p.Ala150Pro | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/23 | 479/3276 | 448/2583 | 150/860 | chr1 | 230954398 | ||
| chr1:230978674
|
A | C | 1 | a0003 | 3 | HG00280.hp2 HG00323.hp2 NA20905.hp2 |
missense_variant | MODERATE | c.157T>G | p.Ser53Ala | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/23 | 188/3276 | 157/2583 | 53/860 | chr1 | 230978674 | ||
| chr1:230978719
|
C | G | 4 | a0002a0003a0009others(1): Show | 83 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
missense_variant | MODERATE | c.112G>C | p.Gly38Arg | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/23 | 143/3276 | 112/2583 | 38/860 | chr1 | 230978719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:230906986
|
T | A | 13 | a0001c0001a0001c0004a0001c0005others(10): Show | 168 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(165): Show |
synonymous_variant | LOW | c.2502A>T | p.Val834Val | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 23/23 | 2533/3276 | 2502/2583 | 834/860 | chr1 | 230906986 | ||
| chr1:230907004
|
A | G | 1 | a0001c0011 | 2 | NA18977.hp2 NA19075.hp1 |
synonymous_variant | LOW | c.2484T>C | p.Tyr828Tyr | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 23/23 | 2515/3276 | 2484/2583 | 828/860 | chr1 | 230907004 | ||
| chr1:230921501
|
A | T | 7 | a0001c0009a0001c0013a0002c0003others(4): Show | 82 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
synonymous_variant | LOW | c.1818T>A | p.Gly606Gly | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 16/23 | 1849/3276 | 1818/2583 | 606/860 | chr1 | 230921501 | ||
| chr1:230929014
|
A | G | 1 | a0001c0005 | 14 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(11): Show |
synonymous_variant | LOW | c.1380T>C | p.Phe460Phe | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/23 | 1411/3276 | 1380/2583 | 460/860 | chr1 | 230929014 | ||
| chr1:230954360
|
T | C | 1 | a0002c0008 | 3 | NA18946.hp1 NA18955.hp1 NA18985.hp1 |
synonymous_variant | LOW | c.486A>G | p.Ala162Ala | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/23 | 517/3276 | 486/2583 | 162/860 | chr1 | 230954360 | ||
| chr1:230961296
|
G | A | 4 | a0001c0004a0001c0013a0005c0022others(1): Show | 19 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(16): Show |
synonymous_variant | LOW | c.279C>T | p.Ser93Ser | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/23 | 310/3276 | 279/2583 | 93/860 | chr1 | 230961296 | ||
| chr1:230978594
|
C | T | 2 | a0001c0017a0001c0018 | 2 | HG02257.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.237G>A | p.Gly79Gly | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/23 | 268/3276 | 237/2583 | 79/860 | chr1 | 230978594 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:230906404
|
C | T | 1 | a0001c0013t0003 | 2 | HG02717.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*501G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 23/23 | 501 | chr1 | 230906404 | |||||
| chr1:230906472
|
G | A | 1 | a0002c0003t0006 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*433C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 23/23 | 433 | chr1 | 230906472 | |||||
| chr1:230906512
|
A | C | 1 | a0001c0017t0007 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 23/23 | 393 | chr1 | 230906512 | |||||
| chr1:230906513
|
G | A | 2 | a0001c0004t0008a0001c0017t0007 | 2 | NA19043.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*392C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 23/23 | 392 | chr1 | 230906513 | |||||
| chr1:230906514
|
TCTTTGAA others(11): Show |
T | 1 | a0001c0017t0007 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373_*390delTCTGGA others(12): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 23/23 | 373 | chr1 | 230906514 | |||||
| chr1:230906683
|
C | T | 1 | a0001c0001t0005 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*222G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 23/23 | 222 | chr1 | 230906683 | |||||
| chr1:230906718
|
G | A | 1 | a0001c0013t0003 | 2 | HG02717.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*187C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 23/23 | 187 | chr1 | 230906718 | |||||
| chr1:230906872
|
C | T | 1 | a0002c0008t0004 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*33G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 23/23 | 33 | chr1 | 230906872 | |||||
| chr1:230978849
|
C | T | 14 | a0001c0001t0001a0001c0001t0005a0001c0002t0001others(11): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
5_prime_UTR_variant | MODIFIER | c.-19G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/23 | 19 | chr1 | 230978849 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:230907131
|
T | A | 1 | a0001c0002t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2469-112A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 22/22 | chr1 | 230907131 | ||||||
| chr1:230907191
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2469-172C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 22/22 | chr1 | 230907191 | ||||||
| chr1:230907336
|
A | G | 3 | a0001c0001t0001g0161a0001c0001t0002g0020a0001c0001t0002g0235 | 4 | HG00673.hp1 HG03490.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.2469-317T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 22/22 | chr1 | 230907336 | ||||||
| chr1:230907470
|
C | T | 1 | a0001c0002t0002g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2469-451G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 22/22 | chr1 | 230907470 | ||||||
| chr1:230907626
|
G | A | 189 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 206 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.2469-607C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 22/22 | chr1 | 230907626 | ||||||
| chr1:230907634
|
T | C | 156 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(153): Show | 168 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.2469-615A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 22/22 | chr1 | 230907634 | ||||||
| chr1:230907812
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2469-793T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 22/22 | chr1 | 230907812 | ||||||
| chr1:230907944
|
G | A | 1 | a0001c0002t0001g0118 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2468+768C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 22/22 | chr1 | 230907944 | ||||||
| chr1:230907985
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2468+727C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 22/22 | chr1 | 230907985 | ||||||
| chr1:230907993
|
T | TAATTCCT others(11): Show |
302 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(299): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.2468+718_2468+719i others(20): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 22/22 | chr1 | 230907993 | ||||||
| chr1:230908271
|
T | C | 2 | a0002c0003t0001g0006a0002c0003t0001g0046 | 3 | NA18978.hp2 NA18989.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2468+441A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 22/22 | chr1 | 230908271 | ||||||
| chr1:230908496
|
G | A | 1 | a0002c0007t0001g0072 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2468+216C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 22/22 | chr1 | 230908496 | ||||||
| chr1:230908636
|
C | T | 1 | a0001c0002t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2468+76G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 22/22 | chr1 | 230908636 | ||||||
| chr1:230908637
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2468+75C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 22/22 | chr1 | 230908637 | ||||||
| chr1:230908929
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2388+13G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 21/22 | chr1 | 230908929 | ||||||
| chr1:230908930
|
G | A | 2 | a0001c0002t0001g0119a0001c0017t0007g0166 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2388+12C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 21/22 | chr1 | 230908930 | ||||||
| chr1:230909145
|
C | A | 1 | a0002c0003t0001g0058 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2310-125G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230909145 | ||||||
| chr1:230909145
|
C | T | 1 | a0001c0002t0002g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2310-125G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230909145 | ||||||
| chr1:230909148
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0158 | 2 | HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2310-128T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230909148 | ||||||
| chr1:230909224
|
C | A | 22 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(19): Show | 26 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.2310-204G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230909224 | ||||||
| chr1:230909278
|
C | T | 5 | a0001c0001t0002g0005a0001c0001t0002g0210a0001c0001t0002g0250others(2): Show | 7 | HG00408.hp2 NA18945.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.2310-258G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230909278 | ||||||
| chr1:230909340
|
C | T | 1 | a0001c0018t0002g0165 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2310-320G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230909340 | ||||||
| chr1:230909370
|
C | T | 1 | a0007c0019t0002g0244 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2310-350G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230909370 | ||||||
| chr1:230909542
|
A | G | 281 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(278): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.2310-522T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230909542 | ||||||
| chr1:230909672
|
A | G | 1 | a0001c0002t0002g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2310-652T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230909672 | ||||||
| chr1:230909824
|
C | T | 1 | a0001c0002t0002g0202 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2310-804G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230909824 | ||||||
| chr1:230909854
|
T | A | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG02630.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2310-834A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230909854 | ||||||
| chr1:230909925
|
C | T | 2 | a0002c0003t0001g0047a0002c0003t0001g0053 | 2 | NA19076.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2310-905G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230909925 | ||||||
| chr1:230909969
|
G | A | 1 | a0001c0002t0001g0119 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2310-949C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230909969 | ||||||
| chr1:230910331
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2309+1139G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910331 | ||||||
| chr1:230910370
|
A | G | 268 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(265): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.2309+1100T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910370 | ||||||
| chr1:230910411
|
C | G | 1 | a0001c0002t0002g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2309+1059G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910411 | ||||||
| chr1:230910437
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2309+1033G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910437 | ||||||
| chr1:230910481
|
G | A | 4 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | HG01496.hp1 HG01952.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.2309+989C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910481 | ||||||
| chr1:230910557
|
G | A | 1 | a0001c0002t0002g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2309+913C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910557 | ||||||
| chr1:230910585
|
C | T | 3 | a0002c0003t0001g0033a0002c0003t0001g0034a0002c0003t0001g0035 | 3 | HG00140.hp1 HG02683.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2309+885G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910585 | ||||||
| chr1:230910650
|
T | C | 1 | a0001c0002t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2309+820A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910650 | ||||||
| chr1:230910658
|
G | A | 22 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(19): Show | 26 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.2309+812C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910658 | ||||||
| chr1:230910673
|
G | A | 21 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(18): Show | 25 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.2309+797C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910673 | ||||||
| chr1:230910673
|
G | C | 1 | a0001c0002t0002g0239 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2309+797C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910673 | ||||||
| chr1:230910940
|
G | A | 189 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 206 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.2309+530C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910940 | ||||||
| chr1:230910978
|
T | TAGCTCTT others(318): Show |
1 | a0001c0002t0002g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2309+491_2309+492i others(327): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910978 | ||||||
| chr1:230910978
|
T | TAGCTCTT others(320): Show |
2 | a0001c0002t0002g0270a0001c0002t0002g0271 | 2 | HG02615.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2309+491_2309+492i others(329): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910978 | ||||||
| chr1:230910978
|
T | TAGCTCTT others(322): Show |
1 | a0001c0002t0002g0272 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2309+491_2309+492i others(331): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910978 | ||||||
| chr1:230910978
|
T | TAGCTCTT others(323): Show |
1 | a0001c0002t0002g0202 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2309+491_2309+492i others(332): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230910978 | ||||||
| chr1:230911268
|
A | G | 1 | a0001c0002t0001g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2309+202T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230911268 | ||||||
| chr1:230911397
|
A | G | 22 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(19): Show | 26 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.2309+73T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 20/22 | chr1 | 230911397 | ||||||
| chr1:230911564
|
TAC | T | 190 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(187): Show | 208 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2230-17_2230-16del others(2): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230911564 | ||||||
| chr1:230911570
|
C | T | 3 | a0001c0002t0001g0014a0001c0002t0001g0090a0001c0002t0002g0225 | 4 | HG02622.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2230-21G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230911570 | ||||||
| chr1:230911646
|
G | A | 189 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(186): Show | 206 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.2230-97C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230911646 | ||||||
| chr1:230911651
|
T | C | 1 | a0001c0002t0001g0149 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2230-102A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230911651 | ||||||
| chr1:230911935
|
C | T | 1 | a0002c0003t0001g0049 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2230-386G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230911935 | ||||||
| chr1:230911948
|
T | G | 22 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(19): Show | 26 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.2230-399A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230911948 | ||||||
| chr1:230911966
|
C | T | 1 | a0001c0001t0005g0102 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2230-417G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230911966 | ||||||
| chr1:230912058
|
C | G | 1 | a0010c0015t0001g0041 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2230-509G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230912058 | ||||||
| chr1:230912063
|
A | G | 3 | a0001c0009t0002g0273a0001c0009t0002g0274a0002c0003t0001g0069 | 3 | HG00408.hp1 HG02015.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.2230-514T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230912063 | ||||||
| chr1:230912085
|
C | A | 1 | a0001c0002t0002g0266 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2230-536G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230912085 | ||||||
| chr1:230912171
|
C | T | 187 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(184): Show | 204 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.2229+452G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230912171 | ||||||
| chr1:230912197
|
A | C | 2 | a0001c0001t0002g0168a0001c0001t0002g0197 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2229+426T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230912197 | ||||||
| chr1:230912305
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0106a0002c0003t0001g0032others(1): Show | 4 | HG01106.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.2229+318C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230912305 | ||||||
| chr1:230912432
|
T | G | 1 | a0001c0002t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2229+191A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230912432 | ||||||
| chr1:230912446
|
A | C | 1 | a0001c0002t0002g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2229+177T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230912446 | ||||||
| chr1:230912507
|
C | T | 3 | a0001c0002t0001g0014a0001c0002t0001g0090a0001c0002t0002g0225 | 4 | HG02622.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2229+116G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230912507 | ||||||
| chr1:230912541
|
T | A | 3 | a0001c0002t0001g0014a0001c0002t0001g0090a0001c0002t0002g0225 | 4 | HG02622.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2229+82A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230912541 | ||||||
| chr1:230912552
|
G | C | 6 | a0001c0002t0001g0119a0001c0002t0002g0174a0001c0002t0002g0176others(3): Show | 6 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2229+71C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 19/22 | chr1 | 230912552 | ||||||
| chr1:230912852
|
C | T | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2094-94G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230912852 | ||||||
| chr1:230913226
|
G | A | 277 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(274): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.2094-468C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230913226 | ||||||
| chr1:230913250
|
C | G | 1 | a0001c0001t0002g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2094-492G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230913250 | ||||||
| chr1:230913394
|
C | T | 2 | a0001c0001t0002g0217a0001c0001t0002g0218 | 2 | NA18993.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2094-636G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230913394 | ||||||
| chr1:230913471
|
C | T | 1 | a0001c0004t0002g0181 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2094-713G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230913471 | ||||||
| chr1:230913472
|
G | A | 7 | a0001c0002t0001g0011a0001c0002t0001g0093a0001c0002t0001g0095others(4): Show | 8 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.2094-714C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230913472 | ||||||
| chr1:230913676
|
G | A | 22 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(19): Show | 26 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.2094-918C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230913676 | ||||||
| chr1:230913777
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2094-1019G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230913777 | ||||||
| chr1:230913788
|
T | C | 3 | a0001c0002t0001g0014a0001c0002t0001g0090a0001c0002t0002g0225 | 4 | HG02622.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2094-1030A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230913788 | ||||||
| chr1:230913803
|
T | C | 3 | a0001c0002t0002g0195a0001c0002t0002g0196a0001c0002t0002g0198 | 3 | HG01243.hp2 HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2094-1045A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230913803 | ||||||
| chr1:230913842
|
C | T | 19 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(16): Show | 20 | HG01109.hp1 HG01243.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.2094-1084G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230913842 | ||||||
| chr1:230913948
|
G | C | 10 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(7): Show | 13 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.2094-1190C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230913948 | ||||||
| chr1:230914020
|
G | A | 1 | a0002c0010t0001g0043 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2094-1262C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914020 | ||||||
| chr1:230914162
|
C | T | 6 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0211others(3): Show | 6 | HG02615.hp1 HG02896.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2094-1404G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914162 | ||||||
| chr1:230914163
|
G | A | 1 | a0001c0002t0001g0119 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2094-1405C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914163 | ||||||
| chr1:230914223
|
T | C | 5 | a0001c0001t0002g0295a0001c0002t0002g0195a0001c0002t0002g0196others(2): Show | 5 | HG00735.hp1 HG02257.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2094-1465A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914223 | ||||||
| chr1:230914247
|
C | T | 1 | a0003c0006t0001g0028 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2094-1489G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914247 | ||||||
| chr1:230914389
|
ATTATT | A | 74 | a0001c0002t0001g0124a0001c0002t0001g0126a0001c0002t0001g0160others(71): Show | 86 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.2094-1636_2094-163 others(9): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914389 | ||||||
| chr1:230914392
|
A | C | 3 | a0001c0001t0001g0016a0001c0013t0003g0091a0001c0013t0003g0092 | 4 | HG00280.hp1 HG01981.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2094-1634T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914392 | ||||||
| chr1:230914398
|
T | C | 1 | a0002c0003t0001g0046 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2094-1640A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914398 | ||||||
| chr1:230914457
|
T | C | 1 | a0001c0001t0002g0245 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2094-1699A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914457 | ||||||
| chr1:230914483
|
G | A | 1 | a0001c0002t0001g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2093+1710C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914483 | ||||||
| chr1:230914498
|
G | A | 1 | a0002c0007t0001g0072 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2093+1695C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914498 | ||||||
| chr1:230914615
|
G | A | 1 | a0001c0002t0002g0223 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2093+1578C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914615 | ||||||
| chr1:230914615
|
G | C | 1 | a0001c0002t0002g0265 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2093+1578C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914615 | ||||||
| chr1:230914636
|
G | T | 3 | a0001c0002t0001g0104a0001c0002t0001g0108a0001c0002t0001g0110 | 3 | HG02602.hp2 HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2093+1557C>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914636 | ||||||
| chr1:230914689
|
G | A | 14 | a0001c0002t0001g0149a0001c0002t0002g0019a0001c0002t0002g0203others(11): Show | 15 | HG00733.hp2 HG01496.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.2093+1504C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914689 | ||||||
| chr1:230914776
|
T | C | 3 | a0001c0002t0001g0014a0001c0002t0001g0090a0001c0002t0002g0225 | 4 | HG02622.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2093+1417A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914776 | ||||||
| chr1:230914789
|
T | C | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2093+1404A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914789 | ||||||
| chr1:230914973
|
C | T | 146 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(143): Show | 158 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.2093+1220G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914973 | ||||||
| chr1:230914979
|
G | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(190): Show | 211 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.2093+1214C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230914979 | ||||||
| chr1:230915356
|
A | ATG | 216 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(213): Show | 240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.2093+835_2093+836d others(4): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915356 | ||||||
| chr1:230915416
|
A | T | 3 | a0001c0002t0001g0014a0001c0002t0001g0090a0001c0002t0002g0225 | 4 | HG02622.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2093+777T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915416 | ||||||
| chr1:230915499
|
A | T | 18 | a0001c0002t0001g0163a0001c0002t0002g0018a0001c0004t0002g0017others(15): Show | 20 | HG01106.hp2 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.2093+694T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915499 | ||||||
| chr1:230915577
|
T | A | 1 | a0001c0005t0002g0169 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2093+616A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915577 | ||||||
| chr1:230915684
|
A | C | 6 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0106others(3): Show | 6 | HG01256.hp1 HG01258.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.2093+509T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915684 | ||||||
| chr1:230915777
|
TTC | T | 49 | a0001c0001t0002g0197a0001c0002t0001g0004a0001c0002t0001g0114others(46): Show | 54 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.2093+414_2093+415d others(4): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915777 | ||||||
| chr1:230915793
|
C | A | 6 | a0001c0002t0002g0019a0001c0002t0002g0022a0001c0002t0002g0179others(3): Show | 8 | HG00741.hp2 HG01192.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.2093+400G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915793 | ||||||
| chr1:230915795
|
C | A | 98 | a0001c0001t0001g0003a0001c0001t0001g0113a0001c0001t0001g0137others(95): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2093+398G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915795 | ||||||
| chr1:230915797
|
C | A | 262 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(259): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.2093+396G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915797 | ||||||
| chr1:230915799
|
A | C | 1 | a0001c0002t0002g0176 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2093+394T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915799 | ||||||
| chr1:230915806
|
T | G | 1 | a0001c0002t0002g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2093+387A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915806 | ||||||
| chr1:230915858
|
G | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.2093+335C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915858 | ||||||
| chr1:230915894
|
G | A | 1 | a0001c0002t0002g0288 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2093+299C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915894 | ||||||
| chr1:230915903
|
G | GC | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.2093+289dupG | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915903 | ||||||
| chr1:230915905
|
C | T | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2093+288G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915905 | ||||||
| chr1:230915909
|
C | A | 68 | a0001c0009t0002g0242a0001c0009t0002g0273a0001c0009t0002g0274others(65): Show | 80 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.2093+284G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915909 | ||||||
| chr1:230915909
|
C | G | 3 | a0001c0002t0001g0095a0001c0002t0001g0096a0002c0007t0001g0044 | 3 | HG00733.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2093+284G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915909 | ||||||
| chr1:230915937
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2093+256C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915937 | ||||||
| chr1:230915961
|
T | C | 146 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(143): Show | 158 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.2093+232A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 18/22 | chr1 | 230915961 | ||||||
| chr1:230916368
|
T | C | 7 | a0001c0001t0001g0137a0001c0002t0001g0124a0001c0002t0001g0126others(4): Show | 7 | NA18956.hp1 NA18963.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.1984-66A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230916368 | ||||||
| chr1:230916437
|
G | T | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1984-135C>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230916437 | ||||||
| chr1:230916460
|
G | A | 3 | a0001c0001t0002g0254a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG00438.hp1 HG02015.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1984-158C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230916460 | ||||||
| chr1:230916550
|
G | A | 21 | a0001c0001t0001g0137a0001c0001t0002g0025a0001c0001t0002g0240others(18): Show | 22 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1984-248C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230916550 | ||||||
| chr1:230916560
|
G | A | 197 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1984-258C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230916560 | ||||||
| chr1:230916989
|
A | T | 1 | a0001c0001t0002g0217 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1984-687T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230916989 | ||||||
| chr1:230916989
|
AT | A | 15 | a0001c0001t0001g0155a0001c0005t0002g0169a0001c0005t0002g0170others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1984-688delA | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230916989 | ||||||
| chr1:230917186
|
C | CA | 13 | a0001c0001t0002g0215a0001c0001t0002g0235a0001c0001t0002g0237others(10): Show | 14 | HG00408.hp1 HG00673.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1984-885dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230917186 | ||||||
| chr1:230917195
|
C | A | 25 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(22): Show | 29 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1984-893G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230917195 | ||||||
| chr1:230917219
|
T | A | 5 | a0001c0002t0002g0174a0001c0002t0002g0175a0001c0002t0002g0176others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1984-917A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230917219 | ||||||
| chr1:230917260
|
A | G | 1 | a0001c0001t0002g0282 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1984-958T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230917260 | ||||||
| chr1:230917317
|
A | G | 146 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(143): Show | 158 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1984-1015T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230917317 | ||||||
| chr1:230917346
|
A | G | 1 | a0001c0001t0001g0141 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1984-1044T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230917346 | ||||||
| chr1:230917402
|
T | C | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1984-1100A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230917402 | ||||||
| chr1:230917608
|
T | C | 1 | a0001c0002t0002g0177 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1984-1306A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230917608 | ||||||
| chr1:230917663
|
C | A | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1984-1361G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230917663 | ||||||
| chr1:230917685
|
G | A | 1 | a0001c0001t0002g0219 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1984-1383C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230917685 | ||||||
| chr1:230918008
|
G | C | 4 | a0002c0003t0001g0037a0002c0003t0001g0080a0002c0003t0001g0081others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1984-1706C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230918008 | ||||||
| chr1:230918028
|
C | G | 1 | a0001c0001t0002g0215 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1984-1726G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230918028 | ||||||
| chr1:230918119
|
T | C | 2 | a0002c0003t0001g0061a0002c0003t0001g0075 | 2 | HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1984-1817A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230918119 | ||||||
| chr1:230918142
|
A | G | 3 | a0001c0001t0002g0254a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG00438.hp1 HG02015.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1984-1840T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230918142 | ||||||
| chr1:230918162
|
G | C | 1 | a0001c0002t0002g0178 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1984-1860C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230918162 | ||||||
| chr1:230918247
|
A | G | 146 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(143): Show | 158 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1984-1945T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230918247 | ||||||
| chr1:230918248
|
T | C | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1984-1946A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230918248 | ||||||
| chr1:230918259
|
G | A | 2 | a0002c0003t0001g0032a0002c0003t0001g0036 | 2 | HG01106.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1984-1957C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230918259 | ||||||
| chr1:230918273
|
G | T | 1 | a0001c0013t0003g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1984-1971C>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230918273 | ||||||
| chr1:230918425
|
C | A | 197 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1983+2085G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230918425 | ||||||
| chr1:230918663
|
A | G | 25 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(22): Show | 29 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1983+1847T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230918663 | ||||||
| chr1:230919002
|
G | C | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1983+1508C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230919002 | ||||||
| chr1:230919065
|
T | C | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1983+1445A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230919065 | ||||||
| chr1:230919148
|
C | T | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1983+1362G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230919148 | ||||||
| chr1:230919226
|
A | G | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1983+1284T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230919226 | ||||||
| chr1:230919411
|
C | T | 70 | a0001c0009t0002g0242a0001c0009t0002g0273a0001c0009t0002g0274others(67): Show | 82 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1983+1099G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230919411 | ||||||
| chr1:230919454
|
T | C | 1 | a0003c0006t0001g0026 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1983+1056A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230919454 | ||||||
| chr1:230919523
|
C | T | 2 | a0001c0002t0002g0179a0001c0002t0002g0269 | 2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1983+987G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230919523 | ||||||
| chr1:230919556
|
A | G | 25 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(22): Show | 29 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1983+954T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230919556 | ||||||
| chr1:230919631
|
C | T | 3 | a0001c0002t0001g0014a0001c0002t0001g0090a0001c0002t0002g0225 | 4 | HG02622.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1983+879G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230919631 | ||||||
| chr1:230919678
|
T | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(142): Show | 157 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1983+832A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230919678 | ||||||
| chr1:230919810
|
G | A | 2 | a0001c0002t0001g0095a0001c0002t0001g0096 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1983+700C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230919810 | ||||||
| chr1:230919974
|
T | G | 25 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(22): Show | 29 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1983+536A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230919974 | ||||||
| chr1:230920055
|
C | T | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1983+455G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230920055 | ||||||
| chr1:230920219
|
G | A | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1983+291C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230920219 | ||||||
| chr1:230920234
|
G | A | 1 | a0001c0002t0002g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1983+276C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230920234 | ||||||
| chr1:230920400
|
A | C | 3 | a0001c0001t0002g0254a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG00438.hp1 HG02015.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1983+110T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 17/22 | chr1 | 230920400 | ||||||
| chr1:230921029
|
T | C | 1 | a0001c0002t0002g0227 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1898+392A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 16/22 | chr1 | 230921029 | ||||||
| chr1:230921118
|
G | A | 197 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1898+303C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 16/22 | chr1 | 230921118 | ||||||
| chr1:230921275
|
G | A | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1898+146C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 16/22 | chr1 | 230921275 | ||||||
| chr1:230921541
|
A | C | 25 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(22): Show | 29 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1815-37T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230921541 | ||||||
| chr1:230921564
|
C | T | 197 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1815-60G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230921564 | ||||||
| chr1:230921774
|
G | C | 145 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(142): Show | 157 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1815-270C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230921774 | ||||||
| chr1:230922085
|
A | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1815-581T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230922085 | ||||||
| chr1:230922092
|
T | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1815-588A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230922092 | ||||||
| chr1:230922129
|
C | T | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1815-625G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230922129 | ||||||
| chr1:230922142
|
C | A | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1815-638G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230922142 | ||||||
| chr1:230922158
|
A | G | 1 | a0001c0002t0002g0018 | 2 | HG01106.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1815-654T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230922158 | ||||||
| chr1:230922255
|
T | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1815-751A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230922255 | ||||||
| chr1:230922329
|
C | T | 1 | a0001c0002t0001g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1815-825G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230922329 | ||||||
| chr1:230922387
|
G | A | 9 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(6): Show | 9 | HG01243.hp1 HG01243.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1815-883C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230922387 | ||||||
| chr1:230922453
|
C | T | 1 | a0001c0001t0005g0102 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1815-949G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230922453 | ||||||
| chr1:230922577
|
T | C | 25 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(22): Show | 29 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1815-1073A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230922577 | ||||||
| chr1:230922666
|
C | G | 1 | a0008c0021t0002g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1815-1162G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230922666 | ||||||
| chr1:230922677
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1814+1164A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230922677 | ||||||
| chr1:230922721
|
T | G | 197 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1814+1120A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230922721 | ||||||
| chr1:230922830
|
A | T | 5 | a0001c0005t0002g0276a0001c0005t0002g0278a0001c0005t0002g0279others(2): Show | 5 | HG02572.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1814+1011T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230922830 | ||||||
| chr1:230923194
|
G | T | 1 | a0001c0002t0002g0198 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1814+647C>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230923194 | ||||||
| chr1:230923214
|
C | T | 197 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1814+627G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230923214 | ||||||
| chr1:230923413
|
G | A | 3 | a0001c0002t0001g0014a0001c0002t0001g0090a0001c0002t0002g0225 | 4 | HG02622.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1814+428C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230923413 | ||||||
| chr1:230923429
|
C | G | 2 | a0001c0002t0001g0013a0001c0002t0001g0115 | 3 | HG02922.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1814+412G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230923429 | ||||||
| chr1:230923496
|
A | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1814+345T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230923496 | ||||||
| chr1:230923689
|
C | T | 1 | a0001c0002t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1814+152G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 15/22 | chr1 | 230923689 | ||||||
| chr1:230924038
|
C | T | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1722-105G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 14/22 | chr1 | 230924038 | ||||||
| chr1:230924051
|
G | A | 4 | a0001c0005t0002g0180a0001c0005t0002g0193a0001c0005t0002g0275others(1): Show | 4 | HG02055.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1722-118C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 14/22 | chr1 | 230924051 | ||||||
| chr1:230924209
|
G | A | 197 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1722-276C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 14/22 | chr1 | 230924209 | ||||||
| chr1:230924334
|
CG | C | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1722-402delC | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 14/22 | chr1 | 230924334 | ||||||
| chr1:230924388
|
A | G | 2 | a0001c0013t0003g0091a0001c0013t0003g0092 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1721+453T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 14/22 | chr1 | 230924388 | ||||||
| chr1:230924455
|
C | T | 3 | a0002c0003t0001g0002a0002c0003t0001g0058a0009c0016t0001g0038 | 5 | HG00621.hp1 HG02132.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.1721+386G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 14/22 | chr1 | 230924455 | ||||||
| chr1:230924497
|
T | G | 12 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(9): Show | 15 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1721+344A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 14/22 | chr1 | 230924497 | ||||||
| chr1:230924518
|
G | C | 1 | a0001c0002t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1721+323C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 14/22 | chr1 | 230924518 | ||||||
| chr1:230924565
|
T | G | 10 | a0001c0002t0001g0149a0001c0002t0002g0019a0001c0002t0002g0203others(7): Show | 11 | HG01496.hp2 HG01516.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1721+276A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 14/22 | chr1 | 230924565 | ||||||
| chr1:230924575
|
G | A | 12 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(9): Show | 15 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1721+266C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 14/22 | chr1 | 230924575 | ||||||
| chr1:230924576
|
C | A | 12 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(9): Show | 15 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1721+265G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 14/22 | chr1 | 230924576 | ||||||
| chr1:230924624
|
G | C | 1 | a0002c0003t0001g0057 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1721+217C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 14/22 | chr1 | 230924624 | ||||||
| chr1:230924787
|
C | T | 1 | a0001c0002t0002g0265 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1721+54G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 14/22 | chr1 | 230924787 | ||||||
| chr1:230924990
|
T | C | 146 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(143): Show | 158 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1589-17A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 13/22 | chr1 | 230924990 | ||||||
| chr1:230925168
|
C | T | 25 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(22): Show | 29 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1589-195G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 13/22 | chr1 | 230925168 | ||||||
| chr1:230925271
|
T | C | 1 | a0001c0002t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1588+246A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 13/22 | chr1 | 230925271 | ||||||
| chr1:230925311
|
A | G | 146 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(143): Show | 158 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1588+206T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 13/22 | chr1 | 230925311 | ||||||
| chr1:230925818
|
A | C | 146 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(143): Show | 158 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1458-171T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230925818 | ||||||
| chr1:230926260
|
G | A | 199 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(196): Show | 218 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.1458-613C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230926260 | ||||||
| chr1:230926279
|
T | C | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1458-632A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230926279 | ||||||
| chr1:230926333
|
G | C | 146 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(143): Show | 158 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1458-686C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230926333 | ||||||
| chr1:230926499
|
T | C | 5 | a0002c0003t0001g0037a0002c0003t0001g0080a0002c0003t0001g0081others(2): Show | 5 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1458-852A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230926499 | ||||||
| chr1:230926529
|
A | G | 18 | a0001c0002t0001g0163a0001c0002t0002g0018a0001c0004t0002g0017others(15): Show | 20 | HG01106.hp2 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1458-882T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230926529 | ||||||
| chr1:230926535
|
A | C | 2 | a0002c0003t0001g0040a0002c0003t0001g0060 | 2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1458-888T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230926535 | ||||||
| chr1:230926682
|
G | A | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1458-1035C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230926682 | ||||||
| chr1:230926936
|
C | A | 25 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(22): Show | 29 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1458-1289G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230926936 | ||||||
| chr1:230927195
|
T | C | 5 | a0001c0005t0002g0276a0001c0005t0002g0278a0001c0005t0002g0279others(2): Show | 5 | HG02572.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1458-1548A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230927195 | ||||||
| chr1:230927593
|
T | A | 1 | a0002c0003t0001g0068 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1457+1344A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230927593 | ||||||
| chr1:230927632
|
C | G | 1 | a0001c0002t0002g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1457+1305G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230927632 | ||||||
| chr1:230927787
|
T | C | 1 | a0001c0001t0002g0199 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1457+1150A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230927787 | ||||||
| chr1:230927799
|
C | A | 2 | a0001c0017t0007g0166a0001c0018t0002g0165 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1457+1138G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230927799 | ||||||
| chr1:230928321
|
T | C | 4 | a0001c0001t0001g0097a0001c0001t0002g0247a0001c0001t0002g0249others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1457+616A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230928321 | ||||||
| chr1:230928478
|
T | C | 1 | a0001c0002t0002g0251 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1457+459A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230928478 | ||||||
| chr1:230928657
|
A | G | 2 | a0001c0002t0002g0179a0001c0002t0002g0269 | 2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1457+280T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230928657 | ||||||
| chr1:230928800
|
T | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(276): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1457+137A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230928800 | ||||||
| chr1:230928832
|
T | TCTC | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1457+104_1457+105i others(5): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230928832 | ||||||
| chr1:230928865
|
G | A | 145 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(142): Show | 157 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1457+72C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 12/22 | chr1 | 230928865 | ||||||
| chr1:230929322
|
A | AT | 68 | a0001c0009t0002g0242a0001c0009t0002g0273a0001c0013t0003g0091others(65): Show | 80 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1301-230dupA | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230929322 | ||||||
| chr1:230929322
|
A | ATTTT | 25 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(22): Show | 29 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1301-233_1301-230d others(6): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230929322 | ||||||
| chr1:230929322
|
A | ATTTTT | 27 | a0001c0001t0002g0197a0001c0002t0001g0163a0001c0002t0002g0018others(24): Show | 29 | HG01106.hp2 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1301-234_1301-230d others(7): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230929322 | ||||||
| chr1:230929322
|
A | ATTTTTT | 138 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(135): Show | 150 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1301-235_1301-230d others(8): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230929322 | ||||||
| chr1:230929335
|
G | C | 12 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(9): Show | 15 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1301-242C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230929335 | ||||||
| chr1:230929370
|
G | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1301-277C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230929370 | ||||||
| chr1:230929752
|
A | G | 1 | a0001c0002t0001g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1301-659T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230929752 | ||||||
| chr1:230929776
|
G | A | 1 | a0001c0001t0002g0289 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1301-683C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230929776 | ||||||
| chr1:230929856
|
C | T | 16 | a0001c0004t0002g0017a0001c0004t0002g0167a0001c0004t0002g0181others(13): Show | 17 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1301-763G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230929856 | ||||||
| chr1:230929879
|
G | GA | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1301-787dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230929879 | ||||||
| chr1:230930004
|
T | C | 2 | a0001c0001t0002g0282a0004c0012t0002g0296 | 2 | HG01167.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1301-911A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230930004 | ||||||
| chr1:230930204
|
G | C | 2 | a0002c0003t0001g0061a0002c0003t0001g0075 | 2 | HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1300+1094C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230930204 | ||||||
| chr1:230930391
|
C | A | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300+907G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230930391 | ||||||
| chr1:230930421
|
A | G | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1300+877T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230930421 | ||||||
| chr1:230930563
|
C | T | 69 | a0001c0009t0002g0242a0001c0009t0002g0273a0001c0013t0003g0091others(66): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1300+735G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230930563 | ||||||
| chr1:230930658
|
G | A | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300+640C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230930658 | ||||||
| chr1:230930744
|
C | A | 1 | a0002c0003t0001g0031 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1300+554G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230930744 | ||||||
| chr1:230930850
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1300+448C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230930850 | ||||||
| chr1:230930951
|
A | G | 16 | a0001c0004t0002g0017a0001c0004t0002g0167a0001c0004t0002g0181others(13): Show | 17 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1300+347T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230930951 | ||||||
| chr1:230930993
|
G | T | 2 | a0001c0002t0001g0163a0001c0002t0002g0018 | 3 | HG01106.hp2 HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1300+305C>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230930993 | ||||||
| chr1:230931036
|
A | G | 172 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(169): Show | 186 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.1300+262T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230931036 | ||||||
| chr1:230931067
|
T | C | 1 | a0001c0002t0001g0119 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1300+231A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230931067 | ||||||
| chr1:230931148
|
G | A | 1 | a0002c0003t0001g0051 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1300+150C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230931148 | ||||||
| chr1:230931205
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1300+93G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 11/22 | chr1 | 230931205 | ||||||
| chr1:230931490
|
C | T | 145 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(142): Show | 157 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1126-18G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 10/22 | chr1 | 230931490 | ||||||
| chr1:230931572
|
G | T | 145 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(142): Show | 157 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1126-100C>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 10/22 | chr1 | 230931572 | ||||||
| chr1:230931607
|
T | C | 2 | a0001c0001t0002g0206a0001c0001t0002g0207 | 2 | HG02523.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1125+129A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 10/22 | chr1 | 230931607 | ||||||
| chr1:230931919
|
C | T | 1 | a0001c0002t0002g0255 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.984-42G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230931919 | ||||||
| chr1:230932003
|
CT | C | 2 | a0002c0003t0001g0006a0002c0003t0001g0046 | 3 | NA18978.hp2 NA18989.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.984-127delA | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230932003 | ||||||
| chr1:230932126
|
G | A | 1 | a0003c0006t0001g0027 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.984-249C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230932126 | ||||||
| chr1:230932295
|
C | T | 2 | a0001c0013t0003g0091a0001c0013t0003g0092 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.984-418G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230932295 | ||||||
| chr1:230932296
|
A | AT | 71 | a0001c0001t0001g0113a0001c0001t0001g0151a0001c0001t0002g0197others(68): Show | 83 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.984-420dupA | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230932296 | ||||||
| chr1:230932296
|
A | ATT | 6 | a0002c0003t0001g0009a0002c0003t0001g0040a0002c0003t0001g0060others(3): Show | 7 | HG02970.hp1 HG03098.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.984-421_984-420dup others(2): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230932296 | ||||||
| chr1:230932296
|
AT | A | 14 | a0001c0001t0001g0097a0001c0001t0001g0164a0001c0001t0002g0247others(11): Show | 17 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.984-420delA | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230932296 | ||||||
| chr1:230932296
|
ATT | A | 18 | a0001c0002t0001g0149a0001c0002t0002g0019a0001c0002t0002g0203others(15): Show | 19 | HG01496.hp2 HG01516.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.984-421_984-420del others(2): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230932296 | ||||||
| chr1:230932451
|
C | T | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.984-574G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230932451 | ||||||
| chr1:230932469
|
G | A | 7 | a0001c0002t0001g0004a0001c0002t0001g0133a0001c0002t0001g0152others(4): Show | 10 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.984-592C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230932469 | ||||||
| chr1:230932545
|
G | A | 1 | a0001c0002t0001g0118 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.984-668C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230932545 | ||||||
| chr1:230932714
|
C | T | 143 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(140): Show | 154 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.984-837G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230932714 | ||||||
| chr1:230933011
|
C | T | 1 | a0001c0004t0008g0184 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.983+768G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230933011 | ||||||
| chr1:230933012
|
G | A | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.983+767C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230933012 | ||||||
| chr1:230933014
|
C | G | 1 | a0001c0002t0002g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.983+765G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230933014 | ||||||
| chr1:230933083
|
C | T | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.983+696G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230933083 | ||||||
| chr1:230933110
|
T | C | 2 | a0001c0001t0002g0217a0001c0001t0002g0218 | 2 | NA18993.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.983+669A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230933110 | ||||||
| chr1:230933145
|
G | A | 18 | a0001c0002t0001g0163a0001c0002t0002g0018a0001c0004t0002g0017others(15): Show | 20 | HG01106.hp2 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.983+634C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230933145 | ||||||
| chr1:230933430
|
A | G | 26 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(23): Show | 30 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.983+349T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230933430 | ||||||
| chr1:230933494
|
G | A | 1 | a0002c0010t0001g0043 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.983+285C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230933494 | ||||||
| chr1:230933594
|
C | T | 60 | a0001c0009t0002g0242a0001c0009t0002g0273a0002c0003t0001g0001others(57): Show | 71 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.983+185G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230933594 | ||||||
| chr1:230933602
|
C | T | 26 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(23): Show | 30 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.983+177G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 9/22 | chr1 | 230933602 | ||||||
| chr1:230933906
|
A | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.901-45T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230933906 | ||||||
| chr1:230934068
|
T | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.901-207A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230934068 | ||||||
| chr1:230934287
|
A | G | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.901-426T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230934287 | ||||||
| chr1:230934390
|
A | C | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.901-529T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230934390 | ||||||
| chr1:230934495
|
C | T | 60 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0105others(57): Show | 66 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.901-634G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230934495 | ||||||
| chr1:230934604
|
A | G | 2 | a0002c0003t0001g0037a0002c0003t0001g0080 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.901-743T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230934604 | ||||||
| chr1:230934768
|
G | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(28): Show | 35 | HG00280.hp1 HG01257.hp2 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.901-907C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230934768 | ||||||
| chr1:230934927
|
A | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.901-1066T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230934927 | ||||||
| chr1:230934949
|
G | A | 1 | a0001c0002t0001g0124 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.901-1088C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230934949 | ||||||
| chr1:230935446
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.901-1585C>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230935446 | ||||||
| chr1:230935667
|
T | C | 3 | a0002c0003t0001g0033a0002c0003t0001g0034a0002c0003t0001g0035 | 3 | HG00140.hp1 HG02683.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.901-1806A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230935667 | ||||||
| chr1:230935957
|
A | G | 1 | a0002c0003t0001g0062 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.901-2096T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230935957 | ||||||
| chr1:230936130
|
C | T | 12 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(9): Show | 15 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.901-2269G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230936130 | ||||||
| chr1:230936342
|
T | C | 1 | a0001c0002t0001g0152 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.901-2481A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230936342 | ||||||
| chr1:230936343
|
C | A | 1 | a0001c0002t0001g0152 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.901-2482G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230936343 | ||||||
| chr1:230936515
|
G | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(190): Show | 211 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.901-2654C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230936515 | ||||||
| chr1:230936590
|
G | A | 14 | a0001c0002t0001g0149a0001c0002t0002g0019a0001c0002t0002g0203others(11): Show | 15 | HG01496.hp2 HG01516.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.901-2729C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230936590 | ||||||
| chr1:230936672
|
C | T | 2 | a0001c0005t0002g0171a0001c0005t0002g0173 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.900+2714G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230936672 | ||||||
| chr1:230936684
|
T | TATTACTA others(20): Show |
67 | a0001c0009t0002g0242a0001c0009t0002g0273a0002c0003t0001g0001others(64): Show | 79 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.900+2701_900+2702i others(29): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230936684 | ||||||
| chr1:230936688
|
G | C | 67 | a0001c0009t0002g0242a0001c0009t0002g0273a0002c0003t0001g0001others(64): Show | 79 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.900+2698C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230936688 | ||||||
| chr1:230936804
|
G | A | 1 | a0001c0004t0008g0184 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.900+2582C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230936804 | ||||||
| chr1:230936865
|
C | T | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+2521G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230936865 | ||||||
| chr1:230936921
|
A | G | 1 | a0001c0001t0002g0240 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.900+2465T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230936921 | ||||||
| chr1:230936925
|
A | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(191): Show | 212 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.900+2461T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230936925 | ||||||
| chr1:230936962
|
TCTAACCT others(7): Show |
T | 18 | a0001c0002t0001g0163a0001c0002t0002g0018a0001c0004t0002g0017others(15): Show | 20 | HG01106.hp2 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.900+2410_900+2423d others(16): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230936962 | ||||||
| chr1:230937022
|
C | T | 2 | a0001c0013t0003g0091a0001c0013t0003g0092 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.900+2364G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230937022 | ||||||
| chr1:230937206
|
T | G | 5 | a0001c0002t0002g0174a0001c0002t0002g0175a0001c0002t0002g0176others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+2180A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230937206 | ||||||
| chr1:230937570
|
G | A | 1 | a0002c0003t0001g0059 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.900+1816C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230937570 | ||||||
| chr1:230937617
|
A | G | 1 | a0001c0001t0002g0219 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.900+1769T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230937617 | ||||||
| chr1:230937670
|
G | T | 14 | a0001c0002t0001g0149a0001c0002t0002g0019a0001c0002t0002g0203others(11): Show | 15 | HG01496.hp2 HG01516.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.900+1716C>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230937670 | ||||||
| chr1:230937702
|
T | C | 1 | a0001c0001t0001g0113 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.900+1684A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230937702 | ||||||
| chr1:230937779
|
C | T | 1 | a0003c0006t0001g0027 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.900+1607G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230937779 | ||||||
| chr1:230937956
|
T | C | 26 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(23): Show | 30 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.900+1430A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230937956 | ||||||
| chr1:230938035
|
C | G | 26 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(23): Show | 30 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.900+1351G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230938035 | ||||||
| chr1:230938143
|
G | A | 1 | a0001c0002t0002g0251 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.900+1243C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230938143 | ||||||
| chr1:230938181
|
C | G | 1 | a0001c0001t0001g0130 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.900+1205G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230938181 | ||||||
| chr1:230938207
|
C | T | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.900+1179G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230938207 | ||||||
| chr1:230938335
|
G | A | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.900+1051C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230938335 | ||||||
| chr1:230938565
|
T | C | 284 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(281): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.900+821A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230938565 | ||||||
| chr1:230938699
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.900+687G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230938699 | ||||||
| chr1:230938992
|
C | G | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+394G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230938992 | ||||||
| chr1:230939037
|
A | C | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+349T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230939037 | ||||||
| chr1:230939068
|
ACT | A | 6 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(3): Show | 6 | HG00408.hp1 HG01243.hp2 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.900+316_900+317del others(2): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230939068 | ||||||
| chr1:230939334
|
A | G | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.900+52T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 8/22 | chr1 | 230939334 | ||||||
| chr1:230939767
|
T | C | 1 | a0002c0003t0001g0065 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.790-271A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 7/22 | chr1 | 230939767 | ||||||
| chr1:230939788
|
G | A | 2 | a0001c0002t0001g0163a0001c0002t0002g0018 | 3 | HG01106.hp2 HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.790-292C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 7/22 | chr1 | 230939788 | ||||||
| chr1:230939828
|
C | T | 277 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(274): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.790-332G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 7/22 | chr1 | 230939828 | ||||||
| chr1:230939865
|
G | A | 2 | a0001c0001t0001g0123a0001c0002t0001g0124 | 2 | NA18963.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.790-369C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 7/22 | chr1 | 230939865 | ||||||
| chr1:230940042
|
C | T | 150 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(147): Show | 162 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.789+398G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 7/22 | chr1 | 230940042 | ||||||
| chr1:230940325
|
C | T | 1 | a0001c0001t0002g0237 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.789+115G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 7/22 | chr1 | 230940325 | ||||||
| chr1:230940431
|
A | G | 18 | a0001c0002t0001g0163a0001c0002t0002g0018a0001c0004t0002g0017others(15): Show | 20 | HG01106.hp2 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.789+9T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 7/22 | chr1 | 230940431 | ||||||
| chr1:230940825
|
T | C | 1 | a0001c0001t0002g0286 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.673-269A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230940825 | ||||||
| chr1:230940834
|
C | T | 194 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(191): Show | 212 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.673-278G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230940834 | ||||||
| chr1:230941078
|
C | T | 4 | a0002c0003t0001g0040a0002c0003t0001g0060a0002c0003t0001g0061others(1): Show | 4 | HG02970.hp1 HG03098.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-522G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230941078 | ||||||
| chr1:230941209
|
G | T | 1 | a0001c0002t0001g0115 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.673-653C>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230941209 | ||||||
| chr1:230941275
|
G | C | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.673-719C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230941275 | ||||||
| chr1:230941380
|
C | T | 1 | a0006c0020t0002g0248 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.673-824G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230941380 | ||||||
| chr1:230941582
|
C | T | 1 | a0001c0004t0002g0185 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.673-1026G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230941582 | ||||||
| chr1:230941934
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.673-1378C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230941934 | ||||||
| chr1:230942006
|
G | A | 26 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(23): Show | 30 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.673-1450C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230942006 | ||||||
| chr1:230942164
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.673-1608C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230942164 | ||||||
| chr1:230942665
|
C | A | 1 | a0001c0002t0002g0228 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.672+1141G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230942665 | ||||||
| chr1:230942746
|
G | T | 26 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(23): Show | 30 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.672+1060C>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230942746 | ||||||
| chr1:230942813
|
T | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0158 | 2 | HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.672+993A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230942813 | ||||||
| chr1:230942827
|
G | A | 1 | a0001c0005t0002g0193 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.672+979C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230942827 | ||||||
| chr1:230942839
|
A | G | 26 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(23): Show | 30 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.672+967T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230942839 | ||||||
| chr1:230942931
|
C | A | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.672+875G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230942931 | ||||||
| chr1:230943248
|
T | A | 6 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0155others(3): Show | 6 | HG01496.hp1 HG01952.hp1 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.672+558A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230943248 | ||||||
| chr1:230943635
|
A | G | 267 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(264): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.672+171T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230943635 | ||||||
| chr1:230943640
|
T | C | 26 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(23): Show | 30 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.672+166A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230943640 | ||||||
| chr1:230943683
|
C | T | 2 | a0001c0002t0002g0204a0001c0002t0002g0239 | 2 | HG01255.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.672+123G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230943683 | ||||||
| chr1:230943704
|
T | G | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.672+102A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230943704 | ||||||
| chr1:230943781
|
G | A | 1 | a0001c0002t0002g0174 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.672+25C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 6/22 | chr1 | 230943781 | ||||||
| chr1:230944136
|
C | G | 1 | a0001c0002t0002g0225 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.580-238G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 5/22 | chr1 | 230944136 | ||||||
| chr1:230944333
|
A | G | 277 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(274): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.580-435T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 5/22 | chr1 | 230944333 | ||||||
| chr1:230944494
|
C | T | 277 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(274): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.580-596G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 5/22 | chr1 | 230944494 | ||||||
| chr1:230944517
|
C | A | 2 | a0001c0002t0001g0163a0001c0002t0002g0018 | 3 | HG01106.hp2 HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.580-619G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 5/22 | chr1 | 230944517 | ||||||
| chr1:230944552
|
C | T | 12 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(9): Show | 15 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.580-654G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 5/22 | chr1 | 230944552 | ||||||
| chr1:230944575
|
T | C | 26 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(23): Show | 30 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.580-677A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 5/22 | chr1 | 230944575 | ||||||
| chr1:230944623
|
A | G | 26 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(23): Show | 30 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.580-725T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 5/22 | chr1 | 230944623 | ||||||
| chr1:230944648
|
AT | A | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+740delA | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 5/22 | chr1 | 230944648 | ||||||
| chr1:230944773
|
T | C | 2 | a0001c0001t0002g0294a0001c0001t0002g0295 | 2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.579+616A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 5/22 | chr1 | 230944773 | ||||||
| chr1:230945184
|
A | G | 1 | a0001c0002t0002g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.579+205T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 5/22 | chr1 | 230945184 | ||||||
| chr1:230945523
|
T | TA | 32 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(29): Show | 36 | HG00280.hp1 HG01358.hp2 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.514-70dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230945523 | ||||||
| chr1:230945558
|
T | G | 167 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(164): Show | 181 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.514-104A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230945558 | ||||||
| chr1:230945660
|
GA | G | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-207delT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230945660 | ||||||
| chr1:230945667
|
A | C | 12 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(9): Show | 15 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.514-213T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230945667 | ||||||
| chr1:230945860
|
T | C | 194 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(191): Show | 212 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.514-406A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230945860 | ||||||
| chr1:230945922
|
G | A | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-468C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230945922 | ||||||
| chr1:230946097
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0002g0237 | 2 | NA18747.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.514-643C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230946097 | ||||||
| chr1:230946234
|
G | T | 26 | a0001c0002t0001g0004a0001c0002t0001g0114a0001c0002t0001g0133others(23): Show | 30 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.514-780C>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230946234 | ||||||
| chr1:230946344
|
C | T | 277 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(274): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.514-890G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230946344 | ||||||
| chr1:230946493
|
A | G | 1 | a0001c0001t0002g0291 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.514-1039T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230946493 | ||||||
| chr1:230946513
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.514-1059A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230946513 | ||||||
| chr1:230946629
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.514-1175G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230946629 | ||||||
| chr1:230946702
|
T | A | 1 | a0001c0002t0002g0201 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.514-1248A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230946702 | ||||||
| chr1:230946708
|
T | C | 136 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(133): Show | 149 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.514-1254A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230946708 | ||||||
| chr1:230946874
|
C | G | 1 | a0001c0011t0002g0205 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.514-1420G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230946874 | ||||||
| chr1:230946972
|
T | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(193): Show | 214 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.514-1518A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230946972 | ||||||
| chr1:230946973
|
A | G | 1 | a0001c0011t0002g0205 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.514-1519T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230946973 | ||||||
| chr1:230947067
|
T | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(193): Show | 214 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.514-1613A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947067 | ||||||
| chr1:230947121
|
C | T | 4 | a0002c0003t0001g0029a0002c0003t0001g0031a0002c0003t0001g0084others(1): Show | 4 | HG00735.hp2 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-1667G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947121 | ||||||
| chr1:230947169
|
A | T | 1 | a0001c0002t0001g0108 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.514-1715T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947169 | ||||||
| chr1:230947262
|
G | A | 3 | a0002c0003t0001g0007a0002c0003t0001g0039a0002c0003t0001g0073 | 4 | NA18941.hp1 NA18986.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-1808C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947262 | ||||||
| chr1:230947293
|
G | A | 26 | a0001c0001t0002g0240a0001c0002t0001g0004a0001c0002t0001g0133others(23): Show | 30 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.514-1839C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947293 | ||||||
| chr1:230947299
|
A | G | 3 | a0001c0002t0002g0222a0001c0002t0002g0264a0001c0002t0002g0265 | 3 | HG02258.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.514-1845T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947299 | ||||||
| chr1:230947535
|
C | T | 15 | a0001c0001t0002g0168a0001c0005t0002g0169a0001c0005t0002g0170others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.514-2081G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947535 | ||||||
| chr1:230947550
|
A | T | 134 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(131): Show | 146 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.514-2096T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947550 | ||||||
| chr1:230947561
|
T | TA | 6 | a0001c0001t0001g0150a0001c0001t0002g0197a0001c0002t0002g0195others(3): Show | 6 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-2108dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947561 | ||||||
| chr1:230947576
|
A | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.514-2122T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947576 | ||||||
| chr1:230947643
|
G | C | 197 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(194): Show | 215 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.514-2189C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947643 | ||||||
| chr1:230947667
|
G | C | 16 | a0001c0004t0002g0017a0001c0004t0002g0167a0001c0004t0002g0181others(13): Show | 17 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.514-2213C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947667 | ||||||
| chr1:230947756
|
C | A | 1 | a0001c0011t0002g0205 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.514-2302G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947756 | ||||||
| chr1:230947769
|
G | A | 14 | a0001c0002t0001g0149a0001c0002t0002g0019a0001c0002t0002g0203others(11): Show | 15 | HG01496.hp2 HG01516.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.514-2315C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947769 | ||||||
| chr1:230947803
|
A | C | 1 | a0001c0011t0002g0205 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.514-2349T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947803 | ||||||
| chr1:230947809
|
T | A | 3 | a0001c0002t0002g0203a0001c0002t0002g0227a0001c0002t0002g0229 | 3 | NA18949.hp2 NA18961.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.514-2355A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947809 | ||||||
| chr1:230947892
|
C | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(126): Show | 141 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.514-2438G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230947892 | ||||||
| chr1:230948211
|
C | T | 2 | a0001c0002t0002g0174a0001c0002t0002g0175 | 2 | HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.514-2757G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230948211 | ||||||
| chr1:230948317
|
G | A | 18 | a0001c0002t0001g0163a0001c0002t0002g0018a0001c0004t0002g0017others(15): Show | 20 | HG01106.hp2 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.514-2863C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230948317 | ||||||
| chr1:230948329
|
T | TA | 193 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(190): Show | 211 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.514-2876dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230948329 | ||||||
| chr1:230948400
|
C | CA | 17 | a0001c0004t0002g0017a0001c0004t0002g0167a0001c0004t0002g0181others(14): Show | 18 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.514-2947dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230948400 | ||||||
| chr1:230948400
|
C | CAAA | 17 | a0001c0001t0002g0168a0001c0002t0001g0163a0001c0002t0002g0018others(14): Show | 18 | HG01106.hp2 HG01109.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.514-2949_514-2947d others(5): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230948400 | ||||||
| chr1:230948400
|
C | CAAAAA | 96 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(93): Show | 106 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.514-2951_514-2947d others(7): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230948400 | ||||||
| chr1:230948400
|
C | CAAAAAA | 29 | a0001c0001t0001g0112a0001c0001t0001g0135a0001c0001t0001g0137others(26): Show | 30 | HG00438.hp1 HG00733.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.514-2952_514-2947d others(8): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230948400 | ||||||
| chr1:230948434
|
T | G | 129 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(126): Show | 141 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.514-2980A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230948434 | ||||||
| chr1:230948783
|
C | A | 1 | a0001c0002t0002g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.514-3329G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230948783 | ||||||
| chr1:230948995
|
T | A | 26 | a0001c0001t0002g0240a0001c0002t0001g0004a0001c0002t0001g0133others(23): Show | 30 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.514-3541A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230948995 | ||||||
| chr1:230949117
|
T | C | 299 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(296): Show | 332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.514-3663A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949117 | ||||||
| chr1:230949120
|
T | C | 1 | a0002c0003t0001g0054 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.514-3666A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949120 | ||||||
| chr1:230949148
|
C | G | 1 | a0001c0002t0002g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.514-3694G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949148 | ||||||
| chr1:230949223
|
A | AC | 67 | a0001c0009t0002g0273a0001c0009t0002g0274a0002c0003t0001g0001others(64): Show | 79 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.514-3770_514-3769i others(3): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949223 | ||||||
| chr1:230949224
|
A | AG | 235 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(232): Show | 256 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.514-3771dupC | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949224 | ||||||
| chr1:230949224
|
A | G | 67 | a0001c0009t0002g0273a0001c0009t0002g0274a0002c0003t0001g0001others(64): Show | 79 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.514-3770T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949224 | ||||||
| chr1:230949258
|
T | C | 1 | a0002c0003t0001g0058 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.514-3804A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949258 | ||||||
| chr1:230949266
|
AG | A | 302 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(299): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.514-3813delC | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949266 | ||||||
| chr1:230949343
|
C | T | 11 | a0001c0001t0002g0240a0001c0002t0001g0004a0001c0002t0001g0133others(8): Show | 13 | HG00140.hp2 HG00639.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.514-3889G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949343 | ||||||
| chr1:230949344
|
G | A | 167 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(164): Show | 181 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.514-3890C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949344 | ||||||
| chr1:230949399
|
T | A | 1 | a0001c0002t0002g0018 | 2 | HG01106.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.514-3945A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949399 | ||||||
| chr1:230949404
|
T | TAAAAAAA others(298): Show |
1 | a0001c0001t0002g0289 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.514-3951_514-3950i others(307): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949404
|
T | TAAAAAAA others(300): Show |
1 | a0001c0004t0002g0185 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.514-3951_514-3950i others(309): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949404
|
T | TAAAAAAA others(298): Show |
1 | a0004c0012t0002g0296 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.514-3951_514-3950i others(307): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949404
|
T | TAAAAAAA others(306): Show |
2 | a0001c0002t0001g0163a0001c0002t0002g0018 | 3 | HG01106.hp2 HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.514-3951_514-3950i others(315): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949404
|
T | TAAAAAAA others(297): Show |
116 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(113): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.514-3951_514-3950i others(306): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949404
|
T | TAAAAAAA others(298): Show |
10 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0125others(7): Show | 10 | HG00597.hp2 HG02145.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.514-3951_514-3950i others(307): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949404
|
T | TAAAAAAA others(300): Show |
13 | a0001c0004t0002g0017a0001c0004t0002g0167a0001c0004t0002g0181others(10): Show | 14 | HG01261.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.514-3951_514-3950i others(309): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949404
|
T | TAAAAAAA others(301): Show |
2 | a0001c0004t0002g0188a0008c0021t0002g0189 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.514-3951_514-3950i others(310): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949404
|
T | TAAAAAAA others(312): Show |
8 | a0001c0001t0002g0168a0001c0005t0002g0169a0001c0005t0002g0170others(5): Show | 8 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-3951_514-3950i others(321): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949404
|
T | TAAAAAAA others(313): Show |
7 | a0001c0002t0002g0201a0001c0005t0002g0171a0001c0005t0002g0172others(4): Show | 7 | HG02572.hp2 HG02965.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.514-3951_514-3950i others(322): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949404
|
T | TAAAAAAA others(314): Show |
1 | a0001c0002t0002g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.514-3951_514-3950i others(323): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949404
|
T | TAAAAAAA others(315): Show |
1 | a0001c0005t0002g0173 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.514-3951_514-3950i others(324): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949404
|
T | TAAAAAAA others(316): Show |
3 | a0001c0002t0002g0202a0001c0002t0002g0271a0001c0002t0002g0272 | 3 | HG01243.hp1 HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.514-3951_514-3950i others(325): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949404
|
T | TAAAAAAA others(297): Show |
1 | a0001c0001t0001g0143 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.514-3951_514-3950i others(306): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949404
|
T | TAAAAAAA others(308): Show |
1 | a0001c0011t0002g0205 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.514-3951_514-3950i others(317): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949404
|
TA | T | 25 | a0001c0001t0002g0240a0001c0002t0001g0004a0001c0002t0001g0133others(22): Show | 29 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.514-3951delT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949404 | ||||||
| chr1:230949478
|
C | A | 5 | a0001c0002t0002g0174a0001c0002t0002g0175a0001c0002t0002g0176others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-4024G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949478 | ||||||
| chr1:230949491
|
G | C | 17 | a0001c0002t0001g0163a0001c0004t0002g0017a0001c0004t0002g0167others(14): Show | 18 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.514-4037C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949491 | ||||||
| chr1:230949562
|
T | C | 1 | a0001c0002t0001g0126 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.514-4108A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949562 | ||||||
| chr1:230949697
|
C | G | 2 | a0001c0017t0007g0166a0001c0018t0002g0165 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.514-4243G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949697 | ||||||
| chr1:230949702
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.514-4248C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949702 | ||||||
| chr1:230949840
|
G | A | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-4386C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949840 | ||||||
| chr1:230949845
|
T | A | 12 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(9): Show | 12 | HG00609.hp2 HG03239.hp1 HG04115.hp1 others(9): Show |
intron_variant | MODIFIER | c.514-4391A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949845 | ||||||
| chr1:230949851
|
A | G | 12 | a0001c0001t0002g0168a0001c0002t0002g0255a0001c0005t0002g0169others(9): Show | 12 | HG01109.hp2 HG02055.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.514-4397T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949851 | ||||||
| chr1:230949865
|
A | G | 69 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0002t0002g0178others(66): Show | 80 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.514-4411T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949865 | ||||||
| chr1:230949871
|
A | C | 1 | a0001c0005t0002g0276 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.514-4417T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949871 | ||||||
| chr1:230949929
|
C | G | 1 | a0001c0001t0002g0286 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.513+4404G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230949929 | ||||||
| chr1:230950164
|
G | T | 11 | a0001c0001t0002g0168a0001c0005t0002g0169a0001c0005t0002g0170others(8): Show | 11 | HG01109.hp2 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.513+4169C>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230950164 | ||||||
| chr1:230950303
|
A | G | 1 | a0001c0002t0002g0227 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.513+4030T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230950303 | ||||||
| chr1:230950305
|
A | G | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+4028T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230950305 | ||||||
| chr1:230950334
|
T | C | 12 | a0001c0001t0002g0240a0001c0002t0001g0004a0001c0002t0001g0133others(9): Show | 15 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.513+3999A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230950334 | ||||||
| chr1:230950427
|
G | T | 198 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(195): Show | 216 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.513+3906C>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230950427 | ||||||
| chr1:230950428
|
C | CA | 26 | a0001c0001t0002g0240a0001c0002t0001g0004a0001c0002t0001g0133others(23): Show | 30 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.513+3904dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230950428 | ||||||
| chr1:230950555
|
T | C | 1 | a0002c0014t0001g0045 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.513+3778A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230950555 | ||||||
| chr1:230950625
|
C | T | 168 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(165): Show | 182 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.513+3708G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230950625 | ||||||
| chr1:230951006
|
A | G | 302 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(299): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.513+3327T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230951006 | ||||||
| chr1:230951098
|
A | G | 1 | a0001c0002t0002g0018 | 2 | HG01106.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.513+3235T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230951098 | ||||||
| chr1:230951273
|
C | A | 1 | a0001c0001t0002g0197 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.513+3060G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230951273 | ||||||
| chr1:230951329
|
A | C | 266 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(263): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.513+3004T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230951329 | ||||||
| chr1:230951340
|
C | A | 1 | a0001c0001t0002g0289 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.513+2993G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230951340 | ||||||
| chr1:230951426
|
T | G | 276 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(273): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.513+2907A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230951426 | ||||||
| chr1:230951592
|
G | A | 1 | a0001c0002t0002g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.513+2741C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230951592 | ||||||
| chr1:230951608
|
A | T | 1 | a0001c0002t0002g0266 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.513+2725T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230951608 | ||||||
| chr1:230951654
|
G | T | 194 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(191): Show | 212 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.513+2679C>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230951654 | ||||||
| chr1:230951725
|
TAC | T | 2 | a0001c0002t0001g0163a0001c0002t0002g0018 | 3 | HG01106.hp2 HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.513+2606_513+2607d others(4): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230951725 | ||||||
| chr1:230951761
|
GAA | G | 2 | a0001c0002t0001g0163a0001c0002t0002g0018 | 3 | HG01106.hp2 HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.513+2570_513+2571d others(4): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230951761 | ||||||
| chr1:230951781
|
G | GA | 194 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(191): Show | 212 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.513+2551dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230951781 | ||||||
| chr1:230951927
|
C | A | 1 | a0001c0001t0002g0295 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.513+2406G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230951927 | ||||||
| chr1:230951976
|
C | G | 168 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(165): Show | 182 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.513+2357G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230951976 | ||||||
| chr1:230951991
|
T | A | 2 | a0001c0009t0002g0273a0002c0003t0001g0069 | 2 | HG00408.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.513+2342A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230951991 | ||||||
| chr1:230952100
|
G | C | 1 | a0002c0007t0001g0072 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.513+2233C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230952100 | ||||||
| chr1:230952149
|
T | A | 1 | a0001c0001t0002g0289 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.513+2184A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230952149 | ||||||
| chr1:230952161
|
G | A | 1 | a0002c0003t0001g0055 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.513+2172C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230952161 | ||||||
| chr1:230952186
|
A | T | 2 | a0001c0002t0001g0163a0001c0002t0002g0018 | 3 | HG01106.hp2 HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.513+2147T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230952186 | ||||||
| chr1:230952238
|
C | T | 194 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(191): Show | 212 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.513+2095G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230952238 | ||||||
| chr1:230952783
|
A | C | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+1550T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230952783 | ||||||
| chr1:230952844
|
A | C | 1 | a0001c0004t0002g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.513+1489T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230952844 | ||||||
| chr1:230953217
|
T | A | 1 | a0001c0002t0002g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.513+1116A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230953217 | ||||||
| chr1:230953307
|
C | G | 14 | a0001c0002t0001g0149a0001c0002t0002g0019a0001c0002t0002g0203others(11): Show | 15 | HG01496.hp2 HG01516.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.513+1026G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230953307 | ||||||
| chr1:230953409
|
C | T | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+924G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230953409 | ||||||
| chr1:230953414
|
A | T | 4 | a0002c0003t0001g0040a0002c0003t0001g0060a0002c0003t0001g0061others(1): Show | 4 | HG02970.hp1 HG03098.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+919T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230953414 | ||||||
| chr1:230953498
|
T | G | 2 | a0001c0002t0001g0012a0001c0002t0001g0116 | 3 | HG02109.hp2 HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.513+835A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230953498 | ||||||
| chr1:230953731
|
G | A | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.513+602C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230953731 | ||||||
| chr1:230953830
|
G | A | 1 | a0001c0001t0002g0237 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.513+503C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230953830 | ||||||
| chr1:230953912
|
T | A | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+421A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230953912 | ||||||
| chr1:230954243
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.513+90T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 4/22 | chr1 | 230954243 | ||||||
| chr1:230954773
|
A | AT | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-371dupA | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230954773 | ||||||
| chr1:230954825
|
A | G | 1 | a0002c0003t0001g0047 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.443-422T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230954825 | ||||||
| chr1:230954832
|
G | A | 218 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(215): Show | 241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.443-429C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230954832 | ||||||
| chr1:230954999
|
T | G | 10 | a0002c0003t0001g0002a0002c0003t0001g0030a0002c0003t0001g0056others(7): Show | 12 | HG00621.hp1 HG02132.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.443-596A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230954999 | ||||||
| chr1:230955052
|
A | T | 1 | a0001c0001t0002g0210 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.443-649T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955052 | ||||||
| chr1:230955144
|
G | A | 108 | a0001c0001t0001g0113a0001c0001t0002g0197a0001c0002t0001g0011others(105): Show | 123 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.443-741C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955144 | ||||||
| chr1:230955155
|
A | T | 3 | a0001c0002t0001g0119a0001c0017t0007g0166a0001c0018t0002g0165 | 3 | HG02257.hp1 HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.443-752T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955155 | ||||||
| chr1:230955258
|
C | T | 44 | a0001c0009t0002g0273a0002c0003t0001g0001a0002c0003t0001g0002others(41): Show | 55 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.443-855G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955258 | ||||||
| chr1:230955353
|
C | T | 218 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(215): Show | 241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.443-950G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955353 | ||||||
| chr1:230955434
|
C | T | 104 | a0001c0001t0001g0113a0001c0002t0001g0011a0001c0002t0001g0012others(101): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.443-1031G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955434 | ||||||
| chr1:230955451
|
CAG | C | 68 | a0001c0009t0002g0273a0001c0013t0003g0091a0001c0013t0003g0092others(65): Show | 80 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.443-1050_443-1049d others(4): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955451 | ||||||
| chr1:230955490
|
C | G | 1 | a0002c0007t0001g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.443-1087G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955490 | ||||||
| chr1:230955507
|
C | CA | 123 | a0001c0001t0001g0113a0001c0001t0002g0221a0001c0001t0002g0299others(120): Show | 139 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.443-1105dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955507 | ||||||
| chr1:230955507
|
C | CAA | 8 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(5): Show | 8 | HG00597.hp1 HG01243.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.443-1106_443-1105d others(4): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955507 | ||||||
| chr1:230955528
|
G | A | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-1125C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955528 | ||||||
| chr1:230955543
|
T | C | 48 | a0001c0009t0002g0273a0002c0003t0001g0001a0002c0003t0001g0002others(45): Show | 59 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.443-1140A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955543 | ||||||
| chr1:230955619
|
C | T | 3 | a0001c0002t0002g0225a0001c0002t0002g0226a0001c0002t0002g0267 | 3 | HG02622.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.443-1216G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955619 | ||||||
| chr1:230955652
|
CAG | C | 103 | a0001c0001t0001g0113a0001c0002t0001g0011a0001c0002t0001g0012others(100): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.443-1251_443-1250d others(4): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955652 | ||||||
| chr1:230955670
|
C | CAAA | 82 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(79): Show | 89 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.443-1270_443-1268d others(5): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955670 | ||||||
| chr1:230955670
|
C | CAAAA | 17 | a0001c0001t0001g0140a0001c0001t0001g0156a0001c0001t0002g0168others(14): Show | 17 | HG01109.hp2 HG01496.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.443-1271_443-1268d others(6): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955670 | ||||||
| chr1:230955670
|
C | CAAAAAA | 13 | a0001c0004t0002g0017a0001c0004t0002g0167a0001c0004t0002g0181others(10): Show | 14 | HG01261.hp1 HG01891.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.443-1273_443-1268d others(8): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955670 | ||||||
| chr1:230955925
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | NA18994.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.443-1522G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230955925 | ||||||
| chr1:230956064
|
C | T | 1 | a0001c0005t0002g0279 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.443-1661G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230956064 | ||||||
| chr1:230956132
|
A | G | 15 | a0001c0001t0002g0168a0001c0005t0002g0169a0001c0005t0002g0170others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.443-1729T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230956132 | ||||||
| chr1:230956226
|
C | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(108): Show | 119 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.443-1823G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230956226 | ||||||
| chr1:230956400
|
G | A | 1 | a0001c0002t0002g0202 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.442+1824C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230956400 | ||||||
| chr1:230956434
|
G | A | 104 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(101): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.442+1790C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230956434 | ||||||
| chr1:230956465
|
T | TG | 108 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(105): Show | 123 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.442+1758dupC | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230956465 | ||||||
| chr1:230956639
|
T | C | 2 | a0002c0003t0001g0030a0002c0003t0001g0083 | 2 | NA19072.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.442+1585A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230956639 | ||||||
| chr1:230956641
|
T | C | 1 | a0002c0003t0001g0035 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.442+1583A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230956641 | ||||||
| chr1:230956834
|
T | A | 217 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(214): Show | 240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.442+1390A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230956834 | ||||||
| chr1:230956911
|
A | G | 1 | a0001c0001t0002g0025 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.442+1313T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230956911 | ||||||
| chr1:230956962
|
T | C | 18 | a0001c0004t0002g0017a0001c0004t0002g0167a0001c0004t0002g0181others(15): Show | 19 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.442+1262A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230956962 | ||||||
| chr1:230957225
|
C | T | 104 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(101): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.442+999G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230957225 | ||||||
| chr1:230957278
|
C | A | 221 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(218): Show | 244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.442+946G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230957278 | ||||||
| chr1:230957556
|
T | C | 104 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(101): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.442+668A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230957556 | ||||||
| chr1:230957663
|
A | T | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+561T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230957663 | ||||||
| chr1:230957762
|
G | A | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+462C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230957762 | ||||||
| chr1:230957825
|
GTAAAATA others(15): Show |
G | 105 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(102): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.442+377_442+398del others(22): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230957825 | ||||||
| chr1:230958039
|
CT | C | 221 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(218): Show | 244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.442+184delA | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230958039 | ||||||
| chr1:230958133
|
C | G | 18 | a0001c0004t0002g0017a0001c0004t0002g0167a0001c0004t0002g0181others(15): Show | 19 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.442+91G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 3/22 | chr1 | 230958133 | ||||||
| chr1:230958304
|
G | GA | 7 | a0001c0001t0001g0138a0001c0001t0001g0158a0001c0001t0002g0253others(4): Show | 7 | HG01361.hp2 HG02258.hp1 HG02738.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.367-6dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230958304 | ||||||
| chr1:230958304
|
GA | G | 98 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(95): Show | 113 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
splice_region_variant&intron_variant | LOW | c.367-6delT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230958304 | ||||||
| chr1:230958548
|
T | C | 217 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(214): Show | 240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.367-249A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230958548 | ||||||
| chr1:230958621
|
C | T | 2 | a0002c0003t0001g0006a0002c0003t0001g0046 | 3 | NA18978.hp2 NA18989.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.367-322G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230958621 | ||||||
| chr1:230958756
|
C | G | 2 | a0001c0013t0003g0091a0001c0013t0003g0092 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.367-457G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230958756 | ||||||
| chr1:230958973
|
G | A | 18 | a0001c0004t0002g0017a0001c0004t0002g0167a0001c0004t0002g0181others(15): Show | 19 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.367-674C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230958973 | ||||||
| chr1:230959127
|
A | T | 104 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(101): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.367-828T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230959127 | ||||||
| chr1:230959236
|
T | C | 1 | a0001c0002t0002g0198 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.367-937A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230959236 | ||||||
| chr1:230959385
|
C | CT | 73 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(70): Show | 79 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.367-1087dupA | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230959385 | ||||||
| chr1:230959467
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.367-1168G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230959467 | ||||||
| chr1:230959587
|
G | A | 3 | a0001c0001t0002g0254a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG00438.hp1 HG02015.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.367-1288C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230959587 | ||||||
| chr1:230959589
|
G | A | 1 | a0001c0004t0008g0184 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.367-1290C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230959589 | ||||||
| chr1:230959628
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.367-1329C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230959628 | ||||||
| chr1:230959661
|
G | A | 1 | a0001c0001t0002g0290 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.367-1362C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230959661 | ||||||
| chr1:230959787
|
G | A | 5 | a0002c0003t0001g0037a0002c0003t0001g0080a0002c0003t0001g0081others(2): Show | 5 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.366+1422C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230959787 | ||||||
| chr1:230960037
|
C | T | 104 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(101): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.366+1172G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230960037 | ||||||
| chr1:230960114
|
C | T | 2 | a0001c0001t0002g0241a0001c0001t0002g0262 | 2 | HG02080.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.366+1095G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230960114 | ||||||
| chr1:230960450
|
G | A | 18 | a0001c0004t0002g0017a0001c0004t0002g0167a0001c0004t0002g0181others(15): Show | 19 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.366+759C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230960450 | ||||||
| chr1:230960487
|
G | A | 1 | a0001c0002t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.366+722C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230960487 | ||||||
| chr1:230960575
|
G | GA | 62 | a0001c0001t0001g0101a0001c0001t0001g0112a0001c0002t0001g0111others(59): Show | 74 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.366+633dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230960575 | ||||||
| chr1:230960576
|
A | G | 5 | a0001c0005t0002g0276a0001c0005t0002g0278a0001c0005t0002g0279others(2): Show | 5 | HG02572.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.366+633T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230960576 | ||||||
| chr1:230960577
|
A | AG | 10 | a0002c0003t0001g0029a0002c0003t0001g0031a0002c0003t0001g0032others(7): Show | 10 | HG00140.hp1 HG00735.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.366+631_366+632ins others(1): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230960577 | ||||||
| chr1:230960615
|
C | A | 1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.366+594G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230960615 | ||||||
| chr1:230960673
|
C | T | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.366+536G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230960673 | ||||||
| chr1:230960935
|
A | C | 217 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(214): Show | 240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.366+274T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230960935 | ||||||
| chr1:230961008
|
A | G | 113 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(110): Show | 121 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.366+201T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230961008 | ||||||
| chr1:230961099
|
T | C | 1 | a0003c0006t0001g0028 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.366+110A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 2/22 | chr1 | 230961099 | ||||||
| chr1:230961448
|
G | A | 18 | a0001c0004t0002g0017a0001c0004t0002g0167a0001c0004t0002g0181others(15): Show | 19 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.272-145C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230961448 | ||||||
| chr1:230961937
|
G | A | 1 | a0001c0002t0002g0202 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.272-634C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230961937 | ||||||
| chr1:230961985
|
C | T | 1 | a0001c0004t0002g0188 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.272-682G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230961985 | ||||||
| chr1:230962070
|
C | G | 2 | a0001c0002t0001g0163a0001c0002t0002g0018 | 3 | HG01106.hp2 HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.272-767G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230962070 | ||||||
| chr1:230962110
|
T | C | 104 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(101): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.272-807A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230962110 | ||||||
| chr1:230962166
|
T | C | 104 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(101): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.272-863A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230962166 | ||||||
| chr1:230962210
|
C | CA | 92 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(89): Show | 98 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.272-908dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230962210 | ||||||
| chr1:230962210
|
C | CAA | 19 | a0001c0001t0001g0153a0001c0002t0001g0163a0001c0002t0002g0018others(16): Show | 21 | HG01106.hp2 HG01109.hp1 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.272-909_272-908dup others(2): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230962210 | ||||||
| chr1:230962353
|
A | G | 73 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(70): Show | 79 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.272-1050T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230962353 | ||||||
| chr1:230962368
|
T | C | 5 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0270others(2): Show | 5 | HG01243.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.272-1065A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230962368 | ||||||
| chr1:230962486
|
C | T | 104 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(101): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.272-1183G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230962486 | ||||||
| chr1:230962550
|
C | T | 1 | a0001c0002t0001g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.272-1247G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230962550 | ||||||
| chr1:230962750
|
C | G | 1 | a0001c0001t0001g0139 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.272-1447G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230962750 | ||||||
| chr1:230962979
|
T | C | 1 | a0002c0003t0001g0082 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.272-1676A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230962979 | ||||||
| chr1:230962989
|
G | A | 1 | a0001c0002t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.272-1686C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230962989 | ||||||
| chr1:230963128
|
CATTAAAT others(33): Show |
C | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.272-1865_272-1826d others(42): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230963128 | ||||||
| chr1:230963430
|
G | GGAGTTTG others(1): Show |
217 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(214): Show | 240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.272-2135_272-2128d others(10): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230963430 | ||||||
| chr1:230963502
|
A | G | 15 | a0001c0001t0002g0168a0001c0005t0002g0169a0001c0005t0002g0170others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.272-2199T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230963502 | ||||||
| chr1:230963524
|
T | C | 16 | a0001c0004t0002g0017a0001c0004t0002g0167a0001c0004t0002g0181others(13): Show | 17 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.272-2221A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230963524 | ||||||
| chr1:230963611
|
G | C | 15 | a0001c0001t0002g0168a0001c0005t0002g0169a0001c0005t0002g0170others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.272-2308C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230963611 | ||||||
| chr1:230963635
|
A | AAAAT | 5 | a0001c0002t0002g0018a0001c0002t0002g0223a0001c0005t0002g0275others(2): Show | 6 | HG01106.hp2 HG02132.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.272-2336_272-2333d others(6): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230963635 | ||||||
| chr1:230963635
|
A | AAAATAAA others(1): Show |
7 | a0001c0001t0002g0168a0001c0002t0001g0163a0001c0002t0002g0198others(4): Show | 8 | HG01243.hp2 HG02109.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.272-2340_272-2333d others(10): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230963635 | ||||||
| chr1:230963635
|
A | AAAATAAA others(5): Show |
24 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(21): Show | 24 | HG01109.hp2 HG01261.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.272-2344_272-2333d others(14): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230963635 | ||||||
| chr1:230963635
|
A | AAAATAAA others(9): Show |
4 | a0001c0004t0002g0185a0001c0004t0002g0186a0001c0004t0002g0187others(1): Show | 4 | HG01109.hp1 HG02486.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.272-2348_272-2333d others(18): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230963635 | ||||||
| chr1:230963635
|
AAAAT | A | 53 | a0001c0001t0001g0112a0001c0001t0001g0127a0001c0001t0001g0154others(50): Show | 62 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.272-2336_272-2333d others(6): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230963635 | ||||||
| chr1:230963635
|
AAAATAAA others(1): Show |
A | 76 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(73): Show | 82 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.272-2340_272-2333d others(10): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230963635 | ||||||
| chr1:230963635
|
AAAATAAA others(5): Show |
A | 2 | a0001c0001t0001g0097a0001c0001t0002g0262 | 2 | HG01516.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.272-2344_272-2333d others(14): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230963635 | ||||||
| chr1:230963635
|
AAAATAAA others(9): Show |
A | 104 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(101): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.272-2348_272-2333d others(18): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230963635 | ||||||
| chr1:230963842
|
G | A | 104 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(101): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.272-2539C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230963842 | ||||||
| chr1:230964149
|
A | C | 105 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(102): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.272-2846T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230964149 | ||||||
| chr1:230964221
|
C | T | 3 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196 | 3 | HG02572.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.272-2918G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230964221 | ||||||
| chr1:230964239
|
G | A | 20 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0002t0001g0011others(17): Show | 22 | HG00642.hp2 HG00733.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.272-2936C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230964239 | ||||||
| chr1:230964511
|
T | C | 26 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(23): Show | 29 | HG00642.hp2 HG00733.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.272-3208A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230964511 | ||||||
| chr1:230964528
|
T | C | 67 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0127others(64): Show | 76 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.272-3225A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230964528 | ||||||
| chr1:230964535
|
C | G | 15 | a0001c0001t0002g0168a0001c0005t0002g0169a0001c0005t0002g0170others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.272-3232G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230964535 | ||||||
| chr1:230964626
|
A | G | 5 | a0002c0003t0001g0037a0002c0003t0001g0080a0002c0003t0001g0081others(2): Show | 5 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.272-3323T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230964626 | ||||||
| chr1:230964661
|
C | T | 10 | a0001c0001t0001g0112a0001c0001t0001g0127a0001c0001t0002g0020others(7): Show | 11 | HG00597.hp2 HG00673.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.272-3358G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230964661 | ||||||
| chr1:230964873
|
C | G | 2 | a0001c0002t0001g0103a0001c0002t0001g0120 | 2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.272-3570G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230964873 | ||||||
| chr1:230964947
|
T | C | 1 | a0001c0001t0005g0102 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.272-3644A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230964947 | ||||||
| chr1:230965036
|
G | A | 215 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(212): Show | 238 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.272-3733C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230965036 | ||||||
| chr1:230965158
|
G | C | 4 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.272-3855C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230965158 | ||||||
| chr1:230965163
|
A | C | 104 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(101): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.272-3860T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230965163 | ||||||
| chr1:230965760
|
C | G | 1 | a0001c0002t0002g0223 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.272-4457G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230965760 | ||||||
| chr1:230965822
|
T | G | 18 | a0001c0004t0002g0017a0001c0004t0002g0167a0001c0004t0002g0181others(15): Show | 19 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.272-4519A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230965822 | ||||||
| chr1:230965825
|
A | AT | 73 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(70): Show | 79 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.272-4523dupA | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230965825 | ||||||
| chr1:230965881
|
G | C | 18 | a0001c0004t0002g0017a0001c0004t0002g0167a0001c0004t0002g0181others(15): Show | 19 | HG01109.hp1 HG01261.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.272-4578C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230965881 | ||||||
| chr1:230966034
|
T | C | 2 | a0002c0003t0001g0070a0002c0003t0001g0074 | 2 | NA19006.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.272-4731A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230966034 | ||||||
| chr1:230966197
|
G | C | 36 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(33): Show | 39 | HG00642.hp2 HG00733.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.272-4894C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230966197 | ||||||
| chr1:230966318
|
T | A | 1 | a0001c0001t0002g0291 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.272-5015A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230966318 | ||||||
| chr1:230966424
|
T | C | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.272-5121A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230966424 | ||||||
| chr1:230966446
|
CTA | C | 113 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(110): Show | 121 | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(118): Show |
intron_variant | MODIFIER | c.272-5145_272-5144d others(4): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230966446 | ||||||
| chr1:230966493
|
T | A | 1 | a0001c0001t0002g0168 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.272-5190A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230966493 | ||||||
| chr1:230966496
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.272-5193T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230966496 | ||||||
| chr1:230967016
|
T | A | 105 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0113others(102): Show | 120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.272-5713A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230967016 | ||||||
| chr1:230967102
|
A | G | 18 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(15): Show | 18 | HG00323.hp1 HG02145.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.272-5799T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230967102 | ||||||
| chr1:230967170
|
CCTT | C | 69 | a0001c0009t0002g0273a0001c0009t0002g0274a0002c0003t0001g0001others(66): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.272-5870_272-5868d others(5): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230967170 | ||||||
| chr1:230967202
|
A | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(215): Show | 241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.272-5899T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230967202 | ||||||
| chr1:230967314
|
T | C | 1 | a0001c0002t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.272-6011A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230967314 | ||||||
| chr1:230967378
|
T | C | 4 | a0002c0003t0001g0030a0002c0003t0001g0064a0002c0003t0001g0065others(1): Show | 4 | NA18964.hp1 NA19007.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.272-6075A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230967378 | ||||||
| chr1:230967403
|
A | AT | 21 | a0001c0001t0002g0025a0001c0001t0002g0212a0001c0001t0002g0233others(18): Show | 22 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.272-6101dupA | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230967403 | ||||||
| chr1:230967403
|
AT | A | 69 | a0001c0009t0002g0273a0001c0009t0002g0274a0002c0003t0001g0001others(66): Show | 81 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.272-6101delA | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230967403 | ||||||
| chr1:230967636
|
T | C | 15 | a0001c0001t0002g0168a0001c0005t0002g0169a0001c0005t0002g0170others(12): Show | 15 | HG01109.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.272-6333A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230967636 | ||||||
| chr1:230967777
|
T | C | 2 | a0001c0001t0002g0005a0001c0001t0002g0263 | 4 | NA18945.hp2 NA19011.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.272-6474A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230967777 | ||||||
| chr1:230967861
|
G | A | 4 | a0001c0001t0001g0151a0001c0002t0001g0004a0001c0002t0001g0133others(1): Show | 6 | HG00140.hp2 HG00639.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.272-6558C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230967861 | ||||||
| chr1:230967931
|
A | G | 1 | a0001c0002t0002g0177 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.272-6628T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230967931 | ||||||
| chr1:230968055
|
A | G | 72 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(69): Show | 78 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.272-6752T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968055 | ||||||
| chr1:230968143
|
TTC | T | 62 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0127others(59): Show | 68 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.272-6842_272-6841d others(4): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968143 | ||||||
| chr1:230968162
|
A | T | 1 | a0001c0001t0002g0232 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.272-6859T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968162 | ||||||
| chr1:230968184
|
T | TG | 54 | a0001c0001t0001g0097a0001c0001t0001g0127a0001c0001t0001g0157others(51): Show | 61 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.272-6882dupC | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968184 | ||||||
| chr1:230968184
|
TG | T | 23 | a0001c0001t0001g0131a0001c0001t0002g0025a0001c0001t0002g0283others(20): Show | 24 | HG00733.hp1 HG01168.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.272-6882delC | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968184 | ||||||
| chr1:230968184
|
TGG | T | 112 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(109): Show | 124 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(121): Show |
intron_variant | MODIFIER | c.272-6883_272-6882d others(4): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968184 | ||||||
| chr1:230968187
|
G | T | 7 | a0001c0001t0001g0113a0001c0001t0002g0168a0001c0005t0002g0169others(4): Show | 7 | HG01109.hp2 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.272-6884C>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968187 | ||||||
| chr1:230968215
|
T | TA | 80 | a0001c0001t0001g0129a0001c0001t0001g0154a0001c0001t0001g0155others(77): Show | 92 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.272-6913dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968215 | ||||||
| chr1:230968215
|
TA | T | 28 | a0001c0001t0001g0137a0001c0001t0002g0025a0001c0001t0002g0168others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.272-6913delT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968215 | ||||||
| chr1:230968291
|
T | C | 1 | a0002c0003t0001g0082 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.272-6988A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968291 | ||||||
| chr1:230968300
|
T | TGATGTGA others(4): Show |
224 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(221): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.272-6998_272-6997i others(13): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968300 | ||||||
| chr1:230968332
|
T | A | 1 | a0001c0001t0001g0159 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.272-7029A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968332 | ||||||
| chr1:230968332
|
T | TA | 151 | a0001c0001t0001g0113a0001c0001t0002g0025a0001c0001t0002g0168others(148): Show | 168 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.272-7030dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968332 | ||||||
| chr1:230968334
|
A | AG | 67 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(64): Show | 75 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.272-7032_272-7031i others(3): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968334 | ||||||
| chr1:230968334
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.272-7031T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968334 | ||||||
| chr1:230968479
|
T | C | 222 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(219): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.272-7176A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968479 | ||||||
| chr1:230968785
|
G | A | 1 | a0003c0006t0001g0028 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.272-7482C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968785 | ||||||
| chr1:230968834
|
C | T | 224 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(221): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.272-7531G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968834 | ||||||
| chr1:230968851
|
C | T | 1 | a0001c0002t0001g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.272-7548G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230968851 | ||||||
| chr1:230969003
|
G | A | 1 | a0001c0004t0002g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.272-7700C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969003 | ||||||
| chr1:230969004
|
G | A | 1 | a0001c0002t0002g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.272-7701C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969004 | ||||||
| chr1:230969045
|
T | C | 224 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(221): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.272-7742A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969045 | ||||||
| chr1:230969070
|
C | T | 1 | a0001c0004t0002g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.272-7767G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969070 | ||||||
| chr1:230969079
|
G | A | 1 | a0001c0002t0002g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.272-7776C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969079 | ||||||
| chr1:230969090
|
G | A | 1 | a0001c0002t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.272-7787C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969090 | ||||||
| chr1:230969094
|
C | T | 39 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(36): Show | 42 | HG00642.hp2 HG01168.hp1 HG01256.hp2 others(39): Show |
intron_variant | MODIFIER | c.272-7791G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969094 | ||||||
| chr1:230969158
|
AG | A | 221 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(218): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.272-7856delC | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969158 | ||||||
| chr1:230969194
|
G | A | 1 | a0001c0002t0001g0119 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.272-7891C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969194 | ||||||
| chr1:230969256
|
C | T | 1 | a0001c0002t0001g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.272-7953G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969256 | ||||||
| chr1:230969264
|
A | AAAAAG | 172 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(169): Show | 190 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.272-7966_272-7962d others(7): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969264 | ||||||
| chr1:230969264
|
A | AAAAAGAA others(3): Show |
4 | a0001c0001t0002g0283a0002c0010t0001g0042a0002c0010t0001g0043others(1): Show | 4 | HG00323.hp1 HG01346.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.272-7971_272-7962d others(12): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969264 | ||||||
| chr1:230969264
|
AAAAAG | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(39): Show | 49 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.272-7966_272-7962d others(7): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969264 | ||||||
| chr1:230969264
|
AAAAAGAA others(3): Show |
A | 2 | a0001c0001t0002g0005a0001c0001t0002g0263 | 4 | NA18945.hp2 NA19011.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.272-7971_272-7962d others(12): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969264 | ||||||
| chr1:230969314
|
A | G | 73 | a0001c0009t0002g0273a0001c0009t0002g0274a0002c0003t0001g0001others(70): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.272-8011T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969314 | ||||||
| chr1:230969506
|
G | A | 2 | a0001c0002t0002g0264a0001c0002t0002g0265 | 2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.272-8203C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969506 | ||||||
| chr1:230969555
|
T | C | 221 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(218): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.272-8252A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969555 | ||||||
| chr1:230969675
|
A | G | 1 | a0001c0002t0001g0122 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.272-8372T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969675 | ||||||
| chr1:230969731
|
C | A | 221 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(218): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.272-8428G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969731 | ||||||
| chr1:230969734
|
C | A | 73 | a0001c0009t0002g0273a0001c0009t0002g0274a0002c0003t0001g0001others(70): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.272-8431G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969734 | ||||||
| chr1:230969757
|
C | T | 224 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(221): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.272-8454G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969757 | ||||||
| chr1:230969762
|
T | C | 73 | a0001c0009t0002g0273a0001c0009t0002g0274a0002c0003t0001g0001others(70): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.272-8459A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969762 | ||||||
| chr1:230969831
|
C | T | 1 | a0001c0002t0002g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.272-8528G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230969831 | ||||||
| chr1:230970011
|
C | A | 1 | a0001c0001t0001g0158 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.271+8549G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970011 | ||||||
| chr1:230970029
|
C | A | 2 | a0001c0002t0001g0013a0001c0002t0001g0115 | 3 | HG02922.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.271+8531G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970029 | ||||||
| chr1:230970143
|
C | T | 1 | a0001c0001t0002g0210 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.271+8417G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970143 | ||||||
| chr1:230970196
|
G | A | 3 | a0001c0002t0001g0163a0001c0013t0003g0091a0001c0013t0003g0092 | 3 | HG02109.hp1 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.271+8364C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970196 | ||||||
| chr1:230970398
|
G | A | 3 | a0001c0002t0001g0163a0001c0013t0003g0091a0001c0013t0003g0092 | 3 | HG02109.hp1 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.271+8162C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970398 | ||||||
| chr1:230970517
|
G | A | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+8043C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970517 | ||||||
| chr1:230970519
|
C | G | 1 | a0002c0003t0001g0009 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.271+8041G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970519 | ||||||
| chr1:230970568
|
G | C | 1 | a0001c0002t0002g0265 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.271+7992C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970568 | ||||||
| chr1:230970569
|
C | G | 3 | a0002c0003t0001g0029a0002c0003t0001g0084a0002c0003t0006g0085 | 3 | HG03688.hp1 HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.271+7991G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970569 | ||||||
| chr1:230970666
|
G | C | 34 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(31): Show | 40 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.271+7894C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970666 | ||||||
| chr1:230970737
|
A | G | 73 | a0001c0009t0002g0273a0001c0009t0002g0274a0002c0003t0001g0001others(70): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.271+7823T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970737 | ||||||
| chr1:230970802
|
G | A | 2 | a0001c0013t0003g0091a0001c0013t0003g0092 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.271+7758C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970802 | ||||||
| chr1:230970808
|
C | A | 1 | a0001c0001t0001g0159 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.271+7752G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970808 | ||||||
| chr1:230970825
|
C | A | 14 | a0001c0001t0002g0168a0001c0002t0002g0174a0001c0002t0002g0175others(11): Show | 14 | HG01109.hp2 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.271+7735G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970825 | ||||||
| chr1:230970833
|
G | A | 2 | a0001c0013t0003g0091a0001c0013t0003g0092 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.271+7727C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970833 | ||||||
| chr1:230970856
|
G | A | 7 | a0001c0005t0002g0275a0001c0005t0002g0276a0001c0005t0002g0277others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.271+7704C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970856 | ||||||
| chr1:230970889
|
G | C | 2 | a0001c0013t0003g0091a0001c0013t0003g0092 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.271+7671C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970889 | ||||||
| chr1:230970926
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.271+7634C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970926 | ||||||
| chr1:230970927
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.271+7633C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970927 | ||||||
| chr1:230970927
|
G | C | 1 | a0001c0004t0002g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.271+7633C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970927 | ||||||
| chr1:230970998
|
G | A | 224 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(221): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.271+7562C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230970998 | ||||||
| chr1:230971073
|
C | T | 73 | a0001c0009t0002g0273a0001c0009t0002g0274a0002c0003t0001g0001others(70): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.271+7487G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971073 | ||||||
| chr1:230971120
|
C | T | 1 | a0005c0022t0002g0183 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.271+7440G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971120 | ||||||
| chr1:230971121
|
G | C | 1 | a0001c0002t0002g0266 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.271+7439C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971121 | ||||||
| chr1:230971189
|
C | CA | 220 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(217): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.271+7370dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971189 | ||||||
| chr1:230971236
|
C | T | 41 | a0001c0001t0002g0025a0001c0001t0002g0282a0001c0001t0002g0283others(38): Show | 43 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.271+7324G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971236 | ||||||
| chr1:230971295
|
G | A | 38 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(35): Show | 41 | HG00642.hp2 HG01168.hp1 HG01256.hp2 others(38): Show |
intron_variant | MODIFIER | c.271+7265C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971295 | ||||||
| chr1:230971345
|
C | CA | 45 | a0001c0001t0002g0025a0001c0001t0002g0268a0001c0001t0002g0283others(42): Show | 47 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.271+7214dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971345 | ||||||
| chr1:230971345
|
C | CAA | 118 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(115): Show | 133 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.271+7213_271+7214d others(4): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971345 | ||||||
| chr1:230971345
|
C | CAAA | 46 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0127others(43): Show | 52 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.271+7212_271+7214d others(5): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971345 | ||||||
| chr1:230971345
|
CAAAAAAA others(3): Show |
C | 6 | a0001c0001t0002g0168a0001c0005t0002g0169a0001c0005t0002g0170others(3): Show | 6 | HG01109.hp2 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.271+7205_271+7214d others(12): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971345 | ||||||
| chr1:230971411
|
G | A | 1 | a0001c0004t0002g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.271+7149C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971411 | ||||||
| chr1:230971416
|
A | G | 14 | a0001c0001t0002g0168a0001c0002t0002g0174a0001c0002t0002g0175others(11): Show | 14 | HG01109.hp2 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.271+7144T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971416 | ||||||
| chr1:230971455
|
A | T | 1 | a0001c0001t0001g0159 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.271+7105T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971455 | ||||||
| chr1:230971531
|
G | A | 221 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(218): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.271+7029C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971531 | ||||||
| chr1:230971541
|
T | C | 1 | a0001c0002t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.271+7019A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971541 | ||||||
| chr1:230971548
|
T | C | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.271+7012A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971548 | ||||||
| chr1:230971563
|
G | A | 7 | a0001c0005t0002g0275a0001c0005t0002g0276a0001c0005t0002g0277others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.271+6997C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971563 | ||||||
| chr1:230971581
|
T | G | 1 | a0002c0003t0001g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.271+6979A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971581 | ||||||
| chr1:230971668
|
A | C | 1 | a0002c0003t0001g0086 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.271+6892T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971668 | ||||||
| chr1:230971718
|
T | G | 1 | a0001c0002t0001g0119 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.271+6842A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971718 | ||||||
| chr1:230971830
|
C | T | 221 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(218): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.271+6730G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971830 | ||||||
| chr1:230971869
|
G | A | 4 | a0002c0003t0001g0076a0002c0003t0001g0077a0002c0003t0001g0078others(1): Show | 4 | NA18968.hp2 NA19055.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+6691C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971869 | ||||||
| chr1:230971869
|
G | C | 2 | a0001c0017t0007g0166a0001c0018t0002g0165 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.271+6691C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971869 | ||||||
| chr1:230971959
|
A | G | 73 | a0001c0009t0002g0273a0001c0009t0002g0274a0002c0003t0001g0001others(70): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.271+6601T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230971959 | ||||||
| chr1:230972040
|
A | T | 42 | a0001c0001t0002g0025a0001c0001t0002g0282a0001c0001t0002g0283others(39): Show | 44 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.271+6520T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972040 | ||||||
| chr1:230972094
|
C | T | 224 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(221): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.271+6466G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972094 | ||||||
| chr1:230972160
|
T | C | 6 | a0001c0001t0002g0168a0001c0005t0002g0169a0001c0005t0002g0170others(3): Show | 6 | HG01109.hp2 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.271+6400A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972160 | ||||||
| chr1:230972252
|
G | A | 41 | a0001c0001t0002g0025a0001c0001t0002g0282a0001c0001t0002g0283others(38): Show | 43 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.271+6308C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972252 | ||||||
| chr1:230972352
|
T | C | 4 | a0001c0005t0002g0278a0001c0005t0002g0279a0001c0005t0002g0280others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.271+6208A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972352 | ||||||
| chr1:230972358
|
C | T | 228 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(225): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.271+6202G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972358 | ||||||
| chr1:230972397
|
C | G | 1 | a0009c0016t0001g0038 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.271+6163G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972397 | ||||||
| chr1:230972456
|
G | A | 221 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(218): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.271+6104C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972456 | ||||||
| chr1:230972529
|
T | C | 11 | a0001c0001t0002g0168a0001c0002t0002g0174a0001c0002t0002g0175others(8): Show | 11 | HG01109.hp2 HG02280.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.271+6031A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972529 | ||||||
| chr1:230972548
|
T | A | 1 | a0001c0001t0001g0159 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.271+6012A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972548 | ||||||
| chr1:230972662
|
A | G | 4 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0002g0208others(1): Show | 4 | HG00609.hp2 HG02523.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+5898T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972662 | ||||||
| chr1:230972696
|
A | C | 221 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(218): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.271+5864T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972696 | ||||||
| chr1:230972731
|
T | C | 4 | a0002c0003t0001g0037a0002c0003t0001g0080a0002c0003t0001g0081others(1): Show | 4 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.271+5829A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972731 | ||||||
| chr1:230972750
|
T | C | 39 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 46 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.271+5810A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972750 | ||||||
| chr1:230972885
|
C | A | 1 | a0002c0003t0001g0009 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.271+5675G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972885 | ||||||
| chr1:230972935
|
G | C | 4 | a0001c0001t0002g0298a0001c0001t0002g0299a0001c0001t0002g0301others(1): Show | 4 | NA18978.hp1 NA18979.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.271+5625C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230972935 | ||||||
| chr1:230973031
|
A | C | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5529T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973031 | ||||||
| chr1:230973033
|
C | A | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5527G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973033 | ||||||
| chr1:230973035
|
A | C | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5525T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973035 | ||||||
| chr1:230973036
|
G | A | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5524C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973036 | ||||||
| chr1:230973059
|
A | T | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5501T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973059 | ||||||
| chr1:230973060
|
C | A | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5500G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973060 | ||||||
| chr1:230973150
|
G | A | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5410C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973150 | ||||||
| chr1:230973152
|
C | T | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5408G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973152 | ||||||
| chr1:230973153
|
T | G | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5407A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973153 | ||||||
| chr1:230973156
|
G | C | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5404C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973156 | ||||||
| chr1:230973160
|
A | AATGAGTC others(10): Show |
1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5399_271+5400i others(19): Show |
TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973160 | ||||||
| chr1:230973167
|
G | A | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5393C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973167 | ||||||
| chr1:230973169
|
T | G | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5391A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973169 | ||||||
| chr1:230973180
|
C | A | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5380G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973180 | ||||||
| chr1:230973191
|
A | T | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5369T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973191 | ||||||
| chr1:230973197
|
G | A | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5363C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973197 | ||||||
| chr1:230973214
|
T | G | 39 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(36): Show | 42 | HG00642.hp2 HG01168.hp1 HG01256.hp2 others(39): Show |
intron_variant | MODIFIER | c.271+5346A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973214 | ||||||
| chr1:230973219
|
T | C | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5341A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973219 | ||||||
| chr1:230973238
|
C | A | 1 | a0001c0002t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.271+5322G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973238 | ||||||
| chr1:230973243
|
A | G | 1 | a0002c0003t0001g0037 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.271+5317T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973243 | ||||||
| chr1:230973266
|
T | C | 1 | a0001c0002t0002g0302 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.271+5294A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973266 | ||||||
| chr1:230973280
|
C | T | 73 | a0001c0009t0002g0273a0001c0009t0002g0274a0002c0003t0001g0001others(70): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.271+5280G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973280 | ||||||
| chr1:230973394
|
C | G | 39 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(36): Show | 42 | HG00642.hp2 HG01168.hp1 HG01256.hp2 others(39): Show |
intron_variant | MODIFIER | c.271+5166G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973394 | ||||||
| chr1:230973547
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.271+5013C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973547 | ||||||
| chr1:230973654
|
A | C | 10 | a0002c0003t0001g0029a0002c0003t0001g0031a0002c0003t0001g0032others(7): Show | 10 | HG00140.hp1 HG00735.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.271+4906T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973654 | ||||||
| chr1:230973800
|
G | A | 2 | a0001c0013t0003g0091a0001c0013t0003g0092 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.271+4760C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973800 | ||||||
| chr1:230973815
|
C | T | 14 | a0001c0001t0002g0168a0001c0002t0002g0174a0001c0002t0002g0175others(11): Show | 14 | HG01109.hp2 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.271+4745G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973815 | ||||||
| chr1:230973816
|
G | A | 2 | a0001c0013t0003g0091a0001c0013t0003g0092 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.271+4744C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973816 | ||||||
| chr1:230973840
|
C | T | 39 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 46 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.271+4720G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973840 | ||||||
| chr1:230973985
|
G | A | 2 | a0001c0013t0003g0091a0001c0013t0003g0092 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.271+4575C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230973985 | ||||||
| chr1:230974076
|
C | CA | 49 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(46): Show | 56 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.271+4483dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230974076 | ||||||
| chr1:230974076
|
CA | C | 10 | a0001c0002t0001g0011a0001c0002t0001g0093a0001c0002t0001g0094others(7): Show | 11 | HG00642.hp2 HG01256.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.271+4483delT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230974076 | ||||||
| chr1:230974098
|
C | G | 124 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(121): Show | 137 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.271+4462G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230974098 | ||||||
| chr1:230974112
|
T | C | 2 | a0001c0013t0003g0091a0001c0013t0003g0092 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.271+4448A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230974112 | ||||||
| chr1:230974417
|
C | T | 1 | a0001c0002t0001g0014 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.271+4143G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230974417 | ||||||
| chr1:230974634
|
G | A | 44 | a0001c0001t0002g0025a0001c0001t0002g0282a0001c0001t0002g0283others(41): Show | 47 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.271+3926C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230974634 | ||||||
| chr1:230974667
|
T | C | 115 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(112): Show | 130 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.271+3893A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230974667 | ||||||
| chr1:230974895
|
T | C | 3 | a0001c0002t0001g0090a0001c0013t0003g0091a0001c0013t0003g0092 | 3 | HG02717.hp2 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.271+3665A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230974895 | ||||||
| chr1:230974929
|
T | C | 45 | a0001c0001t0002g0025a0001c0001t0002g0282a0001c0001t0002g0283others(42): Show | 48 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.271+3631A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230974929 | ||||||
| chr1:230975058
|
T | A | 41 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 48 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.271+3502A>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230975058 | ||||||
| chr1:230975113
|
G | A | 44 | a0001c0001t0002g0025a0001c0001t0002g0282a0001c0001t0002g0283others(41): Show | 47 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.271+3447C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230975113 | ||||||
| chr1:230975155
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0161a0001c0001t0001g0162 | 4 | HG00280.hp1 HG01981.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+3405C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230975155 | ||||||
| chr1:230975211
|
G | GA | 43 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(40): Show | 46 | HG00642.hp2 HG01168.hp1 HG01256.hp2 others(43): Show |
intron_variant | MODIFIER | c.271+3348dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230975211 | ||||||
| chr1:230975211
|
GA | G | 7 | a0001c0001t0002g0168a0001c0002t0002g0203a0001c0005t0002g0169others(4): Show | 7 | HG01109.hp2 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.271+3348delT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230975211 | ||||||
| chr1:230975227
|
A | T | 1 | a0001c0004t0002g0181 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.271+3333T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230975227 | ||||||
| chr1:230975447
|
C | T | 3 | a0001c0002t0001g0090a0001c0013t0003g0091a0001c0013t0003g0092 | 3 | HG02717.hp2 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.271+3113G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230975447 | ||||||
| chr1:230975454
|
A | T | 1 | a0001c0002t0002g0018 | 2 | HG01106.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.271+3106T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230975454 | ||||||
| chr1:230975507
|
G | A | 7 | a0001c0005t0002g0275a0001c0005t0002g0276a0001c0005t0002g0277others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.271+3053C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230975507 | ||||||
| chr1:230975707
|
A | C | 1 | a0001c0004t0002g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.271+2853T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230975707 | ||||||
| chr1:230975723
|
AT | A | 7 | a0001c0005t0002g0275a0001c0005t0002g0276a0001c0005t0002g0277others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.271+2836delA | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230975723 | ||||||
| chr1:230975731
|
C | G | 180 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(177): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.271+2829G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230975731 | ||||||
| chr1:230975833
|
A | G | 1 | a0001c0005t0002g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.271+2727T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230975833 | ||||||
| chr1:230975850
|
T | C | 3 | a0001c0002t0001g0090a0001c0013t0003g0091a0001c0013t0003g0092 | 3 | HG02717.hp2 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.271+2710A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230975850 | ||||||
| chr1:230975966
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.271+2594G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230975966 | ||||||
| chr1:230976176
|
A | C | 115 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(112): Show | 130 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.271+2384T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230976176 | ||||||
| chr1:230976272
|
G | C | 40 | a0001c0001t0002g0025a0001c0001t0002g0282a0001c0001t0002g0283others(37): Show | 42 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.271+2288C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230976272 | ||||||
| chr1:230976315
|
C | T | 4 | a0001c0001t0002g0197a0001c0002t0002g0195a0001c0002t0002g0196others(1): Show | 4 | HG01243.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+2245G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230976315 | ||||||
| chr1:230976364
|
A | C | 115 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(112): Show | 130 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.271+2196T>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230976364 | ||||||
| chr1:230976413
|
G | A | 41 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 48 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.271+2147C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230976413 | ||||||
| chr1:230976451
|
A | G | 54 | a0001c0001t0002g0025a0001c0001t0002g0168a0001c0001t0002g0282others(51): Show | 56 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.271+2109T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230976451 | ||||||
| chr1:230976456
|
C | A | 2 | a0002c0003t0001g0084a0002c0003t0006g0085 | 2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.271+2104G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230976456 | ||||||
| chr1:230976456
|
C | G | 54 | a0001c0001t0002g0025a0001c0001t0002g0168a0001c0001t0002g0282others(51): Show | 56 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.271+2104G>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230976456 | ||||||
| chr1:230976771
|
G | A | 2 | a0001c0001t0002g0303a0002c0003t0001g0086 | 2 | HG01168.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.271+1789C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230976771 | ||||||
| chr1:230976926
|
T | G | 2 | a0001c0017t0007g0166a0001c0018t0002g0165 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.271+1634A>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230976926 | ||||||
| chr1:230976992
|
T | C | 73 | a0001c0009t0002g0273a0001c0009t0002g0274a0002c0003t0001g0001others(70): Show | 85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.271+1568A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230976992 | ||||||
| chr1:230977048
|
C | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(41): Show | 51 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.271+1512G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230977048 | ||||||
| chr1:230977082
|
T | C | 7 | a0001c0005t0002g0275a0001c0005t0002g0276a0001c0005t0002g0277others(4): Show | 7 | HG02572.hp2 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.271+1478A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230977082 | ||||||
| chr1:230977222
|
T | C | 1 | a0001c0002t0001g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.271+1338A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230977222 | ||||||
| chr1:230977316
|
A | T | 41 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 48 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.271+1244T>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230977316 | ||||||
| chr1:230977575
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.271+985G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230977575 | ||||||
| chr1:230977586
|
T | TA | 41 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 48 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.271+973dupT | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230977586 | ||||||
| chr1:230977667
|
T | C | 1 | a0001c0002t0002g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.271+893A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230977667 | ||||||
| chr1:230977691
|
C | A | 113 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(110): Show | 128 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.271+869G>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230977691 | ||||||
| chr1:230977792
|
AT | A | 41 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 48 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.271+767delA | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230977792 | ||||||
| chr1:230977850
|
T | C | 4 | a0002c0003t0001g0010a0002c0008t0001g0088a0002c0008t0001g0089others(1): Show | 5 | HG00609.hp1 HG02155.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.271+710A>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230977850 | ||||||
| chr1:230977985
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.271+575C>G | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230977985 | ||||||
| chr1:230978006
|
A | G | 1 | a0002c0003t0001g0029 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.271+554T>C | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230978006 | ||||||
| chr1:230978150
|
G | A | 23 | a0001c0001t0002g0025a0001c0001t0002g0282a0001c0001t0002g0283others(20): Show | 24 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.271+410C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230978150 | ||||||
| chr1:230978175
|
C | T | 14 | a0001c0001t0002g0168a0001c0002t0002g0174a0001c0002t0002g0175others(11): Show | 14 | HG01109.hp2 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.271+385G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230978175 | ||||||
| chr1:230978217
|
G | A | 41 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 48 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.271+343C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230978217 | ||||||
| chr1:230978250
|
C | T | 113 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(110): Show | 128 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.271+310G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230978250 | ||||||
| chr1:230978315
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.271+245C>T | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230978315 | ||||||
| chr1:230978495
|
C | T | 1 | a0001c0004t0002g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.271+65G>A | TTC13 | ENSG00000143643.13 | transcript | ENST00000366661.9 | protein_coding | 1/22 | chr1 | 230978495 |